Cargando…
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...
Autores principales: | Kim, Doeun, Lee, Yu-Ri, Choi, Tae-Ik, Kim, Se-Hee, Kang, Hoon-Chul, Kim, Cheol-Hee, Lee, Sangkyu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962458/ https://www.ncbi.nlm.nih.gov/pubmed/33800130 http://dx.doi.org/10.3390/ijms22052707 |
Ejemplares similares
-
Zebrafish as an animal model for biomedical research
por: Choi, Tae-Young, et al.
Publicado: (2021) -
Regional vulnerability of brain white matter in vanishing white matter
por: Man, Jodie H.K., et al.
Publicado: (2023) -
Diabetic ketoacidosis in vanishing white matter
por: Alamri, Hannadi, et al.
Publicado: (2016) -
Axonal abnormalities in vanishing white matter
por: Klok, Melanie D., et al.
Publicado: (2018) -
Natural History of Vanishing White Matter
por: Hamilton, Eline M. C., et al.
Publicado: (2018)