Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (18) GO Terms (1) Nucleotides (185) Proteins (59) Interactants (102) Wiki
XB-GENEPAGE-1009710

Papers associated with nup205



???displayGene.coCitedPapers???

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

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.                                                                        


Structure of the cytoplasmic ring of the Xenopus laevis nuclear pore complex., Zhu X, Huang G, Zeng C, Zhan X, Liang K, Xu Q, Zhao Y, Wang P, Wang Q, Zhou Q, Tao Q, Liu M, Lei J, Yan C, Shi Y., Science. June 10, 2022; 376 (6598): eabl8280.


Structure of cytoplasmic ring of nuclear pore complex by integrative cryo-EM and AlphaFold., Fontana P, Dong Y, Pi X, Tong AB, Hecksel CW, Wang L, Fu TM, Bustamante C, Wu H., Science. June 10, 2022; 376 (6598): eabm9326.


Cryo-EM structure of the inner ring from the Xenopus laevis nuclear pore complex., Huang G, Zhan X, Zeng C, Liang K, Zhu X, Zhao Y, Wang P, Wang Q, Zhou Q, Tao Q, Tao Q, Liu M, Lei J, Yan C, Shi Y, Shi Y., Cell Res. May 1, 2022; 32 (5): 451-460.                                              


Cryo-EM structure of the nuclear ring from Xenopus laevis nuclear pore complex., Huang G, Zhan X, Zeng C, Zhu X, Liang K, Zhao Y, Wang P, Wang Q, Zhou Q, Tao Q, Liu M, Lei J, Yan C, Shi Y., Cell Res. April 1, 2022; 32 (4): 349-358.


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


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.                                    


Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome., Braun DA, Lovric S, Schapiro D, Schneider R, Marquez J, Asif M, Hussain MS, Daga A, Widmeier E, Rao J, Ashraf S, Tan W, Lusk CP, Kolb A, Jobst-Schwan T, Schmidt JM, Hoogstraten CA, Eddy K, Kitzler TM, Shril S, Moawia A, Schrage K, Khayyat AIA, Lawson JA, Gee HY, Warejko JK, Hermle T, Majmundar AJ, Hugo H, Budde B, Motameny S, Altmüller J, Noegel AA, Fathy HM, Gale DP, Waseem SS, Khan A, Kerecuk L, Hashmi S, Mohebbi N, Ettenger R, Serdaroğlu E, Alhasan KA, Hashem M, Goncalves S, Ariceta G, Ubetagoyena M, Antonin W, Baig SM, Alkuraya FS, Shen Q, Xu H, Antignac C, Lifton RP, Mane S, Nürnberg P, Khokha MK, Hildebrandt F., 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, Tatarek-Nossol M, Dewor M, Antonin W., J Cell Sci. January 4, 2018; 131 (1):             


Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome., Braun DA, Sadowski CE, Kohl S, Lovric S, Astrinidis SA, Pabst WL, Gee HY, Ashraf S, Lawson JA, Shril S, Airik M, Tan W, Schapiro D, Rao J, Choi WI, Hermle T, Kemper MJ, Pohl M, Ozaltin F, Konrad M, Bogdanovic R, Büscher R, Helmchen U, Serdaroglu E, Lifton RP, Antonin W, Hildebrandt F., Nat Genet. April 1, 2016; 48 (4): 457-65.        


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 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.                


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.              


Nup53 is required for nuclear envelope and nuclear pore complex assembly., Hawryluk-Gara LA, Platani M, Santarella R, Wozniak RW, Mattaj IW., 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, Güttinger S, Hawryluk-Gara LA, Panté N, Mall M, Galy V, Haselmann U, Mühlhäusser P, Wozniak RW, Mattaj IW, Kutay U, Antonin W., 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, Shibuya EK, Wozniak RW., 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, Mattaj IW, Askjaer P., Mol Biol Cell. December 1, 2003; 14 (12): 5104-15.


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.

???pagination.result.page??? 1