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Items: 1 to 20 of 245

1.

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.

Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R.

Nat Genet. 1997 May;16(1):64-7.

PMID:
9140396
2.

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.

Marsh DJ, Coulon V, Lunetta KL, Rocca-Serra P, Dahia PL, Zheng Z, Liaw D, Caron S, Duboué B, Lin AY, Richardson AL, Bonnetblanc JM, Bressieux JM, Cabarrot-Moreau A, Chompret A, Demange L, Eeles RA, Yahanda AM, Fearon ER, Fricker JP, Gorlin RJ, Hodgson SV, Huson S, Lacombe D, Eng C, et al.

Hum Mol Genet. 1998 Mar;7(3):507-15.

PMID:
9467011
3.

Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.

Marsh DJ, Dahia PL, Coulon V, Zheng Z, Dorion-Bonnet F, Call KM, Little R, Lin AY, Eeles RA, Goldstein AM, Hodgson SV, Richardson AL, Robinson BG, Weber HC, Longy M, Eng C.

Genes Chromosomes Cancer. 1998 Jan;21(1):61-9.

PMID:
9443042
4.

Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas.

Rhei E, Kang L, Bogomolniy F, Federici MG, Borgen PI, Boyd J.

Cancer Res. 1997 Sep 1;57(17):3657-9.

5.

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Lynch ED, Ostermeyer EA, Lee MK, Arena JF, Ji H, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Møller P, King MC.

Am J Hum Genet. 1997 Dec;61(6):1254-60.

6.

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

Nelen MR, van Staveren WC, Peeters EA, Hassel MB, Gorlin RJ, Hamm H, Lindboe CF, Fryns JP, Sijmons RH, Woods DG, Mariman EC, Padberg GW, Kremer H.

Hum Mol Genet. 1997 Aug;6(8):1383-7.

PMID:
9259288
7.

Germline mutations of the PTEN/MMAC1 gene in Japanese patients with Cowden disease.

Kohno T, Takahashi M, Fukutomi T, Ushio K, Yokota J.

Jpn J Cancer Res. 1998 May;89(5):471-4.

PMID:
9685848
8.

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.

J Med Genet. 1998 Nov;35(11):881-5.

9.

A heterozygous germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease.

Iida S, Nakamura Y, Fujii H, Kimura M, Moriwaki K.

Int J Mol Med. 1998 Mar;1(3):565-8.

PMID:
9852263
10.

Analysis of the PTEN gene mutation in polyposis syndromes and sporadic gastrointestinal tumors in Japanese patients.

Negoro K, Takahashi S, Kinouchi Y, Takagi S, Hiwatashi N, Ichinohasama R, Shimosegawa T, Toyota T.

Dis Colon Rectum. 2000 Oct;43(10 Suppl):S29-33.

PMID:
11052475
11.

Pten is essential for embryonic development and tumour suppression.

Di Cristofano A, Pesce B, Cordon-Cardo C, Pandolfi PP.

Nat Genet. 1998 Aug;19(4):348-55.

PMID:
9697695
12.

Genetics of Cowden syndrome: through the looking glass of oncology.

Eng C.

Int J Oncol. 1998 Mar;12(3):701-10. Review.

PMID:
9472113
13.

The genetic basis of Cowden's syndrome: three novel mutations in PTEN/MMAC1/TEP1.

Tsou HC, Ping XL, Xie XX, Gruener AC, Zhang H, Nini R, Swisshelm K, Sybert V, Diamond TM, Sutphen R, Peacocke M.

Hum Genet. 1998 Apr;102(4):467-73.

PMID:
9600246
14.

The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases.

Tsou HC, Teng DH, Ping XL, Brancolini V, Davis T, Hu R, Xie XX, Gruener AC, Schrager CA, Christiano AM, Eng C, Steck P, Ott J, Tavtigian SV, Peacocke M.

Am J Hum Genet. 1997 Nov;61(5):1036-43.

15.

Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndrome.

Carethers JM, Furnari FB, Zigman AF, Lavine JE, Jones MC, Graham GE, Teebi AS, Huang HJ, Ha HT, Chauhan DP, Chang CL, Cavenee WK, Boland CR.

Cancer Res. 1998 Jul 1;58(13):2724-6.

16.

Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer.

Cooney KA, Tsou HC, Petty EM, Miesfeldt S, Ping XL, Gruener AC, Peacocke M.

Clin Cancer Res. 1999 Jun;5(6):1387-91.

17.

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, Dunn T, Feit H, Geraghty MT, Graham JM Jr, Hodgson SV, Hunter A, Korf BR, Manchester D, Miesfeldt S, Murday VA, Nathanson KL, Parisi M, Pober B, Romano C, Eng C, et al.

Hum Mol Genet. 1999 Aug;8(8):1461-72.

PMID:
10400993
18.

The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors.

Eng C.

Recent Prog Horm Res. 1999;54:441-52; discussion 453. Review.

PMID:
10548886
19.

Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer.

FitzGerald MG, Marsh DJ, Wahrer D, Bell D, Caron S, Shannon KE, Ishioka C, Isselbacher KJ, Garber JE, Eng C, Haber DA.

Oncogene. 1998 Aug 13;17(6):727-31.

20.

Germline mutations in the PTEN gene in Israeli patients with Bannayan-Riley-Ruvalcaba syndrome and women with familial breast cancer.

Figer A, Kaplan A, Frydman M, Lev D, Paswell J, Papa MZ, Goldman B, Friedman E.

Clin Genet. 2002 Oct;62(4):298-302.

PMID:
12372056

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