Showing results (111-120 of 143) with videos related to
Sort By:
Pageof 15
Clinical Genetics|March 21, 2019
ATP1A3 mosaicism in families with alternating hemiplegia of childhoodXiaoling Yang, Xiaoxu Yang, Jiaoyang Chen, et al.Hepatology Communications|September 1, 2023
The S100 calcium-binding protein A6 plays a crucial role in hepatic steatosis by mediating lipophagyQian Du, Tingting Zhu, Guorong Wen, et al.Neurological Research|July 14, 2020
Arterial spin labeling-MR may be an alternative to SPECT for evaluating cerebral perfusion in patients with unilateral middle cerebral artery stenosisJingyuan Ya, Da Zhou, Jiayue Ding, et al.International Journal of Molecular Sciences|December 4, 2015
ITSN2L Interacts with and Negatively Regulates RABEP1Xiaoxu Yang, Feng Yan, Zhicheng He, et al.Cell Transplantation|March 31, 2010
Shotgun proteomics and network analysis between plasma membrane and extracellular matrix proteins from rat olfactory ensheathing cellsYisong Liu, Xiaohua Teng, Xiaoxu Yang, et al.Human Mutation|June 23, 2015
Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet SyndromeXiaojing Xu, Xiaoxu Yang, Qixi Wu, et al.Database : the Journal of Biological Databases and Curation|October 20, 2018
AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorderChanghong Yang, Jiarui Li, Qixi Wu, et al.Biorxiv : the Preprint Server for Biology|November 14, 2023
Cell-type-resolved somatic mosaicism reveals clonal dynamics of the human forebrainChanguk Chung, Xiaoxu Yang, Robert F Hevner, et al.Brain : a Journal of Neurology|October 25, 2021
Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardationLeonie von Elsner, Guoliang Chai, Pauline E Schneeberger, et al.Journal of Medical Genetics|October 7, 2019
Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephalyShereen Georges Ghosh, Lu Wang, Martin W Breuss, et al.Pageof 15