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Normal Table of Xenopus development: a new graphical resource. , Zahn N ., Development. July 15, 2022; 149 (14):
The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus. , Melchert J., Dev Biol. March 15, 2020; 459 (2): 138-148.
Evaluation of the toxic effects of celecoxib on Xenopus embryo development. , Yoon YH., Biochem Biophys Res Commun. June 22, 2018; 501 (2): 329-335.
Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage. , Kirmizitas A., Proc Natl Acad Sci U S A. June 6, 2017; 114 (23): 5814-5821.
Characterization of ticlopidine-induced developmental and teratogenic defects in Xenopus embryos and human endothelial cells. , Park MS., Chem Biol Interact. October 5, 2015; 240 172-8.
Annexin A3 Regulates Early Blood Vessel Formation. , Meadows SM., PLoS One. July 16, 2015; 10 (7): e0132580.
Predicting Variabilities in Cardiac Gene Expression with a Boolean Network Incorporating Uncertainty. , Grieb M., PLoS One. July 16, 2015; 10 (7): e0131832.
Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4. , Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.
Diverse functions of kindlin/fermitin proteins during embryonic development in Xenopus laevis. , Rozario T., Mech Dev. August 1, 2014; 133 203-17.
Apelin- APJ signaling is a critical regulator of endothelial MEF2 activation in cardiovascular development. , Kang Y., Circ Res. June 21, 2013; 113 (1): 22-31.
CASZ1 promotes vascular assembly and morphogenesis through the direct regulation of an EGFL7/ RhoA-mediated pathway. , Charpentier MS., Dev Cell. April 29, 2013; 25 (2): 132-43.
Regulation of G-protein signaling via Gnas is required to regulate proximal tubular growth in the Xenopus pronephros. , Zhang B., Dev Biol. April 1, 2013; 376 (1): 31-42.
Regulation of primitive hematopoiesis by class I histone deacetylases. , Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
Hippo signaling components, Mst1 and Mst2, act as a switch between self-renewal and differentiation in Xenopus hematopoietic and endothelial progenitors. , Nejigane S., Int J Dev Biol. January 1, 2013; 57 (5): 407-14.
Evolutionarily repurposed networks reveal the well-known antifungal drug thiabendazole to be a novel vascular disrupting agent. , Cha HJ., PLoS Biol. January 1, 2012; 10 (8): e1001379.
Fgf is required to regulate anterior- posterior patterning in the Xenopus lateral plate mesoderm. , Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
Xenopus er71 is involved in vascular development. , Neuhaus H ., Dev Dyn. December 1, 2010; 239 (12): 3436-45.
Notch signaling, wt1 and foxc2 are key regulators of the podocyte gene regulatory network in Xenopus. , White JT ., Development. June 1, 2010; 137 (11): 1863-73.
Claudin-like protein 24 interacts with the VEGFR-2 and VEGFR-3 pathways and regulates lymphatic vessel development. , Saharinen P., Genes Dev. May 1, 2010; 24 (9): 875-80.
Systematic discovery of nonobvious human disease models through orthologous phenotypes. , McGary KL., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9.
ETS family protein ETV2 is required for initiation of the endothelial lineage but not the hematopoietic lineage in the Xenopus embryo. , Salanga MC ., Dev Dyn. April 1, 2010; 239 (4): 1178-87.
XRASGRP2 is essential for blood vessel formation during Xenopus development. , Suzuki K., Int J Dev Biol. January 1, 2010; 54 (4): 609-15.
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.
Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis. , Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.
In vitro organogenesis from undifferentiated cells in Xenopus. , Asashima M ., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
Maturation of blood vessels by haematopoietic stem cells and progenitor cells: involvement of apelin/ APJ and angiopoietin/ Tie2 interactions in vessel caliber size regulation. , Takakura N., Thromb Haemost. June 1, 2009; 101 (6): 999-1005.
Rasip1 is required for endothelial cell motility, angiogenesis and vessel formation. , Xu K., Dev Biol. May 15, 2009; 329 (2): 269-79.
Kruppel-like factor 2 cooperates with the ETS family protein ERG to activate Flk1 expression during vascular development. , Meadows SM., Development. April 1, 2009; 136 (7): 1115-25.
FSHD region gene 1 ( FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy. , Wuebbles RD., Dis Model Mech. January 1, 2009; 2 (5-6): 267-74.
[Effect of apelin in cardiovascular system and water metabolism]. , Corvol P., Therapie. January 1, 2009; 64 (4): 233-9.
The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development. , Kazanskaya O., Development. November 1, 2008; 135 (22): 3655-64.
Fli1 acts at the top of the transcriptional network driving blood and endothelial development. , Liu F., Curr Biol. August 26, 2008; 18 (16): 1234-40.
XRASGRP2 expression during early development of Xenopus embryos. , Nagamine K., Biochem Biophys Res Commun. August 8, 2008; 372 (4): 886-91.
A Myc- Slug ( Snail2)/ Twist regulatory circuit directs vascular development. , Rodrigues CO., Development. June 1, 2008; 135 (11): 1903-11.
A crucial role of a high mobility group protein HMGA2 in cardiogenesis. , Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
SHP-2 is required for the maintenance of cardiac progenitors. , Langdon YG ., Development. November 1, 2007; 134 (22): 4119-30.
Paracrine and autocrine mechanisms of apelin signaling govern embryonic and tumor angiogenesis. , Kälin RE., Dev Biol. May 15, 2007; 305 (2): 599-614.
The g protein-coupled receptor agtrl1b regulates early development of myocardial progenitors. , Scott IC., Dev Cell. March 1, 2007; 12 (3): 403-13.
Xenopus Dab2 is required for embryonic angiogenesis. , Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis. , Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.
Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo. , Cox CM., Dev Biol. August 1, 2006; 296 (1): 177-89.
A novel gene, Ami is expressed in vascular tissue in Xenopus laevis. , Inui M., Gene Expr Patterns. August 1, 2006; 6 (6): 613-9.
The effect of VEGF on blood vessels and blood cells during Xenopus development. , Koibuchi N., Biochem Biophys Res Commun. May 26, 2006; 344 (1): 339-45.
Induction of cells expressing vascular endothelium markers from undifferentiated Xenopus presumptive ectoderm by co-treatment with activin and angiopoietin-2. , Nagamine K., Zoolog Sci. July 1, 2005; 22 (7): 755-61.
Embryonic expression of Xenopus laevis SOX7. , Fawcett SR., Gene Expr Patterns. January 1, 2004; 4 (1): 29-33.
Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus. , Walmsley M., Development. December 1, 2002; 129 (24): 5683-95.
Endoderm is required for vascular endothelial tube formation, but not for angioblast specification. , Vokes SA ., Development. February 1, 2002; 129 (3): 775-85.
Degradation of hyaluronan by a Hyal2-type hyaluronidase affects pattern formation of vitelline vessels during embryogenesis of Xenopus laevis. , Müllegger J., Mech Dev. February 1, 2002; 111 (1-2): 25-35.
The receptor tyrosine kinase EphB4 and ephrin-B ligands restrict angiogenic growth of embryonic veins in Xenopus laevis. , Helbling PM., Development. January 1, 2000; 127 (2): 269-78.
Xl erg: expression pattern and overexpression during development plead for a role in endothelial cell differentiation. , Baltzinger M., Dev Dyn. December 1, 1999; 216 (4-5): 420-33.