| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1106476158 |
| P356 | DOI | 10.1038/S41598-018-31743-5 |
| P932 | PMC publication ID | 6127338 |
| P698 | PubMed publication ID | 30190587 |
| P2093 | author name string | Lance Lee | |
| Randolph S Faustino | |||
| Kathleen M Eyster | |||
| Claudia C Preston | |||
| Casey W McKenzie | |||
| Rozzy Finn | |||
| P2860 | cites work | BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly | Q24295491 |
| All roads lead to ATF4 | Q24299679 | ||
| Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis | Q24309344 | ||
| Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis | Q24310102 | ||
| CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium | Q24310530 | ||
| Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation | Q24319185 | ||
| Molecular basis of tubulin transport within the cilium by IFT74 and IFT81. | Q24320475 | ||
| A SNX10/V-ATPase pathway regulates ciliogenesis in vitro and in vivo | Q24322827 | ||
| Identification of a novel Wnt5a-CK1ɛ-Dvl2-Plk1-mediated primary cilia disassembly pathway | Q24323675 | ||
| The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 | Q24336477 | ||
| The centrosomal kinase Plk1 localizes to the transition zone of primary cilia and induces phosphorylation of nephrocystin-1 | Q24338335 | ||
| Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice | Q24338349 | ||
| CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base | Q24339550 | ||
| Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia | Q24635321 | ||
| Production of Basal Bodies in bulk for dense multicilia formation | Q26740651 | ||
| Genetics and biology of primary ciliary dyskinesia | Q26782119 | ||
| Primary cilia in the developing and mature brain | Q27002324 | ||
| CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies | Q27301023 | ||
| A prefoldin-associated WD-repeat protein (WDR92) is required for the correct architectural assembly of motile cilia | Q27304763 | ||
| CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice | Q27306183 | ||
| Assembly of IFT trains at the ciliary base depends on IFT74 | Q27316132 | ||
| A new mathematical model for relative quantification in real-time RT-PCR | Q27860781 | ||
| MDM1 is a microtubule-binding protein that negatively regulates centriole duplication | Q28116536 | ||
| Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease | Q28118826 | ||
| Subcommissural organ, cerebrospinal fluid circulation, and hydrocephalus | Q28204123 | ||
| Pathophysiology of congenital and neonatal hydrocephalus | Q28271225 | ||
| Neuroanatomical and behavioral deficits in mice haploinsufficient for Pericentriolar material 1 (Pcm1). | Q28505294 | ||
| Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene | Q28506396 | ||
| SDCCAG8 regulates pericentriolar material recruitment and neuronal migration in the developing cortex | Q28507239 | ||
| Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells | Q28509764 | ||
| Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome | Q28509916 | ||
| Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice | Q28512445 | ||
| Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent | Q28585523 | ||
| Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1. | Q28589174 | ||
| Hook3 interacts with PCM1 to regulate pericentriolar material assembly and the timing of neurogenesis | Q28593640 | ||
| Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells | Q28594532 | ||
| The primary cilium as a complex signaling center | Q29615254 | ||
| Hydrocephalus in children | Q30053622 | ||
| Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities | Q30389509 | ||
| Strain-specific modifier genes governing craniofacial phenotypes | Q30457692 | ||
| Centriole maturation requires regulated Plk1 activity during two consecutive cell cycles | Q30588509 | ||
| Identification of candidate susceptibility and resistance genes of mice infected with Streptococcus suis type 2 | Q34182290 | ||
| Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2 | Q34183826 | ||
| Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum | Q34215102 | ||
| Disruption of the mouse L1 gene leads to malformations of the nervous system | Q34444794 | ||
| Ciliary membrane proteins traffic through the Golgi via a Rabep1/GGA1/Arl3-dependent mechanism | Q34541792 | ||
| Microarray analysis of iris gene expression in mice with mutations influencing pigmentation | Q34646618 | ||
| FOP is a centriolar satellite protein involved in ciliogenesis | Q34648100 | ||
| Infantile hydrocephalus: a review of epidemiology, classification and causes | Q35101052 | ||
| Identification of genes with altered expression in male and female Schlager hypertensive mice. | Q35164601 | ||
| A consensus on the classification of hydrocephalus: its utility in the assessment of abnormalities of cerebrospinal fluid dynamics | Q35218195 | ||
| Association of brain immune genes with social behavior of inbred mouse strains. | Q35499613 | ||
| Systems biology surveillance decrypts pathological transcriptome remodeling | Q35693120 | ||
| Cellular damage and prevention in childhood hydrocephalus | Q35901298 | ||
| Molecular characterization of centriole assembly in ciliated epithelial cells | Q36118747 | ||
| Mouse model of Sanfilippo syndrome type B: relation of phenotypic features to background strain. | Q52552931 | ||
| Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus. | Q55365525 | ||
| Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus | Q56532554 | ||
| A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS) | Q70485039 | ||
| Association of SPARC (osteonectin, BM-40) with extracellular and intracellular components of the ciliated surface ectoderm of Xenopus embryos | Q73025519 | ||
| Early response of gene clusters is associated with mouse lung resistance or sensitivity to cigarette smoke | Q83133080 | ||
| Gene expression changes in C57BL/6J and DBA/2J mice following prenatal alcohol exposure | Q36124062 | ||
| Brain development in mice lacking L1-L1 homophilic adhesion | Q36321962 | ||
| Arf-like Protein 3 (ARL3) Regulates Protein Trafficking and Ciliogenesis in Mouse Photoreceptors. | Q36727473 | ||
| Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | Q36855297 | ||
| Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms | Q37217004 | ||
| Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease | Q37304381 | ||
| Enhanced response to pulmonary Streptococcus pneumoniae infection is associated with primary ciliary dyskinesia in mice lacking Pcdp1 and Spef2. | Q37425597 | ||
| Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics | Q37812789 | ||
| Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia | Q38107881 | ||
| Cerebrospinal fluid secretion by the choroid plexus | Q38153679 | ||
| Mechanism of ciliary disassembly. | Q38730540 | ||
| Regulation of centriolar satellite integrity and its physiology | Q38916274 | ||
| The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin | Q39074370 | ||
| Molecular and functional analysis of cadherin-based adherens junctions | Q41689344 | ||
| Flagellar radial spoke protein 3 is an A-kinase anchoring protein (AKAP). | Q42142592 | ||
| The nucleotide-binding proteins Nubp1 and Nubp2 are negative regulators of ciliogenesis. | Q42440588 | ||
| Daple Coordinates Planar Polarized Microtubule Dynamics in Ependymal Cells and Contributes to Hydrocephalus. | Q42512925 | ||
| DAZ-interacting Protein 1 (Dzip1) Phosphorylation by Polo-like Kinase 1 (Plk1) Regulates the Centriolar Satellite Localization of the BBSome Protein during the Cell Cycle | Q42804683 | ||
| PCM1 recruits Plk1 to the pericentriolar matrix to promote primary cilia disassembly before mitotic entry | Q42826397 | ||
| Centriole biogenesis in multiciliated cells | Q43997585 | ||
| Interaction between SPARC and tubulin in Xenopus | Q45025862 | ||
| Adult ependymal cells are postmitotic and are derived from radial glial cells during embryogenesis. | Q45213360 | ||
| Disruption of CDH2/N-cadherin-based adherens junctions leads to apoptosis of ependymal cells and denudation of brain ventricular walls | Q45377825 | ||
| Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development. | Q46651883 | ||
| Mutation in MPDZ causes severe congenital hydrocephalus. | Q47830125 | ||
| L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns. | Q48451285 | ||
| Strain differences of cerebral ventricles in mice: can the MRL/MpJ mouse be a model for hydrocephalus? | Q48526613 | ||
| Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus | Q48697963 | ||
| SPARC/osteonectin, an endogenous mechanism for targeting albumin to the blood-cerebrospinal fluid interface during brain development | Q48912619 | ||
| Arl3 and RP2 regulate the trafficking of ciliary tip kinesins | Q50025735 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 13370 | |
| P577 | publication date | 2018-09-06 | |
| P1433 | published in | Scientific Reports | Q2261792 |
| P1476 | title | Strain-specific differences in brain gene expression in a hydrocephalic mouse model with motile cilia dysfunction | |
| P478 | volume | 8 |
| Q92431399 | Functional loss of Ccdc1 51 leads to hydrocephalus in a mouse model of primary ciliary dyskinesia |
| Q97681288 | Genetic interaction between central pair apparatus genes CFAP221, CFAP54, and SPEF2 in mouse models of primary ciliary dyskinesia |
| Q61799289 | The year in review: progress in brain barriers and brain fluid research in 2018 |
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