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Frontiers in Genetics, ISSN 1664-8021, 03/2019, Volume 10
Alzheimer’s disease (AD) is a progressive and devastating neurodegenerative disorder. It is the leading cause of dementia in the world’s rapidly growing aging... 
microRNAs | pathological process | Alzheimer’s disease | neurofibrillary tangles | amyloid plaques
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 7/2019, Volume 56, Issue 7, pp. 5157 - 5166
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2016, Volume 48, Issue 7, pp. 733 - 739
Journal Article
Frontiers in Molecular Neuroscience, ISSN 1662-5099, 10/2017, Volume 10
Being the most common cause of dementia, AD is a polygenic and neurodegenerative disease. Complex and multiple factors have been shown to be involved in its... 
GWASs | Genetics | Alzheimer’s disease | LOAD | EOAD | Mechanism | genetics | mechanism
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2017, Volume 37, Issue 38, pp. 9101 - 9115
Journal Article
Neurological Sciences, ISSN 1590-1874, 9/2019, Volume 40, Issue 9, pp. 1927 - 1931
Parkinson’s disease (PD) is a common neurodegenerative disorder with multiple factors contributing to disease pathogenesis. Previous studies implicated the... 
Neurology | Medicine & Public Health | Neurosurgery | Psychiatry | HIF1A | Molecular inversion probes | Neuroradiology | Parkinson’s disease | rs11549465 | Parkinson's disease | Next-generation sequencing | Neurodegenerative diseases | Pathogenesis | Gene regulation | Genetic analysis | Inversion | Hypoxia | Minority & ethnic groups | Movement disorders
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 11/2016, Volume 53, Issue 9, pp. 5876 - 5892
Recent evidence suggests that nerve growth factor IB (Nur77) and nuclear receptor related1 (Nurr1) are differentially involved in dopaminergic... 
Neuroprotection | Neurology | Neurosciences | Biomedicine | Memantine | Neurobiology | Nurr1 | Nur77 | Inflammation | Parkinson’s disease | Cell Biology | OXIDATIVE STRESS | Parkinson's disease | DOPAMINERGIC-NEURONS | ALPHA-SYNUCLEIN | NEUROSCIENCES | CELL-DEATH | MITOCHONDRIAL TRANSLOCATION | IN-VITRO | GENE-EXPRESSION | NR4A NUCLEAR RECEPTORS | TRANSCRIPTION FACTOR | PARKINSONS-DISEASE | L-Lactate Dehydrogenase - metabolism | Tumor Necrosis Factor-alpha - metabolism | Dopamine Plasma Membrane Transport Proteins - metabolism | Inflammation - pathology | Tyrosine 3-Monooxygenase - metabolism | Oxidopamine | PC12 Cells | Nerve Degeneration - metabolism | Neuroprotection - drug effects | Gene Knockdown Techniques | Inflammation - metabolism | Interleukin-6 - metabolism | Cell Survival - drug effects | Memantine - pharmacology | Cytochromes c - metabolism | Rats | Mitochondria - metabolism | Mitochondria - drug effects | Subcellular Fractions - metabolism | Nerve Degeneration - pathology | Animals | MAP Kinase Signaling System - drug effects | Nuclear Receptor Subfamily 4, Group A, Member 1 - metabolism | Glutamic Acid - metabolism | Nuclear Receptor Subfamily 4, Group A, Member 2 - metabolism | Post-translational modification | Analysis | Nerve growth factor | Nervous system agents | Alzheimer's disease | Alzheimers disease | Neurodegeneration | Parkinsons disease | Index Medicus
Journal Article
Calcified Tissue International, ISSN 0171-967X, 8/2019, Volume 105, Issue 2, pp. 183 - 192
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, pp. e54792 - e54792
Spinocerebellar ataxia type 3 (SCA3) also known as Machado-Joseph Disease (MJD), is one of nine polyglutamine (polyQ) diseases caused by a CAG-trinucelotide... 
GLYCOGEN-SYNTHASE KINASE-3-BETA | EXPANDED POLYGLUTAMINE | CREB-BINDING PROTEIN | DROSOPHILA-MELANOGASTER | MULTIDISCIPLINARY SCIENCES | MACHADO-JOSEPH-DISEASE | MOUSE MODEL | GENE-EXPRESSION | ALTERED TRANSCRIPTION | ATAXIA TYPE-I | DEACETYLASE INHIBITION | Eye - pathology | Apoptosis - drug effects | Machado-Joseph Disease - metabolism | Humans | Peptides - genetics | Valproic Acid - pharmacology | DNA Repeat Expansion | Peptides - metabolism | Pigmentation - genetics | Life Expectancy | Protein Binding - drug effects | Female | Eye - drug effects | Eye - metabolism | Pigmentation - drug effects | Eye - ultrastructure | Animals, Genetically Modified | Drosophila | Cells, Cultured | Acetylation - drug effects | Phenotype | Animals | Histone Deacetylase Inhibitors - pharmacology | Histones - metabolism | Mutation | Proteins | Medical research | Divalproex | Medicine, Experimental | Genetic engineering | Valproic acid | Health aspects | Apoptosis | Cell culture | Histone deacetylase | Chromatin | Transcription | Medical services | Clinical trials | Transgenic | Kinases | Eye | Ataxin | Neurodegeneration | Coding | Rodents | Ataxia | Acetylation | Trinucleotide repeat diseases | Medical treatment | Trinucleotide repeats | Pharmacology | Polyglutamine diseases | Chemical compounds | Diseases | Histone H4 | Machado-Joseph disease | Inhibitors | Life span | Sodium | Sodium valproate | Histone H3 | Index Medicus
Journal Article