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histidine and Complex IV Deficiency

histidine has been researched along with Complex IV Deficiency in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bax, R; Freisinger, P; Horn, N; Horváth, R; Jaksch, M; Mayr, JA; Merl, T; Moller, LB; Müller-Höcker, J; Pongratz, D; Rubio, R1
Bertini, E; Dionisi-Vici, C; Federici, G; Leuzzi, V; Luchetti, A; Piemonte, F; Rizzo, C; Sabetta, G1
Freisinger, P; Horn, N; Horvath, R; Jaksch, M; Lochmüller, H; Lunkwitz, R; Müller, J; Müller-Höcker, J; Paret, C; Rödel, G; Shoubridge, EA; Stecker, G; Stucka, R; Thirion, C; Trepesch, N1

Other Studies

3 other study(ies) available for histidine and Complex IV Deficiency

ArticleYear
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4

    Topics: Adenosine Triphosphatases; Blotting, Southern; Brain; Cataract; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Cytochrome-c Oxidase Deficiency; Developmental Disabilities; DNA Mutational Analysis; Electrophysiology; Exons; Fibroblasts; Hearing Loss, Sensorineural; Histidine; Humans; Immunoblotting; Immunohistochemistry; Infant; Magnetic Resonance Imaging; Male; Mitochondria; Muscle Hypotonia; Muscle, Skeletal; Muscles; Mutation; Myoblasts; Recombinant Fusion Proteins; Superoxide Dismutase

2005
Oxidative abnormalities in Menkes disease.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:4

    Topics: Cells, Cultured; Ceruloplasmin; Copper; Cytochrome-c Oxidase Deficiency; Fibroblasts; Histidine; Humans; Lactic Acid; Menkes Kinky Hair Syndrome; Organometallic Compounds; Oxidation-Reduction; Treatment Outcome

2000
Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts.
    Human molecular genetics, 2001, Dec-15, Volume: 10, Issue:26

    Topics: Amino Acid Motifs; Carrier Proteins; Cell Line; Cloning, Molecular; Copper; Cytochrome-c Oxidase Deficiency; Electron Transport Complex IV; Fibroblasts; Gene Expression; HeLa Cells; Histidine; Humans; Immunoblotting; Immunohistochemistry; Mitochondria; Mitochondrial Proteins; Molecular Chaperones; Mutation; Organometallic Compounds; Polymerase Chain Reaction; Proteins; Saccharomyces cerevisiae Proteins; Thioredoxins; Transduction, Genetic

2001