Papers associated with hypothalamus (and krt12.4)

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	The appearance and distribution of intermediate filament proteins during differentiation of the central nervous system, skin and notochord of Xenopus laevis., Godsave SF., J Embryol Exp Morphol. September 1, 1986; 97 201-23.
	Immunocytochemical identification of non-neuronal intermediate filament proteins in the developing Xenopus laevis nervous system., Szaro BG., Dev Biol. October 1, 1988; 471 (2): 207-24.
	A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus., Dent JA., Development. January 1, 1989; 105 (1): 61-74.
	Spatial, temporal, and hormonal regulation of epidermal keratin expression during development of the frog, Xenopus laevis., Nishikawa A., Dev Biol. May 1, 1992; 151 (1): 145-53.
	XLPOU-60, a Xenopus POU-domain mRNA, is oocyte-specific from very early stages of oogenesis, and localised to presumptive mesoderm and ectoderm in the blastula., Whitfield T., Dev Biol. February 1, 1993; 155 (2): 361-70.
	Opl: a zinc finger protein that regulates neural determination and patterning in Xenopus., Kuo JS., Development. August 1, 1998; 125 (15): 2867-82.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	In vivo observation of a nuclear channel-like system: evidence for a distinct interchromosomal domain compartment in interphase cells., Reichenzeller M., J Struct Biol. April 1, 2000; 129 (2-3): 175-85.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	Tsukushi functions as an organizer inducer by inhibition of BMP activity in cooperation with chordin., Ohta K., Dev Cell. September 1, 2004; 7 (3): 347-358.
	Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
	The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
	Xenopus Sox3 activates sox2 and geminin and indirectly represses Xvent2 expression to induce neural progenitor formation at the expense of non-neural ectodermal derivatives., Rogers CD., Mech Dev. January 1, 2009; 126 (1-2): 42-55.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	Purinergic receptor-induced Ca2+ signaling in the neuroepithelium of the vomeronasal organ of larval Xenopus laevis., Dittrich K., Purinergic Signal. January 1, 2014; 10 (2): 327-36.
	The neuronal and astrocytic protein SLC38A10 transports glutamine, glutamate, and aspartate, suggesting a role in neurotransmission., Hellsten SV., FEBS Open Bio. April 26, 2017; 7 (6): 730-746.

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