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An integrated modelling framework from cells to organism based on a cohort of digital embryos. , Villoutreix P., Sci Rep. December 2, 2016; 6 37438.
A workflow to process 3D+time microscopy images of developing organisms and reconstruct their cell lineage. , Faure E., Nat Commun. February 25, 2016; 7 8674.
Ca²⁺ influx-linked protein kinase C activity regulates the β- catenin localization, micromere induction signalling and the oral-aboral axis formation in early sea urchin embryos. , Yazaki I., Zygote. June 1, 2015; 23 (3): 426-46.
Mechanisms of the epithelial-to-mesenchymal transition in sea urchin embryos. , Katow H., Tissue Barriers. January 1, 2015; 3 (4): e1059004.
Mesomere-derived glutamate decarboxylase-expressing blastocoelar mesenchyme cells of sea urchin larvae. , Katow H., Biol Open. January 15, 2014; 3 (1): 94-102.
Nuclearization of β- catenin in ectodermal precursors confers organizer-like ability to induce endomesoderm and pattern a pluteus larva. , Byrum CA ., Evodevo. November 4, 2013; 4 (1): 31.
Towards 3D in silico modeling of the sea urchin embryonic development. , Rizzi B., J Chem Biol. September 13, 2013; 7 (1): 17-28.
Atypical protein kinase C controls sea urchin ciliogenesis. , Prulière G., Mol Biol Cell. June 15, 2011; 22 (12): 2042-53.
The echinoid mitotic gradient: effect of cell size on the micromere cleavage cycle. , Duncan RE., Mol Reprod Dev. January 1, 2011; 78 (10-11): 868-78.
Embryonic, larval, and juvenile development of the sea biscuit Clypeaster subdepressus (Echinodermata: Clypeasteroida). , Vellutini BC., PLoS One. March 22, 2010; 5 (3): e9654.
Action at a distance during cytokinesis. , von Dassow G., J Cell Biol. December 14, 2009; 187 (6): 831-45.
Evolutionary modification of specification for the endomesoderm in the direct developing echinoid Peronella japonica: loss of the endomesoderm-inducing signal originating from micromeres. , Iijima M., Dev Genes Evol. May 1, 2009; 219 (5): 235-47.
The micro1 gene is necessary and sufficient for micromere differentiation and mid/ hindgut-inducing activity in the sea urchin embryo. , Yamazaki A., Dev Genes Evol. September 1, 2005; 215 (9): 450-59.
SoxB1 downregulation in vegetal lineages of sea urchin embryos is achieved by both transcriptional repression and selective protein turnover. , Angerer LM ., Development. March 1, 2005; 132 (5): 999-1008.
Structure, regulation, and function of micro1 in the sea urchin Hemicentrotus pulcherrimus. , Nishimura Y., Dev Genes Evol. November 1, 2004; 214 (11): 525-36.
Primary mesenchyme cell patterning during the early stages following ingression. , Peterson RE., Dev Biol. February 1, 2003; 254 (1): 68-78.
Transient activation of the micro1 homeobox gene family in the sea urchin ( Hemicentrotus pulcherrimus) micromere. , Kitamura K., Dev Genes Evol. February 1, 2002; 212 (1): 1-10.
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.
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.
Deuterostome evolution: early development in the enteropneust hemichordate, Ptychodera flava. , Henry JQ., Evol Dev. January 1, 2001; 3 (6): 375-90.
Regulative potential to form an amniotic cavity in mesomeres of a direct developing echinoid, Peronella japonica. , Kitazawa C., Zygote. January 1, 2000; 8 Suppl 1 S79.
SpSoxB1, a maternally encoded transcription factor asymmetrically distributed among early sea urchin blastomeres. , Kenny AP., Development. December 1, 1999; 126 (23): 5473-83.
Timing of the potential of micromere-descendants in echinoid embryos to induce endoderm differentiation of mesomere-descendants. , Minokawa T ., Dev Growth Differ. October 1, 1999; 41 (5): 535-47.
A presumptive developmental role for a sea urchin cyclin B splice variant. , Lozano JC., J Cell Biol. January 26, 1998; 140 (2): 283-93.
Polarized distribution of L-type calcium channels in early sea urchin embryos. , Dale B., Am J Physiol. September 1, 1997; 273 (3 Pt 1): C822-5.
The allocation of early blastomeres to the ectoderm and endoderm is variable in the sea urchin embryo. , Logan CY., Development. June 1, 1997; 124 (11): 2213-23.
Multiple signaling events specify ectoderm and pattern the oral-aboral axis in the sea urchin embryo. , Wikramanayake AH ., Development. January 1, 1997; 124 (1): 13-20.
Transient appearance of Strongylocentrotus purpuratus Otx in micromere nuclei: cytoplasmic retention of SpOtx possibly mediated through an alpha- actinin interaction. , Chuang CK., Dev Genet. January 1, 1996; 19 (3): 231-7.
Autonomous and non-autonomous differentiation of ectoderm in different sea urchin species. , Wikramanayake AH ., Development. May 1, 1995; 121 (5): 1497-505.
Spatial distribution of two maternal messengers in Paracentrotus lividus during oogenesis and embryogenesis. , Di Carlo M ., Proc Natl Acad Sci U S A. June 7, 1994; 91 (12): 5622-6.
Expression of homeobox-containing genes in the sea urchin (Parancentrotus lividus) embryo. , Di Bernardo M., Genetica. January 1, 1994; 94 (2-3): 141-50.
Centrifugal elutriation of large fragile cells: isolation of RNA from fixed embryonic blastomeres. , Nasir A., Anal Biochem. May 15, 1992; 203 (1): 22-6.
Cell movements during the initial phase of gastrulation in the sea urchin embryo. , Burke RD ., Dev Biol. August 1, 1991; 146 (2): 542-57.
Interactions of different vegetal cells with mesomeres during early stages of sea urchin development. , Khaner O., Development. July 1, 1991; 112 (3): 881-90.
The use of confocal microscopy and STERECON reconstructions in the analysis of sea urchin embryonic cell division. , Summers RG., J Electron Microsc Tech. May 1, 1991; 18 (1): 24-30.
The influence of cell interactions and tissue mass on differentiation of sea urchin mesomeres. , Khaner O., Development. July 1, 1990; 109 (3): 625-34.
Range and stability of cell fate determination in isolated sea urchin blastomeres. , Livingston BT ., Development. March 1, 1990; 108 (3): 403-10.
Early inductive interactions are involved in restricting cell fates of mesomeres in sea urchin embryos. , Henry JJ., Dev Biol. November 1, 1989; 136 (1): 140-53.
Embryonic cellular organization: differential restriction of fates as revealed by cell aggregates and lineage markers. , Bernacki SH., J Exp Zool. August 1, 1989; 251 (2): 203-16.
Histone modifications accompanying the onset of developmental commitment. , Chambers SA., Dev Biol. December 1, 1987; 124 (2): 523-31.
Fourth cleavage of sea urchin blastomeres: microtubule patterns and myosin localization in equal and unequal cell divisions. , Schroeder TE., Dev Biol. November 1, 1987; 124 (1): 9-22.
Micromere-specific cell surface proteins of 16-cell stage sea urchin embryos. , De Simone DW., Exp Cell Res. January 1, 1985; 156 (1): 7-14.
Diffusible factors are responsible for differences in nuclease sensitivity among chromatins originating from different cell types. , Chambers SA., Exp Cell Res. September 1, 1984; 154 (1): 213-23.
Structural differences in the chromatin from compartmentalized cells of the sea urchin embryo: differential nuclease accessibility of micromere chromatin. , Cognetti G., Nucleic Acids Res. November 11, 1981; 9 (21): 5609-21.
Changes in cell surface charges during differentiation of isolated micromeres and mesomeres from sea urchin embryos. , Sano K., Dev Biol. October 15, 1977; 60 (2): 404-15.
Distribution of concanavalin A receptor sites on specific populations of embryonic cells. , Roberson M., Science. August 22, 1975; 189 (4203): 639-40.
[Morphological and biochemical characterization of the developmental stages of fertilized eggs inSphaerechinus granularis lam : I. Rearing, Morphology and determination of stages]. , Müller WE., Wilhelm Roux Arch Entwickl Mech Org. June 1, 1971; 167 (2): 99-117.
Cytological and morphological studies of the action of lithium on the development of the sea urchin embryo. , Hagström BE., Wilhelm Roux Arch Entwickl Mech Org. March 1, 1967; 158 (1): 1-12.
Protein synthesis in micromeres of the sea urchin egg. , Spiegel M., Science. March 11, 1966; 151 (3715): 1233-4.