Zhang X - Search Results

1

Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation.

Zhang X, Bogunovic D, Payelle-Brogard B, Francois-Newton V, Speer SD, Yuan C, Volpi S, Li Z, Sanal O, Mansouri D, Tezcan I, Rice GI, Chen C, Mansouri N, Mahdaviani SA, Itan Y, Boisson B, Okada S, Zeng L, Wang X, Jiang H, Liu W, Han T, Liu D, Ma T, Wang B, Liu M, Liu JY, Wang QK, Yalnizoglu D, Radoshevich L, Uzé G, Gros P, Rozenberg F, Zhang SY, Jouanguy E, Bustamante J, García-Sastre A, Abel L, Lebon P, Notarangelo LD, Crow YJ, Boisson-Dupuis S, Casanova JL, Pellegrini S. Zhang X, et al. Among authors: zhang sy. Nature. 2015 Jan 1;517(7532):89-93. doi: 10.1038/nature13801. Epub 2014 Oct 12. Nature. 2015. PMID: 25307056 Free PMC article.

2

Novel HSF4 mutation causes congenital total white cataract in a Chinese family.

Ke T, Wang QK, Ji B, Wang X, Liu P, Zhang X, Tang Z, Ren X, Liu M. Ke T, et al. Among authors: zhang x. Am J Ophthalmol. 2006 Aug;142(2):298-303. doi: 10.1016/j.ajo.2006.03.056. Am J Ophthalmol. 2006. PMID: 16876512

3

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

Zhang XQ, Peng JH, Tang ZH, Xu CQ, Zhou X, Gong SX, Liu JY, Wang Q, Liu MG. Zhang XQ, et al. Yi Chuan Xue Bao. 2006 Aug;33(8):685-91. doi: 10.1016/S0379-4172(06)60100-5. Yi Chuan Xue Bao. 2006. PMID: 16939002

4

A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.

Zhang X, Chen L, Liu J, Zhao Z, Qu E, Wang X, Chang W, Xu C, Wang QK, Liu M. Zhang X, et al. BMC Med Genet. 2007 Aug 8;8:52. doi: 10.1186/1471-2350-8-52. BMC Med Genet. 2007. PMID: 17686168 Free PMC article.

5

Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.

Zhang X, Chen S, Zhang L, Liu M, Redfearn S, Bryant RM, Oberti C, Vincent GM, Wang QK. Zhang X, et al. Among authors: zhang l. BMC Med Genet. 2008 Sep 23;9:87. doi: 10.1186/1471-2350-9-87. BMC Med Genet. 2008. PMID: 18808722 Free PMC article.

6

Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype.

Wu X, Wang QK, Gui L, Liu M, Zhang X, Jin R, Li W, Yan L, Du R, Wang Q, Zhu J, Yang J. Wu X, et al. Among authors: zhang x. J Huazhong Univ Sci Technolog Med Sci. 2010 Feb;30(1):103-7. doi: 10.1007/s11596-010-0119-z. Epub 2010 Feb 14. J Huazhong Univ Sci Technolog Med Sci. 2010. PMID: 20155465

7

Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population.

Wang F, Xu CQ, He Q, Cai JP, Li XC, Wang D, Xiong X, Liao YH, Zeng QT, Yang YZ, Cheng X, Li C, Yang R, Wang CC, Wu G, Lu QL, Bai Y, Huang YF, Yin D, Yang Q, Wang XJ, Dai DP, Zhang RF, Wan J, Ren JH, Li SS, Zhao YY, Fu FF, Huang Y, Li QX, Shi SW, Lin N, Pan ZW, Li Y, Yu B, Wu YX, Ke YH, Lei J, Wang N, Luo CY, Ji LY, Gao LJ, Li L, Liu H, Huang EW, Cui J, Jia N, Ren X, Li H, Ke T, Zhang XQ, Liu JY, Liu MG, Xia H, Yang B, Shi LS, Xia YL, Tu X, Wang QK. Wang F, et al. Among authors: zhang rf, zhang xq. Nat Genet. 2011 Mar 6;43(4):345-9. doi: 10.1038/ng.783. Nat Genet. 2011. PMID: 21378986

8

A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family.

Zeng L, Liu W, Feng W, Wang X, Dang H, Gao L, Yao J, Zhang X. Zeng L, et al. Among authors: zhang x. Mol Vis. 2013 Nov 14;19:2244-9. eCollection 2013. Mol Vis. 2013. PMID: 24319327 Free PMC article.

9

A novel RAB7 mutation in a Chinese family with Charcot-Marie-Tooth type 2B disease.

Wang X, Han C, Liu W, Wang P, Zhang X. Wang X, et al. Among authors: zhang x. Gene. 2014 Jan 25;534(2):431-4. Gene. 2014. PMID: 24498653

10

A novel MIP mutation in a Chinese family with congenital cataract.

Yuan C, Han T, Su P, Liu M, Zhou X, Zhang D, Jia W, Wang A, Yue M, Xiang Z, Chen L, Zhang X. Yuan C, et al. Among authors: zhang d, zhang x. Ophthalmic Genet. 2018 Aug;39(4):473-476. doi: 10.1080/13816810.2018.1484930. Ophthalmic Genet. 2018. PMID: 29947569

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