Zhang M - Search Results

1

[The establishment of four cell lines from Colossoma brachypomum and their growth characteristics under various temperatures].

Zhang M, Chen SH, Zhao XL. Zhang M, et al. Sheng Wu Gong Cheng Xue Bao. 2001 Jan;17(1):105-8. Sheng Wu Gong Cheng Xue Bao. 2001. PMID: 11330178 Chinese.

2

Gene frequencies of alcohol dehydrogenase2 and aldehyde dehydrogenase2 in Northwest Coast Amerindians.

Chen SH, Zhang M, Scott CR. Chen SH, et al. Among authors: zhang m. Hum Genet. 1992 May;89(3):351-2. doi: 10.1007/BF00220558. Hum Genet. 1992. PMID: 1601427 Review.

3

Splice junction mutations in factor IX gene resulting in severe hemophilia B.

Chen SH, Zhang M, Thompson AR, Bray GL, Scott CR. Chen SH, et al. Among authors: zhang m. Nucleic Acids Res. 1991 Mar 11;19(5):1172. doi: 10.1093/nar/19.5.1172. Nucleic Acids Res. 1991. PMID: 2020563 Free PMC article.

4

CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series.

Chen SH, Zhang M, Lovrien EW, Scott CR, Thompson AR. Chen SH, et al. Among authors: zhang m. Hum Genet. 1991 Jun;87(2):177-82. doi: 10.1007/BF00204177. Hum Genet. 1991. PMID: 2066105

5

[Discussion on the significance of detecting ventricular late potential in coronary heart disease].

Zhang M, Chen S. Zhang M, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 1990 Oct;18(5):285-7. Zhonghua Xin Xue Guan Bing Za Zhi. 1990. PMID: 2086192 Chinese. No abstract available.

6

Factor IX Chongqing: a new mutation in the calcium-binding domain of factor IX resulting in severe hemophilia B.

Wang NS, Zhang M, Thompson AR, Chen SH. Wang NS, et al. Among authors: zhang m. Thromb Haemost. 1990 Feb 19;63(1):24-6. Thromb Haemost. 1990. PMID: 2339358

7

Three point mutations in the factor IX genes of five hemophilia B patients. Identification strategy using localization by altered epitopes in their hemophilic proteins.

Chen SH, Thompson AR, Zhang M, Scott CR. Chen SH, et al. Among authors: zhang m. J Clin Invest. 1989 Jul;84(1):113-8. doi: 10.1172/JCI114130. J Clin Invest. 1989. PMID: 2472424 Free PMC article.

8

The factor IX BamHI polymorphism: T-to-G transversion at the nucleotide sequence -561. The BamHI/MSPI haplotypes in blacks and Caucasians.

Zhang M, Chen SH, Scott CR, Thompson AR. Zhang M, et al. Hum Genet. 1989 Jun;82(3):283-4. doi: 10.1007/BF00291171. Hum Genet. 1989. PMID: 2567277

9

Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA).

Zhu Q, Zhang M, Rawlings DJ, Vihinen M, Hagemann T, Saffran DC, Kwan SP, Nilsson L, Smith CI, Witte ON, Chen SH, Ochs HD. Zhu Q, et al. Among authors: zhang m. J Exp Med. 1994 Aug 1;180(2):461-70. doi: 10.1084/jem.180.2.461. J Exp Med. 1994. PMID: 7519238 Free PMC article.

10

The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene.

Zhu Q, Zhang M, Blaese RM, Derry JM, Junker A, Francke U, Chen SH, Ochs HD. Zhu Q, et al. Among authors: zhang m. Blood. 1995 Nov 15;86(10):3797-804. Blood. 1995. PMID: 7579347 Free article.

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