| scholarly article | Q13442814 |
| P50 | author | Diane C Slusarski | Q55127328 |
| Val C. Sheffield | Q61268600 | ||
| P2093 | author name string | Qihong Zhang | |
| Xue Mei | |||
| Alexander G Bassuk | |||
| Trudi A Westfall | |||
| P2860 | cites work | BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly | Q24295491 |
| Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes | Q24298940 | ||
| Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function | Q24300539 | ||
| A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome | Q24310789 | ||
| A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis | Q24311615 | ||
| Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSome | Q24313282 | ||
| BBS mutations modify phenotypic expression of CEP290-related ciliopathies | Q24317466 | ||
| A BBSome subunit links ciliogenesis, microtubule stability, and acetylation | Q24336047 | ||
| The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia | Q24337528 | ||
| Arf, Arl, Arp and Sar proteins: a family of GTP-binding proteins with a structural device for 'front-back' communication | Q24538810 | ||
| Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform | Q27347938 | ||
| Stages of embryonic development of the zebrafish | Q27860947 | ||
| Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome | Q27919661 | ||
| Direct interactions of intraflagellar transport complex B proteins IFT88, IFT52, and IFT46. | Q27967676 | ||
| Ciliogenesis: building the cell's antenna | Q28000047 | ||
| The roles of evolutionarily conserved functional modules in cilia-related trafficking | Q28000150 | ||
| Diego and Prickle regulate Frizzled planar cell polarity signalling by competing for Dishevelled binding | Q28254777 | ||
| Nuclear localization of Prickle2 is required to establish cell polarity during early mouse embryogenesis | Q28259767 | ||
| IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome | Q28307163 | ||
| Planar cell polarity effector gene Fuzzy regulates cilia formation and Hedgehog signal transduction in mouse | Q28505727 | ||
| Wnt5a functions in planar cell polarity regulation in mice | Q28505898 | ||
| Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates | Q28506652 | ||
| Regulation of polarized extension and planar cell polarity in the cochlea by the vertebrate PCP pathway | Q28509023 | ||
| Dishevelled stabilization by the ciliopathy protein Rpgrip1l is essential for planar cell polarity | Q28511174 | ||
| Complex interactions between genes controlling trafficking in primary cilia | Q28512423 | ||
| Ciliary proteins link basal body polarization to planar cell polarity regulation | Q28585995 | ||
| Identification of Vangl2 and Scrb1 as planar polarity genes in mammals | Q28593071 | ||
| The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells | Q28593180 | ||
| Prickle mediates feedback amplification to generate asymmetric planar cell polarity signaling | Q28613827 | ||
| The primary cilium as the cell's antenna: signaling at a sensory organelle | Q29615165 | ||
| Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos | Q29616784 | ||
| Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response | Q29617051 | ||
| Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells | Q30491381 | ||
| The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindness. | Q30499095 | ||
| Prickle1b mediates interpretation of migratory cues during zebrafish facial branchiomotor neuron migration | Q30499504 | ||
| Mechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesis | Q30539146 | ||
| Efficient disruption of Zebrafish genes using a Gal4-containing gene trap | Q30558499 | ||
| Planar cell polarity enables posterior localization of nodal cilia and left-right axis determination during mouse and Xenopus embryogenesis. | Q30977459 | ||
| Regulation of convergence and extension movements during vertebrate gastrulation by the Wnt/PCP pathway | Q33552598 | ||
| Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning | Q33979104 | ||
| Wnt5b-Ryk pathway provides directional signals to regulate gastrulation movement. | Q34092446 | ||
| Mutations in prickle orthologs cause seizures in flies, mice, and humans | Q34560912 | ||
| The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome | Q34679496 | ||
| Zebrafish Prickle1b mediates facial branchiomotor neuron migration via a farnesylation-dependent nuclear activity | Q34856050 | ||
| Stages of ciliogenesis and regulation of ciliary length | Q35718497 | ||
| Prickle and Strabismus form a functional complex to generate a correct axis during planar cell polarity signaling | Q36065784 | ||
| Cooperation of polarized cell intercalations drives convergence and extension of presomitic mesoderm during zebrafish gastrulation | Q36404910 | ||
| Cilia: tuning in to the cell's antenna. | Q36557175 | ||
| Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport. | Q36565794 | ||
| Lethal giant larvae 2 regulates development of the ciliated organ Kupffer's vesicle | Q36682973 | ||
| BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking | Q36920886 | ||
| Dampened Hedgehog signaling but normal Wnt signaling in zebrafish without cilia | Q37314322 | ||
| Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity | Q37321035 | ||
| Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18) | Q37664307 | ||
| Assembly of synaptic laminae by axon guidance molecules | Q38013307 | ||
| Analysis of upstream elements in the HuC promoter leads to the establishment of transgenic zebrafish with fluorescent neurons | Q38306861 | ||
| Ascidian prickle regulates both mediolateral and anterior-posterior cell polarity of notochord cells | Q38330834 | ||
| Prickle 1 regulates cell movements during gastrulation and neuronal migration in zebrafish | Q38352359 | ||
| Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements. | Q38520593 | ||
| A pair of siblings with adiposo-genital dystrophy. 1922. | Q38531638 | ||
| On congenital obesity syndrome with polydactyly and retinitis pigmentosa (a contribution to the study of clinical forms of hypophyseal obesity). 1920. | Q38531644 | ||
| Wnt/PCP proteins regulate stereotyped axon branch extension in Drosophila. | Q39634119 | ||
| The prickle-related gene in vertebrates is essential for gastrulation cell movements | Q39750801 | ||
| The PCP effector Fuzzy controls cilial assembly and signaling by recruiting Rab8 and Dishevelled to the primary cilium | Q42016672 | ||
| Planar polarization of node cells determines the rotational axis of node cilia. | Q42466284 | ||
| Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left-right asymmetry in zebrafish. | Q42474570 | ||
| Requirement for intracellular calcium modulation in zebrafish dorsal-ventral patterning | Q44519129 | ||
| IFT88 plays a cilia- and PCP-independent role in controlling oriented cell divisions during vertebrate embryonic development | Q44809853 | ||
| Ptk7 promotes non-canonical Wnt/PCP-mediated morphogenesis and inhibits Wnt/β-catenin-dependent cell fate decisions during vertebrate development. | Q45237763 | ||
| Planar cell polarity signalling regulates cell adhesion properties in progenitors of the zebrafish laterality organ | Q47073220 | ||
| The zebrafish young mutation acts non-cell-autonomously to uncouple differentiation from specification for all retinal cells | Q47073363 | ||
| Vangl2 directs the posterior tilting and asymmetric localization of motile primary cilia. | Q47073501 | ||
| Calcium fluxes in dorsal forerunner cells antagonize beta-catenin and alter left-right patterning. | Q51971085 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Intraflagellar transport 122 homolog (Chlamydomonas) | Q29827053 |
| P304 | page(s) | 245-255 | |
| P577 | publication date | 2014-06-02 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | Functional characterization of Prickle2 and BBS7 identify overlapping phenotypes yet distinct mechanisms | |
| P478 | volume | 392 |
| Q90564770 | Bardet-Biedl Syndrome in rhesus macaques: A nonhuman primate model of retinitis pigmentosa |
| Q53826883 | High-throughput behavioral assay to investigate seizure sensitivity in zebrafish implicates ZFHX3 in epilepsy. |
| Q37368007 | Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21) |
| Q41327287 | Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. |
| Q36785209 | Prickle3 synergizes with Wtip to regulate basal body organization and cilia growth. |
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