Showing results (841-850 of 1,007) with videos related to

Sort By:
Pageof 101
Human Molecular Genetics|February 11, 2020
Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1Heather M Schmitt, William M Johnson, Inas F Aboobakar, et al.
International Journal of Molecular Sciences|October 13, 2021
Identification of Estrogen Signaling in a Prioritization Study of Intraocular Pressure-Associated GenesHannah A Youngblood, Emily Parker, Jingwen Cai, et al.
Journal of Psychiatric Research|October 5, 2016
Further evidence for a role of the ADRB2 gene in risk for posttraumatic stress disorderMichael A Hauser, Melanie E Garrett, Yutao Liu, et al.
Molecular & Cellular Proteomics : MCP|May 15, 2021
Reverse Phase Protein Array Reveals Correlation of Retinoic Acid Metabolism With Cardiomyopathy in Friedreich's AtaxiaJill S Napierala, Kimal Rajapakshe, Amanda Clark, et al.
The Lancet. Neurology|January 22, 2019
Safety and efficacy of CVT-301 (levodopa inhalation powder) on motor function during off periods in patients with Parkinson's disease: a randomised, double-blind, placebo-controlled phase 3 trialPeter A LeWitt, Robert A Hauser, Rajesh Pahwa, et al.
Nature Plants|January 3, 2025
Pan-phylum genomes of hornworts reveal conserved autosomes but dynamic accessory and sex chromosomesPeter Schafran, Duncan A Hauser, Jessica M Nelson, et al.
The American Journal of Pathology|May 14, 2009
CXCL16 is expressed in podocytes and acts as a scavenger receptor for oxidized low-density lipoproteinPaul Gutwein, Mohamed Sadek Abdel-Bakky, Anja Schramme, et al.
Investigative Ophthalmology & Visual Science|March 16, 2013
A genome-wide association study of central corneal thickness in LatinosXiaoyi Gao, W James Gauderman, Yutao Liu, et al.
Clinical Neuropharmacology|September 15, 2015
Caffeine and Progression of Parkinson Disease: A Deleterious Interaction With CreatineDavid K Simon, Cai Wu, Barbara C Tilley, et al.
Investigative Ophthalmology & Visual Science|June 12, 2014
Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophyYi-Ju Li, Mollie A Minear, Xuejun Qin, et al.
Pageof 101