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Showing results (1051-1060 of 1,115) with videos related to
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Scientific Reports
|
September 8, 2017
Carbonyl reductase 1 catalyzes 20β-reduction of glucocorticoids, modulating receptor activation and metabolic complications of obesity
Ruth A Morgan, Katharina R Beck, Mark Nixon, et al.
Cell
|
March 5, 2019
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2
Christine R Beck, Claudia M B Carvalho, Zeynep C Akdemir, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
March 27, 2025
Gut Microbial Metabolite Imidazole Propionate Impairs Endothelial Cell Function and Promotes the Development of Atherosclerosis
Vanasa Nageswaran, Alba Carreras, Leander Reinshagen, et al.
Human Mutation
|
July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays
Andrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Genome Medicine
|
January 8, 2016
POGZ truncating alleles cause syndromic intellectual disability
Janson White, Christine R Beck, Tamar Harel, et al.
Nature
|
August 23, 2023
Assembly of 43 human Y chromosomes reveals extensive complexity and variation
Pille Hallast, Peter Ebert, Mark Loftus, et al.
Development (Cambridge, England)
|
November 23, 2012
Macrophage migration inhibitory factor acts as a neurotrophin in the developing inner ear
Lisa M Bank, Lynne M Bianchi, Fumi Ebisu, et al.
BMC Genomics
|
April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genome
Adam C English, William J Salerno, Oliver A Hampton, et al.
European Heart Journal
|
August 30, 2025
Gut microbiota-derived imidazole propionate predicts cardiometabolic risk in patients with coronary artery disease
Florian A Wenzl, Peizhi Wang, Florian Kahles, et al.
The Journal of Clinical Investigation
|
January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes
Bo Yuan, Davut Pehlivan, Ender Karaca, et al.
Page
of 112
Search research articles
Search
Showing results (1051-1060 of 1,115) with videos related to
Sort By:
Page
of 112
Scientific Reports
|
September 8, 2017
Carbonyl reductase 1 catalyzes 20β-reduction of glucocorticoids, modulating receptor activation and metabolic complications of obesity
Ruth A Morgan, Katharina R Beck, Mark Nixon, et al.
Cell
|
March 5, 2019
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2
Christine R Beck, Claudia M B Carvalho, Zeynep C Akdemir, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
March 27, 2025
Gut Microbial Metabolite Imidazole Propionate Impairs Endothelial Cell Function and Promotes the Development of Atherosclerosis
Vanasa Nageswaran, Alba Carreras, Leander Reinshagen, et al.
Human Mutation
|
July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays
Andrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Genome Medicine
|
January 8, 2016
POGZ truncating alleles cause syndromic intellectual disability
Janson White, Christine R Beck, Tamar Harel, et al.
Nature
|
August 23, 2023
Assembly of 43 human Y chromosomes reveals extensive complexity and variation
Pille Hallast, Peter Ebert, Mark Loftus, et al.
Development (Cambridge, England)
|
November 23, 2012
Macrophage migration inhibitory factor acts as a neurotrophin in the developing inner ear
Lisa M Bank, Lynne M Bianchi, Fumi Ebisu, et al.
BMC Genomics
|
April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genome
Adam C English, William J Salerno, Oliver A Hampton, et al.
European Heart Journal
|
August 30, 2025
Gut microbiota-derived imidazole propionate predicts cardiometabolic risk in patients with coronary artery disease
Florian A Wenzl, Peizhi Wang, Florian Kahles, et al.
The Journal of Clinical Investigation
|
January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes
Bo Yuan, Davut Pehlivan, Ender Karaca, et al.
Page
of 112