(Q44120017)

English

Identification of the small interstitial deletion at chromosome band 1p34-p35 and its association with poor outcome in oligodendroglial tumors

scientific article published in October 2002

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scholarly article

1 reference

Europe PubMed Central

30 November 2017

Identification of the small interstitial deletion at chromosome band 1p34-p35 and its association with poor outcome in oligodendroglial tumors (English)

1 reference

Europe PubMed Central

30 November 2017

oligodendrocyte

1 reference

based on heuristic

inferred from title

author name string

Toshihiko Iuchi

1

1 reference

Europe PubMed Central

30 November 2017

Hiroki Namba

2

1 reference

Europe PubMed Central

30 November 2017

Yasuo Iwadate

3

1 reference

Europe PubMed Central

30 November 2017

Tomotane Shishikura

4

1 reference

Europe PubMed Central

30 November 2017

Hajime Kageyama

5

1 reference

Europe PubMed Central

30 November 2017

Yoko Nakamura

6

1 reference

Europe PubMed Central

30 November 2017

Miki Ohira

7

1 reference

Europe PubMed Central

30 November 2017

Akira Yamaura

8

1 reference

Europe PubMed Central

30 November 2017

Katsunobu Osato

9

1 reference

Europe PubMed Central

30 November 2017

Shigeru Sakiyama

10

1 reference

Europe PubMed Central

30 November 2017

Akira Nakagawara

11

1 reference

Europe PubMed Central

30 November 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 October 2002

1 reference

Europe PubMed Central

30 November 2017

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

30 November 2017

35

1 reference

Europe PubMed Central

30 November 2017

170-175

1 reference

Europe PubMed Central

30 November 2017

2

1 reference

Europe PubMed Central

30 November 2017

Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

21 January 2018

Identification of two distinct deleted regions on the short arm of chromosome 1 and rare mutation of the CDKN2C gene from 1p32 in oligodendroglial tumors.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

21 January 2018

Magnetic resonance imaging in temporal lobe epilepsy: usefulness for the etiological diagnosis of temporal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

21 January 2018

Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

21 January 2018

Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

7 January 2021

based on heuristic

inferred from DOI database lookup

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

7 January 2021

based on heuristic

inferred from DOI database lookup

There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10080

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.10080

1 reference

Europe PubMed Central

30 November 2017

1 reference

Europe PubMed Central

30 November 2017

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