CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
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Therapy for BRAFi-Resistant Melanomas: Is WNT5A the Answer?The rs11515 Polymorphism Is More Frequent and Associated With Aggressive Breast Tumors with Increased ANRIL and Decreased p16 (INK4a) ExpressionGenetics of familial and sporadic melanoma.Genetics of familial melanoma: 20 years after CDKN2A.Integrative post-genome-wide association analysis of CDKN2A and TP53 SNPs and risk of esophageal adenocarcinoma.Variants at the 9p21 locus and melanoma riskNonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanomaMolecular characterization of melanoma cases in Denmark suspected of genetic predispositionCutaneous melanoma: family screening and genetic testing.High- and low-penetrance cutaneous melanoma susceptibility genes.Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma.The Queensland Study of Melanoma: environmental and genetic associations (Q-MEGA); study design, baseline characteristics, and repeatability of phenotype and sun exposure measures.Genetics and genomics of melanoma.Molecular biology of normal melanocytes and melanoma cells.Radiotherapy for cutaneous melanoma: current and future applications.High incidence of primary melanomas in an MC1R RHC homozygote/CDKN2A mutant genotype patient.Genetic 3'UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight.V600EBraf induces gastrointestinal crypt senescence and promotes tumour progression through enhanced CpG methylation of p16INK4a.Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.The CDKN2A p.A148T variant is associated with cutaneous melanoma in Southern Brazil.A National Budget Impact Analysis of a Specialised Surveillance Programme for Individuals at Very High Risk of Melanoma in Australia.Melanoma in adolescents: a case-control study of risk factors in Queensland, Australia.p16 (CDKN2A) SNP rs11515 was not associated with head and neck carcinoma.Association analysis of p16 (CDKN2A) and RB1 polymorphisms with susceptibility to cervical cancer in Indian population.Prevalence of Germline BAP1, CDKN2A, and CDK4 Mutations in an Australian Population-Based Sample of Cutaneous Melanoma Cases.The genetics of melanomaMutation analysis of theCDKN2A promoter in Australian melanoma familiesMolecular features of primary mediastinal B-cell lymphoma: involvement of p16INK4A, p53 and c-mycClinical course of bladder neoplasms and single nucleotide polymorphisms in theCDKN2Agene
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P2860
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
description
im März 1999 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 March 1999
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в березні 1999
@uk
name
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
@en
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
@nl
type
label
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
@en
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
@nl
prefLabel
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
@en
CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma
@nl
P2093
P2860
P356
P1476
CDKN2A variants in a population-based sample of Queensland families with melanoma
@en
P2093
P2860
P304
P356
10.1093/JNCI/91.5.446
P407
P577
1999-03-01T00:00:00Z