Papers associated with cilium (and tuba4b)

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	INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex., Mascibroda LG., Nat Commun. October 13, 2022; 13 (1): 6054.
	Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):
	Xenopus epidermal and endodermal epithelia as models for mucociliary epithelial evolution, disease, and metaplasia., Walentek P., Genesis. February 1, 2021; 59 (1-2): e23406.
	Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.
	Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
	The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos., Willsey HR., Development. June 22, 2020; 147 (21):
	The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1., Ott T., Front Physiol. January 1, 2019; 10 134.
	A liquid-like organelle at the root of motile ciliopathy., Huizar RL., Elife. December 18, 2018; 7
	WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS., Development. November 28, 2018; 145 (23):
	CDC20B is required for deuterosome-mediated centriole production in multiciliated cells., Revinski DR., Nat Commun. November 7, 2018; 9 (1): 4668.
	Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos., Willsey HR., Dev Biol. October 15, 2018; 442 (2): 276-287.
	The small molecule AMBMP disrupts microtubule growth, ciliogenesis, cell polarity, and cell migration., Werner M., Cytoskeleton (Hoboken). October 1, 2018; 75 (10): 450-457.
	WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation., Kulkarni SS., Dev Cell. September 10, 2018; 46 (5): 595-610.e3.
	A Conserved Role of the Unconventional Myosin 1d in Laterality Determination., Tingler M., Curr Biol. March 5, 2018; 28 (5): 810-816.e3.
	Xenopus: An alternative model system for identifying muco-active agents., Sim HJ., PLoS One. February 14, 2018; 13 (2): e0193310.
	Manipulating and Analyzing Cell Type Composition of the Xenopus Mucociliary Epidermis., Walentek P., Methods Mol Biol. January 1, 2018; 1865 251-263.
	Candidate Heterotaxy Gene FGFR4 Is Essential for Patterning of the Left-Right Organizer in Xenopus., Sempou E., Front Physiol. January 1, 2018; 9 1705.
	Evolutionary Proteomics Uncovers Ancient Associations of Cilia with Signaling Pathways., Sigg MA., Dev Cell. December 18, 2017; 43 (6): 744-762.e11.
	hmmr mediates anterior neural tube closure and morphogenesis in the frog Xenopus., Prager A., Dev Biol. October 1, 2017; 430 (1): 188-201.
	The role of nitric oxide during embryonic epidermis development of Xenopus laevis., Tomankova S., Biol Open. June 15, 2017; 6 (6): 862-871.
	Rfx2 Stabilizes Foxj1 Binding at Chromatin Loops to Enable Multiciliated Cell Gene Expression., Quigley IK., PLoS Genet. January 19, 2017; 13 (1): e1006538.
	RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells., Sedzinski J., J Cell Sci. January 15, 2017; 130 (2): 420-428.
	What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia., Walentek P., Genesis. January 1, 2017; 55 (1-2):
	La-related protein 6 controls ciliated cell differentiation., Manojlovic Z., Cilia. January 1, 2017; 6 4.
	Foxn4 promotes gene expression required for the formation of multiple motile cilia., Campbell EP., Development. December 15, 2016; 143 (24): 4654-4664.
	Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia., Del Viso F., Dev Cell. September 12, 2016; 38 (5): 478-92.
	The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery., Toriyama M., Nat Genet. June 1, 2016; 48 (6): 648-56.
	Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.
	Basal bodies in Xenopus., Zhang S., Cilia. February 3, 2016; 5 2.
	Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program., Zhou F., Curr Biol. December 21, 2015; 25 (24): 3267-73.
	ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia., Walentek P., Dev Biol. December 15, 2015; 408 (2): 292-304.
	TGF-β Signaling Regulates the Differentiation of Motile Cilia., Tözser J., Cell Rep. May 19, 2015; 11 (7): 1000-7.
	ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles., Walentek P., Data Brief. April 20, 2015; 4 22-31.
	The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin., Epting D., Development. January 1, 2015; 142 (1): 174-84.
	miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110., Song R., Nature. June 5, 2014; 510 (7503): 115-20.
	RFX7 is required for the formation of cilia in the neural tube., Manojlovic Z., Mech Dev. May 1, 2014; 132 28-37.
	A novel serotonin-secreting cell type regulates ciliary motility in the mucociliary epidermis of Xenopus tadpoles., Walentek P., Development. April 1, 2014; 141 (7): 1526-33.
	Coordinated genomic control of ciliogenesis and cell movement by RFX2., Chung MI., Elife. January 1, 2014; 3 e01439.
	Stabilization of speckle-type POZ protein (Spop) by Daz interacting protein 1 (Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling., Schwend T., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	Plakophilin-3 is required for late embryonic amphibian development, exhibiting roles in ectodermal and neural tissues., Munoz WA., PLoS One. January 1, 2012; 7 (4): e34342.
	IP3 signaling is required for cilia formation and left-right body axis determination in Xenopus embryos., Hatayama M., Biochem Biophys Res Commun. July 8, 2011; 410 (3): 520-4.
	Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease., Dubaissi E., Dis Model Mech. March 1, 2011; 4 (2): 179-92.
	Specification of ion transport cells in the Xenopus larval skin., Quigley IK., Development. February 1, 2011; 138 (4): 705-14.
	A highly conserved Poc1 protein characterized in embryos of the hydrozoan Clytia hemisphaerica: localization and functional studies., Fourrage C., PLoS One. November 16, 2010; 5 (11): e13994.
	The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation., Dammermann A., Genes Dev. September 1, 2009; 23 (17): 2046-59.
	Localization of Kv2.2 protein in Xenopus laevis embryos and tadpoles., Gravagna NG., J Comp Neurol. October 10, 2008; 510 (5): 508-24.
	Calcium fluxes in dorsal forerunner cells antagonize beta-catenin and alter left-right patterning., Schneider I., Development. January 1, 2008; 135 (1): 75-84.
	PAR1 specifies ciliated cells in vertebrate ectoderm downstream of aPKC., Ossipova O., Development. December 1, 2007; 134 (23): 4297-306.
	Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros., Tran U., Dev Biol. July 1, 2007; 307 (1): 152-64.

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