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Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1. , Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
EphA7 modulates apical constriction of hindbrain neuroepithelium during neurulation in Xenopus. , Wang X ., Biochem Biophys Res Commun. October 28, 2016; 479 (4): 759-765.
Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development. , Buisson I ., Dev Biol. January 15, 2015; 397 (2): 175-90.
Anillin regulates cell-cell junction integrity by organizing junctional accumulation of Rho-GTP and actomyosin. , Reyes CC., Curr Biol. June 2, 2014; 24 (11): 1263-70.
GEF-H1 functions in apical constriction and cell intercalations and is essential for vertebrate neural tube closure. , Itoh K., J Cell Sci. June 1, 2014; 127 (Pt 11): 2542-53.
The Xenopus homologue of Down syndrome critical region protein 6 drives dorsoanterior gene expression and embryonic axis formation by antagonising polycomb group proteins. , Li HY., Development. December 1, 2013; 140 (24): 4903-13.
GlialCAM, a protein defective in a leukodystrophy, serves as a ClC-2 Cl(-) channel auxiliary subunit. , Jeworutzki E., Neuron. March 8, 2012; 73 (5): 951-61.
The tumor-associated EpCAM regulates morphogenetic movements through intracellular signaling. , Maghzal N., J Cell Biol. November 1, 2010; 191 (3): 645-59.
Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling. , Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
Mad is required for wingless signaling in wing development and segment patterning in Drosophila. , Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
N- and E-cadherins in Xenopus are specifically required in the neural and non- neural ectoderm, respectively, for F-actin assembly and morphogenetic movements. , Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
TBX5 is required for embryonic cardiac cell cycle progression. , Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development. , Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
NCAM 180 acting via a conserved C-terminal domain and MLCK is essential for effective transmission with repetitive stimulation. , Polo-Parada L., Neuron. June 16, 2005; 46 (6): 917-31.
The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart. , Smith SJ ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.
Concentric zones of active RhoA and Cdc42 around single cell wounds. , Benink HA., J Cell Biol. January 31, 2005; 168 (3): 429-39.
Localization and functional analyses of the MLC1 protein involved in megalencephalic leukoencephalopathy with subcortical cysts. , Teijido O., Hum Mol Genet. November 1, 2004; 13 (21): 2581-94.
Connective- tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex. , Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.
Xenopus bagpipe-related gene, koza, may play a role in regulation of cell proliferation. , Newman CS., Dev Dyn. December 1, 2002; 225 (4): 571-80.
The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner. , Palmer S., J Cell Biol. May 28, 2001; 153 (5): 985-98.
CARP, a cardiac ankyrin repeat protein, is downstream in the Nkx2-5 homeobox gene pathway. , Zou Y., Development. February 1, 1997; 124 (4): 793-804.
The regulation of MyoD gene expression: conserved elements mediate expression in embryonic axial muscle. , Asakura A., Dev Biol. October 1, 1995; 171 (2): 386-98.