Harrison WR - Search Results

1

Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites.

Sohocki MM, Sullivan LS, Harrison WR, Sodergren EJ, Elder FF, Weinstock G, Tanase S, Daiger SP. Sohocki MM, et al. Among authors: harrison wr. Genomics. 1997 Mar 1;40(2):247-52. doi: 10.1006/geno.1996.4604. Genomics. 1997. PMID: 9119391

2

Genomic DNA sequence, promoter expression, and chromosomal mapping of rat muscle carnitine palmitoyltransferase I.

Wang D, Harrison W, Buja LM, Elder FF, McMillin JB. Wang D, et al. Genomics. 1998 Mar 15;48(3):314-23. doi: 10.1006/geno.1997.5184. Genomics. 1998. PMID: 9545636

3

Characterization of human DSPG3, a small dermatan sulfate proteoglycan.

Deere M, Johnson J, Garza S, Harrison WR, Yoon SJ, Elder FF, Kucherlapati R, Hook M, Hecht JT. Deere M, et al. Among authors: harrison wr. Genomics. 1996 Dec 15;38(3):399-404. doi: 10.1006/geno.1996.0643. Genomics. 1996. PMID: 8975717

4

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.

Hecht JT, Nelson LD, Crowder E, Wang Y, Elder FF, Harrison WR, Francomano CA, Prange CK, Lennon GG, Deere M, et al. Hecht JT, et al. Among authors: harrison wr. Nat Genet. 1995 Jul;10(3):325-9. doi: 10.1038/ng0795-325. Nat Genet. 1995. PMID: 7670471

5

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome.

Lu W, Phillips CL, Killen PD, Hlaing T, Harrison WR, Elder FF, Miner JH, Overbeek PA, Meisler MH. Lu W, et al. Among authors: harrison wr. Genomics. 1999 Oct 15;61(2):113-24. doi: 10.1006/geno.1999.5943. Genomics. 1999. PMID: 10534397

6

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. Sohocki MM, et al. Among authors: harrison wr. Nat Genet. 2000 Jan;24(1):79-83. doi: 10.1038/71732. Nat Genet. 2000. PMID: 10615133 Free PMC article.

7

Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3.

Robinson ML, Allen CE, Davy BE, Durfee WJ, Elder FF, Elliott CS, Harrison WR. Robinson ML, et al. Among authors: harrison wr. Mamm Genome. 2002 Nov;13(11):625-32. doi: 10.1007/s00335-002-2201-8. Mamm Genome. 2002. PMID: 12461648

8

Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse.

Morgan D, Turnpenny L, Goodship J, Dai W, Majumder K, Matthews L, Gardner A, Schuster G, Vien L, Harrison W, Elder FF, Penman-Splitt M, Overbeek P, Strachan T. Morgan D, et al. Nat Genet. 1998 Oct;20(2):149-56. doi: 10.1038/2450. Nat Genet. 1998. PMID: 9771707

9

The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus.

Carrel T, Purandare SM, Harrison W, Elder F, Fox T, Casey B, Herman GE. Carrel T, et al. Hum Mol Genet. 2000 Aug 12;9(13):1937-42. doi: 10.1093/hmg/9.13.1937. Hum Mol Genet. 2000. PMID: 10942421

10

Chromosomes of Brants' whistling rat and genome conservation in the Otomyinae revealed by G-banding and fluorescence in situ hybridization.

Rambau RV, Harrison WR, Elder FF, Robinson TJ. Rambau RV, et al. Among authors: harrison wr. Cytogenet Cell Genet. 1997;78(3-4):216-20. doi: 10.1159/000134660. Cytogenet Cell Genet. 1997. PMID: 9465891

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