BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 14574160)

  • 1. Familial melanoma: a complex disorder leading to controversy on DNA testing.
    de Snoo FA; Bergman W; Gruis NA
    Fam Cancer; 2003; 2(2):109-16. PubMed ID: 14574160
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [From gene to disease; from p16 to melanoma].
    Gruis NA; Bergman W
    Ned Tijdschr Geneeskd; 2000 Oct; 144(44):2100-2. PubMed ID: 11103670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.
    Potjer TP; van der Stoep N; Houwing-Duistermaat JJ; Konings IC; Aalfs CM; van den Akker PC; Ausems MG; Dommering CJ; van der Kolk LE; Maiburg MC; Spruijt L; Wagner A; Vasen HF; Hes FJ
    BMC Res Notes; 2015 Jun; 8():264. PubMed ID: 26111702
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Monitoring of kindreds with hereditary predisposition for cutaneous melanoma and dysplastic nevus syndrome: results of a Swedish preventive program.
    Hansson J; Bergenmar M; Hofer PA; Lundell G; Månsson-Brahme E; Ringborg U; Synnerstad I; Bratel AT; Wennberg AM; Rosdahl I
    J Clin Oncol; 2007 Jul; 25(19):2819-24. PubMed ID: 17602087
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).
    Vasen HF; Gruis NA; Frants RR; van Der Velden PA; Hille ET; Bergman W
    Int J Cancer; 2000 Sep; 87(6):809-11. PubMed ID: 10956390
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetics of hereditary melanoma and nevi. 1998 update.
    Greene MH
    Cancer; 1999 Dec; 86(11 Suppl):2464-77. PubMed ID: 10630172
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic testing for familial melanoma.
    Primiero CA; Maas EJ; Wallingford CK; Soyer HP; McInerney-Leo AM
    Ital J Dermatol Venerol; 2024 Feb; 159(1):34-42. PubMed ID: 38287743
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reply to: "The absence of multiple atypical nevi in germline CDKN2A mutations".
    Soura E; Stratigos AJ; Tsao H
    J Am Acad Dermatol; 2016 Oct; 75(4):e159. PubMed ID: 27646764
    [No Abstract]   [Full Text] [Related]  

  • 9. A review of inherited predisposition to melanoma.
    Cannon-Albright LA; Kamb A; Skolnick M
    Semin Oncol; 1996 Dec; 23(6):667-72. PubMed ID: 8970585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic counseling and DNA testing in patients with increased risks for malignant melanoma].
    Itin PH; Fistarol SK
    Ther Umsch; 2003 Aug; 60(8):469-72. PubMed ID: 14502854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Swedish CDKN2A mutation carriers do not present the atypical mole syndrome phenotype.
    Nielsen K; Harbst K; Måsbäck A; Jönsson G; Borg A; Olsson H; Ingvar C
    Melanoma Res; 2010 Aug; 20(4):266-72. PubMed ID: 20526219
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.
    van der Velden PA; Sandkuijl LA; Bergman W; Hille ET; Frants RR; Gruis NA
    Genome Res; 1999 Jun; 9(6):575-80. PubMed ID: 10400925
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Primary melanoma tumors from CDKN2A mutation carriers do not belong to a distinct molecular subclass.
    Staaf J; Harbst K; Lauss M; Ringnér M; Måsbäck A; Howlin J; Jirström K; Harland M; Zebary A; Palmer JM; Ingvar C; Olsson H; Newton-Bishop J; Hansson J; Hayward N; Gruis N; Jönsson G
    J Invest Dermatol; 2014 Dec; 134(12):3000-3003. PubMed ID: 24999598
    [No Abstract]   [Full Text] [Related]  

  • 14. [Melanoma of the skin: clinico-genetic studies].
    Sitnikova TS; Gar'kavtseva RF; Nefedov MD; Demidov LV
    Vopr Onkol; 1990; 36(8):922-7. PubMed ID: 2219832
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New developments in melanoma genetics.
    Hayward N
    Curr Oncol Rep; 2000 Jul; 2(4):300-6. PubMed ID: 11122857
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CDKN2A germline mutations are not associated with poor survival in an Italian cohort of melanoma patients.
    Dalmasso B; Pastorino L; Ciccarese G; Andreotti V; Grillo F; Mastracci L; Spagnolo F; Ballestrero A; Queirolo P; Bruno W; Ghiorzo P
    J Am Acad Dermatol; 2019 May; 80(5):1263-1271. PubMed ID: 30274933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma.
    Platz A; Hansson J; Månsson-Brahme E; Lagerlof B; Linder S; Lundqvist E; Sevigny P; Inganäs M; Ringborg U
    J Natl Cancer Inst; 1997 May; 89(10):697-702. PubMed ID: 9168184
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Germline p16 mutations in familial melanoma.
    Hussussian CJ; Struewing JP; Goldstein AM; Higgins PA; Ally DS; Sheahan MD; Clark WH; Tucker MA; Dracopoli NC
    Nat Genet; 1994 Sep; 8(1):15-21. PubMed ID: 7987387
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of Heredity in Melanoma Susceptibility: A Primer for the Practicing Surgeon.
    Abdo JF; Sharma A; Sharma R
    Surg Clin North Am; 2020 Feb; 100(1):13-28. PubMed ID: 31753108
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Longitudinal assessment of the nevus phenotype in a melanoma kindred.
    Florell SR; Meyer LJ; Boucher KM; Porter-Gill PA; Hart M; Erickson J; Cannon-Albright LA; Pershing LK; Harris RM; Samlowski WE; Zone JJ; Leachman SA
    J Invest Dermatol; 2004 Sep; 123(3):576-82. PubMed ID: 15304099
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.