Israelisches Militär erschoss Gaza Bauer
The Israeli armed forces shot and killed a twenty-year old Palestinian farmer, while er auf seinem Land arbeitete. Dies geschah am 18.2.2009 in dem Dorf Namens Al-Faraheen, östlich von Khan Younis im Gaza-Streifen.
Die International Human Rights-Aktivisten begleiteten die Bauern während dieser Zeit, als sie etwa 500m vor der Grünen Linie arbeiteten.
Mohammad al - Breem, 20, wurde in das rechte Bein geschossen, als die Bauern, zusammen mit den Menschenrechtsaktivisten, versuchten, sich aus dem Bereich in Sicherheit zubringen, indem sie schon über 2 Stunden unter den Blicken der israelischen Streitkräfte gearbeitet hatten.
Auch nach der Bitte der Menschenrechtsaktivisten an die Israelischen Streitkräfte, das Feuer einzustellen, wurde trotzden weiter geschossen.
Monday, February 23, 2009
Sunday, February 22, 2009
Blender Model From Blueprints
The Crisis of Credit
to explain the complexities of the financial crisis is not easy, then they also do not understand all the more.
But this video by Jonathan Jarvis said the financial crisis on a really clear way. To do this, you do not even understand English perfectly, because the visualization is able to beat me.
And here's the website: http://www.crisisofcredit.com/
to explain the complexities of the financial crisis is not easy, then they also do not understand all the more.
But this video by Jonathan Jarvis said the financial crisis on a really clear way. To do this, you do not even understand English perfectly, because the visualization is able to beat me.
And here's the website: http://www.crisisofcredit.com/
Thursday, February 19, 2009
My Computer Screen Is Split
Sima to genetic engineering: fight to the European Court!
Gemeinsame Kraftanstrengung gegen Aufhebung der Anbauverbote
Bis zum Europäischen Gerichtshof muss laut Umweltstadträtin Ulli Sima der österreichische Kampf gegen die Aufhebung des heimischen für die gentechnisch veränderten Maissorten MON-810 und T 25 gehen. Sie spricht sich für eine gemeinsame Kraftanstrengung gegen den Vormarsch der Gentechnik angesichts der Abstimmungen beim nächsten EU-Landwirtschaftsministerrat aus.
"Österreich hat so viele Jahre erfolgreich die heimische Landwirtschaft gentechnikfrei gehalten und dem Wunsch der Konsumenten und Bauern entsprochen, das muss auch weiter so bleiben. Die Debatte auf EU-Ebene goes in the wrong direction, "said Sima is on Wednesday, the approach at EU level and democratic politics more than questionable.
" There have been countless votes in Causa GM bans, could always be Austria so far to enforce prohibitions. The European Commission clearly wants to vote until their result is acceptable, "criticizes Sima and provides environment ministers Nicholas Berlakovich and Health Minister Alois Stoger full support in this very central issue of the growing bans on.
The local bans on cultivation of genetically modified varieties MON -810 and T 25 must necessarily be maintained, they were from scientific grounds verhängt.
"Österreich hatte all die Jahre starke Verbündete auf EU-Ebene, gemeinsam konnte man den Vormarsch der Gentech-Lobby hintanhalten. Die EU-Kommission stellt sich gegen die Mehrheit der europäischen Konsumenten und Konsumentinnen", kritisiert Sima.
Wien hat indes vorgebaut und schützt die Landwirtschaft vor der Gentechnik durch eine Doppelstrategie: Zum einen mit dem Wiener Gentechnik-Vorsorgegesetz, zum anderen mit der Plattform "Freiwillig ohne Gentechnik", bei der Stadt Wien, Landwirtschaftskammer und LGV eng kooperieren.
-apa, ots
Gemeinsame Kraftanstrengung gegen Aufhebung der Anbauverbote
Bis zum Europäischen Gerichtshof muss laut Umweltstadträtin Ulli Sima der österreichische Kampf gegen die Aufhebung des heimischen für die gentechnisch veränderten Maissorten MON-810 und T 25 gehen. Sie spricht sich für eine gemeinsame Kraftanstrengung gegen den Vormarsch der Gentechnik angesichts der Abstimmungen beim nächsten EU-Landwirtschaftsministerrat aus.
"Österreich hat so viele Jahre erfolgreich die heimische Landwirtschaft gentechnikfrei gehalten und dem Wunsch der Konsumenten und Bauern entsprochen, das muss auch weiter so bleiben. Die Debatte auf EU-Ebene goes in the wrong direction, "said Sima is on Wednesday, the approach at EU level and democratic politics more than questionable.
" There have been countless votes in Causa GM bans, could always be Austria so far to enforce prohibitions. The European Commission clearly wants to vote until their result is acceptable, "criticizes Sima and provides environment ministers Nicholas Berlakovich and Health Minister Alois Stoger full support in this very central issue of the growing bans on.
The local bans on cultivation of genetically modified varieties MON -810 and T 25 must necessarily be maintained, they were from scientific grounds verhängt.
"Österreich hatte all die Jahre starke Verbündete auf EU-Ebene, gemeinsam konnte man den Vormarsch der Gentech-Lobby hintanhalten. Die EU-Kommission stellt sich gegen die Mehrheit der europäischen Konsumenten und Konsumentinnen", kritisiert Sima.
Wien hat indes vorgebaut und schützt die Landwirtschaft vor der Gentechnik durch eine Doppelstrategie: Zum einen mit dem Wiener Gentechnik-Vorsorgegesetz, zum anderen mit der Plattform "Freiwillig ohne Gentechnik", bei der Stadt Wien, Landwirtschaftskammer und LGV eng kooperieren.
-apa, ots
What To Write On A Death Anniversary Invite
government slept introduction of green genetic engineering!
FPÖ fordert mehr Sicherheit für Konsumenten
"Die Regierung and in particular the agriculture and health ministers have missed the quiet and clandestine introduction of agricultural biotechnology. While the government debated and studies announced that the EU creates a reality, "said today the FPÖ NAbg Gerhard Deimeke, a member of the parliamentary Country Economic Committee.
" Long-term studies on the impact of agricultural biotechnology were introduced into only recently commissioned. In addition to advice given by most companies in order, which face the green gene positive.
First, the import bans were killed, 600,000 tonnes of genetically modified soybeans are imported annually for animal feed. Now is the ban fallen und unsere Regierung nimmt das in ihrer EU-Hörigkeit einfach zur Kenntnis", so der Abgeordnete weiter.
"Die FPÖ fordert mehr Sicherheit für die Konsumenten ein, die nicht mehr gewährleistet ist." Man stehe einer unverschämten Machtpolitik der EU und der Konzerne gegenüber, die Bundesregierung sei dabei offensichtlich völlig hilflos.
"Mit dem Vertrag von Lissabon wird diese Entwicklung nicht besser und hier beginnt der Gesinnungsslalom der Grünen, welche mit einem "kritischen Ja" für den Lissabonvertrag auftreten, aber gleichzeitig behaupten, gegen die grüne Gentechnik zu Felde zu ziehen. Das paßt nicht zusammen!" schloss Deimek.
-apa, ots -
FPÖ fordert mehr Sicherheit für Konsumenten
"Die Regierung and in particular the agriculture and health ministers have missed the quiet and clandestine introduction of agricultural biotechnology. While the government debated and studies announced that the EU creates a reality, "said today the FPÖ NAbg Gerhard Deimeke, a member of the parliamentary Country Economic Committee.
" Long-term studies on the impact of agricultural biotechnology were introduced into only recently commissioned. In addition to advice given by most companies in order, which face the green gene positive.
First, the import bans were killed, 600,000 tonnes of genetically modified soybeans are imported annually for animal feed. Now is the ban fallen und unsere Regierung nimmt das in ihrer EU-Hörigkeit einfach zur Kenntnis", so der Abgeordnete weiter.
"Die FPÖ fordert mehr Sicherheit für die Konsumenten ein, die nicht mehr gewährleistet ist." Man stehe einer unverschämten Machtpolitik der EU und der Konzerne gegenüber, die Bundesregierung sei dabei offensichtlich völlig hilflos.
"Mit dem Vertrag von Lissabon wird diese Entwicklung nicht besser und hier beginnt der Gesinnungsslalom der Grünen, welche mit einem "kritischen Ja" für den Lissabonvertrag auftreten, aber gleichzeitig behaupten, gegen die grüne Gentechnik zu Felde zu ziehen. Das paßt nicht zusammen!" schloss Deimek.
-apa, ots -
Wednesday, February 18, 2009
Christian Running Jerseys
ban on genetically modified corn?
Federal Agriculture Minister Ilse Aigner (CSU) has the cultivation of GM crops in Germany called into question. They would consider a ban on cultivation as the only currently approved genetically modified maize in Germany, she announced in the newspaper on Thursday. Environmental groups welcomed the initiative Aigner, she earned criticism from the ranks of the CDU's sister party.
"Green genetic engineering brings to the people in this country so far no apparent benefit," Aigner said the newspaper. " Also rejected the consumers from genetically modified plants, and the farmers they would not. More specifically, the Minister of Agriculture with its plans to genetically modified maize MON 810 of the U.S. manufacturer Monsanto.
The Minister announced to review the approval for the maize and again to withdraw, if it turns out that the manufacturer has failed to fulfill monitoring requirements. "I will now check whether the monitoring requirements are followed. If not, then I will act. "
According to the seed for the approval of competent Bundessortenamt would a ban on MON-810 mean that in Germany any more genetically modified plants may be grown free. The cultivation of GM crops could then only noch unter Laborbedingungen stattfinden, sagte ein Sprecher der Behörde.
Aigner will es einzelnen Bundesländern und Regionen zudem ermöglichen, sich zu komplett gentechnikfreien Zonen zu erklären. Zwar gebe es europarechtlich dafür kaum Spielräume, sagte die Ministerin. Derzeit suche ihr Ministerium aber „fieberhaft nach einer Lösung“. Die Ministerin verlangte außerdem mehr Sensibilität bei der Genehmigung von Freilandversuchen.
Der Naturschutzbund (NABU) wertete den Vorstoß Aigner als „erfreulichen Kurswechsel im Landwirtschaftsministerium“. Ein Verbot von MON-810 sei „überfällig und wäre ein wichtiger Schritt in die richtige Richtung“, NABU said Director Olaf Tschimpke.
criticism of owner thrust exerted Union Group Vice Katherina Reiche. All scientific data and past experience in dealing with GM crops could lead to the conclusion that the so-called green biotechnology 2The safe and controllable high technology should be considered ".
Genetically modified crops could reduce the use of Plant protection products and fertilizers, improve product quality and reduce the burden of production space. They could also make an important contribution to the global fight against hunger.
© afp / www.aerzteblatt.de
Federal Agriculture Minister Ilse Aigner (CSU) has the cultivation of GM crops in Germany called into question. They would consider a ban on cultivation as the only currently approved genetically modified maize in Germany, she announced in the newspaper on Thursday. Environmental groups welcomed the initiative Aigner, she earned criticism from the ranks of the CDU's sister party.
"Green genetic engineering brings to the people in this country so far no apparent benefit," Aigner said the newspaper. " Also rejected the consumers from genetically modified plants, and the farmers they would not. More specifically, the Minister of Agriculture with its plans to genetically modified maize MON 810 of the U.S. manufacturer Monsanto.
The Minister announced to review the approval for the maize and again to withdraw, if it turns out that the manufacturer has failed to fulfill monitoring requirements. "I will now check whether the monitoring requirements are followed. If not, then I will act. "
According to the seed for the approval of competent Bundessortenamt would a ban on MON-810 mean that in Germany any more genetically modified plants may be grown free. The cultivation of GM crops could then only noch unter Laborbedingungen stattfinden, sagte ein Sprecher der Behörde.
Aigner will es einzelnen Bundesländern und Regionen zudem ermöglichen, sich zu komplett gentechnikfreien Zonen zu erklären. Zwar gebe es europarechtlich dafür kaum Spielräume, sagte die Ministerin. Derzeit suche ihr Ministerium aber „fieberhaft nach einer Lösung“. Die Ministerin verlangte außerdem mehr Sensibilität bei der Genehmigung von Freilandversuchen.
Der Naturschutzbund (NABU) wertete den Vorstoß Aigner als „erfreulichen Kurswechsel im Landwirtschaftsministerium“. Ein Verbot von MON-810 sei „überfällig und wäre ein wichtiger Schritt in die richtige Richtung“, NABU said Director Olaf Tschimpke.
criticism of owner thrust exerted Union Group Vice Katherina Reiche. All scientific data and past experience in dealing with GM crops could lead to the conclusion that the so-called green biotechnology 2The safe and controllable high technology should be considered ".
Genetically modified crops could reduce the use of Plant protection products and fertilizers, improve product quality and reduce the burden of production space. They could also make an important contribution to the global fight against hunger.
© afp / www.aerzteblatt.de
Tuesday, February 17, 2009
Women Breast Feeding To Man
gene therapy for HIV possible in principle threatens
A gene therapy can protect CD4 cells from attack by the HIV virus and stabilize the immune system. The effects were evaluated in a randomized clinical study (Nature Medicine 2009; doi: 10.1038/nm.1932) but (still) too weak for a broader clinical application at the present time.
for gene therapy of the 74 HIV-infected participants of the study was first taken from bone marrow. This, the researchers isolated these CD34-positive cells as stem cells, precursors of CD4 cells. The CD34 cells were then in the laboratory - provided in some of the participants with an additional gene - with the help of a virus. For the other participants was a sham treatment.
The therapeutic gene contains the genetic information for the ribozyme OZ1. Ribozymes are molecular scissors that cut specific genes and thereby inactivate. In this case, destroyed OZ1 the tat gene of HIV virus, which is required for virus replication in CD4 cells.
after gene therapy (or sham treatment), the CD34-cells in HIV-infected individuals were re-infused. This is done in the hope that the resulting from them CD4 cells are resistant to HIV and maintain the integrity of the immune system remains.
This seems now to be successful in the first randomized study - albeit with significant compromises. In the first months hatte die Gentherapie keine Auswirkungen auf den Verlauf der HIV-Therapie, wie Ronald Mitsuyasu vom Aids Institute der Universität von Kalifornien in Los Angeles (UCLA) und Mitarbeiter berichten.
Die Konzentration der HI-Viren im Blut waren – gemessen an einer temporären Unterbrechung der antiretroviralen Therapie – nicht niedriger als im Placebo-Arm der Studie. Erst ab der 40. Woche zeichnete sich eine signifikante Abnahme der Viruslast ab.
Die Zahl der CD4-Zellen war im Gentherapie-Arm jedoch während der gesamten 100 Wochen der Studie höher als im Placebo-Arm (gegen Ende soll es dann zu einem Absinken der CD4-Zellen gekommen sein). Die Verträglichkeit wird als gut beschrieben. Spezifische Nebenwirkungen gene therapy will not have seen the group Mitsuyasu.
The results should therefore initially be only a starting point for further experiments. For clinical use, the effects were far too low. A replacement for the long-term anti-retroviral therapy is not gene therapy dar.
Research is expected in the direction of a combination go of gene therapy with a Knochenmarksablation, but this is risky and therefore ethically very questionable, as long as the patients come with anti-retroviral drugs to satisfactory therapeutic results . can heal
that a stem cell therapy for HIV infection, had Gero Hütter of the Berlin Charité - if in a different situation - show recently in a spectacular individual cases. A 40-year-old HIV patient had received due to a recurrent acute myeloid leukemia, an allogeneic stem cell therapy.
happened to be the donor carrier of a mutation in the CCR5 gene that makes the CD4 T cells resistant to HIV infection. The patient is now 20 months since virus-free and therefore in all probability of his HIV infection healed (NEJM 2009, 360: 692-698).
Because of the significant risks that stem cell therapy is currently not eligible. It should however be the starting point for further experiments, like Jay Levy of the University of Southern California in San Francisco in an editorial (NEJM 2009, 360: 724-725) executes. ©
heat / www.aerzteblatt.de
A gene therapy can protect CD4 cells from attack by the HIV virus and stabilize the immune system. The effects were evaluated in a randomized clinical study (Nature Medicine 2009; doi: 10.1038/nm.1932) but (still) too weak for a broader clinical application at the present time.
for gene therapy of the 74 HIV-infected participants of the study was first taken from bone marrow. This, the researchers isolated these CD34-positive cells as stem cells, precursors of CD4 cells. The CD34 cells were then in the laboratory - provided in some of the participants with an additional gene - with the help of a virus. For the other participants was a sham treatment.
The therapeutic gene contains the genetic information for the ribozyme OZ1. Ribozymes are molecular scissors that cut specific genes and thereby inactivate. In this case, destroyed OZ1 the tat gene of HIV virus, which is required for virus replication in CD4 cells.
after gene therapy (or sham treatment), the CD34-cells in HIV-infected individuals were re-infused. This is done in the hope that the resulting from them CD4 cells are resistant to HIV and maintain the integrity of the immune system remains.
This seems now to be successful in the first randomized study - albeit with significant compromises. In the first months hatte die Gentherapie keine Auswirkungen auf den Verlauf der HIV-Therapie, wie Ronald Mitsuyasu vom Aids Institute der Universität von Kalifornien in Los Angeles (UCLA) und Mitarbeiter berichten.
Die Konzentration der HI-Viren im Blut waren – gemessen an einer temporären Unterbrechung der antiretroviralen Therapie – nicht niedriger als im Placebo-Arm der Studie. Erst ab der 40. Woche zeichnete sich eine signifikante Abnahme der Viruslast ab.
Die Zahl der CD4-Zellen war im Gentherapie-Arm jedoch während der gesamten 100 Wochen der Studie höher als im Placebo-Arm (gegen Ende soll es dann zu einem Absinken der CD4-Zellen gekommen sein). Die Verträglichkeit wird als gut beschrieben. Spezifische Nebenwirkungen gene therapy will not have seen the group Mitsuyasu.
The results should therefore initially be only a starting point for further experiments. For clinical use, the effects were far too low. A replacement for the long-term anti-retroviral therapy is not gene therapy dar.
Research is expected in the direction of a combination go of gene therapy with a Knochenmarksablation, but this is risky and therefore ethically very questionable, as long as the patients come with anti-retroviral drugs to satisfactory therapeutic results . can heal
that a stem cell therapy for HIV infection, had Gero Hütter of the Berlin Charité - if in a different situation - show recently in a spectacular individual cases. A 40-year-old HIV patient had received due to a recurrent acute myeloid leukemia, an allogeneic stem cell therapy.
happened to be the donor carrier of a mutation in the CCR5 gene that makes the CD4 T cells resistant to HIV infection. The patient is now 20 months since virus-free and therefore in all probability of his HIV infection healed (NEJM 2009, 360: 692-698).
Because of the significant risks that stem cell therapy is currently not eligible. It should however be the starting point for further experiments, like Jay Levy of the University of Southern California in San Francisco in an editorial (NEJM 2009, 360: 724-725) executes. ©
heat / www.aerzteblatt.de
Betaine Hcl Pregnancy
genetic testing law to fail
the grand coalition at odds over the law on genetic testing.
the Düsseldorf Rheinische Post reported on Saturday, CSU and SPD are divided about whether genetic testing of children in the womb are to be allowed to reveal information about disease risks in later life.
The health spokeswoman for the SPD, Carola Reimann, told the Journal: "I hope that the Union is not insisting that the investigation into possible future outbreak of disease to prohibit and thus endangering the entire legislative package. "
The ethics expert for the CDU parliamentary group, Hubert Hüppe (CDU), said, however, it does not may be that the SPD failed on the law because they necessarily prenatal diagnostics would allow possible diseases like Alzheimer's.
The draft law on genetic testing was adopted in August 2008 by the Cabinet. The law is to comprehensively regulate the handling of investigations on the human genome and should be adopted in this legislative session.
© ddp / www.aerzteblatt.de
bill of the Federal Government: a draft law on genetic studies in man (Gene Diagnostics Law - GenDG), BT-printed matter 16/10532, 13.10.2008
the grand coalition at odds over the law on genetic testing.
the Düsseldorf Rheinische Post reported on Saturday, CSU and SPD are divided about whether genetic testing of children in the womb are to be allowed to reveal information about disease risks in later life.
The health spokeswoman for the SPD, Carola Reimann, told the Journal: "I hope that the Union is not insisting that the investigation into possible future outbreak of disease to prohibit and thus endangering the entire legislative package. "
The ethics expert for the CDU parliamentary group, Hubert Hüppe (CDU), said, however, it does not may be that the SPD failed on the law because they necessarily prenatal diagnostics would allow possible diseases like Alzheimer's.
The draft law on genetic testing was adopted in August 2008 by the Cabinet. The law is to comprehensively regulate the handling of investigations on the human genome and should be adopted in this legislative session.
© ddp / www.aerzteblatt.de
bill of the Federal Government: a draft law on genetic studies in man (Gene Diagnostics Law - GenDG), BT-printed matter 16/10532, 13.10.2008
Saturday, February 14, 2009
Platypus Wings For Sale
genes each of the 99 rhinoviruses deciphered
U.S. researchers have decoded the gene sequence of each of the 99 known rhinovirus, the most frequent causes common colds. Its publication in Science (2009, doi: 10.1126/science.1165557) presents a very joyful virus mutation, but this does not create good conditions for the development of drugs or vaccines.
Human rhinoviruses (HRV) belong to the family of Picornaviridae. They are not just for common cold with a runny nose (rhinitis) responsible. Rhinovirus infections can also der tieferen Atemwege auslösen oder einen Asthmaanfall oder die Exazerbation einer chronisch obstruktiven Lungenerkrankung (COPD) triggern.
Es war bekannt, dass Rhinoviren eine genetisch sehr heterogene Gruppe bilden, weshalb sich die Gruppe um Stephen Liggett von der Universität von Maryland entschloss, das Genom sämtlicher 99 bekannter Serotypen zu sequenzieren.
Dabei bestätigte sie die heutige Einteilung in drei Gruppen. Neben den Gruppen HRV-A und HRV-B wurde kürzlich eine Gruppe von HRV-C postuliert, die für Erkrankungen mit schweren grippeähnlichen Symptomen verantwortlich ist. Die Genforscher vermuten, dass es noch eine vierte Gruppe, HRV-D, gibt. Festlegen wollen sich aber noch nicht.
With about 7,000 base pairs, the genome of the single-stranded RNA virus is relatively small. It encodes a dozen proteins that are sufficient to multiply in the epithelial cells of the mucous membranes. A striking feature is a so-called hypervariable region in 5'UTR section. When poliovirus determined a similar region of the virulence of the pathogen, and the researchers suspect that it is similar for rhinoviruses behave.
The prospects for a vaccine that requires a constancy in the genetic information is diminished by the discovery of no less than 800 mutations that differ between the recent isolates of barely a decade older isolates.
Exchanges von genetischem Material zwischen verschiedenen Virusstämmen, Rekombination genannt, scheint kein seltenes Ereignis zu sein, wenn ein Mensch zufällig mit zwei Schnupfenviren gleichzeitig infiziert ist. Und es steht zu befürchten, dass sich die Viren aufgrund dieser Fähigkeit relativ schnell dem Angriff eines Medikamentes entziehen würden.
Mehr © rme/ www.aerzteblatt.de ebenso weiterfuehrende Links
U.S. researchers have decoded the gene sequence of each of the 99 known rhinovirus, the most frequent causes common colds. Its publication in Science (2009, doi: 10.1126/science.1165557) presents a very joyful virus mutation, but this does not create good conditions for the development of drugs or vaccines.
Human rhinoviruses (HRV) belong to the family of Picornaviridae. They are not just for common cold with a runny nose (rhinitis) responsible. Rhinovirus infections can also der tieferen Atemwege auslösen oder einen Asthmaanfall oder die Exazerbation einer chronisch obstruktiven Lungenerkrankung (COPD) triggern.
Es war bekannt, dass Rhinoviren eine genetisch sehr heterogene Gruppe bilden, weshalb sich die Gruppe um Stephen Liggett von der Universität von Maryland entschloss, das Genom sämtlicher 99 bekannter Serotypen zu sequenzieren.
Dabei bestätigte sie die heutige Einteilung in drei Gruppen. Neben den Gruppen HRV-A und HRV-B wurde kürzlich eine Gruppe von HRV-C postuliert, die für Erkrankungen mit schweren grippeähnlichen Symptomen verantwortlich ist. Die Genforscher vermuten, dass es noch eine vierte Gruppe, HRV-D, gibt. Festlegen wollen sich aber noch nicht.
With about 7,000 base pairs, the genome of the single-stranded RNA virus is relatively small. It encodes a dozen proteins that are sufficient to multiply in the epithelial cells of the mucous membranes. A striking feature is a so-called hypervariable region in 5'UTR section. When poliovirus determined a similar region of the virulence of the pathogen, and the researchers suspect that it is similar for rhinoviruses behave.
The prospects for a vaccine that requires a constancy in the genetic information is diminished by the discovery of no less than 800 mutations that differ between the recent isolates of barely a decade older isolates.
Exchanges von genetischem Material zwischen verschiedenen Virusstämmen, Rekombination genannt, scheint kein seltenes Ereignis zu sein, wenn ein Mensch zufällig mit zwei Schnupfenviren gleichzeitig infiziert ist. Und es steht zu befürchten, dass sich die Viren aufgrund dieser Fähigkeit relativ schnell dem Angriff eines Medikamentes entziehen würden.
Mehr © rme/ www.aerzteblatt.de ebenso weiterfuehrende Links
Wednesday, February 11, 2009
Breastfeeding Husband Her Husband
genes affect willingness to make risky investments
Wie riskant ein Mensch mit Geld umgeht, ist offenbar auch eine Frage des Erbguts. In Experimenten mit Freiwilligen haben Forscher einen Zusammenhang zwischen dem Investitionsverhalten und Genen entdeckt, die den Haushalt von Botenstoffen im Gehirn beeinflussen.
Ist The global financial crisis may also be attributed to specific genetic variants with investors? This suggests a study published Camelia Kuhnen and have Joan Chiao of Northwestern University in Evanston now in the journal PLoS ONE. The researchers studied volunteers who should invest in a money game.
Declining rates: risk-programmed in the genome?
At the beginning of the experiment, participants received each $ 15. With a computer program, they met in 1996 in succession investment decisions. They have always had a choice between two options: a safe investment with low, but guaranteed return and a risky investment with a higher yield and Risk of loss. At the end of the experiment, participants were given the generated amount paid - on average $ 25.
Researchers collected saliva samples from each participant in addition, it isolated the DNA and looked for the genes of 5-HTTLPR and DRD4 lookout. 5-HTTLPR sets the blueprint for a protein that the neurotransmitter serotonin discharged by cell walls, DRD4 the blueprint of a receptor that responds to the neurotransmitter dopamine. Both genes are found in different versions that work differently effective.
When the researchers compared the genetic profile of the participants with their risk appetite in the investment game, there were striking correlations: People with a more efficient serotonin transporter their money invested 28 percent more often in risky assets. Similarly, people went to a particular DRD4 variant 25 percent more often the financial risk.
The researchers believe that it will succeed in the future more and more genetic causes of complex behavior patterns to identify - for example, drug addiction or gambling addiction. They emphasize the same time that experience and cultural background, have also played a big influence.
- hda/ddp-
Wie riskant ein Mensch mit Geld umgeht, ist offenbar auch eine Frage des Erbguts. In Experimenten mit Freiwilligen haben Forscher einen Zusammenhang zwischen dem Investitionsverhalten und Genen entdeckt, die den Haushalt von Botenstoffen im Gehirn beeinflussen.
Ist The global financial crisis may also be attributed to specific genetic variants with investors? This suggests a study published Camelia Kuhnen and have Joan Chiao of Northwestern University in Evanston now in the journal PLoS ONE. The researchers studied volunteers who should invest in a money game.
Declining rates: risk-programmed in the genome?
At the beginning of the experiment, participants received each $ 15. With a computer program, they met in 1996 in succession investment decisions. They have always had a choice between two options: a safe investment with low, but guaranteed return and a risky investment with a higher yield and Risk of loss. At the end of the experiment, participants were given the generated amount paid - on average $ 25.
Researchers collected saliva samples from each participant in addition, it isolated the DNA and looked for the genes of 5-HTTLPR and DRD4 lookout. 5-HTTLPR sets the blueprint for a protein that the neurotransmitter serotonin discharged by cell walls, DRD4 the blueprint of a receptor that responds to the neurotransmitter dopamine. Both genes are found in different versions that work differently effective.
When the researchers compared the genetic profile of the participants with their risk appetite in the investment game, there were striking correlations: People with a more efficient serotonin transporter their money invested 28 percent more often in risky assets. Similarly, people went to a particular DRD4 variant 25 percent more often the financial risk.
The researchers believe that it will succeed in the future more and more genetic causes of complex behavior patterns to identify - for example, drug addiction or gambling addiction. They emphasize the same time that experience and cultural background, have also played a big influence.
- hda/ddp-
Wedding Shower Quotes
genes favoring severe drug allergies
The Stevens-Johnson syndrome and toxic epidermal necrolysis, two of the most feared side effects of medication, have a genetic component. This resulted in investigations by the U.S. Zulassungsbehörde FDA.
Das Stevens-Johnson Syndrom (SJS) und die toxische epidermale Nekrolyse (TEN) gehören zu den allergischen Arzneimittelreaktionen. Beide manifestieren sich an der Haut und den Schleimhäuten.
Nach einem Ausschlag kommt es zur ausgedehnten Blasenbildung, bei der toxischen epidermalen Nekrolyse (manche Experten betrachten sie als Extremvarianten des Stevens-Johnson Syndrom) löst sich die Haut großflächig ab, was – wie bei Verbrennungen – mit einem hohen Risiko lebensgefährlicher Infektionen verbunden ist.
Beide Komplikationen erfordern das sofortige Absetzen der Medikamente. Tests, die diese Reaktion vorhersehbar machen, wären sicherlich ein wichtiger Contribution to drug safety.
SJS and TEN were therefore the first project of the International Serious Adverse Events Consortium (SAEC), which has now been completed. According to the FDA, many genetic associations have been found. Where they exist but have not been betrayed. A publication is planned for later this year. ©
heat / www.aerzteblatt.de
The Stevens-Johnson syndrome and toxic epidermal necrolysis, two of the most feared side effects of medication, have a genetic component. This resulted in investigations by the U.S. Zulassungsbehörde FDA.
Das Stevens-Johnson Syndrom (SJS) und die toxische epidermale Nekrolyse (TEN) gehören zu den allergischen Arzneimittelreaktionen. Beide manifestieren sich an der Haut und den Schleimhäuten.
Nach einem Ausschlag kommt es zur ausgedehnten Blasenbildung, bei der toxischen epidermalen Nekrolyse (manche Experten betrachten sie als Extremvarianten des Stevens-Johnson Syndrom) löst sich die Haut großflächig ab, was – wie bei Verbrennungen – mit einem hohen Risiko lebensgefährlicher Infektionen verbunden ist.
Beide Komplikationen erfordern das sofortige Absetzen der Medikamente. Tests, die diese Reaktion vorhersehbar machen, wären sicherlich ein wichtiger Contribution to drug safety.
SJS and TEN were therefore the first project of the International Serious Adverse Events Consortium (SAEC), which has now been completed. According to the FDA, many genetic associations have been found. Where they exist but have not been betrayed. A publication is planned for later this year. ©
heat / www.aerzteblatt.de
Boxing Gloves Test Fairtex
FDA and International Serious Adverse Events Consortium Release First Data on Genetic Basis of Adverse Drug Events
The first data offering healthcare professionals a better look into the genetic basis of certain types of adverse drug events was released today by the FDA and the International Serious Adverse Events Consortium (SAEC). The data are focused on the genetics associated with drug-induced serious skin rashes, as searchable Stevens-Johnson syndrome and toxic epidermal necrolysis, and helps better predict an individual’s risk of developing these reactions.
Both skin conditions appear as allergic-like skin reactions associated with blistering and peeling, and are considered life-threatening. Medications causing these serious allergic reactions should be discontinued; and if such signs and symptoms are not quickly recognized, these reactions can be fatal.
“The SAEC has fulfilled a key goal of the Critical Path Initiative by providing the research community with public access to new genomic data on adverse drug events,” said Janet Woodcock, M.D., director, the FDA’s Center for Drug Evaluation and Research. “This consortium has taken a significant step forward by promoting open sharing of drug safety data. This type of cooperation has the potential to lead to more personalized approaches to medicine that can reduce a patient’s risk for experiencing an adverse drug event.”
The SAEC is a nonprofit partnership of pharmaceutical companies, the Wellcome Trust, and academic institutions focused on research relating to the genetics of drug-induced serious adverse events. The samples from the initial serious skin rash cases and matched controls were collected by GlaxoSmithKline plc, London, U.K., and donated to the consortium for this research.
By pooling these samples, the SAEC has identified numerous genetic associations that may contribute to an individual’s risk of developing serious drug-induced skin reactions. The data was compiled and analyzed just 16 months after the consortium was launched.
“We are pleased to be able to provide these invaluable data to the research community to both improve the productivity of drug development and to begin the critical process of developing validated biomarkers to forecast patients who may be at risk for drug-induced serious adverse events,” said Arthur Holden, founder and chairman of the SAEC. “We continue to believe the application of genomics to research the genetic basis of serious adverse events will prove to be one the most productive early applications of this technology.”
The consortium will publish its initial research results later this year.
Researchers who enter in to a data use agreement can obtain free access to the data to generate custom data inquiries and obtain immediate results on the genetic basis of adverse drug events.
For more information on the International Serious Adverse Events Consortium, see www.saeconsortium.org.
For information on the FDA's Critical Path Initiative see http://www.fda.gov/oc/initiatives/criticalpath/
The first data offering healthcare professionals a better look into the genetic basis of certain types of adverse drug events was released today by the FDA and the International Serious Adverse Events Consortium (SAEC). The data are focused on the genetics associated with drug-induced serious skin rashes, as searchable Stevens-Johnson syndrome and toxic epidermal necrolysis, and helps better predict an individual’s risk of developing these reactions.
Both skin conditions appear as allergic-like skin reactions associated with blistering and peeling, and are considered life-threatening. Medications causing these serious allergic reactions should be discontinued; and if such signs and symptoms are not quickly recognized, these reactions can be fatal.
“The SAEC has fulfilled a key goal of the Critical Path Initiative by providing the research community with public access to new genomic data on adverse drug events,” said Janet Woodcock, M.D., director, the FDA’s Center for Drug Evaluation and Research. “This consortium has taken a significant step forward by promoting open sharing of drug safety data. This type of cooperation has the potential to lead to more personalized approaches to medicine that can reduce a patient’s risk for experiencing an adverse drug event.”
The SAEC is a nonprofit partnership of pharmaceutical companies, the Wellcome Trust, and academic institutions focused on research relating to the genetics of drug-induced serious adverse events. The samples from the initial serious skin rash cases and matched controls were collected by GlaxoSmithKline plc, London, U.K., and donated to the consortium for this research.
By pooling these samples, the SAEC has identified numerous genetic associations that may contribute to an individual’s risk of developing serious drug-induced skin reactions. The data was compiled and analyzed just 16 months after the consortium was launched.
“We are pleased to be able to provide these invaluable data to the research community to both improve the productivity of drug development and to begin the critical process of developing validated biomarkers to forecast patients who may be at risk for drug-induced serious adverse events,” said Arthur Holden, founder and chairman of the SAEC. “We continue to believe the application of genomics to research the genetic basis of serious adverse events will prove to be one the most productive early applications of this technology.”
The consortium will publish its initial research results later this year.
Researchers who enter in to a data use agreement can obtain free access to the data to generate custom data inquiries and obtain immediate results on the genetic basis of adverse drug events.
For more information on the International Serious Adverse Events Consortium, see www.saeconsortium.org.
For information on the FDA's Critical Path Initiative see http://www.fda.gov/oc/initiatives/criticalpath/
Brown Discharge During Pregnancy With Uti
NWO für Anfänger
Core of Corruption has a new online mini-documentary brought up about the New World Order. There are only information from Core of Corruption. The film shows video segments that have never previously been available over the Internet and no one has seen.
The film is a good start for those who are completely familiar with the information you want to make the NWO.
directed way, led by Jonathan Elinoff Loose Change
Jonathan Elinoff is expected on 27 March 2009, a 5-part film series, Core of public corruption.
The series is a complete and demonstrated a comprehensive case. It's about the biggest case of corruption and conspiracy in the world and evidence exists for it. Videos and news clips that were never look on the Internet: Kennedy, Iran-Contra affair, Watergate, 9 / 11 and even the current economic crisis in which we find ourselves today. And the central theme, as they have gabmacht it is also shown.
more info's and trailer's for the film series at: http://coreofcorruption.com/
Core of Corruption has a new online mini-documentary brought up about the New World Order. There are only information from Core of Corruption. The film shows video segments that have never previously been available over the Internet and no one has seen.
The film is a good start for those who are completely familiar with the information you want to make the NWO.
directed way, led by Jonathan Elinoff Loose Change
Jonathan Elinoff is expected on 27 March 2009, a 5-part film series, Core of public corruption.
The series is a complete and demonstrated a comprehensive case. It's about the biggest case of corruption and conspiracy in the world and evidence exists for it. Videos and news clips that were never look on the Internet: Kennedy, Iran-Contra affair, Watergate, 9 / 11 and even the current economic crisis in which we find ourselves today. And the central theme, as they have gabmacht it is also shown.
more info's and trailer's for the film series at: http://coreofcorruption.com/
Tuesday, February 10, 2009
Canesten Breast-feeding
Scheduled Repeal the GM maize cultivation bans scandalous
securing new attempt by the Commission provide clear rejection
"The project of European Commission, Austria to repeal the ban on the two growing GM maize varieties MON810 and forcing T25 from Monsanto and Bayer, must be resolutely opposed, "says the Agriculture spokesman for the Greens Wolfgang Pirklhuber.
" It is to offer not on ignorance of how the Commission on the wishes of the citizens, on critical expert opinions and unanimous parliamentary decisions ignores. With a slice of tactics it first lifted the Austrian import and sale ban on the two genetic constructs, and now she wants to allow as agent for the genetic engineering companies to the installation and the Austrian fields contaminate, "said Pirklhuber shows stunned.
Pirklhuber calls on Minister of the Environment Berlakovich to look for now the cooperation with other European environment ministers, and to find a clear majority to prevent this planned attack on the Genetic Engineering of the Austrian agriculture.
"The cultivation of GM varieties in Austria would be catastrophic for the small-scale agriculture, organic farming and quality standards in Austria," said Pirklhuber. The Greens, who at the time, to accept the support of all other groups, the cultivation bans, announce massive resistance.
was "Before the summer break in the Austrian Parliament passed a unanimous resolution, in which all the groups for a GM-free agriculture and food production in Austria say. will now be prevented from joining forces, the cultivation of GM varieties in Austria is possible, "said Pirklhuber
-apa, ots -.
securing new attempt by the Commission provide clear rejection
"The project of European Commission, Austria to repeal the ban on the two growing GM maize varieties MON810 and forcing T25 from Monsanto and Bayer, must be resolutely opposed, "says the Agriculture spokesman for the Greens Wolfgang Pirklhuber.
" It is to offer not on ignorance of how the Commission on the wishes of the citizens, on critical expert opinions and unanimous parliamentary decisions ignores. With a slice of tactics it first lifted the Austrian import and sale ban on the two genetic constructs, and now she wants to allow as agent for the genetic engineering companies to the installation and the Austrian fields contaminate, "said Pirklhuber shows stunned.
Pirklhuber calls on Minister of the Environment Berlakovich to look for now the cooperation with other European environment ministers, and to find a clear majority to prevent this planned attack on the Genetic Engineering of the Austrian agriculture.
"The cultivation of GM varieties in Austria would be catastrophic for the small-scale agriculture, organic farming and quality standards in Austria," said Pirklhuber. The Greens, who at the time, to accept the support of all other groups, the cultivation bans, announce massive resistance.
was "Before the summer break in the Austrian Parliament passed a unanimous resolution, in which all the groups for a GM-free agriculture and food production in Austria say. will now be prevented from joining forces, the cultivation of GM varieties in Austria is possible, "said Pirklhuber
-apa, ots -.
Manga Honey Honey Drop
Melde mich zurück.
After a short break I am back writing again.
I needed a break from all this and spent the last week in the mountains. So I could recover myself and my thoughts folders. Now of course I will again have to worry about the blog.
After a short break I am back writing again.
I needed a break from all this and spent the last week in the mountains. So I could recover myself and my thoughts folders. Now of course I will again have to worry about the blog.
Monday, February 9, 2009
Nissan X-trail Roof Rails Remove
First drug from goat milk in the U.S.
The U.S. Drug Administration (FDA) has in some way the stall door to a new era drug therapy should open. A herd of 200 goats to produce future drugs that protect patients with congenital antithrombin deficiency against fatal blood clots. More products will follow.
could
The European Medicines Agency EMEA ATryn ® has indeed in 2006, admitted last year it was in Germany on the market. The turnover is so far small, which is unlikely to change even after the U.S. approval of the drug.
Because treatment with antithrombin alfa, the active substance in ATryn, is rarely necessary. First, the congenital antithrombin deficiency is not very often. The FDA estimates that between one in 5000 adults in the formation of the thrombin antagonist is reduced for genetic reasons.
This requires a degree of thrombophilia. The press release of the producer, half of those affected suffered before 25 Age of thrombosis until the 50th Years it will be even 85 percent.
A therapy for prevention of thromboembolic complications is (currently), however, considered only in high-risk situations as indicated. These are major operations, or (at the U.S. approval) and obstetric interventions, the drug is usually combined with heparin, which improves the protection against thrombosis.
The effectiveness of ATryn was in a relatively small study in only 31 patients examined with congenital antithrombin deficiency, 30 of which were successfully protected against a need of treatment of thrombosis - most common side effect: bleeding and reactions at the injection site.
The specificity of ATryn is the fact that the recombinant protein is not like any other drugs by using genetically engineered bacteria or mammalian cultures is produced, but is made from the milk of goats. The production is not in huge tanks in a sterile factory, but on a small farm in Massachusetts.
The researchers introduced the gene into fertilized eggs and have them fight it, of surrogate animals. Since then, it is in all cells of the genetically modified animals available and later the gene product is excreted in milk, in an amount of 10 grams per liter, as they say. An animal produces in a year, the same amount as antithrombin contained in 90,000 blood units.
The so called pharming bietet sich als eine kostengünstige Alternative zur derzeitigen Produktion an. Denn die Musterfarmen sind (im Prinzip) wesentlich kostengünstiger als die Fabriken. Steigt die Nachfrage an Medikamenten, kann die Produktion durch eine Vergrößerung der Herden jederzeit gesteigert werden (“Breed more if you need more”).
Da sich im Rahmen des Pharmings (im Prinzip) alle gentechnischen Medikamente herstellen lassen, wundert es, dass bisher nicht weitere Firmen ihr Interesse angekündigt haben. Beobachter erwarten, dass die Leitlinien, welche das Center for Veterinary Medicine der FDA im Januar 2009 festgelegt hat, hier einen gewissen Anreiz schaffen, da sie die Bedingungen festlegen.
Pharming, a small company based in Leiden in the Netherlands will, reportedly produced a recombinant human C1 inhibitor (for treatment of hereditary angioedema) using rabbits. PharmAthene of Annapolis, Maryland is planning the production of a recombinant protective antigen as an antidote for anthrax poisoning, which is to be produced in goats. These products would serve only a small niche indication.
would be much larger market for the many monoclonal antibodies, which came in the last few years for the treatment of autoimmune diseases and cancer on the market. But the big manufacturers show little apparent interest.
Whether they will one day competition of biosimilar companies will grow to bring their products cheaply by Pharming in the market, it is difficult to predict. It should, in any case that the high costs are due to the development of drugs than on biotechnology as the clinical development.
Pharming could be associated with its own risks. This should be less in the possibility that some animals escaped into the wilderness and the therapeutic genes to spread in the environment. Much unpleasant could be a scenario where the production of essential medicines for humans fail, because the animals are given because of illness no more milk.
© rme/aerzteblatt.de / FDA
The U.S. Drug Administration (FDA) has in some way the stall door to a new era drug therapy should open. A herd of 200 goats to produce future drugs that protect patients with congenital antithrombin deficiency against fatal blood clots. More products will follow.
could
The European Medicines Agency EMEA ATryn ® has indeed in 2006, admitted last year it was in Germany on the market. The turnover is so far small, which is unlikely to change even after the U.S. approval of the drug.
Because treatment with antithrombin alfa, the active substance in ATryn, is rarely necessary. First, the congenital antithrombin deficiency is not very often. The FDA estimates that between one in 5000 adults in the formation of the thrombin antagonist is reduced for genetic reasons.
This requires a degree of thrombophilia. The press release of the producer, half of those affected suffered before 25 Age of thrombosis until the 50th Years it will be even 85 percent.
A therapy for prevention of thromboembolic complications is (currently), however, considered only in high-risk situations as indicated. These are major operations, or (at the U.S. approval) and obstetric interventions, the drug is usually combined with heparin, which improves the protection against thrombosis.
The effectiveness of ATryn was in a relatively small study in only 31 patients examined with congenital antithrombin deficiency, 30 of which were successfully protected against a need of treatment of thrombosis - most common side effect: bleeding and reactions at the injection site.
The specificity of ATryn is the fact that the recombinant protein is not like any other drugs by using genetically engineered bacteria or mammalian cultures is produced, but is made from the milk of goats. The production is not in huge tanks in a sterile factory, but on a small farm in Massachusetts.
The researchers introduced the gene into fertilized eggs and have them fight it, of surrogate animals. Since then, it is in all cells of the genetically modified animals available and later the gene product is excreted in milk, in an amount of 10 grams per liter, as they say. An animal produces in a year, the same amount as antithrombin contained in 90,000 blood units.
The so called pharming bietet sich als eine kostengünstige Alternative zur derzeitigen Produktion an. Denn die Musterfarmen sind (im Prinzip) wesentlich kostengünstiger als die Fabriken. Steigt die Nachfrage an Medikamenten, kann die Produktion durch eine Vergrößerung der Herden jederzeit gesteigert werden (“Breed more if you need more”).
Da sich im Rahmen des Pharmings (im Prinzip) alle gentechnischen Medikamente herstellen lassen, wundert es, dass bisher nicht weitere Firmen ihr Interesse angekündigt haben. Beobachter erwarten, dass die Leitlinien, welche das Center for Veterinary Medicine der FDA im Januar 2009 festgelegt hat, hier einen gewissen Anreiz schaffen, da sie die Bedingungen festlegen.
Pharming, a small company based in Leiden in the Netherlands will, reportedly produced a recombinant human C1 inhibitor (for treatment of hereditary angioedema) using rabbits. PharmAthene of Annapolis, Maryland is planning the production of a recombinant protective antigen as an antidote for anthrax poisoning, which is to be produced in goats. These products would serve only a small niche indication.
would be much larger market for the many monoclonal antibodies, which came in the last few years for the treatment of autoimmune diseases and cancer on the market. But the big manufacturers show little apparent interest.
Whether they will one day competition of biosimilar companies will grow to bring their products cheaply by Pharming in the market, it is difficult to predict. It should, in any case that the high costs are due to the development of drugs than on biotechnology as the clinical development.
Pharming could be associated with its own risks. This should be less in the possibility that some animals escaped into the wilderness and the therapeutic genes to spread in the environment. Much unpleasant could be a scenario where the production of essential medicines for humans fail, because the animals are given because of illness no more milk.
© rme/aerzteblatt.de / FDA
Converting %w/w To %w/v If You Know The Density
new genes explain the heart attack
Die bei manchen Herzinfarkt-Patienten beobachtete positive Familienanamnese kann vielfältige genetische Ursachen haben, die mit drei Genen in Verbindung stehen, wie eine Publikation in Nature Genetics zeigt – mit neuen Einsichten in die Pathogenese, aber wenig Aussichten auf einen auf breiter Ebene anwendbaren Gentest.
Neben den „traditionellen“ Risikofaktoren wie Alter, arterielle Hypertonie, Fettstoffwechselstörungen, Diabetes mellitus, Rauchen und Übergewicht gibt es auch eine genetische Prädisposition auf den Herzinfarkt. Sie ist häufig bei Patienten vorhanden, die in relativ jungem Alter (Männer unter 50, Frauen diagnosed under 60 years) and that often several family members are affected.
The responsible genes, genetic researchers are trying in so-called genome-wide association studies (GWAS) to track down. Here, the genes of people affected, people here compared with early heart attack, and healthy.
The search focused on a growing number of known single nucleotide polymorphisms (single nucleotide polymorphism, SNP), can assign their variants sometimes certain diseases.
A first variant (PCSK9) was discovered in 2003. The gene plays a role in cholesterol metabolism. Mutations with familial hypercholesterolemia go hand in hand. A number of other risk genes was described two years ago by an international research team led by Heribert Schunkert of the University of Lübeck (NEJM 2007; 357: 443-53).
The recent study of the Myocardial Infarction Genetics Consortium heart attack increases the number of genes to nine, including three previously unknown genes on chromosomes 2, 6 and 21 (Nature Genetics 2009; doi: 10.1038/ng.327). For the current study, the group had to Sekar Kathiresan from the Massachusetts General Hospital in Boston, the genes of 26,000 patients from ten countries can be analyzed.
you had this area not only for SNP but also for so-called CNVs. These are changes in the number of Copies (copy number variants, CNV), in which individual genes on the chromosome are present.
Earlier studies had given differences in the CNV with other diseases. The trigger a heart attack come CNV, at least in the current study, however, not questioned.
contrast, combinations of adjacent SNPs seem to play a role. Such a "cluster" David-Alexandre Trégouët identified by the French research institute INSERM in Paris and employees on the chromosome 6. There, the LPA gene is located.
It regulates the concentration of lipoprotein (a) in the blood. This is one of the transport molecule for cholesterol and as such is an independent risk factor for heart attack (Nature Genetics 2009; doi: 10.1038/ng.314).
Two other risk genes discovered the group to Jeanette Erdmann of the University of Lübeck (Nature Genetics 2009; doi: 10.1038/ng.307n press). This is a variation on the one in the MRAS gene on chromosome 3, which may play a role in vascular biology. The HNF1A gene on chromosome 12 is on the other hand have a close relationship to cholesterol metabolism.
The discovered genes mainly provide new insights into the pathogenesis of heart attack or confirming the known risk constellations. This could possibly be the starting point be applied to develop new drugs.
as the basis for a genetic test to determine individual disease risk, they are likely to qualify only in exceptional cases occur, as Erdman points out in a video with the earlier publication.
the example mentioned in a younger patient with frequent heart attacks young people family tree. For giving a general population screening is currently no reason, the expert said at the time, It is likely also to change anything now. ©
heat / aerzteblatt.de
"Abstract of the study of Myocardial Infarction Genetics Consortium http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.327.html
"Abstract of the study Trégouët et al. http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.314.html
"Abstract of the study Erdmann et al. http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.307.html
»Press Releases of the Massachusetts General Hospital http://www.eurekalert.org/pub_releases/2009- 02/mgh-isi020509.php
»Press release by the University Lübeck http://idw-online.de/pages/de/news299766
» Press Cardiogenics video of the Project (to an earlier publication) http:// www.cardiogenics.eu / web / press.html
Die bei manchen Herzinfarkt-Patienten beobachtete positive Familienanamnese kann vielfältige genetische Ursachen haben, die mit drei Genen in Verbindung stehen, wie eine Publikation in Nature Genetics zeigt – mit neuen Einsichten in die Pathogenese, aber wenig Aussichten auf einen auf breiter Ebene anwendbaren Gentest.
Neben den „traditionellen“ Risikofaktoren wie Alter, arterielle Hypertonie, Fettstoffwechselstörungen, Diabetes mellitus, Rauchen und Übergewicht gibt es auch eine genetische Prädisposition auf den Herzinfarkt. Sie ist häufig bei Patienten vorhanden, die in relativ jungem Alter (Männer unter 50, Frauen diagnosed under 60 years) and that often several family members are affected.
The responsible genes, genetic researchers are trying in so-called genome-wide association studies (GWAS) to track down. Here, the genes of people affected, people here compared with early heart attack, and healthy.
The search focused on a growing number of known single nucleotide polymorphisms (single nucleotide polymorphism, SNP), can assign their variants sometimes certain diseases.
A first variant (PCSK9) was discovered in 2003. The gene plays a role in cholesterol metabolism. Mutations with familial hypercholesterolemia go hand in hand. A number of other risk genes was described two years ago by an international research team led by Heribert Schunkert of the University of Lübeck (NEJM 2007; 357: 443-53).
The recent study of the Myocardial Infarction Genetics Consortium heart attack increases the number of genes to nine, including three previously unknown genes on chromosomes 2, 6 and 21 (Nature Genetics 2009; doi: 10.1038/ng.327). For the current study, the group had to Sekar Kathiresan from the Massachusetts General Hospital in Boston, the genes of 26,000 patients from ten countries can be analyzed.
you had this area not only for SNP but also for so-called CNVs. These are changes in the number of Copies (copy number variants, CNV), in which individual genes on the chromosome are present.
Earlier studies had given differences in the CNV with other diseases. The trigger a heart attack come CNV, at least in the current study, however, not questioned.
contrast, combinations of adjacent SNPs seem to play a role. Such a "cluster" David-Alexandre Trégouët identified by the French research institute INSERM in Paris and employees on the chromosome 6. There, the LPA gene is located.
It regulates the concentration of lipoprotein (a) in the blood. This is one of the transport molecule for cholesterol and as such is an independent risk factor for heart attack (Nature Genetics 2009; doi: 10.1038/ng.314).
Two other risk genes discovered the group to Jeanette Erdmann of the University of Lübeck (Nature Genetics 2009; doi: 10.1038/ng.307n press). This is a variation on the one in the MRAS gene on chromosome 3, which may play a role in vascular biology. The HNF1A gene on chromosome 12 is on the other hand have a close relationship to cholesterol metabolism.
The discovered genes mainly provide new insights into the pathogenesis of heart attack or confirming the known risk constellations. This could possibly be the starting point be applied to develop new drugs.
as the basis for a genetic test to determine individual disease risk, they are likely to qualify only in exceptional cases occur, as Erdman points out in a video with the earlier publication.
the example mentioned in a younger patient with frequent heart attacks young people family tree. For giving a general population screening is currently no reason, the expert said at the time, It is likely also to change anything now. ©
heat / aerzteblatt.de
"Abstract of the study of Myocardial Infarction Genetics Consortium http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.327.html
"Abstract of the study Trégouët et al. http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.314.html
"Abstract of the study Erdmann et al. http://www.nature.com/ng/journal/vaop/ncurrent/abs/ng.307.html
»Press Releases of the Massachusetts General Hospital http://www.eurekalert.org/pub_releases/2009- 02/mgh-isi020509.php
»Press release by the University Lübeck http://idw-online.de/pages/de/news299766
» Press Cardiogenics video of the Project (to an earlier publication) http:// www.cardiogenics.eu / web / press.html
Tuesday, February 3, 2009
Ontario Personalized License Plate Available
European scientists confirm longevity
scientists at the Medical Faculty of the Christian-Albrechts-University Kiel (CAU) have confirmed that the life expectancy of humans by genetic factors.
Some 400 DNA samples from German centenarians had revealed that compared to younger ones, often have a variation in the gene FOXO3A.
in September 2008, an American research team published a study that suggested an accumulation of genetic variation in long Americans of Japanese descent (95 years and older).
"Such a result is only of scientific value if it is in an independent Study population is confirmed, "said Almut Nebel, scientific director of the Kiel-based research group of" healthy aging ".
The relationship between longevity and FOXO3A you can now have any doubts cleared. And French scientists in Paris had come to this conclusion. "This finding is of particular importance, as Japanese and Europeans are genetically quite different. Now we can assume that this gene is likely to reach a great age plays a role in the world, "said Nebel.
FOXO3A for genetic research on aging is of great interest, since it is in the 90s in worm and fly was described as age-relevant. Based on these findings, the Kiel-based research group at the Institute for Clinical Molecular Biology has been a long time with the human variant of the gene.
The study appears this week online in the journal PNAS (Proceedings of the National Academy of Sciences USA). © sc /
www.aerzteblatt.de
scientists at the Medical Faculty of the Christian-Albrechts-University Kiel (CAU) have confirmed that the life expectancy of humans by genetic factors.
Some 400 DNA samples from German centenarians had revealed that compared to younger ones, often have a variation in the gene FOXO3A.
in September 2008, an American research team published a study that suggested an accumulation of genetic variation in long Americans of Japanese descent (95 years and older).
"Such a result is only of scientific value if it is in an independent Study population is confirmed, "said Almut Nebel, scientific director of the Kiel-based research group of" healthy aging ".
The relationship between longevity and FOXO3A you can now have any doubts cleared. And French scientists in Paris had come to this conclusion. "This finding is of particular importance, as Japanese and Europeans are genetically quite different. Now we can assume that this gene is likely to reach a great age plays a role in the world, "said Nebel.
FOXO3A for genetic research on aging is of great interest, since it is in the 90s in worm and fly was described as age-relevant. Based on these findings, the Kiel-based research group at the Institute for Clinical Molecular Biology has been a long time with the human variant of the gene.
The study appears this week online in the journal PNAS (Proceedings of the National Academy of Sciences USA). © sc /
www.aerzteblatt.de
Free South Park Through Quicktime
Cambridge Cognition Welcomes the Launch of the First National Dementia Strategy
UK Strategy Understand the Importance of Early Detection Lines in the Care of Dementia and Alzheimer's Patients
Cambridge Cognition Ltd, developers of a clinical diagnostic product that provides early warning of neurodegenerative conditions including Alzheimer's, welcomes the launch of the National Dementia Strategy. The strategy, unveiled yesterday by Health Secretary, Alan Johnson and Phil Hope, the Care Services Minister, focuses on three key themes: improving public and professional awareness; early diagnosis and intervention; and improving quality of care.
The development of the strategy comes in response to growing concerns over the lack of effective diagnosis and treatment for dementia, a condition suffered by approximately 700,000 Britons, most of whom have Alzheimer's disease.
Current dementia assessment techniques are subjective and time consuming, representing a considerable drain on both financial and human resources. By contrast, Cambridge Cognition's CANTAB(R), the world's leading cognitive testing product for the diagnosis and assessment of important mental health diseases including Alzheimer's disease, is a highly sensitive, objective and cost-effective technology.
Developed at the University of Cambridge, Cambridge Cognition's Paired Associate Learning (PAL) test is widely recognised as being the leading technology for detecting the clinical signs of early stage dementia and Mild Cognitive Impairment, as well as accurately differentiating between demented and healthy patients and those suffering from depression.
Dr Andrew Blackwell, Chief Scientific Officer of Cambridge Cognition, commented: "The devices and tests developed by Cambridge Cognition will assist clinicians in the challenging task of differentiating patients with the early signs of dementia from the 'worried well'. This technology will significantly improve clinical outcomes for older adults experiencing memory problems."
Ian Harris, CEO of Cambridge Cognition, said: "We are delighted with the launch of this strategy, which should make an incredible difference to the lives of people with AD and other forms of dementia. Early detection of dementia is vital to improving the quality of patient care and we look forward to playing a leading role in these important health reforms."
About Cambridge Cognition Ltd.
Cambridge Cognition develops and markets CANTAB(R), the world's leading cognitive testing product for the diagnosis and assessment of important mental health diseases including Alzheimer's, Depression, Schizophrenia and ADHD. The computerised neuropsychological tests in CANTAB(R) are outstandingly sensitive and extensively validated, with a bibliography of over 600 peer-reviewed journal papers. Based in Cambridge, England, and Cambridge, Massachusetts, Cambridge Cognition Ltd supplies its products and services to the pharmaceutical industry and academic researchers across the globe.
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UK Strategy Understand the Importance of Early Detection Lines in the Care of Dementia and Alzheimer's Patients
Cambridge Cognition Ltd, developers of a clinical diagnostic product that provides early warning of neurodegenerative conditions including Alzheimer's, welcomes the launch of the National Dementia Strategy. The strategy, unveiled yesterday by Health Secretary, Alan Johnson and Phil Hope, the Care Services Minister, focuses on three key themes: improving public and professional awareness; early diagnosis and intervention; and improving quality of care.
The development of the strategy comes in response to growing concerns over the lack of effective diagnosis and treatment for dementia, a condition suffered by approximately 700,000 Britons, most of whom have Alzheimer's disease.
Current dementia assessment techniques are subjective and time consuming, representing a considerable drain on both financial and human resources. By contrast, Cambridge Cognition's CANTAB(R), the world's leading cognitive testing product for the diagnosis and assessment of important mental health diseases including Alzheimer's disease, is a highly sensitive, objective and cost-effective technology.
Developed at the University of Cambridge, Cambridge Cognition's Paired Associate Learning (PAL) test is widely recognised as being the leading technology for detecting the clinical signs of early stage dementia and Mild Cognitive Impairment, as well as accurately differentiating between demented and healthy patients and those suffering from depression.
Dr Andrew Blackwell, Chief Scientific Officer of Cambridge Cognition, commented: "The devices and tests developed by Cambridge Cognition will assist clinicians in the challenging task of differentiating patients with the early signs of dementia from the 'worried well'. This technology will significantly improve clinical outcomes for older adults experiencing memory problems."
Ian Harris, CEO of Cambridge Cognition, said: "We are delighted with the launch of this strategy, which should make an incredible difference to the lives of people with AD and other forms of dementia. Early detection of dementia is vital to improving the quality of patient care and we look forward to playing a leading role in these important health reforms."
About Cambridge Cognition Ltd.
Cambridge Cognition develops and markets CANTAB(R), the world's leading cognitive testing product for the diagnosis and assessment of important mental health diseases including Alzheimer's, Depression, Schizophrenia and ADHD. The computerised neuropsychological tests in CANTAB(R) are outstandingly sensitive and extensively validated, with a bibliography of over 600 peer-reviewed journal papers. Based in Cambridge, England, and Cambridge, Massachusetts, Cambridge Cognition Ltd supplies its products and services to the pharmaceutical industry and academic researchers across the globe.
-dpa-
Monday, February 2, 2009
Clothes For Tall Skinny Men
gene therapy for SCID In congenital immunodeficiency a long-term success
Die Langzeitergebnisse einer Gentherapie bei der angeborenen Immunschwächekrankheit SCID sind ausgezeichnet, wenn die Ursache ein Adenosin-Deaminase-Mangel ist. Im Gegensatz zur X-chromosomalen SCID, wo es zu mehreren Todesfällen kam, leben alle zehn Patienten, wie ein Bericht im New England Journal of Medicine (2009; 360:447-458) zeigt.
SCID (für severe combined immunodeficiency) ist eine Sammelbezeichnung für eine Reihe angeborener Erkrankungen mit einem schweren kombinierten Immundefekt, der unbehandelt in der Regel rasch tödlich endet.
Die beste Therapie besteht in einer hämatopoetischen Stammzelltransplantation, die aber nur dann eine sichere Heilungschance bietet, wenn der Spender, in der Regel ein Geschwisterkind, HLA-identisch ist.
Wesentlich riskanter ist die Spende von einem HLA-fremden Spender, die wegen der starken Abstoßungsreaktionen oder einem Fehlschlagen des Transplantates can lead to death. For these patients, gene therapy was devised in the SCID "technically" is easy to perform.
must only stem cells from bone marrow donated by viruses and are equipped with a correct version of the defective gene. This therapy was at the end of the last decade advanced that the first patients were treated.
On Hôpital Necker in Paris were gentherapiert since 2000 children with X-linked SCID. The study was stopped three years later, when several children were suffering from leukemia. With them had imported by the virus gene in the wrong place inserted into the genome.
The "promoter" should stimulate the production of the new gene, suggested the formation of adjacent proto-oncogenes. The likelihood of such insertional oncogenesis was not small: 5 of the 20 previously treated children developed 2 to 5 years after gene therapy a lymphoproliferative syndrome, in which one of them died.
Nevertheless Editorialist Donald Kohn advised the University of Los Angeles and Fabio Candotti by the U.S. National Human Genome Research Institute in Bethesda, Maryland to look at the situation soberly (NEJM 2009, 360: 518-521). Not just because for many children affected with stem cell transplantation (if no suitable HLA-identical donor is available) at least as as risky as gene therapy.
The second reason for optimism is the fact that the long-term results are favorable to a further variant of SCID and have not been overshadowed by cancer.
All ten children between 2000 and 2006 by an Israeli-Italian working group led by Mary Grazie Roncarolo San Raffaele Telethon Institute were from Gene Therapy for deals in Milan, have survived. In nine children, gene therapy has restored the immune system, eight do not require further therapy (2009, 360: 447-458).
was with the children on a defective gene for the enzyme adenosine deaminase. It is the accumulation of toxic metabolic waste and to SCID, which is curable as in the X-SCID only for the lucky children who have an HLA-identical donor. Treatment with bovine adenosine deaminase is rarely satisfactory.
Why in the SCID due to adenosine deaminase deficiency have never came to leukemia is not clear, particularly as the methods for gene transfer were very similar. The results are a motivation for continued therapy.
The Editorialist provide equal opportunities in front of six currently under investigation in order to prevent built-in fuses that the promoters as advised in the patients in Paris out of control. ©
heat / www.aerzteblatt.de
abstract of the study
San Raffaele Foundation
Die Langzeitergebnisse einer Gentherapie bei der angeborenen Immunschwächekrankheit SCID sind ausgezeichnet, wenn die Ursache ein Adenosin-Deaminase-Mangel ist. Im Gegensatz zur X-chromosomalen SCID, wo es zu mehreren Todesfällen kam, leben alle zehn Patienten, wie ein Bericht im New England Journal of Medicine (2009; 360:447-458) zeigt.
SCID (für severe combined immunodeficiency) ist eine Sammelbezeichnung für eine Reihe angeborener Erkrankungen mit einem schweren kombinierten Immundefekt, der unbehandelt in der Regel rasch tödlich endet.
Die beste Therapie besteht in einer hämatopoetischen Stammzelltransplantation, die aber nur dann eine sichere Heilungschance bietet, wenn der Spender, in der Regel ein Geschwisterkind, HLA-identisch ist.
Wesentlich riskanter ist die Spende von einem HLA-fremden Spender, die wegen der starken Abstoßungsreaktionen oder einem Fehlschlagen des Transplantates can lead to death. For these patients, gene therapy was devised in the SCID "technically" is easy to perform.
must only stem cells from bone marrow donated by viruses and are equipped with a correct version of the defective gene. This therapy was at the end of the last decade advanced that the first patients were treated.
On Hôpital Necker in Paris were gentherapiert since 2000 children with X-linked SCID. The study was stopped three years later, when several children were suffering from leukemia. With them had imported by the virus gene in the wrong place inserted into the genome.
The "promoter" should stimulate the production of the new gene, suggested the formation of adjacent proto-oncogenes. The likelihood of such insertional oncogenesis was not small: 5 of the 20 previously treated children developed 2 to 5 years after gene therapy a lymphoproliferative syndrome, in which one of them died.
Nevertheless Editorialist Donald Kohn advised the University of Los Angeles and Fabio Candotti by the U.S. National Human Genome Research Institute in Bethesda, Maryland to look at the situation soberly (NEJM 2009, 360: 518-521). Not just because for many children affected with stem cell transplantation (if no suitable HLA-identical donor is available) at least as as risky as gene therapy.
The second reason for optimism is the fact that the long-term results are favorable to a further variant of SCID and have not been overshadowed by cancer.
All ten children between 2000 and 2006 by an Israeli-Italian working group led by Mary Grazie Roncarolo San Raffaele Telethon Institute were from Gene Therapy for deals in Milan, have survived. In nine children, gene therapy has restored the immune system, eight do not require further therapy (2009, 360: 447-458).
was with the children on a defective gene for the enzyme adenosine deaminase. It is the accumulation of toxic metabolic waste and to SCID, which is curable as in the X-SCID only for the lucky children who have an HLA-identical donor. Treatment with bovine adenosine deaminase is rarely satisfactory.
Why in the SCID due to adenosine deaminase deficiency have never came to leukemia is not clear, particularly as the methods for gene transfer were very similar. The results are a motivation for continued therapy.
The Editorialist provide equal opportunities in front of six currently under investigation in order to prevent built-in fuses that the promoters as advised in the patients in Paris out of control. ©
heat / www.aerzteblatt.de
abstract of the study
San Raffaele Foundation
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