Papers associated with ciliated cell

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	The histone H4K20 methyltransferase SUV4-20H1/KMT5B is required for multiciliated cell differentiation in Xenopus., Angerilli A., Life Sci Alliance. July 1, 2023; 6 (7):
	Kif9 is an active kinesin motor required for ciliary beating and proximodistal patterning of motile axonemes., Konjikusic MJ., J Cell Sci. March 1, 2023; 136 (5):
	Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo., Ventura G., Nat Commun. October 28, 2022; 13 (1): 6423.
	GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base., Jang DG., Elife. August 25, 2022; 11
	Development of a multiciliated cell., Mahjoub MR., Curr Opin Cell Biol. August 1, 2022; 77 102105.
	Evo-Devo of Urbilateria and its larval forms., De Robertis EM., Dev Biol. July 1, 2022; 487 10-20.
	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):
	Male infertility-associated Ccdc108 regulates multiciliogenesis via the intraflagellar transport machinery., Zhao H., EMBO Rep. April 5, 2022; 23 (4): e52775.
	Lrrcc1 and Ccdc61 are conserved effectors of multiciliated cell function., Nommick A., J Cell Sci. February 15, 2022; 135 (4):
	PCD Genes-From Patients to Model Organisms and Back to Humans., Niziolek M., Int J Mol Sci. February 3, 2022; 23 (3):
	CEP97 phosphorylation by Dyrk1a is critical for centriole separation during multiciliogenesis., Lee M., J Cell Biol. January 3, 2022; 221 (1):
	Signaling Control of Mucociliary Epithelia: Stem Cells, Cell Fates, and the Plasticity of Cell Identity in Development and Disease., Walentek P., Cells Tissues Organs. January 1, 2022; 211 (6): 736-753.
	Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates., Szenker-Ravi E., Nat Genet. January 1, 2022; 54 (1): 62-72.
	dmrt2 and myf5 Link Early Somitogenesis to Left-Right Axis Determination in Xenopus laevis., Tingler M., Front Cell Dev Biol. January 1, 2022; 10 858272.
	Fluid Mechanics of Mosaic Ciliated Tissues., Boselli F., Phys Rev Lett. November 5, 2021; 127 (19): 198102.
	Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
	Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. September 20, 2021; 15 722374.
	Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5., Maerker M., Nat Commun. September 16, 2021; 12 (1): 5482.
	Tubulin acetylation promotes penetrative capacity of cells undergoing radial intercalation., Collins C., Cell Rep. August 17, 2021; 36 (7): 109556.
	A polycystin-2 protein with modified channel properties leads to an increased diameter of renal tubules and to renal cysts., Grosch M., J Cell Sci. August 15, 2021; 134 (16):
	Axon terminals control endolysosome diffusion to support synaptic remodelling., Terni B., Life Sci Alliance. July 5, 2021; 4 (8):
	DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J., J Med Genet. July 1, 2021; 58 (7): 453-464.
	Ciliogenesis and autophagy are coordinately regulated by EphA2 in the cornea to maintain proper epithelial architecture., Kaplan N., Ocul Surf. July 1, 2021; 21 193-205.
	Mechanical stretch scales centriole number to apical area via Piezo1 in multiciliated cells., Kulkarni S., Elife. June 29, 2021; 10
	The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus., Beckers A., Sci Rep. June 25, 2021; 11 (1): 13333.
	RNA demethylation by FTO stabilizes the FOXJ1 mRNA for proper motile ciliogenesis., Kim H., Dev Cell. April 19, 2021; 56 (8): 1118-1130.e6.
	The GARP Domain of the Rod CNG Channel's β1-Subunit Contains Distinct Sites for Outer Segment Targeting and Connecting to the Photoreceptor Disk Rim., Pearring JN., J Neurosci. April 7, 2021; 41 (14): 3094-3104.
	A cellular platform for the development of synthetic living machines., Blackiston D., Sci Robot. March 31, 2021; 6 (52):
	A role for Cep70 in centriole amplification in multiciliated cells., Kim SK., Dev Biol. March 1, 2021; 471 10-17.
	Notch signaling induces either apoptosis or cell fate change in multiciliated cells during mucociliary tissue remodeling., Tasca A., Dev Cell. February 22, 2021; 56 (4): 525-539.e6.
	A not-so-simple twist of fate., Long AF., Dev Cell. February 22, 2021; 56 (4): 402-404.
	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.
	Xenopus to the rescue: A model to validate and characterize candidate ciliopathy genes., Rao VG., Genesis. February 1, 2021; 59 (1-2): e23414.
	The molecular dynamics of subdistal appendages in multi-ciliated cells., Ryu H., Nat Commun. January 27, 2021; 12 (1): 612.
	Neural tube closure requires the endocytic receptor Lrp2 and its functional interaction with intracellular scaffolds., Kowalczyk I., Development. January 26, 2021; 148 (2):
	Distinct roles for prominin-1 and photoreceptor cadherin in outer segment disc morphogenesis in CRISPR-altered X. laevis., Carr BJ., J Cell Sci. January 11, 2021; 134 (1):
	Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.
	Building a ciliated epithelium: Transcriptional regulation and radial intercalation of multiciliated cells., Collins C., Curr Top Dev Biol. January 1, 2021; 145 3-39.
	In Xenopus ependymal cilia drive embryonic CSF circulation and brain development independently of cardiac pulsatile forces., Dur AH., Fluids Barriers CNS. December 11, 2020; 17 (1): 72.
	Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins., Lee C, Lee C., Elife. December 2, 2020; 9
	Endoparasites infecting exotic captive amphibian pet and zoo animals (Anura, Caudata) in Germany., Hallinger MJ., Parasitol Res. November 1, 2020; 119 (11): 3659-3673.
	[Analysis of PIH1D3 variant in a Chinese pedigree affected with primary ciliary dyskinesia]., Wang S., Zhonghua Yi Xue Yi Chuan Xue Za Zhi. September 10, 2020; 37 (9): 1021-1024.
	From biomechanics to mechanobiology: Xenopus provides direct access to the physical principles that shape the embryo., Chu CW., Curr Opin Genet Dev. August 1, 2020; 63 71-77.
	Mucociliary Epithelial Organoids from Xenopus Embryonic Cells: Generation, Culture and High-Resolution Live Imaging., Kang HJ., J Vis Exp. July 28, 2020; (161):
	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):
	CAMSAP3 facilitates basal body polarity and the formation of the central pair of microtubules in motile cilia., Robinson AM., Proc Natl Acad Sci U S A. June 16, 2020; 117 (24): 13571-13579.
	The FOXJ1 target Cfap206 is required for sperm motility, mucociliary clearance of the airways and brain development., Beckers A., Development. June 15, 2020; 147 (21):
	CFAP43 modulates ciliary beating in mouse and Xenopus., Rachev E., Dev Biol. March 15, 2020; 459 (2): 109-125.
	Diversity of left-right symmetry breaking strategy in animals., Hamada H., F1000Res. February 19, 2020; 9

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