BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 29381605)

  • 1. Novel PTCH1 Gene Mutation in Nevoid Basal Cell Carcinoma Syndrome.
    Sim YC; Kim GH; Choi SW; Ahn KM
    J Craniofac Surg; 2018 May; 29(3):e252-e255. PubMed ID: 29381605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PTCH1 and SMO gene alterations in keratocystic odontogenic tumors.
    Sun LS; Li XF; Li TJ
    J Dent Res; 2008 Jun; 87(6):575-9. PubMed ID: 18502968
    [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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. [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]  

  • 8. PTCH1 gene mutations in Keratocystic odontogenic tumors: a study of 43 Chinese patients and a systematic review.
    Guo YY; Zhang JY; Li XF; Luo HY; Chen F; Li TJ
    PLoS One; 2013; 8(10):e77305. PubMed ID: 24204797
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12.
    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]  

  • 13. 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]  

  • 14. 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]  

  • 15. [PTCH2 gene alterations in keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome].
    Xu LL; Li TJ
    Beijing Da Xue Xue Bao Yi Xue Ban; 2008 Feb; 40(1):15-8. PubMed ID: 18278130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Somatic mosaicism containing double mutations in
    Ikemoto Y; Takayama Y; Fujii K; Masuda M; Kato C; Hatsuse H; Fujitani K; Nagao K; Kameyama K; Ikehara H; Toyoda M; Umezawa A; Miyashita T
    J Med Genet; 2017 Aug; 54(8):579-584. PubMed ID: 28363938
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data.
    Gianferante DM; Rotunno M; Dean M; Zhou W; Hicks BD; Wyatt K; Jones K; Wang M; Zhu B; Goldstein AM; Mirabello L
    Mol Genet Genomic Med; 2018 Nov; 6(6):1168-1180. PubMed ID: 30411536
    [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. 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]  

  • 20. Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.
    Kato C; Fujii K; Arai Y; Hatsuse H; Nagao K; Takayama Y; Kameyama K; Fujii K; Miyashita T
    Fam Cancer; 2017 Jan; 16(1):131-138. PubMed ID: 27561271
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.