These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 10234502)

  • 21. Effect of nonsense mutations on PTEN mRNA stability.
    Raizis AM; Ferguson MM; George PM
    Hum Genet; 2000 Jul; 107(1):24-7. PubMed ID: 10982030
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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. PubMed ID: 10389923
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Germline PTEN mutations in three families with Cowden syndrome.
    Celebi JT; Ping XL; Zhang H; Remington T; Sulica VI; Tsou HC; Peacocke M
    Exp Dermatol; 2000 Apr; 9(2):152-6. PubMed ID: 10772390
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evaluation of germline PTEN mutations in endometrial cancer patients.
    Black D; Bogomolniy F; Robson ME; Offit K; Barakat RR; Boyd J
    Gynecol Oncol; 2005 Jan; 96(1):21-4. PubMed ID: 15589575
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [Cowden disease and the PTEN gene: a successfully clinical and biological combined approach].
    Longy M
    Bull Cancer; 2001 Dec; 88(12):1153-8. PubMed ID: 11792608
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A heterozygous frameshift mutation of the PTEN/MMAC1 gene in a patient with Lhermitte-Duclos disease - only the mutated allele was expressed in the cerebellar tumor.
    Iida S; Tanaka Y; Fujii H; Hayashi S; Kimura M; Nagareda T; Moriwaki K
    Int J Mol Med; 1998 Jun; 1(6):925-9. PubMed ID: 9852626
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
    Zhou XP; Marsh DJ; Morrison CD; Chaudhury AR; Maxwell M; Reifenberger G; Eng C
    Am J Hum Genet; 2003 Nov; 73(5):1191-8. PubMed ID: 14566704
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel mutation of the PTEN gene in an Italian Cowden's disease kindred.
    Scala S; Bruni P; Lo Muzio L; Mignogna M; Viglietto G; Fusco A
    Int J Oncol; 1998 Oct; 13(4):665-8. PubMed ID: 9735393
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Identification of PTEN mutations in five families with Bannayan-Zonana syndrome.
    Tok Celebi J; Chen FF; Zhang H; Ping XL; Tsou HC; Peacocke M
    Exp Dermatol; 1999 Apr; 8(2):134-9. PubMed ID: 10232405
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Polymorphisms in PTEN in breast cancer families.
    Carroll BT; Couch FJ; Rebbeck TR; Weber BL
    J Med Genet; 1999 Feb; 36(2):94-6. PubMed ID: 10051004
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 14.