Tomlinson IP - Search Results

1

DNA polymerase ε and δ exonuclease domain mutations in endometrial cancer.

Church DN, Briggs SE, Palles C, Domingo E, Kearsey SJ, Grimes JM, Gorman M, Martin L, Howarth KM, Hodgson SV; NSECG Collaborators; Kaur K, Taylor J, Tomlinson IP. Church DN, et al. Among authors: tomlinson ip. Hum Mol Genet. 2013 Jul 15;22(14):2820-8. doi: 10.1093/hmg/ddt131. Epub 2013 Mar 24. Hum Mol Genet. 2013. PMID: 23528559 Free PMC article.

2

Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.

Thomas HJ, Whitelaw SC, Cottrell SE, Murday VA, Tomlinson IP, Markie D, Jones T, Bishop DT, Hodgson SV, Sheer D, Northover JM, Talbot IC, Solomon E, Bodmer WF. Thomas HJ, et al. Among authors: tomlinson ip. Am J Hum Genet. 1996 Apr;58(4):770-6. Am J Hum Genet. 1996. PMID: 8644741 Free PMC article.

3

Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria.

Beck NE, Tomlinson IP, Homfray T, Frayling I, Hodgson SV, Harocopos C, Bodmer WF. Beck NE, et al. Among authors: tomlinson ip. Hum Genet. 1997 Feb;99(2):219-24. doi: 10.1007/s004390050343. Hum Genet. 1997. PMID: 9048925

4

Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilled.

Beck NE, Tomlinson IP, Homfray T, Hodgson SV, Harocopos CJ, Bodmer WF. Beck NE, et al. Among authors: tomlinson ip. Br J Surg. 1997 Feb;84(2):233-7. Br J Surg. 1997. PMID: 9052445

5

Clinical features and molecular analysis of a family with multiple colon tumours and reduced plasminogen activator activity.

Tomlinson IP, Beck NE, Williamson J, Harocopos CJ, Mitchell VE, Hodgson SV, Bodmer WF. Tomlinson IP, et al. Int J Colorectal Dis. 1997;12(1):1-3. doi: 10.1007/s003840050068. Int J Colorectal Dis. 1997. PMID: 9112141

6

Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas.

Beck NE, Tomlinson IP, Homfray TF, Frayling IM, Hodgson SV, Bodmer WF. Beck NE, et al. Among authors: tomlinson ip. Gut. 1997 Aug;41(2):235-8. doi: 10.1136/gut.41.2.235. Gut. 1997. PMID: 9301504 Free PMC article.

7

Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours.

Homfray TF, Cottrell SE, Ilyas M, Rowan A, Talbot IC, Bodmer WF, Tomlinson IP. Homfray TF, et al. Among authors: tomlinson ip. Hum Mutat. 1998;11(2):114-20. doi: 10.1002/(SICI)1098-1004(1998)11:2<114::AID-HUMU3>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9482574

8

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases.

Houlston R, Bevan S, Williams A, Young J, Dunlop M, Rozen P, Eng C, Markie D, Woodford-Richens K, Rodriguez-Bigas MA, Leggett B, Neale K, Phillips R, Sheridan E, Hodgson S, Iwama T, Eccles D, Bodmer W, Tomlinson I. Houlston R, et al. Hum Mol Genet. 1998 Nov;7(12):1907-12. doi: 10.1093/hmg/7.12.1907. Hum Mol Genet. 1998. PMID: 9811934

9

Germline PTEN mutations in Cowden syndrome-like families.

Marsh DJ, Dahia PL, Caron S, Kum JB, Frayling IM, Tomlinson IP, Hughes KS, Eeles RA, Hodgson SV, Murday VA, Houlston R, Eng C. Marsh DJ, et al. Among authors: tomlinson ip. J Med Genet. 1998 Nov;35(11):881-5. doi: 10.1136/jmg.35.11.881. J Med Genet. 1998. PMID: 9832031 Free PMC article.

10

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

Ylikorkala A, Avizienyte E, Tomlinson IP, Tiainen M, Roth S, Loukola A, Hemminki A, Johansson M, Sistonen P, Markie D, Neale K, Phillips R, Zauber P, Twama T, Sampson J, Järvinen H, Mäkelä TP, Aaltonen LA. Ylikorkala A, et al. Among authors: tomlinson ip. Hum Mol Genet. 1999 Jan;8(1):45-51. doi: 10.1093/hmg/8.1.45. Hum Mol Genet. 1999. PMID: 9887330

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