Pages that link to "Q37904442"

The following pages link to Genetic mutations and functions of PINK1. (Q37904442):

Displaying 29 items.

• The Dual Function of Reactive Oxygen/Nitrogen Species in Bioenergetics and Cell Death: The Role of ATP Synthase (Q26749074) (← links)
• The role of free radicals in the aging brain and Parkinson's Disease: convergence and parallelism (Q26852148) (← links)
• Protein Kinases and Parkinson's Disease (Q28067636) (← links)
• A screen for selective killing of cells with chromosomal instability induced by a spindle checkpoint defect (Q28484384) (← links)
• PINK1 positively regulates HDAC3 to suppress dopaminergic neuronal cell death (Q28586619) (← links)
• A synopsis on the role of tyrosine hydroxylase in Parkinson's disease (Q28830946) (← links)
• Decreased approach behavior and nucleus accumbens immediate early gene expression in response to Parkinsonian ultrasonic vocalizations in rats. (Q30377972) (← links)
• Atp13a2 expression in the periaqueductal gray is decreased in the Pink1 -/- rat model of Parkinson disease. (Q30383670) (← links)
• Parkinson's disease-implicated kinases in the brain; insights into disease pathogenesis (Q33797449) (← links)
• The yeast retrograde response as a model of intracellular signaling of mitochondrial dysfunction (Q35966892) (← links)
• The emerging role of proteolysis in mitochondrial quality control and the etiology of Parkinson's disease (Q35986574) (← links)
• The Mitochondrial Permeability Transition Pore: Channel Formation by F-ATP Synthase, Integration in Signal Transduction, and Role in Pathophysiology. (Q36146320) (← links)
• Parkin, PINK1 and mitochondrial integrity: emerging concepts of mitochondrial dysfunction in Parkinson's disease (Q37953288) (← links)
• Oxidative stress in genetic mouse models of Parkinson's disease (Q38029327) (← links)
• Defective autophagy in Parkinson's disease: lessons from genetics (Q38225786) (← links)
• How mitochondrial dynamism orchestrates mitophagy (Q38497008) (← links)
• Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation. (Q38694964) (← links)
• Parkin and PINK1 functions in oxidative stress and neurodegeneration (Q39054548) (← links)
• The Role of Astrocyte Dysfunction in Parkinson's Disease Pathogenesis (Q39319763) (← links)
• A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism (Q41832278) (← links)
• Loss of PINK1 enhances neurodegeneration in a mouse model of Parkinson's disease triggered by mitochondrial stress. (Q41846921) (← links)
• Parkinson's Disease in a Dish: What Patient Specific-Reprogrammed Somatic Cells Can Tell Us about Parkinson's Disease, If Anything? (Q42562656) (← links)
• Characterization of early-onset motor deficits in the Pink1-/- mouse model of Parkinson disease (Q47327885) (← links)
• Genetics and epigenetics of Parkinson's disease. (Q53375184) (← links)
• [PINK1 and the related diseases]. (Q54381681) (← links)
• The changes of mitochondria in substantia nigra and anterior cerebral cortex of hepatic encephalopathy induced by thioacetamide (Q56978185) (← links)
• The Role of TMEM230 Gene in Parkinson's Disease (Q58726908) (← links)
• Early-onset Parkinsonian behaviors in female Pink1-/- rats (Q90201807) (← links)
• A refinement to the formalin test in mice (Q93135958) (← links)