BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 25600101)

  • 1. Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris.
    Goetze S; Raessler F; Hipler UC; Schulz S; Kohlhase J; Elsner P
    J Eur Acad Dermatol Venereol; 2016 Mar; 30(3):493-4. PubMed ID: 25600101
    [No Abstract]   [Full Text] [Related]  

  • 2. Ultraviolet responses of Gorlin syndrome primary skin cells.
    Brellier F; Valin A; Chevallier-Lagente O; Gorry P; Avril MF; Magnaldo T
    Br J Dermatol; 2008 Aug; 159(2):445-52. PubMed ID: 18510667
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Basal cell nevus syndrome: clinical and molecular review and case report.
    Pino LC; Balassiano LK; Sessim M; de Almeida AP; Empinotti VD; Semenovitch I; Treu C; Lupi O
    Int J Dermatol; 2016 Apr; 55(4):367-75. PubMed ID: 26356331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Variable expression of naevoid basal cell carcinoma syndrome in a family with a novel mutation in the PTCH1 gene.
    Alonso-González J; Gutiérrez-González E; Fernández-Redondo V; Vega-Gliemmo A; Toribio J
    Clin Exp Dermatol; 2012 Apr; 37(3):311-3. PubMed ID: 22007994
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome.
    Alonso N; Cañueto J; Ciria S; Bueno E; Palacios-Alvarez I; Alegre M; Badenas C; Barreiro A; Pena L; Maldonado C; Nespeira-Jato MV; Peña-Penabad C; Azon A; Gavrilova M; Ferrer I; Sanmartin O; Robles L; Hernandez-Martin A; Urioste M; Puig S; Puig L; Gonzalez-Sarmiento R
    Br J Dermatol; 2018 Jan; 178(1):198-206. PubMed ID: 28733979
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe Rheumatoid Arthritis Developing in Conjunction with Gorlin Syndrome.
    Scott JF; Bordeaux JS
    J Rheumatol; 2016 Jul; 43(7):1447-9. PubMed ID: 27371652
    [No Abstract]   [Full Text] [Related]  

  • 11. A Japanese case of naevoid basal cell carcinoma syndrome associated with segmental vitiligo.
    Muramatsu S; Suga Y; Mizuno Y; Haseegawa T; Komuro Y; Kubo Y; Imakado S; Ogawa H
    Br J Dermatol; 2005 Apr; 152(4):812-4. PubMed ID: 15840128
    [No Abstract]   [Full Text] [Related]  

  • 12. Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features.
    Valdivielso-Ramos M; Solera J; Mauleon C; Hernanz JM; Amiñoso C; Galiano S; De la Cueva P
    Clin Exp Dermatol; 2014 Apr; 39(3):406-7. PubMed ID: 24635088
    [No Abstract]   [Full Text] [Related]  

  • 13. A novel missense mutation in the PTCH1 gene in a premature case of nevoid basal cell carcinoma syndrome.
    Nakamura M; Tokura Y
    Eur J Dermatol; 2009; 19(3):262-3. PubMed ID: 19213655
    [No Abstract]   [Full Text] [Related]  

  • 14. Gorlin syndrome with an ovarian leiomyoma associated with a PTCH1 second hit.
    Akizawa Y; Miyashita T; Sasaki R; Nagata R; Aoki R; Ishitani K; Nagashima Y; Matsui H; Saito K
    Am J Med Genet A; 2016 Apr; 170A(4):1029-34. PubMed ID: 26782978
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients.
    Ponti G; Bertazzoni G; Pastorino L; Monari E; Cuoghi A; Bergamini S; Bellei E; Benassi L; Azzoni P; Petrachi T; Magnoni C; Pellacani G; Loschi P; Pollio A; Witkowski AM; Tomasi A
    Biomed Res Int; 2013; 2013():794028. PubMed ID: 24369017
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
    Aszterbaum M; Rothman A; Johnson RL; Fisher M; Xie J; Bonifas JM; Zhang X; Scott MP; Epstein EH
    J Invest Dermatol; 1998 Jun; 110(6):885-8. PubMed ID: 9620294
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pediatric nevoid basal cell carcinoma syndrome.
    Pilkington S; McKinley LH; Miller RA
    Cutis; 2017 Dec; 100(6):423-426. PubMed ID: 29360891
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel alterations in IFT172 and KIFAP3 may induce basal cell carcinoma.
    Onodera S; Morita N; Nakamura Y; Takahashi S; Hashimoto K; Nomura T; Katakura A; Kosaki K; Azuma T
    Orphanet J Rare Dis; 2021 Oct; 16(1):443. PubMed ID: 34674729
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.
    Honma M; Ohishi Y; Uehara J; Ibe M; Kinouchi M; Ishida-Yamamoto A; Iizuka H
    J Dermatol Sci; 2008 Apr; 50(1):73-5. PubMed ID: 18068337
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.