Zhao-hui Tang

Ling Liu, Zhao-hui Tang, Qing Zhang, 2015, Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban.

Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.

Mugen Liu, X. Tu, Xu Wang, 2008, Biochemical and biophysical research communications.

Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese family.

Qing Wang, Mugen Liu, Zhao-hui Tang, 2006, Yi chuan xue bao = Acta genetica Sinica.

Knockout of Nr2e3 prevents rod photoreceptor differentiation and leads to selective L-/M-cone photoreceptor degeneration in zebrafish.

Tao Jiang, X. Shu, Mugen Liu, 2019, Biochimica et biophysica acta. Molecular basis of disease.

HSF4 promotes G1/S arrest in human lens epithelial cells by stabilizing p53.

Fei Liu, Mugen Liu, Meng Gao, 2015, Biochimica et biophysica acta.

A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family

Mugen Liu, Xu Wang, Zhao-hui Tang, 2006, Journal of Human Genetics.

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family

Ping Liu, Mugen Liu, T. Ke, 2005, Journal of Molecular Medicine.

Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking.

Mugen Liu, Yuwen Huang, Shanshan Yu, 2019, Biochimica et biophysica acta. Molecular basis of disease.

Mutation c.359_363delGTATTinsATAC in the COL4A5 causes Alport syndrome in a Chinese family.

Qing Wang, Mugen Liu, Zhao-hui Tang, 2013, Gene.

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family.

Changzheng Huang, Qing Wang, Mugen Liu, 2012, Gene.

A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome

Fei Liu, Mugen Liu, Yuwen Huang, 2020, Molecular vision.

Mucolipidosis in a Chinese family with compound heterozygous mutations at the GNPTAB gene.

Mugen Liu, Zhao-hui Tang, Xiukun Cui, 2011, Clinica chimica acta; international journal of clinical chemistry.

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1

Y. Liu, Mugen Liu, Zhao-hui Tang, 2013, Molecular vision.

Prpf31 is essential for the survival and differentiation of retinal progenitor cells by modulating alternative splicing

Fei Liu, X. Shu, Mugen Liu, 2021, Nucleic acids research.

Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration

Fei Liu, X. Shu, Mugen Liu, 2019, The Journal of Biological Chemistry.

Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family

Qing Wang, Mugen Liu, Zhao-hui Tang, 2010, Molecular vision.

BCAS2 is essential for hematopoietic stem and progenitor cell maintenance during zebrafish embryogenesis.

Tao Jiang, Mugen Liu, Daji Luo, 2019, Blood.

Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy

Fei Liu, Tao Jiang, D. Soares, 2017, Scientific Reports.

Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa

Guohua Yang, Mugen Liu, Zhao-hui Tang, 2010, BMC Medical Genetics.

The chromatin remodeler Brg1 is required for formation and maintenance of hematopoietic stem cells

X. Shu, Mugen Liu, H. Jia, 2020, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Loss-of-function Mutation in PMVK Causes Autosomal Dominant Disseminated Superficial Porokeratosis

Changzheng Huang, Mugen Liu, Meng Gao, 2016, Scientific Reports.

Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration

Fei Liu, X. Shu, Mugen Liu, 2022, PLoS genetics.

Rod-genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor compositions and progressive retinal degeneration

X. Shu, Mugen Liu, Daji Luo, 2021, bioRxiv.

Knockout of RP2 decreases GRK1 and rod transducin subunits and leads to photoreceptor degeneration in zebrafish.

X. Shu, Mugen Liu, S. Liao, 2015, Human molecular genetics.

Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa

Fei Liu, Y. Liu, Mugen Liu, 2016, Molecular vision.

Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.

Qing Wang, Mugen Liu, Zhao-hui Tang, 2006, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Knockout of RP 2 decreases GRK 1 and rod transducin subunits and leads to photoreceptor degeneration in zebra fi sh

X. Shu, Mugen Liu, S. Liao, 2015 .

A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families

Qinbo Yang, Qing Wang, Mugen Liu, 2006, American journal of medical genetics. Part A.

Retinal degeneration in rpgra mutant zebrafish

Fei Liu, Mugen Liu, Yuwen Huang, 2023, Frontiers in Cell and Developmental Biology.

Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy

Fei Liu, Tao Jiang, Mugen Liu, 2018, Human Genetics.

Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafish

Tao Jiang, X. Shu, D. Soares, 2017, The Journal of Biological Chemistry.

Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese family.

Mugen Liu, T. Ke, Zhao-hui Tang, 2009, Archives of ophthalmology.