Involvement of the mitochondrial compartment in human NCL fibroblasts.
about
An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1 mutation.Proteomic Profiling in the Brain of CLN1 Disease Model Reveals Affected Functional Modules.Different molecular mechanisms involved in spontaneous and oxidative stress-induced mitochondrial fragmentation in tripeptidyl peptidase-1 (TPP-1)-deficient fibroblasts.P-glycoprotein mediates drug resistance via a novel mechanism involving lysosomal sequestration.Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrum.Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).Decreased sensitivity of palmitoyl protein thioesterase 1-deficient neurons to chemical anoxia.
P2860
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P2860
Involvement of the mitochondrial compartment in human NCL fibroblasts.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@en
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@nl
type
label
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@en
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@nl
prefLabel
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@en
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@nl
P2093
P1476
Involvement of the mitochondrial compartment in human NCL fibroblasts.
@en
P2093
Alessandra Tessa
Alessandro Simonati
Filippo M Santorelli
Floriana Gismondi
Francesco Pezzini
Paola Tonin
P304
P356
10.1016/J.BBRC.2011.11.016
P407
P577
2011-11-11T00:00:00Z