BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 16675912)

  • 1. 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; 27(4):175-80. PubMed ID: 16675912
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. 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; 14(2):174-9. PubMed ID: 18302678
    [TBL] [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; 79(6):1418-22. PubMed ID: 10890722
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 27(1):21-6. PubMed ID: 11457640
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 102(11):793-7. PubMed ID: 14724726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Detection of PTCH gene mutations in odontogenic keratocysts by SSCP and DNA sequencing].
    Gu XM; Li TJ
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2006 Aug; 24(4):293-6. PubMed ID: 16999341
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of BRAFV600E mutation in odontogenic keratocysts.
    França JA; de Sousa SF; Diniz MG; Pereira TDSF; de Resende TAC; Santos JND; Gomez RS; Gomes CC
    J Oral Pathol Med; 2018 Feb; 47(2):186-191. PubMed ID: 29272070
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 95(4):548-53. PubMed ID: 16909134
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 121(2):118-21. PubMed ID: 18272036
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 24(5):441. PubMed ID: 15459969
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 296(7):303-8. PubMed ID: 15565302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 56(20):4562-5. PubMed ID: 8840960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. One germline mutation of PTCH gene in a Chinese family with non-syndromic keratocystic odontogenic tumours.
    Wang X; Lu Y; Shen G; Chen W
    Int J Oral Maxillofac Surg; 2011 Aug; 40(8):829-33. PubMed ID: 21507611
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic screening for nevoid basal cell carcinoma syndrome in patients with a solitary keratocystic odontogenic tumour is not useful.
    Karagozoglu KH; Van Hagen JM; Baart JA; Van Der Waal I
    Minerva Stomatol; 2011; 60(1-2):1-4. PubMed ID: 21252844
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 26(3):283. PubMed ID: 16088933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts.
    Gu XM; Zhao HS; Sun LS; Li TJ
    J Dent Res; 2006 Sep; 85(9):859-63. PubMed ID: 16931872
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 60(1):21-6. PubMed ID: 8981943
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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; 149(2):78-81. PubMed ID: 15688838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The immunoprofile of odontogenic keratocyst (keratocystic odontogenic tumor) that includes expression of PTCH, SMO, GLI-1 and bcl-2 is similar to ameloblastoma but different from odontogenic cysts.
    Vered M; Peleg O; Taicher S; Buchner A
    J Oral Pathol Med; 2009 Aug; 38(7):597-604. PubMed ID: 19473442
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.