Papers associated with progenitor cell (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.
	Structure of cytoplasmic ring of nuclear pore complex by integrative cryo-EM and AlphaFold., Fontana P., Science. June 10, 2022; 376 (6598): eabm9326.
	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 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.
	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):
	Karyopherins regulate nuclear pore complex barrier and transport function., Kapinos LE., J Cell Biol. November 6, 2017; 216 (11): 3609-3624.
	The Nup62 Coiled-Coil Motif Provides Plasticity for Triple-Helix Bundle Formation., Dewangan PS., Biochemistry. June 6, 2017; 56 (22): 2803-2811.
	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.
	Crystal structure of the metazoan Nup62•Nup58•Nup54 nucleoporin complex., Chug H., Science. October 2, 2015; 350 (6256): 106-10.
	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.
	Structural organization of the nuclear pore permeability barrier., Liashkovich I., J Control Release. June 28, 2012; 160 (3): 601-8.
	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.
	ER membrane-bending proteins are necessary for de novo nuclear pore formation., Dawson TR., J Cell Biol. March 9, 2009; 184 (5): 659-75.
	Individual binding pockets of importin-beta for FG-nucleoporins have different binding properties and different sensitivities to RanGTP., Otsuka S., Proc Natl Acad Sci U S A. October 21, 2008; 105 (42): 16101-6.
	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.
	High-resolution near-field optical imaging of single nuclear pore complexes under physiological conditions., Höppener C., Biophys J. May 1, 2005; 88 (5): 3681-8.
	Reconstitution of nuclear protein export in isolated nuclear envelopes., Siebrasse JP., J Cell Biol. September 2, 2002; 158 (5): 849-54.
	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.
	The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates., Bachi A., RNA. January 1, 2000; 6 (1): 136-58.
	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.
	Interactions and three-dimensional localization of a group of nuclear pore complex proteins., Panté N., J Cell Biol. August 1, 1994; 126 (3): 603-17.
	Intranuclear filaments containing a nuclear pore complex protein., Cordes VC., J Cell Biol. December 1, 1993; 123 (6 Pt 1): 1333-44.
	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.
	Protein import through the nuclear pore complex is a multistep process., Akey CW., J Cell Biol. September 1, 1989; 109 (3): 971-82.

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