BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 17171691)

  • 1. The M53I mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestry.
    Lang J; Hayward N; Goldgar D; Tsao H; Hogg D; Palmer J; Stark M; Tobias ES; MacKie R
    Genes Chromosomes Cancer; 2007 Mar; 46(3):277-87. PubMed ID: 17171691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations.
    Pollock PM; Spurr N; Bishop T; Newton-Bishop J; Gruis N; van der Velden PA; Goldstein AM; Tucker MA; Foulkes WD; Barnhill R; Haber D; Fountain J; Hayward NK
    Hum Mutat; 1998; 11(6):424-31. PubMed ID: 9603434
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families.
    Ciotti P; Struewing JP; Mantelli M; Chompret A; Avril MF; Santi PL; Tucker MA; Bianchi-Scarrà G; Bressac-de Paillerets B; Goldstein AM
    Am J Hum Genet; 2000 Aug; 67(2):311-9. PubMed ID: 10869234
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and molecular characterization of patients at risk for hereditary melanoma in southern Brazil.
    Ashton-Prolla P; Bakos L; Junqueira G; Giugliani R; Azevedo SJ; Hogg D
    J Invest Dermatol; 2008 Feb; 128(2):421-5. PubMed ID: 17713569
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.
    Goldstein AM; Liu L; Shennan MG; Hogg D; Tucker MA; Struewing JP
    Br J Cancer; 2001 Aug; 85(4):527-30. PubMed ID: 11506491
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect.
    Auroy S; Avril MF; Chompret A; Pham D; Goldstein AM; Bianchi-Scarrà G; Frebourg T; Joly P; Spatz A; Rubino C; Demenais F; Bressac-de Paillerets B;
    Genes Chromosomes Cancer; 2001 Nov; 32(3):195-202. PubMed ID: 11579459
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families.
    Lang J; Boxer M; MacKie RM
    Br J Dermatol; 2005 Dec; 153(6):1121-5. PubMed ID: 16307646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients.
    Mantelli M; Pastorino L; Ghiorzo P; Barile M; Bruno W; Gargiulo S; Sormani MP; Gliori S; Vecchio S; Ciotti P; Sertoli MR; Queirolo P; Goldstein AM; Bianchi-Scarrà G;
    Melanoma Res; 2004 Dec; 14(6):443-8. PubMed ID: 15577313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel CDKN2A mutation detected in Spanish melanoma pedigree.
    de Torre C; Martínez-Escribano J
    Exp Dermatol; 2010 Aug; 19(8):e333-5. PubMed ID: 20653773
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers.
    Gironi LC; Colombo E; Pasini B; Giorgione R; Farinelli P; Zottarelli F; Esposto E; Zavattaro E; Allara E; Ogliara P; Betti M; Dianzani I; Savoia P
    Arch Dermatol Res; 2018 Dec; 310(10):769-784. PubMed ID: 30218143
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas.
    Hashemi J; Platz A; Ueno T; Stierner U; Ringborg U; Hansson J
    Cancer Res; 2000 Dec; 60(24):6864-7. PubMed ID: 11156381
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families.
    Hashemi J; Bendahl PO; Sandberg T; Platz A; Linder S; Stierner U; Olsson H; Ingvar C; Hansson J; Borg A
    Genes Chromosomes Cancer; 2001 Jun; 31(2):107-16. PubMed ID: 11319798
    [TBL] [Abstract][Full Text] [Related]  

  • 13. First detection of the melanoma-predisposing proline-48-threonine mutation of p16 in Hungarians: was there a common founder either in Italy or in Hungary?
    Széll M; Balogh K; Dobozy A; Kemény L; Oláh J
    Melanoma Res; 2007 Aug; 17(4):251-4. PubMed ID: 17625456
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CDKN2A and CDK4 variants in Latvian melanoma patients: analysis of a clinic-based population.
    Pjanova D; Engele L; Randerson-Moor JA; Harland M; Bishop DT; Newton Bishop JA; Taylor C; Debniak T; Lubinski J; Kleina R; Heisele O
    Melanoma Res; 2007 Jun; 17(3):185-91. PubMed ID: 17505264
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of Latvian familial melanoma patients shows novel variants in the noncoding regions of CDKN2A and that the CDK4 mutation R24H is a founder mutation.
    Veinalde R; Ozola A; Azarjana K; Molven A; Akslen LA; Doniņa S; Proboka G; Cēma I; Baginskis A; Pjanova D
    Melanoma Res; 2013 Jun; 23(3):221-6. PubMed ID: 23546221
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation.
    Della Torre G; Pasini B; Frigerio S; Donghi R; Rovini D; Delia D; Peters G; Huot TJ; Bianchi-Scarra G; Lantieri F; Rodolfo M; Parmiani G; Pierotti MA
    Br J Cancer; 2001 Sep; 85(6):836-44. PubMed ID: 11556834
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel CDKN2A mutations detected in western Swedish families with hereditary malignant melanoma.
    Erlandson A; Appelqvist F; Wennberg AM; Holm J; Enerbäck C
    J Invest Dermatol; 2007 Jun; 127(6):1465-7. PubMed ID: 17255954
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
    Goldstein AM; Chan M; Harland M; Hayward NK; Demenais F; Bishop DT; Azizi E; Bergman W; Bianchi-Scarra G; Bruno W; Calista D; Albright LA; Chaudru V; Chompret A; Cuellar F; Elder DE; Ghiorzo P; Gillanders EM; Gruis NA; Hansson J; Hogg D; Holland EA; Kanetsky PA; Kefford RF; Landi MT; Lang J; Leachman SA; MacKie RM; Magnusson V; Mann GJ; Bishop JN; Palmer JM; Puig S; Puig-Butille JA; Stark M; Tsao H; Tucker MA; Whitaker L; Yakobson E; ;
    J Med Genet; 2007 Feb; 44(2):99-106. PubMed ID: 16905682
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma.
    Ghiorzo P; Gargiulo S; Pastorino L; Nasti S; Cusano R; Bruno W; Gliori S; Sertoli MR; Burroni A; Savarino V; Gensini F; Sestini R; Queirolo P; Goldstein AM; Scarrà GB
    Hum Mol Genet; 2006 Sep; 15(18):2682-9. PubMed ID: 16893909
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    Tovar-Parra JD; Gutiérrez-Castañeda LD; Gil-Quiñones SR; Nova JA; Pulido L
    Biomed Res Int; 2020; 2020():7458917. PubMed ID: 33102592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.