Papers associated with brain (and hoxb4)

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	Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH., Dev Biol. March 1, 2022; 483 157-168.
	Reduced Retinoic Acid Signaling During Gastrulation Induces Developmental Microcephaly., Gur M., Front Cell Dev Biol. January 1, 2022; 10 844619.
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	What are the roles of retinoids, other morphogens, and Hox genes in setting up the vertebrate body axis?, Durston AJ., Genesis. July 1, 2019; 57 (7-8): e23296.
	Time space translation: a hox mechanism for vertebrate a-p patterning., Durston A., Curr Genomics. June 1, 2012; 13 (4): 300-7.
	XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010.
	Xwnt8 directly initiates expression of labial Hox genes., In der Rieden PM., Dev Dyn. January 1, 2010; 239 (1): 126-39.
	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.
	Ethanol exposure affects gene expression in the embryonic organizer and reduces retinoic acid levels., Yelin R., Dev Biol. March 1, 2005; 279 (1): 193-204.
	The Meis3 protein and retinoid signaling interact to pattern the Xenopus hindbrain., Dibner C., Dev Biol. July 1, 2004; 271 (1): 75-86.
	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.
	Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.
	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.
	The small GTPase Rap1 is an immediate downstream target for Hoxb4 transcriptional regulation., Morsi El-Kadi AS., Mech Dev. May 1, 2002; 113 (2): 131-9.
	Regulatory analysis of the mouse Hoxb3 gene: multiple elements work in concert to direct temporal and spatial patterns of expression., Kwan CT., Dev Biol. April 1, 2001; 232 (1): 176-90.
	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.
	Graded retinoid responses in the developing hindbrain., Godsave SF., Dev Dyn. September 1, 1998; 213 (1): 39-49.
	Initiation of rhombomeric Hoxb4 expression requires induction by somites and a retinoid pathway., Gould A., Neuron. July 1, 1998; 21 (1): 39-51.
	Positive cross-regulation and enhancer sharing: two mechanisms for specifying overlapping Hox expression patterns., Gould A., Genes Dev. April 1, 1997; 11 (7): 900-13.
	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.
	Microinjection of synthetic Xhox-1A homeobox mRNA disrupts somite formation in developing Xenopus embryos., Harvey RP., Cell. June 3, 1988; 53 (5): 687-97.

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