(Q37523394)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19536551%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

review article

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title

The genetic and epigenetic basis of ependymoma (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19536551%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1

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31 January 2020

author name string

Michael D Taylor

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19536551%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

language of work or name

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18 June 2009

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19536551%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

published in

Child's Nervous System

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19536551%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

volume

25

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31 January 2020

issue

10

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31 January 2020

page(s)

1195-1201

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https://scigraph.springernature.com/pub.10.1007/s00381-009-0928-1

31 January 2020

exact match

0 references

cites work

Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups

1 reference

https://api.crossref.org/works/10.1007%2FS00381-009-0928-1

Genomic imbalances in pediatric intracranial ependymomas define clinically relevant groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-009-0928-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-009-0928-1

Identification of novel chromosomal abnormalities and prognostic cytogenetics markers in intracranial pediatric ependymoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-009-0928-1

Epigenetic silencing of the HIC-1 gene in human medulloblastomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-009-0928-1

Epigenetic inactivation of the RASSF1A tumour suppressor gene in ependymoma.

21 January 2018

1 reference

12 December 2020

Postoperative chemotherapy without irradiation for ependymoma in children under 5 years of age: a multicenter trial of the French Society of Pediatric Oncology.

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular genetic analysis of non-astrocytic gliomas

1 reference

12 December 2020

Genetic abnormalities detected in ependymomas by comparative genomic hybridisation

1 reference

12 December 2020

Prognostic factors in infants and very young children with intracranial ependymomas

1 reference

12 December 2020

Correlation between localization, age, and chromosomal imbalances in ependymal tumours as detected by CGH.

1 reference

12 December 2020

Identification of tumor-specific molecular signatures in intracranial ependymoma and association with clinical characteristics.

1 reference

12 December 2020

Chemotherapy for intracranial ependymomas

1 reference

12 December 2020

Low frequency of chromosomal imbalances in anaplastic ependymomas as detected by comparative genomic hybridization.

1 reference

12 December 2020

Cytogenetic abnormalities in human ependymomas.

1 reference

12 December 2020

Cytogenetic analysis of 109 pediatric central nervous system tumors.

1 reference

12 December 2020

Human ependymomas reveal frequent deletions on chromosomes 6 and 9.

1 reference

12 December 2020

Identification of gains on 1q and epidermal growth factor receptor overexpression as independent prognostic markers in intracranial ependymoma

1 reference

12 December 2020

Methylation of RASSF1A and TRAIL pathway-related genes is frequent in childhood intracranial ependymomas and benign choroid plexus papilloma.

1 reference

12 December 2020

Infrequency of p53 gene mutations in ependymomas

1 reference

12 December 2020

Epigenetic inactivation of MCJ (DNAJD1) in malignant paediatric brain tumours.

1 reference

12 December 2020

Radiation dosimetry predicts IQ after conformal radiation therapy in pediatric patients with localized ependymoma.

1 reference

12 December 2020

Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas

1 reference

12 December 2020

Karyotype studies in 18 ependymomas with literature review of 107 cases

1 reference

12 December 2020

Ependymoma: new therapeutic approaches including radiation and chemotherapy

1 reference

12 December 2020

1 reference

12 December 2020

Chromosome abnormalities in low-grade central nervous system tumors

1 reference

12 December 2020

Cytogenetic investigation in subependymoma.

1 reference

12 December 2020

Late neurocognitive sequelae in survivors of brain tumours in childhood

1 reference

12 December 2020

Preliminary results from a phase II trial of conformal radiation therapy and evaluation of radiation-related CNS effects for pediatric patients with localized ependymoma

1 reference

12 December 2020

Cytogenetics of pediatric central nervous system tumors.

1 reference

12 December 2020

Karyotypes in 90 human gliomas

1 reference

12 December 2020

Serial evaluation of academic and behavioral outcome after treatment with cranial radiation in childhood.

1 reference

12 December 2020

Cytogenetic study of 33 ependymomas.

1 reference

12 December 2020

Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas

1 reference

12 December 2020

Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma

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

Involvement of chromosome 22 in ependymomas.

1 reference

12 December 2020

Infrequent alterations of the p15, p16, CDK4 and cyclin D1 genes in non-astrocytic human brain tumors.

1 reference

12 December 2020

A multicenter retrospective study of chemotherapy for recurrent intracranial ependymal tumors in adults by the Gruppo Italiano Cooperativo di Neuro-Oncologia.

1 reference

12 December 2020

Identification of novel regions of allelic loss in ependymomas by high-resolution allelotyping with 384 microsatellite markers.

1 reference

12 December 2020

Analysis of HIC-1 methylation and transcription in human ependymomas

1 reference

12 December 2020

Molecular genetic alterations on chromosomes 11 and 22 in ependymomas.

1 reference

12 December 2020

Neurofibromatosis type 2

1 reference

12 December 2020

Microsatellite analysis of childhood brain tumors

1 reference

12 December 2020

Molecular cytogenetic analysis of glial tumors using spectral karyotyping and comparative genomic hybridization

1 reference

12 December 2020

Radial glia cells are candidate stem cells of ependymoma

1 reference

12 December 2020

CDKN2A, CDKN2B and p14ARF are frequently and differentially methylated in ependymal tumours.

1 reference

12 December 2020

Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.

1 reference

12 December 2020

Chromosomes in the genesis and progression of ependymomas.

1 reference

12 December 2020

Multiagent chemotherapy and deferred radiotherapy in infants with malignant brain tumors: a report from the Children's Cancer Group

1 reference

12 December 2020

Chromosomal characteristics of childhood brain tumors

1 reference

12 December 2020

CDKN2A/p16 in ependymomas.

1 reference

12 December 2020

Molecular cytogenetic studies of pediatric ependymomas

1 reference

12 December 2020

Aberrant promoter methylation of multiple genes in oligodendrogliomas and ependymomas.

1 reference

12 December 2020

Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma.

1 reference

12 December 2020

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

1 reference

12 December 2020

Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma

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

PTEN mutations in gliomas and glioneuronal tumors.

1 reference

12 December 2020

Cytogenetic studies in 45 pediatric brain tumors

1 reference

12 December 2020

Evaluation of NF2 gene deletion in sporadic schwannomas, meningiomas, and ependymomas by chromogenic in situ hybridization

1 reference

12 December 2020

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

1 reference

12 December 2020

Change in neurocognitive functioning after treatment with cranial radiation in childhood.

1 reference

12 December 2020

Production and characterization of two ependymoma xenografts

1 reference

12 December 2020

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

1 reference

12 December 2020

Aberrant CpG island methylation of multiple genes in ependymal tumors.

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas

1 reference

12 December 2020

The role of chemotherapy in newly diagnosed ependymoma of childhood.

1 reference

12 December 2020

Molecular analysis of genetic changes in ependymomas.

1 reference

12 December 2020

Ependymomas in children

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12 December 2020

10.1007/S00381-009-0928-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19536551%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference