Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Melanoma and CDKN2B[original query] |
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A single nucleotide polymorphism in the 3'untranslated region of the CDKN2A gene is common in sporadic primary melanomas but mutations in the CDKN2B, CDKN2C, CDK4 and p53 genes are rare. International journal of cancer. Journal international du cancer 2001 Nov 95 (6): 388-93. Kumar R, Smeds J, Berggren P, Straume O, Rozell B L, Akslen L A, Hemminki |
New common variants affecting susceptibility to basal cell carcinoma. Nature genetics 2009 Aug 41 (8): 909-14. Stacey Simon N, Sulem Patrick, Masson Gisli, Gudjonsson Sigurjon A, Thorleifsson Gudmar, Jakobsdottir Margret, Sigurdsson Asgeir, Gudbjartsson Daniel F, Sigurgeirsson Bardur, Benediktsdottir Kristrun R, Thorisdottir Kristin, Ragnarsson Rafn, Scherer Dominique, Hemminki Kari, Rudnai Peter, Gurzau Eugene, Koppova Kvetoslava, Botella-Estrada Rafael, Soriano Virtudes, Juberias Pablo, Saez Berta, Gilaberte Yolanda, Fuentelsaz Victoria, Corredera Cristina, Grasa Matilde, Höiom Veronica, Lindblom Annika, Bonenkamp Johannes J, van Rossum Michelle M, Aben Katja K H, de Vries Esther, Santinami Mario, Di Mauro Maria G, Maurichi Andrea, Wendt Judith, Hochleitner Pia, Pehamberger Hubert, Gudmundsson Julius, Magnusdottir Droplaug N, Gretarsdottir Solveig, Holm Hilma, Steinthorsdottir Valgerdur, Frigge Michael L, Blondal Thorarinn, Saemundsdottir Jona, Bjarnason Hjördis, Kristjansson Kristleifur, Bjornsdottir Gyda, Okamoto Ichiro, Rivoltini Licia, Rodolfo Monica, Kiemeney Lambertus A, Hansson Johan, Nagore Eduardo, Mayordomo José I, Kumar Rajiv, Karagas Margaret R, Nelson Heather H, Gulcher Jeffrey R, Rafnar Thorunn, Thorsteinsdottir Unnur, Olafsson Jon H, Kong Augustine, Stefansson Ka |
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression. PLoS genetics 2010 Apr 6 (4): e1000899. Cunnington Michael S, Santibanez Koref Mauro, Mayosi Bongani M, Burn John, Keavney Berna |
Deletion at chromosome arm 9p in relation to BRAF/NRAS mutations and prognostic significance for primary melanoma. Genes, chromosomes & cancer 2010 May 49 (5): 425-38. Conway Caroline, Beswick Samantha, Elliott Faye, Chang Yu-Mei, Randerson-Moor Juliette, Harland Mark, Affleck Paul, Marsden Jerry, Sanders D Scott, Boon Andy, Knowles Margaret A, Bishop D Timothy, Newton-Bishop Julia |
Common genetic variants in the 9p21 region and their associations with multiple tumours. British journal of cancer 2013 Jan . Gu F, Pfeiffer RM, Bhattacharjee S, Han SS, Taylor PR, Berndt S, Yang H, Sigurdson AJ, Toro J, Mirabello L, Greene MH, Freedman ND, Abnet CC, Dawsey SM, Hu N, Qiao YL, Ding T, Brenner AV, Garcia-Closas M, Hayes R, Brinton LA, Lissowska J, Wentzensen N, Kratz C, Moore LE, Ziegler RG, Chow WH, Savage SA, Burdette L, Yeager M, Chanock SJ, Chatterjee N, Tucker MA, Goldstein AM, Yang XR |
Clinical histopathological features and CDKN2A/CDK4/MITF mutational status of patients with multiple primary melanomas from Bologna: Italy is a fascinating but complex mosaic. Italian journal of dermatology and venereology 2020 Mar . Dika Emi, Patrizi Annalisa, Rossi Cesare, Turchetti Daniela, Miccoli Sara, Ferracin Manuela, Veronesi Giulia, Scarfì Federica, Lambertini Marti |
Disease-Associated Risk Variants in ANRIL Are Associated with Tumor-Infiltrating Lymphocyte Presence in Primary Melanomas in the Population-Based GEM Study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2021 Oct . Davari Danielle R, Orlow Irene, Kanetsky Peter A, Luo Li, Edmiston Sharon N, Conway Kathleen, Parrish Eloise A, Hao Honglin, Busam Klaus J, Sharma Ajay, Kricker Anne, Cust Anne E, Anton-Culver Hoda, Gruber Stephen B, Gallagher Richard P, Zanetti Roberto, Rosso Stefano, Sacchetto Lidia, Dwyer Terence, Ollila David W, Begg Colin B, Berwick Marianne, Thomas Nancy E, |
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- Page last updated:Apr 16, 2024
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