SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas (Q36466870)

14 August 2017

SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas (English)

1 reference

14 August 2017

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Willeke A.M. Blokx

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

author name string

Heidi V N Küsters-Vandevelde

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

David Creytens

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Adriana C H van Engen-van Grunsven

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Marcel Jeunink

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Veronique Winnepenninckx

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Patricia J T A Groenen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Benno Küsters

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Clemens F M Prinsen

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

publication date

15 January 2016

1 reference

Acta Neuropathologica Communications

14 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

page(s)

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1186/s40478-016-0272-0

10 June 2020

exact match

0 references

cites work

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Whole-genome copy-number analysis identifies new leads for chromosomal aberrations involved in the oncogenesis and metastastic behavior of uveal melanomas

30 September 2017

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30 September 2017

1 reference

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SF3B1 mutations constitute a novel therapeutic target in breast cancer

30 September 2017

1 reference

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TERT promoter mutation status as an independent prognostic factor in cutaneous melanoma

30 September 2017

1 reference

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Prognostic parameters in uveal melanoma and their association with BAP1 expression

30 September 2017

1 reference

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Lack of BAP1 protein expression in uveal melanoma is associated with increased metastatic risk and has utility in routine prognostic testing

30 September 2017

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30 September 2017

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Rare SF3B1 R625 mutations in cutaneous melanoma.

30 September 2017

1 reference

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Splicing factor mutations and cancer

30 September 2017

1 reference

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BAP1 protein loss by immunohistochemistry: a potentially useful tool for prognostic prediction in patients with uveal melanoma

30 September 2017

1 reference

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SF3B1 mutations are associated with alternative splicing in uveal melanoma

30 September 2017

1 reference

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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

30 September 2017

1 reference

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

30 September 2017

1 reference

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Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytes.

30 September 2017

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Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

30 September 2017

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BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs

30 September 2017

1 reference

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GNAQ and GNA11 mutations in melanocytomas of the central nervous system

30 September 2017

1 reference

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SF3B1 and other novel cancer genes in chronic lymphocytic leukemia

30 September 2017

1 reference

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Histone deacetylase inhibitors induce growth arrest and differentiation in uveal melanoma

30 September 2017

1 reference

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Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

30 September 2017

1 reference

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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

30 September 2017

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Mutations in GNA11 in uveal melanoma

30 September 2017

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Frequent mutation of BAP1 in metastasizing uveal melanomas

30 September 2017

1 reference

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Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis.

30 September 2017

1 reference

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Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB

30 September 2017

1 reference

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Activating mutations of the GNAQ gene: a frequent event in primary melanocytic neoplasms of the central nervous system

30 September 2017

1 reference

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Frequent somatic mutations of GNAQ in uveal melanoma and blue naevi

30 September 2017

1 reference

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Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936.

30 September 2017

1 reference

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Absence of TERT promoter mutations in primary melanocytic tumours of the central nervous system.

30 September 2017

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Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter in a single case of uveal melanoma

28 June 2018

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Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma.

28 June 2018

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Mutations in g protein encoding genes and chromosomal alterations in primary leptomeningeal melanocytic neoplasms.

28 June 2018

1 reference

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Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma.

21 September 2018

1 reference

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Pathology databanking and biobanking in The Netherlands, a central role for PALGA, the nationwide histopathology and cytopathology data network and archive.

21 September 2018

1 reference

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Function of eukaryotic translation initiation factor 1A (eIF1A) (formerly called eIF-4C) in initiation of protein synthesis.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4714515

Primary leptomeningeal melanoma is part of the BAP1-related cancer syndrome

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26769193

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chromosome 3 status combined with BAP1 and EIF1AX mutation profiles are associated with metastasis in uveal melanoma

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26769193

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S40478-016-0272-0

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

10 June 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26769193%20AND%20SRC:MED&resulttype=core&format=json