(Q36641299)

English

Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes

scientific article published on February 2000

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1 reference

based on heuristic

inferred from title

Dominique Stoppa-Lyonnet

8

object named as

Stoppa-Lyonnet D

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Brigitte Bressac-de Paillerets

2

object named as

Bressac-de Paillerets B

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

author name string

Soufir N

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Desjardins L

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Lévy C

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Bombled J

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Gorin I

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Schlienger P

7

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

language of work or name

0 references

publication date

1 February 2000

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

British Journal of Cancer

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

82

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

818-822

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Selective deletion of exon 1 beta of the p19ARF gene in metastatic melanoma cell lines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Tumor suppressor p16INK4A: determination of solution structure and analyses of its interaction with cyclin-dependent kinase 4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Differential expression of G1 cyclins and cyclin-dependent kinase inhibitors in normal and transformed melanocytes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Identification of CDK4 sequences involved in cyclin D1 and p16 binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Constitutional alterations in p16 in patients with uveal melanoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

CDKN2 mutations in melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Heredity and intraocular malignant melanoma. Study of two families and review of forty-five cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Familial uveal melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene, CDK4I, in melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

30 September 2017

Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

28 June 2018

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374387

4 December 2018

Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family studies in melanoma: identification of the atypical mole syndrome (AMS) phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial uveal melanoma. Clinical observations on 56 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial uveal melanoma: absence of germline mutations involving the cyclin-dependent kinase-4 inhibitor gene (p16)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial uveal melanoma, III. Is the occurrence of familial uveal melanoma coincidental?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informative MspI polymorphism adjacent to exon 3 of the p16INK4 (MTS1) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Affected members of melanoma‐prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in the p16/CDKN2A binding region of the cyclin-dependent kinase-4 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID 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://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Occurrence of cutaneous and uveal melanoma in patients with uveal melanoma and their first degree relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of p16 (CDKN2/MTS-1/INK4A) alterations in primary sporadic uveal melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Five cases of coexistent primary ocular and cutaneous melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline brca2 sequence variants in patients with ocular melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two subclones in a case of uveal melanoma. Relevance of monosomy 3 and multiplication of chromosome 8q

1 reference

https://pubmed.ncbi.nlm.nih.gov/10732752

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1054/BJOC.1999.1005

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36641299&oldid=2199128470"