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Briefings in Bioinformatics|June 30, 2011
Ortholog identification in the presence of domain architecture rearrangementKimmen Sjölander, Ruchira S Datta, Yaoqing Shen, et al.Genetics|December 17, 2013
Genome destabilizing mutator alleles drive specific mutational trajectories in Saccharomyces cerevisiaePeter C Stirling, Yaoqing Shen, Richard Corbett, et al.Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
Hypermutation signature reveals a slippage and realignment model of translesion synthesis by Rev3 polymerase in cisplatin-treated yeastRomulo Segovia, Yaoqing Shen, Scott A Lujan, et al.Neurology. Genetics|January 3, 2024
Mitofusin 2 Variant Presenting With a Phenotype of Multiple System Atrophy of Cerebellar SubtypeAdrienne Elbert, Katherine Dixon, Yaoqing Shen, et al.Journal of Human Genetics|March 20, 2015
A novel mutation in EED associated with overgrowthAna S A Cohen, Beyhan Tuysuz, Yaoqing Shen, et al.Neuro-Oncology|August 7, 2015
Comparative genomic and genetic analysis of glioblastoma-derived brain tumor-initiating cells and their parent tumorsBrad Davis, Yaoqing Shen, Candice C Poon, et al.American Journal of Medical Genetics. Part A|November 26, 2021
An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?Hui-Lin Chin, Stephanie Huynh, Jahanshah Ashkani, et al.American Journal of Medical Genetics. Part A|February 5, 2022
Long-read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmiaPierre K Boerkoel, Katherine Dixon, Carrie Fitzsimons, et al.Cold Spring Harbor Molecular Case Studies|August 3, 2019
The pivotal role of sampling recurrent tumors in the precision care of patients with tumors of the central nervous systemDerek Wong, Yaoqing Shen, Adrian B Levine, et al.Journal of Medical Genetics|November 13, 2024
Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromesVahid Akbari, Sarah Dada, Yaoqing Shen, et al.Pageof 6