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American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 11/2011, Volume 301, Issue 5, pp. H1924 - H1931
Lee Y, Lee HY, Hanna RA, Gustafsson angstrom B. Mitochondrial autophagy by Bnip3 involves Drp1-mediated mitochondrial fission and recruitment of Parkin in... 
Bcl-2/adeno-virus E1B 19-kDa interacting protein 3 | Mitochondria | Mitofusin 1 | Dynamin-related protein 1 | APOPTOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | FUSION | mitochondria | dynamin-related protein 1 | MAMMALIAN-CELLS | Bcl-2/adenovirus E1B 19-kDa interacting protein 3 | mitofusin 1 | CELL-DEATH | DRP1 | OPA1 | NEURONS | PERIPHERAL VASCULAR DISEASE | STRESS | Dynamins - metabolism | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Mitochondria, Heart - pathology | Male | Mitochondrial Proteins - genetics | Autophagy | Myocytes, Cardiac - enzymology | Transfection | RNA Interference | Mitochondrial Proteins - metabolism | Membrane Proteins - metabolism | Proto-Oncogene Proteins - metabolism | Membrane Proteins - genetics | Mice, Inbred C57BL | Cells, Cultured | Mitochondria, Heart - enzymology | Ubiquitin-Protein Ligases - metabolism | Dynamins - genetics | Rats | Proto-Oncogene Proteins - genetics | Rats, Sprague-Dawley | Mice, Knockout | Protein Transport | Myocytes, Cardiac - pathology | Animals | GTP Phosphohydrolases - metabolism | GTP Phosphohydrolases - genetics | Ubiquitin-Protein Ligases - deficiency | Mice | Mutation | Ubiquitin-Protein Ligases - genetics | Autophagy (Cytology) | Ligases | Physiological aspects | Research | Health aspects | Heart muscle | Proteins | Cardiomyocytes | Physiology | Gene expression | Index Medicus | Bcl-2 | Signaling and Stress Response | adenovirus E1B 19-kDa interacting protein 3
Journal Article
Neuron, ISSN 0896-6273, 08/2012, Volume 75, Issue 4, pp. 618 - 632
Mitochondrial abnormalities have been documented in Alzheimer’s disease and related neurodegenerative disorders, but the causal relationship between... 
ALZHEIMERS-DISEASE BRAIN | DOMINANT OPTIC ATROPHY | MITOCHONDRIAL-FUNCTION | MOUSE MODEL | LIGHT-CHAIN | FRONTOTEMPORAL DEMENTIA | AXONAL-TRANSPORT | NEUROSCIENCES | DYNAMIN-RELATED PROTEIN | PHOSPHORYLATION SITES | TRANSGENIC MICE | Neurons - pathology | Microtubule-Associated Proteins - genetics | Tauopathies - genetics | Cytoskeletal Proteins - genetics | Gelsolin - metabolism | Microtubule-Associated Proteins - metabolism | Humans | Actins - metabolism | Tauopathies - pathology | Cytoplasm - metabolism | MicroRNAs - metabolism | Green Fluorescent Proteins - genetics | Mitochondrial Proteins - genetics | Drosophila Proteins - metabolism | GTP-Binding Proteins - genetics | Nerve Degeneration - metabolism | Neurons - ultrastructure | tau Proteins - genetics | Cell Death - genetics | Mitochondria - genetics | Mitochondrial Proteins - metabolism | ATP Synthetase Complexes - metabolism | Cell Cycle Proteins - genetics | Tauopathies - complications | Cytoskeletal Proteins - metabolism | Myosins - metabolism | Cytoplasm - genetics | RNA Interference - physiology | Disease Models, Animal | In Situ Nick-End Labeling | Green Fluorescent Proteins - metabolism | Animals, Genetically Modified | Gene Expression Regulation - genetics | Drosophila | Cell Cycle Proteins - metabolism | Mitochondria - metabolism | Mitochondria - pathology | Mutation - genetics | Animals | GTP Phosphohydrolases - metabolism | Analysis of Variance | GTP Phosphohydrolases - genetics | Gelsolin - genetics | Mice | Drosophila Proteins - genetics | Nerve Degeneration - etiology | Voltage-Dependent Anion Channels - metabolism | GTP-Binding Proteins - metabolism | Nervous system diseases | Actin | Neurons | Utrophin | Myosin | Mitochondrial DNA | Alzheimer's disease | Proteins | Phosphorylation | Mitochondria | Neurotoxicity | Insects | Microscopy | Neurodegeneration | Pathogenesis | Morphology | Mutation | Defects | Index Medicus | Neurodegenerative diseases | Tau protein | Cell death | Elongation
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 9/2005, Volume 170, Issue 7, pp. 1067 - 1078
Mutations in GDAP1 lead to severe forms of the peripheral motor and sensory neuropathy, Charcot-Marie-Tooth disease (CMT), which is characterized by... 
COS cells | Mitochondria | Transfection | Neurons | Charcot Marie Tooth disease | Schwann cells | HeLa cells | Genetic mutation | Peripheral nervous system diseases | Cells | OUTER-MEMBRANE | FUSION | NEUROPATHY | SCHWANN-CELLS | FISSION | GDAP1 GENE | MAMMALIAN-CELLS | DYNAMIN-RELATED PROTEIN | ETHACRYNIC-ACID | AUTOSOMAL RECESSIVE CMT | CELL BIOLOGY | Humans | Nerve Tissue Proteins - analysis | Microtubule-Associated Proteins - pharmacology | Neurons - cytology | Schwann Cells - cytology | Charcot-Marie-Tooth Disease - genetics | Mitochondrial Membrane Transport Proteins - genetics | Mitochondrial Membrane Transport Proteins - physiology | Mitochondrial Proteins - metabolism | Membrane Transport Proteins - metabolism | Membrane Proteins - metabolism | Neurons - metabolism | Mitochondria - chemistry | Charcot-Marie-Tooth Disease - metabolism | Nerve Tissue Proteins - physiology | Cells, Cultured | Gene Expression Regulation | Rats | Schwann Cells - metabolism | Mitochondria - pathology | Intracellular Membranes - chemistry | Nerve Tissue Proteins - genetics | Mitochondrial Proteins - pharmacology | Animals | Charcot-Marie-Tooth Disease - etiology | GTP Phosphohydrolases - metabolism | Models, Biological | Mice | Mutation | Mitochondria - physiology | GTP Phosphohydrolases - pharmacology | Proteins | Care and treatment | Research | Gangliosides | Charcot-Marie-Tooth disease | Mitochondrial DNA | Gene expression | Ribonucleic acid--RNA | Ribonucleic acid | Index Medicus
Journal Article
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 09/2009, Volume 186, Issue 6, pp. 793 - 803
Journal Article
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 4/2004, Volume 165, Issue 2, pp. 167 - 173
Mitochondrial morphology and inheritance of mitochondrial DNA in yeast depend on the dynamin-like GTPase Mgm1. It is present in two isoforms in the... 
Protein isoforms | Yeasts | Mitochondria | Motor ability | Fluorescence | Reports | Mitochondrial DNA | Gene expression regulation | Imports | Hydrophobicity | Down regulation | Mitochondrial fusion | Mitochondrial diseases | Rhomboid protease | Dynamin-like protein | Protein import | rhomboid protease | TRANSLOCASE | FUSION | MEMBRANE | mitochondrial fusion | SACCHAROMYCES-CEREVISIAE | CELL BIOLOGY | YEAST | MAINTENANCE | mitochondrial diseases | DOMINANT OPTIC ATROPHY | DYNAMIN-RELATED GTPASE | dynamin-like protein | protein import | PROTEINS | Protein Structure, Tertiary | Humans | Models, Molecular | Nuclear Proteins - metabolism | Protein Transport - physiology | Mitochondria - metabolism | Mitochondrial Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | GTP-Binding Proteins - genetics | Saccharomyces cerevisiae - cytology | Saccharomyces cerevisiae - metabolism | Protein Isoforms - metabolism | Mitochondrial Proteins - metabolism | Adenosine Triphosphate - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Molecular Motor Proteins - metabolism | Serine Endopeptidases | GTP-Binding Proteins - metabolism | Protein Isoforms - genetics | Physiological aspects | Chemical properties | Adenosine triphosphate | Cytology | Proteins | Enzymes | Disease | Adenosine triphosphatase | Index Medicus | mitochondrial fusion; protein import; mitochondrial diseases; rhomboid protease; dynamin-like protein | Report
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2015, Volume 290, Issue 36, pp. 22005 - 22018
Efficient apoptosis requires Bax/Bak-mediated mitochondrial outer membrane permeabilization (MOMP), which releases death-promoting proteins cytochrome c and... 
BCL-2 | DOMAIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | IAP | BAX | SMAC | CYTOCHROME-C RELEASE | CLEAVAGE | CHEMOTHERAPY | CELL-DEATH PROTEASES | FAMILY | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | bcl-2 Homologous Antagonist-Killer Protein - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Mitochondrial Proteins - genetics | bcl-2 Homologous Antagonist-Killer Protein - metabolism | Caspases - metabolism | MCF-7 Cells | Mitochondrial Proteins - metabolism | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | HEK293 Cells | Intracellular Signaling Peptides and Proteins - genetics | bcl-2-Associated X Protein - genetics | Fibroblasts - metabolism | Permeability - drug effects | Cytochromes c - secretion | Cells, Cultured | bcl-2-Associated X Protein - metabolism | Mitochondria - metabolism | Blotting, Western | X-Linked Inhibitor of Apoptosis Protein - genetics | Mice, Knockout | Mitochondrial Membranes - metabolism | Protein Transport | Animals | GTP Phosphohydrolases - metabolism | Embryo, Mammalian - cytology | GTP Phosphohydrolases - genetics | Fibroblasts - drug effects | X-Linked Inhibitor of Apoptosis Protein - metabolism | Enzyme Activation | HeLa Cells | Microscopy, Fluorescence | Index Medicus | tumor necrosis factor (TNF) | dynamin-related protein 1 (Drp1) | cell death | mitochondria | mitochondrial apoptosis | mitochondrial outer membrane permeabilization (MOMP) | E3 ubiquitin ligase | X-linked inhibitor of apoptosis protein (XIAP) | Cell Biology
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2017, Volume 12, Issue 6, pp. e0179397 - e0179397
Mitochondria are dynamic organelles that continually adapt their morphology by fusion and fission events. An imbalance between fusion and fission has been... 
CLATHRIN-MEDIATED ENDOCYTOSIS | GTPASE ACTIVITY | CONFORMATIONAL-CHANGES | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | MEMBRANE FISSION | PLECKSTRIN HOMOLOGY DOMAIN | MITOCHONDRIAL FISSION MACHINERY | DYNAMIN-RELATED PROTEIN-1 | ELECTRON-MICROSCOPY | NEURONAL MITOCHONDRIA | Microtubule-Associated Proteins - chemistry | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | Recombinant Proteins - chemistry | Guanosine Triphosphate - metabolism | Mitochondria - metabolism | Mitochondrial Proteins - genetics | Recombinant Proteins - biosynthesis | Cryoelectron Microscopy | GTP Phosphohydrolases - chemistry | Recombinant Proteins - isolation & purification | GTP Phosphohydrolases - metabolism | Protein Isoforms - metabolism | GTP Phosphohydrolases - genetics | Mitochondrial Proteins - metabolism | Protein Isoforms - chemistry | Mitochondrial Proteins - chemistry | Protein Structure, Quaternary | Protein Binding | Guanosine Triphosphate - chemistry | Protein Isoforms - genetics | Usage | Physiological aspects | Nervous system | Genetic aspects | Degeneration | Research | Diagnosis | Electron microscopy | Membrane proteins | Self assembly | Membranes | GTP | Lipids | Biology | Monomers | Fission | Proteins | Oligomers | Mitochondria | Mathematical analysis | Dimensional analysis | Tomography | Tubes | Crystal structure | Neurodegenerative diseases | Incubation | Cell division | Organelles | Diseases | Neurological diseases | Self-assembly | Transmission electron microscopy | Dynamin | Mutation | Alzheimers disease | In vitro methods and tests | Guanosinetriphosphatase | Index Medicus
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Journal Article