(Q48613043)

13 February 2018

title

Analysis of the NF2 gene in oligodendrogliomas and ependymomas (English)

1 reference

13 February 2018

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M Eva Alonso

1

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13 February 2018

M Josefa Bello

2

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13 February 2018

Dolores Arjona

3

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13 February 2018

Pilar Gonzalez-Gomez

4

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13 February 2018

Jesus Lomas

5

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13 February 2018

Jose M de Campos

6

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13 February 2018

M Elena Kusak

7

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13 February 2018

Alberto Isla

8

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13 February 2018

Juan A Rey

9

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13 February 2018

publication date

1 April 2002

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13 February 2018

Cancer Genetics and Cytogenetics

published in

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13 February 2018

volume

134

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13 February 2018

issue

1

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13 February 2018

page(s)

1-5

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13 February 2018

Chromosomal patterns in human malignant astrocytomas

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Chromosome abnormalities in low-grade central nervous system tumors

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7 January 2021

Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas

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7 January 2021

Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo‐astrocytomas

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7 January 2021

A cytogenetic study of 19 recurrent gliomas.

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7 January 2021

Chromosome studies in 70 brain tumors with special attention to sex chromosome loss and single autosomal trisomy

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7 January 2021

Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma

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7 January 2021

Chromosomes in the genesis and progression of ependymomas.

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7 January 2021

Involvement of chromosome 22 in ependymomas.

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7 January 2021

Chromosome aberrations in four ependymomas

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7 January 2021

Constitutional de novo t(1;22)(p22;q11.2) and ependymoma.

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7 January 2021

Cytogenetic study of 33 ependymomas.

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7 January 2021

Molecular analysis of genetic changes in ependymomas.

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7 January 2021

Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma

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7 January 2021

Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups

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7 January 2021

Loss of heterozygosity for distal markers on 22q in human gliomas

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7 January 2021

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

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7 January 2021

Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene.

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7 January 2021

Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2.

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7 January 2021

Common regions of deletion on chromosome 22q12.3-q13.1 and 22q13.2 in human astrocytomas appear related to malignancy grade.

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7 January 2021

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

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7 January 2021

Combined molecular genetic studies of chromosome 22q and the neurofibromatosis type 2 gene in central nervous system tumors.

1 reference

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7 January 2021

Frequent type 2 neurofibromatosis gene transcript mutations in sporadic intramedullary spinal cord ependymomas

1 reference

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7 January 2021

Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Exon scanning for mutation of the NF2 gene in schwannomas

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https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

Molecular genetic alterations on chromosomes 11 and 22 in ependymomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900591-X

7 January 2021

10.1016/S0165-4608(01)00591-X

Identifiers

DOI

1 reference

13 February 2018

1 reference

13 February 2018