MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
about
Melanoma: from melanocyte to genetic alterations and clinical optionsThe genetics of sun sensitivity in humans.A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colorSignificance of the Melanocortin 1 and Endothelin B Receptors in Melanocyte Homeostasis and Prevention of Sun-Induced GenotoxicityCapturing the biological impact of CDKN2A and MC1R genes as an early predisposing event in melanoma and non melanoma skin cancerSome molecular and clinical aspects of genetic predisposition to malignant melanoma and tumours of various site of originFamilial malignant melanoma - overviewHereditary genodermatoses with cancer predispositionDistinct pigmentary and melanocortin 1 receptor-dependent components of cutaneous defense against ultraviolet radiation.Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes.Vitamin D receptor gene polymorphisms, serum 25-hydroxyvitamin D levels, and melanoma: UK case-control comparisons and a meta-analysis of published VDR dataPopulation-based, case-control-family design to investigate genetic and environmental influences on melanoma risk: Australian Melanoma Family StudyMelanoma epidemiology, biology and prognosis.Melanoma genetics and the development of rational therapeutics.Localization of a novel melanoma susceptibility locus to 1p22MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2)Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.A comparative study of gene-expression data of basal cell carcinoma and melanoma reveals new insights about the two cancers.Estimating CDKN2A carrier probability and personalizing cancer risk assessments in hereditary melanoma using MelaPRO.Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.Epidemiology of invasive cutaneous melanoma.Stepping up melanocytes to the challenge of UV exposure.Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish populationMelanoma: Molecular Pathogenesis and Therapeutic ManagementMolecular characterization of melanoma cases in Denmark suspected of genetic predispositionPharmacogenetic candidate genes for melanoma.Melanocortin 1 receptor genotype: an important determinant of the damage response of melanocytes to ultraviolet radiation.Selection criteria for genetic assessment of patients with familial melanomaMelanocortin 1 receptor variants, pigmentation, and skin cancer susceptibility.Benefits of oral Polypodium Leucotomos extract in MM high-risk patientsAssociations between environmental factors and incidence of cutaneous melanoma. ReviewGermline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.Tumor suppressor genetics.Genetic counseling in melanoma.Cutaneous melanoma: family screening and genetic testing.A single-nucleotide polymorphism (SNP) multiplex system: the association of five SNPs with human eye and hair color in the Slovenian population and comparison using a Bayesian network and logistic regression model.High- and low-penetrance cutaneous melanoma susceptibility genes.Role of MC1R variants in uveal melanoma.Red hair--a desirable mutation?Melanoma genetic testing, counseling, and adherence to skin cancer prevention and detection behaviors.
P2860
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P2860
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
description
2001 nî lūn-bûn
@nan
2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@ast
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@en
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@nl
type
label
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@ast
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@en
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@nl
prefLabel
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@ast
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@en
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@nl
P2093
P2860
P50
P356
P1476
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
@en
P2093
P2860
P304
P356
10.1086/323412
P407
P577
2001-08-08T00:00:00Z