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Summary Anatomy Item Literature (2386) Expression Attributions Wiki
XB-ANAT-509

Papers associated with epithelium∨derBy=4 (and mapt)

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Large, long range tensile forces drive convergence during Xenopus blastopore closure and body axis elongation., Shook DR., Elife. March 13, 2018; 7                           

Malaria parasite CelTOS targets the inner leaflet of cell membranes for pore-dependent disruption., Jimah JR., Elife. December 1, 2016; 5                   

Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.                                              

Development of a novel selective inhibitor of the Down syndrome-related kinase Dyrk1A., Ogawa Y., Nat Commun. October 5, 2010; 1 86.  

MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.                                                      

Developmental regulation of central spindle assembly and cytokinesis during vertebrate embryogenesis., Kieserman EK., Curr Biol. January 22, 2008; 18 (2): 116-23.            

Block of hERG channel by ziprasidone: biophysical properties and molecular determinants., Su Z., Biochem Pharmacol. January 12, 2006; 71 (3): 278-86.

The circadian clock-containing photoreceptor cells in Xenopus laevis express several isoforms of casein kinase I., Constance CM., Brain Res Mol Brain Res. May 20, 2005; 136 (1-2): 199-211.            

State-dependent trapping of flecainide in the cardiac sodium channel., Ramos E., J Physiol. October 1, 2004; 560 (Pt 1): 37-49.

Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen., Phiel CJ., J Biol Chem. September 28, 2001; 276 (39): 36734-41.              

Sodium channel isoform-specific effects of halothane: protein kinase C co-expression and slow inactivation gating., Patel MK., Br J Pharmacol. August 1, 2000; 130 (8): 1785-92.

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