Papers associated with egg (and nup153)

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	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.
	The Cytoskeleton and Its Roles in Self-Organization Phenomena: Insights from Xenopus Egg Extracts., Geisterfer ZM., Cells. August 26, 2021; 10 (9):
	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):
	The Spindle Assembly Checkpoint Functions during Early Development in Non-Chordate Embryos., Chenevert J., Cells. April 28, 2020; 9 (5):
	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.
	Nanobodies: site-specific labeling for super-resolution imaging, rapid epitope-mapping and native protein complex isolation., Pleiner T., Elife. January 6, 2015; 4 e11349.
	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.
	Transportin mediates nuclear entry of DNA in vertebrate systems., Lachish-Zalait A., Traffic. October 1, 2009; 10 (10): 1414-28.
	Leader-induced phosphorylation of nucleoporins correlates with nuclear trafficking inhibition by cardioviruses., Porter FW., J Virol. February 1, 2009; 83 (4): 1941-51.
	ELYS/MEL-28 chromatin association coordinates nuclear pore complex assembly and replication licensing., Gillespie PJ., Curr Biol. October 9, 2007; 17 (19): 1657-62.
	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.
	Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export., Vasu S., J Cell Biol. October 29, 2001; 155 (3): 339-54.
	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.
	Direct and indirect association of the small GTPase ran with nuclear pore proteins and soluble transport factors: studies in Xenopus laevis egg extracts., Saitoh H., Mol Biol Cell. September 1, 1996; 7 (9): 1319-34.
	Nuclear pore complex assembly studied with a biochemical assay for annulate lamellae formation., Meier E., J Cell Biol. June 1, 1995; 129 (6): 1459-72.

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