Wang QK - 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: wang x, wang b, wang qk. 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: wang x, wang qk. Am J Ophthalmol. 2006 Aug;142(2):298-303. doi: 10.1016/j.ajo.2006.03.056. Am J Ophthalmol. 2006. PMID: 16876512

3

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

Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK. Liu M, et al. Among authors: wang x, wang z, wang t, wang qk. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6. doi: 10.1167/iovs.05-1438. Invest Ophthalmol Vis Sci. 2006. PMID: 16877416

4

A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families.

Wang X, Xiao F, Yang Q, Liang B, Tang Z, Jiang L, Zhu Q, Chang W, Jiang J, Jiang C, Ren X, Liu JY, Wang QK, Liu M. Wang X, et al. Among authors: wang qk. Am J Med Genet A. 2006 Sep 1;140A(17):1846-53. doi: 10.1002/ajmg.a.31372. Am J Med Genet A. 2006. PMID: 16892395

5

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. Among authors: wang x, wang qk. BMC Med Genet. 2007 Aug 8;8:52. doi: 10.1186/1471-2350-8-52. BMC Med Genet. 2007. PMID: 17686168 Free PMC article.

6

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

Chang W, Ding Q, Tang Z, Liu P, Jiang F, Ke T, Ren X, Wang Z, Liu J, Wang QK, Liu M. Chang W, et al. Among authors: wang z, wang qk. Mol Vis. 2007 Aug 30;13:1548-54. Mol Vis. 2007. PMID: 17893654

7

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

Li H, Li C, Lu Q, Su T, Ke T, Li DW, Yuan M, Liu J, Ren X, Zhang Z, Zeng S, Wang QK, Liu M. Li H, et al. Among authors: wang qk. Biochim Biophys Acta. 2008 May;1782(5):303-9. doi: 10.1016/j.bbadis.2008.01.011. Epub 2008 Feb 20. Biochim Biophys Acta. 2008. PMID: 18343237 Free article.

8

T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.

Zhang S, Wang L, Hao Y, Wang P, Hao P, Yin K, Wang QK, Liu M. Zhang S, et al. Among authors: wang l, wang p, wang qk. Mitochondrion. 2008 Jun;8(3):205-10. doi: 10.1016/j.mito.2008.02.003. Epub 2008 Mar 6. Mitochondrion. 2008. PMID: 18440284

9

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: wang qk. BMC Med Genet. 2008 Sep 23;9:87. doi: 10.1186/1471-2350-9-87. BMC Med Genet. 2008. PMID: 18808722 Free PMC article.

10

A novel mutation in the ATP2C1 gene is associated with Hailey-Hailey disease in a Chinese family.

Liu JZ, Yang T, Li X, Liu M, Wang QK, Liu JY. Liu JZ, et al. Among authors: wang qk. Int J Dermatol. 2009 Jan;48(1):47-51. doi: 10.1111/j.1365-4632.2009.03878.x. Int J Dermatol. 2009. PMID: 19126050

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