Papers associated with 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, 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.
	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.
	The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice., Beckers A, Ott T, Schuster-Gossler K, Boldt K, Alten L, Ueffing M, Blum M, Gossler A., Sci Rep. October 2, 2018; 8 (1): 14678.
	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):
	Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia., Del Viso F, Huang F, Myers J, Chalfant M, Zhang Y, Reza N, Bewersdorf J, Lusk CP, Khokha MK., 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, 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.
	Crystal structure of the metazoan Nup62•Nup58•Nup54 nucleoporin complex., Chug H, Trakhanov S, Hülsmann BB, Pleiner T, Görlich D., 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, 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.
	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 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.
	PACSIN2 is a regulator of the metalloprotease/disintegrin ADAM13., Cousin H, Gaultier A, Bleux C, Darribère T, Alfandari D, Alfandari D., Dev Biol. November 1, 2000; 227 (1): 197-210.
	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.
	Incorporation of the nuclear pore basket protein nup153 into nuclear pore structures is dependent upon lamina assembly: evidence from cell-free extracts of Xenopus eggs., Smythe C, Jenkins HE, Hutchison CJ., EMBO J. August 1, 2000; 19 (15): 3918-31.
	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.
	Nup93, a vertebrate homologue of yeast Nic96p, forms a complex with a novel 205-kDa protein and is required for correct nuclear pore assembly., Grandi P, Dang T, Pané N, Shevchenko A, Mann M, Forbes D, Hurt E., Mol Biol Cell. October 1, 1997; 8 (10): 2017-38.
	Identification of new localized RNAs in the Xenopus oocyte by differential display PCR., Hudson JW, Alarcón VB, Elinson RP., Dev Genet. January 1, 1996; 19 (3): 190-8.

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