Papers associated with mesenchyme

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	Electron microscopic study on the early histogenesis of thymus in the toad, Xenopus laevis., Nagata S., Cell Tissue Res. March 30, 1977; 179 (1): 87-96.
	The changing morphology of the epithelium-mesenchyme interface in the differentiation zone of growing teeth of selected vertebrates and its relationship to possible mechanisms of differentiation., Kallenbach E., J Biol Buccale. September 1, 1978; 6 (3): 229-40.
	Direct observation of cell migration into Xenopus thymus rudiments through mesenchyme., Tochinai S., Dev Comp Immunol. January 1, 1980; 4 (2): 273-82.
	An atlas of notochord and somite morphogenesis in several anuran and urodelean amphibians., Youn BW., J Embryol Exp Morphol. October 1, 1980; 59 223-47.
	Axis determination in eggs of Xenopus laevis: a critical period before first cleavage, identified by the common effects of cold, pressure and ultraviolet irradiation., Scharf SR., Dev Biol. September 1, 1983; 99 (1): 75-87.
	Lineage segregation and developmental autonomy in expression of functional muscle acetylcholinesterase mRNA in the ascidian embryo., Meedel TH., Dev Biol. October 1, 1984; 105 (2): 479-87.
	Differential participation of ventral and dorsolateral mesoderms in the hemopoiesis of Xenopus, as revealed in diploid-triploid or interspecific chimeras., Maéno M., Dev Biol. August 1, 1985; 110 (2): 503-8.
	Mesoderm induction in Xenopus laevis: a quantitative study using a cell lineage label and tissue-specific antibodies., Dale L., J Embryol Exp Morphol. October 1, 1985; 89 289-312.
	A mesoderm-inducing factor is produced by Xenopus cell line., Smith JC., Development. January 1, 1987; 99 (1): 3-14.
	Development of the connective tissue in the digestive tract of the larval and metamorphosing Xenopus laevis., Ishizuya-Oka A., Anat Anz. January 1, 1987; 164 (2): 81-93.
	Fates of the blastomeres of the 16-cell stage Xenopus embryo., Moody SA., Dev Biol. February 1, 1987; 119 (2): 560-78.
	Fate map for the 32-cell stage of Xenopus laevis., Dale L., Development. April 1, 1987; 99 (4): 527-51.
	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.
	Induction of mesodermal tissues by acidic and basic heparin binding growth factors., Grunz H., Cell Differ. February 1, 1988; 22 (3): 183-9.
	Mesoderm-inducing factors: a small class of molecules., Godsave SF., Development. March 1, 1988; 102 (3): 555-66.
	Purification, partial characterization and biological effects of the XTC mesoderm-inducing factor., Smith JC., Development. July 1, 1988; 103 (3): 591-600.
	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.
	Characterization of a murine homeo box gene, Hox-2.6, related to the Drosophila Deformed gene., Graham A., Genes Dev. November 1, 1988; 2 (11): 1424-38.
	A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus., Dent JA., Development. January 1, 1989; 105 (1): 61-74.
	Amphibian (urodele) myotomes display transitory anterior/posterior and medial/lateral differentiation patterns., Neff AW., Dev Biol. April 1, 1989; 132 (2): 529-43.
	Complementary homeo protein gradients in developing limb buds., Oliver G., Genes Dev. May 1, 1989; 3 (5): 641-50.
	Ontogeny and tissue distribution of leukocyte-common antigen bearing cells during early development of Xenopus laevis., Ohinata H., Development. November 1, 1989; 107 (3): 445-52.
	[The differentiation factor in the bone marrow and blood serum of healthy subjects and in acute leukemia]., Khoperskaia OA., Biull Eksp Biol Med. December 1, 1989; 108 (12): 732-4.
	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.
	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.
	Ultrastructural comparison between regenerating and developing hindlimbs of Xenopus laevis tadpoles., Khan PA., Growth Dev Aging. January 1, 1990; 54 (4): 173-81.
	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.
	Mesodermal induction in early amphibian embryos by activin A (erythroid differentiation factor)., Asashima M., Rouxs Arch Dev Biol. March 1, 1990; 198 (6): 330-335.
	Enhanced c-myc gene expression during forelimb regenerative outgrowth in the young Xenopus laevis., Géraudie J., Proc Natl Acad Sci U S A. May 1, 1990; 87 (10): 3797-801.
	Occurrence of nonlymphoid leukocytes that are not derived from blood islands in Xenopus laevis larvae., Ohinata H., Dev Biol. September 1, 1990; 141 (1): 123-9.
	A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H., Genes Dev. January 1, 1991; 5 (1): 94-104.
	Local fate and distribution of locally infused basic FGF. The example of the rat brain and the Xenopus tail mesenchyme., Gonzalez AM., Ann N Y Acad Sci. January 1, 1991; 638 416-9.
	Examining pattern formation in mouse, chicken and frog embryos with an En-specific antiserum., Davis CA., Development. February 1, 1991; 111 (2): 287-98.
	Prolactin inhibits both thyroid hormone-induced morphogenesis and cell death in cultured amphibian larval tissues., Tata JR., Dev Biol. July 1, 1991; 146 (1): 72-80.
	Distribution and expression of two interactive extracellular matrix proteins, cytotactin and cytotactin-binding proteoglycan, during development of Xenopus laevis. II. Metamorphosis., Williamson DA., J Morphol. August 1, 1991; 209 (2): 203-13.
	Distribution and expression of two interactive extracellular matrix proteins, cytotactin and cytotactin-binding proteoglycan, during development of Xenopus laevis. I. Embryonic development., Williamson DA., J Morphol. August 1, 1991; 209 (2): 189-202.
	Concentration-dependent inducing activity of activin A., Ariizumi T., Rouxs Arch Dev Biol. September 1, 1991; 200 (4): 230-233.
	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.
	Analysis of Xwnt-4 in embryos of Xenopus laevis: a Wnt family member expressed in the brain and floor plate., McGrew LL., Development. June 1, 1992; 115 (2): 463-73.
	Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development., Del Amo FF., Development. July 1, 1992; 115 (3): 737-44.
	Developmental expression of the Xenopus int-2 (FGF-3) gene: activation by mesodermal and neural induction., Tannahill D., Development. July 1, 1992; 115 (3): 695-702.
	N-cadherin transcripts in Xenopus laevis from early tailbud to tadpole., Simonneau L., Dev Dyn. August 1, 1992; 194 (4): 247-60.
	Mesoderm and Neural Inductions on Newt Ectoderm by Activin A: (mesoderm induction/newt embryo/activin/EDF)., Moriya N., Dev Growth Differ. October 1, 1992; 34 (5): 589-594.
	Isolation of Sna, a mouse gene homologous to the Drosophila genes snail and escargot: its expression pattern suggests multiple roles during postimplantation development., Smith DE., Development. December 1, 1992; 116 (4): 1033-9.
	Morphological response of extending spinal neuritic growth cones to peripheral target tissue., Somasekhar T., J Comp Neurol. December 8, 1992; 326 (2): 314-26.
	[The role of mechanical stresses in the formation and orientation of vessel-like structures in explants of clawed toad embryos]., Fesenko IV., Ontogenez. January 1, 1993; 24 (4): 19-28.
	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.
	Expression patterns of the activin receptor IIA and IIB genes during chick limb development., Nohno T., Prog Clin Biol Res. January 1, 1993; 383B 705-14.

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