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PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, pp. e9313 - e9313
Background: Lewy body disease is a heterogeneous group of neurodegenerative disorders characterized by alpha-synuclein accumulation that includes dementia with... 
WILD-TYPE | CHAPERONE-MEDIATED AUTOPHAGY | ALZHEIMERS-DISEASE | MOUSE MODEL | FRONTOTEMPORAL DEMENTIA | BIOLOGY | AGGREGATE-PRONE PROTEINS | NEURONAL EXPRESSION | PARKINSONS-DISEASE | TRANSGENIC MICE | GAUCHER-DISEASE | Pyramidal Cells - metabolism | Humans | Nerve Degeneration - genetics | Male | Autophagy | Nerve Degeneration - metabolism | Alzheimer Disease - pathology | Brain - metabolism | Lewy Body Disease - genetics | RNA Interference | Brain - ultrastructure | Aged, 80 and over | Female | alpha-Synuclein - genetics | Pyramidal Cells - ultrastructure | Disease Models, Animal | Cell Line | Ubiquitin-Activating Enzymes - genetics | Signal Transduction | Lewy Body Disease - pathology | Mice, Transgenic | Microscopy, Electron | Ubiquitin-Activating Enzymes - metabolism | Blotting, Western | Nerve Degeneration - pathology | Lewy Body Disease - metabolism | Microscopy, Confocal | Autophagy-Related Protein 7 | Animals | Alzheimer Disease - metabolism | Brain - pathology | Cell Line, Tumor | Pyramidal Cells - pathology | Aged | Mice | Alzheimer Disease - genetics | alpha-Synuclein - metabolism | TOR protein | Neurosciences | Animal models | Parkinson's disease | Pathogenesis | Toxicity | Parkinsons disease | Phagosomes | Nervous system | Synuclein | Neuromodulation | Accumulation | Modulators | Proteins | Infusion | Alterations | Neurodegeneration | Dementia disorders | Alzheimer's disease | Movement disorders | Enzymes | Neurodegenerative diseases | Neurons | Immunomodulation | Lewy body disease | Transgenic mice | Rapamycin | Patients | Lewy bodies | Studies | Pathology | Mutation | Alzheimers disease | Phagocytosis | Apoptosis | Dementia | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2013, Volume 110, Issue 3, pp. 1041 - 1046
The molecular etiology of human progenitor reprogramming into self-renewing leukemia stem cells (LSC) has remained elusive. Although DNA sequencing has... 
Protein isoforms | Up regulation | RNA editing | Cord blood | Genes | Leukemia | Stem cells | Chronic myeloid leukemia | Progenitor cells | Cells | CHRONIC MYELOGENOUS LEUKEMIA | ADENOSINE-DEAMINASE | CML | MESSENGER-RNA | GENE | MULTIDISCIPLINARY SCIENCES | HEMATOPOIETIC STEM-CELLS | IMATINIB | HUMAN TRANSCRIPTOME | ACCURATE IDENTIFICATION | EDITING SITES | Alternative Splicing | Adenosine Deaminase - metabolism | RNA Editing | Humans | Leukemia, Myeloid, Chronic-Phase - pathology | Transcriptome | Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics | Glycogen Synthase Kinase 3 beta | Transplantation, Heterologous | RNA-Binding Proteins | Gene Knockdown Techniques | Neoplastic Stem Cells - metabolism | Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology | Inflammation Mediators - metabolism | Neoplastic Stem Cells - pathology | Leukemia, Myeloid, Chronic-Phase - metabolism | Tumor Stem Cell Assay | Blast Crisis - pathology | Adenosine Deaminase - genetics | Blast Crisis - etiology | Glycogen Synthase Kinase 3 - metabolism | Disease Progression | Fusion Proteins, bcr-abl - genetics | Animals | Glycogen Synthase Kinase 3 - genetics | Cell Transformation, Neoplastic | Leukemia, Myelogenous, Chronic, BCR-ABL Positive - metabolism | Blast Crisis - genetics | Mice | Blast Crisis - metabolism | Fusion Proteins, bcr-abl - metabolism | Leukemia, Myeloid, Chronic-Phase - genetics | Physiological aspects | Nuclear reprogramming | Research | Adenosine deaminase | Health aspects | Enzymes | Mutation | Gene expression | Ribonucleic acid--RNA | Index Medicus | Biological Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 4, pp. e19338 - e19338
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1922 - 10
Journal Article
Nature Neuroscience, ISSN 1097-6256, 10/2005, Volume 8, Issue 10, pp. 1343 - 1349
In Alzheimer disease, increased beta-secretase (BACE1) activity has been associated with neurodegeneration and accumulation of amyloid precursor protein (APP)... 
RNA INTERFERENCE | CLEAVING ENZYME | BETA-SECRETASE ACTIVITY | CARBOXYL-TERMINAL FRAGMENT | IN-VIVO | LENTIVIRAL VECTOR | MICE | AMYLOID PRECURSOR PROTEIN | EXPRESSION | NEUROSCIENCES | BRAIN | Microtubule-Associated Proteins - metabolism | Humans | Lentivirus - physiology | Brain - virology | Molecular Sequence Data | Glial Fibrillary Acidic Protein - metabolism | Alzheimer Disease - pathology | Brain - metabolism | Endopeptidases - chemistry | Time Factors | Aspartic Acid Endopeptidases | Amyloid Precursor Protein Secretases | Amyloid beta-Protein Precursor - metabolism | Cloning, Molecular | Spatial Behavior - drug effects | Disease Models, Animal | Cell Line | Endopeptidases - metabolism | Maze Learning - physiology | Alzheimer Disease - drug therapy | Gene Expression Regulation - physiology | Mice, Transgenic | Maze Learning - drug effects | Brain - drug effects | Gene Expression Regulation - drug effects | Immunohistochemistry - methods | Amyloid beta-Protein Precursor - genetics | Animals | Endopeptidases - genetics | Analysis of Variance | RNA, Small Interfering - therapeutic use | Alzheimer Disease - metabolism | Brain - pathology | Genetic Vectors - physiology | Mice | Alzheimer Disease - genetics | Neurons | Physiological aspects | Genetic aspects | Diagnosis | Research | Gene expression | Alzheimer's disease | Risk factors | Index Medicus
Journal Article
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 03/2009, Volume 108, Issue 6, pp. 1561 - 1574
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2008, Volume 3, Issue 9, pp. e3135 - e3135
Background: Misfolding and pathological aggregation of neuronal proteins has been proposed to play a critical role in the pathogenesis of neurodegenerative... 
IN-VITRO | LIPID RAFTS | BIOLOGY | A-BETA | AMYLOID-BETA-PROTEIN | PRECURSOR PROTEIN | ION CHANNELS | LEWY-BODY-DISEASE | MOLECULAR-DYNAMICS SIMULATION | PROTOFIBRILLAR ALPHA-SYNUCLEIN | TRANSGENIC MICE | Protein Structure, Tertiary | Humans | Mice, Transgenic | Parkinson Disease - genetics | Calcium - chemistry | Protein Folding | alpha-Synuclein - chemistry | Brain - metabolism | Lewy Body Disease - metabolism | Animals | Electrophysiology - methods | Computer Simulation | Alzheimer Disease - metabolism | Protein Denaturation | Mice | Parkinson Disease - metabolism | Alzheimer Disease - genetics | Proteins | Oligomers | Advertising executives | Genetic engineering | Alzheimer's disease | Analysis | Brain | Neurosciences | Parkinson's disease | Calcium | Pathogenesis | Parkinsons disease | Disorders | Agglomeration | Synuclein | Accumulation | Calcium influx | Monomers | Consortia | Neurodegeneration | Protein folding | Aging | Biocompatibility | Amyloid | Modelling | Movement disorders | Computer simulation | Neurodegenerative diseases | Lewy body disease | Hexamers | Transgenic mice | Forming | Trimers | C-Terminus | Lewy bodies | Neurological diseases | Pathology | Molecular modelling | N-Terminus | In vivo methods and tests | Dimers | Computer centers | Porosity | Gene therapy | Alzheimers disease | Dementia | Index Medicus
Journal Article