Derry JM - Search Results

1

Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins.

Huang MM, Tsuboi S, Wong A, Yu XJ, Oh-Eda M, Derry JM, Francke U, Fukuda M, Weinberg KI, Kohn DB. Huang MM, et al. Among authors: derry jm. Gene Ther. 2000 Feb;7(4):314-20. doi: 10.1038/sj.gt.3301085. Gene Ther. 2000. PMID: 10694812

2

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Derry JM, Kerns JA, Weinberg KI, Ochs HD, Volpini V, Estivill X, Walker AP, Francke U. Derry JM, et al. Hum Mol Genet. 1995 Jul;4(7):1127-35. doi: 10.1093/hmg/4.7.1127. Hum Mol Genet. 1995. PMID: 8528199

3

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

Derry JM, Ochs HD, Francke U. Derry JM, et al. Cell. 1994 Aug 26;78(4):635-44. doi: 10.1016/0092-8674(94)90528-2. Cell. 1994. PMID: 8069912

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

5

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

Derry JM, Ochs HD, Francke U. Derry JM, et al. Cell. 1994 Dec 2;79(5):following 922. Cell. 1994. PMID: 8001129 No abstract available.

6

Pillars Article: Isolation of a Novel Gene Mutated in Wiskott-Aldrich Syndrome. Cell. 1994. 78: 635-644.

Derry JMJ, Ochs HD, Francke U. Derry JMJ, et al. J Immunol. 2018 Jun 1;200(11):3671-3680. J Immunol. 2018. PMID: 29784763 No abstract available.

7

The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome.

Derry JM, Wiedemann P, Blair P, Wang Y, Kerns JA, Lemahieu V, Godfrey VL, Wilkinson JE, Francke U. Derry JM, et al. Genomics. 1995 Sep 20;29(2):471-7. doi: 10.1006/geno.1995.9979. Genomics. 1995. PMID: 8666397 Free article.

8

Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization.

Symons M, Derry JM, Karlak B, Jiang S, Lemahieu V, Mccormick F, Francke U, Abo A. Symons M, et al. Among authors: derry jm. Cell. 1996 Mar 8;84(5):723-34. doi: 10.1016/s0092-8674(00)81050-8. Cell. 1996. PMID: 8625410 Free article.

9

RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain.

Derry JM, Kerns JA, Francke U. Derry JM, et al. Hum Mol Genet. 1995 Dec;4(12):2307-11. doi: 10.1093/hmg/4.12.2307. Hum Mol Genet. 1995. PMID: 8634703

10

Cloning and characterization of a novel zinc finger gene in Xp11.2.

Derry JM, Jess U, Francke U. Derry JM, et al. Genomics. 1995 Nov 20;30(2):361-5. doi: 10.1006/geno.1995.0031. Genomics. 1995. PMID: 8586441 Free article.

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