Papers associated with trunk (and hoxb4)

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	Retinoic acid control of pax8 during renal specification of Xenopus pronephros involves hox and meis3., Durant-Vesga J., Dev Biol. January 1, 2023; 493 17-28.
	Reduced Retinoic Acid Signaling During Gastrulation Induces Developmental Microcephaly., Gur M., Front Cell Dev Biol. January 1, 2022; 10 844619.
	Retinoic Acid Fluctuation Activates an Uneven, Direction-Dependent Network-Wide Robustness Response in Early Embryogenesis., Parihar M., Front Cell Dev Biol. January 1, 2021; 9 747969.
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	ADHFe1: a novel enzyme involved in retinoic acid-dependent Hox activation., Shabtai Y., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 303-310.
	Genome evolution in the allotetraploid frog Xenopus laevis., Session AM., Nature. October 20, 2016; 538 (7625): 336-343.
	A time space translation hypothesis for vertebrate axial patterning., Durston AJ., Semin Cell Dev Biol. June 1, 2015; 42 86-93.
	Vertical signalling involves transmission of Hox information from gastrula mesoderm to neurectoderm., Bardine N., PLoS One. January 1, 2014; 9 (12): e115208.
	Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.
	XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010.
	Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.
	Interaction between X-Delta-2 and Hox genes regulates segmentation and patterning of the anteroposterior axis., Peres JN., Mech Dev. April 1, 2006; 123 (4): 321-33.
	Timed interactions between the Hox expressing non-organiser mesoderm and the Spemann organiser generate positional information during vertebrate gastrulation., Wacker SA., Dev Biol. April 1, 2004; 268 (1): 207-19.
	Initiating Hox gene expression: in the early chick neural tube differential sensitivity to FGF and RA signaling subdivides the HoxB genes in two distinct groups., Bel-Vialar S., Development. November 1, 2002; 129 (22): 5103-15.
	Xenopus embryonic E2F is required for the formation of ventral and posterior cell fates during early embryogenesis., Suzuki A., Mol Cell. February 1, 2000; 5 (2): 217-29.
	Inhibition of Xhox1A gene expression in Xenopus embryos by antisense RNA produced from an expression vector read by RNA polymerase III., Nichols A., Mech Dev. July 1, 1995; 52 (1): 37-49.
	Expression patterns of Hoxb genes in the Xenopus embryo suggest roles in anteroposterior specification of the hindbrain and in dorsoventral patterning of the mesoderm., Godsave S., Dev Biol. December 1, 1994; 166 (2): 465-76.
	Overexpression of a cellular retinoic acid binding protein (xCRABP) causes anteroposterior defects in developing Xenopus embryos., Dekker EJ., Development. April 1, 1994; 120 (4): 973-85.
	Hox-5.1 defines a homeobox-containing gene locus on mouse chromosome 2., Featherstone MS., Proc Natl Acad Sci U S A. July 1, 1988; 85 (13): 4760-4.

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