BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 17328283)

  • 1. Multifocal desmoplastic medulloblastoma in an african-american child with nevoid basal cell carcinoma (gorlin) syndrome. Case report.
    Smucker PS; Smith JL
    J Neurosurg; 2006 Oct; 105(4 Suppl):315-20. PubMed ID: 17328283
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nevoid basal cell carcinoma syndrome: relation with desmoplastic medulloblastoma in infancy. A population-based study and review of the literature.
    Amlashi SF; Riffaud L; Brassier G; Morandi X
    Cancer; 2003 Aug; 98(3):618-24. PubMed ID: 12879481
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
    Vortmeyer AO; Stavrou T; Selby D; Li G; Weil RJ; Park WS; Moon YW; Chandra R; Goldstein AM; Zhuang Z
    Cancer; 1999 Jun; 85(12):2662-7. PubMed ID: 10375116
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction.
    Korczak JF; Brahim JS; DiGiovanna JJ; Kase RG; Wexler LH; Goldstein AM
    Am J Med Genet; 1997 Mar; 69(3):309-14. PubMed ID: 9096762
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.
    Lacombe D; Chateil JF; Fontan D; Battin J
    Genet Couns; 1990; 1(3-4):273-7. PubMed ID: 2098052
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.
    Garavelli L; Piemontese MR; Cavazza A; Rosato S; Wischmeijer A; Gelmini C; Albertini E; Albertini G; Forzano F; Franchi F; Carella M; Zelante L; Superti-Furga A
    Am J Med Genet A; 2013 Nov; 161A(11):2894-901. PubMed ID: 24124115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [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]  

  • 13. 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]  

  • 14. Basal cell nevus syndrome and medulloblastoma: a case report.
    Romero Pérez JA; Lleras Santana I
    Bol Asoc Med P R; 1993; 85(1-3):24-6. PubMed ID: 8060441
    [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. Nevoid basal cell carcinoma syndrome (Gorlin syndrome).
    Lo Muzio L
    Orphanet J Rare Dis; 2008 Nov; 3():32. PubMed ID: 19032739
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.
    Hasan Ali O; Yurchenko AA; Pavlova O; Sartori A; Bomze D; Higgins R; Ring SS; Hartmann F; Bühler D; Fritzsche FR; Jochum W; Navarini AA; Kim A; French LE; Dermitzakis E; Christiano AM; Hohl D; Bickers DR; Nikolaev SI; Flatz L
    J Eur Acad Dermatol Venereol; 2021 Feb; 35(2):396-402. PubMed ID: 32564428
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.