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Xian-Ning Zhang

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Publications

TOP 3
Wei-zhen Xu; Yan Zhao; Chun-yue Chen; Xiao-ling Chen; Zhen-fang Du; Wen-ting Liu; Xian-Ning Zhang
A novel de novo mutation of the Nipped-B-like gene in an isolated Chinese patient with Cornelia de Lange syndrome.
Xiao-Ling Chen; Zhen-Fang Du; Hai-Ping Ke; Wen-Ting Liu; Yan Zhao; Xian-Ning Zhang
Detection of somatic and germline mosaicism for the LAMP2 gene mutation c.808dupG in a Chinese family with Danon disease.
Zhen-Fang Du; Hong Fang; Hai-Ping Ke; Wen-Ting Liu; Chen-Ming Xu; Chun-Yue Chen; Xiao-Ling Chen; Yan Zhao; Xian-Ning Zhang
Two novel de novo mutations of KRT6A and KRT16 genes in two Chinese pachyonychia congenita pedigrees with fissured tongue or diffuse plantar keratoderma.

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All Publications

2013: Wei-zhen Xu; Yan Zhao; Chun-yue Chen; Xiao-ling Chen; Zhen-fang Du; Wen-ting Liu; Xian-Ning Zhang
A novel de novo mutation of the Nipped-B-like gene in an isolated Chinese patient with Cornelia de Lange syndrome.
Chinese medical journal 2013;126(1):191-2.
2012: Xiao-Ling Chen; Zhen-Fang Du; Hai-Ping Ke; Wen-Ting Liu; Yan Zhao; Xian-Ning Zhang
Detection of somatic and germline mosaicism for the LAMP2 gene mutation c.808dupG in a Chinese family with Danon disease.
Gene 2012;507(2):174-6.
2012: Zhen-Fang Du; Hong Fang; Hai-Ping Ke; Wen-Ting Liu; Chen-Ming Xu; Chun-Yue Chen; Xiao-Ling Chen; Yan Zhao; Xian-Ning Zhang
Two novel de novo mutations of KRT6A and KRT16 genes in two Chinese pachyonychia congenita pedigrees with fissured tongue or diffuse plantar keratoderma.
European journal of dermatology : EJD 2012;22(4):476-80.
2012: Wen-Ting Liu; Jia-Jun Lu; Dan Yu; Xiao-Ling Chen; Zheng-Fang Du; Hai-Ping Ke; Yan Zhao; Xian-Ning Zhang
The most common mutation of KRT9, c.C487T (p.R163W), in epidermolytic palmoplantar keratoderma in two large Chinese pedigrees.
Anatomical record (Hoboken, N.J. : 2007) 2012;295(4):604-9.
2012: Lei Shu; Chun-Yue Chen; Xiao-Xiao Huang; Yong-Ming Zhang; Xian-Ning Zhang
Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation.
International journal of ophthalmology 2012;5(1):28-31.
2011: Zhen-Fang Du; Hong Fang; Wen-Ting Liu; Jia-Jun Lu; Lian-Gen Mao; Yi-Fan Wang; Wei Wei; Chen-Ming Xu; Chun-Yue Chen; Xiao-Ling Chen; Xian-Ning Zhang
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.
European journal of dermatology : EJD 2011;21(5):675-9.
2011: Xiao-Ping Qi; Jin-Quan Wang; Rong-Biao Ying; Jian-Guo Zhang; Chun-Yue Chen; Xiao-Ling Chen; Zhen-Fang Du; Jun Fei; Jian-Shan Han; Hang-Yang Jin; Wen-Ting Liu; Jia-Jun Lu; Ju-Ming Ma; Xian-Ning Zhang
RET germline mutations identified by exome sequencing in a Chinese multiple endocrine neoplasia type 2A/familial medullary thyroid carcinoma family.
PloS one 2011;6(5):e20353.
2010: Chun-Yue Chen; Chen-Ming Xu; Zhen-Fang Du; Xiao-Ling Chen; Guo-Liang Ren; Xian-Ning Zhang
A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree.
Genetic testing and molecular biomarkers 2010;14(2):193-6.
2009: Xian-Ning Zhang; Lou-Yang Qi; Da-Yuan Zhu; Yi-Jia Lou
[Effect of concanavalin A on expression of MAPEG mRNA in Balb/c mouse brain].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2009;38(3):255-9.
2009: Yu-hua Liang; Xiao-ling Chen; Zhong-sheng Yu; Chun-yue Chen; Sheng Bi; Lian-gen Mao; Bo-lin Zhou; Xian-Ning Zhang
Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy.
Journal of Zhejiang University. Science. B 2009;10(1):29-34.
2008: Xian-Ning Zhang; Ming Qi
Mitochondrion and its related disorders: making a comeback.
Journal of Zhejiang University. Science. B 2008;9(2):90-2.
2007: Xian-Ning Zhang; Miao-ni Zhou; Yun-Qing Qiu; Shi-Ping Ding; Ming Qi; Ji Cheng Li
Genetic analysis of RET, EDNRB, and EDN3 genes and three SNPs in MCS + 9.7 in Chinese Patients with isolated Hirschsprung disease.
Biochemical genetics 2007;45(7-8):523-7.
2007: Rui Yu; Xian-Ning Zhang; Xiao-Xiao Huang; Shi-Ping Ding; Ji Cheng Li
Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: a case-control study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(4):570-3.
2007: Xian-Ning Zhang; Huan-huan Wang; Zhi-qiang Wang
[Protective effect of icaritin on apoptosis of primarily cultured rat neurons induced by Abeta25-35 peptide].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2007;36(3):224-8.
2007: Da-Yuan Zhu; Xian-Ning Zhang; Yue Du
[Directed differentiation of mouse embryonic stem cells into neuronal cells induced by icaritin in vitro].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2007;36(3):217-23.
2007: Dong-Dong Ti; Xian-Ning Zhang
[Research advances in human mitochondrial DNA with aging and degenerative diseases].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2007;36(1):93-7.
2006: Rui Yu; Zheng Lai; Wei Zhou; Dong-Dong Ti; Xian-Ning Zhang
Recurrent FBN1 mutation (R62C) in a Chinese family with isolated ectopia lentis.
American journal of ophthalmology 2006;141(6):1136-8.
2006: Jun-Ming Guo; Bing-Xiu Xiao; G Z Kang; Dong-Hai Liu; H Chen; Shun Zhang; Xian-Ning Zhang
Suppression of telomerase activity and arrest at G1 phase in human cervical cancer HeLa cells by all-trans retinoic acid.
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2006;16(1):341-6.
2005: Zheng Lai; Xian-Ning Zhang; Wei Zhou; Rui Yu; Yan-Ping Le
Evaluation of the ELOVL4 gene in a Chinese family with autosomal dominant STGD3-like macular dystrophy.
Journal of cellular and molecular medicine 2005;9(4):961-5.
2005: Xian-Ning Zhang; Xin-hui He; Ji Cheng Li
[PCR products with heterozygous mutations containing two types of heteroduplexes].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2005;34(5):417-20.
2005: Xian-Ning Zhang; Xin-Hui He; Z Lai; W-G Yin; Yan-ping Le; Jun-Ming Guo; Wei Mao; X-L He; J-C Li
An insertion-deletion mutation in keratin 9 in three Chinese families with epidermolytic palmoplantar keratoderma.
The British journal of dermatology 2005;152(4):804-6.
2004: Xian-Ning Zhang; Wei Mao; Xin-hui He; Zheng Lai
[Present status of the molecular genetics in epidermolytic palmoplantar keratoderma].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2004;21(4):372-5.
2004: Xin-Hui He; Xian-Ning Zhang; Wei Mao; H-P Chen; L-R Xu; H Chen; X-L He; Yan-ping Le
A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.
The British journal of dermatology 2004;150(4):647-51.
2004: Xian-Ning Zhang; San-Duo Jiang; Xin-Hui He; Li-Na Zhang
102T/C SNP in the 5-hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern Han Chinese populations: lack of association.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;126B(1):16-8.
2003: Xian-Ning Zhang; Lie-min Ruan; Yan-ping Le; Ye Zhang
[Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2003;20(4):322-4.