The neurofibromatosis type 2 gene is mutated in perineurial cell tumors: a molecular genetic study of eight cases. (Q35842044)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11290539%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

The neurofibromatosis type 2 gene is mutated in perineurial cell tumors: a molecular genetic study of eight cases (English)

1 reference

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neurofibromatosis type II

6 November 2019

main subject

1 reference

3

1 reference

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6 November 2019

Bartosz Wasąg

series ordinal

4

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6 November 2019

6

M Miettinen

1 reference

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6 November 2019

1

J Lasota

1 reference

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6 November 2019

author name string

J F Fetsch

series ordinal

2

1 reference

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6 November 2019

R Sciot

series ordinal

5

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6 November 2019

language of work or name

English

0 references

publication date

1 April 2001

1 reference

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The American Journal of Pathology

6 November 2019

published in

1 reference

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6 November 2019

volume

158

1 reference

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6 November 2019

issue

4

1 reference

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6 November 2019

page(s)

1223-1229

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Characterisation of 16 polymorphic markers in the NF2 gene: application to hemizygosity detection

6 November 2019

cites work

1 reference

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The involvement of calpain-dependent proteolysis of the tumor suppressor NF2 (merlin) in schwannomas and meningiomas

11 July 2018

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Detection of the SYT-SSX fusion transcripts in formaldehyde-fixed, paraffin-embedded tissue: a reverse transcription polymerase chain reaction amplification assay useful in the diagnosis of synovial sarcoma.

11 July 2018

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Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations

11 July 2018

1 reference

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Universal absence of merlin, but not other ERM family members, in schwannomas.

11 July 2018

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Loss of merlin expression in sporadic meningiomas, ependymomas and schwannomas

11 July 2018

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Reduced expression of schwannomin/merlin in human sporadic meningiomas

11 July 2018

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Soft-tissue perineurioma. Evidence for an abnormality of chromosome 22, criteria for diagnosis, and review of the literature

11 July 2018

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Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease

11 July 2018

1 reference

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Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.

11 July 2018

1 reference

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Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma.

11 July 2018

1 reference

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Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

11 July 2018

1 reference

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Intraneural perineurioma. A clonal neoplasm associated with abnormalities of chromosome 22.

11 July 2018

1 reference

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Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma

11 July 2018

1 reference

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Mutation and cancer: statistical study of retinoblastoma

11 July 2018

1 reference

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Perineurial cells coexpress genes encoding interstitial collagens and basement membrane zone components

11 July 2018

1 reference

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The enigmatic perineurial cell and its participation in tumors and in tumorlike entities

11 July 2018

1 reference

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Perineurioma: an uncommon soft tissue neoplasm distinct from localized hypertrophic neuropathy and neurofibroma

11 July 2018

1 reference

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NF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas.

11 July 2018

1 reference

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NF2 gene in neurofibromatosis type 2 patients.

24 September 2018

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

24 September 2018

1 reference

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The neurofibromatosis type 2 gene is inactivated in schwannomas

24 September 2018

1 reference

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Screening for germ-line mutations in the NF2 gene

24 September 2018

1 reference

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Immunohistochemical detection of epithelial membrane antigen in normal perineurial cells and perineurioma

24 September 2018

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https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964072-2

Epithelial membrane antigen expression by the perineurial cell: further studies of peripheral nerve lesions

7 January 2021

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Sclerosing perineurioma: a clinicopathologic study of 19 cases of a distinctive soft tissue lesion with a predilection for the fingers and palms of young adults

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964072-2

Ultrastructural identification of a benign perineurial cell tumor

7 January 2021

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Extraneural retiform perineuriomas. A report of four cases

7 January 2021

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Perineurial malignant peripheral nerve sheath tumor (MPNST): a clinicopathologic, immunohistochemical, and ultrastructural study of seven cases

7 January 2021

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Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion

7 January 2021

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

7 January 2021

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Analysis of mutations in theSCH gene in schwannomas

7 January 2021

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Molecular characterization of germline NF2 gene rearrangements

7 January 2021

1 reference

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A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene

7 January 2021

1 reference

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Tight association of loss of merlin expression with loss of heterozygosity at chromosome 22q in sporadic meningiomas

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11290539

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular diagnosis of mantle cell lymphoma in paraffin-embedded tissue

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11290539

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)64072-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11290539%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11290539%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

PubMed publication ID

11290539

1 reference