Chen SH - Search Results

1

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: chen sh. 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.

2

Unique mutations of Bruton's tyrosine kinase in fourteen unrelated X-linked agammaglobulinemia families.

Zhu Q, Zhang M, Winkelstein J, Chen SH, Ochs HD. Zhu Q, et al. Among authors: chen sh. Hum Mol Genet. 1994 Oct;3(10):1899-900. doi: 10.1093/hmg/3.10.1899. Hum Mol Genet. 1994. PMID: 7849721 No abstract available.

3

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: chen sh. Thromb Haemost. 1990 Feb 19;63(1):24-6. Thromb Haemost. 1990. PMID: 2339358

4

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: chen sh. Blood. 1995 Nov 15;86(10):3797-804. Blood. 1995. PMID: 7579347 Free article.

5

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. J Clin Invest. 1989 Jul;84(1):113-8. doi: 10.1172/JCI114130. J Clin Invest. 1989. PMID: 2472424 Free PMC article.

6

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. 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.

7

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

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

8

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. Hum Genet. 1991 Jun;87(2):177-82. doi: 10.1007/BF00204177. Hum Genet. 1991. PMID: 2066105

9

Gene frequencies of alcohol dehydrogenase2 (ADH2) and aldehyde dehydrogenase2 (ALDH2) in five Chinese minorities.

Chen SH, Zhang M, Wang NS, Scott CR. Chen SH, et al. Hum Genet. 1994 Nov;94(5):571-2. doi: 10.1007/BF00211030. Hum Genet. 1994. PMID: 7959698

10

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. Among authors: chen sh. Hum Genet. 1989 Jun;82(3):283-4. doi: 10.1007/BF00291171. Hum Genet. 1989. PMID: 2567277

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