(Q45167839)

10 December 2017

title

Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas (English)

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10 December 2017

9

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10 December 2017

12

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10 December 2017

13

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10 December 2017

8

Diana Eccles

1 reference

10 December 2017

1

Miriam J Smith

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10 December 2017

4

Kristen D Hadfield

1 reference

10 December 2017

11

Daniel du Plessis

1 reference

10 December 2017

James O'Sullivan

2

1 reference

10 December 2017

Sanjeev S Bhaskar

3

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10 December 2017

Gemma Poke

5

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10 December 2017

John Caird

6

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10 December 2017

Saba Sharif

7

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10 December 2017

Daniel Rawluk

10

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10 December 2017

language of work or name

English

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publication date

3 February 2013

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10 December 2017

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10 December 2017

volume

45

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10 December 2017

issue

3

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10 December 2017

page(s)

295-298

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Epidemiology and etiology of intracranial meningiomas: a review

10 December 2017

cites work

1 reference

Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset.

21 January 2018

1 reference

Multiple meningiomas: differential involvement of the NF2 gene in children and adults

21 January 2018

1 reference

Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas

21 January 2018

1 reference

Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri

21 January 2018

1 reference

Molecular heterogeneity of meningioma with INI1 mutation

21 January 2018

1 reference

INI1 mutations in meningiomas at a potential hotspot in exon 9

21 January 2018

1 reference

SMARCB1 mutations are not a common cause of multiple meningiomas

21 January 2018

1 reference

Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas

21 January 2018

1 reference

Common variation at 10p12.31 near MLLT10 influences meningioma risk

21 January 2018

1 reference

Reciprocal regulation of CD4/CD8 expression by SWI/SNF-like BAF complexes

21 January 2018

1 reference

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review

21 January 2018

1 reference

Architectural DNA binding by a high-mobility-group/kinesin-like subunit in mammalian SWI/SNF-related complexes

21 January 2018

1 reference

N-terminally truncated BAF57 isoforms contribute to the diversity of SWI/SNF complexes in neurons

21 January 2018

1 reference

The BRG1- and hBRM-associated factor BAF57 induces apoptosis by stimulating expression of the cylindromatosis tumor suppressor gene

21 January 2018

1 reference

The SWI/SNF chromatin remodeling subunit BAF57 is a critical regulator of estrogen receptor function in breast cancer cells

21 January 2018

1 reference

Targeting of SWI/SNF chromatin remodelling complexes to estrogen-responsive genes

21 January 2018

1 reference

Identification of BAF57 mutations in human breast cancer cell lines

21 January 2018

1 reference

Highly parallel identification of essential genes in cancer cells

21 January 2018

1 reference

Identification and characterization of novel potentially oncogenic mutations in the human BAF57 gene in a breast cancer patient.

21 January 2018

1 reference

Loss of the tumor suppressor Snf5 leads to aberrant activation of the Hedgehog-Gli pathway.

21 January 2018

1 reference

Loss of SUFU function in familial multiple meningioma.

21 January 2018

1 reference

ARID1A mutations in endometriosis-associated ovarian carcinomas

21 January 2018

1 reference

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

21 January 2018

1 reference

Frequent mutations of chromatin remodeling gene ARID1A in ovarian clear cell carcinoma

21 January 2018

1 reference

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

21 January 2018

1 reference

Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

21 January 2018

1 reference

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

21 January 2018

1 reference

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

21 January 2018

1 reference

Incidence and clinical features of asymptomatic meningiomas

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23377182

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial risks in nervous system tumors.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23377182

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Population-based analysis of sporadic and type 2 neurofibromatosis-associated meningiomas and schwannomas

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23377182

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.2552

1 reference

Dimensions Publication ID

10 December 2017

1040590247

0 references

1 reference