???pagination.result.count???
???pagination.result.page???
1
Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates. , Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
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.
Leukemia inhibitory factor signaling in Xenopus embryo: Insights from gain of function analysis and dominant negative mutant of the receptor. , Jalvy S., Dev Biol. March 15, 2019; 447 (2): 200-213.
Models of convergent extension during morphogenesis. , Shindo A., Wiley Interdiscip Rev Dev Biol. January 1, 2018; 7 (1):
The Lhx9-integrin pathway is essential for positioning of the proepicardial organ. , Tandon P ., Development. March 1, 2016; 143 (5): 831-40.
A distinct mechanism of vascular lumen formation in Xenopus requires EGFL7. , Charpentier MS., PLoS One. February 6, 2015; 10 (2): e0116086.
A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. , Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/ β-catenin-mediated lung specification in Xenopus. , Rankin SA , Rankin SA ., Development. August 1, 2012; 139 (16): 3010-20.
Dystroglycan is involved in skin morphogenesis downstream of the Notch signaling pathway. , Sirour C., Mol Biol Cell. August 15, 2011; 22 (16): 2957-69.
Inversin relays Frizzled-8 signals to promote proximal pronephros development. , Lienkamp S ., Proc Natl Acad Sci U S A. November 23, 2010; 107 (47): 20388-93.
MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization. , Suzuki M ., Development. July 1, 2010; 137 (14): 2329-39.
In vivo analyzes of dystroglycan function during somitogenesis in Xenopus laevis. , Hidalgo M., Dev Dyn. June 1, 2009; 238 (6): 1332-45.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development. , Urban AE ., Dev Biol. September 1, 2006; 297 (1): 103-17.
Syndecan-4 regulates non-canonical Wnt signalling and is essential for convergent and extension movements in Xenopus embryos. , Muñoz R., Nat Cell Biol. May 1, 2006; 8 (5): 492-500.
Nuclear translocation of Xenopus laevis paxillin. , Ogawa M., Biochem Biophys Res Commun. May 16, 2003; 304 (4): 676-83.
The Wnt/Wg signal transducer beta-catenin controls fibronectin expression. , Gradl D ., Mol Cell Biol. August 1, 1999; 19 (8): 5576-87.
Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning. , Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
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.
Integrin alpha 6 expression is required for early nervous system development in Xenopus laevis. , Lallier TE., Development. August 1, 1996; 122 (8): 2539-54.
Dorsalizing and neuralizing properties of Xdsh, a maternally expressed Xenopus homolog of dishevelled. , Sokol SY ., Development. June 1, 1995; 121 (6): 1637-47.
Appearance and distribution of laminin during development of Xenopus laevis. , Fey J., Differentiation. February 1, 1990; 42 (3): 144-52.
Regional specificity of glycoconjugates in Xenopus and axolotl embryos. , Slack JM ., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 137-53.