Scott RJ - Search Results

1

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.

Reeves SG, Meldrum C, Groombridge C, Spigelman AD, Suchy J, Kurzawski G, Lubinski J, McElduff P, Scott RJ. Reeves SG, et al. Among authors: scott rj. Eur J Hum Genet. 2009 May;17(5):629-35. doi: 10.1038/ejhg.2008.239. Epub 2009 Jan 21. Eur J Hum Genet. 2009. PMID: 19156174 Free PMC article.

2

Tumour site, sex, and survival in colorectal cancer.

Scott RJ, Spigelman AD. Scott RJ, et al. Lancet. 2000 Sep 2;356(9232):857; author reply 858. doi: 10.1016/S0140-6736(05)73439-5. Lancet. 2000. PMID: 11022958 No abstract available.

3

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.

Scott RJ, McPhillips M, Meldrum CJ, Fitzgerald PE, Adams K, Spigelman AD, du Sart D, Tucker K, Kirk J. Scott RJ, et al. Am J Hum Genet. 2001 Jan;68(1):118-127. doi: 10.1086/316942. Epub 2000 Dec 7. Am J Hum Genet. 2001. PMID: 11112663 Free PMC article.

4

Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes.

Jakubowska A, Górski B, Kurzawski G, Debniak T, Hadaczek P, Cybulski C, Kladny J, Oszurek O, Scott RJ, Lubinski J. Jakubowska A, et al. Among authors: scott rj. Hum Mutat. 2001;17(1):52-60. doi: 10.1002/1098-1004(2001)17:1<52::AID-HUMU6>3.0.CO;2-E. Hum Mutat. 2001. PMID: 11139242

5

Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity.

Scott RJ, Meldrum C, Crooks R, Spigelman AD, Kirk J, Tucker K, Koorey D; Hunter Family Cancer Service. Scott RJ, et al. Gut. 2001 Apr;48(4):508-14. doi: 10.1136/gut.48.4.508. Gut. 2001. PMID: 11247895 Free PMC article.

6

Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography.

Kurzawski G, Safranow K, Suchy J, Chlubek D, Scott RJ, Lubiński J. Kurzawski G, et al. Among authors: scott rj. J Biochem Biophys Methods. 2002 Mar 4;51(1):89-100. doi: 10.1016/s0165-022x(02)00003-9. J Biochem Biophys Methods. 2002. PMID: 11879922

7

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.

Scott RJ, Crooks R, Meldrum CJ, Thomas L, Smith CJ, Mowat D, McPhillips M, Spigelman AD. Scott RJ, et al. Clin Genet. 2002 Oct;62(4):282-7. doi: 10.1034/j.1399-0004.2002.620405.x. Clin Genet. 2002. PMID: 12372054

8

BRCA2 gene mutations in families with aggregations of breast and stomach cancers.

Jakubowska A, Nej K, Huzarski T, Scott RJ, Lubiński J. Jakubowska A, et al. Among authors: scott rj. Br J Cancer. 2002 Oct 7;87(8):888-91. doi: 10.1038/sj.bjc.6600562. Br J Cancer. 2002. PMID: 12373604 Free PMC article.

9

BRCA2 mutations in a population-based series of patients with ocular melanoma.

Scott RJ, Vajdic CM, Armstrong BK, Ainsworth CJ, Meldrum CJ, Aitken JF, Kricker A. Scott RJ, et al. Int J Cancer. 2002 Nov 10;102(2):188-91. doi: 10.1002/ijc.10693. Int J Cancer. 2002. PMID: 12385017

10

Electro-oculographic and electroretinographic studies in HNPCC gene mutation carriers.

Lubiński W, Kurzawski G, Suchy J, Szych Z, Penkala K, Palacz O, Scott RJ, Lubiński J. Lubiński W, et al. Among authors: scott rj. Ophthalmic Res. 2003 Sep-Oct;35(5):281-94. doi: 10.1159/000072149. Ophthalmic Res. 2003. PMID: 12920342

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