glutamine and Hereditary Optic Atrophy

glutamine has been researched along with Hereditary Optic Atrophy in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Barquera, B; Finel, M; Wikström, M; Zickermann, V	1
Birch, DG; Bowne, SJ; Daiger, SP; Heckenlively, JR; Lewis, RA; Mintz-Hittner, H; Northrup, H; Rodriquez, JA; Ruiz, RS; Saperstein, DA; Sohocki, MM; Sullivan, LS	1

Other Studies

2 other study(ies) available for glutamine and Hereditary Optic Atrophy

Article	Year
Analysis of the pathogenic human mitochondrial mutation ND1/3460, and mutations of strictly conserved residues in its vicinity, using the bacterium Paracoccus denitrificans. Biochemistry, 1998, Aug-25, Volume: 37, Issue:34 Topics: Alanine; Amino Acid Sequence; Animals; Aspartic Acid; Conserved Sequence; DNA, Mitochondrial; Electron Transport Complex I; Glutamine; Humans; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; NAD(P)H Dehydrogenase (Quinone); NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Paracoccus denitrificans; Quinone Reductases	1998
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Human mutation, 2001, Volume: 17, Issue:1 Topics: Amino Acid Substitution; Animals; Arginine; Cysteine; Genetic Variation; Glutamine; Homeodomain Proteins; Humans; Intermediate Filament Proteins; Leucine; Membrane Glycoproteins; Mutation; Nerve Tissue Proteins; Optic Atrophies, Hereditary; Peripherins; Prevalence; Proline; Retinal Degeneration; Retinal Diseases; Retinitis Pigmentosa; Rhodopsin; Trans-Activators; Tyrosine	2001

Article

Year

Analysis of the pathogenic human mitochondrial mutation ND1/3460, and mutations of strictly conserved residues in its vicinity, using the bacterium Paracoccus denitrificans.

Biochemistry, 1998, Aug-25, Volume: 37, Issue:34

Topics: Alanine; Amino Acid Sequence; Animals; Aspartic Acid; Conserved Sequence; DNA, Mitochondrial; Electron Transport Complex I; Glutamine; Humans; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; NAD(P)H Dehydrogenase (Quinone); NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Paracoccus denitrificans; Quinone Reductases

1998

Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.

Human mutation, 2001, Volume: 17, Issue:1

Topics: Amino Acid Substitution; Animals; Arginine; Cysteine; Genetic Variation; Glutamine; Homeodomain Proteins; Humans; Intermediate Filament Proteins; Leucine; Membrane Glycoproteins; Mutation; Nerve Tissue Proteins; Optic Atrophies, Hereditary; Peripherins; Prevalence; Proline; Retinal Degeneration; Retinal Diseases; Retinitis Pigmentosa; Rhodopsin; Trans-Activators; Tyrosine

2001