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Journal Abstract Search

692 related items for PubMed ID: 8658145

  • 1. Human homolog of patched, a candidate gene for the basal cell nevus syndrome.
    Johnson RL, Rothman AL, Xie J, Goodrich LV, Bare JW, Bonifas JM, Quinn AG, Myers RM, Cox DR, Epstein EH, Scott MP.
    Science; 1996 Jun 14; 272(5268):1668-71. PubMed ID: 8658145
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  • 2. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
    Aszterbaum M, Rothman A, Johnson RL, Fisher M, Xie J, Bonifas JM, Zhang X, Scott MP, Epstein EH.
    J Invest Dermatol; 1998 Jun 14; 110(6):885-8. PubMed ID: 9620294
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  • 6. 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. 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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  • 9. Novel mutations in the PATCHED gene in basal cell nevus syndrome.
    Lam CW, Leung CY, Lee KC, Xie J, Lo FM, Au TS, Tong SF, Poon MK, Chan LY, Luk NM.
    Mol Genet Metab; 2002 May 17; 76(1):57-61. PubMed ID: 12175781
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  • 10. The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas.
    Gailani MR, Ståhle-Bäckdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, Undén AB, Dean M, Brash DE, Bale AE, Toftgård R.
    Nat Genet; 1996 Sep 17; 14(1):78-81. PubMed ID: 8782823
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  • 13. Tumour suppressors. Dispatches from patched.
    Shilo BZ.
    Nature; 1996 Jul 11; 382(6587):115-6. PubMed ID: 8700198
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  • 15. PTC gene mutations and expression of SHH, PTC, SMO, and GLI-1 in odontogenic keratocysts.
    Ohki K, Kumamoto H, Ichinohasama R, Sato T, Takahashi N, Ooya K.
    Int J Oral Maxillofac Surg; 2004 Sep 11; 33(6):584-92. PubMed ID: 15308259
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  • 16. Variable expressivity of patched mutations in flies and humans.
    Bale AE.
    Am J Hum Genet; 1997 Jan 11; 60(1):10-2. PubMed ID: 8981940
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  • 17. PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.
    Santos DC, Zaphiropoulos PG, Neto CF, Pimentel ER, Sanches JA, Ruiz IR.
    Int J Dermatol; 2011 Jul 11; 50(7):838-43. PubMed ID: 21699520
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  • 18. Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.
    Boutet N, Bignon YJ, Drouin-Garraud V, Sarda P, Longy M, Lacombe D, Gorry P.
    J Invest Dermatol; 2003 Sep 11; 121(3):478-81. PubMed ID: 12925203
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  • 19. The hedgehog pathway and basal cell carcinomas.
    Bale AE, Yu KP.
    Hum Mol Genet; 2001 Apr 11; 10(7):757-62. PubMed ID: 11257109
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  • 20. Germline PTCH1 mutations in Japanese basal cell nevus syndrome patients.
    Takahashi C, Kanazawa N, Yoshikawa Y, Yoshikawa R, Saitoh Y, Chiyo H, Tanizawa T, Hashimoto-Tamaoki T, Nakano Y.
    J Hum Genet; 2009 Jul 11; 54(7):403-8. PubMed ID: 19557015
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