Showing results (371-380 of 399) with videos related to

Sort By:
Pageof 40
Nature Communications|April 29, 2018
Manipulation of insulin signaling phenocopies evolution of a host-associated polyphenismMeghan M Fawcett, Mary C Parks, Alice E Tibbetts, et al.
Peerj|January 4, 2021
The Aichi Biodiversity Targets: achievements for marine conservation and priorities beyond 2020Hannah Carr, Marina Abas, Loubna Boutahar, et al.
Science Advances|June 1, 2019
Oxygen tension-mediated erythrocyte membrane interactions regulate cerebral capillary hyperemiaSitong Zhou, Michael Giannetto, James DeCourcey, et al.
Plos One|August 3, 2016
Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy MetabolismC Alexander Valencia, Xinjian Wang, Jin Wang, et al.
European Journal of Human Genetics : EJHG|March 20, 2023
A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severityKevin M Flanigan, Megan A Waldrop, Paul T Martin, et al.
Molecular Therapy. Methods & Clinical Development|August 11, 2022
Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouseNicolas Wein, Tatyana A Vetter, Adeline Vulin, et al.
Molecular Therapy. Nucleic Acids|November 24, 2022
Systemic PPMO-mediated dystrophin expression in the Dup2 mouse model of Duchenne muscular dystrophyLiubov V Gushchina, Tatyana A Vetter, Emma C Frair, et al.
Pediatric Research|March 30, 2017
Hepatic MDR3 expression impacts lipid homeostasis and susceptibility to inflammatory bile duct obstruction in neonatesAlexandra N Carey, Wujuan Zhang, Kenneth D R Setchell, et al.
Molecular Pharmaceutics|July 23, 2019
Central Nervous System Delivery and Biodistribution Analysis of an Antibody-Enzyme Fusion for the Treatment of Lafora DiseaseGrant L Austin, Zoe R Simmons, Jack E Klier, et al.
Plant Physiology|June 10, 2010
A customized gene expression microarray reveals that the brittle stem phenotype fs2 of barley is attributable to a retroelement in the HvCesA4 cellulose synthase geneRachel A Burton, Gang Ma, Ute Baumann, et al.
Pageof 40