Papers associated with cytoplasm (and nup62)

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	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):
	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.
	Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery., Zuleger N., Genome Biol. February 15, 2013; 14 (2): R14.
	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.
	ER membrane-bending proteins are necessary for de novo nuclear pore formation., Dawson TR., J Cell Biol. March 9, 2009; 184 (5): 659-75.
	Domain topology of the p62 complex within the 3-D architecture of the nuclear pore complex., Schwarz-Herion K., J Mol Biol. July 20, 2007; 370 (4): 796-806.
	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.
	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.
	Nuclear pore localization and nucleocytoplasmic transport of eIF-5A: evidence for direct interaction with the export receptor CRM1., Rosorius O., J Cell Sci. July 1, 1999; 112 ( Pt 14) 2369-80.
	Phosphorylation and glycosylation of nucleoporins., Miller MW., Arch Biochem Biophys. July 1, 1999; 367 (1): 51-60.
	The nucleoporin nup153 plays a critical role in multiple types of nuclear export., Ullman KS., Mol Biol Cell. March 1, 1999; 10 (3): 649-64.
	An evaluation of sialation of the nucleoporin p62., Fang B., Arch Biochem Biophys. September 1, 1998; 357 (1): 95-100.
	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.
	Direct interaction of nucleoporin p62 with mRNA during its export from the nucleus., Dargemont C., J Cell Sci. January 1, 1995; 108 ( Pt 1) 257-63.
	Intranuclear filaments containing a nuclear pore complex protein., Cordes VC., J Cell Biol. December 1, 1993; 123 (6 Pt 1): 1333-44.
	Structural requirements of 5S rRNA for nuclear transport, 7S ribonucleoprotein particle assembly, and 60S ribosomal subunit assembly in Xenopus oocytes., Allison LA., Mol Cell Biol. November 1, 1993; 13 (11): 6819-31.
	Cytoplasmic transport of ribosomal subunits microinjected into the Xenopus laevis oocyte nucleus: a generalized, facilitated process., Bataillé N., J Cell Biol. October 1, 1990; 111 (4): 1571-82.
	Monoclonal antibodies identify a group of nuclear pore complex glycoproteins., Snow CM., J Cell Biol. May 1, 1987; 104 (5): 1143-56.

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