???pagination.result.count???
???pagination.result.page???
1
Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway. , Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
TAK1 promotes BMP4/ Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network. , Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
Protein 4.1 and its interaction with other cytoskeletal proteins in Xenopus laevis oogenesis. , Carotenuto R., Eur J Cell Biol. June 1, 2009; 88 (6): 343-56.
Phosphorylation of p27( BBP)/ eIF6 and its association with the cytoskeleton are developmentally regulated in Xenopus oogenesis. , Carotenuto R., Cell Mol Life Sci. July 1, 2005; 62 (14): 1641-52.
A novel G protein-coupled receptor, related to GPR4, is required for assembly of the cortical actin skeleton in early Xenopus embryos. , Tao Q , Tao Q ., Development. June 1, 2005; 132 (12): 2825-36.
Cytokeratin intermediate filament organisation and dynamics in the vegetal cortex of living Xenopus laevis oocytes and eggs. , Clarke EJ., Cell Motil Cytoskeleton. September 1, 2003; 56 (1): 13-26.
Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis. , Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
A role for GATA5 in Xenopus endoderm specification. , Weber H., Development. October 1, 2000; 127 (20): 4345-60.
Organization and characterization of the keratin cytoskeleton in the previtellogenic ovarian follicle of the lizard Podarcis sicula raf. , Maurizii MG., Mol Reprod Dev. October 1, 2000; 57 (2): 159-66.
The Xenopus homologue of Bicaudal-C is a localized maternal mRNA that can induce endoderm formation. , Wessely O ., Development. May 1, 2000; 127 (10): 2053-62.
The organization and animal-vegetal asymmetry of cytokeratin filaments in stage VI Xenopus oocytes is dependent upon F-actin and microtubules. , Gard DL ., Dev Biol. April 1, 1997; 184 (1): 95-114.
Establishment of the dorso- ventral axis in Xenopus embryos is presaged by early asymmetries in beta-catenin that are modulated by the Wnt signaling pathway. , Larabell CA ., J Cell Biol. March 10, 1997; 136 (5): 1123-36.
Immunodetection of cytoskeletal structures and the Eg5 motor protein on deep-etch replicas of Xenopus egg cortices isolated during the cortical rotation. , Chang P., Biol Cell. January 1, 1996; 88 (3): 89-98.
Reattachment of retinas to cultured pigment epithelial monolayers from Xenopus laevis. , Defoe DM., Invest Ophthalmol Vis Sci. April 1, 1994; 35 (5): 2466-76.
XLPOU-60, a Xenopus POU-domain mRNA, is oocyte-specific from very early stages of oogenesis, and localised to presumptive mesoderm and ectoderm in the blastula. , Whitfield T., Dev Biol. February 1, 1993; 155 (2): 361-70.
The role of intermediate filaments in early Xenopus development studied by antisense depletion of maternal mRNA. , Heasman J ., Dev Suppl. January 1, 1992; 119-25.
Evidence for the involvement of microtubules, ER, and kinesin in the cortical rotation of fertilized frog eggs. , Houliston E ., J Cell Biol. September 1, 1991; 114 (5): 1017-28.
Cytokeratin filaments and desmosomes in the epithelioid cells of the perineurial and arachnoidal sheaths of some vertebrate species. , Achtstätter T., Differentiation. May 1, 1989; 40 (2): 129-49.
Expression of intermediate filament proteins during development of Xenopus laevis. I. cDNA clones encoding different forms of vimentin. , Herrmann H ., Development. February 1, 1989; 105 (2): 279-98.
Analysis of cytokeratin domains by cloning and expression of intact and deleted polypeptides in Escherichia coli. , Magin TM., EMBO J. September 1, 1987; 6 (9): 2607-15.
Genesis and regression of the figures of Eberth and occurrence of cytokeratin aggregates in the epidermis of anuran larvae. , Fox H., Anat Embryol (Berl). January 1, 1986; 174 (1): 73-82.
The cytoskeleton of Xenopus oocytes and its role in development. , Wylie CC ., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 1-15.
Oocytes and early embryos of Xenopus laevis contain intermediate filaments which react with anti-mammalian vimentin antibodies. , Godsave SF., J Embryol Exp Morphol. October 1, 1984; 83 169-87.