Francke U - Search Results

1

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

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

2

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

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

3

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. Among authors: francke u. Genomics. 1995 Sep 20;29(2):471-7. doi: 10.1006/geno.1995.9979. Genomics. 1995. PMID: 8666397 Free article.

4

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

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

5

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. Among authors: francke u. Hum Mol Genet. 1995 Jul;4(7):1127-35. doi: 10.1093/hmg/4.7.1127. Hum Mol Genet. 1995. PMID: 8528199

6

Molecular cloning of the human homolog of a striatum-enriched phosphatase (STEP) gene and chromosomal mapping of the human and murine loci.

Li X, Luna J, Lombroso PJ, Francke U. Li X, et al. Among authors: francke u. Genomics. 1995 Aug 10;28(3):442-9. doi: 10.1006/geno.1995.1173. Genomics. 1995. PMID: 7490079 Free article.

7

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: francke u. Cell. 1996 Mar 8;84(5):723-34. doi: 10.1016/s0092-8674(00)81050-8. Cell. 1996. PMID: 8625410 Free article.

8

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

9

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

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

10

Characterization of the human gene for microfibril-associated glycoprotein (MFAP2), assignment to chromosome 1p36.1-p35, and linkage to D1S170.

Faraco J, Bashir M, Rosenbloom J, Francke U. Faraco J, et al. Among authors: francke u. Genomics. 1995 Feb 10;25(3):630-7. doi: 10.1016/0888-7543(95)80004-6. Genomics. 1995. PMID: 7759096

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