High-resolution analysis of chromosome arm 1p alterations in meningioma (Q74063057)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10913674%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

High-resolution analysis of chromosome arm 1p alterations in meningioma (English)

1 reference

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8 November 2019

M J Bello

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8 November 2019

J M de Campos

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8 November 2019

J Vaquero

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8 November 2019

M E Kusak

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8 November 2019

J L Sarasa

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8 November 2019

J A Rey

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8 November 2019

publication date

1 July 2000

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Cancer Genetics and Cytogenetics

8 November 2019

published in

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8 November 2019

volume

120

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8 November 2019

issue

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8 November 2019

page(s)

30-36

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Analysis of genomic alterations in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression

8 November 2019

cites work

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

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

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Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression.

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7 January 2021

Allelic loss at 1p is associated with tumor progression of meningiomas.

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Allelic status of chromosome 1 in neoplasms of the nervous system.

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7 January 2021

Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putative 'tumor progression' locus

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7 January 2021

Loss of heterozygosity of chromosome 14q in low- and high-grade meningiomas

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7 January 2021

Deletion mapping of the short arm of chromosome 1 identifies a common region of deletion distal to D1S496 in human meningiomas.

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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

Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma

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Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches

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7 January 2021

Chromosomal involvement secondary to -22 in human meningiomas

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7 January 2021

Karyotypic evolution of human meningioma. Progression through malignancy

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7 January 2021

Correlation between cytogenetic and histopathological findings in 75 human meningiomas

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7 January 2021

Chromosome abnormalities in meningeal neoplasms: do they correlate with histology?

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7 January 2021

Cytogenetic, molecular genetic and pathological analyses in 126 meningiomas

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7 January 2021

Monosomy 1p is correlated with enhanced in vivo glucose metabolism in meningiomas

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7 January 2021

Cytogenetical findings of recurrent meningiomas. A study of 10 tumors

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7 January 2021

Cytogenetic analysis of aggressive meningiomas: Possible diagnostic and prognostic implications

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7 January 2021

Chromosomal losses and gains in meningiomas: comparative genomic hybridization (CGH) study of the whole genome

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7 January 2021

Deletion mapping of chromosomal region 1p32-pter in primary breast cancer

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7 January 2021

Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers

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7 January 2021

1p36: every subband a suppressor?

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7 January 2021

Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

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7 January 2021

hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas

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7 January 2021

Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32

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7 January 2021

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

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7 January 2021

10.1016/S0165-4608(99)00249-6

Identifiers

DOI

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8 November 2019

1 reference

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