Papers associated with oocyte (and h4c4)

Limit to papers also referencing gene:
Show all oocyte papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	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.
	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.
	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.
	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.
	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.
	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.
	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.
	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.
	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.

???pagination.result.page??? 1