Li C - Search Results

1

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: li c, li dw. 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.

2

Repression of MHC class I transcription by HPV16E7 through interaction with a putative RXRbeta motif and NF-kappaB cytoplasmic sequestration.

Li H, Zhan T, Li C, Liu M, Wang QK. Li H, et al. Among authors: li c. Biochem Biophys Res Commun. 2009 Oct 16;388(2):383-8. doi: 10.1016/j.bbrc.2009.08.019. Epub 2009 Aug 8. Biochem Biophys Res Commun. 2009. PMID: 19665994

3

Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family.

Liu X, Tang Z, Li C, Yang K, Gan G, Zhang Z, Liu J, Jiang F, Wang Q, Liu M. Liu X, et al. Among authors: li c. Mol Vis. 2010 Mar 17;16:454-61. doi: 10.1167/3.9.454. Mol Vis. 2010. PMID: 20309401 Free PMC article.

4

[Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema].

Sheng JQ, Zeng F, Li C, Liu JY, Wang Q, Liu MG. Sheng JQ, et al. Among authors: li c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):371-5. doi: 10.3760/cma.j.issn.1003-9406.2010.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20677139 Chinese.

5

Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa.

Huang Y, Zhang J, Li C, Yang G, Liu M, Wang QK, Tang Z. Huang Y, et al. Among authors: li c. BMC Med Genet. 2010 Aug 10;11:121. doi: 10.1186/1471-2350-11-121. BMC Med Genet. 2010. PMID: 20696082 Free PMC article.

6

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family.

Liu Y, Yu X, Wang L, Li C, Archacki S, Huang C, Liu JY, Wang Q, Liu M, Tang Z. Liu Y, et al. Among authors: li c. Gene. 2012 Jan 10;491(2):246-50. doi: 10.1016/j.gene.2011.10.009. Epub 2011 Oct 10. Gene. 2012. PMID: 22008666

7

HSF4 is involved in DNA damage repair through regulation of Rad51.

Cui X, Zhang J, Du R, Wang L, Archacki S, Zhang Y, Yuan M, Ke T, Li H, Li D, Li C, Li DW, Tang Z, Yin Z, Liu M. Cui X, et al. Among authors: li c, li d, li dw, li h. Biochim Biophys Acta. 2012 Aug;1822(8):1308-15. doi: 10.1016/j.bbadis.2012.05.005. Epub 2012 May 14. Biochim Biophys Acta. 2012. PMID: 22587838 Free article.

8

HSF4 regulates DLAD expression and promotes lens de-nucleation.

Cui X, Wang L, Zhang J, Du R, Liao S, Li D, Li C, Ke T, Li DW, Huang H, Yin Z, Tang Z, Liu M. Cui X, et al. Among authors: li c, li d, li dw. Biochim Biophys Acta. 2013 Aug;1832(8):1167-72. doi: 10.1016/j.bbadis.2013.03.007. Epub 2013 Mar 16. Biochim Biophys Acta. 2013. PMID: 23507146 Free article.

9

Mutations in ABCB6 cause dyschromatosis universalis hereditaria.

Zhang C, Li D, Zhang J, Chen X, Huang M, Archacki S, Tian Y, Ren W, Mei A, Zhang Q, Fang M, Su Z, Yin Y, Liu D, Chen Y, Cui X, Li C, Yang H, Wang Q, Wang J, Liu M, Deng Y. Zhang C, et al. Among authors: li c, li d. J Invest Dermatol. 2013 Sep;133(9):2221-8. doi: 10.1038/jid.2013.145. Epub 2013 Mar 21. J Invest Dermatol. 2013. PMID: 23519333 Free article.

10

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.

Liu F, Li P, Liu Y, Li W, Wong F, Du R, Wang L, Li C, Jiang F, Tang Z, Liu M. Liu F, et al. Among authors: li c, li w, li p. Mol Vis. 2013;19:695-701. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559863 Free PMC article.

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