Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.
about
Cytoplasmic dynein regulation by subunit heterogeneity and its role in apical transportMutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosaIdentification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration CA dual role for EDEM1 in the processing of rod opsinAlternative RNA splicing of the human endothelin-A receptor generates multiple transcriptsStructural and functional impairment of endocytic pathways by retinitis pigmentosa mutant rhodopsin-arrestin complexesGenetic heterogeneity among blue-cone monochromatsFine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17pBinding-, intracellular transport-, and biosynthesis-defective mutants of vasopressin type 2 receptor in patients with X-linked nephrogenic diabetes insipidusInterconversion of red opsin isoforms by the cyclophilin-related chaperone protein Ran-binding protein 2Pharmacoperones: a new therapeutic approach for diseases caused by misfolded G protein-coupled receptorsInactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in DrosophilaThe roles of evolutionarily conserved functional modules in cilia-related trafficking.Export from the endoplasmic reticulum represents the limiting step in the maturation and cell surface expression of the human delta opioid receptorThe chaperone environment at the cytoplasmic face of the endoplasmic reticulum can modulate rhodopsin processing and inclusion formationA novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defectAHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisisLocalization of Tctex-1, a cytoplasmic dynein light chain, to the Golgi apparatus and evidence for dynein complex heterogeneityEvolution of mammalian Opn5 as a specialized UV-absorbing pigment by a single amino acid mutationThe effects of IRE1, ATF6, and PERK signaling on adRP-linked rhodopsinsDifferential light-induced responses in sectorial inherited retinal degeneration.Rhodopsin: the functional significance of asn-linked glycosylation and other post-translational modificationsIdentification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinRestoration of the majority of the visual spectrum by using modified Volvox channelrhodopsin-1.Functional rescue of the nephrogenic diabetes insipidus-causing vasopressin V2 receptor mutants G185C and R202C by a second site suppressor mutation.Transport of truncated rhodopsin and its effects on rod function and degeneration.Q344ter mutation causes mislocalization of rhodopsin molecules that are catalytically active: a mouse model of Q344ter-induced retinal degeneration.Adaptive optics retinal imaging: emerging clinical applications.Human herpesvirus 6 open reading frame U12 encodes a functional beta-chemokine receptor.Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice.Blocking transcription of the human rhodopsin gene by triplex-mediated DNA photocrosslinkingSite-directed mutagenesis of highly conserved amino acids in the first cytoplasmic loop of Drosophila Rh1 opsin blocks rhodopsin synthesis in the nascent stateAbnormalities in G protein-coupled signal transduction pathways in human disease.Specificity in intracellular protein aggregation and inclusion body formation.Calpain and PARP activation during photoreceptor cell death in P23H and S334ter rhodopsin mutant ratsXenopus laevis P23H rhodopsin transgene causes rod photoreceptor degeneration that is more severe in the ventral retina and is modulated by light.Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosaGene augmentation for adRP mutations in RHO.Electrostatic compensation restores trafficking of the autosomal recessive retinitis pigmentosa E150K opsin mutant to the plasma membrane.Time-resolved rhodopsin activation currents in a unicellular expression system.
P2860
Q24291366-50E25E18-446F-411D-A2B9-ED957BC8B84CQ24303572-2F86C70F-ABEE-4031-BF99-10D5D88E77E0Q24317208-C95F7E57-11BB-41D5-925A-E4567366EAFDQ24320047-98509252-7FC8-40DC-A257-AE3F764BACFBQ24324601-403C4FE6-5E43-4CD7-BB67-E9B63DF0823DQ24563320-4F033B82-4D03-443A-B3EE-214AB35FB236Q24671042-D950BBBD-EE1B-4227-8D34-F5CCFD2EB0E8Q24671325-BA1A9394-254F-4BCB-B01C-F1B392CAE302Q24678213-104D9387-4F7B-4C55-B72E-DC03E1A9644DQ24683146-7BE3D6DE-A566-42D1-BE76-AC226A49D724Q26992276-32291DAA-E851-42E0-A5BF-8A180880F61DQ27346679-ED0236CF-30D6-4211-8836-A4201573B050Q28000150-67CA84CA-6C46-4B68-A688-1A227CDC2F75Q28115723-ACA04FDF-216D-47DB-AA84-11237D74F90EQ28117679-31F04477-AE73-4C0E-A360-456C2B54F0E3Q28262688-C9B79DA0-52CA-4320-8EF4-99F960045083Q28509528-1447E816-FBCF-41CB-BFFE-CB7BF0184E4BQ28511577-D510DC43-57D8-4692-864D-405F295BE67FQ28584729-2FE4B396-878B-47B6-B6F7-5B52AB42DC92Q28820980-53874387-B346-4F08-A884-459B4058625FQ30368295-C6C430AC-4187-4608-8835-BBE5A92E6DA3Q30382885-AA1ABDEF-2A28-493F-AE15-A679C80466BFQ30445562-570DE087-5DEB-447B-BCEE-3BFB3FF8DB80Q30650951-E612C9A1-DEE4-4816-A05A-7A3C0D17E003Q31695973-3EE2718D-AC51-4C7F-B097-CECA140CA512Q33285745-03996C8D-FAD6-4853-9BC5-D1D1BF0F2231Q33598499-9A0AF3E6-9DF1-4BA2-A1AA-7E2283EC3ADFQ33740576-57C06D9E-B1BB-428C-AA0C-A5CF293173ADQ33785746-40407AC4-85E7-41AB-AFFE-8BED892E074BQ33825000-FEEAD27B-959F-475F-ABD2-4F6F9BC876BCQ33825913-D8FB08FF-A409-447E-ADE7-889021E02A68Q33886329-02FEE998-EF4D-4048-95D7-350D1FCB8F07Q33900844-685B36F7-A518-4281-AF52-A3EB2030B27FQ33949081-706DD27D-31B3-4CDE-AD9F-5FBA33D4C9F2Q33963936-F0BF4FE3-AA24-4E66-BF38-7CC4CDC2765EQ34024392-38B51AD6-EE36-4A1F-99F4-710E21A4F008Q34029081-4B197073-804A-40C4-BCCE-AC192C586540Q34083185-F4DE826D-A8AD-4905-88D4-AF9F6D15FB75Q34121624-845A66AB-4BC1-402D-8446-12B70D353FF8Q34171251-6E0AD0CF-5C20-4014-B70D-95FA3C98DB28
P2860
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.
description
1991 nî lūn-bûn
@nan
1991 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@ast
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@en
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@nl
type
label
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@ast
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@en
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@nl
prefLabel
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@ast
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@en
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@nl
P2093
P2860
P356
P1476
Functional heterogeneity of mu ...... dominant retinitis pigmentosa.
@en
P2093
B G Schneider
D S Papermaster
P2860
P304
P356
10.1073/PNAS.88.19.8840
P407
P577
1991-10-01T00:00:00Z