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Journal of Human Genetics|January 13, 2017
Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated casesXiaomei Luo, Yongyi Zou, Bo Tan, et al.
Plos One|December 2, 2016
The Effects of Irreversible Electroporation on the Colon in a Porcine ModelXiaomei Luo, Xianjun Liang, Jiannan Li, et al.
Biochemical Pharmacology|May 14, 2026
Dual-targeting evodiamine analogue overcomes pancreatic cancer immunotherapy resistance by inducing immunogenic cell deathXiaomei Luo, Changling Yang, Xiaoting Chen, et al.
Neuroimage. Clinical|October 5, 2018
Disruption of superficial white matter in the emotion regulation network in bipolar disorderShufei Zhang, Ying Wang, Feng Deng, et al.
The Journal of Clinical Endocrinology and Metabolism|July 25, 2024
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency CohortRuifang Wang, Xiaomei Luo, Yu Sun, et al.
Journal of Human Genetics|January 15, 2016
A novel de novo POGZ mutation in a patient with intellectual disabilityBo Tan, Yongyi Zou, Yue Zhang, et al.
The Journal of Molecular Diagnostics : JMD|July 25, 2025
Additional Diagnostic Yield through the Analysis of Short Tandem Repeats Based on Exome Sequencing DataShiyi Xu, Xiaomei Luo, Bing Xiao, et al.
Clinical Chemistry|February 8, 2020
High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective StudyYu Sun, Xiantao Ye, Yanjie Fan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 5, 2026
Low-Dose AAV9-SMN1 with CNS-Selective Expression Delivers Efficacy and Favorable Safety in Spinal Muscular AtrophyYongguo Yu, Xiji Qin, Mengxia Jing, et al.
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