BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 25727044)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome.
    Matsuzawa N; Nagao T; Shimozato K; Niikawa N; Yoshiura KI
    J Clin Pathol; 2006 Oct; 59(10):1084-6. PubMed ID: 17021131
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Basal cell nevus syndrome: clinical and genetic diagnosis.
    García de Marcos JA; Dean-Ferrer A; Arroyo Rodríguez S; Calderón-Polanco J; Alamillos Granados FJ; Poblet E
    Oral Maxillofac Surg; 2009 Dec; 13(4):225-30. PubMed ID: 19795138
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome.
    Durmaz CD; Evans G; Smith MJ; Ertop P; Akay BN; Tuncalı T
    Cytogenet Genome Res; 2018; 154(2):57-61. PubMed ID: 29544218
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Nevoid basal cell carcinoma syndrome with corpus callosum agenesis, PTCH1 mutation and absence of basal cell carcinoma].
    Mazzuoccolo LD; Martínez MF; Muchnik C; Azurmendi PJ; Stengel F
    Medicina (B Aires); 2014; 74(4):307-10. PubMed ID: 25188659
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome.
    Pastorino L; Pollio A; Pellacani G; Guarneri C; Ghiorzo P; Longo C; Bruno W; Giusti F; Bassoli S; Bianchi-Scarrà G; Ruini C; Seidenari S; Tomasi A; Ponti G
    PLoS One; 2012; 7(8):e43827. PubMed ID: 22952776
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation.
    Ponti G; Ruini C; Pastorino L; Loschi P; Pecchi A; Malagoli M; Mandel VD; Boano R; Conti A; Pellacani G; Tomasi A
    Future Oncol; 2014 May; 10(6):917-25. PubMed ID: 24941978
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.
    Fujii K; Ohashi H; Suzuki M; Hatsuse H; Shiohama T; Uchikawa H; Miyashita T
    Fam Cancer; 2013 Dec; 12(4):611-4. PubMed ID: 23479190
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.
    Santos DC; Zaphiropoulos PG; Neto CF; Pimentel ER; Sanches JA; Ruiz IR
    Int J Dermatol; 2011 Jul; 50(7):838-43. PubMed ID: 21699520
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome.
    Ponti G; Pollio A; Mignogna MD; Pellacani G; Pastorino L; Bianchi-Scarrà G; Di Gregorio C; Magnoni C; Azzoni P; Greco M; Seidenari S
    Cancer Genet; 2012 Apr; 205(4):177-81. PubMed ID: 22559979
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations: a case report.
    Sasaki R; Miyashita T; Matsumoto N; Fujii K; Saito K; Ando T
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 Aug; 110(2):e41-6. PubMed ID: 20659694
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Analysis of mutation in exon 17 of PTCH in patients with nevoid basal cell carcinoma syndrome.
    Li J; Wang J; Liu Y; Wang W
    Mol Biol Rep; 2010 Jan; 37(1):359-62. PubMed ID: 19728145
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.