(Q34626994)

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New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment.

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30 December 2019

New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment (English)

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Europe PubMed Central

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30 December 2019

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Stéphane Dalle

2

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30 December 2019

Fabienne Lesueur

10

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30 December 2019

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Alain Sarasin

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30 December 2019

Brigitte Bressac-de Paillerets

13

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Brigitte Bressac-de Paillerets

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30 December 2019

Christine Lasset

7

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Christine Lasset

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30 December 2019

author name string

Caroline Kannengiesser

1

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30 December 2019

Marie-Thérèse Leccia

3

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30 December 2019

Marie Françoise Avril

4

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30 December 2019

Valerie Bonadona

5

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30 December 2019

Agnès Chompret

6

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30 December 2019

Dominique Leroux

8

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30 December 2019

Luc Thomas

9

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30 December 2019

Gilbert Lenoir

11

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30 December 2019

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1 August 2007

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30 December 2019

Genes, Chromosomes and Cancer

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30 December 2019

46

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30 December 2019

8

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30 December 2019

751-760

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PubMed publication ID

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30 December 2019

Geographical variation in the penetrance of CDKN2A mutations for melanoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

21 January 2018

Functional analysis of wild-type and malignant glioma derived CDKN2Abeta alleles: evidence for an RB-independent growth suppressive pathway

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Sporadic multiple primary melanoma cases:CDKN2Agermline mutations with a founder effect

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Human melanocyte senescence and melanoma susceptibility genes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

INK4a-deficient human diploid fibroblasts are resistant to RAS-induced senescence

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of Genes, Nevi, and Sun Sensitivity on Melanoma Risk in a Family Sample Unselected by Family History and in Melanoma-Prone Families

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple primary melanoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinicopathological features of and risk factors for multiple primary melanomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Malignant melanoma and levodopa in Parkinson's disease: causality or coincidence?

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of melanoma predisposition

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Biallelic mutations in p16(INK4a) confer resistance to Ras- and Ets-induced senescence in human diploid fibroblasts

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic susceptibility in familial melanoma from northeastern Italy.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

The M53I mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestry

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

CDKN2A: the IVS2-105A/G intronic mutation found in an Italian patient affected by eight primary melanomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of 9p21 deletions in UK melanoma families.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

CDKN2A mutations in multiple primary melanomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Haplotype analysis of two recurrentCDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of the CDKN2A locus in patients with multiple primary melanomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of the INK4a locus in tumor suppression and cell mortality.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

CDK inhibitors: positive and negative regulators of G1-phase progression

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Levodopa therapy and the risk of malignant melanoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

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]

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Skin colour and skin cancer - MC1R, the genetic link

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitogenic signalling and the p16INK4a-Rb pathway cooperate to enforce irreversible cellular senescence

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Nucleolar Arf sequesters Mdm2 and activates p53

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Melanoma, Parkinson's disease and levodopa: causal or spurious link? A review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20461

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.20461

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17492760%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

release_tbl7zn3asjaqdawyuspotleeta

1 reference

https://api.fatcat.wiki/v0/release/tbl7zn3asjaqdawyuspotleeta

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17492760%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

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