Papers associated with embryo

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	Heads or tails? Amphioxus and the evolution of anterior-posterior patterning in deuterostomes., Holland LZ., Dev Biol. January 15, 2002; 241 (2): 209-28.
	Spicule matrix protein LSM34 is essential for biomineralization of the sea urchin spicule., Peled-Kamar M., Exp Cell Res. January 1, 2002; 272 (1): 56-61.
	Molecular patterning along the sea urchin animal-vegetal axis., Brandhorst BP., Int Rev Cytol. January 1, 2002; 213 183-232.
	The beginnings of developmental biology in Swiss universities., Weber R., Int J Dev Biol. January 1, 2002; 46 (1): 15-22.
	Potential of veg2 blastomeres to induce endoderm differentiation in sea urchin embryos., Iijima M., Zoolog Sci. January 1, 2002; 19 (1): 81-5.
	Behavior of pigment cells in gastrula-stage embryos of Hemicentrotus pulcherrimus and Scaphechinus mirabilis., Kominami T., Dev Growth Differ. December 1, 2001; 43 (6): 699-707.
	Expression pattern of Brachyury in the embryo of the sea urchin Paracentrotus lividus., Croce J., Dev Genes Evol. December 1, 2001; 211 (12): 617-9.
	Design and synthesis of fluoroquinophenoxazines that interact with human telomeric G-quadruplexes and their biological effects., Duan W., Mol Cancer Ther. December 1, 2001; 1 (2): 103-20.
	Displacement of the mitotic apparatus which induces ectopic polar body formation or parthenogenetic cleavage in starfish oocytes., Hamaguchi Y., Dev Biol. November 15, 2001; 239 (2): 364-75.
	The role of Brachyury (T) during gastrulation movements in the sea urchin Lytechinus variegatus., Gross JM., Dev Biol. November 1, 2001; 239 (1): 132-47.
	[Serotoninergic processes in cells of early embryos of the sea urchin Paracentrotus lividus]., Shmukler IuB., Ross Fiziol Zh Im I M Sechenova. November 1, 2001; 87 (11): 1557-64.
	[Cholinergic regulation of the sea urchin embryonic and larval development]., Buznikov GA., Ross Fiziol Zh Im I M Sechenova. November 1, 2001; 87 (11): 1548-56.
	Combined toxicity of dissolved mercury with copper, lead and cadmium on embryogenesis and early larval growth of the Paracentrotus lividus sea-urchin., Fernández N., Ecotoxicology. October 1, 2001; 10 (5): 263-71.
	An RGDS peptide-binding receptor, FR-1R, localizes to the basal side of the ectoderm and to primary mesenchyme cells in sand dollar embryos., Katow H., Dev Growth Differ. October 1, 2001; 43 (5): 601-10.
	ske-T, a T-box gene expressed in the skeletogenic mesenchyme lineage of the sea urchin embryo., Croce J., Mech Dev. September 1, 2001; 107 (1-2): 159-62.
	Evidence for a mesodermal embryonic regulator of the sea urchin CyIIa gene., Martin EL., Dev Biol. August 1, 2001; 236 (1): 46-63.
	Calcium-mediated inactivation of the MAP kinase pathway in sea urchin eggs at fertilization., Kumano M., Dev Biol. August 1, 2001; 236 (1): 244-57.
	Inhibitors of procollagen C-terminal proteinase block gastrulation and spicule elongation in the sea urchin embryo., Huggins LG., Dev Growth Differ. August 1, 2001; 43 (4): 415-24.
	Protein translation during early cell divisions of sea urchin embryos regulated at the level of polypeptide chain elongation and highly sensitive to natural polyamines., Monnier A., Zygote. August 1, 2001; 9 (3): 229-36.
	MUP-4 is a novel transmembrane protein with functions in epithelial cell adhesion in Caenorhabditis elegans., Hong L., J Cell Biol. July 23, 2001; 154 (2): 403-14.
	mua-3, a gene required for mechanical tissue integrity in Caenorhabditis elegans, encodes a novel transmembrane protein of epithelial attachment complexes., Bercher M., J Cell Biol. July 23, 2001; 154 (2): 415-26.
	DNA (cytosine-5) methyltransferase turnover and cellular localization in developing Paracentrotus lividus sea urchin embryo., Di Giaimo R., Gene. July 11, 2001; 272 (1-2): 199-208.
	A large-scale analysis of mRNAs expressed by primary mesenchyme cells of the sea urchin embryo., Zhu X., Development. July 1, 2001; 128 (13): 2615-27.
	Skeletogenesis in sea urchin interordinal hybrid embryos., Brandhorst BP., Cell Tissue Res. July 1, 2001; 305 (1): 159-67.
	Cyclin E and its associated cdk activity do not cycle during early embryogenesis of the sea Urchin., Sumerel JL., Dev Biol. June 15, 2001; 234 (2): 425-40.
	Conserved regions of the Drosophila erect wing protein contribute both positively and negatively to transcriptional activity., Fazio IK., J Biol Chem. June 1, 2001; 276 (22): 18710-6.
	Bep4 protein is involved in patterning along the animal-vegetal axis in the Paracentrotus lividus embryo., Romancino DP., Dev Biol. June 1, 2001; 234 (1): 107-19.
	Evaluation and use of sediment toxicity reference sites for statistical comparisons in regional assessments., Hunt JW., Environ Toxicol Chem. June 1, 2001; 20 (6): 1266-75.
	Ectoderm exerts the driving force for gastrulation in the sand dollar Scaphechinus mirabilis., Takata H., Dev Growth Differ. June 1, 2001; 43 (3): 265-74.
	Nucleus: cell volume ratio directs the timing of the increase in blastomere adhesiveness in starfish embryos., Masui M., Dev Growth Differ. June 1, 2001; 43 (3): 295-304.
	LvNotch signaling plays a dual role in regulating the position of the ectoderm-endoderm boundary in the sea urchin embryo., Sherwood DR., Development. June 1, 2001; 128 (12): 2221-32.
	p62/p56 are cortical granule proteins that contribute to formation of the cortical granule envelope and play a role in mammalian preimplantation development., Hoodbhoy T., Mol Reprod Dev. May 1, 2001; 59 (1): 78-89.
	Correct Expression of spec2a in the sea urchin embryo requires both Otx and other cis-regulatory elements., Yuh CH., Dev Biol. April 15, 2001; 232 (2): 424-38.
	Characterization and developmental expression of the amphioxus homolog of Notch (AmphiNotch): evolutionary conservation of multiple expression domains in amphioxus and vertebrates., Holland LZ., Dev Biol. April 15, 2001; 232 (2): 493-507.
	Influence of sample manipulation on contaminant flux and toxicity at the sediment-water interface., Anderson BS., Mar Environ Res. April 1, 2001; 51 (3): 191-211.
	The role of oxidative stress in developmental and reproductive toxicity of tamoxifen., Pagano G., Life Sci. March 2, 2001; 68 (15): 1735-49.
	A mammalian oocyte-specific linker histone gene H1oo: homology with the genes for the oocyte-specific cleavage stage histone (cs-H1) of sea urchin and the B4/H1M histone of the frog., Tanaka M., Development. March 1, 2001; 128 (5): 655-64.
	Ca(2+) in specification of vegetal cell fate in early sea urchin embryos., Yazaki I., J Exp Biol. March 1, 2001; 204 (Pt 5): 823-34.
	Structure-activity relationship for bromoindole carbaldehydes: effects on the sea urchin embryo cell cycle., Moubax I., Environ Toxicol Chem. March 1, 2001; 20 (3): 589-96.
	Bioaccumulation and toxicity of four dissolved metals in Paracentrotus lividus sea-urchin embryo., Radenac G., Mar Environ Res. March 1, 2001; 51 (2): 151-66.
	Change in the adhesive properties of blastomeres during early cleavage stages in sea urchin embryo., Masui M., Dev Growth Differ. February 1, 2001; 43 (1): 43-53.
	Regulating potential in development of a direct developing echinoid, Peronella japonica., Kitazawa C., Dev Growth Differ. February 1, 2001; 43 (1): 73-82.
	Disappearance of an epithelial cell surface-specific glycoprotein (Epith-1) associated with epithelial-mesenchymal conversion in sea urchin embryogenesis., Kanoh K., Dev Growth Differ. February 1, 2001; 43 (1): 83-95.
	Oral-aboral axis specification in the sea urchin embryo. I. Axis entrainment by respiratory asymmetry., Coffman JA., Dev Biol. February 1, 2001; 230 (1): 18-28.
	Calcium and mitosis., Whitaker M., Semin Cell Dev Biol. February 1, 2001; 12 (1): 53-8.
	Micromere descendants at the blastula stage are involved in normal archenteron formation in sea urchin embryos., Ishizuka Y., Dev Genes Evol. February 1, 2001; 211 (2): 83-8.
	Syntaxin, VAMP, and Rab3 are selectively expressed during sea urchin embryogenesis., Conner SD., Mol Reprod Dev. January 1, 2001; 58 (1): 22-9.
	Characterization of matrix metalloprotease activities induced in the sea urchin extraembryonic matrix, the hyaline layer., Sharpe C., Biochem Cell Biol. January 1, 2001; 79 (4): 461-8.
	Brachyury homolog (HpTa) is involved in the formation of archenteron and secondary mesenchyme cell differentiation in the sea urchin embryo., Mitsunaga-Nakatsubo K., Zoology (Jena). January 1, 2001; 104 (2): 99-102.
	Cytoplasm of sea urchin unfertilized eggs contains a nucleosome remodeling activity., Medina R., J Cell Biochem. January 1, 2001; 83 (4): 554-62.

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