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Nature Communications|December 31, 2024
Robust ferromagnetism in wafer-scale Fe3GaTe2 above room-temperatureShuxiang Wu, Zhihao He, Minghui Gu, et al.European Urology Oncology|January 18, 2020
Rare Germline Pathogenic Mutations of DNA Repair Genes Are Most Strongly Associated with Grade Group 5 Prostate CancerYishuo Wu, Hongjie Yu, Shuwei Li, et al.The Prostate|December 1, 2020
Validation of a prostate cancer polygenic risk scoreMary H Black, Shuwei Li, Holly LaDuca, et al.Translational Stroke Research|November 23, 2018
From Analysis of Ischemic Mouse Brain Proteome to Identification of Human Serum Clusterin as a Potential Biomarker for Severity of Acute Ischemic StrokeHailong Song, Hui Zhou, Zhe Qu, et al.Science Advances|July 17, 2020
Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancerMulong Du, Rui Zheng, Gaoxiang Ma, et al.Neuron|November 12, 2024
Potassium ion channel modulation at cancer-neural interface enhances neuronal excitability in epileptogenic glioblastoma multiformeYe Zhang, Wei Duan, Lingchao Chen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.Cell Genomics|June 30, 2023
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs target discovery in ankylosing spondylitisAndrew C Brown, Carla J Cohen, Olga Mielczarek, et al.Human Mutation|October 13, 2018
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variantsKristy Lee, Kate Krempely, Maegan E Roberts, et al.Pageof 32