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Journal Abstract Search

114 related items for PubMed ID: 9354420

  • 1. Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis.
    Vorechovský I, Undén AB, Sandstedt B, Toftgård R, Ståhle-Bäckdahl M.
    Cancer Res; 1997 Nov 01; 57(21):4677-81. PubMed ID: 9354420
    [Abstract] [Full Text] [Related]

  • 2. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.
    Vorechovský I, Tingby O, Hartman M, Strömberg B, Nister M, Collins VP, Toftgård R.
    Oncogene; 1997 Jul 17; 15(3):361-6. PubMed ID: 9233770
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  • 3. Patched (ptch)-associated preferential expression of smoothened (smoh) in human basal cell carcinoma of the skin.
    Kallassy M, Toftgård R, Ueda M, Nakazawa K, Vorechovský I, Yamasaki H, Nakazawa H.
    Cancer Res; 1997 Nov 01; 57(21):4731-5. PubMed ID: 9354432
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  • 4. Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.
    Wolter M, Reifenberger J, Sommer C, Ruzicka T, Reifenberger G.
    Cancer Res; 1997 Jul 01; 57(13):2581-5. PubMed ID: 9205058
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  • 5. Human patched (PTCH) mRNA is overexpressed consistently in tumor cells of both familial and sporadic basal cell carcinoma.
    Undén AB, Zaphiropoulos PG, Bruce K, Toftgård R, Ståhle-Bäckdahl M.
    Cancer Res; 1997 Jun 15; 57(12):2336-40. PubMed ID: 9192803
    [Abstract] [Full Text] [Related]

  • 6. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
    Vortmeyer AO, Stavrou T, Selby D, Li G, Weil RJ, Park WS, Moon YW, Chandra R, Goldstein AM, Zhuang Z.
    Cancer; 1999 Jun 15; 85(12):2662-7. PubMed ID: 10375116
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  • 7. Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.
    Unden AB, Holmberg E, Lundh-Rozell B, Stähle-Bäckdahl M, Zaphiropoulos PG, Toftgård R, Vorechovsky I.
    Cancer Res; 1996 Oct 15; 56(20):4562-5. PubMed ID: 8840960
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  • 8. Mutations in SUFU predispose to medulloblastoma.
    Taylor MD, Liu L, Raffel C, Hui CC, Mainprize TG, Zhang X, Agatep R, Chiappa S, Gao L, Lowrance A, Hao A, Goldstein AM, Stavrou T, Scherer SW, Dura WT, Wainwright B, Squire JA, Rutka JT, Hogg D.
    Nat Genet; 2002 Jul 15; 31(3):306-10. PubMed ID: 12068298
    [Abstract] [Full Text] [Related]

  • 9. Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma.
    Maesawa C, Tamura G, Iwaya T, Ogasawara S, Ishida K, Sato N, Nishizuka S, Suzuki Y, Ikeda K, Aoki K, Saito K, Satodate R.
    Genes Chromosomes Cancer; 1998 Mar 15; 21(3):276-9. PubMed ID: 9523206
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  • 14. Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas.
    Reifenberger J, Wolter M, Knobbe CB, Köhler B, Schönicke A, Scharwächter C, Kumar K, Blaschke B, Ruzicka T, Reifenberger G.
    Br J Dermatol; 2005 Jan 15; 152(1):43-51. PubMed ID: 15656799
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  • 15. Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.
    Reifenberger J, Wolter M, Weber RG, Megahed M, Ruzicka T, Lichter P, Reifenberger G.
    Cancer Res; 1998 May 01; 58(9):1798-803. PubMed ID: 9581815
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  • 16. Functional analysis of novel sonic hedgehog gene mutations identified in basal cell carcinomas from xeroderma pigmentosum patients.
    Couvé-Privat S, Le Bret M, Traiffort E, Queille S, Coulombe J, Bouadjar B, Avril MF, Ruat M, Sarasin A, Daya-Grosjean L.
    Cancer Res; 2004 May 15; 64(10):3559-65. PubMed ID: 15150112
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  • 17. Brooke-Spiegler syndrome: report of a case with a novel mutation in the CYLD gene and different types of somatic mutations in benign and malignant tumors.
    Kazakov DV, Schaller J, Vanecek T, Kacerovska D, Michal M.
    J Cutan Pathol; 2010 Aug 15; 37(8):886-90. PubMed ID: 20132422
    [Abstract] [Full Text] [Related]

  • 18. PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.
    Soufir N, Gerard B, Portela M, Brice A, Liboutet M, Saiag P, Descamps V, Kerob D, Wolkenstein P, Gorin I, Lebbe C, Dupin N, Crickx B, Basset-Seguin N, Grandchamp B.
    Br J Cancer; 2006 Aug 21; 95(4):548-53. PubMed ID: 16909134
    [Abstract] [Full Text] [Related]

  • 19. Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors.
    Dahia PL, Marsh DJ, Zheng Z, Zedenius J, Komminoth P, Frisk T, Wallin G, Parsons R, Longy M, Larsson C, Eng C.
    Cancer Res; 1997 Nov 01; 57(21):4710-3. PubMed ID: 9354427
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  • 20. UV-specific p53 and PTCH mutations in sporadic basal cell carcinoma of sun-exposed skin.
    Ratner D, Peacocke M, Zhang H, Ping XL, Tsou HC.
    J Am Acad Dermatol; 2001 Feb 01; 44(2):293-7. PubMed ID: 11174390
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