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 Anatomy Item Literature (4079) Expression Attributions Wiki
XB-ANAT-3714

Papers associated with right (and kmt2d)

Limit to papers also referencing gene:
Show all right papers
???pagination.result.count???

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

Sort Newest To Oldest Sort Oldest To Newest

A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.            


Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J., Genesis. February 1, 2021; 59 (1-2): e23404.      


Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J., Dev Dyn. June 1, 2019; 248 (6): 465-476.                  


A phospho-dependent mechanism involving NCoR and KMT2D controls a permissive chromatin state at Notch target genes., Oswald F., Nucleic Acids Res. June 2, 2016; 44 (10): 4703-20.                              


WDR5 associates with histone H3 methylated at K4 and is essential for H3 K4 methylation and vertebrate development., Wysocka J., Cell. June 17, 2005; 121 (6): 859-72.  

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