Pages that link to "Q21115193"

The following pages link to ATPase cation transporting 13A2 (Q21115193):

Displaying 25 items.

• ATP13A2 (Q18037150) (← links)
• Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism (Q24301367) (← links)
• The role of oxidative stress in Parkinson's disease (Q24307946) (← links)
• Interaction of divalent cations with peptide fragments from Parkinson's disease genes (Q27930795) (← links)
• Parkinson's disease-linked human PARK9/ATP13A2 maintains zinc homeostasis and promotes α-Synuclein externalization via exosomes (Q27932080) (← links)
• Mn(II) and Zn(II) interactions with peptide fragments from Parkinson's disease genes (Q27932738) (← links)
• A lipid switch unlocks Parkinson's disease-associated ATP13A2 (Q28115404) (← links)
• Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove (Q28115428) (← links)
• Parkinson's disease-associated human P5B-ATPase ATP13A2 increases spermidine uptake (Q28115696) (← links)
• Zn²⁺ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation (Q28116171) (← links)
• ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy (Q28116203) (← links)
• ATP13A2 regulates mitochondrial bioenergetics through macroautophagy (Q28116275) (← links)
• Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase (Q28116395) (← links)
• PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity (Q28117134) (← links)
• Regulation of ATP13A2 via PHD2-HIF1α Signaling Is Critical for Cellular Iron Homeostasis: Implications for Parkinson's Disease (Q28118364) (← links)
• ATP13A2/PARK9 regulates secretion of exosomes and α-synuclein (Q28118666) (← links)
• ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese (Q28118761) (← links)
• Unlocking ATP13A2/PARK9 activity (Q28118908) (← links)
• ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons (Q28119120) (← links)
• The Parkinson's disease-associated genes ATP13A2 and SYT11 regulate autophagy via a common pathway (Q42576627) (← links)
• ATP13A2 transports cations from cytosol to lysosomal lumen (Q50299651) (← links)
• Modeling Parkinson's Disease in C. elegans (Q51767278) (← links)
• The Parkinson-associated human P5B-ATPase ATP13A2 modifies lipid homeostasis (Q64764741) (← links)
• ATP13A2 facilitates HDAC6 recruitment to lysosome to promote autophagosome-lysosome fusion (Q90411150) (← links)
• ATP13A2 deficiency disrupts lysosomal polyamine export (Q93040411) (← links)