Xian-ning Zhang

发表

Brief Research Communication Association Analysis of COMT Polymorphisms and Schizophrenia in a Chinese Han Population

A. Case-Control, Rui Yu, Xian-ning Zhang, 2007 .

Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: A case‐control study

Jicheng Li, Rui Yu, Xian-ning Zhang, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

CRISPR/Cas9-Mediated Treatment Ameliorates the Phenotype of the Epidermolytic Palmoplantar Keratoderma-like Mouse

Xian-ning Zhang, Xiao-Rui Luan, Xiao-ling Chen, 2018, Molecular therapy. Nucleic acids.

Genetic Analysis of RET, EDNRB, and EDN3 Genes and Three SNPs in MCS + 9.7 in Chinese Patients with Isolated Hirschsprung Disease

Jicheng Li, M. Qi, Y. Qiu, 2007, Biochemical Genetics.

Detection of somatic and germline mosaicism for the LAMP2 gene mutation c.808dupG in a Chinese family with Danon disease.

Xian-ning Zhang, Xiao-ling Chen, H. Ke, 2012, Gene.

KRT9 gene mutation as a reliable indicator in the prenatal molecular diagnosis of epidermolytic palmoplantar keratoderma.

Rong-Rong Liu, Xian-ning Zhang, Chenming Xu, 2014, Gene.

Correlation between human seizure-related gene 6 variants and idiopathic generalized epilepsy in a Southern Chinese Han population☆

Xian-ning Zhang, Yan Han, Jianming Jiang, 2012, Neural regeneration research.

p.N78S and p.R161Q germline mutations of the VHL gene are present in von Hippel-Lindau syndrome in two pedigrees.

Xian-ning Zhang, Xiao-ling Chen, Jinyu Li, 2013, Molecular medicine reports.

Genetic diagnosis of autosomal dominant polycystic kidney disease by targeted capture and next-generation sequencing: utility and limitations.

W. Dong, Zheng Su, Xian-ning Zhang, 2013, Gene.

A novel CRX mutation by whole-exome sequencing in an autosomal dominant cone-rod dystrophy pedigree.

Rong-Rong Liu, M. Fang, Jian-Guo Zhang, 2015, International journal of ophthalmology.

RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family

Jian-Guo Zhang, Xian-ning Zhang, Xiao-ling Chen, 2011, PloS one.

Eukaryotic translation initiation factor 5A2 regulates the migration and invasion of hepatocellular carcinoma cells via pathways involving reactive oxygen species

Rong-Rong Liu, Xian-ning Zhang, Xiaocui Zheng, 2016, Oncotarget.

102T/C SNP in the 5‐hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern han chinese populations: Lack of association

Xian-ning Zhang, San-duo Jiang, Li-na Zhang, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Recurrent FBN1 mutation (R62C) in a Chinese family with isolated ectopia lentis.

W. Zhou, Rui Yu, Xian-ning Zhang, 2006, American journal of ophthalmology.

Deletion analysis of SMN1 and NAIP genes in southern Chinese children with spinal muscular atrophy

Y. Liang, Xian-ning Zhang, Xiao-ling Chen, 2009, Journal of Zhejiang University SCIENCE B.

RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China.

Jun Cheng, Xian-ning Zhang, Xiao-ling Chen, 2012, Thyroid : official journal of the American Thyroid Association.

Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation.

Lei Shu, Xian-ning Zhang, Xiao-Xiao Huang, 2012, International journal of ophthalmology.

A Small Indel Mutant Mouse Model of Epidermolytic Palmoplantar Keratoderma and Its Application to Mutant-specific shRNA Therapy

Rong-Rong Liu, Jing Zhao, Xian-ning Zhang, 2016, Molecular therapy. Nucleic acids.

Mitochondrion and its related disorders: Making a comeback

M. Qi, Xian-ning Zhang, 2008, Journal of Zhejiang University SCIENCE B.

The Most Common Mutation of KRT9, c.C487T (p.R163W), in Epidermolytic Palmoplantar Keratoderma in Two Large Chinese Pedigrees

Xian-ning Zhang, Xiao-ling Chen, H. Ke, 2012, Anatomical record.

A novel mutation within the 2B rod domain of keratin 9 in a Chinese pedigree with epidermolytic palmoplantar keratoderma combined with knuckle pads and camptodactyly.

Wei Wei, Xian-ning Zhang, Chenming Xu, 2011, EJD. European journal of dermatology.

A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree.

Xian-ning Zhang, Chenming Xu, Xiao-ling Chen, 2010, Genetic testing and molecular biomarkers.

Evaluation of the ELOVL4 gene in a Chinese family with autosomal dominant STGD3‐like macular dystrophy

W. Zhou, Rui Yu, Xian-ning Zhang, 2005, Journal of cellular and molecular medicine.