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	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.
	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.
	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 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.
	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.
	Modulation of nuclear pore topology by transport modifiers., Jäggi RD., Biophys J. January 1, 2003; 84 (1): 665-70.
	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.
	Reconstitution of nuclear protein export in isolated nuclear envelopes., Siebrasse JP., J Cell Biol. September 2, 2002; 158 (5): 849-54.
	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.
	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.
	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.
	Aldosterone signaling pathway across the nuclear envelope., Schäfer C., Proc Natl Acad Sci U S A. May 14, 2002; 99 (10): 7154-9.
	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.
	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.
	Electrophoretic plugging of nuclear pores by using the nuclear hourglass technique., Danker T., J Membr Biol. November 15, 2001; 184 (2): 91-9.
	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.
	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.
	Evidence for Ca2+- and ATP-sensitive peripheral channels in nuclear pore complexes., Shahin V., FASEB J. September 1, 2001; 15 (11): 1895-901.
	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 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.
	Monitoring biomolecular interactions by time-lapse atomic force microscopy., Stolz M., J Struct Biol. September 1, 2000; 131 (3): 171-80.
	Ran alters nuclear pore complex conformation., Goldberg MW, Goldberg MW., J Mol Biol. July 14, 2000; 300 (3): 519-29.
	Recombinant Nup153 incorporates in vivo into Xenopus oocyte nuclear pore complexes., Panté N., J Struct Biol. April 1, 2000; 129 (2-3): 306-12.
	Calcium, ATP and nuclear pore channel gating., Bustamante JO., Pflugers Arch. February 1, 2000; 439 (4): 433-44.
	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.
	Nuclear hourglass technique: an approach that detects electrically open nuclear pores in Xenopus laevis oocyte., Danker T., Proc Natl Acad Sci U S A. November 9, 1999; 96 (23): 13530-5.
	Optical recording of signal-mediated protein transport through single nuclear pore complexes., Keminer O., Proc Natl Acad Sci U S A. October 12, 1999; 96 (21): 11842-7.
	Dbp5, a DEAD-box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p., Schmitt C., EMBO J. August 2, 1999; 18 (15): 4332-47.
	Conformational changes of the in situ nuclear pore complex., Wang H., Biophys J. July 1, 1999; 77 (1): 241-7.
	Permeability of single nuclear pores., Keminer O., Biophys J. July 1, 1999; 77 (1): 217-28.
	CRM1-mediated recycling of snurportin 1 to the cytoplasm., Paraskeva E., J Cell Biol. April 19, 1999; 145 (2): 255-64.
	RAE1 is a shuttling mRNA export factor that binds to a GLEBS-like NUP98 motif at the nuclear pore complex through multiple domains., Pritchard CE., J Cell Biol. April 19, 1999; 145 (2): 237-54.
	Calcium-mediated structural changes of native nuclear pore complexes monitored by time-lapse atomic force microscopy., Stoffler D., J Mol Biol. April 9, 1999; 287 (4): 741-52.
	Molecular segments of protein Tpr that confer nuclear targeting and association with the nuclear pore complex., Cordes VC., Exp Cell Res. November 25, 1998; 245 (1): 43-56.
	Molecular architecture of the yeast nuclear pore complex: localization of Nsp1p subcomplexes., Fahrenkrog B., J Cell Biol. November 2, 1998; 143 (3): 577-88.
	The role of the ran GTPase in nuclear assembly and DNA replication: characterisation of the effects of Ran mutants., Hughes M., J Cell Sci. October 1, 1998; 111 ( Pt 20) 3017-26.
	Regulated expression of neurogenic basic helix-loop-helix transcription factors during differentiation of the immortalized neuronal progenitor cell line HC2S2 into neurons., Ohtsuka T., Cell Tissue Res. July 1, 1998; 293 (1): 23-9.
	Interaction of the human immunodeficiency virus type 1 Vpr protein with the nuclear pore complex., Fouchier RA., J Virol. July 1, 1998; 72 (7): 6004-13.
	ATP-Induced shape change of nuclear pores visualized with the atomic force microscope., Rakowska A., J Membr Biol. May 15, 1998; 163 (2): 129-36.
	Nup116p and nup100p are interchangeable through a conserved motif which constitutes a docking site for the mRNA transport factor gle2p., Bailer SM., EMBO J. February 16, 1998; 17 (4): 1107-19.

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