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Summary Anatomy Item Literature (14956) Expression Attributions Wiki
XB-ANAT-468

Papers associated with whole organism (and nup93)

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Nucleoporin NUP205 plays a critical role in cilia and congenital disease., Marquez J., 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., Sci Rep. October 2, 2018; 8 (1): 14678.            

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

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.        

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

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

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.                    

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