Papers associated with cardiovascular system (and actl6a)

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	The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
	Effects of Roundup and glyphosate formulations on intracellular transport, microtubules and actin filaments in Xenopus laevis melanophores., Hedberg D., Toxicol In Vitro. April 1, 2010; 24 (3): 795-802.
	Lymph heart musculature is under distinct developmental control from lymphatic endothelium., Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.
	Isolation and characterization of cytoplasmic cofilin-actin rods., Minamide LS., J Biol Chem. February 19, 2010; 285 (8): 5450-60.
	Proteomic analysis of blastema formation in regenerating axolotl limbs., Rao N., BMC Biol. November 30, 2009; 7 83.
	Arsenic transport by zebrafish aquaglyceroporins., Hamdi M., BMC Mol Biol. November 3, 2009; 10 104.
	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.
	Connexin 43 regulates epicardial cell polarity and migration in coronary vascular development., Rhee DY., Development. September 1, 2009; 136 (18): 3185-93.
	Interactions between beta subunits of the KCNMB family and Slo3: beta4 selectively modulates Slo3 expression and function., Yang CT., PLoS One. July 3, 2009; 4 (7): e6135.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Highly specific responses to amine odorants of individual olfactory receptor neurons in situ., Gliem S., Eur J Neurosci. June 1, 2009; 29 (12): 2315-26.
	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.
	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.
	The extracellular domain of Lrp5/6 inhibits noncanonical Wnt signaling in vivo., Bryja V., Mol Biol Cell. February 1, 2009; 20 (3): 924-36.
	Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	Induction and modulation of smooth muscle differentiation in Xenopus embryonic cells., Barillot W., Dev Dyn. November 1, 2008; 237 (11): 3373-86.
	Tumor necrosis factor-alpha attenuates thyroid hormone-induced apoptosis in vascular endothelial cell line XLgoo established from Xenopus tadpole tails., Mawaribuchi S., Endocrinology. July 1, 2008; 149 (7): 3379-89.
	XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage., Ito Y., Dev Biol. July 1, 2008; 319 (1): 34-45.
	Pleiotropic effects in Eya3 knockout mice., Söker T., BMC Dev Biol. June 23, 2008; 8 118.
	Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.
	The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.
	Patterning the embryonic kidney: BMP signaling mediates the differentiation of the pronephric tubules and duct in Xenopus laevis., Bracken CM., Dev Dyn. January 1, 2008; 237 (1): 132-44.
	H,K-ATPase protein localization and Kir4.1 function reveal concordance of three axes during early determination of left-right asymmetry., Aw S., Mech Dev. January 1, 2008; 125 (3-4): 353-72.
	The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development., Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.
	Small heat shock protein Hsp27 is required for proper heart tube formation., Brown DD., Genesis. November 1, 2007; 45 (11): 667-78.
	Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
	ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.
	Intrinsic chiral properties of the Xenopus egg cortex: an early indicator of left-right asymmetry?, Danilchik MV., Development. November 1, 2006; 133 (22): 4517-26.
	Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.
	Transgenic Xenopus laevis strain expressing cre recombinase in muscle cells., Waldner C., Dev Dyn. August 1, 2006; 235 (8): 2220-8.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.
	Cofilin mediates ATP depletion-induced endothelial cell actin alterations., Suurna MV., Am J Physiol Renal Physiol. June 1, 2006; 290 (6): F1398-407.
	Aquaporin-11: a channel protein lacking apparent transport function expressed in brain., Gorelick DA., BMC Biochem. May 1, 2006; 7 14.
	Early, H+-V-ATPase-dependent proton flux is necessary for consistent left-right patterning of non-mammalian vertebrates., Adams DS., Development. May 1, 2006; 133 (9): 1657-71.
	Bves, a member of the Popeye domain-containing gene family., Osler ME., Dev Dyn. March 1, 2006; 235 (3): 586-93.
	Protein phosphatase activity is necessary for myofibrillogenesis., Terry M., Cell Biochem Biophys. January 1, 2006; 45 (3): 265-78.
	The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis., Huot ME., Mol Biol Cell. September 1, 2005; 16 (9): 4350-61.
	Organization and developmental expression of an amphibian vascular smooth muscle alpha-actin gene., Warkman AS., Dev Dyn. August 1, 2005; 233 (4): 1546-53.
	Cloning and developmental expression of Xenopus Enabled (Xena)., Xanthos JB., Dev Dyn. June 1, 2005; 233 (2): 631-7.
	Transgenic frogs expressing the highly fluorescent protein venus under the control of a strong mammalian promoter suitable for monitoring living cells., Sakamaki K., Dev Dyn. June 1, 2005; 233 (2): 562-9.
	Identification and characterization of a novel mammalian Mg2+ transporter with channel-like properties., Goytain A., BMC Genomics. April 1, 2005; 6 48.
	Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.
	Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis., Brown DD., Development. February 1, 2005; 132 (3): 553-63.
	An in vitro analysis of myocardial potential indicates that phenotypic plasticity is an innate property of early embryonic tissue., Eisenberg LM., Stem Cells Dev. December 1, 2004; 13 (6): 614-24.
	Function and regulation of FoxF1 during Xenopus gut development., Tseng HT., Development. August 1, 2004; 131 (15): 3637-47.
	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.
	Connective-tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex., Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.
	Calcium transients regulate patterned actin assembly during myofibrillogenesis., Li H., Dev Dyn. February 1, 2004; 229 (2): 231-42.

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