(Q44718402)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

multiple meningiomas

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

author name string

Pepijn van den Munckhof

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Imke Christiaans

2

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Susan B Kenter

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Theo J M Hulsebos

5

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

publication date

26 October 2011

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

13

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

1-7

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

https://scigraph.springernature.com/pub.10.1007/s10048-011-0300-y

0 references

Germline mutation of INI1/SMARCB1 in familial schwannomatosis

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Falx Meningiomas: Surgical Results and Lessons Learned from 68 Cases

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Anatomic location is a risk factor for atypical and malignant meningiomas

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomas

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

SMARCB1 mutations are not a common cause of multiple meningiomas

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0300-Y

21 January 2018

Analysis of mutations in theSCH gene in schwannomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/22038540

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22038540

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-011-0300-Y

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

release_txw3chtutjbyrciiviikijiss4

1 reference

https://api.fatcat.wiki/v0/release/txw3chtutjbyrciiviikijiss4

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

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