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Possible role of mitochondrial permeability transition pore in the pathogenesis of Huntington disease
Fecha de emisión
2017
Autor(es)
Quintanilla R.A.
Tapia C.
Pérez M.J.
DOI
10.1016/j.bbrc.2016.09.054
Temas
Calcium
Huntington disease
Mitochondria
Mitochondrial permeab...
Oxidative stress
calcium
huntingtin
lead
mitochondrial permeab...
carrier protein
HTT protein, human
huntingtin
mitochondrial permeab...
bioenergy
brain dysfunction
brain function
clinical feature
human
Huntington chorea
mitochondrial respira...
neuropathology
neurotoxicity
nonhuman
priority journal
Review
genetics
Huntington chorea
pathology
pathophysiology
physiology
Humans
Huntingtin Protein
Huntington Disease
Mitochondrial Membran...
Archivo(s)