Zhang J - Search Results

1

Damaged Keratin Filament Network Caused by KRT5 Mutations in Localized Recessive Epidermolysis Bullosa Simplex.

Chen F, Yao L, Zhang X, Gu Y, Yu H, Yao Z, Zhang J, Li M. Chen F, et al. Among authors: zhang j, zhang x. Front Genet. 2021 Nov 29;12:736610. doi: 10.3389/fgene.2021.736610. eCollection 2021. Front Genet. 2021. PMID: 34912369 Free PMC article.

2

Genome sequence of a novel recombinant coxsackievirus a6 strain from shanghai, china, 2013.

Feng X, Guan W, Guo Y, Yu H, Zhang X, Cheng R, Wang Z, Zhang Z, Zhang J, Li H, Zhuang Y, Zhang H, Lu Z, Li M, Yu H, Bao Y, Hu Y, Yao Z. Feng X, et al. Among authors: zhang z, zhang j, zhang x, zhang h. Genome Announc. 2015 Jan 8;3(1):e01347-14. doi: 10.1128/genomeA.01347-14. Genome Announc. 2015. PMID: 25573929 Free PMC article.

3

Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population.

Zhang J, Tong H, Fu X, Zhang Y, Liu J, Cheng R, Liang J, Peng J, Sun Z, Liu H, Zhang F, Lu W, Li M, Yao Z. Zhang J, et al. Among authors: zhang f, zhang y. Sci Rep. 2015 Jun 9;5:11291. doi: 10.1038/srep11291. Sci Rep. 2015. PMID: 26056819 Free PMC article.

4

A novel recombinant lineage's contribution to the outbreak of coxsackievirus A6-associated hand, foot and mouth disease in Shanghai, China, 2012-2013.

Feng X, Guan W, Guo Y, Yu H, Zhang X, Cheng R, Wang Z, Zhang Z, Zhang J, Li H, Zhuang Y, Zhang H, Lu Z, Li M, Yu H, Bao Y, Hu Y, Yao Z. Feng X, et al. Among authors: zhang z, zhang j, zhang x, zhang h. Sci Rep. 2015 Jun 30;5:11700. doi: 10.1038/srep11700. Sci Rep. 2015. PMID: 26121916 Free PMC article.

5

Novel in-frame deletion mutation c.177_179delTAC of neurofibromatosis type 1 in a Chinese 4-year-old boy with binocular blindness.

Peng J, Zhang J, Zhang Q, Zhao PQ, Yao ZR. Peng J, et al. Among authors: zhang q, zhang j. Int J Ophthalmol. 2015 Oct 18;8(5):1078-9. doi: 10.3980/j.issn.2222-3959.2015.05.39. eCollection 2015. Int J Ophthalmol. 2015. PMID: 26558229 Free PMC article. No abstract available.

6

A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome.

Ni C, Yan M, Zhang J, Cheng R, Liang J, Deng D, Wang Z, Li M, Yao Z. Ni C, et al. Among authors: zhang j. Sci Rep. 2016 Feb 23;6:21815. doi: 10.1038/srep21815. Sci Rep. 2016. PMID: 26902751 Free PMC article.

7

Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.

Li M, Wang J, Li Z, Zhang J, Ni C, Cheng R, Yao Z. Li M, et al. Among authors: zhang j. Eur J Hum Genet. 2016 Aug;24(9):1367-70. doi: 10.1038/ejhg.2016.15. Epub 2016 Mar 2. Eur J Hum Genet. 2016. PMID: 26932190 Free PMC article.

8

[Molecular analysis of two pediatric cases with sporadic neurofibromatosis type 1].

Zhang J, Li M, Yao Z. Zhang J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):200-2. doi: 10.3760/cma.j.issn.1003-9406.2016.02.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27060315 Chinese.

9

Report of Chinese family with severe dermatitis, multiple allergies and metabolic wasting syndrome caused by novel homozygous desmoglein-1 gene mutation.

Cheng R, Yan M, Ni C, Zhang J, Li M, Yao Z. Cheng R, et al. Among authors: zhang j. J Dermatol. 2016 Oct;43(10):1201-1204. doi: 10.1111/1346-8138.13431. J Dermatol. 2016. PMID: 27154412

10

Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome.

Zhang J, Shen J, Cheng R, Ni C, Liang J, Li M, Yao Z. Zhang J, et al. Mol Med Rep. 2016 Sep;14(3):2639-43. doi: 10.3892/mmr.2016.5547. Epub 2016 Jul 27. Mol Med Rep. 2016. PMID: 27484170 Review.

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