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Diabetes
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May 26, 2019
A Genetic Locus on Chromosome 2q24 Predicting Peripheral Neuropathy Risk in Type 2 Diabetes: Results From the ACCORD and BARI 2D Studies
Yaling Tang, Petra A Lenzini, Rodica Pop-Busui, et al.
BMC Medical Genetics
|
October 1, 2011
Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome
Thomas M Morgan, John A House, Sharon Cresci, et al.
Journal of the American College of Cardiology
|
April 10, 2024
Safety and Efficacy of Metabolic Modulation With Ninerafaxstat in Patients With Nonobstructive Hypertrophic Cardiomyopathy
Martin S Maron, Masliza Mahmod, Azlan Helmy Abd Samat, et al.
Diabetes
|
January 25, 2020
<i>PPARA</i> Polymorphism Influences the Cardiovascular Benefit of Fenofibrate in Type 2 Diabetes: Findings From ACCORD-Lipid
Mario Luca Morieri, Hetal S Shah, Jennifer Sjaarda, et al.
Frontiers in Physiology
|
July 11, 2022
Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis
Tessa Schillemans, Vinicius Tragante, Buamina Maitusong, et al.
European Heart Journal
|
March 22, 2021
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality
Stefan J Schunk, Marcus E Kleber, Winfried März, et al.
The New England Journal of Medicine
|
November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease
, Nathan O Stitziel, Hong-Hee Won, et al.
Circulation
|
July 14, 2020
Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data
Bakhtawar K Mahmoodi, Vinicius Tragante, Marcus E Kleber, et al.
Nature
|
December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do, Nathan O Stitziel, Hong-Hee Won, et al.
The Lancet. Diabetes & Endocrinology
|
June 2, 2017
Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study
Stephen Zewinger, Marcus E Kleber, Vinicius Tragante, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 72) with videos related to
Sort By:
Page
of 8
Diabetes
|
May 26, 2019
A Genetic Locus on Chromosome 2q24 Predicting Peripheral Neuropathy Risk in Type 2 Diabetes: Results From the ACCORD and BARI 2D Studies
Yaling Tang, Petra A Lenzini, Rodica Pop-Busui, et al.
BMC Medical Genetics
|
October 1, 2011
Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome
Thomas M Morgan, John A House, Sharon Cresci, et al.
Journal of the American College of Cardiology
|
April 10, 2024
Safety and Efficacy of Metabolic Modulation With Ninerafaxstat in Patients With Nonobstructive Hypertrophic Cardiomyopathy
Martin S Maron, Masliza Mahmod, Azlan Helmy Abd Samat, et al.
Diabetes
|
January 25, 2020
<i>PPARA</i> Polymorphism Influences the Cardiovascular Benefit of Fenofibrate in Type 2 Diabetes: Findings From ACCORD-Lipid
Mario Luca Morieri, Hetal S Shah, Jennifer Sjaarda, et al.
Frontiers in Physiology
|
July 11, 2022
Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis
Tessa Schillemans, Vinicius Tragante, Buamina Maitusong, et al.
European Heart Journal
|
March 22, 2021
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality
Stefan J Schunk, Marcus E Kleber, Winfried März, et al.
The New England Journal of Medicine
|
November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease
, Nathan O Stitziel, Hong-Hee Won, et al.
Circulation
|
July 14, 2020
Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data
Bakhtawar K Mahmoodi, Vinicius Tragante, Marcus E Kleber, et al.
Nature
|
December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do, Nathan O Stitziel, Hong-Hee Won, et al.
The Lancet. Diabetes & Endocrinology
|
June 2, 2017
Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study
Stephen Zewinger, Marcus E Kleber, Vinicius Tragante, et al.
Page
of 8