Papers associated with cell (and h4c4)

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	The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus., Melchert J., Dev Biol. March 15, 2020; 459 (2): 138-148.
	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	A cell-free CENP-A assembly system defines the chromatin requirements for centromere maintenance., Westhorpe FG., J Cell Biol. June 22, 2015; 209 (6): 789-801.
	HDAC1 Regulates the Proliferation of Radial Glial Cells in the Developing Xenopus Tectum., Tao Y., PLoS One. March 16, 2015; 10 (3): e0120118.
	Histone titration against the genome sets the DNA-to-cytoplasm threshold for the Xenopus midblastula transition., Amodeo AA., Proc Natl Acad Sci U S A. March 10, 2015; 112 (10): E1086-95.
	Quantitative proteomics of Xenopus laevis embryos: expression kinetics of nearly 4000 proteins during early development., Sun L., Sci Rep. February 26, 2014; 4 4365.
	The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.
	MicroRNA-mediated mRNA translation activation in quiescent cells and oocytes involves recruitment of a nuclear microRNP., Truesdell SS., Sci Rep. January 1, 2012; 2 842.
	The development of the adult intestinal stem cells: Insights from studies on thyroid hormone-dependent amphibian metamorphosis., Shi YB., Cell Biosci. September 6, 2011; 1 (1): 30.
	Histone deacetylase activity is necessary for left-right patterning during vertebrate development., Carneiro K., BMC Dev Biol. May 20, 2011; 11 29.
	EBF factors drive expression of multiple classes of target genes governing neuronal development., Green YS., Neural Dev. April 30, 2011; 6 19.
	Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation., Juraver-Geslin HA., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.
	HDAC activity is required during Xenopus tail regeneration., Tseng AS., PLoS One. January 1, 2011; 6 (10): e26382.
	Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.
	Novel functions of protein arginine methyltransferase 1 in thyroid hormone receptor-mediated transcription and in the regulation of metamorphic rate in Xenopus laevis., Matsuda H., Mol Cell Biol. February 1, 2009; 29 (3): 745-57.
	Analysis of histones in Xenopus laevis. I. A distinct index of enriched variants and modifications exists in each cell type and is remodeled during developmental transitions., Shechter D., J Biol Chem. January 9, 2009; 284 (2): 1064-74.
	A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
	XMam1, Xenopus Mastermind1, induces neural gene expression in a Notch-independent manner., Katada T., Mech Dev. November 1, 2006; 123 (11): 851-9.
	The intracellular domain of X-Serrate-1 is cleaved and suppresses primary neurogenesis in Xenopus laevis., Kiyota T., Mech Dev. June 1, 2004; 121 (6): 573-85.
	Regulation of Msx genes by a Bmp gradient is essential for neural crest specification., Tribulo C., Development. December 1, 2003; 130 (26): 6441-52.
	The APC regulator CDH1 is essential for the progression of embryonic cell cycles in Xenopus., Zhou Y., Biochem Biophys Res Commun. May 31, 2002; 294 (1): 120-6.
	foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
	The pitx2 homeobox protein is required early for endoderm formation and nodal signaling. ., Faucourt M., Dev Biol. January 15, 2001; 229 (2): 287-306.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	Xoom is required for epibolic movement of animal ectodermal cells in Xenopus laevis gastrulation., Hasegawa K., Dev Growth Differ. August 1, 2000; 42 (4): 337-46.
	Is chordin a long-range- or short-range-acting factor? Roles for BMP1-related metalloproteases in chordin and BMP4 autofeedback loop regulation., Blitz IL., Dev Biol. July 1, 2000; 223 (1): 120-38.
	Purification and properties of the Xenopus Hat1 acetyltransferase: association with the 14-3-3 proteins in the oocyte nucleus., Imhof A., Biochemistry. October 5, 1999; 38 (40): 13085-93.
	Functional analysis of the SIN3-histone deacetylase RPD3-RbAp48-histone H4 connection in the Xenopus oocyte., Vermaak D., Mol Cell Biol. September 1, 1999; 19 (9): 5847-60.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF., Dev Biol. March 15, 1999; 207 (2): 350-63.
	Transcriptionally active Xenopus laevis somatic 5 S ribosomal RNA genes are packaged with hyperacetylated histone H4, whereas transcriptionally silent oocyte genes are not., Howe L., J Biol Chem. August 14, 1998; 273 (33): 20693-6.
	Xenopus Zic family and its role in neural and neural crest development., Nakata K., Mech Dev. July 1, 1998; 75 (1-2): 43-51.
	A Xenopus homologue of aml-1 reveals unexpected patterning mechanisms leading to the formation of embryonic blood., Tracey WD., Development. April 1, 1998; 125 (8): 1371-80.
	Requirement for Xvent-1 and Xvent-2 gene function in dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. April 1, 1998; 125 (8): 1447-56.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	Regulated unmasking of in vivo synthesized maternal mRNA at oocyte maturation. A role for the chaperone nucleoplasmin., Meric F., J Biol Chem. May 9, 1997; 272 (19): 12840-6.
	Early expression of a novel nucleotide receptor in the neural plate of Xenopus embryos., Bogdanov YD., J Biol Chem. May 9, 1997; 272 (19): 12583-90.
	Combinatorial signalling by Xwnt-11 and Xnr3 in the organizer epithelium., Glinka A., Mech Dev. December 1, 1996; 60 (2): 221-31.
	Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S., Genes Dev. November 1, 1996; 10 (21): 2805-17.
	The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. October 1, 1996; 122 (10): 3045-53.
	Anterior neurectoderm is progressively induced during gastrulation: the role of the Xenopus homeobox gene orthodenticle., Blitz IL., Development. April 1, 1995; 121 (4): 993-1004.
	Effects of oligo sequence and chemistry on the efficiency of oligodeoxyribonucleotide-mediated mRNA cleavage., Baker C., Nucleic Acids Res. June 25, 1990; 18 (12): 3537-43.
	The maternal store of the xlgv7 mRNA in full-grown oocytes is not required for normal development in Xenopus., Kloc M., Development. December 1, 1989; 107 (4): 899-907.
	The assembly of regularly spaced nucleosomes in the Xenopus oocyte S-150 extract is accompanied by deacetylation of histone H4., Shimamura A., J Biol Chem. August 25, 1989; 264 (24): 14524-30.
	Assembly of transcriptionally active chromatin in Xenopus oocytes requires specific DNA binding factors., Gargiulo G., Cell. September 1, 1984; 38 (2): 511-21.
	Transcription of a cloned Xenopus laevis H4 histone gene in the homologous frog oocyte system depends on an evolutionary conserved sequence motif in the -50 region., Clerc RG., Nucleic Acids Res. December 20, 1983; 11 (24): 8641-57.

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