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Summary Anatomy Item Literature (235) Expression Attributions Wiki
XB-ANAT-3742

Papers associated with neural progenitor cell (and nup93)

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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., Protein Cell. October 1, 2022; 13 (10): 760-777.                                                                        


Structure of the cytoplasmic ring of the Xenopus laevis nuclear pore complex., Zhu X., Science. June 10, 2022; 376 (6598): eabl8280.


Cryo-EM structure of the inner ring from the Xenopus laevis nuclear pore complex., Huang G., Cell Res. May 1, 2022; 32 (5): 451-460.                                              


Cryo-EM structure of the nuclear ring from Xenopus laevis nuclear pore complex., Huang G., Cell Res. April 1, 2022; 32 (4): 349-358.


Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., Dev Biol. January 1, 2021; 469 46-53.                        


Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome., Braun DA., J Clin Invest. October 1, 2018; 128 (10): 4313-4328.


A self-inhibitory interaction within Nup155 and membrane binding are required for nuclear pore complex formation., De Magistris P., J Cell Sci. January 4, 2018; 131 (1):             


Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia., Del Viso F., Dev Cell. September 12, 2016; 38 (5): 478-92.                        


Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome., Braun DA., Nat Genet. April 1, 2016; 48 (4): 457-65.        


Crystal structure of the metazoan Nup62•Nup58•Nup54 nucleoporin complex., Chug H., Science. October 2, 2015; 350 (6256): 106-10.


Nanobodies: site-specific labeling for super-resolution imaging, rapid epitope-mapping and native protein complex isolation., Pleiner T., Elife. January 6, 2015; 4 e11349.                


Dimerization and direct membrane interaction of Nup53 contribute to nuclear pore complex assembly., Vollmer B., EMBO J. October 17, 2012; 31 (20): 4072-84.              


The C-terminal domain of Nup93 is essential for assembly of the structural backbone of nuclear pore complexes., Sachdev R., Mol Biol Cell. February 1, 2012; 23 (4): 740-9.                


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


Nup53 is required for nuclear envelope and nuclear pore complex assembly., Hawryluk-Gara LA., Mol Biol Cell. April 1, 2008; 19 (4): 1753-62.                


The conserved transmembrane nucleoporin NDC1 is required for nuclear pore complex assembly in vertebrate cells., Mansfeld J., Mol Cell. April 7, 2006; 22 (1): 93-103.


Vertebrate Nup53 interacts with the nuclear lamina and is required for the assembly of a Nup93-containing complex., Hawryluk-Gara LA., Mol Biol Cell. May 1, 2005; 16 (5): 2382-94.


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.

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