Jingyu Liu

发表

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family

Mugen Liu, Stephen Archacki, Zhao-hui Tang, 2011, Neuroscience Letters.

Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

Qinbo Yang, Mugen Liu, T. Ke, 2006, Investigative ophthalmology & visual science.

CERKL regulates autophagy via the NAD-dependent deacetylase SIRT1

Fei Liu, Tao Jiang, X. Shu, 2018, Autophagy.

Heterogeneity of clinical features and mutation analysis of NTRK1 in Han Chinese patients with congenital insensitivity to pain with anhidrosis

Guangyou Duan, Jiaoli Sun, Jingyu Liu, 2019, Journal of pain research.

Cataract mutation P20S of alphaB-crystallin impairs chaperone activity of alphaA-crystallin and induces apoptosis of human lens epithelial cells.

Mugen Liu, T. Ke, Chang Li, 2008, Biochimica et biophysica acta.

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

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

Cataract mutation P20S of (cid:11) B-crystallin impairs chaperone activity of (cid:11) A-crystallin and induces apoptosis of human lens epithelial cells

Mugen Liu, T. Ke, Chang Li, 2018 .

A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family

Mugen Liu, Chengqi Xu, Q. Wang, 2007, BMC Medical Genetics.

Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.

H. Shang, T. Ashizawa, Baorong Zhang, 2017, Brain : a journal of neurology.

Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population

Dan Wang, Xin Tu, Lisong Shi, 2009, Human Genetics.

Exosomes from patients with Parkinson’s disease are pathological in mice

Zhentao Zhang, Ling Liu, N. Xiong, 2019, Journal of Molecular Medicine.

Molecular genetic analysis of partial 9p trisomy in two Chinese families with mental retardation and facial anomaly

Ai-ping Feng, N. Zhang, Jingyu Liu, 2011, 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.

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

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

Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.

Qing Wang, Mugen Liu, Ping Liu, 2008, Journal of genetics and genomics = Yi chuan xue bao.

(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.

H. Shang, T. Klockgether, T. Ashizawa, 2016, Brain : a journal of neurology.

A novel de novo frameshift mutation of RPGR ORF15 is associated with X-linked retinitis pigmentosa in a Chinese family.

Mugen Liu, T. Ke, Zhao-hui Tang, 2007, Molecular vision.

Identification of a novel NOG mutation in a Chinese family with proximal symphalangism.

Zhen Qu, Zhao-hui Tang, Chang Li, 2014, Clinica chimica acta; international journal of clinical chemistry.

Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation

Y. Liu, Yi Xiao, Mugen Liu, 2018, Scientific Reports.