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Journal of Biological Chemistry, ISSN 0021-9258, 05/2012, Volume 287, Issue 19, pp. 15345 - 15364
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 08/2014, Volume 289, Issue 32, pp. 21856 - 21876
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 17, pp. 4491 - 4509
A novel mutation in the alpha-Synuclein (alpha-Syn) gene "G51D" was recently identified in two familial cases exhibiting features of Parkinson's disease (PD)... 
WILD-TYPE | INCLUSION FORMATION | OXIDATIVE STRESS | HUMAN PLASMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | RAT-BRAIN NEURONS | MONOCLONAL-ANTIBODY | SOLUTION NMR-SPECTROSCOPY | PULSED ESR MEASUREMENTS | TRANSGENIC MICE | PHOSPHOLIPID-BINDING | Neurons - pathology | Humans | alpha-Synuclein - ultrastructure | Saccharomyces cerevisiae - drug effects | Protein Transport - drug effects | Brain - metabolism | Saccharomyces cerevisiae - metabolism | Cell Nucleus - metabolism | Protein Binding - drug effects | Sodium Dodecyl Sulfate - pharmacology | Cell Membrane - metabolism | Neurons - metabolism | alpha-Synuclein - genetics | Phosphorylation - drug effects | Buffers | Inclusion Bodies - metabolism | Neurons - drug effects | Protein Aggregation, Pathological - genetics | Cell Membrane - drug effects | Neuroblastoma - pathology | Protein Aggregates - drug effects | Cell Line | Parkinson Disease - pathology | Protein Structure, Secondary | Subcellular Fractions - drug effects | Cells, Cultured | Inclusion Bodies - drug effects | Mitochondria - metabolism | alpha-Synuclein - secretion | Mitochondria - drug effects | Parkinson Disease - genetics | Mutation - genetics | Subcellular Fractions - metabolism | alpha-Synuclein - chemistry | Brain - drug effects | Unilamellar Liposomes - metabolism | Nuclear Envelope - metabolism | Nuclear Envelope - drug effects | Cell Differentiation - drug effects | Brain - pathology | Cell Nucleus - drug effects | Index Medicus
Journal Article
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 08/2014, Volume 289, Issue 32, pp. 21856 - 21876
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2010, Volume 285, Issue 4, pp. 2807 - 2822
Phosphorylation of α-synuclein (α-syn) at Ser-129 is a hallmark of Parkinson disease and related synucleinopathies. However, the identity of the natural... 
INCLUSION FORMATION | NERVOUS-SYSTEM | HUMAN ALPHA-SYNUCLEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-PROLIFERATION | PROTEIN-SERINE/THREONINE KINASE | DROSOPHILA-POLO | SYNAPTIC PLASTICITY | RAT MODEL | PARKINSONS-DISEASE | TRANSGENIC MICE | Phosphorylation - physiology | Humans | Molecular Sequence Data | Cytoplasm - metabolism | Neurons - cytology | Cell Nucleus - metabolism | Transfection | Intermediate Filament Proteins - genetics | Cell Cycle Proteins - genetics | Nuclear Magnetic Resonance, Biomolecular | Cell Membrane - metabolism | Parkinson Disease - metabolism | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Protein-Serine-Threonine Kinases - metabolism | Proto-Oncogene Proteins - metabolism | Amino Acid Sequence | Cell Line | Cell Cycle Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Mice, Transgenic | Proto-Oncogene Proteins - genetics | Kidney - cytology | beta-Synuclein - genetics | Animals | Neurons - enzymology | Alzheimer Disease - metabolism | Mice | RNA, Small Interfering | beta-Synuclein - metabolism | Intermediate Filament Proteins - metabolism | Neurochemistry | Nucleus | Fractionation | Phosphorylation | RNAi | RNA | Neurobiology | Kinases | Protein | Diseases | Neuroscience | Protein Synthesis, Post-Translational Modification, and Degradation | Serine-Threonine | Amyloid | Structure | Cell
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 770 - 776
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, p. 770
  Cone-rod degeneration (CRD) belongs to the disease spectrum of retinal degenerations, a group of hereditary disorders characterized by an extreme clinical... 
Deafness | Genetic disorders | Eye diseases | Mutation | Cells
Journal Article
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