???pagination.result.count???
???pagination.result.page???
1
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.
The Inner Nuclear Membrane Protein Nemp1 Is a New Type of RanGTP-Binding Protein in Eukaryotes. , Shibano T., PLoS One. May 6, 2015; 10 (5): e0127271.
Nanobodies: site-specific labeling for super-resolution imaging, rapid epitope-mapping and native protein complex isolation. , Pleiner T., Elife. January 6, 2015; 4 e11349.
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.
Nucleoporin 153 arrests the nuclear import of hepatitis B virus capsids in the nuclear basket. , Schmitz A., PLoS Pathog. January 29, 2010; 6 (1): e1000741.
ER membrane-bending proteins are necessary for de novo nuclear pore formation. , Dawson TR., J Cell Biol. March 9, 2009; 184 (5): 659-75.
Nanomechanical basis of selective gating by the nuclear pore complex. , Lim RY., Science. October 26, 2007; 318 (5850): 640-3.
Changes in nucleoporin domain topology in response to chemical effectors. , Paulillo SM., J Mol Biol. October 13, 2006; 363 (1): 39-50.
Nucleoporin domain topology is linked to the transport status of the nuclear pore complex. , Paulillo SM., J Mol Biol. August 26, 2005; 351 (4): 784-98.
The RNA binding domain within the nucleoporin Nup153 associates preferentially with single-stranded RNA. , Ball JR., RNA. January 1, 2004; 10 (1): 19-27.
RanGTP mediates nuclear pore complex assembly. , Walther TC., Nature. August 7, 2003; 424 (6949): 689-94.
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.
RNA association defines a functionally conserved domain in the nuclear pore protein Nup153. , Dimaano C., J Biol Chem. November 30, 2001; 276 (48): 45349-57.
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.
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.
Recombinant Nup153 incorporates in vivo into Xenopus oocyte nuclear pore complexes. , Panté N., J Struct Biol. April 1, 2000; 129 (2-3): 306-12.
The nucleoporin nup153 plays a critical role in multiple types of nuclear export. , Ullman KS ., Mol Biol Cell. March 1, 1999; 10 (3): 649-64.
Nucleoporins nup98 and nup214 participate in nuclear export of human immunodeficiency virus type 1 Rev. , Zolotukhin AS., J Virol. January 1, 1999; 73 (1): 120-7.
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.