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Xiang-Ping Yao

Showing results (11-20 of 25) with videos related to

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Frontiers in Genetics|November 8, 2021
Mutation Analysis of <i>MYORG</i> in a Chinese Cohort With Primary Familial Brain CalcificationYi-Heng Zeng, Bi-Wei Lin, Hui-Zhen Su, et al.
Molecular Brain|July 23, 2022
Knockdown of myorg leads to brain calcification in zebrafishMiao Zhao, Xiao-Hong Lin, Yi-Heng Zeng, et al.
Journal of Human Genetics|March 17, 2017
Novel mutations of PDGFRB cause primary familial brain calcification in Chinese familiesChong Wang, Xiang-Ping Yao, Hai-Ting Chen, et al.
Gene|December 17, 2016
Mutation screening of PDGFB gene in Chinese population with primary familial brain calcificationXiang-Ping Yao, Chong- Wang, Hui-Zhen Su, et al.
Cell and Tissue Research|August 3, 2017
Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcificationXiang-Ping Yao, Miao Zhao, Chong Wang, et al.
Gene|August 14, 2013
Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcificationWan-Jin Chen, Xiang-Ping Yao, Qi-Jie Zhang, et al.
Infection and Drug Resistance|November 24, 2025
Exploring the Spectrum of Microbiota in Central Nervous System Infections Through Metagenomic Next-Generation SequencingJun-Mei Wang, Yu-Ying Pan, Jian-Chen Hong, et al.
Microbiology Spectrum|December 4, 2023
Systemic and cerebrospinal fluid biomarkers for tuberculous meningitis identification and treatment monitoringXiang-Ping Yao, Jian-Chen Hong, Zai-Jie Jiang, et al.
Clinical Genetics|March 21, 2019
Identification of SLC20A2 deletions in patients with primary familial brain calcificationXin-Xin Guo, Hui-Zhen Su, Xiao-Huan Zou, et al.
Annals of Clinical and Translational Neurology|November 1, 2024
Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutationJingjing Lin, Yun-Lu Li, Bo-Li Chen, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Frontiers in Genetics|November 8, 2021
Mutation Analysis of <i>MYORG</i> in a Chinese Cohort With Primary Familial Brain CalcificationYi-Heng Zeng, Bi-Wei Lin, Hui-Zhen Su, et al.
Molecular Brain|July 23, 2022
Knockdown of myorg leads to brain calcification in zebrafishMiao Zhao, Xiao-Hong Lin, Yi-Heng Zeng, et al.
Journal of Human Genetics|March 17, 2017
Novel mutations of PDGFRB cause primary familial brain calcification in Chinese familiesChong Wang, Xiang-Ping Yao, Hai-Ting Chen, et al.
Gene|December 17, 2016
Mutation screening of PDGFB gene in Chinese population with primary familial brain calcificationXiang-Ping Yao, Chong- Wang, Hui-Zhen Su, et al.
Cell and Tissue Research|August 3, 2017
Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcificationXiang-Ping Yao, Miao Zhao, Chong Wang, et al.
Gene|August 14, 2013
Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcificationWan-Jin Chen, Xiang-Ping Yao, Qi-Jie Zhang, et al.
Infection and Drug Resistance|November 24, 2025
Exploring the Spectrum of Microbiota in Central Nervous System Infections Through Metagenomic Next-Generation SequencingJun-Mei Wang, Yu-Ying Pan, Jian-Chen Hong, et al.
Microbiology Spectrum|December 4, 2023
Systemic and cerebrospinal fluid biomarkers for tuberculous meningitis identification and treatment monitoringXiang-Ping Yao, Jian-Chen Hong, Zai-Jie Jiang, et al.
Clinical Genetics|March 21, 2019
Identification of SLC20A2 deletions in patients with primary familial brain calcificationXin-Xin Guo, Hui-Zhen Su, Xiao-Huan Zou, et al.
Annals of Clinical and Translational Neurology|November 1, 2024
Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutationJingjing Lin, Yun-Lu Li, Bo-Li Chen, et al.
Pageof 3