BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

364 related articles for article (PubMed ID: 25117323)

  • 21. [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]  

  • 22. Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome.
    Kosaki R; Nagao K; Kameyama K; Suzuki M; Fujii K; Miyashita T
    Am J Med Genet A; 2012 Jul; 158A(7):1724-8. PubMed ID: 22711650
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Heterozygous PTCH1 Mutations Impact the Bone Metabolism in Patients With Nevoid Basal Cell Carcinoma Syndrome Likely by Regulating SPARC Expression.
    Hong Y; Zhang J; Zhang H; Li X; Qu J; Zhai J; Zhang L; Chen F; Li T
    J Bone Miner Res; 2016 Jul; 31(7):1413-28. PubMed ID: 26890308
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome.
    Ozcan G; Balta B; Sekerci AE; Etoz OA; Martinuzzi C; Kara O; Pastorino L; Kocoglu F; Ulker O; Erdogan M
    Indian J Pathol Microbiol; 2016; 59(3):335-8. PubMed ID: 27510672
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. The large intracellular loop of ptch1 mediates the non-canonical Hedgehog pathway through cyclin B1 in nevoid basal cell carcinoma syndrome.
    Yu FY; Hong YY; Qu JF; Chen F; Li TJ
    Int J Mol Med; 2014 Aug; 34(2):507-12. PubMed ID: 24840883
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic and clinicopathologic aspects of Gorlin-Goltz syndrome (NBCCS): presentation of two case reports and literature review.
    Acocella A; Sacco R; Bertolai R; Sacco N
    Minerva Stomatol; 2009; 58(1-2):43-53. PubMed ID: 19234436
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Manifestations of Gorlin-Goltz syndrome.
    Larsen AK; Mikkelsen DB; Hertz JM; Bygum A
    Dan Med J; 2014 May; 61(5):A4829. PubMed ID: 24814739
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New mutations and an updated database for the patched-1 (PTCH1) gene.
    Reinders MG; van Hout AF; Cosgun B; Paulussen AD; Leter EM; Steijlen PM; Mosterd K; van Geel M; Gille JJ
    Mol Genet Genomic Med; 2018 May; 6(3):409-415. PubMed ID: 29575684
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. Myogenic tumors in nevoid Basal cell carcinoma syndrome.
    Hettmer S; Teot LA; Kozakewich H; Werger AM; Davies KJ; Fletcher CD; Grier HE; Rodriguez-Galindo C; Wagers AJ
    J Pediatr Hematol Oncol; 2015 Mar; 37(2):147-9. PubMed ID: 24517962
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. Radiological features in 82 patients with nevoid basal cell carcinoma (NBCC or Gorlin) syndrome.
    Kimonis VE; Mehta SG; Digiovanna JJ; Bale SJ; Pastakia B
    Genet Med; 2004; 6(6):495-502. PubMed ID: 15545745
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Intronic splicing mutations in PTCH1 cause Gorlin syndrome.
    Bholah Z; Smith MJ; Byers HJ; Miles EK; Evans DG; Newman WG
    Fam Cancer; 2014 Sep; 13(3):477-80. PubMed ID: 24659465
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.