Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes (Q33370678)

26 July 2017

Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes (English)

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26 July 2017

David Ng

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26 July 2017

Xiaohong R Yang

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2

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26 July 2017

Margaret A Tucker

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3

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26 July 2017

Alisa M Goldstein

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4

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26 July 2017

19 September 2008

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26 July 2017

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26 July 2017

1

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26 July 2017

86

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https://scigraph.springernature.com/pub.10.1186/1756-0500-1-86

26 July 2017

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cites work

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Expression and sequence analysis of candidates for the 1p36.31 tumor suppressor gene deleted in neuroblastomas

21 June 2018

1 reference

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CHD5 is a tumor suppressor at human 1p36

21 June 2018

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An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers

21 June 2018

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A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation

21 June 2018

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PMUT: a web-based tool for the annotation of pathological mutations on proteins.

21 June 2018

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Localization of a novel melanoma susceptibility locus to 1p22

21 June 2018

1 reference

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Genetics of melanoma predisposition

21 June 2018

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

21 June 2018

1 reference

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MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

21 June 2018

1 reference

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Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

21 June 2018

1 reference

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Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi.

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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Chromosomal aberrations in human neuroblastomas

21 June 2018

1 reference

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CDKN2A and CDK4 variants in Latvian melanoma patients: analysis of a clinic-based population

21 June 2018

1 reference

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

31 October 2018

1 reference

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Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations

31 October 2018

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

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma

1 reference

12 December 2020

Identification of novel deletion Loci at 1p36 and 9p22-21 in melanocytic dysplastic nevi and cutaneous malignant melanomas

1 reference

12 December 2020

Microsatellite analysis at 1p36.3 in malignant melanoma of the skin: fine mapping in search of a possible tumour suppressor gene region

1 reference

12 December 2020

Identifiers

DOI

10.1186/1756-0500-1-86

1 reference

Dimensions Publication ID

26 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1756-0500-1-86

9 September 2019

1 reference

26 July 2017

1 reference