Prowse AH - Search Results

1

Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis.

Clifford SC, Prowse AH, Affara NA, Buys CH, Maher ER. Clifford SC, et al. Among authors: prowse ah. Genes Chromosomes Cancer. 1998 Jul;22(3):200-9. doi: 10.1002/(sici)1098-2264(199807)22:3<200::aid-gcc5>3.0.co;2-#. Genes Chromosomes Cancer. 1998. PMID: 9624531

2

Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.

Prowse AH, Webster AR, Richards FM, Richard S, Olschwang S, Resche F, Affara NA, Maher ER. Prowse AH, et al. Am J Hum Genet. 1997 Apr;60(4):765-71. Am J Hum Genet. 1997. PMID: 9106522 Free PMC article.

3

Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma.

Foster K, Prowse A, van den Berg A, Fleming S, Hulsbeek MM, Crossey PA, Richards FM, Cairns P, Affara NA, Ferguson-Smith MA, et al. Foster K, et al. Hum Mol Genet. 1994 Dec;3(12):2169-73. doi: 10.1093/hmg/3.12.2169. Hum Mol Genet. 1994. PMID: 7881415

4

Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype.

Crossey PA, Richards FM, Foster K, Green JS, Prowse A, Latif F, Lerman MI, Zbar B, Affara NA, Ferguson-Smith MA, et al. Crossey PA, et al. Hum Mol Genet. 1994 Aug;3(8):1303-8. doi: 10.1093/hmg/3.8.1303. Hum Mol Genet. 1994. PMID: 7987306

5

Molecular genetic evidence that endometriosis is a precursor of ovarian cancer.

Prowse AH, Manek S, Varma R, Liu J, Godwin AK, Maher ER, Tomlinson IP, Kennedy SH. Prowse AH, et al. Int J Cancer. 2006 Aug 1;119(3):556-62. doi: 10.1002/ijc.21845. Int J Cancer. 2006. PMID: 16506222 Free article.

6

Molecular genetic analysis of the 3p- syndrome.

Phipps ME, Latif F, Prowse A, Payne SJ, Dietz-Band J, Leversha M, Affara NA, Moore AT, Tolmie J, Schinzel A, et al. Phipps ME, et al. Hum Mol Genet. 1994 Jun;3(6):903-8. doi: 10.1093/hmg/3.6.903. Hum Mol Genet. 1994. PMID: 7951234 Free article. Clinical Trial.

7

Mutational analysis of the von hippel lindau gene in clear cell renal carcinomas from tuberous sclerosis complex patients.

Duffy K, Al-Saleem T, Karbowniczek M, Ewalt D, Prowse AH, Henske EP. Duffy K, et al. Among authors: prowse ah. Mod Pathol. 2002 Mar;15(3):205-10. doi: 10.1038/modpathol.3880517. Mod Pathol. 2002. PMID: 11904337

8

DNA array-based method for detection of large rearrangements in the BRCA1 gene.

Frolov A, Prowse AH, Vanderveer L, Bove B, Wu H, Godwin AK. Frolov A, et al. Among authors: prowse ah. Genes Chromosomes Cancer. 2002 Nov;35(3):232-41. doi: 10.1002/gcc.10109. Genes Chromosomes Cancer. 2002. PMID: 12353265

9

Allelic loss studies do not provide evidence for the "endometriosis-as-tumor" theory.

Prowse AH, Fakis G, Manek S, Churchman M, Edwards S, Rowan A, Koninckx P, Kennedy S, Tomlinson IP. Prowse AH, et al. Fertil Steril. 2005 Apr;83 Suppl 1:1134-43. doi: 10.1016/j.fertnstert.2004.07.982. Fertil Steril. 2005. PMID: 15831286 Free article.

10

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PL, O'Riordan JL, Toledo SP, et al. Eng C, et al. J Med Genet. 1995 Dec;32(12):934-7. doi: 10.1136/jmg.32.12.934. J Med Genet. 1995. PMID: 8825918 Free PMC article.

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