199 related articles for article (PubMed ID: 10051160)
21. Mutations of the human PTEN gene.
Bonneau D; Longy M
Hum Mutat; 2000; 16(2):109-22. PubMed ID: 10923032
[TBL] [Abstract][Full Text] [Related]
22. 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. PubMed ID: 11052475
[TBL] [Abstract][Full Text] [Related]
23. Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.
Kim DK; Myung SJ; Yang SK; Hong SS; Kim KJ; Byeon JS; Lee GH; Kim JH; Min YI; Lee SM; Jeong JY; Song K; Jung SA
Dis Colon Rectum; 2005 Sep; 48(9):1714-22. PubMed ID: 16007494
[TBL] [Abstract][Full Text] [Related]
24. Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
Nelen MR; Kremer H; Konings IB; Schoute F; van Essen AJ; Koch R; Woods CG; Fryns JP; Hamel B; Hoefsloot LH; Peeters EA; Padberg GW
Eur J Hum Genet; 1999 Apr; 7(3):267-73. PubMed ID: 10234502
[TBL] [Abstract][Full Text] [Related]
25. Association between Cowden syndrome and Lhermitte-Duclos disease: report of two cases and review of the literature.
Derrey S; Proust F; Debono B; Langlois O; Layet A; Layet V; Longy M; Fréger P; Laquerrière A
Surg Neurol; 2004 May; 61(5):447-54; discussion 454. PubMed ID: 15120218
[TBL] [Abstract][Full Text] [Related]
26. Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.
Zhou X; Hampel H; Thiele H; Gorlin RJ; Hennekam RC; Parisi M; Winter RM; Eng C
Lancet; 2001 Jul; 358(9277):210-1. PubMed ID: 11476841
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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. PubMed ID: 9697695
[TBL] [Abstract][Full Text] [Related]
29. Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.
Zhou XP; Waite KA; Pilarski R; Hampel H; Fernandez MJ; Bos C; Dasouki M; Feldman GL; Greenberg LA; Ivanovich J; Matloff E; Patterson A; Pierpont ME; Russo D; Nassif NT; Eng C
Am J Hum Genet; 2003 Aug; 73(2):404-11. PubMed ID: 12844284
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. PTEN inactivation by germline/somatic c.950_953delTACT mutation in patients with Lhermitte-Duclos disease manifesting progressive phenotypes.
Chen XY; Lu F; Wang YM; Yang Y; Wei GQ; Wu D; Wang LF; Wu YM
Clin Genet; 2014 Oct; 86(4):349-54. PubMed ID: 24102544
[TBL] [Abstract][Full Text] [Related]
32. Novel germline mutation of the PTEN gene in a Japanese family with Cowden disease.
Harada N; Sugimura T; Yoshimura R; Motomura S; Shirahama S; Naramoto J; Chijiiwa Y; Nakamura K; Ito K; Nawata H
J Gastroenterol; 2003; 38(1):87-91. PubMed ID: 12560928
[TBL] [Abstract][Full Text] [Related]
33. Germline mutations in PTEN are present in Bannayan-Zonana syndrome.
Marsh DJ; Dahia PL; Zheng Z; Liaw D; Parsons R; Gorlin RJ; Eng C
Nat Genet; 1997 Aug; 16(4):333-4. PubMed ID: 9241266
[No Abstract] [Full Text] [Related]
34. 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]
35. Identification of germline mutation of PTEN gene and analysis of apoptosis resistance of the lymphocytes in a patient with Cowden disease.
Kanaseki T; Torigoe T; Hirohashi Y; Hirai I; Himi T; Sato N
Pathobiology; 2002; 70(1):34-9. PubMed ID: 12415190
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Lhermitte-Duclos Disease (Dysplastic Gangliocytoma of the Cerebellum) and Cowden Syndrome: Clinical Experience From a Single Institution with Long-Term Follow-Up.
Jiang T; Wang J; Du J; Luo S; Liu R; Xie J; Wang Y; Li C
World Neurosurg; 2017 Aug; 104():398-406. PubMed ID: 28479525
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. PTEN mutations in eight Spanish families and one Brazilian family with Cowden syndrome.
Bussaglia E; Pujol RM; Gil MJ; Martí RM; Tuneu A; Febrer MI; Garcia-Patos V; Ruiz EM; Barnadas M; Alegre M; Serrano S; Matias-Guiu X
J Invest Dermatol; 2002 Apr; 118(4):639-44. PubMed ID: 11918710
[TBL] [Abstract][Full Text] [Related]
40. Brain magnetic resonance imaging in patients with Cowden syndrome.
Lok C; Viseux V; Avril MF; Richard MA; Gondry-Jouet C; Deramond H; Desfossez-Tribout C; Courtade S; Delaunay M; Piette F; Legars D; Dreno B; Saïag P; Longy M; Lorette G; Laroche L; Caux F;
Medicine (Baltimore); 2005 Mar; 84(2):129-136. PubMed ID: 15758842
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
