(Q34388064)

English

Infrequency of p53 gene mutations in ependymomas

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

1 August 2017

Infrequency of p53 gene mutations in ependymomas (English)

1 reference

Europe PubMed Central

1 August 2017

author name string

Fink KL

1

1 reference

Europe PubMed Central

1 August 2017

Rushing EJ

2

1 reference

Europe PubMed Central

1 August 2017

Schold SC Jr

3

1 reference

Europe PubMed Central

1 August 2017

Nisen PD

4

1 reference

Europe PubMed Central

1 August 2017

publication date

1 February 1996

1 reference

Europe PubMed Central

1 August 2017

Journal of Neuro-Oncology

1 reference

Europe PubMed Central

1 August 2017

27

1 reference

Europe PubMed Central

1 August 2017

2

1 reference

Europe PubMed Central

1 August 2017

111-115

1 reference

Europe PubMed Central

1 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00177473

0 references

Ependymoma: a follow-up study of 101 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ependymomas: a clinicopathologic study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic abnormalities in human ependymomas.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deadly inheritance

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology, cytogenetics, and molecular biology of brain tumors.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of the short arm of chromosome 1 in a myxopapillary ependymoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of histopathological correlation of malignant ependymomas with postoperative survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in low-grade central nervous system tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

p53 mutations in human cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic alterations in glioma and medulloblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

p53 mutations in nonastrocytic human brain tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of genetic information in central nervous system tumors common to children and young adults.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotypes in 90 human gliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple chromosome rearrangements in a childhood ependymoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infrequent p53 gene mutations in medulloblastomas.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent intracranial ependymomas in children. Survival, patterns of failure, and prognostic factors.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overexpression of multiple oncogenes related to histological grade of astrocytic glioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of p53 gene mutations in human gliomas by polymerase chain reaction-based single-strand conformation polymorphism and DNA sequencing.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cellular myb oncogene is amplified, rearranged and activated in human glioblastoma cell lines.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clonal expansion of p53 mutant cells is associated with brain tumour progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Posterior fossa ependymomas: report of 30 cases and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A correlative study of p53 protein alteration and p53 gene mutation in glioblastoma multiforme.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8699232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00177473

1 reference

Europe PubMed Central

1 August 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

1 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34388064&oldid=1549450205"