About: CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma

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scientific article published on 01 March 1999

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1999 (uk) article scientifique publié en 1999 (fr) im März 1999 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1999 (ast) scientific article published on 01 March 1999 (en)
publication date	wds:Q57391793-B3A560DA-7A40-4123-8099-763AC71CC893
publication date	1999-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57391793-E9A179D5-CBA6-4507-AB92-3947DB40D33B
language of work or name	English
cites work	wds:Q57391793-0314A9D1-C883-4CFE-B928-750CADE5D4CC wds:Q57391793-15AEC279-FBEF-49EA-A26A-22249DE0038A wds:Q57391793-16692267-6E71-40BD-ABE9-A28DF3DA8405 wds:Q57391793-21221CBA-D50A-4F68-A4B6-B7C44861CE1C wds:Q57391793-25D534F0-CEDF-468C-A98F-5EF60C046B4D wds:Q57391793-3859012A-519C-4908-A872-1FC522043263 wds:Q57391793-3FAD095F-71BD-4EC0-8DF8-1F4D7B5A015F wds:Q57391793-51CF299B-5497-4A18-A25B-B10BFFEFA681 wds:Q57391793-55203CEC-FF6A-4517-B8C9-DC45C99264F6 wds:Q57391793-5716187E-5246-40FB-B9F3-914E46EC7731 wds:Q57391793-6CCE6B71-B985-4404-9C76-6B247979AF58 wds:Q57391793-7C28DD40-BFED-4686-A508-A483BB87260D wds:Q57391793-85AD704F-D906-4E78-BA3E-D25A0C901674 wds:Q57391793-997CDE3D-B9AD-4237-ADCF-C81621372D43 wds:Q57391793-B28D0C83-5FF9-4347-93EB-D4C0EA85ADB0 wds:Q57391793-C7F982EE-7D6C-48BF-BEB8-050AE9DE3347 wds:Q57391793-D44A5B9D-7123-427F-A1AF-C9185E7D4775 wds:Q57391793-EAD90464-EB7D-4004-B3FE-DE8335DF518F wds:Q57391793-F32949B8-EAA7-47D6-A02A-887CDF49F8FD wds:Q57391793-FEC86637-9460-4B2E-A48F-6F2EC4E35838
cites work	Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair Heterogeneity of melanoma risk in families of melanoma patients. Mutations associated with familial melanoma impair p16INK4 function. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941] Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men. A cell cycle regulator potentially involved in genesis of many tumor types The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma Comparability of surrogate and self-reported information on melanoma risk factors. A simple salting out procedure for extracting DNA from human nucleated cells Germline p16 mutations in familial melanoma Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibition CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Germline Mutations of the CDKN2 Gene in UK Melanoma Families Risk of cutaneous melanoma associated with a family history of the disease Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds Risk of cutaneous melanoma associated with pigmentation characteristics and freckling: systematic overview of 10 case-control studies. The International Melanoma Analysis Group (IMAGE). Compilation of somatic mutations of the CDKN2 gene in human cancers: non-random distribution of base substitutions
author name string	wds:Q57391793-25660205-D0AA-41B4-AC0A-8165F3CFEA50 wds:Q57391793-4824A71B-37D8-4279-8859-5439C1BF376C wds:Q57391793-5CA751F2-C650-4C58-AB8F-65BBF9D5D0A2 wds:Q57391793-68424310-1164-4B46-A9D1-E8BCE8E56A4B wds:Q57391793-D577D605-3A10-4719-95A1-1D1BA21BC271
author name string	A Green N Martin J Welch A Milligan N Hayward
rdfs: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)
skos: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)
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)
author	wds:Q57391793-1F238C20-9AC9-4737-BA00-F55763E09F9B wds:Q57391793-A531F327-AF61-4C58-AAA5-B9DA06F8737B
author	David L. Duffy Joanne F Aitken
title	wds:Q57391793-CBCF44F6-17BB-45F2-926B-6A4AF32F9394
title	CDKN2A variants in a population-based sample of Queensland families with melanoma (en)
page(s)	wds:Q57391793-7EBBA4B6-9212-4A1E-BED9-407B0EF4C594
page(s)	446-452
instance of	wds:Q57391793-8CD5B6BA-C856-4459-849D-3FDCC2D96C87
instance of	scholarly article
main subject	wds:Q57391793-8F86177A-6046-4ECD-B1C3-4122C4791723
main subject	Queensland
PubMed ID	wds:Q57391793-B3774435-B800-4905-A576-07BFDD2BB810
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10070944
PubMed ID	10070944
published in	wds:Q57391793-81F6762A-A114-477A-A6FC-354EDDC6294E
published in	Journal of the National Cancer Institute
issue	wds:Q57391793-65561D81-9C12-4A9D-8909-E3DF2BA21950
volume	wds:Q57391793-1CCC903C-BC37-48B5-8F3F-D409CA98B00F
issue	5
volume	91
DOI	wds:Q57391793-092A80E8-6FA0-42B8-B92E-37BAA819B46A
DOI	http://dx.doi.org/10.1093/JNCI/91.5.446
DOI	10.1093/JNCI/91.5.446
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57391793
is cites work of	Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma Polymorphisms of the BRAF gene predispose males to malignant melanoma Molecular biology of normal melanocytes and melanoma cells MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype? Genetics of melanoma predisposition The Queensland Study of Melanoma: environmental and genetic associations (Q-MEGA); study design, baseline characteristics, and repeatability of phenotype and sun exposure measures A common variant of CDKN2A (p16) predisposes to breast cancer

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