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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

154 related items for PubMed ID: 12175781

  • 1. 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; 76(1):57-61. PubMed ID: 12175781
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles.
    Savino M, d'Apolito M, Formica V, Baorda F, Mari F, Renieri A, Carabba E, Tarantino E, Andreucci E, Belli S, Lo Muzio L, Dallapiccola B, Zelante L, Savoia A.
    Hum Mutat; 2004 Nov 15; 24(5):441. PubMed ID: 15459969
    [Abstract] [Full Text] [Related]

  • 4. PTCH gene mutations in odontogenic keratocysts.
    Barreto DC, Gomez RS, Bale AE, Boson WL, De Marco L.
    J Dent Res; 2000 Jun 15; 79(6):1418-22. PubMed ID: 10890722
    [Abstract] [Full Text] [Related]

  • 5. Expression of the Sonic Hedgehog receptor "PATCHED" in basal cell carcinomas and odontogenic keratocysts.
    Zedan W, Robinson PA, Markham AF, High AS.
    J Pathol; 2001 Aug 15; 194(4):473-7. PubMed ID: 11523056
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 110(6):885-8. PubMed ID: 9620294
    [Abstract] [Full Text] [Related]

  • 7. Basal cell nevus syndrome: clinical and genetic diagnosis.
    García de Marcos JA, Dean-Ferrer A, Arroyo Rodríguez S, Calderón-Polanco J, Alamillos Granados FJ, Poblet E.
    Oral Maxillofac Surg; 2009 Dec 15; 13(4):225-30. PubMed ID: 19795138
    [Abstract] [Full Text] [Related]

  • 8. Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory.
    Klein RD, Dykas DJ, Bale AE.
    Genet Med; 2005 Dec 15; 7(9):611-9. PubMed ID: 16301862
    [Abstract] [Full Text] [Related]

  • 9. Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.
    Minami M, Urano Y, Ishigami T, Tsuda H, Kusaka J, Arase S.
    J Dermatol Sci; 2001 Sep 15; 27(1):21-6. PubMed ID: 11457640
    [Abstract] [Full Text] [Related]

  • 10. Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients.
    Chidambaram A, Goldstein AM, Gailani MR, Gerrard B, Bale SJ, DiGiovanna JJ, Bale AE, Dean M.
    Cancer Res; 1996 Oct 15; 56(20):4599-601. PubMed ID: 8840969
    [Abstract] [Full Text] [Related]

  • 11. PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients.
    Li TJ, Yuan JW, Gu XM, Sun LS, Zhao HS.
    Oral Dis; 2008 Mar 15; 14(2):174-9. PubMed ID: 18302678
    [Abstract] [Full Text] [Related]

  • 12. Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome.
    Song YL, Zhang WF, Peng B, Wang CN, Wang Q, Bian Z.
    Tumour Biol; 2006 Mar 15; 27(4):175-80. PubMed ID: 16675912
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. DHPLC analysis of patients with Nevoid Basal Cell Carcinoma Syndrome reveals novel PTCH missense mutations in the sterol-sensing domain.
    Marsh A, Wicking C, Wainwright B, Chenevix-Trench G.
    Hum Mutat; 2005 Sep 14; 26(3):283. PubMed ID: 16088933
    [Abstract] [Full Text] [Related]

  • 15. [From gene to disease: basal cell naevus syndrome].
    de Meij TG, Baars MJ, Gille JJ, Hack WW, Haasnoot K, van Hagen JM.
    Ned Tijdschr Geneeskd; 2005 Jan 08; 149(2):78-81. PubMed ID: 15688838
    [Abstract] [Full Text] [Related]

  • 16. The effects of splice site mutations in patients with naevoid basal cell carcinoma syndrome.
    Smyth I, Wicking C, Wainwright B, Chenevix-Trench G.
    Hum Genet; 1998 May 08; 102(5):598-601. PubMed ID: 9654212
    [Abstract] [Full Text] [Related]

  • 17. 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 08; 33(6):584-92. PubMed ID: 15308259
    [Abstract] [Full Text] [Related]

  • 18. Nevoid basal cell carcinoma syndrome - clinical manifestations and mutation analysis of a Taiwanese family.
    Chung CH, Wong TY, Shieh TY, Shieh DB, Chao SC.
    J Formos Med Assoc; 2003 Nov 08; 102(11):793-7. PubMed ID: 14724726
    [Abstract] [Full Text] [Related]

  • 19. Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.
    Pastorino L, Cusano R, Nasti S, Faravelli F, Forzano F, Baldo C, Barile M, Gliori S, Muggianu M, Ghigliotti G, Lacaita MG, Lo Muzio L, Bianchi-Scarra G.
    Hum Mutat; 2005 Mar 08; 25(3):322-3. PubMed ID: 15712338
    [Abstract] [Full Text] [Related]

  • 20. A new mutation of PTCH gene in a Chinese family with nevoid basal cell carcinoma syndrome.
    Lü Y, Zhu HG, Ye WM, Zhang MB, He D, Chen WT.
    Chin Med J (Engl); 2008 Jan 20; 121(2):118-21. PubMed ID: 18272036
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.