proline and 11-cis-retinal

proline has been researched along with 11-cis-retinal in 38 studies

Research

Studies (38)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	17 (44.74)	18.2507
2000's	15 (39.47)	29.6817
2010's	4 (10.53)	24.3611
2020's	2 (5.26)	2.80

Authors

Authors	Studies
Berson, EL; Cowley, GS; Dryja, TP; Gordon, JW; Hayes, A; Molday, RS; Mukai, S; Olsson, JE; Pawlyk, BS; Roof, D	1
Apfelstedt-Sylla, E; Gal, A; Horn, M; Kunisch, M; Rüther, K; Zrenner, E	1
Jacobson, SG; Kemp, CM; Nathans, J; Roman, AJ; Sung, CH	1
Gal, A; Niemeyer, G; Schinzel, A; Trüb, P	1
Fishman, GA; Khadivi, P; Kimura, AE; Nichols, BE; Sheffield, VC; Stone, EM	1
Berson, EL; Dryja, TP; Rosner, B; Sandberg, MA	1
Berson, EL; Dryja, TP; Rosner, B; Sandberg, MA; Weigel-DiFranco, C	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
Birch, DG; Hood, DC; Nusinowitz, S; Pepperberg, DR	1
Hennessey, JC; Macke, JP; Nathans, J	1
Berson, EL; Dryja, TP; Sandberg, MA; Weigel-DiFranco, C	1
Baverstock, J; Davies, A; Langmack, K; Marsh, D; Saibil, H; Venien-Bryan, C; Watts, A	1
Al-Maghtheh, M; Bhattacharya, S; Inglehearn, C; Keen, J; Tarttelin, E	1
Dryja, TP; Li, T; Olsson, JE; Snyder, WK	1
Abrahamson, M; Andréasson, S; Ehinger, B; Fex, G; Polland, W; Ponjavic, V	1
Drenser, KA; Flannery, JG; Hauswirth, WW; LaVail, MM; Lewin, AS; Nishikawa, S; Yasumura, D	1
Albert, AD; Alderfer, JA; Chopra, A; Yeagle, PL	1
Bush, RA; Kononen, L; Machida, S; Sieving, PA	1
Berson, EL; Dryja, TP; McEvoy, JA; McGee, TL	1
Ayuso, C; Garcia-Sandoval, B; Gimenez, A; Gonzalez-Gonzalez, MC; Ibañez, A; Lorda-Sanchez, I; Ramos, C; Sanz, R; Trujillo, MJ	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
Hirano, T; Imai, H; Kandori, H; Shichida, Y; Terakita, A	1
Krishna, AG; Marin, EP; Sakmar, TP	1
Barnett-Norris, J; Guarnieri, F; Hurst, DP; Lynch, DL; Reggio, PH; Singh, R	1
Hirano, T; Imai, H; Kuwayama, S; Shichida, Y; Terakita, A	1
Geller, S; LaVail, M; Lee, D; Matthes, M; Stone, J; Valter, K; Walsh, N; Yasumura, D	1
Deng, N; Ding, J; Gan, X; Li, L; Ma, Z; Wang, J	1
Allen, D; Hao, Y; Kraft, TW; Peng, YW; Petters, RM; Wong, F	1
Allocca, M; Auricchio, A; Bozzoni, I; Denti, MA; Di Vicino, U; Domenici, L; Parisi, F; Tessitore, A	1
Moritz, OL; Tam, BM	1
Kaushal, S; Krebs, MP; McDowell, JH; Noorwez, SM; Ostrov, DA	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
Acosta, ML; Fletcher, EL; Kalloniatis, M; Misra, S; Mistra, S; Nivison-Smith, L; Zhu, Y	1
Shah, SP; Sharp, DM; Vincent, AL; Wong, F	1
Pope, AL; Reeves, PJ; Sanchez-Reyes, OB; Smith, SO; South, K; Vogel, R; Zaitseva, E; Ziliox, M	1
Girach, A; Justin, GA; Maldonado, RS	1

Reviews

1 review(s) available for proline and 11-cis-retinal

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

37 other study(ies) available for proline and 11-cis-retinal

Article	Year
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa. Neuron, 1992, Volume: 9, Issue:5 Topics: Animals; Codon; Disease Models, Animal; Electroretinography; Fundus Oculi; Humans; Mice; Mice, Transgenic; Microscopy, Electron; Mutation; Ophthalmoscopy; Photoreceptor Cells; Proline; Restriction Mapping; Retina; Retinal Vessels; Retinitis Pigmentosa; Rhodopsin; Rod Opsins	1992
Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin. German journal of ophthalmology, 1992, Volume: 1, Issue:5 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
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
Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene. Documenta ophthalmologica. Advances in ophthalmology, 1992, Volume: 79, Issue:4 Topics: Adolescent; Adult; Arginine; Electroretinography; Humans; Male; Middle Aged; Mutagenesis, Site-Directed; Pedigree; Photoreceptor Cells; Proline; Retinitis Pigmentosa; Rhodopsin	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
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine. American journal of ophthalmology, 1991, May-15, Volume: 111, Issue:5 Topics: Adolescent; Adult; Amino Acid Sequence; Chromosome Aberrations; Chromosome Disorders; Dark Adaptation; Electroretinography; Female; Fundus Oculi; Humans; Leucine; Male; Middle Aged; Molecular Sequence Data; Mutation; Night Blindness; Pedigree; Proline; Retinitis Pigmentosa; Rhodopsin; 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
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
Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347. Human molecular genetics, 1995, Volume: 4, Issue:4 Topics: Alanine; Amino Acid Sequence; Base Sequence; DNA; Female; Genes, Dominant; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Proline; Retinitis Pigmentosa; Rhodopsin	1995
Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa. Investigative ophthalmology & visual science, 1995, Volume: 36, Issue:9 Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Child; Codon; Dark Adaptation; Electroretinography; Humans; Middle Aged; Molecular Sequence Data; Mutation; Proline; Retina; Retinitis Pigmentosa; Rhodopsin; Structure-Activity Relationship; Visual Acuity; Visual Fields	1995
Effect of the C-terminal proline repeats on ordered packing of squid rhodopsin and its mobility in membranes. FEBS letters, 1995, Feb-06, Volume: 359, Issue:1 Topics: Animals; Cell Membrane; Decapodiformes; Electron Spin Resonance Spectroscopy; Hot Temperature; Microscopy, Electron; Peptide Fragments; Photoreceptor Cells, Invertebrate; Proline; Repetitive Sequences, Nucleic Acid; Rhodopsin	1995
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
Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments. Proceedings of the National Academy of Sciences of the United States of America, 1996, Nov-26, Volume: 93, Issue:24 Topics: Animals; Electroretinography; Genes, Dominant; Humans; Mice; Mice, Transgenic; Microscopy, Confocal; Microscopy, Electron; Microscopy, Electron, Scanning; Point Mutation; Proline; Retinal Degeneration; Rhodopsin; Rod Cell Outer Segment; Serine	1996
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu. Ophthalmic genetics, 1997, Volume: 18, Issue:2 Topics: Adult; Chromosome Aberrations; Chromosome Disorders; Electroretinography; Exons; Eye Diseases, Hereditary; Family Health; Female; Genes, Dominant; Genetic Testing; Heterozygote; Humans; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Proline; Retinitis Pigmentosa; Rhodopsin; Sequence Analysis, DNA; Sweden; Visual Acuity	1997
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
Solution structure of the sixth transmembrane helix of the G-protein-coupled receptor, rhodopsin. Biochimica et biophysica acta, 2000, Jan-15, Volume: 1463, Issue:1 Topics: Amino Acid Sequence; Humans; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Sequence Data; Peptide Fragments; Proline; Protein Structure, Secondary; Rhodopsin	2000
The effect of calcium channel blocker diltiazem on photoreceptor degeneration in the rhodopsin Pro213His rat. Investigative ophthalmology & visual science, 2000, Volume: 41, Issue:9 Topics: Animals; Calcium Channel Blockers; Cell Count; Cell Survival; Diltiazem; Electroretinography; Female; Histidine; Injections, Intraperitoneal; Male; Point Mutation; Proline; Rats; Rats, Mutant Strains; Rats, Sprague-Dawley; Retinal Degeneration; Rhodopsin; Rod Cell Outer Segment	2000
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa. Investigative ophthalmology & visual science, 2000, Volume: 41, Issue:10 Topics: DNA Mutational Analysis; Female; Glutamine; Glycine; Humans; Male; Mutation, Missense; Pedigree; Polymorphism, Single-Stranded Conformational; Proline; Retinitis Pigmentosa; Rhodopsin; Valine	2000
Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family. Ophthalmic genetics, 2000, Volume: 21, Issue:4 Topics: Adult; DNA Mutational Analysis; Electroretinography; Female; Fundus Oculi; Genes, Dominant; Genotype; Humans; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Proline; Retinitis Pigmentosa; Rhodopsin; Serine; Spain; Visual Fields	2000
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Human mutation, 2001, Volume: 17, Issue:1 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
Difference in molecular structure of rod and cone visual pigments studied by Fourier transform infrared spectroscopy. Biochemistry, 2001, Mar-06, Volume: 40, Issue:9 Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Avian Proteins; Cattle; Chickens; Eye Proteins; Imides; Light; Molecular Sequence Data; Mutagenesis, Site-Directed; Photoreceptor Cells, Vertebrate; Proline; Protein Structure, Secondary; Retinal Pigments; Rhodopsin; Spectroscopy, Fourier Transform Infrared	2001
Disruption of the alpha5 helix of transducin impairs rhodopsin-catalyzed nucleotide exchange. Biochemistry, 2002, Jun-04, Volume: 41, Issue:22 Topics: Alanine; Amino Acid Sequence; Amino Acid Substitution; Animals; Cattle; Gene Deletion; Molecular Sequence Data; Mutagenesis; Mutagenesis, Insertional; Nucleotides; Proline; Protein Structure, Secondary; Rhodopsin; Transducin	2002
Activation of the cannabinoid CB1 receptor may involve a W6 48/F3 36 rotamer toggle switch. The journal of peptide research : official journal of the American Peptide Society, 2002, Volume: 60, Issue:6 Topics: Amino Acid Sequence; Amino Acids, Aromatic; Computer Simulation; Humans; Hydrogen Bonding; Membrane Proteins; Models, Molecular; Molecular Sequence Data; Monte Carlo Method; Mutation; Probability; Proline; Protein Structure, Secondary; Receptors, Cannabinoid; Receptors, Drug; Rhodopsin; Rotation; Thermodynamics	2002
Conserved proline residue at position 189 in cone visual pigments as a determinant of molecular properties different from rhodopsins. Biochemistry, 2002, Dec-24, Volume: 41, Issue:51 Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Avian Proteins; Cell Line; Chickens; Conserved Sequence; Epitopes; Eye Proteins; Genetic Vectors; Glycine; Humans; Isoleucine; Leucine; Mice; Proline; Retinal Cone Photoreceptor Cells; Retinal Pigments; Rhodopsin; Serine; Spectrophotometry; Thermodynamics; Valine	2002
Photoreceptor degeneration in Pro23His and S334ter transgenic rats. Advances in experimental medicine and biology, 2003, Volume: 533 Topics: Animals; Animals, Genetically Modified; Animals, Newborn; Apoptosis; Histidine; In Situ Nick-End Labeling; Mutation; Peptide Fragments; Photoreceptor Cells, Vertebrate; Proline; Rats; Retinal Degeneration; Rhodopsin; Serine	2003
Involvement of the C-terminal proline-rich motif of G protein-coupled receptor kinases in recognition of activated rhodopsin. The Journal of biological chemistry, 2004, Nov-26, Volume: 279, Issue:48 Topics: Amino Acid Motifs; Animals; beta-Adrenergic Receptor Kinases; Binding Sites; Cattle; Cyclic AMP-Dependent Protein Kinases; Eye Proteins; G-Protein-Coupled Receptor Kinase 1; G-Protein-Coupled Receptor Kinase 5; Light; Mutation; Phosphorylation; Proline; Protein Kinases; Protein Serine-Threonine Kinases; Protein Structure, Tertiary; Receptors, G-Protein-Coupled; Rhodopsin	2004
Altered light responses of single rod photoreceptors in transgenic pigs expressing P347L or P347S rhodopsin. Molecular vision, 2005, Dec-31, Volume: 11 Topics: Amino Acid Substitution; Animals; Animals, Genetically Modified; Electrophysiology; Immunohistochemistry; Kinetics; Leucine; Light; Mutation; Proline; Retinal Degeneration; Retinal Rod Photoreceptor Cells; Rhodopsin; Swine; Vision, Ocular	2005
Preferential silencing of a common dominant rhodopsin mutation does not inhibit retinal degeneration in a transgenic model. Molecular therapy : the journal of the American Society of Gene Therapy, 2006, Volume: 14, Issue:5 Topics: Alleles; Animals; Animals, Genetically Modified; Base Sequence; Dependovirus; Gene Silencing; Genetic Vectors; Mice; Models, Animal; Molecular Sequence Data; Mutation; Proline; Rats; Retinal Degeneration; Rhodopsin; RNA, Small Interfering	2006
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
A high-throughput screening method for small-molecule pharmacologic chaperones of misfolded rhodopsin. Investigative ophthalmology & visual science, 2008, Volume: 49, Issue:7 Topics: Animals; Cattle; Cell Line; Histidine; Molecular Chaperones; Molecular Weight; Mutation; Norisoprenoids; Proline; Protein Folding; Pyrazoles; Rhodopsin	2008
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
Mapping cation entry in photoreceptors and inner retinal neurons during early degeneration in the P23H-3 rat retina. Visual neuroscience, 2013, Volume: 30, Issue:3 Topics: Age Factors; Agmatine; Animals; Apoptosis; Gene Expression Regulation, Developmental; Histidine; Humans; Mutation; Nerve Tissue Proteins; Neurons; Photoreceptor Cells; Proline; Rats; Rats, Sprague-Dawley; Rats, Transgenic; Retina; Retinal Degeneration; Rhodopsin; Silver Staining	2013
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
A Conserved Proline Hinge Mediates Helix Dynamics and Activation of Rhodopsin. Structure (London, England : 1993), 2020, 09-01, Volume: 28, Issue:9 Topics: HEK293 Cells; Humans; Hydrogen Bonding; Magnetic Resonance Spectroscopy; Models, Molecular; Mutation; Proline; Protein Conformation; Rhodopsin; Spectroscopy, Fourier Transform Infrared; Tryptophan; Tyrosine	2020