Papers associated with cardiovascular system (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.
	DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes., Marquez J., J Med Genet. July 1, 2021; 58 (7): 453-464.
	Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.
	Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo., Bharathan NK., Dev Biol. June 15, 2019; 450 (2): 115-131.
	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 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.
	c21orf59/kurly Controls Both Cilia Motility and Polarization., Jaffe KM., Cell Rep. March 1, 2016; 14 (8): 1841-9.
	Mechanical strain determines the axis of planar polarity in ciliated epithelia., Chien YH., Curr Biol. November 2, 2015; 25 (21): 2774-2784.
	Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral-right blastomere., Tingler M., Genesis. June 1, 2014; 52 (6): 588-99.
	Myb promotes centriole amplification and later steps of the multiciliogenesis program., Tan FE., Development. October 1, 2013; 140 (20): 4277-86.
	Global hyper-synchronous spontaneous activity in the developing optic tectum., Imaizumi K., Sci Rep. January 1, 2013; 3 1552.

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