(Q35447197)

8 August 2017

title

A common variant of CDKN2A (p16) predisposes to breast cancer (English)

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8 August 2017

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Cybulski C

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Byrski T

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Narod SA

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Lubinski J

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Szczylik C

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Haus O

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Gronwald J

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Huzarski T

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8 August 2017

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Górski B

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Debniak T

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Gozdecka-Grodecka S

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Góźdź S

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8 August 2017

Mackiewicz A

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8 August 2017

Kowalska E

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8 August 2017

Grzybowska E

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8 August 2017

Stawicka M

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8 August 2017

Swiec M

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8 August 2017

Urbański K

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Niepsuj S

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8 August 2017

Waśko B

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8 August 2017

Wandzel P

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8 August 2017

Surdyka D

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8 August 2017

Rozmiarek A

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8 August 2017

Zambrano O

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8 August 2017

Posmyk M

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8 August 2017

language of work or name

English

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publication date

6 May 2005

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Journal of Medical Genetics

8 August 2017

published in

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8 August 2017

volume

42

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8 August 2017

issue

10

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8 August 2017

page(s)

763-765

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CHEK2 is a multiorgan cancer susceptibility gene

8 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Identification of a splice acceptor site mutation in p16INK4A/p14ARF within a breast cancer, melanoma, neurofibroma prone kindred

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Methylation silencing and mutations of the p14ARF and p16INK4a genes in colon cancer

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Alterations of p16-pRb pathway and chromosome locus 9p21-22 in sporadic invasive breast carcinomas.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Aberrant methylation of p16(INK4a) is an early event in lung cancer and a potential biomarker for early diagnosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Hypomethylation and increased gene expression of p16INK4a in primary and metastatic breast carcinoma as compared to normal breast tissue

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Cancer-associated mis-sense and deletion mutations impair p16INK4 CDK inhibitory activity

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

CDKN2A common variants and their association with melanoma risk: a population-based study.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Inactivation of the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene in squamous cell carcinoma of the larynx.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Hereditary p16-Leiden mutation in a patient with multiple head and neck tumors

26 September 2018

1 reference

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An assessment of the CDKN2A variant Ala148Thr as a nevus/melanoma susceptibility allele.

26 September 2018

1 reference

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Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers.

26 September 2018

1 reference

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The p16INK4a/CDKN2A tumor suppressor and its relatives.

26 September 2018

1 reference

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A Familial Syndrome of Pancreatic Cancer and Melanoma with a Mutation in theCDKN2Tumor-Suppressor Gene

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

Mutations associated with familial melanoma impair p16INK4 function.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735931

High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families

26 September 2018

1 reference

12 December 2020

Methylation of the p16(Ink4a) tumor suppressor gene 5'-CpG island in breast cancer

1 reference

12 December 2020

Analysis of mutations in the p16/CDKN2A gene in sporadic and familial melanoma in the Polish population

1 reference

12 December 2020

Alterations of the p16INK4a/p14ARF pathway in clear cell sarcoma

1 reference

12 December 2020

CDKN2A mutations in multiple primary melanomas

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of ligurian melanoma families and risk of occurrence of other neoplasia

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.2005.031476

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8 August 2017

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8 August 2017

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