Lysosomal function in macromolecular homeostasis and bioenergetics in Parkinson's disease.
about
Autophagy, mitochondria and oxidative stress: cross-talk and redox signallingGenetically engineered mouse models of Parkinson's diseaseThe Fab1/PIKfyve phosphoinositide phosphate kinase is not necessary to maintain the pH of lysosomes and of the yeast vacuole.The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson diseaseGenetic variation in neurodegenerative diseases and its accessibility in the model organism Caenorhabditis elegans.BAG3 expression in glioblastoma cells promotes accumulation of ubiquitinated clients in an Hsp70-dependent manner.Systems biology of the autophagy-lysosomal pathway.Loss of leucine-rich repeat kinase 2 causes age-dependent bi-phasic alterations of the autophagy pathwayCln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disordersDiscerning the Chemistry in Individual Organelles with Small-Molecule Fluorescent Probes.Tet3 Reads 5-Carboxylcytosine through Its CXXC Domain and Is a Potential Guardian against NeurodegenerationActivator of G-Protein Signaling 3-Induced Lysosomal Biogenesis Limits Macrophage Intracellular Bacterial Infection.Beyond ubiquitination: the atypical functions of Fbxo7 and other F-box proteins.Over-expression of an inactive mutant cathepsin D increases endogenous alpha-synuclein and cathepsin B activity in SH-SY5Y cells.Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond.Reduction of mutant huntingtin accumulation and toxicity by lysosomal cathepsins D and B in neurons.Membrane lipids as therapeutic targets for Parkinson's disease: a possible link between Lewy pathology and membrane lipids.Mild MPP+ exposure impairs autophagic degradation through a novel lysosomal acidity-independent mechanism.The Underexploited Role of Non-Coding RNAs in Lysosomal Storage Diseases.Is trehalose an autophagic inducer? Unraveling the roles of non-reducing disaccharides on autophagic flux and alpha-synuclein aggregation.Mitochondrial function and autophagy: integrating proteotoxic, redox, and metabolic stress in Parkinson's disease.Haplodeficiency of Cathepsin D does not affect cerebral amyloidosis and autophagy in APP/PS1 transgenic mice.Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways.Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations.SIRT3 Protects Rotenone-induced Injury in SH-SY5Y Cells by Promoting Autophagy through the LKB1-AMPK-mTOR Pathway.
P2860
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P2860
Lysosomal function in macromolecular homeostasis and bioenergetics in Parkinson's disease.
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Lysosomal function in macromol ...... getics in Parkinson's disease.
@en
type
label
Lysosomal function in macromol ...... getics in Parkinson's disease.
@en
prefLabel
Lysosomal function in macromol ...... getics in Parkinson's disease.
@en
P2860
P356
P1476
Lysosomal function in macromol ...... getics in Parkinson's disease.
@en
P2093
Jianhua Zhang
Lonnie Schneider
P2860
P2888
P356
10.1186/1750-1326-5-14
P577
2010-04-13T00:00:00Z
P5875
P6179
1022009143