Papers associated with lateral plate mesoderm

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	Alteration of structure and penetrability of the vitelline envelope after passage of eggs from coelom to oviduct in Xenopus laevis., Grey RD., J Exp Zool. July 1, 1977; 201 (1): 73-83.
	The free swimming Pipa larvae, with a review of pipid larvae and pipid phylogeny (Anura: Pipidae)., Sokol OM., J Morphol. December 1, 1977; 154 (3): 357-425.
	Dual contribution of embryonic ventral blood island and dorsal lateral plate mesoderm during ontogeny of hemopoietic cells in Xenopus laevis., Kau CL., J Immunol. November 1, 1983; 131 (5): 2262-6.
	Dorsalization and neural induction: properties of the organizer in Xenopus laevis., Smith JC., J Embryol Exp Morphol. December 1, 1983; 78 299-317.
	Different modes of pronephric duct origin among vertebrates., Poole TJ., Scan Electron Microsc. January 1, 1984; (Pt 1): 475-82.
	A flow cytometric analysis of the embryonic origin of lymphocytes in diploid/triploid chimeric Xenopus laevis., Flajnik MF., Dev Biol. July 1, 1984; 104 (1): 247-54.
	Dorsal lateral plate mesoderm influences proliferation and differentiation of hemopoietic stem cells derived from ventral lateral plate mesoderm during early development of Xenopus laevis embryos., Turpen JB., J Leukoc Biol. September 1, 1985; 38 (3): 415-27.
	Regional specification within the mesoderm of early embryos of Xenopus laevis., Dale L., Development. June 1, 1987; 100 (2): 279-95.
	Fates of the blastomeres of the 32-cell-stage Xenopus embryo., Moody SA., Dev Biol. August 1, 1987; 122 (2): 300-19.
	The development of an assay to detect mRNAs that affect early development., Woodland HR., Development. December 1, 1987; 101 (4): 925-30.
	Induction of mesodermal tissues by acidic and basic heparin binding growth factors., Grunz H., Cell Differ. February 1, 1988; 22 (3): 183-9.
	The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos., Kao KR., Dev Biol. May 1, 1988; 127 (1): 64-77.
	Microinjection of synthetic Xhox-1A homeobox mRNA disrupts somite formation in developing Xenopus embryos., Harvey RP., Cell. June 3, 1988; 53 (5): 687-97.
	Inductive effects of fibroblast growth factor and lithium ion on Xenopus blastula ectoderm., Slack JM., Development. July 1, 1988; 103 (3): 581-90.
	The distribution of fibronectin and tenascin along migratory pathways of the neural crest in the trunk of amphibian embryos., Epperlein HH., Development. August 1, 1988; 103 (4): 743-56.
	Accumulation and decay of DG42 gene products follow a gradient pattern during Xenopus embryogenesis., Rosa F., Dev Biol. September 1, 1988; 129 (1): 114-23.
	Gene expression in the embryonic nervous system of Xenopus laevis., Richter K., Proc Natl Acad Sci U S A. November 1, 1988; 85 (21): 8086-90.
	A gradient of homeodomain protein in developing forelimbs of Xenopus and mouse embryos., Oliver G., Cell. December 23, 1988; 55 (6): 1017-24.
	Dorsalization of mesoderm induction by lithium., Kao KR., Dev Biol. March 1, 1989; 132 (1): 81-90.
	Determination of axial polarity in the vertebrate embryo: homeodomain proteins and homeogenetic induction., De Robertis EM., Cell. April 21, 1989; 57 (2): 189-91.
	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.
	Segregation of fate during cleavage of frog (Xenopus laevis) blastomeres., Moody SA., Anat Embryol (Berl). January 1, 1990; 182 (4): 347-62.
	Origin and distribution of enteric neurones in Xenopus., Epperlein HH., Anat Embryol (Berl). January 1, 1990; 182 (1): 53-67.
	Distribution of integrins and their ligands in the trunk of Xenopus laevis during neural crest cell migration., Krotoski D., J Exp Zool. February 1, 1990; 253 (2): 139-50.
	Comparative studies on the vascular organization of carotid labyrinths of anurans and caudates., Kusakabe T., J Morphol. April 1, 1990; 204 (1): 47-55.
	The Xenopus XIHbox 6 homeo protein, a marker of posterior neural induction, is expressed in proliferating neurons., Wright CV., Development. May 1, 1990; 109 (1): 225-34.
	The restriction of the heart morphogenetic field in Xenopus laevis., Sater AK., Dev Biol. August 1, 1990; 140 (2): 328-36.
	[Self-organization in the determination of the size of the axial structures in the embryogenesis of the clawed toad]., Zaraĭskiĭ AG., Ontogenez. January 1, 1991; 22 (4): 365-74.
	Expression of a leukocyte-specific antigen during ontogeny in Xenopus laevis., Smith PB., Dev Immunol. January 1, 1991; 1 (4): 295-307.
	Xwnt-8, a Xenopus Wnt-1/int-1-related gene responsive to mesoderm-inducing growth factors, may play a role in ventral mesodermal patterning during embryogenesis., Christian JL., Development. April 1, 1991; 111 (4): 1045-55.
	Progressively restricted expression of a new homeobox-containing gene during Xenopus laevis embryogenesis., Su MW., Development. April 1, 1991; 111 (4): 1179-87.
	Xenopus dorsal pattern formation is lithium-sensitive., Klein SL., Rouxs Arch Dev Biol. July 1, 1991; 199 (7): 427-436.
	The switch from larval to adult globin gene expression in Xenopus laevis is mediated by erythroid cells from distinct compartments., Weber R., Development. August 1, 1991; 112 (4): 1021-9.
	Expression of two nonallelic type II procollagen genes during Xenopus laevis embryogenesis is characterized by stage-specific production of alternatively spliced transcripts., Su MW., J Cell Biol. October 1, 1991; 115 (2): 565-75.
	Transient expression of XMyoD in non-somitic mesoderm of Xenopus gastrulae., Frank D., Development. December 1, 1991; 113 (4): 1387-93.
	Dissecting Wnt signalling pathways and Wnt-sensitive developmental processes through transient misexpression analyses in embryos of Xenopus laevis., Moon RT., Dev Suppl. January 1, 1992; 85-94.
	Induction of dorsal and ventral mesoderm by ectopically expressed Xenopus basic fibroblast growth factor., Kimelman D., Development. January 1, 1992; 114 (1): 261-9.
	The marginal zone of the 32-cell amphibian embryo contains all the information required for chordamesoderm development., Pierce KE., J Exp Zool. April 15, 1992; 262 (1): 40-50.
	Secretory and inductive properties of Drosophila wingless protein in Xenopus oocytes and embryos., Chakrabarti A., Development. May 1, 1992; 115 (1): 355-69.
	Expression of RNA isolated from the water-shunting complex of a sap-sucking insect increases the membrane permeability for water in Xenopus oocytes., Guillam MT., Exp Cell Res. June 1, 1992; 200 (2): 301-5.
	Bone morphogenetic protein 4: a ventralizing factor in early Xenopus development., Dale L., Development. June 1, 1992; 115 (2): 573-85.
	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.
	Suramin changes the fate of Spemann's organizer and prevents neural induction in Xenopus laevis., Grunz H., Mech Dev. August 1, 1992; 38 (2): 133-41.
	A novel homeobox gene expressed in the anterior neural plate of the Xenopus embryo., Zaraisky AG., Dev Biol. August 1, 1992; 152 (2): 373-82.
	N-cadherin transcripts in Xenopus laevis from early tailbud to tadpole., Simonneau L., Dev Dyn. August 1, 1992; 194 (4): 247-60.
	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.
	Interactions between Xwnt-8 and Spemann organizer signaling pathways generate dorsoventral pattern in the embryonic mesoderm of Xenopus., Christian JL., Genes Dev. January 1, 1993; 7 (1): 13-28.
	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.
	[Regionalization of the expression of tenascin as a response to the inducers of mesoderm]., Umbhauer M., C R Seances Soc Biol Fil. January 1, 1993; 187 (3): 341-55.
	Evidence that the border of the neural plate may be positioned by the interaction between signals that induce ventral and dorsal mesoderm., Zhang J., Dev Dyn. February 1, 1993; 196 (2): 79-90.

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