Ashley JA - Search Results

1

Identification of the homologous beige and Chediak-Higashi syndrome genes.

Barbosa MD, Nguyen QA, Tchernev VT, Ashley JA, Detter JC, Blaydes SM, Brandt SJ, Chotai D, Hodgman C, Solari RC, Lovett M, Kingsmore SF. Barbosa MD, et al. Among authors: ashley ja. Nature. 1996 Jul 18;382(6588):262-5. doi: 10.1038/382262a0. Nature. 1996. PMID: 8717042 Free PMC article.

2

Physical mapping of the beige critical region on mouse chromosome 13.

Kingsmore SF, Barbosa MD, Nguyen QA, Ashley JA, Blaydes SM, Tchernev VT, Detter JC, Lovett M. Kingsmore SF, et al. Among authors: ashley ja. Mamm Genome. 1996 Oct;7(10):773-5. doi: 10.1007/s003359900231. Mamm Genome. 1996. PMID: 8854868 No abstract available.

3

The structure of the human multiple exostoses 2 gene and characterization of homologs in mouse and Caenorhabditis elegans.

Clines GA, Ashley JA, Shah S, Lovett M. Clines GA, et al. Among authors: ashley ja. Genome Res. 1997 Apr;7(4):359-67. doi: 10.1101/gr.7.4.359. Genome Res. 1997. PMID: 9110175 Free PMC article.

4

TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.

Wise CA, Chiang LC, Paznekas WA, Sharma M, Musy MM, Ashley JA, Lovett M, Jabs EW. Wise CA, et al. Among authors: ashley ja. Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3110-5. doi: 10.1073/pnas.94.7.3110. Proc Natl Acad Sci U S A. 1997. PMID: 9096354 Free PMC article.

5

A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region.

Guimerá J, Casas C, Pucharcòs C, Solans A, Domènech A, Planas AM, Ashley J, Lovett M, Estivill X, Pritchard MA. Guimerá J, et al. Hum Mol Genet. 1996 Sep;5(9):1305-10. doi: 10.1093/hmg/5.9.1305. Hum Mol Genet. 1996. PMID: 8872470

6

Human chromosome-specific cDNA libraries: new tools for gene identification and genome annotation.

Del Mastro RG, Wang L, Simmons AD, Gallardo TD, Clines GA, Ashley JA, Hilliard CJ, Wasmuth JJ, McPherson JD, Lovett M. Del Mastro RG, et al. Among authors: ashley ja. Genome Res. 1995 Sep;5(2):185-94. doi: 10.1101/gr.5.2.185. Genome Res. 1995. PMID: 9132272 Free article.

7

Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection.

Guimera J, Pucharcós C, Domènech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M. Guimera J, et al. Genomics. 1997 Oct 1;45(1):59-67. doi: 10.1006/geno.1997.4861. Genomics. 1997. PMID: 9339361

8

Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome.

Nichols KE, Harkin DP, Levitz S, Krainer M, Kolquist KA, Genovese C, Bernard A, Ferguson M, Zuo L, Snyder E, Buckler AJ, Wise C, Ashley J, Lovett M, Valentine MB, Look AT, Gerald W, Housman DE, Haber DA. Nichols KE, et al. Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13765-70. doi: 10.1073/pnas.95.23.13765. Proc Natl Acad Sci U S A. 1998. PMID: 9811875 Free PMC article.

9

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.

Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ. Chen A, et al. Am J Med Genet. 1997 Sep 5;71(4):467-71. Am J Med Genet. 1997. PMID: 9286457

10

Suppression of psychoactive effects of cocaine by active immunization.

Carrera MR, Ashley JA, Parsons LH, Wirsching P, Koob GF, Janda KD. Carrera MR, et al. Among authors: ashley ja. Nature. 1995 Dec 14;378(6558):727-30. doi: 10.1038/378727a0. Nature. 1995. PMID: 7501020

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