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Human Genetics|July 29, 2015
Mutations in human IFT140 cause non-syndromic retinal degenerationMingchu Xu, Lizhu Yang, Feng Wang, et al.Retina (Philadelphia, Pa.)|August 23, 2018
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHYXuan Zou, Qing Fu, Sha Fang, et al.Genome Research|February 26, 2016
Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genesLi Zhao, Yiyun Chen, Amol Onkar Bajaj, et al.Investigative Ophthalmology & Visual Science|June 13, 2015
ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular InvolvementMingchu Xu, Violet Gelowani, Aiden Eblimit, et al.Cell Reports|April 5, 2018
Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer TypesZhongqi Ge, Jake S Leighton, Yumeng Wang, et al.NPJ Breast Cancer|May 10, 2022
Identification of biomarkers of response to preoperative talazoparib monotherapy in treatment naïve gBRCA+ breast cancersXuan Liu, Zhongqi Ge, Fei Yang, et al.JAMA Ophthalmology|June 4, 2016
Molecular and Clinical Findings in Patients With Knobloch SyndromeSarah Hull, Gavin Arno, Cristy A Ku, et al.Cell Reports|November 24, 2021
Reprogramming of H3K9bhb at regulatory elements is a key feature of fasting in the small intestineChristopher J Terranova, Kristina M Stemler, Praveen Barrodia, et al.Cell Reports|April 5, 2018
Molecular Characterization and Clinical Relevance of Metabolic Expression Subtypes in Human CancersXinxin Peng, Zhongyuan Chen, Farshad Farshidfar, et al.Nature Medicine|May 9, 2018
ARID1A deficiency promotes mutability and potentiates therapeutic antitumor immunity unleashed by immune checkpoint blockadeJianfeng Shen, Zhenlin Ju, Wei Zhao, et al.Pageof 4