Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors - Wikidata - wikimedia - TriplyDB

Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors

Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors

http://www.wikidata.org/entity/Q36117350

about

A partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticles No evidence for a genetic blueprint: The case of the "complex" mammalian photoreceptor Structural and functional relationships between photoreceptor tetraspanins and other superfamily members Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus cones Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy Quantitative Fundus Autofluorescence and Optical Coherence Tomography in PRPH2/RDS- and ABCA4-Associated Disease Exhibiting Phenotypic Overlap.Efficient non-viral ocular gene transfer with compacted DNA nanoparticles.Structure of cone photoreceptors.Ocular delivery of compacted DNA-nanoparticles does not elicit toxicity in the mouse retina Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS.Initiation of rod outer segment disc formation requires RDS.Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa.Rim formation is not a prerequisite for distribution of cone photoreceptor outer segment proteins.A 350 bp region of the proximal promoter of Rds drives cell-type specific gene expression.Deciphering the structure and function of Als2cr4 in the mouse retina.Defects in the outer limiting membrane are associated with rosette development in the Nrl-/- retina.Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS Gene therapy for PRPH2-associated ocular disease: challenges and prospects The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse.Overexpression of retinal degeneration slow (RDS) protein adversely affects rods in the rd7 model of enhanced S-cone syndrome Early-onset, slow progression of cone photoreceptor dysfunction and degeneration in CNG channel subunit CNGB3 deficiency.Rod phosphodiesterase-6 (PDE6) catalytic subunits restore cone function in a mouse model lacking cone PDE6 catalytic subunit.The tetraspanin protein peripherin-2 forms a complex with melanoregulin, a putative membrane fusion regulator SNAREs Interact with Retinal Degeneration Slow and Rod Outer Segment Membrane Protein-1 during Conventional and Unconventional Outer Segment Targeting.Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy.Endoplasmic reticulum stress-associated cone photoreceptor degeneration in cyclic nucleotide-gated channel deficiency.Effect of Rds abundance on cone outer segment morphogenesis, photoreceptor gene expression, and outer limiting membrane integrity Retinal Degeneration Slow (RDS) Glycosylation Plays a Role in Cone Function and in the Regulation of RDS·ROM-1 Protein Complex Formation.Varying the GARP2-to-RDS Ratio Leads to Defects in Rim Formation and Rod and Cone Function.Role of RDS and Rhodopsin in Cngb1-Related Retinal Degeneration.The role of Rds in outer segment morphogenesis and human retinal disease.Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina.PRPH2/RDS and ROM-1: Historical context, current views and future considerations.The B3 Subunit of the Cone Cyclic Nucleotide-gated Channel Regulates the Light Responses of Cones and Contributes to the Channel Structural Flexibility A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas.Protein sorting, targeting and trafficking in photoreceptor cells cGMP accumulation causes photoreceptor degeneration in CNG channel deficiency: evidence of cGMP cytotoxicity independently of enhanced CNG channel function.Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments Native cone photoreceptor cyclic nucleotide-gated channel is a heterotetrameric complex comprising both CNGA3 and CNGB3: a study using the cone-dominant retina of Nrl-/- mice.

P2860

Q27349737-C4D198C5-AA39-4136-A127-C4C3370D4D71 Q28080564-4F46466F-E508-4EBB-BDB1-E088D907A9EB Q28742243-7B5966A7-9822-44CA-B2B2-0445010CCA63 Q30464083-38CDAA15-9B8D-4A1C-8761-9011DFA7DE04 Q30485964-42C28C45-6F6B-42FB-BB9C-215CBAD0E5A7 Q30498337-43AB4A8C-00ED-4BC1-BF62-88DA6A43DE4F Q30652635-36CF43E8-8DA2-4AEF-9B0F-9AF4036C9427 Q33267297-800F512F-1B90-41AB-A85F-5A4EBFE340BF Q33462272-C9616D58-17DC-4B0F-8298-A02C3D17C97B Q33510137-C1681BD6-E0CA-42F4-B0C5-D13E2CA83776 Q33649255-9A2109B7-C90B-4B41-A58F-8FA9C2522D27 Q33712465-AE50204D-E7FD-42EF-BFB3-81FE36E5B3F3 Q33752902-A05271F8-1D60-48BE-A2FC-DC73689D8A04 Q33913251-EE8C2B4C-072E-4C0A-A693-58F9997AEA6D Q34119861-AC827895-5ADF-4B14-8B6A-6D273D95425E Q34135553-9761D792-3171-4276-8579-F2A01E1C9CF5 Q34199858-8A11FE17-3DA8-4FBD-BCDE-310CC66AF07B Q34341141-82D63EEA-C42E-464D-9701-28F61F78E1B3 Q34400262-C4950DF2-677F-4E5B-B6BF-C3DF4F290226 Q34463210-0C33AFC7-F1F6-4E63-BA5C-466670C2BEE7 Q34708558-318B9960-4EF1-4CFE-BAAB-8680B7E8D0C3 Q35027626-012A0657-2394-458F-A02C-358168C170F6 Q35311820-12CB9D96-2FCF-4078-9D79-5ABE85282AB2 Q35754832-3ACEE117-FBE8-48C3-AE74-18547237BA60 Q35788032-F095EDC6-AD05-432C-BA5B-C34BB76C1A53 Q35957421-DAB3016F-F3AB-4EFF-9CBC-CCA100B88093 Q36002797-DD852755-9DE9-42A5-A60A-8919A5089DA8 Q36130673-6E82D18B-635E-43C9-8C7E-7B4A45140698 Q36282945-DACB8A0B-8F5E-46D9-96F7-37ECEF79AD7A Q36425001-89CE2E40-3F11-4F75-827F-998B032B8E20 Q36648914-1B77CF53-7591-4B79-847B-7604102B81D7 Q36674594-E91CE37A-0B05-4F9B-A391-C1C51537A248 Q36676811-F56E0490-0F0F-4AE2-A2D8-2BE142FC1D19 Q36829127-745C0C47-AA92-487E-B093-638F4756B0B2 Q36884703-83929361-5214-4543-A69C-0D2C3F6A4DF5 Q37012902-B580EB9C-9211-40A3-A826-CBA64A709748 Q37138123-EC35A27A-725D-4608-A139-7B16E46765E5 Q37165487-3A53C5B3-4B0F-455C-AC62-B7A877031BEC Q37307190-95C1D5FE-EB8B-40BE-8CC1-4089284CE709 Q37372752-D235F867-6245-45F7-B9CB-20C2698D0C36

P2860

Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors

http://www.wikidata.org/entity/Q36117350

description

2006 nî lūn-bûn

@nan

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

2006年论文

@zh

2006年论文

@zh-cn

name

Retention of function without ...... one but not rod photoreceptors

@ast

Retention of function without ...... one but not rod photoreceptors

@en

type

label

Retention of function without ...... one but not rod photoreceptors

@ast

Retention of function without ...... one but not rod photoreceptors

@en

prefLabel

Retention of function without ...... one but not rod photoreceptors

@ast

Retention of function without ...... one but not rod photoreceptors

@en

P1433

Q36117350-9A2735B2-92BC-41CF-93BF-2195E0A086F7

P1476

Q36117350-65BDFDD1-E3A0-40D3-8C20-9949BD092CF6

P2093

Q36117350-493BCB12-4D51-46B8-A9FC-C4F924C20337

Q36117350-749480E3-1472-4577-8FFA-7C092CF9F7D3

Q36117350-9F877AD5-3C39-4105-81AE-47198C9CE5EB

Q36117350-DA74BFD7-0620-49DE-B53A-C558D3EBDDAE

Q36117350-E9C70CF5-4B6A-4880-AB18-17485E5EE14F

Q36117350-FB6F816C-40FF-4560-90AD-EC43A3304CB7

Q36117350-FDB9FF7B-555A-4E3E-A8B0-3B3E91912C7B

P2860

Q36117350-0681DD3B-C2B8-48D7-AC41-21EE7145A27D

Q36117350-0F48EDB9-C7B3-4563-9DCF-4D1B24A83BA4

Q36117350-4D10B14A-178A-473A-8D16-C6A1831BC485

Q36117350-4FF49DC8-7896-49FF-BBD3-4443B78919D8

Q36117350-6173FF4C-F23A-4E19-A614-D0722BED60DB

Q36117350-61D6D7DC-68A2-4EB7-93CA-E18FB2FAC989

Q36117350-61E6B973-C077-4090-8F39-461BA5C7EBB1

Q36117350-68651882-402A-4E3B-BA63-A7C26F16CA3C

Q36117350-6CA0D69E-A044-4F90-943A-B8C70921FAEE

Q36117350-6DF13A32-16CE-420D-9C82-44BA168570B9

P304

Q36117350-BB9214F1-200F-4EB8-814B-3FFAC7419476

P31

Q36117350-E7AE3C2C-6B79-43FC-9731-67177B4A2CF2

P356

Q36117350-E50FE114-71A3-4116-90F0-76405030139B

P407

Q36117350-93D2E1B5-4A4F-4D30-85C9-A93E5D746C0B

P433

Q36117350-CFF0B73F-4F4C-4F06-AE84-5F10D8AC1551

P478

Q36117350-663D94BB-F863-4705-93DF-CFF0117E1DB9

P577

Q36117350-0CC5EF69-E366-471B-9F2B-FDACE2847980

P5875

Q36117350-8EF2B112-0FCA-4373-AA58-95A146F48B04

P698

Q36117350-749B3721-3CCC-40D3-8549-0474547F3890

P921

Q36117350-7CCFC328-405C-4243-ADD1-DA56A34CBC97

Q36117350-BE16DF7F-727A-414E-87AF-5478FED3D3A4

P932

Q36117350-7E9E70D3-A226-461A-B2DA-405BEB2622A8

P356

P1433

Journal of Cell Biology

P1476

Retention of function without ...... one but not rod photoreceptors

@en

P2093

Alexander B Quiambao

http://www.w3.org/2001/XMLSchema#string

Barbara A Nagel

http://www.w3.org/2001/XMLSchema#string

Jeff S Skaggs

http://www.w3.org/2001/XMLSchema#string

Muna I Naash

http://www.w3.org/2001/XMLSchema#string

Rafal Farjo

http://www.w3.org/2001/XMLSchema#string

Steven J Fliesler

http://www.w3.org/2001/XMLSchema#string

Zack A Nash

http://www.w3.org/2001/XMLSchema#string

P2860

Photoreceptor renewal: a role for peripherin/rds

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl

Nrl is required for rod photoreceptor development

Photoreceptor renewal: A role for peripherin/rds

Molecular characterization and expression of the (Na+ + K+)-ATPase alpha-subunit in Drosophila melanogaster.

Retinitis pigmentosa: defined from a molecular point of view.

Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression.

Uncoupling of photoreceptor peripherin/rds fusogenic activity from biosynthesis, subunit assembly, and targeting: a potential mechanism for pathogenic effects.

Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane.

P304

59-68

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1083/JCB.200509036

http://www.w3.org/2001/XMLSchema#string

P407

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

173

http://www.w3.org/2001/XMLSchema#string

P577

2006-04-03T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

7195296

http://www.w3.org/2001/XMLSchema#string

P698

16585269

http://www.w3.org/2001/XMLSchema#string

P921

Photoreceptor protein

P932

2063789

http://www.w3.org/2001/XMLSchema#string