(Q54239316)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24129063%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

title

NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi (English)

1 reference

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27 February 2020

6

1 reference

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27 February 2020

Jorg Tost

10

1 reference

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27 February 2020

Selim Aractingi

12

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27 February 2020

Romain H Fontaine

2

1 reference

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27 February 2020

Gabriel G Malouf

3

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27 February 2020

Sarah Guegan

13

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27 February 2020

author name string

Christelle Charbel

1

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27 February 2020

Arnaud Picard

4

1 reference

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27 February 2020

Natacha Kadlub

5

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27 February 2020

Alexandre How-Kit

7

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27 February 2020

Xiaoping Su

8

1 reference

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27 February 2020

Aurore Coulomb-L'Hermine

9

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27 February 2020

Samia Mourah

11

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27 February 2020

language of work or name

English

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publication date

15 October 2013

1 reference

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Journal of Investigative Dermatology

27 February 2020

published in

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27 February 2020

volume

134

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27 February 2020

page(s)

1067-1074

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27 February 2020

issue

4

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https://scigraph.springernature.com/pub.10.1038/jid.2013.429

27 February 2020

exact match

0 references

cites work

Large congenital melanocytic nevi and the risk for the development of malignant melanoma. A prospective study.

1 reference

12 December 2020

The genomic complexity of primary human prostate cancer

1 reference

12 December 2020

Neurocutaneous melanosis: clinical features of large congenital melanocytic nevi in patients with manifest central nervous system melanosis

1 reference

12 December 2020

Melanoma risk in congenital melanocytic naevi: a systematic review

1 reference

12 December 2020

Genotypic and gene expression studies in congenital melanocytic nevi: insight into initial steps of melanotumorigenesis

1 reference

12 December 2020

Genetic alterations in melanocytic tumors

1 reference

12 December 2020

Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development

1 reference

12 December 2020

Lack of BRAF(V600E) mutations in giant congenital melanocytic nevi in a Chinese population.

1 reference

12 December 2020

Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS

1 reference

12 December 2020

Sensitive detection of KRAS mutations using enhanced-ice-COLD-PCR mutation enrichment and direct sequence identification

1 reference

12 December 2020

High frequency of BRAF mutations in nevi

1 reference

12 December 2020

Initial genome sequencing and analysis of multiple myeloma

1 reference

12 December 2020

Hallmarks of Cancer: The Next Generation

1 reference

12 December 2020

Molecular nevogenesis

1 reference

12 December 2020

Mutational analysis of the BRAF gene in human congenital and dysplastic melanocytic naevi.

1 reference

12 December 2020

Distribution of BRAF T1799A(V600E) mutations across various types of benign nevi: implications for melanocytic tumorigenesis

1 reference

12 December 2020

Familial site-specific congenital melanocytic nevus: report of two families

1 reference

12 December 2020

Understanding the progression of melanocytic neoplasia using genomic analysis: from fields to cancer

1 reference

12 December 2020

Next generation sequencing in cancer research and clinical application

1 reference

12 December 2020

MEK162 for patients with advanced melanoma harbouring NRAS or Val600 BRAF mutations: a non-randomised, open-label phase 2 study

1 reference

12 December 2020

BRAF and NRAS mutations in melanoma and melanocytic nevi

1 reference

12 December 2020

Association of melanoma and neurocutaneous melanocytosis with large congenital melanocytic naevi-results from the NYU-LCMN registry

1 reference

12 December 2020

Clinical outcome and pathological features associated with NRAS mutation in cutaneous melanoma.

1 reference

12 December 2020

High frequency of BRAFV600E mutation in acquired nevi and small congenital nevi, but low frequency of mutation in medium-sized congenital nevi

1 reference

12 December 2020

Point mutations in the N-ras oncogene in malignant melanoma and congenital naevi

1 reference

12 December 2020

Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naevi

1 reference

12 December 2020

Familial clustering of giant congenital melanocytic nevi

1 reference

12 December 2020

A general approach to single-nucleotide polymorphism discovery.

1 reference

12 December 2020

Congenital melanocytic nevi frequently harbor NRAS mutations but no BRAF mutations

1 reference

12 December 2020

BRAF exon 15 T1799A mutation is common in melanocytic nevi, but less prevalent in cutaneous malignant melanoma, in Chinese Han.

1 reference

12 December 2020

A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers

1 reference

12 December 2020

DNA methylation analysis by pyrosequencing

1 reference

12 December 2020

Large or multiple congenital melanocytic nevi: occurrence of neurocutaneous melanocytosis in 1008 persons

1 reference

12 December 2020

Molecular cytogenetic analysis of Spitz nevi shows clear differences to melanoma

1 reference

12 December 2020

Measuring congenital melanocytic nevi

1 reference

12 December 2020

The mutational landscape of head and neck squamous cell carcinoma

1 reference

12 December 2020

Identifiers

DOI

10.1038/JID.2013.429

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24129063%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

1 reference

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