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Journal Abstract Search

154 related items for PubMed ID: 18476955

  • 1. 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; 159(1):222-7. PubMed ID: 18476955
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  • 2. 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
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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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  • 9. 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
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  • 11. 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 Jun 15; 11(6):480. PubMed ID: 10200051
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  • 12. 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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  • 16. Is PATCHED an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report.
    Roudgari H, Farndon PA, Murray AD, Hardy C, Miedzybrodzka Z.
    Clin Genet; 2012 Jul 17; 82(1):71-6. PubMed ID: 21651513
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  • 18. 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 17; 21(4):451-2. PubMed ID: 12655573
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  • 19. Patched mutations and hairy skin patches: a new sign in Gorlin syndrome.
    Wilson LC, Ajayi-Obe E, Bernhard B, Maas SM.
    Am J Med Genet A; 2006 Dec 01; 140(23):2625-30. PubMed ID: 16906569
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  • 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
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