heme has been researched along with Leigh Disease in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cannon, A; Fox, JL; Harris, NJ; Khalimonchuk, O; Swenson, S; Taylor, NG | 1 |
| Anderka, O; Bundschuh, FA; Hannappel, A; Ludwig, B | 1 |
| Rustin, P; Taanman, JW; Valnot, I; Williams, SL | 1 |
| Shoubridge, EA | 1 |
1 review(s) available for heme and Leigh Disease
| Article | Year |
|---|---|
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 |
3 other study(ies) available for heme and Leigh Disease
| Article | Year |
|---|---|
Analysis of Oligomerization Properties of Heme a Synthase Provides Insights into Its Function in Eukaryotes.
Topics: Amino Acid Sequence; Animals; Blotting, Western; Cardiomyopathy, Hypertrophic; Case-Control Studies; Cells, Cultured; Crystallography, X-Ray; Electron Transport Complex IV; Eukaryota; Fibroblasts; Heme; Humans; Immunoprecipitation; Leigh Disease; Membrane Proteins; Models, Molecular; Molecular Sequence Data; Mutation; Protein Conformation; Protein Folding; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Skin; Substrate Specificity; Swine | 2016 |
Surf1, associated with Leigh syndrome in humans, is a heme-binding protein in bacterial oxidase biogenesis.
Topics: Bacterial Proteins; Electron Transport Complex IV; Heme; Humans; Leigh Disease; Membrane Proteins; Mitochondrial Proteins; Paracoccus denitrificans; Protein Binding | 2009 |
Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1.
Topics: Alkyl and Aryl Transferases; Cells, Cultured; Copper; Cytochrome c Group; Electron Transport Complex IV; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Heme; Humans; Leigh Disease; Membrane Proteins; Mitochondrial Proteins; Molecular Chaperones; Mutation; Oxidation-Reduction; Protein Subunits | 2004 |