Papers associated with brain (and mcc)

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	CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability., Deniz E., Dev Biol. July 1, 2023; 499 75-88.
	INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex., Mascibroda LG., Nat Commun. October 13, 2022; 13 (1): 6054.
	Development of a multiciliated cell., Mahjoub MR., Curr Opin Cell Biol. August 1, 2022; 77 102105.
	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):
	DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J., J Med Genet. July 1, 2021; 58 (7): 453-464.
	Xenopus to the rescue: A model to validate and characterize candidate ciliopathy genes., Rao VG., Genesis. February 1, 2021; 59 (1-2): e23414.
	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.
	Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance., Bustamante-Marin XM., Am J Hum Genet. February 7, 2019; 104 (2): 229-245.
	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.
	The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice., Beckers A., Sci Rep. October 2, 2018; 8 (1): 14678.
	La-related protein 6 controls ciliated cell differentiation., Manojlovic Z., Cilia. January 1, 2017; 6 4.
	Ciliary transcription factors and miRNAs precisely regulate Cp110 levels required for ciliary adhesions and ciliogenesis., Walentek P., Elife. September 13, 2016; 5
	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.
	The involvement of PCP proteins in radial cell intercalations during Xenopus embryonic development., Ossipova O., Dev Biol. December 15, 2015; 408 (2): 316-27.
	miR-34/449 control apical actin network formation during multiciliogenesis through small GTPase pathways., Chevalier B., Nat Commun. September 18, 2015; 6 8386.
	TGF-β Signaling Regulates the Differentiation of Motile Cilia., Tözser J., Cell Rep. May 19, 2015; 11 (7): 1000-7.
	The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T., Development. September 1, 2014; 141 (18): 3505-16.
	miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110., Song R., Nature. June 5, 2014; 510 (7503): 115-20.
	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.
	Myb promotes centriole amplification and later steps of the multiciliogenesis program., Tan FE., Development. October 1, 2013; 140 (20): 4277-86.
	Ciliogenesis and cerebrospinal fluid flow in the developing Xenopus brain are regulated by foxj1., Hagenlocher C., Cilia. April 29, 2013; 2 (1): 12.
	Global hyper-synchronous spontaneous activity in the developing optic tectum., Imaizumi K., Sci Rep. January 1, 2013; 3 1552.
	Multicilin promotes centriole assembly and ciliogenesis during multiciliate cell differentiation., Stubbs JL., Nat Cell Biol. January 8, 2012; 14 (2): 140-7.

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