PCR- and restriction endonuclease-based detection of IDH1 mutations

Hotspot mutations in codon 132 of the gene encoding isocitrate dehydrogenase 1 (IDH1) have emerged as the most frequent DNA alteration in astrocytomas, oligodendrogliomas and oligoastrocytomas. These mutations have been shown to be of significant diagnostic and prognostic value. So far, assessment o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Meyer, Jochen (VerfasserIn) , Pusch, Stefan (VerfasserIn) , Balß, Jörg (VerfasserIn) , Capper, David (VerfasserIn) , Müller, Wolf C. (VerfasserIn) , Christians, Arne (VerfasserIn) , Hartmann, Christian (VerfasserIn) , Deimling, Andreas von (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 02 February 2010
In: Brain pathology
Year: 2010, Jahrgang: 20, Heft: 2, Pages: 298-300
ISSN:1750-3639
DOI:10.1111/j.1750-3639.2009.00327.x
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1111/j.1750-3639.2009.00327.x
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1750-3639.2009.00327.x
Volltext
Verfasserangaben:Jochen Meyer; Stefan Pusch; Jörg Balss; David Capper; Wolf Mueller; Arne Christians; Christian Hartmann; Andreas Von Deimling
Beschreibung
Zusammenfassung:Hotspot mutations in codon 132 of the gene encoding isocitrate dehydrogenase 1 (IDH1) have emerged as the most frequent DNA alteration in astrocytomas, oligodendrogliomas and oligoastrocytomas. These mutations have been shown to be of significant diagnostic and prognostic value. So far, assessment of IDH1 mutation relied on DNA sequencing techniques. We generated a set of primers suitable for endonuclease-based detection of hotspot mutations in codon 132 of IDH1. This primer set will allow determining these mutations without the need of DNA sequencing. One set of primer sets is designed to detect the presence or absence of IDH1 mutations in codon 132, while the other primer sets individually recognize the R132H, R132C, R132S, R132G and R132L mutations.
Beschreibung:Gesehen am 20.04.2023
Beschreibung:Online Resource
ISSN:1750-3639
DOI:10.1111/j.1750-3639.2009.00327.x