Compounds > histidine
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histidine and Hereditary Optic Atrophy

histidine has been researched along with Hereditary Optic Atrophy in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's2 (40.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chalukya, M; Donoso, L; Hussles Maumenee, I; Nusinowitz, S; Silva-Garcia, R; Small, KW; Udar, N; Vrabec, T; Yelchits, S; Yellore, V1
Carelli, V; Cortelli, P; Crimi, M; Degli Esposti, M; Ghelli, A; Lenaz, G; Lugaresi, E; Montagna, P; Ratta, M; Sangiorgi, S1
Isashiki, Y; Nakagawa, M; Ohba, N; Uto, M1
Fujiki, K; Hayakawa, M; Hotta, Y; Kanai, A; Nakajima, A; Saito, K1
Elsas, LJ; Hodge, JA; Lezza, AM; Lott, MT; Nikoskelainen, EK; Schurr, TG; Singh, G; Wallace, DC1

Other Studies

5 other study(ies) available for histidine and Hereditary Optic Atrophy

ArticleYear
Identification of GUCY2D gene mutations in CORD5 families and evidence of incomplete penetrance.
    Human mutation, 2003, Volume: 21, Issue:2

    Topics: Adolescent; Adult; Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Cattle; Child; Child, Preschool; Dogs; Echinacea; Female; Genes, Dominant; Genetic Markers; Guanylate Cyclase; Histidine; Humans; Male; Mice; Middle Aged; Molecular Sequence Data; Mutation; Optic Atrophies, Hereditary; Pedigree; Penetrance; Plant Proteins; Rats; Recombination, Genetic

2003
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.
    FEBS letters, 1994, Oct-03, Volume: 352, Issue:3

    Topics: Amino Acid Sequence; Arginine; Base Sequence; Blood Platelets; Conserved Sequence; DNA, Mitochondrial; Electron Transport Complex I; Female; Histidine; Humans; Kinetics; Macromolecular Substances; Male; Mitochondria; Molecular Sequence Data; NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Pedigree; Point Mutation; Polymerase Chain Reaction; Rotenone

1994
Sequence homology of NADH CoQ reductase subunit IV with nucleotide-requiring enzymes.
    Japanese journal of ophthalmology, 1993, Volume: 37, Issue:1

    Topics: Adenosine Triphosphatases; Adenylate Kinase; Amino Acid Sequence; Arginine; Argininosuccinate Synthase; DNA, Mitochondrial; Electron Transport Complex I; Histidine; Humans; Molecular Sequence Data; NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Point Mutation; Sequence Homology, Amino Acid

1993
Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification.
    American journal of ophthalmology, 1989, Nov-15, Volume: 108, Issue:5

    Topics: Adult; Arginine; DNA Mutational Analysis; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Gene Amplification; Hereditary Sensory and Motor Neuropathy; Histidine; Humans; Male; Optic Atrophies, Hereditary; Pedigree; Polymerase Chain Reaction; Visual Acuity

1989
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
    Science (New York, N.Y.), 1988, Dec-09, Volume: 242, Issue:4884

    Topics: Animals; Arginine; Black People; Cytochrome Reductases; DNA, Mitochondrial; Female; Genes; Georgia; Hereditary Sensory and Motor Neuropathy; Histidine; Humans; Macromolecular Substances; Male; Mutation; NADH Dehydrogenase; Optic Atrophies, Hereditary; Pedigree; Reference Values; White People

1988