Papers associated with right (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.
	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.
	A self-inhibitory interaction within Nup155 and membrane binding are required for nuclear pore complex formation., De Magistris P., J Cell Sci. January 4, 2018; 131 (1):
	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.
	The Autophagy Receptor TAX1BP1 and the Molecular Motor Myosin VI Are Required for Clearance of Salmonella Typhimurium by Autophagy., Tumbarello DA., PLoS Pathog. October 1, 2015; 11 (10): e1005174.
	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.
	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.
	ER membrane-bending proteins are necessary for de novo nuclear pore formation., Dawson TR., J Cell Biol. March 9, 2009; 184 (5): 659-75.
	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.
	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.
	Chromosomal proteins HMG-14 and HMG-17 are released from mitotic chromosomes and imported into the nucleus by active transport., Hock R., J Cell Biol. December 14, 1998; 143 (6): 1427-36.

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