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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2008, Volume 105, Issue 49, pp. 19318 - 19323
Journal Article
Journal Article
The EMBO Journal, ISSN 0261-4189, 01/2008, Volume 27, Issue 2, pp. 433 - 446
Journal Article
Open Biology, ISSN 2046-2441, 2012, Volume 2, Issue MAY, pp. 120080 - 120080
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 4/2010, Volume 189, Issue 2, pp. 211 - 221
Parkinson's disease (PD) is a prevalent neuro-degenerative disorder. Recent identification of genes linked to familial forms of PD such as Parkin and PINK1... 
Mitochondria | Report | Ubiquitins | Mitochondrial membranes | HeLa cells | Parkinson disease | Antibodies | Immunoblotting | Genetic mutation | Cytoplasm | Perceptual localization | UBIQUITIN-PROTEIN LIGASE | DISEASE | DEGRADATION | PROTEASOME SYSTEM | MUTATIONS | DYSFUNCTION | AUTOPHAGY | RECESSIVE PARKINSONISM | DROSOPHILA-PINK1 | IMPAIRMENT | CELL BIOLOGY | Protein Kinases - metabolism | Protein Kinases - genetics | Uncoupling Agents - pharmacology | Humans | Fluorescent Dyes - metabolism | Dimethyl Sulfoxide - pharmacology | Mitochondrial Proteins - genetics | Recombinant Fusion Proteins - metabolism | Solvents - pharmacology | Mitochondrial Proteins - metabolism | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | Membrane Potential, Mitochondrial - physiology | Parkinson Disease - metabolism | Fibroblasts - metabolism | Biomarkers - metabolism | Parkinson Disease - pathology | Ubiquitin-Protein Ligases - metabolism | Receptors, Cytoplasmic and Nuclear - genetics | Mitochondria - drug effects | Mitochondria - pathology | Mice, Knockout | Animals | Recombinant Fusion Proteins - genetics | Fibroblasts - cytology | Mice | HeLa Cells | Mitochondria - physiology | Ubiquitin-Protein Ligases - genetics | Receptors, Cytoplasmic and Nuclear - metabolism | Ubiquitin | Properties | Mitochondrial DNA | Enzymes | Membranes | Cellular biology | Parkinsons disease | Gene expression | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 7, pp. e11468 - e11468
Background: Aging results in a progressive loss of skeletal muscle, a condition known as sarcopenia. Mitochondrial DNA (mtDNA) mutations accumulate with aging... 
POINT MUTATIONS | LIFE-SPAN | OXIDATIVE STRESS | DELETION MUTATIONS | CAUSAL ROLE | MULTIDISCIPLINARY SCIENCES | CALORIC RESTRICTION | HYDROGEN-PEROXIDE | ELECTRON-TRANSPORT | CELL-DEATH | AGE | Sarcopenia - genetics | Caspase 9 - metabolism | Reactive Oxygen Species - metabolism | Oligonucleotide Array Sequence Analysis | Caspase 3 - metabolism | Apoptosis - genetics | Male | Mice, Transgenic | Muscle, Skeletal - metabolism | Mitochondria - pathology | Reverse Transcriptase Polymerase Chain Reaction | Animals | DNA, Mitochondrial - genetics | Mitochondria - genetics | Sarcopenia - pathology | Membrane Potential, Mitochondrial - physiology | Female | Mice | Apoptosis - physiology | Muscle, Skeletal - pathology | Mutation | Sarcopenia | Gene mutations | Analysis | Genes | Genetic research | Muscles | DNA polymerases | Genetic aspects | Mitochondrial DNA | Gene expression | Apoptosis | Oxidative stress | Reactive oxygen species | Phosphorylation | DNA polymerase | Parametric analysis | Liver | Biology | Mutation rates | Proteins | Electron transport chain | Mitochondria | Bioenergetics | Proofreading | Older people | Rodents | Aging | Membrane potential | Deoxyribonucleic acid--DNA | Age | Aging (artificial) | Skeletal muscle | Medicine | Polymerase | Musculoskeletal system | Hypotheses | Brain research | Oxidative phosphorylation | Insects | Growth hormones | Genetic engineering | Electron transport | DNA-directed DNA polymerase | Geriatrics | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
Nature, ISSN 0028-0836, 11/2012, Volume 491, Issue 7423, pp. 269 - 273
Myocardial cell death is initiated by excessive mitochondrial Ca2+ entry causing Ca2+ overload, mitochondrial permeability transition pore (mPTP) opening and... 
OXIDATION | HYPERTROPHY | APOPTOSIS | INNER MEMBRANE | II INHIBITION PROTECTS | MULTIDISCIPLINARY SCIENCES | CALCIUM UNIPORTER | IN-VIVO | CALMODULIN KINASE | FAILURE | KINASE-II | Mitochondria, Heart - metabolism | Apoptosis - drug effects | Calcium - metabolism | Cyclosporine - pharmacology | Mitochondria, Heart - pathology | Membrane Potential, Mitochondrial - drug effects | Heart Failure - prevention & control | Myocardium - metabolism | Membrane Potential, Mitochondrial - physiology | Female | Stress, Physiological - drug effects | Reperfusion Injury - metabolism | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism | Heart - physiopathology | Mitochondrial Membrane Transport Proteins - metabolism | Calcium - pharmacology | Reperfusion Injury - pathology | Reperfusion Injury - enzymology | Mice, Inbred C57BL | Mitochondria, Heart - enzymology | Mice, Transgenic | Myocardium - pathology | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - antagonists & inhibitors | Serine - metabolism | Heart Failure - drug therapy | Myocardium - enzymology | Animals | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - chemistry | Myocardial Infarction - drug therapy | Reperfusion Injury - prevention & control | Heart - drug effects | Mice | Myocardial Infarction - prevention & control | Heart failure | Cell death | Heart cells | Research | Mitochondrial myopathies | Properties | Observations | Protein kinases | Calmodulin | Proteins | Heart | Mitochondria | Heart attacks | Rodents | Homeostasis | Apoptosis | Index Medicus
Journal Article