Compounds > histidine

Page last updated: 2024-08-17

histidine and Pigmentary Retinopathy

histidine has been researched along with Pigmentary Retinopathy in 16 studies

Research

Studies (16)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	9 (56.25)	18.2507
2000's	2 (12.50)	29.6817
2010's	4 (25.00)	24.3611
2020's	1 (6.25)	2.80

Authors

Authors	Studies
Girach, A; Justin, GA; Maldonado, RS	1
Shah, SP; Sharp, DM; Vincent, AL; Wong, F	1
Arehart, E; Byington, D; Gleim, S; Hwa, J; Stojanovic, A	1
Acosta, ML; Christie, DL; Fletcher, EL; Kalloniatis, M; Ready, S; Shin, YS	1
Chan, F; Price, BA; Sandoval, IM; Simons, DL; Wensel, TG; Wilson, JH; Wu, SM	1
Ferrell, WD; Jones, BW; Lee, DC; Marc, RE; Moritz, OL; Tam, BM; Vazquez-Chona, FR	1
Moritz, OL; Tam, BM	1
Birch, DG; Hood, DC; Nusinowitz, S; Pepperberg, DR	1
Antich, J; Carballo, M; Gean, E; Llecha, N; Molina, M; Reig, C; Reventós, J; Tejada, I	1
Al-Maghtheh, M; Bhattacharya, S; Inglehearn, C; Keen, J; Tarttelin, E	1
Drenser, KA; Flannery, JG; Hauswirth, WW; LaVail, MM; Lewin, AS; Nishikawa, S; Yasumura, D	1
Jacobson, SG; Kemp, CM; Nathans, J; Roman, AJ; Sung, CH	1
Fishman, GA; Khadivi, P; Kimura, AE; Nichols, BE; Sheffield, VC; Stone, EM	1
Berson, EL; Dryja, TP; Rosner, B; Sandberg, MA	1
Bashir, R; Bradley, DG; Farrar, GJ; Humphries, MM; Inglehearn, CF; Jay, M; Kenna, P; McWilliam, P; Redmond, R; Sharp, EM	1
Ehinger, B	1

Reviews

1 review(s) available for histidine and Pigmentary Retinopathy

Article	Year
Antisense oligonucleotide therapy for proline-23-histidine autosomal dominant retinitis pigmentosa. Current opinion in ophthalmology, 2023, May-01, Volume: 34, Issue:3 Topics: Animals; Histidine; Humans; Mutation; Oligonucleotides, Antisense; Proline; Retinitis Pigmentosa; Rhodopsin	2023

Other Studies

15 other study(ies) available for histidine and Pigmentary Retinopathy

Article	Year
A novel rhodopsin point mutation, proline-170-histidine, associated with sectoral retinitis pigmentosa. Ophthalmic genetics, 2014, Volume: 35, Issue:4 Topics: Adult; Electrophysiology; Histidine; Humans; Male; Pedigree; Point Mutation; Proline; Retinitis Pigmentosa; Rhodopsin; Visual Acuity; Visual Fields; White People	2014
Conserved rhodopsin intradiscal structural motifs mediate stabilization: effects of zinc. Biochemistry, 2009, Mar-03, Volume: 48, Issue:8 Topics: Amino Acid Motifs; Amino Acid Sequence; Chelating Agents; Conserved Sequence; Crystallography, X-Ray; Histidine; Humans; Hydrogen Bonding; Molecular Sequence Data; Mutant Proteins; Mutation; Opsins; Protein Stability; Retinitis Pigmentosa; Rhodopsin; Sequence Analysis, Protein; Temperature; Time Factors; Zinc	2009
Retinal metabolic state of the proline-23-histidine rat model of retinitis pigmentosa. American journal of physiology. Cell physiology, 2010, Volume: 298, Issue:3 Topics: Adenosine Triphosphate; Age Factors; Animals; Apoptosis; Ca(2+) Mg(2+)-ATPase; Coumaric Acids; Creatine; Creatine Kinase; Disease Models, Animal; Disease Progression; Energy Metabolism; Histidine; L-Lactate Dehydrogenase; Membrane Transport Proteins; Monocarboxylic Acid Transporters; Mutation; Phosphocreatine; Phosphodiesterase Inhibitors; Piperazines; Proline; Purines; Rats; Rats, Sprague-Dawley; Rats, Transgenic; Retina; Retinitis Pigmentosa; Sensory Rhodopsins; Sildenafil Citrate; Sodium-Potassium-Exchanging ATPase; Sulfones	2010
Mislocalization and degradation of human P23H-rhodopsin-GFP in a knockin mouse model of retinitis pigmentosa. Investigative ophthalmology & visual science, 2011, Dec-28, Volume: 52, Issue:13 Topics: Animals; Blotting, Northern; Codon; Disease Models, Animal; Electroretinography; Gene Expression Regulation; Gene Knock-In Techniques; Genotyping Techniques; Green Fluorescent Proteins; Histidine; Mice; Mice, Inbred C57BL; Microscopy, Confocal; Mutagenesis, Site-Directed; Mutation; Proline; Recombinant Fusion Proteins; Retinal Photoreceptor Cell Inner Segment; Retinal Photoreceptor Cell Outer Segment; Retinitis Pigmentosa; Rhodopsin	2011
Dysmorphic photoreceptors in a P23H mutant rhodopsin model of retinitis pigmentosa are metabolically active and capable of regenerating to reverse retinal degeneration. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012, Feb-08, Volume: 32, Issue:6 Topics: Amino Acid Substitution; Animals; Animals, Genetically Modified; Disease Models, Animal; Histidine; Mutation; Nerve Regeneration; Proline; Retinal Degeneration; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Rhodopsin; Xenopus laevis	2012
Dark rearing rescues P23H rhodopsin-induced retinal degeneration in a transgenic Xenopus laevis model of retinitis pigmentosa: a chromophore-dependent mechanism characterized by production of N-terminally truncated mutant rhodopsin. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, Aug-22, Volume: 27, Issue:34 Topics: Animals; Animals, Genetically Modified; Cattle; Cell Line, Transformed; Darkness; Disease Models, Animal; Gene Expression Regulation; Histidine; Humans; Mice; Microscopy, Electron, Scanning; Mutation; Peptide Fragments; Proline; Retinal Rod Photoreceptor Cells; Retinaldehyde; Retinitis Pigmentosa; Rhodopsin; Transfection; Xenopus laevis	2007
Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation. Investigative ophthalmology & visual science, 1995, Volume: 36, Issue:8 Topics: Adolescent; Adult; Dark Adaptation; Electroretinography; Female; Histidine; Humans; Male; Middle Aged; Mutation; Photic Stimulation; Proline; Retinal Cone Photoreceptor Cells; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Rhodopsin; Signal Transduction; Structure-Activity Relationship	1995
A missense mutation (211His-->Arg) and a silent (160Thr) mutation within the rhodopsin gene in a spanish autosomal dominant retinitis pigmentosa family. Human molecular genetics, 1994, Volume: 3, Issue:1 Topics: Amino Acid Sequence; Arginine; Base Sequence; DNA; Exons; Female; Genes, Dominant; Histidine; Humans; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Retinitis Pigmentosa; Rhodopsin; Spain; Threonine	1994
Simple tests for rhodopsin involvement in retinitis pigmentosa. Journal of medical genetics, 1996, Volume: 33, Issue:3 Topics: Female; Genetic Markers; Histidine; Humans; Leucine; Male; Mutation; Pedigree; Point Mutation; Polymorphism, Restriction Fragment Length; Proline; Retinitis Pigmentosa; Rhodopsin	1996
Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa. Nature medicine, 1998, Volume: 4, Issue:8 Topics: Animals; Animals, Genetically Modified; Dependovirus; Disease Models, Animal; Genes, Dominant; Genetic Therapy; Histidine; Photoreceptor Cells; Point Mutation; Proline; Promoter Regions, Genetic; Rats; Rats, Sprague-Dawley; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Rhodopsin; RNA, Catalytic; Rod Opsins	1998
Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation. American journal of ophthalmology, 1992, Feb-15, Volume: 113, Issue:2 Topics: Adolescent; Adult; Aged; Codon; Dark Adaptation; Electroretinography; Female; Histidine; Humans; Male; Middle Aged; Mutation; Pedigree; Photoreceptor Cells; Proline; Retinitis Pigmentosa; Rhodopsin; Visual Fields	1992
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene. Ophthalmology, 1991, Volume: 98, Issue:12 Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Base Sequence; Codon; DNA; Female; Histidine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Proline; Retinal Degeneration; Retinitis Pigmentosa; Rhodopsin; Visual Fields	1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His). Archives of ophthalmology (Chicago, Ill. : 1960), 1991, Volume: 109, Issue:1 Topics: Adolescent; Adult; Base Sequence; Codon; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Histidine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Pedigree; Polymerase Chain Reaction; Proline; Retinitis Pigmentosa; Rhodopsin; Visual Acuity; Visual Fields	1991
Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from Europe. American journal of human genetics, 1990, Volume: 47, Issue:6 Topics: Amino Acid Sequence; Base Sequence; Codon; Europe; Exons; Female; Genes, Dominant; Histidine; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Proline; Retinitis Pigmentosa; Rhodopsin	1990
[Unexpected findings partly explain the causes of retinitis pigmentosa]. Lakartidningen, 1990, Apr-25, Volume: 87, Issue:17 Topics: Base Sequence; Histidine; Humans; Molecular Conformation; Molecular Sequence Data; Photoreceptor Cells; Proline; Retinal Pigments; Retinitis Pigmentosa; Rhodopsin	1990