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Nature Genetics
|
November 8, 2016
Prospective functional classification of all possible missense variants in PPARG
Amit R Majithia, Ben Tsuda, Maura Agostini, et al.
Nature Immunology
|
November 21, 2025
Pseudokinase STK40 limits T cell exhaustion through COP1-dependent degradation of AP1-family transcription factors
Svetlana Altshuler-Keylin, Nicole Caduff, Isabel E Ishizuka, et al.
Obesity (Silver Spring, Md.)
|
April 19, 2013
Racial/ethnic differences in clinical and biochemical type 2 diabetes mellitus risk factors in children
Michael Rosenbaum, Ilene Fennoy, Siham Accacha, et al.
Nature Genetics
|
December 9, 2008
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion
Valeriya Lyssenko, Cecilia L F Nagorny, Michael R Erdos, et al.
Nature Genetics
|
January 24, 2009
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus
Robert R Graham, Chris Cotsapas, Leela Davies, et al.
Science (New York, N.Y.)
|
May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
Jacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
The New England Journal of Medicine
|
January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A Weiss, Yiping Shen, Joshua M Korn, et al.
Human Molecular Genetics
|
May 16, 2013
MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension
Ryan S Friese, Angelina E Altshuler, Kuixing Zhang, et al.
Nature Communications
|
July 7, 2025
Protozoal populations drive system-wide variation in the rumen microbiome
Carl M Kobel, Andy Leu, Arturo Vera-Ponce de León, et al.
International Journal of Cancer
|
August 28, 2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts
Daphne W Bell, Sang H Kim, Andrew K Godwin, et al.
Page
of 123
Search research articles
Search
Showing results (1101-1110 of 1,225) with videos related to
Sort By:
Page
of 123
Nature Genetics
|
November 8, 2016
Prospective functional classification of all possible missense variants in PPARG
Amit R Majithia, Ben Tsuda, Maura Agostini, et al.
Nature Immunology
|
November 21, 2025
Pseudokinase STK40 limits T cell exhaustion through COP1-dependent degradation of AP1-family transcription factors
Svetlana Altshuler-Keylin, Nicole Caduff, Isabel E Ishizuka, et al.
Obesity (Silver Spring, Md.)
|
April 19, 2013
Racial/ethnic differences in clinical and biochemical type 2 diabetes mellitus risk factors in children
Michael Rosenbaum, Ilene Fennoy, Siham Accacha, et al.
Nature Genetics
|
December 9, 2008
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion
Valeriya Lyssenko, Cecilia L F Nagorny, Michael R Erdos, et al.
Nature Genetics
|
January 24, 2009
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus
Robert R Graham, Chris Cotsapas, Leela Davies, et al.
Science (New York, N.Y.)
|
May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
Jacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
The New England Journal of Medicine
|
January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A Weiss, Yiping Shen, Joshua M Korn, et al.
Human Molecular Genetics
|
May 16, 2013
MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension
Ryan S Friese, Angelina E Altshuler, Kuixing Zhang, et al.
Nature Communications
|
July 7, 2025
Protozoal populations drive system-wide variation in the rumen microbiome
Carl M Kobel, Andy Leu, Arturo Vera-Ponce de León, et al.
International Journal of Cancer
|
August 28, 2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts
Daphne W Bell, Sang H Kim, Andrew K Godwin, et al.
Page
of 123