heme has been researched along with Mitochondrial Diseases in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 5 (55.56) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, P; Li, Y; Lu, L; Wang, H; Wei, X; Zhang, C; Zhang, Y | 1 |
| Furuyama, K; Kaneko, K | 1 |
| Fushimi, T; Ichimoto, K; Ishii, T; Kishita, Y; Matsunaga, A; Murayama, K; Nakajima, M; Nozawa, N; Ogawa-Tominaga, M; Ohtake, A; Okazaki, Y; Shimura, M; Tajika, M; Takahashi, K; Tanaka, T; Tsuruoka, T | 1 |
| Andrews, NC; Barrientos, T; Xu, W | 1 |
| Bauer, JW; Feichtinger, RG; Kofler, B; Sperl, W | 1 |
| Ferguson, SJ; Moore, RL; Stevens, JM | 1 |
| Fischer, JH; Hayashi, J; Schauen, M; Schubert, J; Spitkovsky, D; Wiesner, RJ | 1 |
| Wilson, RB | 1 |
| Shoubridge, EA | 1 |
4 review(s) available for heme and Mitochondrial Diseases
| Article | Year |
|---|---|
Iron metabolism in erythroid cells and patients with congenital sideroblastic anemia.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Anemia, Sideroblastic; Cerebellar Ataxia; Chromosomes, Human, X; Congenital Bone Marrow Failure Syndromes; Electron Transport Complex I; Erythroid Cells; Female; Glutaredoxins; Heme; HSP70 Heat-Shock Proteins; Humans; Iron; Lipid Metabolism, Inborn Errors; Male; MELAS Syndrome; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Muscular Diseases; Mutation | 2018 |
Mitochondrial dysfunction: a neglected component of skin diseases.
Topics: Autoimmune Diseases; Cockayne Syndrome; Deoxyribonucleotides; DNA Repair; DNA, Mitochondrial; Energy Metabolism; Fatty Acids; Genes, Mitochondrial; Heme; Humans; Intermediate Filaments; Iron-Sulfur Proteins; MAP Kinase Signaling System; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Mutation; Oxidative Phosphorylation; Skin Aging; Skin Diseases; Skin Neoplasms | 2014 |
Iron dysregulation in Friedreich ataxia.
Topics: Amino Acid Sequence; Animals; Frataxin; Friedreich Ataxia; Heme; Humans; Iron; Iron Metabolism Disorders; Iron-Binding Proteins; Manganese; Mice; Mice, Knockout; Mitochondria; Mitochondrial Diseases; Molecular Sequence Data; Oxygen Consumption; Sulfur; Superoxide Dismutase | 2006 |
Cytochrome c oxidase deficiency.
Topics: Adult; Carrier Proteins; Catalysis; Child; Cytochrome-c Oxidase Deficiency; DNA, Complementary; DNA, Mitochondrial; Electron Transport Complex IV; Genotype; Heme; Humans; Leigh Disease; Membrane Proteins; Mitochondrial Diseases; Mitochondrial Proteins; Models, Biological; Molecular Chaperones; Mutation; Phenotype; Protein Structure, Tertiary; Proteins | 2001 |
5 other study(ies) available for heme and Mitochondrial Diseases
| Article | Year |
|---|---|
Mitochondrial dysfunctions trigger the calcium signaling-dependent fungal multidrug resistance.
Topics: Alkyl and Aryl Transferases; Antifungal Agents; Aspergillus fumigatus; Calcium Chelating Agents; Calcium Signaling; Chitin Synthase; Drug Resistance, Fungal; Fungal Proteins; Gene Expression Regulation, Fungal; Heme; Humans; Membrane Proteins; Mitochondria; Mitochondrial Diseases; Phosphoprotein Phosphatases; Reactive Oxygen Species; Transcription Factors; Triazoles | 2020 |
Effects of 5-aminolevulinic acid and sodium ferrous citrate on fibroblasts from individuals with mitochondrial diseases.
Topics: Adenosine Triphosphate; Aminolevulinic Acid; Biosynthetic Pathways; Case-Control Studies; Citric Acid; DNA Copy Number Variations; DNA, Mitochondrial; Female; Ferrous Compounds; Fibroblasts; Heme; Heme Oxygenase-1; Humans; In Vitro Techniques; Infant; Infant, Newborn; Male; Mitochondrial Diseases; Oxidative Phosphorylation; Oxygen Consumption; RNA, Messenger; Sodium Citrate; Up-Regulation | 2019 |
Iron and copper in mitochondrial diseases.
Topics: Heme; Homeostasis; Humans; Iron; Iron-Sulfur Proteins; Mitochondrial Diseases; Models, Biological | 2013 |
Mitochondrial cytochrome c synthase: CP motifs are not necessary for heme attachment to apocytochrome c.
Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Conserved Sequence; Cytochromes c; Heme; Humans; Lyases; Mice; Mitochondria; Mitochondrial Diseases; Molecular Sequence Data; Mutation; Protein Binding; Saccharomyces cerevisiae | 2011 |
Respiratory chain deficiency slows down cell-cycle progression via reduced ROS generation and is associated with a reduction of p21CIP1/WAF1.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Cell Cycle; Cell Cycle Proteins; Cell Enlargement; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21; Down-Regulation; Ethidium; Extracellular Signal-Regulated MAP Kinases; HeLa Cells; Heme; Humans; Mitochondrial Diseases; Proto-Oncogene Proteins c-akt; Reactive Oxygen Species; Signal Transduction; Uridine; Uridine Triphosphate | 2006 |