(Q48593235)

13 February 2018

title

Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas. (English)

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13 February 2018

author

Martin Hasselblatt

4

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13 February 2018

Christian Beetz

12

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13 February 2018

William G. Newman

15

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13 February 2018

Gareth Evans

object named as

D Gareth Evans

16

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Miriam J Smith

1

object named as

Miriam J Smith

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13 February 2018

Daniel Du Plessis

13

object named as

Daniel du Plessis

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13 February 2018

author name string

Andrew J Wallace

2

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13 February 2018

Chris Bennett

3

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13 February 2018

Ewelina Elert-Dobkowska

5

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13 February 2018

Linton T Evans

6

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13 February 2018

William F Hickey

7

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Jack van Hoff

8

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13 February 2018

David Bauer

9

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13 February 2018

Amy Lee

10

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Robert F Hevner

11

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John-Paul Kilday

14

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publication date

6 October 2014

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13 February 2018

published in

Journal of Pathology

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13 February 2018

volume

234

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13 February 2018

issue

4

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13 February 2018

page(s)

436-440

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13 February 2018

NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update

cites work

1 reference

INI1 mutations in meningiomas at a potential hotspot in exon 9

21 January 2018

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SMARCB1 mutations are not a common cause of multiple meningiomas

21 January 2018

1 reference

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

21 January 2018

1 reference

Loss of SUFU function in familial multiple meningioma.

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

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

21 January 2018

1 reference

Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO

21 January 2018

1 reference

Genomic sequencing of meningiomas identifies oncogenic SMO and AKT1 mutations

21 January 2018

1 reference

Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PATH.4427

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13 February 2018

PubMed ID

25143307

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13 February 2018