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Nature Neuroscience|April 5, 2022
Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onsetBranduff McAllister, Jasmine Donaldson, Caroline S Binda, et al.
International Journal for Parasitology|July 3, 2016
Cryptic Eimeria genotypes are common across the southern but not northern hemisphereEmily L Clark, Sarah E Macdonald, V Thenmozhi, et al.
American Journal of Human Genetics|March 29, 2002
PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD studyAnita L DeStefano, Mark F Lew, Lawrence I Golbe, et al.
Biorxiv : the Preprint Server for Biology|July 1, 2024
HumanIslets: An integrated platform for human islet data access and analysisJessica D Ewald, Yao Lu, Cara E Ellis, et al.
American Journal of Human Genetics|March 6, 2012
Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene regionJong-Min Lee, Tammy Gillis, Jayalakshmi Srinidhi Mysore, et al.
Cell Metabolism|October 2, 2024
HumanIslets.com: Improving accessibility, integration, and usability of human research islet dataJessica D Ewald, Yao Lu, Cara E Ellis, et al.
Nature Communications|February 9, 2022
Beta-cell specific Insr deletion promotes insulin hypersecretion and improves glucose tolerance prior to global insulin resistanceSøs Skovsø, Evgeniy Panzhinskiy, Jelena Kolic, et al.
American Journal of Human Genetics|July 10, 2012
Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomaliesHyung-Goo Kim, Hyun-Taek Kim, Natalia T Leach, et al.
Human Genetics|July 25, 2012
Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onsetEliana Marisa Ramos, Jeanne C Latourelle, Ji-Hyun Lee, et al.
Nature Communications|October 1, 2020
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2DAna Viñuela, Arushi Varshney, Martijn van de Bunt, et al.
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