Papers associated with left (and nup62)

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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.
	The TFIIH complex is required to establish and maintain mitotic chromosome structure., Haase J., Elife. March 16, 2022; 11
	The nucleoporin Nup50 activates the Ran guanine nucleotide exchange factor RCC1 to promote NPC assembly at the end of mitosis., Holzer G., EMBO J. December 1, 2021; 40 (23): e108788.
	ZC3HC1 Is a Novel Inherent Component of the Nuclear Basket, Resident in a State of Reciprocal Dependence with TPR., Gunkel P., Cells. July 30, 2021; 10 (8):
	Structure of the cytoplasmic ring of the Xenopus laevis nuclear pore complex by cryo-electron microscopy single particle analysis., Huang G., Cell Res. June 1, 2020; 30 (6): 520-531.
	Conservation and divergence of protein pathways in the vertebrate heart., Federspiel JD., PLoS Biol. September 6, 2019; 17 (9): e3000437.
	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.
	Identification of p62/SQSTM1 as a component of non-canonical Wnt VANGL2-JNK signalling in breast cancer., Puvirajesinghe TM., Nat Commun. January 12, 2016; 7 10318.
	Nucleoporin gene expression in Xenopus tropicalis embryonic development., Reza N., Int J Dev Biol. January 1, 2016; 60 (4-6): 181-8.
	Nup153 Recruits the Nup107-160 Complex to the Inner Nuclear Membrane for Interphasic Nuclear Pore Complex Assembly., Vollmer B., Dev Cell. June 22, 2015; 33 (6): 717-28.
	Parvoviruses cause nuclear envelope breakdown by activating key enzymes of mitosis., Porwal M., PLoS Pathog. October 1, 2013; 9 (10): e1003671.
	Systematic analysis of barrier-forming FG hydrogels from Xenopus nuclear pore complexes., Labokha AA., EMBO J. January 23, 2013; 32 (2): 204-18.
	The permeability of reconstituted nuclear pores provides direct evidence for the selective phase model., Hülsmann BB., Cell. August 17, 2012; 150 (4): 738-51.
	Embryonic and adult isoforms of XLAP2 form microdomains associated with chromatin and the nuclear envelope., Chmielewska M., Cell Tissue Res. April 1, 2011; 344 (1): 97-110.
	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.
	The XMAP215-family protein DdCP224 is required for cortical interactions of microtubules., Hestermann A., BMC Cell Biol. June 8, 2004; 5 24.
	The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import., Walther TC., J Cell Biol. July 8, 2002; 158 (1): 63-77.
	Interference with the cytoplasmic tail of gp210 disrupts "close apposition" of nuclear membranes and blocks nuclear pore dilation., Drummond SP., J Cell Biol. July 8, 2002; 158 (1): 53-62.
	Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells., Daigle N., J Cell Biol. July 9, 2001; 154 (1): 71-84.
	A role for nuclear lamins in nuclear envelope assembly., Lopez-Soler RI., J Cell Biol. July 9, 2001; 154 (1): 61-70.
	Cofactor requirements for nuclear export of Rev response element (RRE)- and constitutive transport element (CTE)-containing retroviral RNAs. An unexpected role for actin., Hofmann W., J Cell Biol. March 5, 2001; 152 (5): 895-910.
	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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