(Q34403463)

1 August 2017

title

Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis (English)

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1 August 2017

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Tzer Jing Seng

1

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1 August 2017

Koichi Ichimura

2

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1 August 2017

Lu Liu

3

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1 August 2017

Ola Tingby

4

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1 August 2017

Danita M Pearson

5

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1 August 2017

V Peter Collins

6

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1 August 2017

publication date

1 June 2005

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Genes, Chromosomes and Cancer

1 August 2017

published in

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1 August 2017

volume

43

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1 August 2017

issue

2

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1 August 2017

page(s)

181-193

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

1 August 2017

cites work

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The complexity of the 7p12 amplicon in human astrocytic gliomas: detailed mapping of 246 tumors.

21 January 2018

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Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomas

21 January 2018

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Acetylation of importin-alpha nuclear import factors by CBP/p300.

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7 January 2021

Analysis of mutations in theSCH gene in schwannomas

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7 January 2021

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

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7 January 2021

Reevaluating human gene annotation: a second-generation analysis of chromosome 22

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7 January 2021

The DNA sequence of human chromosome 22

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7 January 2021

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

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7 January 2021

Mutations truncating the EP300 acetylase in human cancers

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7 January 2021

Fine mapping of chromosome 22q tumor suppressor gene candidate regions in astrocytoma

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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

Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades.

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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

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7 January 2021

Allelotype and replication error phenotype of small cell lung carcinoma.

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7 January 2021

Comparative genomic hybridization in glioma: a meta-analysis of 509 cases.

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7 January 2021

Analysis of p53 mutation and epidermal growth factor receptor amplification in recurrent gliomas with malignant progression.

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7 January 2021

Identification and validation of tumor suppressor genes

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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

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

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7 January 2021

Mutational profile of the PTEN gene in primary human astrocytic tumors and cultivated xenografts.

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7 January 2021

Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations

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7 January 2021

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

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7 January 2021

Mutational analysis of INI1 in sporadic human brain tumors

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7 January 2021

Chromosome 22q in pancreatic endocrine tumors: identification of a homozygous deletion and potential prognostic associations of allelic deletions

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7 January 2021

Frequent loss of heterozygosity at telomeric loci on 22q in sporadic colorectal cancers

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7 January 2021

Identifiers

DOI

10.1002/GCC.20181

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1 August 2017

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