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Summary Expression Phenotypes Gene Literature (40) GO Terms (5) Nucleotides (267) Proteins (56) Interactants (285) Wiki
XB--6450415

Papers associated with nup98



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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, Zhu Y, Ren H, Huang X, Zhang C, Sun F., Protein Cell. October 1, 2022; 13 (10): 760-777.                                                                        


ZC3HC1 Is a Novel Inherent Component of the Nuclear Basket, Resident in a State of Reciprocal Dependence with TPR., Gunkel P, Iino H, Krull S, Cordes VC., Cells. July 30, 2021; 10 (8):               


Exportins can inhibit major mitotic assembly events in vitro: membrane fusion, nuclear pore formation, and spindle assembly., Nord MS, Bernis C, Carmona S, Garland DC, Travesa A, Forbes DJ., Nucleus. December 1, 2020; 11 (1): 178-193.            


Structure of the cytoplasmic ring of the Xenopus laevis nuclear pore complex by cryo-electron microscopy single particle analysis., Huang G, Zhang Y, Zhang Y, Zhu X, Zeng C, Wang Q, Zhou Q, Tao Q, Tao Q, Liu M, Lei J, Yan C, Shi Y, Shi Y., Cell Res. June 1, 2020; 30 (6): 520-531.                                    


Conservation and divergence of protein pathways in the vertebrate heart., Federspiel JD, Tandon P, Wilczewski CM, Wasson L, Herring LE, Venkatesh SS, Cristea IM, Conlon FL., PLoS Biol. September 6, 2019; 17 (9): e3000437.                                                    


Toxic PRn poly-dipeptides encoded by the C9orf72 repeat expansion block nuclear import and export., Shi KY, Mori E, Nizami ZF, Lin Y, Kato M, Xiang S, Wu LC, Ding M, Yu Y, Gall JG, McKnight SL., Proc Natl Acad Sci U S A. February 14, 2017; 114 (7): E1111-E1117.


Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy., Duncan AR, Khokha MK., Semin Cell Dev Biol. March 1, 2016; 51 73-9.    


Nucleoporin gene expression in Xenopus tropicalis embryonic development., Reza N, Khokha MK, Del Viso F., Int J Dev Biol. January 1, 2016; 60 (4-6): 181-8.            


The NIMA-like kinase Nek2 is a key switch balancing cilia biogenesis and resorption in the development of left-right asymmetry., Endicott SJ, Basu B, Khokha M, Brueckner M., Development. December 1, 2015; 142 (23): 4068-79.                                  


Prediction of Functionally Important Phospho-Regulatory Events in Xenopus laevis Oocytes., Johnson JR, Santos SD, Johnson T, Pieper U, Strumillo M, Wagih O, Sali A, Krogan NJ, Beltrao P., PLoS Comput Biol. August 27, 2015; 11 (8): e1004362.                            


Nup98 FG domains from diverse species spontaneously phase-separate into particles with nuclear pore-like permselectivity., Schmidt HB, Görlich D., Elife. January 6, 2015; 4                                   


Nanobodies: site-specific labeling for super-resolution imaging, rapid epitope-mapping and native protein complex isolation., Pleiner T, Bates M, Trakhanov S, Lee CT, Lee CT, Schliep JE, Chug H, Böhning M, Stark H, Urlaub H, Görlich D., Elife. January 6, 2015; 4 e11349.                


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.


Systematic analysis of barrier-forming FG hydrogels from Xenopus nuclear pore complexes., Labokha AA, Gradmann S, Frey S, Hülsmann BB, Urlaub H, Baldus M, Görlich D., EMBO J. January 23, 2013; 32 (2): 204-18.              


Dimerization and direct membrane interaction of Nup53 contribute to nuclear pore complex assembly., Vollmer B, Schooley A, Sachdev R, Eisenhardt N, Schneider AM, Sieverding C, Madlung J, Gerken U, Macek B, Antonin W., EMBO J. October 17, 2012; 31 (20): 4072-84.              


The permeability of reconstituted nuclear pores provides direct evidence for the selective phase model., Hülsmann BB, Labokha AA, Görlich D., Cell. August 17, 2012; 150 (4): 738-51.          


Structural organization of the nuclear pore permeability barrier., Liashkovich I, Meyring A, Oberleithner H, Shahin V., 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, Sieverding C, Flötenmeyer M, Antonin W., Mol Biol Cell. February 1, 2012; 23 (4): 740-9.                


Domain topology of nucleoporin Nup98 within the nuclear pore complex., Chatel G, Desai SH, Mattheyses AL, Powers MA, Fahrenkrog B., J Struct Biol. January 1, 2012; 177 (1): 81-9.


POM121 and Sun1 play a role in early steps of interphase NPC assembly., Talamas JA, Hetzer MW., J Cell Biol. July 11, 2011; 194 (1): 27-37.          


Nup98 regulates bipolar spindle assembly through association with microtubules and opposition of MCAK., Cross MK, Powers MA., Mol Biol Cell. March 1, 2011; 22 (5): 661-72.            


The nucleoporin Nup188 controls passage of membrane proteins across the nuclear pore complex., Theerthagiri G, Eisenhardt N, Schwarz H, Antonin W., J Cell Biol. June 28, 2010; 189 (7): 1129-42.              


Vesicular stomatitis virus inhibits mitotic progression and triggers cell death., Chakraborty P, Seemann J, Mishra RK, Wei JH, Weil L, Nussenzveig DR, Heiber J, Barber GN, Dasso M, Fontoura BM., EMBO Rep. October 1, 2009; 10 (10): 1154-60.


Leader-induced phosphorylation of nucleoporins correlates with nuclear trafficking inhibition by cardioviruses., Porter FW, Palmenberg AC., J Virol. February 1, 2009; 83 (4): 1941-51.


Single bead affinity detection (SINBAD) for the analysis of protein-protein interactions., Schulte R, Talamas J, Doucet C, Hetzer MW., PLoS One. April 9, 2008; 3 (4): e2061.      


Complex formation among the RNA export proteins Nup98, Rae1/Gle2, and TAP., Blevins MB, Smith AM, Phillips EM, Powers MA., J Biol Chem. June 6, 2003; 278 (23): 20979-88.


The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import., Walther TC, Pickersgill HS, Cordes VC, Goldberg MW, Allen TD, Mattaj IW, Fornerod M., 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, Wilson KL., J Cell Biol. July 8, 2002; 158 (1): 53-62.              


Nup98 is a mobile nucleoporin with transcription-dependent dynamics., Griffis ER, Altan N, Lippincott-Schwartz J, Powers MA., Mol Biol Cell. April 1, 2002; 13 (4): 1282-97.


Novel vertebrate nucleoporins Nup133 and Nup160 play a role in mRNA export., Vasu S, Shah S, Orjalo A, Park M, Fischer WH, Forbes DJ., J Cell Biol. October 29, 2001; 155 (3): 339-54.                    


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, Reichart B, Ewald A, Müller E, Schmitt I, Stauber RH, Lottspeich F, Jockusch BM, Scheer U, Hauber J, Dabauvalle MC., J Cell Biol. March 5, 2001; 152 (5): 895-910.                  


Identification of a new vertebrate nucleoporin, Nup188, with the use of a novel organelle trap assay., Miller BR, Powers M, Park M, Fischer W, Forbes DJ., Mol Biol Cell. October 1, 2000; 11 (10): 3381-96.


The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates., Bachi A, Braun IC, Rodrigues JP, Panté N, Ribbeck K, von Kobbe C, Kutay U, Wilm M, Görlich D, Carmo-Fonseca M, Izaurralde E., RNA. January 1, 2000; 6 (1): 136-58.


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, Fornerod M, Kasper LH, van Deursen JM., J Cell Biol. April 19, 1999; 145 (2): 237-54.                  


The nucleoporin nup153 plays a critical role in multiple types of nuclear export., Ullman KS, Shah S, Powers MA, Forbes DJ., 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, Felber BK., 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, Tugendreich S, Forbes D., J Cell Biol. April 6, 1998; 141 (1): 31-49.                    


Nup116p and nup100p are interchangeable through a conserved motif which constitutes a docking site for the mRNA transport factor gle2p., Bailer SM, Siniossoglou S, Podtelejnikov A, Hellwig A, Mann M, Hurt E., EMBO J. February 16, 1998; 17 (4): 1107-19.


The vertebrate GLFG nucleoporin, Nup98, is an essential component of multiple RNA export pathways., Powers MA, Forbes DJ, Dahlberg JE, Lund E., J Cell Biol. January 27, 1997; 136 (2): 241-50.            


Identification of a protein complex that is required for nuclear protein import and mediates docking of import substrate to distinct nucleoporins., Radu A, Blobel G, Moore MS., Proc Natl Acad Sci U S A. February 28, 1995; 92 (5): 1769-73.

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