VESELSKÁ, Renata, Jan ŠKODA, Tomáš LOJA, Karel ZITTERBART, Zdeněk PAVELKA, Jana ŠMARDOVÁ, Iveta VALÁŠKOVÁ, Markéta HERMANOVÁ and Jaroslav ŠTĚRBA. 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. Child's Nervous System. Berlin / Heidelberg: Springer, 2010, vol. 26, No 6, p. 841-846. ISSN 0256-7040.
Other formats:   BibTeX LaTeX RIS
Basic information
Original 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
Authors VESELSKÁ, Renata (203 Czech Republic, guarantor, belonging to the institution), Jan ŠKODA (203 Czech Republic, belonging to the institution), Tomáš LOJA (703 Slovakia, belonging to the institution), Karel ZITTERBART (203 Czech Republic, belonging to the institution), Zdeněk PAVELKA (203 Czech Republic, belonging to the institution), Jana ŠMARDOVÁ (203 Czech Republic, belonging to the institution), Iveta VALÁŠKOVÁ (203 Czech Republic, belonging to the institution), Markéta HERMANOVÁ (203 Czech Republic, belonging to the institution) and Jaroslav ŠTĚRBA (203 Czech Republic, belonging to the institution).
Edition Child's Nervous System, Berlin / Heidelberg, Springer, 2010, 0256-7040.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.314
RIV identification code RIV/00216224:14310/10:00040768
Organization unit Faculty of Science
UT WoS 000277595300022
Keywords in English glioblastoma multiforme; EGFR ; p53; FISH; FASAY; karyotyping
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Renata Veselská, Ph.D., M.Sc., učo 1260. Changed: 24/1/2011 09:59.
Abstract
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.
Abstract (in Czech)
Tato studie popisuje případ multiformního glioblastomu s polyploidním karyotypem včetně velmi neobvyklé genetické aberace - ztráty kopie genu EGFR v lokusu 7p11.2; tento nádor byl diagnostikován u chlapce ve věku 14,5 roku. K datu odeslání publikace tento pacient žije bez příznaků nemoci 34 měsíců od diagnozy. Byla rovněž provedena detailní analýza buněčné linie HGG-02, která byla derivována z tohoto primárního nádoru.
Links
NR9125, research and development projectName: Diagnostický a prediktivní význam molekulárně cytogenetických markerů u embryonálních nádorů dětského věku.
Investor: Ministry of Health of the CR
PrintDisplayed: 19/9/2024 01:07