Rong Xiang (R Xiang)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 19

Top Topics

Hypertrophic Cardiomyopathy

Top Venues

BioMed research international

The journal of gene medicine

Translational neurodegeneration

QJM : monthly journal of the Association of Physicians

This page only lists publications with an associated author ORCID identifier.

Publications

Hao Huang, Rong Xiang, Riqiang Yan
Linking APOE4/4 genotype to microglial lipid droplets and neurotoxicity in Alzheimer's disease. Translational neurodegeneration 13 (1) (2024)
Hao Huang, Rong Xiang, Riqiang Yan
Linking APOE4/4 genotype to microglial lipid droplets and neurotoxicity in Alzheimer's disease. Translational neurodegeneration 13 (1) (2024)
Hao Huang, Rong Xiang, Riqiang Yan
Linking APOE4/4 genotype to microglial lipid droplets and neurotoxicity in Alzheimer's disease. Translational neurodegeneration 13 (1) (2024)
Yi-Lei Lu, Qin Wang, Min Wang, Si-Hua Chang, Ji-Qiang He, Rong Xiang, Ju-Yu Tang, Jie-Yuan Jin
Identification of A Novel Variant of Filamin A Destroying the Attraction Between Benzene Rings and Sulfhydryl in Developmental Dysplasia of the Hip. DNA and cell biology 42 (10) (2023)
Jie-Yuan Jin, Li-Yang Zhang, Shuai Guo, Ke Tang, Lei Zeng, Rong Xiang, Jie-Yu Liang
Genetic analysis combined with 3D-printing assistant surgery in diagnosis and treatment for an X-linked hypophosphatemia patient. Journal of clinical laboratory analysis 36 (3) (2022)
Liang-Liang Fan, Ran Du, Ji-Shi Liu, Jie-Yuan Jin, Chen-Yu Wang, Yi Dong, Wan-Xia He, Ri-Qiang Yan, Rong Xiang
Loss of RTN3 phenocopies chronic kidney disease and results in activation of the IGF2-JAK2 pathway in proximal tubular epithelial cells. Experimental & molecular medicine 54 (5) (2022)
J-Y Jin, L-P Wu, Y Dong, H-C Pi, H-F Wu, Rong Xiang
Identification of a novel GATA binding protein 5 variant (c.830C>T/p.P277L) damaging the nuclear translocation and causing tetralogy of Fallot. QJM : monthly journal of the Association of Physicians 115 (4) (2022)
Rong Xiang, Yuxing Liu, Liangliang Fan, Boyue Jiang, Fang Wang
RNA adenosine deaminase (ADAR1) alleviates high-fat diet-induced nonalcoholic fatty liver disease by inhibiting NLRP3 inflammasome. Laboratory investigation; a journal of technical methods and pathology 102 (10) (2022)
Yi Dong, Ran Du, Liang-Liang Fan, Jie-Yuan Jin, Hao Huang, Ya-Qin Chen, Dan-Dong Bi, Rong Xiang
Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block. BioMed research international 2021 (2021)
Hao Huang, Yaqin Chen, Jieyuan Jin, Ran Du, Ke Tang, Liang-Liang Fan, Rong Xiang
CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family. The journal of gene medicine (2021)
Bing-Bing Guo, Jie-Yuan Jin, Zhuang-Zhuang Yuan, Lei Zeng, Rong Xiang
A Novel COMP Mutated Allele Identified in a Chinese Family with Pseudoachondroplasia. BioMed research international 2021 (2021)
Jie-Yuan Jin, Dan-Yu Liu, Zi-Jun Jiao, Yi Dong, Jie Li, Rong Xiang
The Novel Compound Heterozygous Mutations of ECEL1 Identified in a Family with Distal Arthrogryposis Type 5D. BioMed research international 2020 (2020)
Jian-Xia Tang, Xiang-Shui Xiao, Kai Wang, Jie-Yuan Jin, Liang-Liang Fan, Rong Xiang
Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate. BioMed research international 2020 (2020)
Jie-Yuan Jin, Lei Zeng, Ke Li, Ji-Qiang He, Xiaoyang Pang, Hao Huang, Rong Xiang, Ju-Yu Tang
A novel mutation (c.1010G>T; p.R337L) in TP63 as a cause of split-hand/foot malformation with hypodontia. The journal of gene medicine 21 (10) (2019)
Liang-Liang Fan, Ji-Shi Liu, Hao Huang, Ran Du, Rong Xiang
Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis. The journal of gene medicine 21 (2-3) (2019)
Liang-Liang Fan, Ya-Qin Chen, Hao Huang, Zhuang-Zhuang Yuan, Jie-Yuan Jin, Min Hu, Rong Xiang
Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope. Journal of human genetics 64 (3) (2018)
Shuai Guo, Xue-Feng Fan, Jie-Yuan Jin, Liang-Liang Fan, Lei Zeng, Zheng-Bing Zhou, Rong Xiang, Ju-Yu Tang
A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel's deformity. Molecular cytogenetics 11 (2018)
Shu-Bing Zhang, Yu-Xing Liu, Liang-Liang Fan, Hao Huang, Jing-Jing Li, Jie-Yuan Jin, Rong Xiang
A novel heterozygous variant p.(Trp538Arg) of SYNM is identified by whole-exome sequencing in a Chinese family with dilated cardiomyopathy. Annals of human genetics 83 (2) (2018)
Hao Huang, Ya-Qin Chen, Liang-Liang Fan, Shuai Guo, Jing-Jing Li, Jie-Yuan Jin, Rong Xiang
Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death. Journal of cellular and molecular medicine 22 (2) (2017)