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	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.
	Nuclear pores collapse in response to CO2 imaged with atomic force microscopy., Oberleithner H., Pflugers Arch. January 1, 2000; 439 (3): 251-5.
	Calcium, ATP and nuclear pore channel gating., Bustamante JO., Pflugers Arch. February 1, 2000; 439 (4): 433-44.
	Recombinant Nup153 incorporates in vivo into Xenopus oocyte nuclear pore complexes., Panté N., J Struct Biol. April 1, 2000; 129 (2-3): 306-12.
	Ran alters nuclear pore complex conformation., Goldberg MW, Goldberg MW., J Mol Biol. July 14, 2000; 300 (3): 519-29.
	Monitoring biomolecular interactions by time-lapse atomic force microscopy., Stolz M., J Struct Biol. September 1, 2000; 131 (3): 171-80.
	The matrix protein of vesicular stomatitis virus inhibits nucleocytoplasmic transport when it is in the nucleus and associated with nuclear pore complexes., Petersen JM., Mol Cell Biol. November 1, 2000; 20 (22): 8590-601.
	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 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.
	Evidence for Ca2+- and ATP-sensitive peripheral channels in nuclear pore complexes., Shahin V., FASEB J. September 1, 2001; 15 (11): 1895-901.
	The nucleoporin Nup153 is required for nuclear pore basket formation, nuclear pore complex anchoring and import of a subset of nuclear proteins., Walther TC., EMBO J. October 15, 2001; 20 (20): 5703-14.
	Adenovirus hexon protein enhances nuclear delivery and increases transgene expression of polyethylenimine/plasmid DNA vectors., Carlisle RC., Mol Ther. November 1, 2001; 4 (5): 473-83.
	Electrophoretic plugging of nuclear pores by using the nuclear hourglass technique., Danker T., J Membr Biol. November 15, 2001; 184 (2): 91-9.
	Nuclear transport kinetics in microarrays of nuclear envelope patches., Peters R., J Struct Biol. January 1, 2002; 140 (1-3): 268-78.
	Domain-specific antibodies reveal multiple-site topology of Nup153 within the nuclear pore complex., Fahrenkrog B., J Struct Biol. January 1, 2002; 140 (1-3): 254-67.
	Nuclear pore complex is able to transport macromolecules with diameters of about 39 nm., Panté N., Mol Biol Cell. February 1, 2002; 13 (2): 425-34.
	Aldosterone signaling pathway across the nuclear envelope., Schäfer C., Proc Natl Acad Sci U S A. May 14, 2002; 99 (10): 7154-9.
	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.
	Steady-state nuclear localization of exportin-t involves RanGTP binding and two distinct nuclear pore complex interaction domains., Kuersten S., Mol Cell Biol. August 1, 2002; 22 (16): 5708-20.
	Nuclear export of mRNA by TAP/NXF1 requires two nucleoporin-binding sites but not p15., Braun IC., Mol Cell Biol. August 1, 2002; 22 (15): 5405-18.
	Regulation of nuclear pore complex conformation by IP(3) receptor activation., Moore-Nichols D., Biophys J. September 1, 2002; 83 (3): 1421-8.
	Enzymes of the SUMO modification pathway localize to filaments of the nuclear pore complex., Zhang H., Mol Cell Biol. September 1, 2002; 22 (18): 6498-508.
	Rapid translocation of NTF2 through the nuclear pore of isolated nuclei and nuclear envelopes., Siebrasse JP., EMBO Rep. September 1, 2002; 3 (9): 887-92.
	Reconstitution of nuclear protein export in isolated nuclear envelopes., Siebrasse JP., J Cell Biol. September 2, 2002; 158 (5): 849-54.
	Concentration of Ran on chromatin induces decondensation, nuclear envelope formation and nuclear pore complex assembly., Zhang C., Eur J Cell Biol. November 1, 2002; 81 (11): 623-33.
	Modulation of nuclear pore topology by transport modifiers., Jäggi RD., Biophys J. January 1, 2003; 84 (1): 665-70.
	Real-time imaging of nuclear permeation by EGFP in single intact cells., Wei X., Biophys J. February 1, 2003; 84 (2 Pt 1): 1317-27.
	Route of steroid-activated macromolecules through nuclear pores imaged with atomic force microscopy., Oberleithner H., Biochem Soc Trans. February 1, 2003; 31 (Pt 1): 71-5.
	The strategy for coupling the RanGTP gradient to nuclear protein export., Becskei A., Proc Natl Acad Sci U S A. February 18, 2003; 100 (4): 1717-22.
	Polyproline type II conformation in the C-terminal domain of the nuclear pore complex protein gp210., Pilpel Y., Biochemistry. April 1, 2003; 42 (12): 3519-26.
	The conserved Nup107-160 complex is critical for nuclear pore complex assembly., Walther TC., Cell. April 18, 2003; 113 (2): 195-206.
	Cryo-electron tomography provides novel insights into nuclear pore architecture: implications for nucleocytoplasmic transport., Stoffler D., J Mol Biol. April 18, 2003; 328 (1): 119-30.
	Importin beta-depending nuclear import pathways: role of the adapter proteins in the docking and releasing steps., Rollenhagen C., Mol Biol Cell. May 1, 2003; 14 (5): 2104-15.
	RanGTP mediates nuclear pore complex assembly., Walther TC., Nature. August 7, 2003; 424 (6949): 689-94.
	Optical microwell assay of membrane transport kinetics., Kiskin NI., Biophys J. October 1, 2003; 85 (4): 2311-22.
	Importin beta negatively regulates nuclear membrane fusion and nuclear pore complex assembly., Harel A., Mol Biol Cell. November 1, 2003; 14 (11): 4387-96.
	Passive transport of macromolecules through Xenopus laevis nuclear envelope., Enss K., J Membr Biol. December 1, 2003; 196 (3): 147-55.
	Quantitative topographical analysis of nuclear pore complex function using scanning force microscopy., Jäggi RD., Biophys J. December 1, 2003; 85 (6): 4093-8.
	Caenorhabditis elegans nucleoporins Nup93 and Nup205 determine the limit of nuclear pore complex size exclusion in vivo., Galy V., Mol Biol Cell. December 1, 2003; 14 (12): 5104-15.
	Spatial and temporal control of nuclear envelope assembly by Ran GTPase., Clarke PR., Symp Soc Exp Biol. January 1, 2004; (56): 193-204.
	Nup358/RanBP2 attaches to the nuclear pore complex via association with Nup88 and Nup214/CAN and plays a supporting role in CRM1-mediated nuclear protein export., Bernad R., Mol Cell Biol. March 1, 2004; 24 (6): 2373-84.
	Yeast nuclear pore complexes have a cytoplasmic ring and internal filaments., Kiseleva E., J Struct Biol. March 1, 2004; 145 (3): 272-88.
	Evolution of neural precursor selection: functional divergence of proneural proteins., Quan XJ., Development. April 1, 2004; 131 (8): 1679-89.
	Nuclear side conformational changes in the nuclear pore complex following calcium release from the nuclear membrane., Mooren OL., Phys Biol. June 1, 2004; 1 (1-2): 125-34.
	Intranuclear membrane structure formations by CaaX-containing nuclear proteins., Ralle T., J Cell Sci. December 1, 2004; 117 (Pt 25): 6095-104.
	Activation of ryanodine receptors in the nuclear envelope alters the conformation of the nuclear pore complex., Erickson ES., Biophys Chem. December 1, 2004; 112 (1): 1-7.
	The SWI/SNF chromatin remodeling protein Brg1 is required for vertebrate neurogenesis and mediates transactivation of Ngn and NeuroD., Seo S., Development. January 1, 2005; 132 (1): 105-15.
	The integral membrane nucleoporin pom121 functionally links nuclear pore complex assembly and nuclear envelope formation., Antonin W., Mol Cell. January 7, 2005; 17 (1): 83-92.

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