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Biorxiv : the Preprint Server for Biology|November 24, 2025
Transcriptomic and protein analysis of human cortex reveals genes and pathways linked to NPTX2 disruption in Alzheimer's diseaseYuelin Lao, Mei-Fang Xiao, Shiyu Ji, et al.International Journal of Molecular Sciences|April 17, 2025
Characterization of Isolated Human Astrocytes from Aging BrainGeidy E Serrano, Sidra Aslam, Jessica E Walker, et al.American Journal of Medical Genetics. Part A|February 1, 2017
A de novo splice site mutation in CASK causes FG syndrome-4 and congenital nystagmusP Dunn, G P Prigatano, S Szelinger, et al.Cells|July 6, 2023
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental DisordersEric Frankel, Avijit Podder, Megan Sharifi, et al.Frontiers in Immunology|October 31, 2022
The double-sided of human leukocyte antigen-G molecules in type 1 autoimmune hepatitisRoberto Littera, Andrea Perra, Michela Miglianti, et al.Nature Communications|May 1, 2014
Geographic population structure analysis of worldwide human populations infers their biogeographical originsEran Elhaik, Tatiana Tatarinova, Dmitri Chebotarev, et al.American Journal of Human Genetics|August 20, 2019
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA DysregulationChris Balak, Marianne Benard, Elise Schaefer, et al.Journal of Neuropathology and Experimental Neurology|July 12, 2022
SARS-CoV-2 Brain Regional Detection, Histopathology, Gene Expression, and Immunomodulatory Changes in Decedents with COVID-19Geidy E Serrano, Jessica E Walker, Cécilia Tremblay, et al.Pageof 16