Papers associated with hindbrain (and lhx1)

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	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
	Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.
	In Xenopus ependymal cilia drive embryonic CSF circulation and brain development independently of cardiac pulsatile forces., Dur AH., Fluids Barriers CNS. December 11, 2020; 17 (1): 72.
	Amphibian thalamic nuclear organization during larval development and in the adult frog Xenopus laevis: Genoarchitecture and hodological analysis., Morona R., J Comp Neurol. October 1, 2020; 528 (14): 2361-2403.
	Probing forebrain to hindbrain circuit functions in Xenopus., Kelley DB., Genesis. January 1, 2017; 55 (1-2):
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus., Thélie A., Development. October 1, 2015; 142 (19): 3416-28.
	Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.
	Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
	Variation in the schedules of somite and neural development in frogs., Sáenz-Ponce N., Proc Natl Acad Sci U S A. December 11, 2012; 109 (50): 20503-7.
	Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Embryogenesis and laboratory maintenance of the foam-nesting túngara frogs, genus Engystomops (= Physalaemus)., Romero-Carvajal A., Dev Dyn. June 1, 2009; 238 (6): 1444-54.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.
	LIM-homeodomain genes as territory markers in the brainstem of adult and developing Xenopus laevis., Moreno N., J Comp Neurol. May 9, 2005; 485 (3): 240-54.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
	The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development., Barreto G., Mech Dev. April 1, 2003; 120 (4): 415-28.
	The Xenopus receptor tyrosine kinase Xror2 modulates morphogenetic movements of the axial mesoderm and neuroectoderm via Wnt signaling., Hikasa H., Development. November 1, 2002; 129 (22): 5227-39.
	Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney., Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.
	Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation., Lamar E., Development. April 1, 2001; 128 (8): 1335-46.
	A study of Xlim1 function in the Spemann-Mangold organizer., Kodjabachian L., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Expression of murine Lhx5 suggests a role in specifying the forebrain., Sheng HZ., Dev Dyn. February 1, 1997; 208 (2): 266-77.
	The LIM homeodomain protein Lim-1 is widely expressed in neural, neural crest and mesoderm derivatives in vertebrate development., Karavanov AA., Int J Dev Biol. April 1, 1996; 40 (2): 453-61.
	The LIM class homeobox gene lim5: implied role in CNS patterning in Xenopus and zebrafish., Toyama R., Dev Biol. August 1, 1995; 170 (2): 583-93.
	XIPOU 2, a noggin-inducible gene, has direct neuralizing activity., Witta SE., Development. March 1, 1995; 121 (3): 721-30.
	Expression of the LIM class homeobox gene Xlim-1 in pronephros and CNS cell lineages of Xenopus embryos is affected by retinoic acid and exogastrulation., Taira M., Development. June 1, 1994; 120 (6): 1525-36.
	Embryonic expression of Lim-1, the mouse homolog of Xenopus Xlim-1, suggests a role in lateral mesoderm differentiation and neurogenesis., Barnes JD., Dev Biol. January 1, 1994; 161 (1): 168-78.
	Expression of LIM class homeobox gene Xlim-3 in Xenopus development is limited to neural and neuroendocrine tissues., Taira M., Dev Biol. September 1, 1993; 159 (1): 245-56.

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