Papers associated with germ cell (and eef1a1)

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	Reference gene identification and validation for quantitative real-time PCR studies in developing Xenopus laevis., Mughal BB., Sci Rep. January 11, 2018; 8 (1): 496.
	Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development., Owens ND., Cell Rep. January 26, 2016; 14 (3): 632-47.
	Validation of novel reference genes for RT-qPCR studies of gene expression in Xenopus tropicalis during embryonic and post-embryonic development., Dhorne-Pollet S., Dev Dyn. June 1, 2013; 242 (6): 709-17.
	Physiological responses of Xenopus laevis tadpoles exposed to cyanobacterial biomass containing microcystin-LR., Ziková A., Aquat Toxicol. March 15, 2013; 128-129 25-33.
	Single blastomere expression profiling of Xenopus laevis embryos of 8 to 32-cells reveals developmental asymmetry., Flachsova M., Sci Rep. January 1, 2013; 3 2278.
	Regulation of thyroid hormone sensitivity by differential expression of the thyroid hormone receptor during Xenopus metamorphosis., Nakajima K., Genes Cells. August 1, 2012; 17 (8): 645-59.
	Early, nonciliary role for microtubule proteins in left-right patterning is conserved across kingdoms., Lobikin M., Proc Natl Acad Sci U S A. July 31, 2012; 109 (31): 12586-91.
	Identification and expression analysis of GPAT family genes during early development of Xenopus laevis., Bertolesi GE., Gene Expr Patterns. January 1, 2012; 12 (7-8): 219-27.
	Evolutionary importance of translation elongation factor eEF1A variant switching: eEF1A1 down-regulation in muscle is conserved in Xenopus but is controlled at a post-transcriptional level., Newbery HJ., Biochem Biophys Res Commun. July 22, 2011; 411 (1): 19-24.
	Xenopus tropicalis transgenic lines and their use in the study of embryonic induction., Hirsch N., Dev Dyn. December 1, 2002; 225 (4): 522-35.
	Balbiani bodies in cricket oocytes: development, ultrastructure, and presence of localized RNAs., Bradley JT., Differentiation. June 1, 2001; 67 (4-5): 117-27.
	The role of maternal VegT in establishing the primary germ layers in Xenopus embryos., Zhang J., Cell. August 21, 1998; 94 (4): 515-24.
	Katanin is responsible for the M-phase microtubule-severing activity in Xenopus eggs., McNally FJ., Mol Biol Cell. July 1, 1998; 9 (7): 1847-61.
	Thyroid hormone regulation of germ cell-specific EF-1 alpha expression during metamorphosis of Xenopus laevis., Abdallah B., Int J Dev Biol. April 1, 1996; 40 (2): 507-14.
	Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos., Smith WC., Cell. September 4, 1992; 70 (5): 829-40.
	Isolation and characterization of the gene encoding EF-1 alpha O, an elongation factor 1-alpha expressed during early development of Xenopus laevis., Frydenberg J., Gene. December 30, 1991; 109 (2): 185-92.
	Two forms of elongation factor 1 alpha (EF-1 alpha O and 42Sp50), present in oocytes, but absent in somatic cells of Xenopus laevis., Deschamps S., J Cell Biol. September 1, 1991; 114 (6): 1109-11.
	Purification and characterization of a germ cell-specific form of elongation factor 1 alpha (EF-1 alpha) from Xenopus laevis., Morales J., Biochimie. September 1, 1991; 73 (9): 1249-53.
	Elongation factor 1 alpha (EF-1 alpha) is concentrated in the Balbiani body and accumulates coordinately with the ribosomes during oogenesis of Xenopus laevis., Viel A., Dev Biol. October 1, 1990; 141 (2): 270-8.

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