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Summary Anatomy Item Literature (2353) Expression Attributions Wiki
XB-ANAT-4083

Papers associated with tadpole (and fn1)

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Inhibition of the serine protease HtrA1 by SerpinE2 suggests an extracellular proteolytic pathway in the control of neural crest migration., Pera EM., Elife. April 18, 2024; 12                                               


Overlapping action of T3 and T4 during Xenopus laevis development., Tribondeau A., Front Endocrinol (Lausanne). January 1, 2024; 15 1360188.      


Impaired negative feedback and death following acute stress in glucocorticoid receptor knockout Xenopus tropicalis tadpoles., Paul B., Gen Comp Endocrinol. September 15, 2022; 326 114072.      


Lysosomes are required for early dorsal signaling in the Xenopus embryo., Tejeda-Muñoz N., Proc Natl Acad Sci U S A. April 26, 2022; 119 (17): e2201008119.                          


Stage-dependent cardiac regeneration in Xenopus is regulated by thyroid hormone availability., Marshall LN., Proc Natl Acad Sci U S A. February 26, 2019; 116 (9): 3614-3623.          


Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo., Gouignard N., PLoS One. January 18, 2018; 13 (1): e0191751.                                                          


EphA7 regulates claudin6 and pronephros development in Xenopus., Sun J., Biochem Biophys Res Commun. January 8, 2018; 495 (2): 1580-1587.        


PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.                                


Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.                                


Spatiotemporally Controlled Mechanical Cues Drive Progenitor Mesenchymal-to-Epithelial Transition Enabling Proper Heart Formation and Function., Jackson TR., Curr Biol. May 8, 2017; 27 (9): 1326-1335.                            


Controlled levels of canonical Wnt signaling are required for neural crest migration., Maj E., Dev Biol. September 1, 2016; 417 (1): 77-90.                          


Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              


Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin., Gouignard N., Dis Model Mech. June 1, 2016; 9 (6): 607-20.                                      


The Lhx9-integrin pathway is essential for positioning of the proepicardial organ., Tandon P., Development. March 1, 2016; 143 (5): 831-40.                                    


Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.                                        


Snail2/Slug cooperates with Polycomb repressive complex 2 (PRC2) to regulate neural crest development., Tien CL., Development. February 15, 2015; 142 (4): 722-31.                


A distinct mechanism of vascular lumen formation in Xenopus requires EGFL7., Charpentier MS., PLoS One. February 6, 2015; 10 (2): e0116086.              


Hedgehog activity controls opening of the primary mouth., Tabler JM., Dev Biol. December 1, 2014; 396 (1): 1-7.            


The need of MMP-2 on the sperm surface for Xenopus fertilization: its role in a fast electrical block to polyspermy., Iwao Y., Mech Dev. November 1, 2014; 134 80-95.                  


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


NEDD4L regulates convergent extension movements in Xenopus embryos via Disheveled-mediated non-canonical Wnt signaling., Zhang Y., Dev Biol. August 1, 2014; 392 (1): 15-25.                              


Ric-8A, a guanine nucleotide exchange factor for heterotrimeric G proteins, is critical for cranial neural crest cell migration., Fuentealba J., Dev Biol. June 15, 2013; 378 (2): 74-82.          


Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.                      


Thyroid hormone-dependent development in Xenopus laevis: a sensitive screen of thyroid hormone signaling disruption by municipal wastewater treatment plant effluent., Searcy BT., Gen Comp Endocrinol. May 1, 2012; 176 (3): 481-92.


The cytoplasmic tyrosine kinase Arg regulates gastrulation via control of actin organization., Bonacci G., Dev Biol. April 1, 2012; 364 (1): 42-55.                                        


Histology of plastic embedded amphibian embryos and larvae., Kurth T., Genesis. March 1, 2012; 50 (3): 235-50.                                


The involvement of Eph-Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements., Park EC., Dev Biol. February 15, 2011; 350 (2): 441-50.                          


Rapid differential transport of Nodal and Lefty on sulfated proteoglycan-rich extracellular matrix regulates left-right asymmetry in Xenopus., Marjoram L., Development. February 1, 2011; 138 (3): 475-85.            


Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.            


Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.      


TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.                


Integrin alpha5beta1 and fibronectin regulate polarized cell protrusions required for Xenopus convergence and extension., Davidson LA, Davidson LA., Curr Biol. May 9, 2006; 16 (9): 833-44.                


Xenopus ILK (integrin-linked kinase) is required for morphogenetic movements during gastrulation., Yasunaga T., Genes Cells. April 1, 2005; 10 (4): 369-79.          


Assembly and remodeling of the fibrillar fibronectin extracellular matrix during gastrulation and neurulation in Xenopus laevis., Davidson LA., Dev Dyn. December 1, 2004; 231 (4): 888-95.      


Patterning and tissue movements in a novel explant preparation of the marginal zone of Xenopus laevis., Davidson LA., Gene Expr Patterns. July 1, 2004; 4 (4): 457-66.        


PKC delta is essential for Dishevelled function in a noncanonical Wnt pathway that regulates Xenopus convergent extension movements., Kinoshita N., Genes Dev. July 1, 2003; 17 (13): 1663-76.                    


The function of Xenopus germ cell nuclear factor (xGCNF) in morphogenetic movements during neurulation., Barreto G., Dev Biol. May 15, 2003; 257 (2): 329-42.            


Exposure to the herbicide acetochlor alters thyroid hormone-dependent gene expression and metamorphosis in Xenopus Laevis., Crump D., Environ Health Perspect. December 1, 2002; 110 (12): 1199-205.


Molecular cloning, expression and partial characterization of Xksy, Xenopus member of the Sky family of receptor tyrosine kinases., Kishi YA., Gene. April 17, 2002; 288 (1-2): 29-40.              


The expression pattern of thyroid hormone response genes in remodeling tadpole tissues defines distinct growth and resorption gene expression programs., Berry DL., Dev Biol. November 1, 1998; 203 (1): 24-35.                  


The expression pattern of thyroid hormone response genes in the tadpole tail identifies multiple resorption programs., Berry DL., Dev Biol. November 1, 1998; 203 (1): 12-23.                


Molecular cloning and developmental expression of the Xenopus homolog of integrin alpha 4., Whittaker CA., Ann N Y Acad Sci. October 23, 1998; 857 56-73.


Thyroid hormone induces apoptosis in primary cell cultures of tadpole intestine: cell type specificity and effects of extracellular matrix., Su Y., J Cell Biol. December 15, 1997; 139 (6): 1533-43.                


Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain., Landesman Y., Mech Dev. May 1, 1997; 63 (2): 199-209.            


ADAM 13: a novel ADAM expressed in somitic mesoderm and neural crest cells during Xenopus laevis development., Alfandari D, Alfandari D., Dev Biol. February 15, 1997; 182 (2): 314-30.      


Cloning of a Xenopus laevis cDNA encoding focal adhesion kinase (FAK) and expression during early development., Zhang X., Gene. July 28, 1995; 160 (2): 219-22.


The SH2-containing protein-tyrosine phosphatase SH-PTP2 is required upstream of MAP kinase for early Xenopus development., Tang TL., Cell. February 10, 1995; 80 (3): 473-83.              


Follistatin, an antagonist of activin, is expressed in the Spemann organizer and displays direct neuralizing activity., Hemmati-Brivanlou A., Cell. April 22, 1994; 77 (2): 283-95.                    


Xwnt-11: a maternally expressed Xenopus wnt gene., Ku M., Development. December 1, 1993; 119 (4): 1161-73.              


V(+)-fibronectin expression and localization prior to gastrulation in Xenopus laevis embryos., Danker K., Mech Dev. December 1, 1993; 44 (2-3): 155-65.

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