BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 37504252)

  • 1. Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the
    Pál M; Vetró É; Nagy N; Nagy D; Horváth E; Bokor BA; Varga A; Seres L; Oláh J; Piffkó J; Széll M
    Curr Issues Mol Biol; 2023 Jun; 45(7):5293-5304. PubMed ID: 37504252
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. PTCH2 is not a strong candidate gene for gorlin syndrome predisposition.
    Smith MJ; Evans DG
    Fam Cancer; 2022 Jul; 21(3):343-346. PubMed ID: 34170463
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of
    Roemen GMJM; Theunissen TEJ; Hoezen WWJ; Steyls ARM; Paulussen ADC; Mosterd K; Rahikkala E; Zur Hausen A; Speel EJM; van Geel M
    Biomedicines; 2024 Jan; 12(2):. PubMed ID: 38397932
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Basal cell nevus syndrome or Gorlin syndrome.
    Thalakoti S; Geller T
    Handb Clin Neurol; 2015; 132():119-28. PubMed ID: 26564075
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel PTCH1 Mutation Causes Gorlin-Goltz Syndrome.
    Yue HT; Cao HY; He M
    Chin J Dent Res; 2024 Mar; 27(1):83-88. PubMed ID: 38546523
    [TBL] [Abstract][Full Text] [Related]  

  • 11. "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]  

  • 12. Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.
    Casano K; Meddaugh H; Zambrano RM; Marble M; Torres JI; Lacassie Y
    Eur J Med Genet; 2020 Apr; 63(4):103842. PubMed ID: 31945512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population.
    Lu N; Wang J; Zhu B; Zhang M; Qi F; Wang X; Gu J
    Cancer Biomark; 2017 Dec; 21(1):161-168. PubMed ID: 29081410
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Medulloblastoma and other neoplasms in patients with heterozygous germline SUFU variants: A scoping review.
    Lee SG; Evans G; Stephen M; Goren R; Bondy M; Goodman S
    Am J Med Genet A; 2024 Jun; 194(6):e63496. PubMed ID: 38282294
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome.
    Matsudate Y; Naruto T; Hayashi Y; Minami M; Tohyama M; Yokota K; Yamada D; Imoto I; Kubo Y
    J Dermatol Sci; 2017 Jun; 86(3):206-211. PubMed ID: 28342698
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development of a targeted gene panel for the diagnosis of Gorlin syndrome.
    Nakamura Y; Onodera S; Takano M; Katakura A; Nomura T; Azuma T
    Int J Oral Maxillofac Surg; 2022 Nov; 51(11):1431-1444. PubMed ID: 35437209
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 8.