Page last updated: 2024-08-23

heme and Leigh Disease

heme has been researched along with Leigh Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cannon, A; Fox, JL; Harris, NJ; Khalimonchuk, O; Swenson, S; Taylor, NG1
Anderka, O; Bundschuh, FA; Hannappel, A; Ludwig, B1
Rustin, P; Taanman, JW; Valnot, I; Williams, SL1
Shoubridge, EA1

Reviews

1 review(s) available for heme and Leigh Disease

ArticleYear
Cytochrome c oxidase deficiency.
    American journal of medical genetics, 2001,Spring, Volume: 106, Issue:1

    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

Other Studies

3 other study(ies) available for heme and Leigh Disease

ArticleYear
Analysis of Oligomerization Properties of Heme a Synthase Provides Insights into Its Function in Eukaryotes.
    The Journal of biological chemistry, 2016, May-06, Volume: 291, Issue:19

    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.
    The Journal of biological chemistry, 2009, Sep-18, Volume: 284, Issue:38

    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.
    The Journal of biological chemistry, 2004, Feb-27, Volume: 279, Issue:9

    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