(Q71131047)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8655144%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

title

Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8655144%20AND%20SRC:MED&resulttype=core&format=json

neurofibromatosis type II

16 October 2019

main subject

1 reference

8

1 reference

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16 October 2019

author name string

L R De Vitis

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8655144%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

A Tedde

2

1 reference

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16 October 2019

F Vitelli

3

1 reference

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16 October 2019

F Ammannati

4

1 reference

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16 October 2019

P Mennonna

5

1 reference

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16 October 2019

U Bigozzi

6

1 reference

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16 October 2019

E Montali

7

1 reference

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16 October 2019

publication date

1 May 1996

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16 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8655144%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

volume

97

1 reference

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16 October 2019

page(s)

632-637

1 reference

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16 October 2019

issue

5

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf02281874

16 October 2019

exact match

0 references

cites work

Mutational analysis of patients with neurofibromatosis 2

1 reference

12 December 2020

Analysis of mutations in theSCH gene in schwannomas

1 reference

12 December 2020

Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE

1 reference

12 December 2020

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene

1 reference

12 December 2020

Search for putative suppressor genes in meningioma: significance of chromosome 22

1 reference

12 December 2020

Effect of 5' splice site mutations on splicing of the preceding intron

1 reference

12 December 2020

Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas

1 reference

12 December 2020

Exon scanning for mutation of the NF2 gene in schwannomas.

1 reference

12 December 2020

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

1 reference

12 December 2020

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

1 reference

12 December 2020

A microsatellite-based multipoint index map of human chromosome 22.

1 reference

12 December 2020

A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity

1 reference

12 December 2020

Multifocal meningiomas in a patient with a constitutional ring chromosome 22.

1 reference

12 December 2020

Suppression of tumorigenicity in transformed cells after transfection with vinculin cDNA

1 reference

12 December 2020

Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma

1 reference

12 December 2020

Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.

1 reference

12 December 2020

Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors

1 reference

12 December 2020

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene

1 reference

12 December 2020

Expression of transduced tropomyosin 1 cDNA suppresses neoplastic growth of cells transformed by the ras oncogene

1 reference

12 December 2020

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

12 December 2020

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

1 reference

12 December 2020

Deletions on chromosome 22 in sporadic meningioma

1 reference

12 December 2020

Tumor-suppressive function of mutated gelsolin in ras-transformed cells.

1 reference

12 December 2020

An anti-Ras function of neurofibromatosis type 2 gene product (NF2/Merlin).

1 reference

12 December 2020

High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons

1 reference

12 December 2020

Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers

1 reference

12 December 2020

Suppression of tumorigenicity in simian virus 40-transformed 3T3 cells transfected with alpha-actinin cDNA.

1 reference

12 December 2020

1 reference

12 December 2020

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

1 reference

12 December 2020

Screening for germ-line mutations in the NF2 gene.

1 reference

12 December 2020

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

1 reference

12 December 2020

Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas

1 reference

12 December 2020

The neurofibromatosis type 2 gene is inactivated in schwannomas

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the D22S268 locus

1 reference

12 December 2020

Deletion mapping of the long arm of chromosome 22 in human meningiomas

1 reference

12 December 2020

Molecular genetic analysis of chromosome 22 in 81 cases of meningioma

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02281874

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8655144%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference