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Jeanette Erdmann

Showing results (81-90 of 284) with videos related to

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Clinical Science (London, England : 1979)|May 3, 2007
The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factorsKlaus Stark, Katharina Neureuther, Kamil Sedlacek, et al.
Plos One|April 10, 2008
Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control studyKlaus Stark, Wibke Reinhard, Katharina Neureuther, et al.
Scientific Reports|March 1, 2019
A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1ATill Joscha Demal, Melina Heise, Benedikt Reiz, et al.
Hypertension (Dallas, Tex. : 1979)|August 3, 2002
Relation of the G protein beta3-subunit polymorphism with left ventricle structure and functionKamil Sedlácek, Marcus Fischer, Jeanette Erdmann, et al.
Lipids in Health and Disease|April 8, 2009
Macrophage cholesterol efflux correlates with lipoprotein subclass distribution and risk of obstructive coronary artery disease in patients undergoing coronary angiographyPatrick Linsel-Nitschke, Henning Jansen, Zouhair Aherrarhou, et al.
European Journal of Human Genetics : EJHG|June 4, 2015
Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarctionIngrid Brænne, Mariana Kleinecke, Benedikt Reiz, et al.
European Journal of Preventive Cardiology|November 2, 2019
Long-term prevention after myocardial infarction in young patients ≤45 years: the Intensive Prevention Program in the Young (IPP-Y) studyAndreas Fach, Rico Osteresch, Jeanette Erdmann, et al.
Human Molecular Genetics|February 28, 2007
Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery diseaseAndrea Baessler, Marcus Fischer, Bjoern Mayer, et al.
Circulation|August 23, 2021
Identification of a Functional <i>PDE5A</i> Variant at the Chromosome 4q27 Coronary Artery Disease Locus in an Extended Myocardial Infarction FamilyTan An Dang, Thorsten Kessler, Jana Wobst, et al.
Physiological Genomics|August 24, 2006
Ultrafine mapping of Dyscalc1 to an 80-kb chromosomal segment on chromosome 7 in mice susceptible for dystrophic calcificationZouhair Aherrahrou, Lars C Doehring, Piotr M Kaczmarek, et al.
Pageof 29

Showing results (81-90 of 284) with videos related to

Sort By:
Pageof 29
Clinical Science (London, England : 1979)|May 3, 2007
The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factorsKlaus Stark, Katharina Neureuther, Kamil Sedlacek, et al.
Plos One|April 10, 2008
Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control studyKlaus Stark, Wibke Reinhard, Katharina Neureuther, et al.
Scientific Reports|March 1, 2019
A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1ATill Joscha Demal, Melina Heise, Benedikt Reiz, et al.
Hypertension (Dallas, Tex. : 1979)|August 3, 2002
Relation of the G protein beta3-subunit polymorphism with left ventricle structure and functionKamil Sedlácek, Marcus Fischer, Jeanette Erdmann, et al.
Lipids in Health and Disease|April 8, 2009
Macrophage cholesterol efflux correlates with lipoprotein subclass distribution and risk of obstructive coronary artery disease in patients undergoing coronary angiographyPatrick Linsel-Nitschke, Henning Jansen, Zouhair Aherrarhou, et al.
European Journal of Human Genetics : EJHG|June 4, 2015
Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarctionIngrid Brænne, Mariana Kleinecke, Benedikt Reiz, et al.
European Journal of Preventive Cardiology|November 2, 2019
Long-term prevention after myocardial infarction in young patients ≤45 years: the Intensive Prevention Program in the Young (IPP-Y) studyAndreas Fach, Rico Osteresch, Jeanette Erdmann, et al.
Human Molecular Genetics|February 28, 2007
Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery diseaseAndrea Baessler, Marcus Fischer, Bjoern Mayer, et al.
Circulation|August 23, 2021
Identification of a Functional <i>PDE5A</i> Variant at the Chromosome 4q27 Coronary Artery Disease Locus in an Extended Myocardial Infarction FamilyTan An Dang, Thorsten Kessler, Jana Wobst, et al.
Physiological Genomics|August 24, 2006
Ultrafine mapping of Dyscalc1 to an 80-kb chromosomal segment on chromosome 7 in mice susceptible for dystrophic calcificationZouhair Aherrahrou, Lars C Doehring, Piotr M Kaczmarek, et al.
Pageof 29