Papers associated with embryonic structure (and gnat1)

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	Müller glia reactivity follows retinal injury despite the absence of the glial fibrillary acidic protein gene in Xenopus., Martinez-De Luna RI., Dev Biol. June 15, 2017; 426 (2): 219-235.
	Tbx3 represses bmp4 expression and, with Pax6, is required and sufficient for retina formation., Motahari Z., Development. October 1, 2016; 143 (19): 3560-3572.
	Genome-Wide Identification and Expression of Xenopus F-Box Family of Proteins., Saritas-Yildirim B., PLoS One. September 1, 2015; 10 (9): e0136929.
	A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit., Manes G., PLoS One. January 1, 2014; 9 (4): e95768.
	Cell type-specific translational profiling in the Xenopus laevis retina., Watson FL., Dev Dyn. December 1, 2012; 241 (12): 1960-72.
	Early onset and differential temporospatial expression of melanopsin isoforms in the developing chicken retina., Verra DM., Invest Ophthalmol Vis Sci. July 29, 2011; 52 (8): 5111-20.
	Mislocalized rhodopsin does not require activation to cause retinal degeneration and neurite outgrowth in Xenopus laevis., Tam BM., J Neurosci. January 4, 2006; 26 (1): 203-9.
	Identification of new localized RNAs in the Xenopus oocyte by differential display PCR., Hudson JW., Dev Genet. January 1, 1996; 19 (3): 190-8.
	A unique mutation in the Enhancer of split gene complex affects the fates of the mystery cells in the developing Drosophila eye., Fischer-Vize JA., Development. May 1, 1992; 115 (1): 89-101.

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