(Q48946827)

17 February 2018

title

Analysis of chromosome 7 in adult and pediatric ependymomas using chromogenic in situ hybridization. (English)

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17 February 2018

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2

Martha Quezado

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17 February 2018

author name string

Mariarita Santi

series ordinal

1

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17 February 2018

Rubin Ronchetti

series ordinal

3

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17 February 2018

Elisabeth J Rushing

series ordinal

4

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17 February 2018

publication date

1 March 2005

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17 February 2018

Journal of Neuro-Oncology

published in

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17 February 2018

volume

72

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17 February 2018

issue

1

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17 February 2018

page(s)

25-28

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17 February 2018

https://scigraph.springernature.com/pub.10.1007/s11060-004-3117-9

exact match

0 references

cites work

Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups

1 reference

https://api.crossref.org/works/10.1007%2FS11060-004-3117-9

Structural genomic abnormalities of chromosomes 9 and 18 in myxopapillary ependymomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11060-004-3117-9

Interphase cytogenetic (in situ hybridization) analysis of astrocytomas using archival, formalin-fixed, paraffin-embedded tissue and nonfluorescent light microscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11060-004-3117-9

Amplification of c-myc oncogene by chromogenic and fluorescence in situ hybridization in archival breast cancer tissue array samples.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11060-004-3117-9

Gain of chromosome 7, as detected by in situ hybridization, strongly correlates with shorter survival in astrocytoma grade 2.

21 January 2018

1 reference

12 December 2020

Interphase cytogenetics: a new tool for the study of genetic changes in brain tumors

1 reference

12 December 2020

Analysis of HER-2/neu amplification in endometrial carcinoma by chromogenic in situ hybridization. Correlation with fluorescence in situ hybridization, HER-2/neu, p53 and Ki-67 protein expression, and outcome

1 reference

12 December 2020

Chromosome abnormalities in low-grade central nervous system tumors

1 reference

12 December 2020

Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics.

1 reference

12 December 2020

Epidemiology of central nervous system tumors in childhood and adolescence based on the new WHO classification

1 reference

12 December 2020

Differential involvement of protein 4.1 family members DAL-1 and NF2 in intracranial and intraspinal ependymomas.

1 reference

12 December 2020

Molecular cytogenetic studies of pediatric ependymomas

1 reference

12 December 2020

Clear cell ependymoma: A clinicopathologic and radiographic analysis of 10 patients

1 reference

12 December 2020

Metastatic trophoblastic disease after an initial diagnosis of partial hydatidiform mole: genotyping and chromosome in situ hybridization analysis

1 reference

12 December 2020

Comparative genomic hybridization detects losses of chromosomes 22 and 16 as the most common recurrent genetic alterations in primary ependymomas.

1 reference

12 December 2020

Detection of numerical alterations of chromosome 1 in cytopathological specimens of breast tumors by chromogen in situ hybridization

1 reference

12 December 2020

Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas.

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S11060-004-3117-9

Identifiers

DOI

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17 February 2018

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17 February 2018