Prosser J - Search Results

1

Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3).

Dry KL, Aldred MA, Edgar AJ, Brown J, Manson FD, Ho MF, Prosser J, Hardwick LJ, Lennon AA, Thomson K, et al. Dry KL, et al. Among authors: prosser j. Hum Mol Genet. 1995 Dec;4(12):2347-53. doi: 10.1093/hmg/4.12.2347. Hum Mol Genet. 1995. PMID: 8634709

2

Degeneracy in human multicopy RBM (YRRM), a candidate spermatogenesis gene.

Prosser J, Inglis JD, Condie A, Ma K, Kerr S, Thakrar R, Taylor K, Cameron JM, Cooke HJ. Prosser J, et al. Mamm Genome. 1996 Nov;7(11):835-42. doi: 10.1007/s003359900246. Mamm Genome. 1996. PMID: 8875892

3

The human PAX6 gene is mutated in two patients with aniridia.

Jordan T, Hanson I, Zaletayev D, Hodgson S, Prosser J, Seawright A, Hastie N, van Heyningen V. Jordan T, et al. Among authors: prosser j. Nat Genet. 1992 Aug;1(5):328-32. doi: 10.1038/ng0892-328. Nat Genet. 1992. PMID: 1302030

4

The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.

Axton R, Hanson I, Danes S, Sellar G, van Heyningen V, Prosser J. Axton R, et al. Among authors: prosser j. J Med Genet. 1997 Apr;34(4):279-86. doi: 10.1136/jmg.34.4.279. J Med Genet. 1997. PMID: 9138149 Free PMC article.

5

Zinc finger point mutations within the WT1 gene in Wilms tumor patients.

Little MH, Prosser J, Condie A, Smith PJ, Van Heyningen V, Hastie ND. Little MH, et al. Among authors: prosser j. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4791-5. doi: 10.1073/pnas.89.11.4791. Proc Natl Acad Sci U S A. 1992. PMID: 1317572 Free PMC article.

6

Detection of point mutations in the p53 gene: comparison of single-strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques.

Condie A, Eeles R, Borresen AL, Coles C, Cooper C, Prosser J. Condie A, et al. Among authors: prosser j. Hum Mutat. 1993;2(1):58-66. doi: 10.1002/humu.1380020111. Hum Mutat. 1993. PMID: 8477265

7

Mouse small eye results from mutations in a paired-like homeobox-containing gene.

Hill RE, Favor J, Hogan BL, Ton CC, Saunders GF, Hanson IM, Prosser J, Jordan T, Hastie ND, van Heyningen V. Hill RE, et al. Among authors: prosser j. Nature. 1991 Dec 19-26;354(6354):522-5. doi: 10.1038/354522a0. Nature. 1991. PMID: 1684639

8

Evidence that p53 behaves as a tumour suppressor gene in sporadic breast tumours.

Prosser J, Thompson AM, Cranston G, Evans HJ. Prosser J, et al. Oncogene. 1990 Oct;5(10):1573-9. Oncogene. 1990. PMID: 2250913

9

APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis.

Prosser J, Condie A, Wright M, Horn JM, Fantes JA, Wyllie AH, Dunlop MG. Prosser J, et al. Br J Cancer. 1994 Nov;70(5):841-6. doi: 10.1038/bjc.1994.408. Br J Cancer. 1994. PMID: 7524601 Free PMC article.

10

PAX6 mutations reviewed.

Prosser J, van Heyningen V. Prosser J, et al. Hum Mutat. 1998;11(2):93-108. doi: 10.1002/(SICI)1098-1004(1998)11:2<93::AID-HUMU1>3.0.CO;2-M. Hum Mutat. 1998. PMID: 9482572 Review.

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