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Journal Abstract Search

130 related items for PubMed ID: 9654212

  • 1. 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; 102(5):598-601. PubMed ID: 9654212
    [Abstract] [Full Text] [Related]

  • 2. Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients.
    Fujii K, Kohno Y, Sugita K, Nakamura M, Moroi Y, Urabe K, Furue M, Yamada M, Miyashita T.
    Hum Mutat; 2003 Apr; 21(4):451-2. PubMed ID: 12655573
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Nonsense-associated altered splicing of the Patched gene fails to suppress carcinogenesis in Gorlin syndrome.
    Laimer M, Onder K, Schlager P, Lanschuetzer CM, Emberger M, Selhofer S, Hintner H, Bauer JW.
    Br J Dermatol; 2008 Jul 15; 159(1):222-7. PubMed ID: 18476955
    [Abstract] [Full Text] [Related]

  • 5. Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays.
    Nagao K, Togawa N, Fujii K, Uchikawa H, Kohno Y, Yamada M, Miyashita T.
    Hum Mol Genet; 2005 Nov 15; 14(22):3379-88. PubMed ID: 16203740
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Gorlin syndrome: identification of 4 novel germ-line mutations of the human patched (PTCH) gene. Mutations in brief no. 137. Online.
    Hasenpusch-Theil K, Bataille V, Laehdetie J, Obermayr F, Sampson JR, Frischauf AM.
    Hum Mutat; 1998 Jul 17; 11(6):480. PubMed ID: 10200051
    [Abstract] [Full Text] [Related]

  • 8. New mutation of the patched homologue 1 gene in a Chinese family with naevoid basal cell carcinoma syndrome.
    Wang W, Wang J, Li J, Mao L, Guo F, Zhang B.
    Br J Oral Maxillofac Surg; 2009 Jul 17; 47(5):366-9. PubMed ID: 19008023
    [Abstract] [Full Text] [Related]

  • 9.
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  • 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. A new germline mutation of the PTCH gene in a Japanese patient with nevoid basal cell carcinoma syndrome associated with meningioma.
    Tate G, Li M, Suzuki T, Mitsuya T.
    Jpn J Clin Oncol; 2003 Jan 15; 33(1):47-50. PubMed ID: 12604725
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 76(1):57-61. PubMed ID: 12175781
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 102(11):793-7. PubMed ID: 14724726
    [Abstract] [Full Text] [Related]

  • 17. [PTCH gene mutations in odontogenic keratocysts].
    Yuan JW, Li TJ, Zhong HH, Zhao HS.
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2006 Jan 15; 41(1):41-4. PubMed ID: 16620627
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 25(3):322-3. PubMed ID: 15712338
    [Abstract] [Full Text] [Related]

  • 19. Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.
    Tanioka M, Takahashi K, Kawabata T, Kosugi S, Murakami K, Miyachi Y, Nishigori C, Iizuka T.
    Arch Dermatol Res; 2005 Jan 15; 296(7):303-8. PubMed ID: 15565302
    [Abstract] [Full Text] [Related]

  • 20. 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]

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