Papers associated with egg (and nup62)

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	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):
	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):
	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.
	Transportin acts to regulate mitotic assembly events by target binding rather than Ran sequestration., Bernis C., Mol Biol Cell. April 1, 2014; 25 (7): 992-1009.
	The permeability of reconstituted nuclear pores provides direct evidence for the selective phase model., Hülsmann BB., Cell. August 17, 2012; 150 (4): 738-51.
	The C-terminal domain of Nup93 is essential for assembly of the structural backbone of nuclear pore complexes., Sachdev R., Mol Biol Cell. February 1, 2012; 23 (4): 740-9.
	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.
	Leader-induced phosphorylation of nucleoporins correlates with nuclear trafficking inhibition by cardioviruses., Porter FW., J Virol. February 1, 2009; 83 (4): 1941-51.
	Pre-M phase-promoting factor associates with annulate lamellae in Xenopus oocytes and egg extracts., Beckhelling C., Mol Biol Cell. March 1, 2003; 14 (3): 1125-37.
	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.
	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.
	Identification of a new vertebrate nucleoporin, Nup188, with the use of a novel organelle trap assay., Miller BR., Mol Biol Cell. October 1, 2000; 11 (10): 3381-96.
	Nuclear glycogen and glycogen synthase kinase 3., Ragano-Caracciolo M., Biochem Biophys Res Commun. August 19, 1998; 249 (2): 422-7.
	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.
	Nup93, a vertebrate homologue of yeast Nic96p, forms a complex with a novel 205-kDa protein and is required for correct nuclear pore assembly., Grandi P., Mol Biol Cell. October 1, 1997; 8 (10): 2017-38.
	High content of a nuclear pore complex protein in cytoplasmic annulate lamellae of Xenopus oocytes., Cordes VC., Eur J Cell Biol. November 1, 1995; 68 (3): 240-55.
	Intranuclear filaments containing a nuclear pore complex protein., Cordes VC., J Cell Biol. December 1, 1993; 123 (6 Pt 1): 1333-44.
	Regulation of nuclear envelope precursor functions during cell division., Vigers GP., J Cell Sci. June 1, 1992; 102 ( Pt 2) 273-84.

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