(Q57304749)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7669741%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas (English)

1 reference

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23 October 2019

0 references

4

1 reference

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Xavier Estivill i Pallejà

23 October 2019

10

1 reference

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23 October 2019

author name string

Mérel P

1

1 reference

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23 October 2019

Hoang-Xuan K

2

1 reference

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23 October 2019

Sanson M

3

1 reference

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23 October 2019

Bijlsma EK

5

1 reference

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23 October 2019

Lazaro C

6

1 reference

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23 October 2019

Moisan JP

7

1 reference

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23 October 2019

Resche F

8

1 reference

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23 October 2019

Nishisho I

9

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23 October 2019

publication date

1 July 1995

1 reference

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Genes, Chromosomes and Cancer

23 October 2019

published in

1 reference

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23 October 2019

volume

13

1 reference

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23 October 2019

page(s)

211-216

1 reference

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23 October 2019

issue

3

1 reference

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Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

23 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

Alternative splicing of the NF2 gene and its mutation analysis of breast and colorectal cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Analysis of mutations in theSCH gene in schwannomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Analysis of theNF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Exon scanning for mutation of the NF2 gene in schwannomas.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

DNA diagnosis of neurofibromatosis 2. Altered coding sequence of the merlin tumor suppressor in an extended pedigree.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Screening for germ-line mutations in the NF2 gene.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

The neurofibromatosis type 2 gene is inactivated in schwannomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Cytological and cytogenetical studies on human meningioma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Chromosomal Constitution of Meningiomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870130311

7 January 2021

Identifiers

DOI

10.1002/GCC.2870130311

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7669741%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference