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XB--855724
Papers associated with kmt2d (and Disease Ontology)
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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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The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration., Schwenty-Lara J, Nehl D, Borchers A., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.  |
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Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J, Nürnberger A, Borchers A., Dev Dyn. June 1, 2019; 248 (6): 465-476.  |
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