Compounds > threonine

threonine and Night Blindness

threonine has been researched along with Night Blindness in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bojang, P; Furukawa, T; Goldberg, AF; Gregg, RG; Hirschtritt, ME; Koike, C; McCall, MA; Nawy, S; Nishina, PM; Peachey, NS; Pearring, JN; Ray, TA; Shen, Y; Sturgill-Short, G1
Gross, AK; Oprian, DD; Xie, G1
Gross, AK; Oprian, DD; Rao, VR1
Bessant, DA; Bhattacharya, SS; Bird, AC; Fitzke, FW; Holder, GE; Payne, AM1
al-Jandal, N; Bannon, N; Farrar, GJ; Findlay, JB; Humphries, MM; Humphries, P; Kenna, PF; Kiang, AS1

Other Studies

5 other study(ies) available for threonine and Night Blindness

ArticleYear
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
    Journal of neurophysiology, 2012, Volume: 108, Issue:9

    Topics: Action Potentials; Amino Acid Sequence; Amino Acids; Animals; Capsaicin; Chromosome Mapping; Chromosomes, Mammalian; Dendrites; Disease Models, Animal; Exons; Eye Diseases, Hereditary; Genetic Diseases, X-Linked; Heterozygote; Mice; Mice, Transgenic; Molecular Sequence Data; Mutation, Missense; Myopia; Night Blindness; Point Mutation; Retina; Retinal Bipolar Cells; Sequence Analysis, DNA; Threonine; TRPM Cation Channels; Xanthenes

2012
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
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.
    Archives of ophthalmology (Chicago, Ill. : 1960), 2003, Volume: 121, Issue:6

    Topics: Adolescent; Adult; Basic-Leucine Zipper Transcription Factors; Child; Dark Adaptation; DNA-Binding Proteins; Electroretinography; Eye Proteins; Female; Fluorescein Angiography; Humans; Leucine Zippers; Male; Middle Aged; Mutation; Night Blindness; Ophthalmoscopy; Pedigree; Phenotype; Photoreceptor Cells, Vertebrate; Retinitis Pigmentosa; Serine; Threonine; Transcription Factors; Visual Acuity; Visual Fields

2003
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness.
    Human mutation, 1999, Volume: 13, Issue:1

    Topics: Amino Acid Substitution; Computer Simulation; Dark Adaptation; Female; Humans; Ireland; Isoleucine; Male; Middle Aged; Mutation, Missense; Night Blindness; Pedigree; Polymerase Chain Reaction; Rhodopsin; Threonine

1999