Papers associated with forebrain (and actc1)

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	Development of a heat-stable alkaline phosphatase reporter system for cis-regulatory analysis and its application to 3D digital imaging of Xenopus embryonic tissues., Sakagami K., Dev Growth Differ. March 4, 2024;
	Predation threats for a 24-h period activated the extension of axons in the brains of Xenopus tadpoles., Mori T., Sci Rep. July 16, 2020; 10 (1): 11737.
	DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain., Kyono Y., Dev Biol. June 15, 2020; 462 (2): 180-196.
	Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.
	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	Cell-fate determination by ubiquitin-dependent regulation of translation., Werner A., Nature. September 24, 2015; 525 (7570): 523-7.
	Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.
	Expression cloning of camelid nanobodies specific for Xenopus embryonic antigens., Itoh K., PLoS One. January 1, 2014; 9 (10): e107521.
	Maturin is a novel protein required for differentiation during primary neurogenesis., Martinez-De Luna RI., Dev Biol. December 1, 2013; 384 (1): 26-40.
	Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
	Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.
	XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development., Ori M., Development. February 1, 2006; 133 (4): 631-40.
	BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.
	Transgenic frogs expressing the highly fluorescent protein venus under the control of a strong mammalian promoter suitable for monitoring living cells., Sakamaki K., Dev Dyn. June 1, 2005; 233 (2): 562-9.
	Identification and characterisation of the posteriorly-expressed Xenopus neurotrophin receptor homolog genes fullback and fullback-like., Bromley E., Gene Expr Patterns. November 1, 2004; 5 (1): 135-40.
	The E3 ubiquitin ligase GREUL1 anteriorizes ectoderm during Xenopus development., Borchers AG., Dev Biol. November 15, 2002; 251 (2): 395-408.
	Distinct enhancers regulate skeletal and cardiac muscle-specific expression programs of the cardiac alpha-actin gene in Xenopus embryos., Latinkić BV., Dev Biol. May 1, 2002; 245 (1): 57-70.
	Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.
	Post-transcriptional regulation of Xwnt-8 expression is required for normal myogenesis during vertebrate embryonic development., Tian Q., Development. August 1, 1999; 126 (15): 3371-80.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	A novel BMP expressed in developing mouse limb, spinal cord, and tail bud is a potent mesoderm inducer in Xenopus embryos., Gamer LW., Dev Biol. April 1, 1999; 208 (1): 222-32.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	Mesoderm induction by heterodimeric AP-1 (c-Jun and c-Fos) and its involvement in mesoderm formation through the embryonic fibroblast growth factor/Xbra autocatalytic loop during the early development of Xenopus embryos., Kim J., J Biol Chem. January 16, 1998; 273 (3): 1542-50.
	The role of intracellular alkalinization in the establishment of anterior neural fate in Xenopus., Uzman JA., Dev Biol. January 1, 1998; 193 (1): 10-20.
	Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus., McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Epidermal induction and inhibition of neural fate by translation initiation factor 4AIII., Weinstein DC., Development. November 1, 1997; 124 (21): 4235-42.
	Caudalization of neural fate by tissue recombination and bFGF., Cox WG., Development. December 1, 1995; 121 (12): 4349-58.
	The Xenopus homologue of Otx2 is a maternal homeobox gene that demarcates and specifies anterior body regions., Pannese M., Development. March 1, 1995; 121 (3): 707-20.
	XFKH2, a Xenopus HNF-3 alpha homologue, exhibits both activin-inducible and autonomous phases of expression in early embryos., Bolce ME., Dev Biol. December 1, 1993; 160 (2): 413-23.
	Localized expression of a Xenopus POU gene depends on cell-autonomous transcriptional activation and induction-dependent inactivation., Frank D., Development. June 1, 1992; 115 (2): 439-48.
	Expression of Xenopus N-CAM RNA in ectoderm is an early response to neural induction., Kintner CR., Development. March 1, 1987; 99 (3): 311-25.

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