New developments in melanoma genetics (Q34107950)

31 July 2017

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title

New developments in melanoma genetics (English)

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31 July 2017

Hayward N

1

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31 July 2017

publication date

1 July 2000

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31 July 2017

published in

Current Oncology Reports

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31 July 2017

volume

2

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31 July 2017

issue

4

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31 July 2017

page(s)

300-306

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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

31 July 2017

cites work

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12 December 2020

Familial melanoma and pancreatic cancer. Ligurian Skin Tumor Study Group

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12 December 2020

Genetic and environmental influences in the development of multiple primary melanoma

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12 December 2020

Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds

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12 December 2020

Functional evidence of novel tumor suppressor genes for cutaneous malignant melanoma.

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12 December 2020

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

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12 December 2020

The Atypical-Mole Syndrome and Predisposition to Melanoma

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12 December 2020

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

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12 December 2020

Increasing incidence of cutaneous melanoma in Queensland, Australia

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12 December 2020

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

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12 December 2020

Tumor spectrum in ARF-deficient mice.

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12 December 2020

CDKN2A Germline Mutations in U.K. Patients with Familial Melanoma and Multiple Primary Melanomas

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12 December 2020

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

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12 December 2020

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]

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12 December 2020

Familial tumor syndrome associated with a germline nonfunctional p16INK4a allele

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12 December 2020

A novel p16INK4A transcript

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12 December 2020

Novel germline p16 mutation in familial malignant melanoma in southern Sweden

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12 December 2020

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).

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12 December 2020

p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

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12 December 2020

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

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12 December 2020

Lack of germ-line mutations of CDK4, p16(INK4A), and p15(INK4B) in families with glioma.

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12 December 2020

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

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12 December 2020

Genomic structure, expression and mutational analysis of the P15 (MTS2) gene

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12 December 2020

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

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12 December 2020

Melanoma development in relation to non-functional p16/INK4A protein and dysplastic naevus syndrome in Swedish melanoma kindreds

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12 December 2020

Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma

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12 December 2020

CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas

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12 December 2020

CDKN2a/p16INK4a Mutations and Lack of p19ARF Involvement in Familial Melanoma Kindreds

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12 December 2020

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12 December 2020

Germline p16 mutations in familial melanoma

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12 December 2020

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

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12 December 2020

Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A ( P16INK4A ) gene

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12 December 2020

The p16INK4a/CDKN2A tumor suppressor and its relatives.

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12 December 2020

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

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12 December 2020

Screening for tumour suppressor p16(CDKN2A) germline mutations in Israeli melanoma families

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12 December 2020

CDKN2AMutations in Multiple Primary Melanomas

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12 December 2020

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

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12 December 2020

Origin of familial malignant melanomas from heritable melanocytic lesions. 'The B-K mole syndrome'

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12 December 2020

Complex structure and regulation of the P16 (MTS1) locus

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12 December 2020

A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families

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12 December 2020

10.1007/S11912-000-0022-Z

Identifiers

DOI

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Dimensions Publication ID

31 July 2017

1039703480

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