Compounds > glutamine

glutamine and Night Blindness

glutamine has been researched along with Night Blindness in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dryja, TP; Fishman, GA; Hajali, M; Lindeman, M; Sweeney, MO1
Gross, AK; Oprian, DD; Xie, G1
Gross, AK; Oprian, DD; Rao, VR1
Gekka, T; Hayashi, T; Kitahara, K; Kozaki, K; Kubo, A; Nakamura, Y; Omoto, S; Takeuchi, T; Toda, K; Watanabe, A1

Other Studies

4 other study(ies) available for glutamine and Night Blindness

ArticleYear
Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.
    Documenta ophthalmologica. Advances in ophthalmology, 2009, Volume: 118, Issue:3

    Topics: Alcohol Oxidoreductases; Arginine; Child; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Glutamine; Glycine; Humans; Hypopigmentation; Mutation, Missense; Night Blindness; Photic Stimulation; Retina; Retinal Cone Photoreceptor Cells; Retinal Pigments; Retinal Rod Photoreceptor Cells; Sensory Thresholds; Tryptophan; Vision, Ocular; Visual Fields

2009
Slow binding of retinal to rhodopsin mutants G90D and T94D.
    Biochemistry, 2003, Feb-25, Volume: 42, Issue:7

    Topics: Alanine; Amino Acid Sequence; Animals; Aspartic Acid; Glutamic Acid; Glutamine; Glycine; Humans; Molecular Sequence Data; Mutagenesis, Insertional; Night Blindness; Protein Binding; Protein Denaturation; Retinaldehyde; Rhodopsin; Schiff Bases; Spectrophotometry, Ultraviolet; Threonine

2003
Characterization of rhodopsin congenital night blindness mutant T94I.
    Biochemistry, 2003, Feb-25, Volume: 42, Issue:7

    Topics: Amino Acid Sequence; Animals; Cattle; COS Cells; Glutamic Acid; Glutamine; Humans; Hydrogen-Ion Concentration; Isoleucine; Kinetics; Light; Molecular Sequence Data; Mutagenesis, Insertional; Night Blindness; Rhodopsin; Schiff Bases; Threonine; Transducin; Transfection

2003
Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).
    Acta ophthalmologica Scandinavica, 2004, Volume: 82, Issue:5

    Topics: Adolescent; Asian People; Base Sequence; Codon, Nonsense; Codon, Terminator; Color Vision Defects; Electroretinography; Fundus Oculi; Glutamine; Humans; Male; Night Blindness; Orphan Nuclear Receptors; Pedigree; Receptors, Cytoplasmic and Nuclear; Retinal Cone Photoreceptor Cells; Retinal Diseases; Syndrome; Transcription Factors; Visual Acuity

2004