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Michael M Hoffmann

Showing results (61-70 of 98) with videos related to

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BMC Medical Genetics|June 2, 2009
Genetic variation in Fc gamma receptor IIa and risk of coronary heart disease: negative results from two large independent populationsMahir Karakas, Michael M Hoffmann, Caren Vollmert, et al.
Atherosclerosis|October 20, 2009
Association of the single nucleotide polymorphism rs599839 in the vicinity of the sortilin 1 gene with LDL and triglyceride metabolism, coronary heart disease and myocardial infarction. The Ludwigshafen Risk and Cardiovascular Health StudyMarcus E Kleber, Wilfried Renner, Tanja B Grammer, et al.
European Journal of Human Genetics : EJHG|December 8, 2005
Hidden population substructures in an apparently homogeneous population bias association studiesMario Berger, Hans H Stassen, Karola Köhler, et al.
Diabetes/Metabolism Research and Reviews|March 9, 2011
Association of TCF7L2 SNPs with age at onset of type 2 diabetes and proinsulin/insulin ratio but not with glucagon-like peptide 1Guenther Silbernagel, Wilfried Renner, Tanja B Grammer, et al.
Orphanet Journal of Rare Diseases|August 8, 2013
A mutation in the c-fos gene associated with congenital generalized lipodystrophyBirgit Knebel, Jorg Kotzka, Stefan Lehr, et al.
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 25, 2003
The variable number of tandem repeat polymorphism in the P-selectin glycoprotein ligand-1 gene is not associated with coronary heart diseasePeter Bugert, Michael M Hoffmann, Bernhard R Winkelmann, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.
Annals of Human Genetics|January 12, 2010
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndromeMaren Sullivan, Zoran Erlic, Michael M Hoffmann, et al.
European Heart Journal. Cardiovascular Imaging|December 24, 2025
Wall shear stress and oscillatory shear index are independently associated with complicated carotid artery plaquesJonathan Andrae, Andreas Schindler, Christoph Strecker, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
BMC Medical Genetics|June 2, 2009
Genetic variation in Fc gamma receptor IIa and risk of coronary heart disease: negative results from two large independent populationsMahir Karakas, Michael M Hoffmann, Caren Vollmert, et al.
Atherosclerosis|October 20, 2009
Association of the single nucleotide polymorphism rs599839 in the vicinity of the sortilin 1 gene with LDL and triglyceride metabolism, coronary heart disease and myocardial infarction. The Ludwigshafen Risk and Cardiovascular Health StudyMarcus E Kleber, Wilfried Renner, Tanja B Grammer, et al.
European Journal of Human Genetics : EJHG|December 8, 2005
Hidden population substructures in an apparently homogeneous population bias association studiesMario Berger, Hans H Stassen, Karola Köhler, et al.
Diabetes/Metabolism Research and Reviews|March 9, 2011
Association of TCF7L2 SNPs with age at onset of type 2 diabetes and proinsulin/insulin ratio but not with glucagon-like peptide 1Guenther Silbernagel, Wilfried Renner, Tanja B Grammer, et al.
Orphanet Journal of Rare Diseases|August 8, 2013
A mutation in the c-fos gene associated with congenital generalized lipodystrophyBirgit Knebel, Jorg Kotzka, Stefan Lehr, et al.
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 25, 2003
The variable number of tandem repeat polymorphism in the P-selectin glycoprotein ligand-1 gene is not associated with coronary heart diseasePeter Bugert, Michael M Hoffmann, Bernhard R Winkelmann, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.
Annals of Human Genetics|January 12, 2010
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndromeMaren Sullivan, Zoran Erlic, Michael M Hoffmann, et al.
European Heart Journal. Cardiovascular Imaging|December 24, 2025
Wall shear stress and oscillatory shear index are independently associated with complicated carotid artery plaquesJonathan Andrae, Andreas Schindler, Christoph Strecker, et al.
Pageof 10