glycine has been researched along with Retinitis Pigmentosa in 13 studies
Retinitis Pigmentosa: Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
| Excerpt | Relevance | Reference |
|---|---|---|
| "A large family affected with autosomal dominant retinitis pigmentosa (ADRP) with a sectorial phenotype showed a previously described (G to A) mutation in the rhodopsin gene resulting in the substitution of a glycine residue by an arginine in codon 106 of rhodopsin." | 3.69 | G106R rhodopsin mutation is also present in Spanish ADRP patients. ( Antiñolo, G; Ayuso, C; Borrego, S; Carballo, M; Garcia-Sandoval, B; Reig, C; Trujillo, MJ, 1996) |
| "We show that disease progression in the TgP347L rabbit closely tracks human cone-sparing RP, including the cone-associated preservation of bipolar cell signaling and triggering of reprogramming." | 1.37 | Retinal remodeling in the Tg P347L rabbit, a large-eye model of retinal degeneration. ( Anderson, J; Jones, BW; Kondo, M; Lin, Y; Marc, RE; Rapp, K; Shaw, MV; Terasaki, H; Watt, CB; Yang, JH, 2011) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (7.69) | 18.7374 |
| 1990's | 4 (30.77) | 18.2507 |
| 2000's | 3 (23.08) | 29.6817 |
| 2010's | 3 (23.08) | 24.3611 |
| 2020's | 2 (15.38) | 2.80 |
| Authors | Studies |
|---|---|
| Gehlen, J | 1 |
| Esser, S | 1 |
| Schaffrath, K | 1 |
| Johnen, S | 1 |
| Walter, P | 1 |
| Müller, F | 1 |
| Sterrett, MC | 1 |
| Enyenihi, L | 1 |
| Leung, SW | 1 |
| Hess, L | 1 |
| Strassler, SE | 1 |
| Farchi, D | 1 |
| Lee, RS | 1 |
| Withers, ES | 1 |
| Kremsky, I | 1 |
| Baker, RE | 1 |
| Basrai, MA | 1 |
| van Hoof, A | 1 |
| Fasken, MB | 1 |
| Corbett, AH | 1 |
| Jones, BW | 1 |
| Kondo, M | 1 |
| Terasaki, H | 1 |
| Watt, CB | 1 |
| Rapp, K | 1 |
| Anderson, J | 1 |
| Lin, Y | 1 |
| Shaw, MV | 1 |
| Yang, JH | 1 |
| Marc, RE | 1 |
| Jensen, RJ | 1 |
| Ahmedli, NB | 1 |
| Gribanova, Y | 1 |
| Njoku, CC | 1 |
| Naidu, A | 1 |
| Young, A | 1 |
| Mendoza, E | 1 |
| Yamashita, CK | 1 |
| Özgül, RK | 1 |
| Johnson, JE | 1 |
| Fox, DA | 1 |
| Farber, DB | 1 |
| Gire, AI | 1 |
| Sullivan, LS | 1 |
| Bowne, SJ | 1 |
| Birch, DG | 1 |
| Hughbanks-Wheaton, D | 1 |
| Heckenlively, JR | 1 |
| Daiger, SP | 1 |
| Millán, JM | 1 |
| Fuchs, S | 1 |
| Paricio, N | 1 |
| Wedemann, H | 1 |
| Gal, A | 1 |
| Nájera, C | 1 |
| Prieto, F | 1 |
| Ayuso, C | 1 |
| Reig, C | 1 |
| Garcia-Sandoval, B | 1 |
| Trujillo, MJ | 1 |
| Antiñolo, G | 1 |
| Borrego, S | 1 |
| Carballo, M | 1 |
| Rabier, D | 1 |
| Diry, C | 1 |
| Rotig, A | 1 |
| Rustin, P | 1 |
| Heron, B | 1 |
| Bardet, J | 1 |
| Parvy, P | 1 |
| Ponsot, G | 1 |
| Marsac, C | 1 |
| Saudubray, JM | 1 |
| Munnich, A | 1 |
| Kamoun, P | 1 |
| Fishman, GA | 1 |
| Grover, S | 1 |
| Jacobson, SG | 1 |
| Alexander, KR | 1 |
| Derlacki, DJ | 1 |
| Wu, W | 1 |
| Buraczynska, M | 1 |
| Swaroop, A | 1 |
| Fletcher, EL | 1 |
| Dryja, TP | 1 |
| McEvoy, JA | 1 |
| McGee, TL | 1 |
| Berson, EL | 1 |
| Onisawa, J | 1 |
| Lee, TY | 1 |
1 review available for glycine and Retinitis Pigmentosa
| Article | Year |
|---|---|
Alterations in neurochemistry during retinal degeneration.
Topics: Animals; Animals, Newborn; Aspartic Acid; gamma-Aminobutyric Acid; Glutamic Acid; Glutamine; Glycine | 2000 |
12 other studies available for glycine and Retinitis Pigmentosa
| Article | Year |
|---|---|
Blockade of Retinal Oscillations by Benzodiazepines Improves Efficiency of Electrical Stimulation in the Mouse Model of RP, rd10.
Topics: Action Potentials; Animals; Benzodiazepines; Disease Models, Animal; Electric Stimulation Therapy; F | 2020 |
A budding yeast model for human disease mutations in the
Topics: Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Dwarfism; Exoribonucleases; Exosome Mul | 2021 |
Retinal remodeling in the Tg P347L rabbit, a large-eye model of retinal degeneration.
Topics: Adult; Animals; Animals, Genetically Modified; Disease Models, Animal; Disease Progression; Electror | 2011 |
Activation of ganglion cells in wild-type and P23H rat retinas with a small subretinal electrode.
Topics: Action Potentials; Animals; Disease Models, Animal; Electric Stimulation; Evoked Potentials, Visual; | 2012 |
Dynamics of the rhomboid-like protein RHBDD2 expression in mouse retina and involvement of its human ortholog in retinitis pigmentosa.
Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Cell Membrane; Endopeptidases; Female; Gene Express | 2013 |
The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.
Topics: Adult; Arginine; Child; Cohort Studies; Female; Gene Frequency; Genes, Dominant; Glycine; Humans; Ma | 2007 |
Gly114Asp mutation of rhodopsin in autosomal dominant retinitis pigmentosa.
Topics: Adolescent; Adult; Amino Acid Sequence; Aspartic Acid; Base Sequence; Codon; Female; Genes, Dominant | 1995 |
G106R rhodopsin mutation is also present in Spanish ADRP patients.
Topics: Adolescent; Adult; Aged; Arginine; Child; Child, Preschool; DNA; Electroretinography; Female; Glycin | 1996 |
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
Topics: Abnormalities, Multiple; Ataxia; Biomarkers; Child, Preschool; Citrulline; DNA, Mitochondrial; Femal | 1998 |
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
Topics: Adolescent; Adult; Aged; Carrier Proteins; Child, Preschool; Codon; DNA Mutational Analysis; Electro | 1998 |
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
Topics: DNA Mutational Analysis; Female; Glutamine; Glycine; Humans; Male; Mutation, Missense; Pedigree; Pol | 2000 |
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Pr | 1970 |