Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study. - Wikidata - awgldk - TriplyDB

Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.

Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.

http://www.wikidata.org/entity/Q34212766

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Melanoma: from mutations to medicine Capturing the biological impact of CDKN2A and MC1R genes as an early predisposing event in melanoma and non melanoma skin cancer Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma Implementing an Internet-Delivered Skin Cancer Genetic Testing Intervention to Improve Sun Protection Behavior in a Diverse Population: Protocol for a Randomized Controlled Trial.Melanoma epidemiology, biology and prognosis.Malignant melanoma and melanocortin 1 receptor.GPCRs and cancer Rare presentations of primary melanoma and special populations: a systematic review.Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study.Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants.Absence of germline CDKN2A mutation in Sicilian patients with familial malignant melanoma: Could it be a population-specific genetic signature?Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors.Clinical applications of melanoma genetics.MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentation Variants of the melanocortin-1 receptor: do they matter clinically?Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF.Germline CDKN2A Mutation Status and Survival in Familial Melanoma Cases.Characterization of patients at high risk of melanoma in Austria.A large French case-control study emphasizes the role of rare Mc1R variants in melanoma risk [MITF: a genetic key to melanoma and renal cell carcinoma?].Phenocopies in melanoma-prone families with germ-line CDKN2A mutations.Rare germline variants in known melanoma susceptibility genes in familial melanoma.Pathways from senescence to melanoma: focus on MITF sumoylation.Genetic and functional evaluation of MITF as a candidate gene for cutaneous melanoma predisposition in pigs.MC1R, ASIP, TYR, and TYRP1 gene variants in a population-based series of multiple primary melanomas.CDKN2A and MC1R variants found in Cypriot patients diagnosed with cutaneous melanoma.A short acidic motif in ARF guards against mitochondrial dysfunction and melanoma susceptibility.Interest and Uptake of MC1R Testing for Melanoma Risk in a Diverse Primary Care Population: A Randomized Clinical Trial Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

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Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.

http://www.wikidata.org/entity/Q34212766

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2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Journal of the National Cancer Institute

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P2860

Melanocortin-1 receptor signaling markedly induces the expression of the NR4A nuclear receptor subgroup in melanocytic cells

ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways

A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4

The genetics of sun sensitivity in humans.

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

Quantifying heterogeneity in a meta-analysis

Genetic determinants of hair, eye and skin pigmentation in Europeans

The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.

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1568-1583

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20

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102

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Nelleke A Gruis

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Florence Demenais

Lorenza Pastorino

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