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Diabetes
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June 28, 2014
Genetic determinants of circulating interleukin-1 receptor antagonist levels and their association with glycemic traits
Christian Herder, Marja-Liisa Nuotio, Sonia Shah, et al.
Hepatology (Baltimore, Md.)
|
September 11, 2012
Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease
Mercedes Vazquez-Chantada, Aintzane Gonzalez-Lahera, Ibon Martinez-Arranz, et al.
Nature Genetics
|
June 30, 2019
Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes
Irene Miguel-Escalada, Silvia Bonàs-Guarch, Inês Cebola, et al.
Nature Genetics
|
September 7, 2010
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
Toshimasa Yamauchi, Kazuo Hara, Shiro Maeda, et al.
Nature Communications
|
January 24, 2018
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Communications
|
June 1, 2018
Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Communications
|
January 29, 2016
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Minako Imamura, Atsushi Takahashi, Toshimasa Yamauchi, et al.
Diabetes
|
April 29, 2018
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
Natalie R van Zuydam, Emma Ahlqvist, Niina Sandholm, et al.
Journal of the American College of Cardiology
|
August 18, 2012
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism
Anna Helgadottir, Solveig Gretarsdottir, Gudmar Thorleifsson, et al.
Nature Genetics
|
September 28, 2011
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
Simon N Stacey, Patrick Sulem, Aslaug Jonasdottir, et al.
Page
of 21
Search research articles
Search
Showing results (171-180 of 204) with videos related to
Sort By:
Page
of 21
Diabetes
|
June 28, 2014
Genetic determinants of circulating interleukin-1 receptor antagonist levels and their association with glycemic traits
Christian Herder, Marja-Liisa Nuotio, Sonia Shah, et al.
Hepatology (Baltimore, Md.)
|
September 11, 2012
Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease
Mercedes Vazquez-Chantada, Aintzane Gonzalez-Lahera, Ibon Martinez-Arranz, et al.
Nature Genetics
|
June 30, 2019
Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes
Irene Miguel-Escalada, Silvia Bonàs-Guarch, Inês Cebola, et al.
Nature Genetics
|
September 7, 2010
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
Toshimasa Yamauchi, Kazuo Hara, Shiro Maeda, et al.
Nature Communications
|
January 24, 2018
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Communications
|
June 1, 2018
Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Sílvia Bonàs-Guarch, Marta Guindo-Martínez, Irene Miguel-Escalada, et al.
Nature Communications
|
January 29, 2016
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Minako Imamura, Atsushi Takahashi, Toshimasa Yamauchi, et al.
Diabetes
|
April 29, 2018
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
Natalie R van Zuydam, Emma Ahlqvist, Niina Sandholm, et al.
Journal of the American College of Cardiology
|
August 18, 2012
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism
Anna Helgadottir, Solveig Gretarsdottir, Gudmar Thorleifsson, et al.
Nature Genetics
|
September 28, 2011
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
Simon N Stacey, Patrick Sulem, Aslaug Jonasdottir, et al.
Page
of 21