BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 9685848)

  • 1. 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. PubMed ID: 9685848
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 9443042
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 9259288
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    Hum Mol Genet; 1998 Mar; 7(3):507-15. PubMed ID: 9467011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 9140396
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 57(17):3657-9. PubMed ID: 9288766
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 9600246
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel PTEN mutation in a Japanese patient with Cowden disease.
    Kubo Y; Urano Y; Hida Y; Ikeuchi T; Nomoto M; Kunitomo K; Arase S
    Br J Dermatol; 2000 Jun; 142(6):1100-5. PubMed ID: 10848731
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 9852263
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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. PubMed ID: 9399897
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 58(13):2724-6. PubMed ID: 9661881
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of the PTEN / MMAC1 gene in Japanese patients with Cowden disease.
    Sawada T; Hamano N; Satoh H; Okada T; Takeda Y; Mabuchi H
    Jpn J Cancer Res; 2000 Jul; 91(7):700-5. PubMed ID: 10920277
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease.
    Sanson M; Zhou XP; Brault JL; Hoang-Xuan K; Hamelin R
    Acta Oncol; 1999; 38(7):973-5. PubMed ID: 10606430
    [No Abstract]   [Full Text] [Related]  

  • 14. Mutational abrogation of the PTEN/MMAC1 gene in gastrointestinal polyps in patients with Cowden disease.
    Chi SG; Kim HJ; Park BJ; Min HJ; Park JH; Kim YW; Dong SH; Kim BH; Lee JI; Chang YW; Chang R; Kim WK; Yang MH
    Gastroenterology; 1998 Nov; 115(5):1084-9. PubMed ID: 9797362
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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. PubMed ID: 9345101
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two novel mutations of PTEN gene in Japanese patients with Cowden syndrome.
    Sawada T; Okada T; Miwa K; Satoh H; Asano A; Mabuchi H
    Am J Med Genet A; 2004 Jul; 128A(1):12-4. PubMed ID: 15211648
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 9832031
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome.
    Raizis AM; Ferguson MM; Robinson BA; Atkinson CH; George PM
    Mol Pathol; 1998 Dec; 51(6):339-41. PubMed ID: 10193515
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline mutation of the PTEN gene in a Japanese patient with Cowden's disease.
    Kato N; Kimura K; Sugawara H; Aoyagi S; Ikeda T; Horii A
    Int J Oncol; 2001 May; 18(5):1017-22. PubMed ID: 11295050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.
    Dahia PM; Gimm O; Chi H; Marsh DJ; Reynolds PR; Eng C
    J Med Genet; 2000 Sep; 37(9):715-7. PubMed ID: 11182934
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.