Xiang-Ping Yao

发表

Knock-down Sox5 suppresses porcine adipogenesis through BMP R-Smads signal pathway.

Gongshe Yang, Ying Peng, Xin-e Shi, 2020, Biochemical and biophysical research communications.

Knockdown of myorg leads to brain calcification in zebrafish

Wanjin Chen, Miao Zhao, Chong Wang, 2022, Molecular Brain.

Mutation screening of PDGFB gene in Chinese population with primary familial brain calcification.

Wanjin Chen, Ning Wang, Xin-Xin Guo, 2017, Gene.

Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification

Wanjin Chen, Ning Wang, Xin-Xin Guo, 2017, Cell and Tissue Research.

Noninvasive urine-derived cell lines derived from neurological genetic patients

Wanjin Chen, Min-ting Lin, S. Murong, 2013, Neuroreport.

Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families

Wanjin Chen, Ning Wang, Xin-Xin Guo, 2017, Journal of Human Genetics.

Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

Z. Xiong, Ning Wang, Hongjie Yu, 2018, Neuron.

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

S. Murong, Ning Wang, W. Ni, 2013, Gene.

Advances in gene therapy for neurogenetic diseases: a brief review

Miao Zhao, Xiang-Ping Yao, Yi-Kun Chen, 2021, Journal of Molecular Medicine.

Identification of SLC20A2 deletions in patients with primary familial brain calcification

Ning Wang, Xin-Xin Guo, Jie Lin, 2019, Clinical genetics.

Mutation Analysis of MYORG in a Chinese Cohort With Primary Familial Brain Calcification

Xin-Xin Guo, Miao Zhao, Yun-Lu Li, 2021, Frontiers in Genetics.

Idiopathic basal ganglia calcification associated with new MYORG mutation site: A case report

Jing Ding, Xin Wang, Hui-Zhen Su, 2021, World journal of clinical cases.

Loss of function of CMPK2 causes mitochondria deficiency and brain calcification

Z. Xiong, Min-ting Lin, C. Liou, 2022, Cell Discovery.

Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification

Ning Wang, Xin-Xin Guo, Q. Yao, 2019, Human mutation.

Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification

Ning Wang, Xin-Xin Guo, Miao Zhao, 2017, Cell and Tissue Research.

[Construction of a striatum-specific Slc20a2 gene knockout mice model by CRISPR/Cas9 AAV system].

Min-ting Lin, Miao Zhao, Lu-Lu Lai, 2020, Yi chuan = Hereditas.

Astrocytes modulate brain phosphate homeostasis via polarized distribution of phosphate uptake transporter PiT2 and exporter XPR1

Yong-Chuan Zhu, Miao Zhao, Xiang-Ping Yao, 2024, Neuron.