Comparative Proteome Research in a Zebrafish Model for Vanishing White Matter Disease

Vanishing white matter (VWM) disease is a genetic leukodystrophy leading to severe neurological disease and early death. VWM is caused by bi-allelic mutations in any of the five genes encoding the subunits of the eukaryotic translation factor 2B (EIF2B). Previous studies have attempted to investigat...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	International journal of molecular sciences 2021-03, Vol.22 (5), p.2707
Hauptverfasser:	Kim, Doeun, Lee, Yu-Ri, Choi, Tae-Ik, Kim, Se-Hee, Kang, Hoon-Chul, Kim, Cheol-Hee, Lee, Sangkyu
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Transport System ASC - genetics Amino Acid Transport System ASC - metabolism Animals Animals, Genetically Modified Disease Models, Animal Eukaryotic Initiation Factor-2B - deficiency Eukaryotic Initiation Factor-2B - metabolism Humans Leukoencephalopathies - genetics Leukoencephalopathies - metabolism Leukoencephalopathies - pathology Proteome - genetics Proteome - metabolism Proteomics Zebrafish - genetics Zebrafish - metabolism Zebrafish Proteins - genetics Zebrafish Proteins - metabolism
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!