Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.
about
A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescenceThe dynamic cilium in human diseasesBBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assemblyA novel protein LZTFL1 regulates ciliary trafficking of the BBSome and SmoothenedBardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypesBardet-Biedl syndrome proteins 1 and 3 regulate the ciliary trafficking of polycystic kidney disease 1 proteinCharacterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndromeBardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionBBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesSpata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retinaIntrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSomeThe Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formationRequirement of Bardet-Biedl syndrome proteins for leptin receptor signalingLoss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epitheliaCiliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)The blind leading the obese: the molecular pathophysiology of a human obesity syndromeImpaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndromeIn-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouseLoss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and functionMechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors.Specialized Cilia in Mammalian Sensory SystemsThe role of primary cilia in the development and disease of the retinaCilia in vertebrate development and diseaseSmelling the roses and seeing the light: gene therapy for ciliopathiesWnt and planar cell polarity signaling in cystic renal diseaseAcute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypesIqcg is essential for sperm flagellum formation in miceMutations in a guanylate cyclase GCY-35/GCY-36 modify Bardet-Biedl syndrome-associated phenotypes in Caenorhabditis elegansIdentification and functional analysis of the vision-specific BBS3 (ARL6) long isoformMouse models of ciliopathies: the state of the art.The nonmotile ciliopathies.The BBSome controls IFT assembly and turnaround in cilia.CP110 and its network of partners coordinately regulate cilia assembly.Biology and therapy of inherited retinal degenerative disease: insights from mouse modelsA novel H395R mutation in MKKS/BBS6 causes retinitis pigmentosa and polydactyly without other findings of Bardet-Biedl or McKusick-Kaufman syndromeCilia and developmental signalingLeptin resistance is a secondary consequence of the obesity in ciliopathy mutant miceDisruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesBardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia
P2860
Q21092494-AD85FCD0-0A0D-4ACA-B4FB-E3AF28C8DDDBQ21202039-3254B839-3F8D-415F-85E4-BB91F5F3D33FQ24295491-69667F62-E504-47CC-99B9-5E1B8DAE2E9AQ24296671-9498709E-082E-4514-8639-B75C325975E3Q24298940-88121722-D6F6-43B3-8A3A-2B426C12DCC8Q24299480-6A80B0E8-D453-4001-AF4D-09F8208F73D1Q24299600-CBE36031-7DF1-4D18-BB53-E5BC821A893FQ24300539-67CB898C-BE44-4539-839F-D6E17381ED35Q24301377-5F81445A-48C4-41BF-BFBE-3759A43578CEQ24306695-D343DE17-D41B-42AC-B323-203BE2966FA4Q24313282-CCDE7F45-55E8-4238-BB05-FE6CC1B732B8Q24316483-E57C8BB6-62F3-4873-B6CC-DB80457022E0Q24317488-76C0F8C2-746F-46F6-9146-FC305F29F51FQ24317556-E932F11D-A3C9-4151-8C2B-C650CD666701Q24337720-F7372A7D-39F6-4F3C-9287-3617BFDD5C60Q24546392-00DE5282-ED09-4EEC-B1E4-B71A61C7F188Q24595694-04CA4F26-0F1B-42BF-BB1C-D2D69FE15EECQ24652543-4D616F49-EACD-4373-A408-EE43EC32E77EQ24671808-B5DA4960-DC4D-493B-B788-35E2384CAC59Q24678735-E6CE7A84-8D67-42E8-A303-C2E791431142Q24682888-EF87F0B2-7C18-43A5-ABA3-A7ECBC533ACAQ26785912-417E476B-D6AF-48E2-97EC-61E5DB83EB04Q26822720-34D10D3B-3D11-4102-A03A-D9F7385CDDCFQ26829114-51270E38-1B57-4470-A7C9-B73F0A68018CQ26829936-83DF3FD5-6BF0-4849-9426-3134712519CAQ26999700-6F24597C-56E0-43A8-B58A-3A2D743CF48AQ27319882-3572E538-FAE5-40FB-A355-1438F22948C8Q27330274-8268D76C-BABC-4B5E-8345-C51CB2B61C83Q27335893-473C476C-8E37-4C04-B752-E24098547C9FQ27347938-E29721E5-EA51-4F60-A27B-EB780F87D137Q27692039-422CB38C-9735-45A8-B211-7DE8478F5DB8Q27967648-E709405D-D546-401B-802A-C05441F4D638Q28000109-C8141C53-273A-430F-84CB-BC99138AC4EEQ28000138-6CC79C94-0DBF-46EE-BB92-8CFC396D3017Q28084726-A216424F-1FD4-4F3A-B728-A37EFE779BF8Q28116066-B66342B1-3C79-446B-A729-6FC677E081A5Q28302606-B767EA06-C714-4D0C-BFCA-35585D4873FCQ28504740-42B9246A-ADF6-4CCF-B13A-A51894703DE0Q28506652-1EA7A822-D186-40D6-A79A-26D24B0EC02CQ28506905-D39138DD-C22C-4CD7-8C57-8307DAF760C2
P2860
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.
description
2004 nî lūn-bûn
@nan
2004 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Bbs2-null mice have neurosenso ...... h mislocalization of rhodopsin
@nl
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@ast
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@en
type
label
Bbs2-null mice have neurosenso ...... h mislocalization of rhodopsin
@nl
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@ast
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@en
prefLabel
Bbs2-null mice have neurosenso ...... h mislocalization of rhodopsin
@nl
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@ast
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@en
P2093
P2860
P50
P3181
P356
P1476
Bbs2-null mice have neurosenso ...... mislocalization of rhodopsin.
@en
P2093
Baoli Yang
Charles Searby
Darryl Y Nishimura
Jeaneen L Andorf
Michael Andrews
Rivka Carmi
Roger Davis
Ruth E Swiderski
Val C Sheffield
P2860
P304
16588-16593
P3181
P356
10.1073/PNAS.0405496101
P407
P577
2004-11-11T00:00:00Z