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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 by cryo-electron microscopy single particle analysis. , Huang G., Cell Res. June 1, 2020; 30 (6): 520-531.
Parvoviruses cause nuclear envelope breakdown by activating key enzymes of mitosis. , Porwal M., PLoS Pathog. October 1, 2013; 9 (10): e1003671.
The permeability of reconstituted nuclear pores provides direct evidence for the selective phase model. , Hülsmann BB., Cell. August 17, 2012; 150 (4): 738-51.
Indian hedgehog signaling is required for proper formation, maintenance and migration of Xenopus neural crest. , Agüero TH., Dev Biol. April 15, 2012; 364 (2): 99-113.
Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left- Right Asymmetry. , Pai VP ., Stem Cells Int. January 1, 2012; 2012 353491.
Transmembrane potential of GlyCl-expressing instructor cells induces a neoplastic-like conversion of melanocytes via a serotonergic pathway. , Blackiston D ., Dis Model Mech. January 1, 2011; 4 (1): 67-85.
PIASy-dependent SUMOylation regulates DNA topoisomerase IIalpha activity. , Ryu H., J Cell Biol. November 15, 2010; 191 (4): 783-94.
ER membrane-bending proteins are necessary for de novo nuclear pore formation. , Dawson TR., J Cell Biol. March 9, 2009; 184 (5): 659-75.
A new role for the Endothelin-1/Endothelin-A receptor signaling during early neural crest specification. , Bonano M., Dev Biol. November 1, 2008; 323 (1): 114-29.
Hairy2- Id3 interactions play an essential role in Xenopus neural crest progenitor specification. , Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.
Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. , Aoki Y., Dev Biol. July 1, 2003; 259 (1): 19-33.