Compounds > asparagine

asparagine and Retinitis Pigmentosa

asparagine has been researched along with Retinitis Pigmentosa in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's3 (60.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chou, CL; Lin, CS; Palmer, N; Tsang, SH; Tsui, I1
Horrigan, DM; Kim, JA; Tetreault, ML; Zimmerman, AL1
Chida, Y; Kamio, K; Kikawa, E; Nakazawa, M; Shiono, T; Tamai, M1
Akeo, K; Kudoh, J; Mashima, Y; Oguchi, Y; Saga, M; Shimizu, N1
Birch, DG; Blackshaw, S; Blanton, SH; Bowne, SJ; Cepko, CL; Daiger, SP; Heckenlively, JR; Hughbanks-Wheaton, D; Sullivan, LS1

Other Studies

5 other study(ies) available for asparagine and Retinitis Pigmentosa

ArticleYear
Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N.
    Current eye research, 2008, Volume: 33, Issue:11

    Topics: Adolescent; Adult; Asparagine; Aspartic Acid; Child; Electroretinography; Fluorescence; Fundus Oculi; Genes, Dominant; Genotype; Humans; Male; Middle Aged; Mutation; Pedigree; Phenotype; Retinal Pigment Epithelium; Retinitis Pigmentosa; Rhodopsin; Visual Acuity; Visual Fields; Young Adult

2008
Retinoids restore normal cyclic nucleotide sensitivity of mutant ion channels associated with cone dystrophy.
    Molecular vision, 2006, Dec-29, Volume: 12

    Topics: Animals; Asparagine; Cattle; Cyclic GMP; Cyclic Nucleotide-Gated Cation Channels; Humans; Ion Channels; Mutation; Oocytes; Patch-Clamp Techniques; Retinitis Pigmentosa; Retinoids; Serine; Transduction, Genetic; Vitamin A; Xenopus

2006
Ocular findings in patients with autosomal dominant retinitis pigmentosa and transversion mutation in codon 244 (Asn244Lys) of the peripherin/RDS gene.
    Archives of ophthalmology (Chicago, Ill. : 1960), 1994, Volume: 112, Issue:12

    Topics: Adult; Asparagine; Base Sequence; Child; Codon; Female; Genes, Dominant; Humans; Intermediate Filament Proteins; Lysine; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Neuropeptides; Pedigree; Peripherins; Retinitis Pigmentosa

1994
A novel homozygous Ile535Asn mutation in the rod cGMP phosphodiesterase beta-subunit gene in two brothers of a Japanese family with autosomal recessive retinitis pigmentosa.
    Current eye research, 1998, Volume: 17, Issue:3

    Topics: 3',5'-Cyclic-GMP Phosphodiesterases; Adult; Asparagine; Codon; Cyclic Nucleotide Phosphodiesterases, Type 6; Fundus Oculi; Humans; Isoleucine; Japan; Male; Middle Aged; Pedigree; Phosphoric Diester Hydrolases; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Visual Fields

1998
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.
    Human molecular genetics, 2002, Mar-01, Volume: 11, Issue:5

    Topics: Amino Acid Motifs; Amino Acid Sequence; Amino Acid Substitution; Asparagine; Chromosomes, Human, Pair 7; Conserved Sequence; Gene Frequency; Genes, Dominant; Genetic Linkage; Humans; IMP Dehydrogenase; Molecular Sequence Data; Mutation, Missense; Pedigree; Promoter Regions, Genetic; Retinitis Pigmentosa; Sequence Alignment

2002