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Monika Stoll

Showing results (21-30 of 171) with videos related to

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International Journal of Cardiology|May 20, 2008
Platelet reactivity and clopidogrel resistance are associated with the H2 haplotype of the P2Y12-ADP receptor genePeter Staritz, Kerstin Kurz, Monika Stoll, et al.
Journal of the American Society of Nephrology : JASN|November 26, 2003
A major gene locus links early onset albuminuria with renal interstitial fibrosis in the MWF rat with polygenetic albuminuriaAngela Schulz, Dorothea Standke, Larisa Kovacevic, et al.
Plos One|February 4, 2015
Fetal-adult cardiac transcriptome analysis in rats with contrasting left ventricular mass reveals new candidates for cardiac hypertrophyKatja Grabowski, Mona Riemenschneider, Leonard Schulte, et al.
The American Journal of Gastroenterology|December 13, 2006
DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's diseaseVincent Biank, Frauke Friedrichs, Umesh Babusukumar, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 28, 2014
The contribution of genetic factors to phenotype and progression of drusen in early age-related macular degenerationMartha Dietzel, Daniel Pauleikhoff, Astrid Arning, et al.
Blood|June 12, 2009
Fibrinogen alpha and gamma genes and factor VLeiden in children with thromboembolism: results from 2 family-based association studiesUlrike Nowak-Göttl, Hartmut Weiler, Irene Hernandez, et al.
Circulation. Cardiovascular Genetics|July 15, 2016
Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric StrokeMonika Stoll, Frank Rühle, Anika Witten, et al.
Journal of Clinical Medicine|January 11, 2024
Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database StudySusan Halimeh, Lydia Koch, Gili Kenet, et al.
Human Genetics|November 9, 2015
Pathway-based variant enrichment analysis on the example of dilated cardiomyopathyChristina Backes, Benjamin Meder, Alan Lai, et al.
Journal of Hypertension|October 9, 2007
Induction of C1q expression in glomerular endothelium in a rat model with arterial hypertension and albuminuriaReinhold Kreutz, Angela Schulz, Anika Sietmann, et al.
Pageof 18

Showing results (21-30 of 171) with videos related to

Sort By:
Pageof 18
International Journal of Cardiology|May 20, 2008
Platelet reactivity and clopidogrel resistance are associated with the H2 haplotype of the P2Y12-ADP receptor genePeter Staritz, Kerstin Kurz, Monika Stoll, et al.
Journal of the American Society of Nephrology : JASN|November 26, 2003
A major gene locus links early onset albuminuria with renal interstitial fibrosis in the MWF rat with polygenetic albuminuriaAngela Schulz, Dorothea Standke, Larisa Kovacevic, et al.
Plos One|February 4, 2015
Fetal-adult cardiac transcriptome analysis in rats with contrasting left ventricular mass reveals new candidates for cardiac hypertrophyKatja Grabowski, Mona Riemenschneider, Leonard Schulte, et al.
The American Journal of Gastroenterology|December 13, 2006
DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's diseaseVincent Biank, Frauke Friedrichs, Umesh Babusukumar, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 28, 2014
The contribution of genetic factors to phenotype and progression of drusen in early age-related macular degenerationMartha Dietzel, Daniel Pauleikhoff, Astrid Arning, et al.
Blood|June 12, 2009
Fibrinogen alpha and gamma genes and factor VLeiden in children with thromboembolism: results from 2 family-based association studiesUlrike Nowak-Göttl, Hartmut Weiler, Irene Hernandez, et al.
Circulation. Cardiovascular Genetics|July 15, 2016
Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric StrokeMonika Stoll, Frank Rühle, Anika Witten, et al.
Journal of Clinical Medicine|January 11, 2024
Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database StudySusan Halimeh, Lydia Koch, Gili Kenet, et al.
Human Genetics|November 9, 2015
Pathway-based variant enrichment analysis on the example of dilated cardiomyopathyChristina Backes, Benjamin Meder, Alan Lai, et al.
Journal of Hypertension|October 9, 2007
Induction of C1q expression in glomerular endothelium in a rat model with arterial hypertension and albuminuriaReinhold Kreutz, Angela Schulz, Anika Sietmann, et al.
Pageof 18