Shao MH - Search Results

1

[Mutation analysis of ATP2C1 gene in a Chinese family with Hailey-Hailey disease].

Zhang GL, Sun YT, Shi HJ, Gu Y, Shao MH, Du XF. Zhang GL, et al. Among authors: shao mh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):414-6. doi: 10.3760/cma.j.issn.1003-9406.2010.04.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20677148 Chinese.

2

Two novel ATP2C1 mutations in patients with Hailey-Hailey disease and a literature review of sequence variants reported in the Chinese population.

Meng L, Gu Y, Du XF, Shao MH, Zhang LL, Zhang GL, Wang XL. Meng L, et al. Among authors: shao mh. Genet Mol Res. 2015 Dec 29;14(4):19349-59. doi: 10.4238/2015.December.29.45. Genet Mol Res. 2015. PMID: 26782588 Free article. Review.

3

[An incontinentia pigmenti family with deletion in both NEMO gene and pseudogene DeltaNEMO].

Zhang G, Shi H, Du X, Shao M, Zhou Q. Zhang G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Oct;25(5):573-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18841575 Chinese.

4

[Mutation analysis of FLG gene in 10 Chinese families with ichthyosis vulgaris].

Gu Y, Shao M, Du X, Li M, Shi H, Zhang G. Gu Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):257-60. doi: 10.3760/cma.j.issn.1003-9406.2013.03.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744309 Chinese.

5

Genetic spectrum of dyschromatosis symmetrica hereditaria in Chinese patients including a novel nonstop mutation in ADAR1 gene.

Zhang G, Shao M, Li Z, Gu Y, Du X, Wang X, Li M. Zhang G, et al. BMC Med Genet. 2016 Feb 18;17:14. doi: 10.1186/s12881-015-0255-1. BMC Med Genet. 2016. PMID: 26892242 Free PMC article.

6

[Analysis of ATP2A2 gene mutations in a pedigree and a sporadic case with Darier disease].

Zhao X, Gu Y, Du X, Shao M, Luo H, Zhu L, Zhou Q, Zhang G. Zhao X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):641-4. doi: 10.3760/cma.j.issn.1003-9406.2016.05.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577212 Chinese.

7

Identification of one Novel complex delins mutation and one recurrent mutation of ERCC8 gene in a Chinese family with Cockayne Syndrome A.

Gu Y, Bhatta AK, Du X, Shao M, Keyal U, Zhang G, Hua Y. Gu Y, et al. J Eur Acad Dermatol Venereol. 2017 Sep;31(9):e394-e395. doi: 10.1111/jdv.14201. Epub 2017 Apr 5. J Eur Acad Dermatol Venereol. 2017. PMID: 28273366 No abstract available.

8

Mutations in the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.

Zhang GL, Shi HJ, Shao MH, Li M, Mu HJ, Gu Y, Du XF, Xie P. Zhang GL, et al. Among authors: shao mh. Genet Mol Res. 2013 Jan 4;12(3):2794-9. doi: 10.4238/2013.January.4.18. Genet Mol Res. 2013. PMID: 23315877 Free article.

9

Association of the NFKBIA gene polymorphisms with susceptibility to autoimmune and inflammatory diseases: a meta-analysis.

Zhang GL, Zou YF, Feng XL, Shi HJ, Du XF, Shao MH, Gu Y, Zhou Q. Zhang GL, et al. Among authors: shao mh. Inflamm Res. 2011 Jan;60(1):11-8. doi: 10.1007/s00011-010-0216-2. Epub 2010 May 21. Inflamm Res. 2011. PMID: 20495844

10

A novel point mutation at donor splice-site in intron 18 of ATP2A2 gene resulting in the insertion of 27 nucleotides into the mature mRNA in a Chinese patient with severe Darier's disease.

Zhang GL, Li M, Du XF, Shi HJ, Shao MH, Mu HJ, Gu Y, Yang SD. Zhang GL, et al. Among authors: shao mh. J Dermatol Sci. 2011 Oct;64(1):72-5. doi: 10.1016/j.jdermsci.2011.06.014. Epub 2011 Jul 6. J Dermatol Sci. 2011. PMID: 21784620 No abstract available.

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