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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 9341860)

  • 1. Characterisation of human patched germ line mutations in naevoid basal cell carcinoma syndrome.
    Lench NJ; Telford EA; High AS; Markham AF; Wicking C; Wainwright BJ
    Hum Genet; 1997 Oct; 100(5-6):497-502. PubMed ID: 9341860
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. 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]  

  • 4. 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; 11(6):480. PubMed ID: 10200051
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.
    Wicking C; Gillies S; Smyth I; Shanley S; Fowles L; Ratcliffe J; Wainwright B; Chenevix-Trench G
    Am J Med Genet; 1997 Dec; 73(3):304-7. PubMed ID: 9415689
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of known and novel PTCH mutations in both syndromic and non-syndromic keratocystic odontogenic tumors.
    Pan S; Xu LL; Sun LS; Li TJ
    Int J Oral Sci; 2009 Mar; 1(1):34-8. PubMed ID: 20690502
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 56(20):4599-601. PubMed ID: 8840969
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. 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; 47(5):366-9. PubMed ID: 19008023
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Identification of a novel mutation in the PTCH gene in a Korean family with naevoid basal cell carcinoma syndrome.
    Lee YW; Roh BH; Ki CS; Park YL; Shin HB; Lee YK; Choi TY; Whang KU
    Clin Exp Dermatol; 2007 Mar; 32(2):202-3. PubMed ID: 16780502
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. 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; 15(3):361-6. PubMed ID: 9233770
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.