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425 related items for PubMed ID: 21412176

  • 1. Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition.
    Abdel-Rahman MH, Pilarski R, Massengill JB, Christopher BN, Noss R, Davidorf FH.
    Melanoma Res; 2011 Jun; 21(3):175-9. PubMed ID: 21412176
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  • 2. Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes.
    Soufir N, Bressac-de Paillerets B, Desjardins L, Lévy C, Bombled J, Gorin I, Schlienger P, Stoppa-Lyonnet D.
    Br J Cancer; 2000 Feb; 82(4):818-22. PubMed ID: 10732752
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  • 6. Contribution of germline mutations in BRCA2, P16(INK4A), P14(ARF) and P15 to uveal melanoma.
    Hearle N, Damato BE, Humphreys J, Wixey J, Green H, Stone J, Easton DF, Houlston RS.
    Invest Ophthalmol Vis Sci; 2003 Feb; 44(2):458-62. PubMed ID: 12556369
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  • 7. Prevalence of variations in melanoma susceptibility genes among Slovenian melanoma families.
    Peric B, Cerkovnik P, Novakovic S, Zgajnar J, Besic N, Hocevar M.
    BMC Med Genet; 2008 Sep 19; 9():86. PubMed ID: 18803811
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  • 8. CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas.
    Holland EA, Schmid H, Kefford RF, Mann GJ.
    Genes Chromosomes Cancer; 1999 Aug 19; 25(4):339-48. PubMed ID: 10398427
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  • 9. Genetic study of familial uveal melanoma: association of uveal and cutaneous melanoma with cutaneous and ocular nevi.
    Smith JH, Padnick-Silver L, Newlin A, Rhodes K, Rubinstein WS.
    Ophthalmology; 2007 Apr 19; 114(4):774-9. PubMed ID: 17207529
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  • 10. Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma.
    Soufir N, Lacapere JJ, Bertrand G, Matichard E, Meziani R, Mirebeau D, Descamps V, Gérard B, Archimbaud A, Ollivaud L, Bouscarat F, Baccard M, Lanternier G, Saïag P, Lebbé C, Basset-Seguin N, Crickx B, Cave H, Grandchamp B.
    Br J Cancer; 2004 Jan 26; 90(2):503-9. PubMed ID: 14735200
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  • 11. 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 26; 23(3):221-6. PubMed ID: 23546221
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  • 13. 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 14; 85(6):836-44. PubMed ID: 11556834
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  • 14. 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 15; 60(24):6864-7. PubMed ID: 11156381
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  • 15. 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 15; 17(3):185-91. PubMed ID: 17505264
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  • 16. Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma.
    Abdel-Rahman MH, Sample KM, Pilarski R, Walsh T, Grosel T, Kinnamon D, Boru G, Massengill JB, Schoenfield L, Kelly B, Gordon D, Johansson P, DeBenedictis MJ, Singh A, Casadei S, Davidorf FH, White P, Stacey AW, Scarth J, Fewings E, Tischkowitz M, King MC, Hayward NK, Cebulla CM.
    Ophthalmology; 2020 May 15; 127(5):668-678. PubMed ID: 32081490
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  • 17. CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.
    Pastorino L, Bonelli L, Ghiorzo P, Queirolo P, Battistuzzi L, Balleari E, Nasti S, Gargiulo S, Gliori S, Savoia P, Abate Osella S, Bernengo MG, Bianchi Scarrà G.
    Pigment Cell Melanoma Res; 2008 Dec 15; 21(6):700-9. PubMed ID: 18983535
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  • 18. Novel and recurrent p14 mutations in Italian familial melanoma.
    Binni F, Antigoni I, De Simone P, Majore S, Silipo V, Crisi A, Amantea A, Pacchiarini D, Castori M, De Bernardo C, Catricalà C, Grammatico P.
    Clin Genet; 2010 Jun 15; 77(6):581-6. PubMed ID: 20132244
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  • 19. A novel type of deletion in the CDKN2A gene identified in a melanoma-prone family.
    Knappskog S, Geisler J, Arnesen T, Lillehaug JR, Lønning PE.
    Genes Chromosomes Cancer; 2006 Dec 15; 45(12):1155-63. PubMed ID: 17001621
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  • 20. High prevalence of the G101W germline mutation in the CDKN2A (P16(ink4a)) gene in 62 Italian malignant melanoma families.
    Mantelli M, Barile M, Ciotti P, Ghiorzo P, Lantieri F, Pastorino L, Catricalà C, Torre GD, Folco U, Grammatico P, Padovani L, Pasini B, Rovini D, Queirolo P, Rainero ML, Santi PL, Sertoli RM, Goldstein AM, Bianchi-Scarrà G, Società Italiana Dermatologia, Gruppo Italiano Studi Epidemiologici in Dermatologia.
    Am J Med Genet; 2002 Jan 22; 107(3):214-21. PubMed ID: 11807902
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