Papers associated with embryonic structure (and actl6a)

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	Translation of Xenopus liver messenger RNA in Xenopus oocytes: vitellogenin synthesis and conversion to yolk platelet proteins., Berridge MV., Cell. June 1, 1976; 8 (2): 283-97.
	Localization of myosin and actin in ocular nonmuscle cells. Immunofluorescence-microscopic, biochemical, and electron-microscopic studies., Drenckhahn D., Cell Tissue Res. July 19, 1977; 181 (4): 493-503.
	Monoclonal antibodies against myofibrillar components of rat skeletal muscle decorate the intermediate filaments of cultured cells., Lin JJ., Proc Natl Acad Sci U S A. April 1, 1981; 78 (4): 2335-9.
	A subcortical, pigment-containing structure in Xenopus eggs with contractile properties., Merriam RW., Dev Biol. February 1, 1983; 95 (2): 439-46.
	Interaction of metabolic inhibitors with actin fibrils., Bereiter-Hahn J., Cell Tissue Res. January 1, 1984; 238 (1): 129-34.
	Differential induction of vitellogenin gene transcription and total transcriptional activity by estrogen in Xenopus laevis liver., Martin MB., J Biol Chem. February 15, 1986; 261 (5): 2355-61.
	Tissue-specific expression of actin genes injected into Xenopus embryos., Wilson C., Cell. November 21, 1986; 47 (4): 589-99.
	Expression of Xenopus N-CAM RNA in ectoderm is an early response to neural induction., Kintner CR., Development. March 1, 1987; 99 (3): 311-25.
	Autoantibodies in hypertrophic cardiomyopathy and their clinical significance., Gregor P., Eur Heart J. July 1, 1987; 8 (7): 773-8.
	A processed gene coding for a sarcomeric actin in Xenopus laevis and Xenopus tropicalis., Stutz F., EMBO J. July 1, 1987; 6 (7): 1989-95.
	An amphibian cytoskeletal-type actin gene is expressed exclusively in muscle tissue., Mohun TJ., Development. October 1, 1987; 101 (2): 393-402.
	Synergistic induction of mesoderm by FGF and TGF-beta and the identification of an mRNA coding for FGF in the early Xenopus embryo., Kimelman D., Cell. December 4, 1987; 51 (5): 869-77.
	Expression and segregation of nucleoplasmin during development in Xenopus., Litvin J., Development. January 1, 1988; 102 (1): 9-21.
	Increase of cytosolic calcium results in formation of F-actin aggregates in endothelial cells., Stolz B., Cell Biol Int Rep. April 1, 1988; 12 (4): 321-9.
	Structure, chromosome location, and expression of the human gamma-actin gene: differential evolution, location, and expression of the cytoskeletal beta- and gamma-actin genes., Erba HP., Mol Cell Biol. April 1, 1988; 8 (4): 1775-89.
	Microinjection of synthetic Xhox-1A homeobox mRNA disrupts somite formation in developing Xenopus embryos., Harvey RP., Cell. June 3, 1988; 53 (5): 687-97.
	Proteins regulating actin assembly in oogenesis and early embryogenesis of Xenopus laevis: gelsolin is the major cytoplasmic actin-binding protein., Ankenbauer T., J Cell Biol. October 1, 1988; 107 (4): 1489-98.
	Expression of intermediate filament proteins during development of Xenopus laevis. III. Identification of mRNAs encoding cytokeratins typical of complex epithelia., Fouquet B., Development. December 1, 1988; 104 (4): 533-48.
	Amphibian (urodele) myotomes display transitory anterior/posterior and medial/lateral differentiation patterns., Neff AW., Dev Biol. April 1, 1989; 132 (2): 529-43.
	XlHbox 8: a novel Xenopus homeo protein restricted to a narrow band of endoderm., Wright CV., Development. April 1, 1989; 105 (4): 787-94.
	Bimodal and graded expression of the Xenopus homeobox gene Xhox3 during embryonic development., Ruiz i Altaba A., Development. May 1, 1989; 106 (1): 173-83.
	The appearance of acetylated alpha-tubulin during early development and cellular differentiation in Xenopus., Chu DT., Dev Biol. November 1, 1989; 136 (1): 104-17.
	MyoD expression in the forming somites is an early response to mesoderm induction in Xenopus embryos., Hopwood ND., EMBO J. November 1, 1989; 8 (11): 3409-17.
	A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest., Hopwood ND., Cell. December 1, 1989; 59 (5): 893-903.
	Molecular approach to dorsoanterior development in Xenopus laevis., Sato SM., Dev Biol. January 1, 1990; 137 (1): 135-41.
	Spreading of trypsinized cells: cytoskeletal dynamics and energy requirements., Bereiter-Hahn J., J Cell Sci. May 1, 1990; 96 ( Pt 1) 171-88.
	Localization of specific mRNAs in Xenopus embryos by whole-mount in situ hybridization., Hemmati-Brivanlou A., Development. October 1, 1990; 110 (2): 325-30.
	A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H., Genes Dev. January 1, 1991; 5 (1): 94-104.
	Gene activation in the amphibian mesoderm., Hopwood ND., Dev Suppl. January 1, 1991; 1 95-104.
	Variant cDNAs encoding proteins similar to the alpha subunit of chicken CapZ., Cooper JA., Cell Motil Cytoskeleton. January 1, 1991; 18 (3): 204-14.
	Xenopus Myf-5 marks early muscle cells and can activate muscle genes ectopically in early embryos., Hopwood ND., Development. February 1, 1991; 111 (2): 551-60.
	Coordinate estrogen-regulated instability of serum protein-coding messenger RNAs in Xenopus laevis., Pastori RL., Mol Endocrinol. April 1, 1991; 5 (4): 461-8.
	Progressively restricted expression of a new homeobox-containing gene during Xenopus laevis embryogenesis., Su MW., Development. April 1, 1991; 111 (4): 1179-87.
	Expression of SPARC/osteonectin in tissues of bony and cartilaginous vertebrates., Ringuette M., Biochem Cell Biol. April 1, 1991; 69 (4): 245-50.
	Developmental and regional expression of thyroid hormone receptor genes during Xenopus metamorphosis., Kawahara A., Development. August 1, 1991; 112 (4): 933-43.
	Antimicrobial peptides in the stomach of Xenopus laevis., Moore KS., J Biol Chem. October 15, 1991; 266 (29): 19851-7.
	Transient expression of XMyoD in non-somitic mesoderm of Xenopus gastrulae., Frank D., Development. December 1, 1991; 113 (4): 1387-93.
	Localized expression of a Xenopus POU gene depends on cell-autonomous transcriptional activation and induction-dependent inactivation., Frank D., Development. June 1, 1992; 115 (2): 439-48.
	Ventrolateral regionalization of Xenopus laevis mesoderm is characterized by the expression of alpha-smooth muscle actin., Saint-Jeannet JP., Development. August 1, 1992; 115 (4): 1165-73.
	Expression of tenascin mRNA in mesoderm during Xenopus laevis embryogenesis: the potential role of mesoderm patterning in tenascin regionalization., Umbhauer M., Development. September 1, 1992; 116 (1): 147-57.
	Amphibian intestinal villin: isolation and expression during embryonic and larval development., Heusser S., J Cell Sci. November 1, 1992; 103 ( Pt 3) 699-708.
	A carboxyl-terminal truncated version of the activin receptor mediates activin signals in early Xenopus embryos., Nishimatsu S., FEBS Lett. November 9, 1992; 312 (2-3): 169-73.
	Characterization of the Xenopus Hox 2.4 gene and identification of control elements in its intron., Bittner D., Dev Dyn. January 1, 1993; 196 (1): 11-24.
	Polarized distribution of vinculin epitopes in Xenopus laevis embryos., Levi G., C R Acad Sci III. January 1, 1993; 316 (4): 359-65.
	Characterization of the GArC motif. A novel cis-acting element of the human cardiac myosin heavy chain genes., Mably JD., J Biol Chem. January 5, 1993; 268 (1): 476-82.
	Xenopus Distal-less related homeobox genes are expressed in the developing forebrain and are induced by planar signals., Papalopulu N., Development. March 1, 1993; 117 (3): 961-75.
	Induction of cardiac muscle differentiation in isolated animal pole explants of Xenopus laevis embryos., Logan M., Development. July 1, 1993; 118 (3): 865-75.
	Mesoderm formation in Xenopus ectodermal explants overexpressing Xwnt8: evidence for a cooperating signal reaching the animal pole by gastrulation., Sokol SY., Development. August 1, 1993; 118 (4): 1335-42.
	Competence prepattern in the animal hemisphere of the 8-cell-stage Xenopus embryo., Kinoshita K., Dev Biol. November 1, 1993; 160 (1): 276-84.
	XFKH2, a Xenopus HNF-3 alpha homologue, exhibits both activin-inducible and autonomous phases of expression in early embryos., Bolce ME., Dev Biol. December 1, 1993; 160 (2): 413-23.

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