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526 results
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ATM and genome maintenance: defining its role in breast cancer susceptibility.
Khanna KK, Chenevix-Trench G. Khanna KK, et al. J Mammary Gland Biol Neoplasia. 2004 Jul;9(3):247-62. doi: 10.1023/B:JOMG.0000048772.92326.a1. J Mammary Gland Biol Neoplasia. 2004. PMID: 15557798 Review.
Glutathione S-transferase M1 and T1 polymorphisms: susceptibility to colon cancer and age of onset.
Chenevix-Trench G, Young J, Coggan M, Board P. Chenevix-Trench G, et al. Carcinogenesis. 1995 Jul;16(7):1655-7. doi: 10.1093/carcin/16.7.1655. Carcinogenesis. 1995. PMID: 7614702
Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas.
Shanley SM, Dawkins H, Wainwright BJ, Wicking C, Heenan P, Eldon M, Searle J, Chenevix-Trench G. Shanley SM, et al. Hum Mol Genet. 1995 Jan;4(1):129-33. doi: 10.1093/hmg/4.1.129. Hum Mol Genet. 1995. PMID: 7711724
Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome.
Wicking C, Berkman J, Wainwright B, Chenevix-Trench G. Wicking C, et al. Genomics. 1994 Aug;22(3):505-11. doi: 10.1006/geno.1994.1423. Genomics. 1994. PMID: 8001963
Exclusion of APC and MCC as the gene defect in one family with familial juvenile polyposis.
Leggett BA, Thomas LR, Knight N, Healey S, Chenevix-Trench G, Searle J. Leggett BA, et al. Gastroenterology. 1993 Nov;105(5):1313-6. doi: 10.1016/0016-5085(93)90134-x. Gastroenterology. 1993. PMID: 8224634
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.
Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Hockey A, Haan E, Oley C, Ravine D, Turner A, Goldgar D, et al. Chenevix-Trench G, et al. Am J Hum Genet. 1993 Sep;53(3):760-7. Am J Hum Genet. 1993. PMID: 8352281 Free PMC article.
Rare mutations and no hypermethylation at the CDKN2A locus in epithelial ovarian tumours.
Shih YC, Kerr J, Liu J, Hurst T, Khoo SK, Ward B, Wainwright B, Chenevix-Trench G. Shih YC, et al. Int J Cancer. 1997 Mar 4;70(5):508-11. doi: 10.1002/(sici)1097-0215(19970304)70:5<508::aid-ijc3>3.0.co;2-1. Int J Cancer. 1997. PMID: 9052747
Relationship between number of ovulatory cycles and accumulation of mutant p53 in epithelial ovarian cancer.
Webb PM, Green A, Cummings MC, Purdie DM, Walsh MD, Chenevix-Trench G. Webb PM, et al. J Natl Cancer Inst. 1998 Nov 18;90(22):1729-34. doi: 10.1093/jnci/90.22.1729. J Natl Cancer Inst. 1998. PMID: 9827528
Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.
Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C, Wainwright BJ. Smyth I, et al. Hum Mol Genet. 1999 Feb;8(2):291-7. doi: 10.1093/hmg/8.2.291. Hum Mol Genet. 1999. PMID: 9931336
Androgen receptor exon 1 CAG repeat length and breast cancer in women before age forty years.
Spurdle AB, Dite GS, Chen X, Mayne CJ, Southey MC, Batten LE, Chy H, Trute L, McCredie MR, Giles GG, Armes J, Venter DJ, Hopper JL, Chenevix-Trench G. Spurdle AB, et al. J Natl Cancer Inst. 1999 Jun 2;91(11):961-6. doi: 10.1093/jnci/91.11.961. J Natl Cancer Inst. 1999. PMID: 10359549
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