An unusual loss of EGFR gene copy in glioblastoma multiforme in a child: a case report and analysis of a successfully derived HGG-02 cell line
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F10%3A00040768" target="_blank" >RIV/00216224:14310/10:00040768 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
An unusual loss of EGFR gene copy in glioblastoma multiforme in a child: a case report and analysis of a successfully derived HGG-02 cell line
Original language description
This study report on a case of glioblastoma multiforme with a polyploid karyotype including a very unusual genetic change - the loss of a copy of the EGFR gene at locus 7p11.2 (EGFR gene) - diagnosed in a 14.5-year-old boy. To date, this patient has survived event-free for 34 months. A detailed analysis of the HGG-02 cell line, which was derived from this primary tumor, was also performed.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
<a href="/en/project/NR9125" target="_blank" >NR9125: Importance of molecular cytogenetic markers for diagnosis and prediction of embryonal childhood tumors.</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Child's Nervous System
ISSN
0256-7040
e-ISSN
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Volume of the periodical
26
Issue of the periodical within the volume
6
Country of publishing house
DE - GERMANY
Number of pages
6
Pages from-to
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UT code for WoS article
000277595300022
EID of the result in the Scopus database
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