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Journal Abstract Search

179 related items for PubMed ID: 10554356

  • 1. Involvement of patched (PTCH) gene in Gorlin syndrome and related disorders: three family cases.
    Situm M, Levanat S, Crnic I, Pavelic B, Macan D, Grgurević J, Mubrin-Koncar M, Lipozencić J.
    Croat Med J; 1999 Dec; 40(4):533-8. PubMed ID: 10554356
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  • 2. 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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  • 3. The patched/hedgehog/smoothened signalling pathway in human breast cancer: no evidence for H133Y SHH, PTCH and SMO mutations.
    Vorechovský I, Benediktsson KP, Toftgård R.
    Eur J Cancer; 1999 May 15; 35(5):711-3. PubMed ID: 10505029
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  • 4. Analysis of PTCH/SMO/SHH pathway genes in medulloblastoma.
    Zurawel RH, Allen C, Chiappa S, Cato W, Biegel J, Cogen P, de Sauvage F, Raffel C.
    Genes Chromosomes Cancer; 2000 Jan 15; 27(1):44-51. PubMed ID: 10564585
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  • 7. Analysis of mutation in exon 17 of PTCH in patients with nevoid basal cell carcinoma syndrome.
    Li J, Wang J, Liu Y, Wang W.
    Mol Biol Rep; 2010 Jan 15; 37(1):359-62. PubMed ID: 19728145
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  • 10. Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.
    Wicking C, Shanley S, Smyth I, Gillies S, Negus K, Graham S, Suthers G, Haites N, Edwards M, Wainwright B, Chenevix-Trench G.
    Am J Hum Genet; 1997 Jan 15; 60(1):21-6. PubMed ID: 8981943
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  • 13. De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.
    Wicking C, Gillies S, Smyth I, Shanley S, Fowles L, Ratcliffe J, Wainwright B, Chenevix-Trench G.
    Am J Med Genet; 1997 Dec 19; 73(3):304-7. PubMed ID: 9415689
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  • 14. 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. The sebaceous nevus: a nevus with deletions of the PTCH gene.
    Xin H, Matt D, Qin JZ, Burg G, Böni R.
    Cancer Res; 1999 Apr 15; 59(8):1834-6. PubMed ID: 10213487
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