BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 28328116)

  • 1. Brain morphology in children with nevoid basal cell carcinoma syndrome.
    Shiohama T; Fujii K; Miyashita T; Mizuochi H; Uchikawa H; Shimojo N
    Am J Med Genet A; 2017 Apr; 173(4):946-952. PubMed ID: 28328116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Role of Dermal Fibroblasts in Nevoid Basal Cell Carcinoma Syndrome Patients: An Overview.
    Bellei B; Caputo S; Carbone A; Silipo V; Papaccio F; Picardo M; Eibenschutz L
    Int J Mol Sci; 2020 Jan; 21(3):. PubMed ID: 31979112
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. [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]  

  • 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. Mechanisms of inactivation of PTCH1 gene in nevoid basal cell carcinoma syndrome: modification of the two-hit hypothesis.
    Pan S; Dong Q; Sun LS; Li TJ
    Clin Cancer Res; 2010 Jan; 16(2):442-50. PubMed ID: 20068110
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome.
    Zhou J; Zhang G; Shi M; Liu Z; Xiao M; Fu S; Gong X; Shi X
    Med Mol Morphol; 2019 Dec; 52(4):235-237. PubMed ID: 30997576
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Immunohistochemical evaluation of Sonic Hedgehog signaling pathway proteins (Shh, Ptch1, Ptch2, Smo, Gli1, Gli2, and Gli3) in sporadic and syndromic odontogenic keratocysts.
    Hoyos Cadavid AM; Kaminagakura E; Rodrigues MFSD; Pinto CAL; Teshima THN; Alves FA
    Clin Oral Investig; 2019 Jan; 23(1):153-159. PubMed ID: 29564556
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Basal Cell Carcinoma in Gorlin's Patients: a Matter of Fibroblasts-Led Protumoral Microenvironment?
    Gache Y; Brellier F; Rouanet S; Al-Qaraghuli S; Goncalves-Maia M; Burty-Valin E; Barnay S; Scarzello S; Ruat M; Sevenet N; Avril MF; Magnaldo T
    PLoS One; 2015; 10(12):e0145369. PubMed ID: 26694869
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. [Skeletal and dermatological manifestations of the nevoid Basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Results of 8 patients in 12 years].
    Rupprecht M; Mensing CH; Barvencik F; Ittrich H; Heiland M; Rueger JM; Amling M; Pogoda P
    Rofo; 2007 Jun; 179(6):618-26. PubMed ID: 17492539
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Ponti G; Manfredini M; Pastorino L; Maccaferri M; Tomasi A; Pellacani G
    Anticancer Res; 2018 Jan; 38(1):471-476. PubMed ID: 29277811
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Elucidating the role of molecular signaling pathways in the tumorigenesis of basal cell carcinoma.
    Tang JY
    Semin Cutan Med Surg; 2011 Dec; 30(4 Suppl):S6-9. PubMed ID: 22177103
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. PTCH1 +/- dermal fibroblasts isolated from healthy skin of Gorlin syndrome patients exhibit features of carcinoma associated fibroblasts.
    Valin A; Barnay-Verdier S; Robert T; Ripoche H; Brellier F; Chevallier-Lagente O; Avril MF; Magnaldo T
    PLoS One; 2009; 4(3):e4818. PubMed ID: 19287498
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.