Papers associated with tail (and nucb1)

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	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
	Drosha protein levels are translationally regulated during Xenopus oocyte maturation., Muggenhumer D., Mol Biol Cell. July 1, 2014; 25 (13): 2094-104.
	Germline Transgenic Methods for Tracking Cells and Testing Gene Function during Regeneration in the Axolotl., Khattak S., Stem Cell Reports. June 4, 2013; 1 (1): 90-103.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Histology of plastic embedded amphibian embryos and larvae., Kurth T., Genesis. March 1, 2012; 50 (3): 235-50.
	The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate., Li Y., J Biol Chem. December 4, 2009; 284 (49): 34283-95.
	Developmental expression of Xenopus myosin 1d and identification of a myo1d tail homology that overlaps TH1., LeBlanc-Straceski JM., Dev Growth Differ. May 1, 2009; 51 (4): 443-51.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	Exploration of the extracellular space by a large-scale secretion screen in the early Xenopus embryo., Pera EM., Int J Dev Biol. January 1, 2005; 49 (7): 781-96.

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