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British Journal of Pharmacology|June 26, 2019
Inhibitors of class I histone deacetylases attenuate thioacetamide-induced liver fibrosis in mice by suppressing hepatic type 2 inflammationZhixuan Loh, Rebecca L Fitzsimmons, Robert C Reid, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Nucleic Acids Research|January 7, 2026
Multimodal bHLH-PAS DNA binding controls specificity and drives obesityDavid C Bersten, Daniel P McDougal, Adrienne E Sullivan, et al.
HGG Advances|July 17, 2023
Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
American Journal of Human Genetics|May 11, 2015
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3Jessica X Chong, Lindsay C Burrage, Anita E Beck, et al.
American Journal of Human Genetics|December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5DMargaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
Cell Reports|July 16, 2013
Caveolin-1 is necessary for hepatic oxidative lipid metabolism: evidence for crosstalk between caveolin-1 and bile acid signalingManuel A Fernández-Rojo, Milena Gongora, Rebecca L Fitzsimmons, et al.
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