Papers associated with animal cap

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	Are the primordial germ cells (PGCs) in urodela formed by the inductive action of the vegetative yolk mass?, Michael P., Dev Biol. May 1, 1984; 103 (1): 109-16.
	Development of the ectoderm in Xenopus: tissue specification and the role of cell association and division., Jones EA., Cell. January 31, 1986; 44 (2): 345-55.
	The midblastula cell cycle transition and the character of mesoderm in u.v.-induced nonaxial Xenopus development., Cooke J., Development. February 1, 1987; 99 (2): 197-210.
	The organization of mesodermal pattern in Xenopus laevis: experiments using a Xenopus mesoderm-inducing factor., Cooke J., Development. December 1, 1987; 101 (4): 893-908.
	The development of an assay to detect mRNAs that affect early development., Woodland HR., Development. December 1, 1987; 101 (4): 925-30.
	Gastrulation and larval pattern in Xenopus after blastocoelic injection of a Xenopus-derived inducing factor: experiments testing models for the normal organization of mesoderm., Cooke J., Dev Biol. February 1, 1989; 131 (2): 383-400.
	Potentiation by the lithium ion of morphogenetic responses to a Xenopus inducing factor., Cooke J., Development. March 1, 1989; 105 (3): 549-58.
	Mesoderm-inducing factors and Spemann's organiser phenomenon in amphibian development., Cooke J., Development. October 1, 1989; 107 (2): 229-41.
	Mesoderm-inducing factor from bovine amniotic fluid: purification and N-terminal amino acid sequence determination., Chertov OYu., Biomed Sci. January 1, 1990; 1 (5): 499-506.
	Activins are expressed early in Xenopus embryogenesis and can induce axial mesoderm and anterior structures., Thomsen G., Cell. November 2, 1990; 63 (3): 485-93.
	Growth-factor-related proteins that are inducers in early amphibian development may mediate similar steps in amniote (bird) embryogenesis., Cooke J., Development. January 1, 1991; 111 (1): 197-212.
	Gene activation in the amphibian mesoderm., Hopwood ND., Dev Suppl. January 1, 1991; 1 95-104.
	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.
	Retinoic acid modifies mesodermal patterning in early Xenopus embryos., Ruiz i Altaba A., Genes Dev. February 1, 1991; 5 (2): 175-87.
	Differential expression of two cadherins in Xenopus laevis., Angres B., Development. March 1, 1991; 111 (3): 829-44.
	Bone morphogenetic protein 4 (BMP-4), a member of the TGF-beta family, in early embryos of Xenopus laevis: analysis of mesoderm inducing activity., Köster M., Mech Dev. March 1, 1991; 33 (3): 191-9.
	Changes in neural and lens competence in Xenopus ectoderm: evidence for an autonomous developmental timer., Servetnick M., Development. May 1, 1991; 112 (1): 177-88.
	Autonomous differentiation of dorsal axial structures from an animal cap cleavage stage blastomere in Xenopus., Gallagher BC., Development. August 1, 1991; 112 (4): 1103-14.
	Xwnt-8 modifies the character of mesoderm induced by bFGF in isolated Xenopus ectoderm., Christian JL., EMBO J. January 1, 1992; 11 (1): 33-41.
	The patterning and functioning of protrusive activity during convergence and extension of the Xenopus organiser., Keller R., Dev Suppl. January 1, 1992; 81-91.
	Secretory and inductive properties of Drosophila wingless protein in Xenopus oocytes and embryos., Chakrabarti A., Development. May 1, 1992; 115 (1): 355-69.
	Xenopus blastulae show regional differences in competence for mesoderm induction: correlation with endogenous basic fibroblast growth factor levels., Godsave SF., Dev Biol. June 1, 1992; 151 (2): 506-15.
	DVR-4 (bone morphogenetic protein-4) as a posterior-ventralizing factor in Xenopus mesoderm induction., Jones CM., Development. June 1, 1992; 115 (2): 639-47.
	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.
	Ectopic induction of dorsal mesoderm by overexpression of Xwnt-8 elevates the neural competence of Xenopus ectoderm., Otte AP., Dev Biol. July 1, 1992; 152 (1): 184-7.
	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.
	[Function, molecular structure and gene expression of fibroblast growth factor (FGF/HBGF)]., Shiokawa K., Nihon Rinsho. August 1, 1992; 50 (8): 1893-901.
	Activin A induced expression of a fork head related gene in posterior chordamesoderm (notochord) of Xenopus laevis embryos., Knöchel S., Mech Dev. August 1, 1992; 38 (2): 157-65.
	Over-expression of fibroblast growth factors in Xenopus embryos., Thompson J., Mech Dev. September 1, 1992; 38 (3): 175-82.
	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.
	Xenopus Gastrulation without a blastocoel roof., Keller R., Dev Dyn. November 1, 1992; 195 (3): 162-76.
	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.
	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.
	The Xenopus platelet-derived growth factor alpha receptor: cDNA cloning and demonstration that mesoderm induction establishes the lineage-specific pattern of ligand and receptor gene expression., Jones SD., Dev Genet. January 1, 1993; 14 (3): 185-93.
	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.
	Activin is produced by rat Sertoli cells in vitro and can act as an autocrine regulator of Sertoli cell function., de Winter JP., Endocrinology. March 1, 1993; 132 (3): 975-82.
	Integrin alpha subunit mRNAs are differentially expressed in early Xenopus embryos., Whittaker CA., Development. April 1, 1993; 117 (4): 1239-49.
	A Xenopus homebox gene defines dorsal-ventral domains in the developing brain., Saha MS., Development. May 1, 1993; 118 (1): 193-202.
	Raf-1 kinase is essential for early Xenopus development and mediates the induction of mesoderm by FGF., MacNicol AM., Cell. May 7, 1993; 73 (3): 571-83.
	Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos., Coffman CR., Cell. May 21, 1993; 73 (4): 659-71.
	The mechanism of gastrulation in the white sturgeon., Bolker JA., J Exp Zool. June 1, 1993; 266 (2): 132-45.
	Alternative splicing of a neural-specific Src mRNA (Src+) is a rapid and protein synthesis-independent response to neural induction in Xenopus laevis., Collett JW., Dev Biol. August 1, 1993; 158 (2): 487-95.
	The Brachyury gene encodes a novel DNA binding protein., Kispert A., EMBO J. August 1, 1993; 12 (8): 3211-20.
	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.
	Processed Vg1 protein is an axial mesoderm inducer in Xenopus., Thomsen GH., Cell. August 13, 1993; 74 (3): 433-41.
	Expression of Xenopus snail in mesoderm and prospective neural fold ectoderm., Essex LJ., Dev Dyn. October 1, 1993; 198 (2): 108-22.
	Suramin prevents transcription of dorsal marker genes in Xenopus laevis embryos, isolated dorsal blastopore lips and activin A induced animal caps., Oschwald R., Mech Dev. October 1, 1993; 43 (2-3): 121-33.
	Competence prepattern in the animal hemisphere of the 8-cell-stage Xenopus embryo., Kinoshita K., Dev Biol. November 1, 1993; 160 (1): 276-84.
	Distinct elements of the xsna promoter are required for mesodermal and ectodermal expression., Mayor R., Development. November 1, 1993; 119 (3): 661-71.
	The expression of a zebrafish gene homologous to Drosophila snail suggests a conserved function in invertebrate and vertebrate gastrulation., Hammerschmidt M., Development. December 1, 1993; 119 (4): 1107-18.

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