Pages that link to "Q24680250"
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The following pages link to Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27 (Q24680250):
Displaying 50 items.
- The genetic epidemiology of neurodegenerative disease (Q22306301) (← links)
- Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36 (Q24536382) (← links)
- Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study (Q24539105) (← links)
- Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease (Q24656075) (← links)
- A Mechanistic Review of Mitophagy and Its Role in Protection against Alcoholic Liver Disease (Q26778940) (← links)
- Pathologic and therapeutic implications for the cell biology of parkin (Q27010567) (← links)
- Targeting Pink1-Parkin-mediated mitophagy for treating liver injury (Q28082937) (← links)
- Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease (Q28280353) (← links)
- The aetiology of idiopathic Parkinson's disease (Q28365451) (← links)
- Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease (Q28764371) (← links)
- Neuronal Mitophagy in Neurodegenerative Diseases (Q29248361) (← links)
- The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity. (Q30357944) (← links)
- Parkin disease: a clinicopathologic entity? (Q30594306) (← links)
- Cul4B regulates neural progenitor cell growth (Q31095156) (← links)
- Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism (Q33393439) (← links)
- Increasing the Coding Potential of Genomes Through Alternative Splicing: The Case of PARK2 Gene. (Q33782133) (← links)
- Alternative splicing generates different parkin protein isoforms: evidences in human, rat, and mouse brain. (Q34014415) (← links)
- Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region (Q34386289) (← links)
- Identification of biomarkers of human skin ageing in both genders. Wnt signalling - a label of skin ageing? (Q34505325) (← links)
- Acetaminophen from liver to brain: New insights into drug pharmacological action and toxicity (Q34516005) (← links)
- PARK2 mediates interleukin 6 and monocyte chemoattractant protein 1 production by human macrophages (Q34563658) (← links)
- The genetics of Parkinson disease (Q34604083) (← links)
- The genetic basis of Parkinson's disease (Q34863976) (← links)
- Metabolomics and in-silico analysis reveal critical energy deregulations in animal models of Parkinson's disease (Q34919307) (← links)
- Rare genetic mutations shed light on the pathogenesis of Parkinson disease (Q35047289) (← links)
- Chasing genes in Alzheimer's and Parkinson's disease (Q35681844) (← links)
- Unfolded protein stress in the endoplasmic reticulum and mitochondria: a role in neurodegeneration (Q35911798) (← links)
- Splicing: is there an alternative contribution to Parkinson's disease? (Q36069844) (← links)
- The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane (Q36100136) (← links)
- Regulation of RNF144A E3 Ubiquitin Ligase Activity by Self-association through Its Transmembrane Domain (Q36281694) (← links)
- The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease (Q36611426) (← links)
- α-Synuclein oligomers and clinical implications for Parkinson disease (Q36718306) (← links)
- Genome-wide analysis of copy number variants in age-related macular degeneration (Q36732124) (← links)
- Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease (Q37027318) (← links)
- Progress in the pathogenesis and genetics of Parkinson's disease (Q37143657) (← links)
- Targeting the progression of Parkinson's disease. (Q37299619) (← links)
- Association of regions on chromosomes 6 and 7 with blood pressure in Nigerian families (Q37347621) (← links)
- Priorities in Parkinson's disease research (Q37870670) (← links)
- Kynurenines in Parkinson's disease: therapeutic perspectives. (Q37920750) (← links)
- The neuropathology of genetic Parkinson's disease (Q37997386) (← links)
- The role of central nervous system development in late-onset neurodegenerative disorders (Q38008841) (← links)
- Genetic basis of Parkinson's disease: inheritance, penetrance, and expression (Q38115298) (← links)
- RBR E3-ligases at work (Q38182404) (← links)
- Reduced expression of PARK2 in manganese-exposed smelting workers (Q38615741) (← links)
- The Effects of Variants in the Parkin, PINK1, and DJ-1 Genes along with Evidence for their Pathogenicity (Q38769351) (← links)
- Twenty years since the discovery of the parkin gene (Q39377582) (← links)
- Neuroprotective therapy in Parkinson's disease: current status and new directions from experimental and genetic clues (Q40027470) (← links)
- Parkinson's disease candidate gene prioritization based on expression profile of midbrain dopaminergic neurons (Q41764118) (← links)
- Merging mouse transcriptome analyses with Parkinson's disease linkage studies (Q41902132) (← links)
- Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease (Q41954719) (← links)