(Q34107950)

31 July 2017

1 reference

title

New developments in melanoma genetics (English)

1 reference

31 July 2017

Hayward N

1

1 reference

31 July 2017

1 July 2000

1 reference

31 July 2017

Current Oncology Reports

1 reference

31 July 2017

2

1 reference

31 July 2017

300-306

1 reference

31 July 2017

4

1 reference

https://scigraph.springernature.com/pub.10.1007/s11912-000-0022-z

31 July 2017

0 references

cites work

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

12 December 2020

Familial melanoma and pancreatic cancer. Ligurian Skin Tumor Study Group

1 reference

12 December 2020

Genetic and environmental influences in the development of multiple primary melanoma

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The Atypical-Mole Syndrome and Predisposition to Melanoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Increasing incidence of cutaneous melanoma in Queensland, Australia

1 reference

12 December 2020

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

1 reference

12 December 2020

Tumor spectrum in ARF-deficient mice.

1 reference

12 December 2020

CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.

1 reference

12 December 2020

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

1 reference

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]

1 reference

12 December 2020

Familial tumor syndrome associated with a germline nonfunctional p16INK4a allele

1 reference

12 December 2020

A novel p16INK4A transcript

1 reference

12 December 2020

Novel germline p16 mutation in familial malignant melanoma in southern Sweden

1 reference

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).

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Germline p16 mutations in familial melanoma

1 reference

12 December 2020

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

1 reference

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

1 reference

12 December 2020

The p16INK4a/CDKN2A tumor suppressor and its relatives.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

CDKN2A mutations in multiple primary melanomas

1 reference

12 December 2020

Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Complex structure and regulation of the P16 (MTS1) locus

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S11912-000-0022-Z

Identifiers

DOI

1 reference

PubMed ID

11122857

Dimensions Publication ID

31 July 2017

0 references

1 reference

PubMed ID

11122857