Pages that link to "Q57419094"
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The following pages link to Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation (Q57419094):
Displaying 50 items.
- Transgenic rodent models of Parkinson’s disease (Q22252835) (← links)
- Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update (Q22252904) (← links)
- Mitochondrial dysfunction and loss of Parkinson's disease-linked proteins contribute to neurotoxicity of manganese-containing welding fumes (Q23916368) (← links)
- Parkinson disease protein DJ-1 binds metals and protects against metal-induced cytotoxicity (Q24296667) (← links)
- Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition (Q24300958) (← links)
- Parkinson disease protein DJ-1 converts from a zymogen to a protease by carboxyl-terminal cleavage (Q24304102) (← links)
- Oxidative status of DJ-1-dependent activation of dopamine synthesis through interaction of tyrosine hydroxylase and 4-dihydroxy-L-phenylalanine (L-DOPA) decarboxylase with DJ-1 (Q24309004) (← links)
- Sensitivity to oxidative stress in DJ-1-deficient dopamine neurons: an ES- derived cell model of primary Parkinsonism (Q24797276) (← links)
- Evolutionary and functional relationships within the DJ1 superfamily (Q24803493) (← links)
- Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease (Q28237811) (← links)
- Role of DJ-1 in Parkinson's disease (Q28272473) (← links)
- Gene-environment interactions: key to unraveling the mystery of Parkinson's disease (Q28388674) (← links)
- Age-dependent motor deficits and dopaminergic dysfunction in DJ-1 null mice (Q28507691) (← links)
- DJ-1 gene deletion reveals that DJ-1 is an atypical peroxiredoxin-like peroxidase (Q28513159) (← links)
- Structural effects of Parkinson's disease linked DJ-1 mutations. (Q30369057) (← links)
- Genetic mouse models of parkinsonism: strengths and limitations (Q30537732) (← links)
- Quantitative proteomic analysis of single pancreatic islets (Q33511709) (← links)
- DJ-1, PINK1, and their effects on mitochondrial pathways (Q33733264) (← links)
- DJ-1 deficient mice demonstrate similar vulnerability to pathogenic Ala53Thr human alpha-syn toxicity (Q33755817) (← links)
- Engineered disulfide bonds restore chaperone-like function of DJ-1 mutants linked to familial Parkinson's disease (Q34078603) (← links)
- Parkinson's disease: Exit toxins, enter genetics (Q34140428) (← links)
- Astrocytes and Therapeutics for Parkinson's Disease (Q34168266) (← links)
- Human DJ-1-specific Transcriptional Activation of Tyrosine Hydroxylase Gene (Q34400824) (← links)
- The genetics of Parkinson disease (Q34604083) (← links)
- Transgenic animal models of neurodegeneration based on human genetic studies. (Q34890228) (← links)
- Assessing causal relationships in genomics: From Bradford-Hill criteria to complex gene-environment interactions and directed acyclic graphs (Q35122574) (← links)
- Mutations in DJ-1 are rare in familial Parkinson disease (Q35231079) (← links)
- A DJ-1 Based Peptide Attenuates Dopaminergic Degeneration in Mice Models of Parkinson's Disease via Enhancing Nrf2. (Q35646201) (← links)
- Chasing genes in Alzheimer's and Parkinson's disease (Q35681844) (← links)
- Accelerated formation of alpha-synuclein oligomers by concerted action of the 20S proteasome and familial Parkinson mutations (Q35698432) (← links)
- Parkinson's Disease in Saudi Patients: A Genetic Study (Q35746162) (← links)
- A Physical Interaction between the Dopamine Transporter and DJ-1 Facilitates Increased Dopamine Reuptake (Q35754644) (← links)
- Absence of the Yeast Hsp31 Chaperones of the DJ-1 Superfamily Perturbs Cytoplasmic Protein Quality Control in Late Growth Phase (Q35806855) (← links)
- Genetic clues to the pathogenesis of Parkinson's disease (Q35844782) (← links)
- DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism (Q36022165) (← links)
- Neurodegenerative disorders: Parkinson's disease and Huntington's disease (Q36198011) (← links)
- Progressive dopaminergic cell loss with unilateral-to-bilateral progression in a genetic model of Parkinson disease (Q36300804) (← links)
- Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism (Q36424540) (← links)
- Recessive Parkinson's disease (Q36449306) (← links)
- Genetic findings in Parkinson's disease and translation into treatment: a leading role for mitochondria? (Q36499640) (← links)
- Octanoic acid in alcohol-responsive essential tremor: a randomized controlled study (Q36841527) (← links)
- Genetics of Parkinson disease (Q37037053) (← links)
- Progress in the pathogenesis and genetics of Parkinson's disease (Q37143657) (← links)
- Emerging pathways in genetic Parkinson's disease: autosomal-recessive genes in Parkinson's disease--a common pathway? (Q37330543) (← links)
- DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients. (Q37427193) (← links)
- A critical evaluation of the ubiquitin-proteasome system in Parkinson's disease (Q37472304) (← links)
- Genetic insights into sporadic Parkinson's disease pathogenesis (Q37583402) (← links)
- Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases (Q37775036) (← links)
- Milestones in PD genetics (Q37882589) (← links)
- Synaptic protein alterations in Parkinson's disease. (Q37972089) (← links)