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R Beck

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 obesityRuth A Morgan, Katharina R Beck, Mark Nixon, et al.
Cell|March 5, 2019
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2Christine 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 AtherosclerosisVanasa 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 delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Genome Medicine|January 8, 2016
POGZ truncating alleles cause syndromic intellectual disabilityJanson White, Christine R Beck, Tamar Harel, et al.
Nature|August 23, 2023
Assembly of 43 human Y chromosomes reveals extensive complexity and variationPille 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 earLisa 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 genomeAdam 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 diseaseFlorian 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 phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
Pageof 112

Showing results (1051-1060 of 1,115) with videos related to

Sort By:
Pageof 112
Scientific Reports|September 8, 2017
Carbonyl reductase 1 catalyzes 20β-reduction of glucocorticoids, modulating receptor activation and metabolic complications of obesityRuth A Morgan, Katharina R Beck, Mark Nixon, et al.
Cell|March 5, 2019
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2Christine 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 AtherosclerosisVanasa 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 delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Genome Medicine|January 8, 2016
POGZ truncating alleles cause syndromic intellectual disabilityJanson White, Christine R Beck, Tamar Harel, et al.
Nature|August 23, 2023
Assembly of 43 human Y chromosomes reveals extensive complexity and variationPille 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 earLisa 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 genomeAdam 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 diseaseFlorian 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 phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
Pageof 112