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 *

236 related articles for article (PubMed ID: 12925203)

  • 1. Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.
    Boutet N; Bignon YJ; Drouin-Garraud V; Sarda P; Longy M; Lacombe D; Gorry P
    J Invest Dermatol; 2003 Sep; 121(3):478-81. PubMed ID: 12925203
    [TBL] [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; 56(20):4562-5. PubMed ID: 8840960
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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; 25(3):322-3. PubMed ID: 15712338
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.
    Musani V; Ozretić P; Trnski D; Sabol M; Poduje S; Tošić M; Šitum M; Levanat S
    Croat Med J; 2018 Feb; 59(1):20-24. PubMed ID: 29498494
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report.
    Škodrić-Trifunović V; Stjepanović M; Savić Ž; Ilić M; Kavečan I; Jovanović Privrodski J; Spasovski V; Stojiljković M; Pavlović S
    Croat Med J; 2015 Feb; 56(1):63-7. PubMed ID: 25727044
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. [PTCH1 gene analysis in 25 Japanese patients with Gorlin syndrome].
    Endo M; Fujii K; Miyashita T; Uchikawa H; Tanabe R; Sugita K; Arai H; Kohno Y
    No To Hattatsu; 2009 Jul; 41(4):259-63. PubMed ID: 19618880
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An 8.9 year old girl with autism and Gorlin syndrome.
    Delbroek H; Steyaert J; Legius E
    Eur J Paediatr Neurol; 2011 May; 15(3):268-70. PubMed ID: 21190878
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. PTCH mutations: distribution and analyses.
    Lindström E; Shimokawa T; Toftgård R; Zaphiropoulos PG
    Hum Mutat; 2006 Mar; 27(3):215-9. PubMed ID: 16419085
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients: two familial and three sporadic cases including the first Japanese patient with medulloblastoma.
    Fujii M; Noguchi K; Urade M; Muraki Y; Moridera K; Kishimoto H; Hashimoto-Tamaoki T; Nakano Y
    J Hum Genet; 2011 Apr; 56(4):277-83. PubMed ID: 21368767
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel missense mutation in the PTCH1 gene in a premature case of nevoid basal cell carcinoma syndrome.
    Nakamura M; Tokura Y
    Eur J Dermatol; 2009; 19(3):262-3. PubMed ID: 19213655
    [No Abstract]   [Full Text] [Related]  

  • 18. Nevoid Basal Cell Carcinoma Syndrome:
    Martinez MF; Romano MV; Martinez AP; González A; Muchnik C; Stengel FM; Mazzuoccolo LD; Azurmendi PJ
    Cells; 2019 Feb; 8(2):. PubMed ID: 30754660
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation.
    Rodrigues AL; Carvalho A; Cabral R; Carneiro V; Gilardi P; Duarte CP; Puente-Prieto J; Santos P; Mota-Vieira L
    Genet Mol Res; 2014 Jul; 13(3):5654-63. PubMed ID: 25117323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.