BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 29575684)

  • 1. 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]  

  • 2. Germline PTCH1 mutations in Japanese basal cell nevus syndrome patients.
    Takahashi C; Kanazawa N; Yoshikawa Y; Yoshikawa R; Saitoh Y; Chiyo H; Tanizawa T; Hashimoto-Tamaoki T; Nakano Y
    J Hum Genet; 2009 Jul; 54(7):403-8. PubMed ID: 19557015
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic profiling of basal cell carcinomas detects postzygotic mosaicism in basal cell naevus syndrome.
    Reinders MGHC; Cosgun B; Gijezen LMC; van Oosterhoud CN; Kelleners-Smeets NWJ; Vermander E; Vreeburg M; Steijlen PM; Mosterd K; van Geel M
    Br J Dermatol; 2019 Sep; 181(3):587-591. PubMed ID: 30520020
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.
    Smith MJ; Beetz C; Williams SG; Bhaskar SS; O'Sullivan J; Anderson B; Daly SB; Urquhart JE; Bholah Z; Oudit D; Cheesman E; Kelsey A; McCabe MG; Newman WG; Evans DG
    J Clin Oncol; 2014 Dec; 32(36):4155-61. PubMed ID: 25403219
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome.
    Gielen RCAM; Reinders MGHC; Koillinen HK; Paulussen ADC; Mosterd K; van Geel M
    J Hum Genet; 2018 Sep; 63(9):965-969. PubMed ID: 29930296
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unexpected phenotype in a frameshift mutation of PTCH1.
    Beltrami B; Prada E; Tolva G; Scuvera G; Silipigni R; Graziani D; Bulfamante G; Gervasini C; Marchisio P; Milani D
    Mol Genet Genomic Med; 2020 Jan; 8(1):e987. PubMed ID: 31578813
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [PTCH1 gene analysis in 25 Japanese patients with Gorlin syndrome].
    Endo M; Fujii K; Miyashita T; Uchikawa H; Tanabe R; Sugita K; Arai H; Kohno Y
    No To Hattatsu; 2009 Jul; 41(4):259-63. PubMed ID: 19618880
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.
    Musani V; Ozretić P; Trnski D; Sabol M; Poduje S; Tošić M; Šitum M; Levanat S
    Croat Med J; 2018 Feb; 59(1):20-24. PubMed ID: 29498494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome.
    Kaibuchi-Ando K; Takeichi T; Ito Y; Takeuchi S; Yamashita Y; Yamada M; Muro Y; Ogi T; Akiyama M
    Nagoya J Med Sci; 2021 May; 83(2):393-396. PubMed ID: 34239189
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Postzygotic mosaicism in basal cell naevus syndrome.
    Reinders MGHC; Boersma HJ; Leter EM; Vreeburg M; Paulussen ADC; Arits AHMM; Roemen GMJM; Speel EJM; Steijlen PM; van Geel M; Mosterd K
    Br J Dermatol; 2017 Jul; 177(1):249-252. PubMed ID: 27658957
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. "PTCH"-ing it together: a basal cell nevus syndrome review.
    Lam C; Ou JC; Billingsley EM
    Dermatol Surg; 2013 Nov; 39(11):1557-72. PubMed ID: 23725561
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Retrospective analysis of the histopathologic features of basal cell carcinomas in pediatric patients with basal cell nevus syndrome.
    Nguyen CV; Rubin AI; Smith A; Castelo-Soccio L
    J Cutan Pathol; 2021 Mar; 48(3):390-395. PubMed ID: 33063358
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.
    Onodera S; Saito A; Hasegawa D; Morita N; Watanabe K; Nomura T; Shibahara T; Ohba S; Yamaguchi A; Azuma T
    PLoS One; 2017; 12(9):e0184702. PubMed ID: 28915250
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.