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Methods in Molecular Biology (Clifton, N.J.)|August 4, 2015
Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer's DiseaseSheng Chih Jin, Bruno A Benitez, Yuetiva Deming, et al.Plos Pathogens|April 6, 2019
Unique features in the intracellular transport of typhoid toxin revealed by a genome-wide screenShu-Jung Chang, Sheng Chih Jin, Xuyao Jiao, et al.Trends in Molecular Medicine|March 2, 2019
EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and DiseaseXue Zeng, Ava Hunt, Sheng Chih Jin, et al.Plos Genetics|June 7, 2022
Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart diseaseYuhan Xie, Wei Jiang, Weilai Dong, et al.Ebiomedicine|July 6, 2024
Potential clinical applications of advanced genomic analysis in cerebral palsySara A Lewis, Andrew Ruttenberg, Tuğçe Iyiyol, et al.Neurobiology of Aging|February 9, 2013
TREM2 is associated with the risk of Alzheimer's disease in Spanish populationBruno A Benitez, Breanna Cooper, Pau Pastor, et al.Cold Spring Harbor Molecular Case Studies|April 27, 2018
A novel association of campomelic dysplasia and hydrocephalus with an unbalanced chromosomal translocation upstream of SOX9Prince Antwi, Christopher S Hong, Daniel Duran, et al.Annals of Clinical and Translational Neurology|March 24, 2025
Unleashing the Power of Multiomics: Unraveling the Molecular Landscape of Peripheral NeuropathyJulie Choi, Zitian Tang, Wendy Dong, et al.Alzheimer'S Research & Therapy|August 22, 2012
Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohortSheng Chih Jin, Pau Pastor, Breanna Cooper, et al.Quantitative Biology (Beijing, China)|April 13, 2022
Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart diseaseMo Li, Xue Zeng, Chentian Jin, et al.Pageof 10