proline has been researched along with Retinal Diseases in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, KJ; Han, WH; Kao, LY; Lin, KK; Pang, JH; Sun, MH; Tsao, YP | 1 |
| Edwards, AO; Zhuk, SA | 1 |
| Muthulakshmi, R; Nallathambi, J; Namperumalsamy, P; Rajendran, A; Shukla, D; Sundaresan, P | 1 |
| Boman, H; Bredrup, C; Knappskog, PM; Rødahl, E | 1 |
| Hayasaka, S; Mizuno, K; Saito, T; Tada, K; Yabata, K | 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 |
| Apfelstedt-Sylla, E; Gal, A; Horn, M; Kunisch, M; Rüther, K; Zrenner, E | 1 |
7 other study(ies) available for proline and Retinal Diseases
| Article | Year |
|---|---|
Down-regulation of matrix metalloproteinase-9 by pyrrolidine dithiocarbamate prevented retinal ganglion cell death after transection of optic nerve in rats.
Topics: Animals; Antioxidants; Apoptosis; Blotting, Western; Cell Count; Disease Models, Animal; Down-Regulation; Immunohistochemistry; In Situ Nick-End Labeling; Male; Matrix Metalloproteinase 9; Optic Nerve; Proline; Rats; Rats, Sprague-Dawley; Retinal Diseases; Retinal Ganglion Cells; Thiocarbamates | 2011 |
Peripherin/RDS and VMD2 mutations in macular dystrophies with adult-onset vitelliform lesion.
Topics: Age of Onset; Aged; Aged, 80 and over; Arginine; Atrophy; Bestrophins; Chloride Channels; Eye Proteins; Female; Fundus Oculi; Humans; Intermediate Filament Proteins; Macula Lutea; Male; Membrane Glycoproteins; Middle Aged; Nerve Tissue Proteins; Peripherins; Proline; Prospective Studies; Retinal Diseases; Visual Acuity | 2006 |
Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.
Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Asian People; Cysteine; Exons; Exudates and Transudates; Eye Diseases; Fluorescein Angiography; Frizzled Receptors; Fundus Oculi; Humans; India; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Phenylalanine; Proline; Receptors, G-Protein-Coupled; Retinal Diseases; Serine; Vitreous Body | 2006 |
Clinical manifestation of a novel PAX6 mutation Arg128Pro.
Topics: Adult; Aged; Arginine; Cataract; Corneal Opacity; Eye Diseases, Hereditary; Eye Proteins; Female; Fovea Centralis; Homeodomain Proteins; Humans; Iris; Male; Middle Aged; Mutation, Missense; Nystagmus, Pathologic; Paired Box Transcription Factors; PAX6 Transcription Factor; Pedigree; Proline; Repressor Proteins; Retinal Diseases; Tomography, Optical Coherence | 2008 |
Atypical gyrate atrophy of the choroid and retina associated with iminoglycinuria.
Topics: Adult; Atrophy; Choroid; Glycine; Humans; Hydroxyproline; Imino Acids; Macula Lutea; Male; Proline; Retinal Diseases; Uveal Diseases | 1982 |
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.
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 |
Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin.
Topics: Adult; Aged; Dark Adaptation; DNA Mutational Analysis; Electroretinography; Female; Fundus Oculi; Humans; Leucine; Male; Middle Aged; Mutation; Pedigree; Photoreceptor Cells; Proline; Retinal Diseases; Retinitis Pigmentosa; Rhodopsin; Visual Fields | 1992 |