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XB-GENEPAGE-960315
Papers associated with kdm6a
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A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB, Willsey HR, Xu Y, Xu Y, Mei Y, Dea J, Wang S, Curtis C, Sempou E, Khokha MK, Chi NC, Willsey AJ, Fisch KM, Ideker T., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.  |
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Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J, Pauli S, Borchers A., Genesis. February 1, 2021; 59 (1-2): e23404.  |
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Role of epigenetics and miRNAs in orofacial clefts., Garland MA, Sun B, Zhang S, Reynolds K, Ji Y, Zhou CJ., Birth Defects Res. November 1, 2020; 112 (19): 1635-1659. |
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Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos., Naert T, Tulkens D, Edwards NA, Carron M, Shaidani NI, Wlizla M, Boel A, Demuynck S, Horb ME, Coucke P, Willaert A, Zorn AM, Vleminckx K, Vleminckx K., Sci Rep. September 4, 2020; 10 (1): 14662.  |
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A phospho-dependent mechanism involving NCoR and KMT2D controls a permissive chromatin state at Notch target genes., Oswald F, Rodriguez P, Giaimo BD, Antonello ZA, Mira L, Mittler G, Thiel VN, Collins KJ, Tabaja N, Cizelsky W, Rothe M, Kühl SJ, Kühl SJ, Kühl M, Ferrante F, Hein K, Kovall RA, Dominguez M, Borggrefe T., Nucleic Acids Res. June 2, 2016; 44 (10): 4703-20.  |
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Comparative expression analysis of the H3K27 demethylases, JMJD3 and UTX, with the H3K27 methylase, EZH2, in Xenopus., Kawaguchi A, Ochi H, Sudou N, Ogino H., Int J Dev Biol. January 1, 2012; 56 (4): 295-300.  |
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