Prosser J - Search Results

1

A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.

Weir-Thompson E, Condie A, Leonard RC, Prosser J. Weir-Thompson E, et al. Among authors: prosser j. Oncogene. 1991 Dec;6(12):2353-6. Oncogene. 1991. PMID: 1662795

2

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

3

Exclusion of constitutional p53 mutations as a cause of genetic susceptibility to colorectal cancer.

Bhagirath T, Condie A, Dunlop MG, Wyllie AH, Prosser J. Bhagirath T, et al. Among authors: prosser j. Br J Cancer. 1993 Oct;68(4):712-4. doi: 10.1038/bjc.1993.415. Br J Cancer. 1993. PMID: 8398698 Free PMC article. No abstract available.

4

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

5

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.

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

Detecting single-base mutations.

Prosser J. Prosser J. Trends Biotechnol. 1993 Jun;11(6):238-46. doi: 10.1016/0167-7799(93)90135-V. Trends Biotechnol. 1993. PMID: 7763820 Review.

8

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.

9

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

10

Mutations in p53 do not account for heritable breast cancer: a study in five affected families.

Prosser J, Elder PA, Condie A, MacFadyen I, Steel CM, Evans HJ. Prosser J, et al. Br J Cancer. 1991 Feb;63(2):181-4. doi: 10.1038/bjc.1991.44. Br J Cancer. 1991. PMID: 1997094 Free PMC article. No abstract available.

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