heme has been researched along with Complex IV Deficiency in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (28.57) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Brown, DR; Chen, J; Chen, WW; Del Rosario, A; Dong, T; Hammond, PT; He, Y; Hu, G; Ivica, NA; Kleyman, M; Li, Y; Papageorgiou, DP; Sullivan, LB; Vander Heiden, MG | 1 |
| Hegg, EL; Herwaldt, EJ; Rivett, ED; White, AJ | 1 |
| Barrientos, A; Fontanesi, F; Gouget, K; Horn, D; Soto, IC | 1 |
| Elliott, JL; Haller, RG; Leary, SC; Pierrel, F; Romain, N; Son, M; Winge, DR | 1 |
| Behr, J; Hellwig, P; Mäntele, W; Michel, H | 1 |
| Capaldi, RA; Cooper, JM; García, JJ; Hanna, MG; Hargreaves, I; Lake, BD; Leonard, JV; Meunier, B; Nelson, I; Rahman, S; Schapira, AH; Taanman, JW | 1 |
| Shoubridge, EA | 1 |
2 review(s) available for heme and Complex IV Deficiency
| Article | Year |
|---|---|
Suppression mechanisms of COX assembly defects in yeast and human: insights into the COX assembly process.
Topics: Animals; Cytochrome-c Oxidase Deficiency; Electron Transport Complex IV; Heme; Humans; Mammals; Models, Biological; Saccharomyces cerevisiae | 2009 |
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 Complex IV Deficiency
| Article | Year |
|---|---|
MFSD7C switches mitochondrial ATP synthesis to thermogenesis in response to heme.
Topics: Adenosine Triphosphate; Animals; Cytochrome-c Oxidase Deficiency; Electron Transport Complex III; Electron Transport Complex IV; Energy Metabolism; Gene Knockout Techniques; HEK293 Cells; Heme; Humans; Membrane Transport Proteins; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondria; Mitochondrial Membranes; Protein Domains; Receptors, Virus; Sarcoplasmic Reticulum Calcium-Transporting ATPases; Signal Transduction; Thermogenesis; THP-1 Cells | 2020 |
Cox15 interacts with the cytochrome
Topics: Cytochrome-c Oxidase Deficiency; Electron Transport Complex III; Electron Transport Complex IV; Heme; Membrane Proteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins | 2018 |
Isolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS protein.
Topics: Alanine; Amino Acid Substitution; Animals; Cytochrome-c Oxidase Deficiency; Electrophoresis, Polyacrylamide Gel; Glycine; Heme; Humans; Kidney; Mice; Mice, Transgenic; Molecular Chaperones; Organ Specificity; Oxidative Phosphorylation; Protein Subunits; Spinal Cord; Superoxide Dismutase | 2008 |
Redox dependent changes at the heme propionates in cytochrome c oxidase from Paracoccus denitrificans: direct evidence from FTIR difference spectroscopy in combination with heme propionate 13C labeling.
Topics: 5-Aminolevulinate Synthetase; Carbon Isotopes; Cytochrome-c Oxidase Deficiency; Electron Transport Complex IV; Gene Deletion; Heme; Isotope Labeling; Mutagenesis, Site-Directed; Oxidation-Reduction; Paracoccus denitrificans; Spectroscopy, Fourier Transform Infrared | 1998 |
A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy.
Topics: Acidosis, Lactic; Adolescent; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Blotting, Western; Cell Nucleus; Cell Respiration; Cells, Cultured; Cytochrome-c Oxidase Deficiency; DNA, Mitochondrial; Electron Transport Complex IV; Enzyme Stability; Heme; Holoenzymes; Humans; Immunohistochemistry; Male; Mitochondria; Models, Molecular; Molecular Sequence Data; Muscles; Muscular Diseases; Mutation, Missense; Photolysis; Polarography; Protein Structure, Quaternary; Sequence Alignment | 1999 |