(Q49018540)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15731777%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Alterations of protein 4.1 family members in ependymomas: a study of 84 cases (English)

1 reference

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8 January 2020

5

1 reference

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8 January 2020

David H. Gutmann

series ordinal

2

1 reference

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8 January 2020

4

David B Mansur

1 reference

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8 January 2020

author name string

Veena Rajaram

series ordinal

1

1 reference

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8 January 2020

Srinivas K Prasad

series ordinal

3

1 reference

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8 January 2020

publication date

1 July 2005

1 reference

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8 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15731777%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

volume

18

1 reference

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8 January 2020

issue

7

1 reference

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8 January 2020

page(s)

991-997

1 reference

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https://scigraph.springernature.com/pub.10.1038/modpathol.3800390

8 January 2020

exact match

0 references

cites work

Histologic prognostic factors in ependymoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Intracranial ependymomas of childhood: long-term outcome and prognostic factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

The clinical and prognostic relevance of grading in intracranial ependymomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Survival and prognostic factors following radiation therapy and chemotherapy for ependymomas in children: a report of the Children's Cancer Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Prognostic factors in intracranial ependymomas in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

9p21 and 13q14 dosages in ependymomas. A clinicopathologic study of 101 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Karyotype studies in 18 ependymomas with literature review of 107 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Loss of merlin expression in sporadic meningiomas, ependymomas and schwannomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

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/10.1038%2FMODPATHOL.3800390

Molecular genetic alterations on chromosomes 11 and 22 in ependymomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

The neurofibromatoses: when less is more

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

ERM proteins: from cellular architecture to cell signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Cloning and characterization of 4.1G (EPB41L2), a new member of the skeletal protein 4.1 (EPB41) gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Loss of DAL-1, a protein 4.1-related tumor suppressor, is an important early event in the pathogenesis of meningiomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Aggressive phenotypic and genotypic features in pediatric and NF2-associated meningiomas: a clinicopathologic study of 53 cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Identification of a third Protein 4.1 tumor suppressor, Protein 4.1R, in meningioma pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Gene Expression Patterns in Ependymomas Correlate with Tumor Location, Grade, and Patient Age

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

Protein 4.1 in forebrain postsynaptic density preparations: enrichment of 4.1 gene products and detection of 4.1R binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

inferred from DOI database lookup

7 January 2021

based on heuristic

Merlin, DAL-1, and progesterone receptor expression in clinicopathologic subsets of meningioma: a correlative immunohistochemical study of 175 cases

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800390

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/MODPATHOL.3800390

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15731777%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

8 January 2020

1001927528

0 references

1 reference