Papers associated with left (and nup93)

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	8 Å structure of the outer rings of the Xenopus laevis nuclear pore complex obtained by cryo-EM and AI., Tai L., Protein Cell. October 1, 2022; 13 (10): 760-777.
	Cryo-EM structure of the inner ring from the Xenopus laevis nuclear pore complex., Huang G., Cell Res. May 1, 2022; 32 (5): 451-460.
	Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.
	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.
	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.
	Nucleoporin gene expression in Xenopus tropicalis embryonic development., Reza N., Int J Dev Biol. January 1, 2016; 60 (4-6): 181-8.
	Dimerization and direct membrane interaction of Nup53 contribute to nuclear pore complex assembly., Vollmer B., EMBO J. October 17, 2012; 31 (20): 4072-84.
	The nucleoporin Nup188 controls passage of membrane proteins across the nuclear pore complex., Theerthagiri G., J Cell Biol. June 28, 2010; 189 (7): 1129-42.
	PACSIN2 is a regulator of the metalloprotease/disintegrin ADAM13., Cousin H., Dev Biol. November 1, 2000; 227 (1): 197-210.
	Major binding sites for the nuclear import receptor are the internal nucleoporin Nup153 and the adjacent nuclear filament protein Tpr., Shah S., J Cell Biol. April 6, 1998; 141 (1): 31-49.

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