Papers associated with napsa

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	Kap-β2/Transportin mediates β-catenin nuclear transport in Wnt signaling., Hwang WY, Kostiuk V, González DP, Lusk CP, Khokha MK., Elife. October 27, 2022; 11
	Importin-9 wraps around the H2A-H2B core to act as nuclear importer and histone chaperone., Padavannil A, Sarkar P, Kim SJ, Cagatay T, Jiou J, Brautigam CA, Tomchick DR, Sali A, D'Arcy S, Chook YM., Elife. March 11, 2019; 8
	Effects of histone H2B ubiquitylation on the nucleosome structure and dynamics., Krajewski WA, Li J, Dou Y., Nucleic Acids Res. September 6, 2018; 46 (15): 7631-7642.
	Karyopherins regulate nuclear pore complex barrier and transport function., Kapinos LE, Huang B, Rencurel C, Lim RYH., J Cell Biol. November 6, 2017; 216 (11): 3609-3624.
	Glutamylation of Nap1 modulates histone H1 dynamics and chromosome condensation in Xenopus., Miller KE, Heald R., J Cell Biol. April 27, 2015; 209 (2): 211-20.
	Karyopherin-centric control of nuclear pores based on molecular occupancy and kinetic analysis of multivalent binding with FG nucleoporins., Kapinos LE, Schoch RL, Wagner RS, Schleicher KD, Lim RY., Biophys J. April 15, 2014; 106 (8): 1751-62.
	Limiting Ago protein restricts RNAi and microRNA biogenesis during early development in Xenopus laevis., Lund E, Sheets MD, Imboden SB, Dahlberg JE., Genes Dev. June 1, 2011; 25 (11): 1121-31.
	Brownian dynamics simulation of nucleocytoplasmic transport: a coarse-grained model for the functional state of the nuclear pore complex., Moussavi-Baygi R, Jamali Y, Karimi R, Mofrad MR., PLoS Comput Biol. June 1, 2011; 7 (6): e1002049.
	Biophysical coarse-grained modeling provides insights into transport through the nuclear pore complex., Moussavi-Baygi R, Jamali Y, Karimi R, Mofrad MR., Biophys J. March 16, 2011; 100 (6): 1410-9.
	The histone chaperone Nap1 promotes nucleosome assembly by eliminating nonnucleosomal histone DNA interactions., Andrews AJ, Chen X, Zevin A, Stargell LA, Luger K., Mol Cell. March 26, 2010; 37 (6): 834-42.
	A thermodynamic model for Nap1-histone interactions., Andrews AJ, Downing G, Brown K, Park YJ, Luger K., J Biol Chem. November 21, 2008; 283 (47): 32412-8.
	Phosphorylation and functions of inhibitor-2 family of proteins., Li M, Satinover DL, Brautigan DL., Biochemistry. March 6, 2007; 46 (9): 2380-9.
	Preferential binding of the histone (H3-H4)2 tetramer by NAP1 is mediated by the amino-terminal histone tails., McBryant SJ, Park YJ, Abernathy SM, Laybourn PJ, Nyborg JK, Luger K., J Biol Chem. November 7, 2003; 278 (45): 44574-83.
	Expression and partial characterization of kinesin-related proteins in differentiating and adult skeletal muscle., Ginkel LM, Wordeman L., Mol Biol Cell. December 1, 2000; 11 (12): 4143-58.
	Photoreceptor localization of the KIF3A and KIF3B subunits of the heterotrimeric microtubule motor kinesin II in vertebrate retina., Whitehead JL, Wang SY, Bost-Usinger L, Hoang E, Frazer KA, Burnside B., Exp Eye Res. November 1, 1999; 69 (5): 491-503.
	Heterotrimeric kinesin II is the microtubule motor protein responsible for pigment dispersion in Xenopus melanophores., Tuma MC, Zill A, Le Bot N, Vernos I, Gelfand V., J Cell Biol. December 14, 1998; 143 (6): 1547-58.

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