Papers associated with oocyte (and nodal1)

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	The early dorsal signal in vertebrate embryos requires endolysosomal membrane trafficking., Azbazdar Y., Bioessays. January 1, 2024; 46 (1): e2300179.
	Subunit-specific effects of poricoic acid A on NMDA receptors., Lee J., Pharmacol Rep. April 1, 2020; 72 (2): 472-480.
	Genome organization of the vg1 and nodal3 gene clusters in the allotetraploid frog Xenopus laevis., Suzuki A., Dev Biol. June 15, 2017; 426 (2): 236-244.
	A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.
	Possible regulation of Oct60 transcription by a positive feedback loop in Xenopus oocytes., Morichika K., Zygote. May 1, 2014; 1-9.
	Foxi2 is an animally localized maternal mRNA in Xenopus, and an activator of the zygotic ectoderm activator Foxi1e., Cha SW., PLoS One. January 1, 2012; 7 (7): e41782.
	Membrane trauma and Na+ leak from Nav1.6 channels., Wang JA., Am J Physiol Cell Physiol. October 1, 2009; 297 (4): C823-34.
	Maternal Tgif1 regulates nodal gene expression in Xenopus., Kerr TC., Dev Dyn. October 1, 2008; 237 (10): 2862-73.
	The role of FoxC1 in early Xenopus development., Cha JY., Dev Dyn. October 1, 2007; 236 (10): 2731-41.
	Xenopus Lefty requires proprotein cleavage but not N-linked glycosylation to inhibit nodal signaling., Westmoreland JJ., Dev Dyn. August 1, 2007; 236 (8): 2050-61.
	Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant., Fein AJ., BMC Genomics. May 16, 2007; 8 226.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Xantivin suppresses the activity of EGF-CFC genes to regulate nodal signaling., Tanegashima K., Int J Dev Biol. June 1, 2004; 48 (4): 275-83.
	Differential modulation of NR1-NR2A and NR1-NR2B subtypes of NMDA receptor by PDZ domain-containing proteins., Iwamoto T., J Neurochem. April 1, 2004; 89 (1): 100-8.
	Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.
	Effects of heterodimerization and proteolytic processing on Derrière and Nodal activity: implications for mesoderm induction in Xenopus., Eimon PM., Development. July 1, 2002; 129 (13): 3089-103.
	Characterization and comparison of the NR3A subunit of the NMDA receptor in recombinant systems and primary cortical neurons., Sasaki YF., J Neurophysiol. April 1, 2002; 87 (4): 2052-63.
	Overexpression of the Xenopus tight-junction protein claudin causes randomization of the left-right body axis., Brizuela BJ., Dev Biol. February 15, 2001; 230 (2): 217-29.
	Zic3 is involved in the left-right specification of the Xenopus embryo., Kitaguchi T., Development. November 1, 2000; 127 (22): 4787-95.
	Internal Mg2+ block of recombinant NMDA channels mutated within the selectivity filter and expressed in Xenopus oocytes., Kupper J., J Physiol. February 15, 1998; 507 ( Pt 1) 1-12.
	Stoichiometry of recombinant N-methyl-D-aspartate receptor channels inferred from single-channel current patterns., Premkumar LS., J Gen Physiol. November 1, 1997; 110 (5): 485-502.
	Expression cloning of a Xenopus T-related gene (Xombi) involved in mesodermal patterning and blastopore lip formation., Lustig KD., Development. December 1, 1996; 122 (12): 4001-12.
	A Xenopus nodal-related gene that acts in synergy with noggin to induce complete secondary axis and notochord formation., Lustig KD., Development. October 1, 1996; 122 (10): 3275-82.

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