Li W - Search Results

1

Genetic analyses of Chinese patients with digenic oculocutaneous albinism.

Wei AH, Yang XM, Lian S, Li W. Wei AH, et al. Among authors: li w. Chin Med J (Engl). 2013 Jan;126(2):226-30. Chin Med J (Engl). 2013. PMID: 23324268

2

Four novel mutations of TYR gene in Chinese OCA1 patients.

Wang Y, Guo X, Li W, Lian S. Wang Y, et al. Among authors: li w. J Dermatol Sci. 2009 Jan;53(1):80-1. doi: 10.1016/j.jdermsci.2008.07.002. Epub 2008 Aug 12. J Dermatol Sci. 2009. PMID: 18701257 No abstract available.

3

The first case report of a Chinese Hermansky-Pudlak syndrome patient with a novel mutation on HPS1 gene.

Wei A, Lian S, Wang L, Li W. Wei A, et al. Among authors: li w. J Dermatol Sci. 2009 Nov;56(2):130-2. doi: 10.1016/j.jdermsci.2009.07.007. Epub 2009 Aug 7. J Dermatol Sci. 2009. PMID: 19665357 No abstract available.

4

A comprehensive analysis reveals mutational spectra and common alleles in Chinese patients with oculocutaneous albinism.

Wei A, Wang Y, Long Y, Wang Y, Guo X, Zhou Z, Zhu W, Liu J, Bian X, Lian S, Li W. Wei A, et al. Among authors: li w. J Invest Dermatol. 2010 Mar;130(3):716-24. doi: 10.1038/jid.2009.339. Epub 2009 Oct 29. J Invest Dermatol. 2010. PMID: 19865097 Free article.

5

Implementation of an optimized strategy for genetic testing of the Chinese patients with oculocutaneous albinism.

Wei A, Yang X, Lian S, Li W. Wei A, et al. Among authors: li w. J Dermatol Sci. 2011 May;62(2):124-7. doi: 10.1016/j.jdermsci.2011.02.009. Epub 2011 Mar 5. J Dermatol Sci. 2011. PMID: 21458243

6

The BLOS1-interacting protein KXD1 is involved in the biogenesis of lysosome-related organelles.

Yang Q, He X, Yang L, Zhou Z, Cullinane AR, Wei A, Zhang Z, Hao Z, Zhang A, He M, Feng Y, Gao X, Gahl WA, Huizing M, Li W. Yang Q, et al. Among authors: li w. Traffic. 2012 Aug;13(8):1160-9. doi: 10.1111/j.1600-0854.2012.01375.x. Epub 2012 May 28. Traffic. 2012. PMID: 22554196 Free PMC article.

7

Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis.

Wei AH, Li W. Wei AH, et al. Among authors: li w. Pigment Cell Melanoma Res. 2013 Mar;26(2):176-92. doi: 10.1111/pcmr.12051. Epub 2012 Dec 31. Pigment Cell Melanoma Res. 2013. PMID: 23171219 Review.

8

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.

Wei AH, Zang DJ, Zhang Z, Liu XZ, He X, Yang L, Wang Y, Zhou ZY, Zhang MR, Dai LL, Yang XM, Li W. Wei AH, et al. Among authors: li w. J Invest Dermatol. 2013 Jul;133(7):1834-40. doi: 10.1038/jid.2013.49. Epub 2013 Jan 30. J Invest Dermatol. 2013. PMID: 23364476 Free article.

9

Hypopigmentation in Hermansky-Pudlak syndrome.

Wei AH, He X, Li W. Wei AH, et al. Among authors: li w. J Dermatol. 2013 May;40(5):325-9. doi: 10.1111/1346-8138.12025. J Dermatol. 2013. PMID: 23668540 Review.

10

Increasing the complexity: new genes and new types of albinism.

Montoliu L, Grønskov K, Wei AH, Martínez-García M, Fernández A, Arveiler B, Morice-Picard F, Riazuddin S, Suzuki T, Ahmed ZM, Rosenberg T, Li W. Montoliu L, et al. Among authors: li w. Pigment Cell Melanoma Res. 2014 Jan;27(1):11-8. doi: 10.1111/pcmr.12167. Epub 2013 Oct 17. Pigment Cell Melanoma Res. 2014. PMID: 24066960 Review.

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