Papers associated with posterior (and tubb2b)

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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. April 1, 2024; 66 (3): 256-265.
	Patterns of tubb2b Promoter-Driven Fluorescence in the Forebrain of Larval Xenopus laevis., Daume D., Front Neuroanat. January 1, 2022; 16 914281.
	Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors., Kakebeen AD., Elife. April 27, 2020; 9
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	Xenopus slc7a5 is essential for notochord function and eye development., Katada T., Mech Dev. February 1, 2019; 155 48-59.
	Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
	Alteration of the Retinoid Acid-CBP Signaling Pathway in Neural Crest Induction Contributes to Enteric Nervous System Disorder., Li C., Front Pediatr. December 3, 2018; 6 382.
	Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14., Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.
	Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo., Gouignard N., PLoS One. January 18, 2018; 13 (1): e0191751.
	Six1 and Eya1 both promote and arrest neuronal differentiation by activating multiple Notch pathway genes., Riddiford N., Dev Biol. November 15, 2017; 431 (2): 152-167.
	Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration., Simon E., Biol Open. October 15, 2017; 6 (10): 1528-1540.
	Developmental neurogenesis in mouse and Xenopus is impaired in the absence of Nosip., Hoffmeister M., Dev Biol. September 1, 2017; 429 (1): 200-212.
	N1-Src Kinase Is Required for Primary Neurogenesis in Xenopus tropicalis., Lewis PA., J Neurosci. August 30, 2017; 37 (35): 8477-8485.
	sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis., Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.
	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.
	Tbx3 represses bmp4 expression and, with Pax6, is required and sufficient for retina formation., Motahari Z., Development. October 1, 2016; 143 (19): 3560-3572.
	The positive transcriptional elongation factor (P-TEFb) is required for neural crest specification., Hatch VL., Dev Biol. August 15, 2016; 416 (2): 361-72.
	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.
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y., Development. October 1, 2014; 141 (19): 3740-51.
	Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
	The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.
	FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.
	Maturin is a novel protein required for differentiation during primary neurogenesis., Martinez-De Luna RI., Dev Biol. December 1, 2013; 384 (1): 26-40.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	The Xenopus doublesex-related gene Dmrt5 is required for olfactory placode neurogenesis., Parlier D., Dev Biol. January 1, 2013; 373 (1): 39-52.
	Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development., Xu Y, Xu Y., Cell. December 7, 2012; 151 (6): 1200-13.
	Involvement of XZFP36L1, an RNA-binding protein, in Xenopus neural development., Xia YJ., Dongwuxue Yanjiu. December 1, 2012; 33 (E5-6): E82-8.
	Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus., Park BY., Dev Biol. February 1, 2012; 362 (1): 65-75.
	Genomic targets of Brachyury (T) in differentiating mouse embryonic stem cells., Evans AL., PLoS One. January 1, 2012; 7 (3): e33346.
	Focal adhesion kinase protein regulates Wnt3a gene expression to control cell fate specification in the developing neural plate., Fonar Y., Mol Biol Cell. July 1, 2011; 22 (13): 2409-21.
	hnRNP K post-transcriptionally co-regulates multiple cytoskeletal genes needed for axonogenesis., Liu Y., Development. July 1, 2011; 138 (14): 3079-90.
	Interaction of Sox1, Sox2, Sox3 and Oct4 during primary neurogenesis., Archer TC., Dev Biol. February 15, 2011; 350 (2): 429-40.
	MicroRNA-9 reveals regional diversity of neural progenitors along the anterior-posterior axis., Bonev B., Dev Cell. January 18, 2011; 20 (1): 19-32.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	Histone XH2AX is required for Xenopus anterior neural development: critical role of threonine 16 phosphorylation., Lee SY., J Biol Chem. September 17, 2010; 285 (38): 29525-34.
	Delta-Notch signaling is involved in the segregation of the three germ layers in Xenopus laevis., Revinski DR., Dev Biol. March 15, 2010; 339 (2): 477-92.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
	Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis., Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.
	Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis., Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.
	Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development., Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
	BDNF promotes target innervation of Xenopus mandibular trigeminal axons in vivo., Huang JK., BMC Dev Biol. May 31, 2007; 7 59.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	Novel Daple-like protein positively regulates both the Wnt/beta-catenin pathway and the Wnt/JNK pathway in Xenopus., Kobayashi H., Mech Dev. October 1, 2005; 122 (10): 1138-53.

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