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Plos One|April 26, 2014
Molecular diagnosis of putative Stargardt disease by capture next generation sequencingXiao Zhang, Xianglian Ge, Wei Shi, et al.
Scientific Reports|November 7, 2014
A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese familyLiping Zhang, Wei Shi, Liming Song, et al.
Signal Transduction and Targeted Therapy|August 15, 2023
CDK7-YAP-LDHD axis promotes D-lactate elimination and ferroptosis defense to support cancer stem cell-like propertiesMengzhu Lv, Ying Gong, Xuesong Liu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 6, 2025
Loss of MNX1 Sensitizes Tumors to Cytotoxic T Cells by Degradation of PD-L1 mRNAZhengzheng Li, Lei Chen, Ge Zhang, et al.
Medical Review (2021)|June 26, 2024
Genomic characterization and risk stratification of esophageal squamous dysplasiaQingjie Min, Min Zhang, Dongmei Lin, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|November 6, 2018
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencingJinyu Wu, Ping Yu, Xin Jin, et al.
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