Papers associated with septum (and otx2)

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	Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells., Okuno H., Regen Ther. August 24, 2021; 18 275-280.
	Coordinating heart morphogenesis: A novel role for hyperpolarization-activated cyclic nucleotide-gated (HCN) channels during cardiogenesis in Xenopus laevis., Pitcairn E., Commun Integr Biol. May 10, 2017; 10 (3): e1309488.
	Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.
	cnrip1 is a regulator of eye and neural development in Xenopus laevis., Zheng X., Genes Cells. April 1, 2015; 20 (4): 324-39.
	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.
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
	Scaling of dorsal-ventral patterning by embryo size-dependent degradation of Spemann's organizer signals., Inomata H., Cell. June 6, 2013; 153 (6): 1296-311.
	Xnr3 affects brain patterning via cell migration in the neural-epidermal tissue boundary during early Xenopus embryogenesis., Morita M., Int J Dev Biol. January 1, 2013; 57 (9-10): 779-86.
	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.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus., Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.
	Regulation of TCF3 by Wnt-dependent phosphorylation during vertebrate axis specification., Hikasa H., Dev Cell. October 19, 2010; 19 (4): 521-32.
	Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.
	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	MicroRNAs couple cell fate and developmental timing in retina., Decembrini S., Proc Natl Acad Sci U S A. December 15, 2009; 106 (50): 21179-84.
	The role of miR-124a in early development of the Xenopus eye., Qiu R., Mech Dev. October 1, 2009; 126 (10): 804-16.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	FAM/USP9x, a deubiquitinating enzyme essential for TGFbeta signaling, controls Smad4 monoubiquitination., Dupont S., Cell. January 9, 2009; 136 (1): 123-35.
	Expression study of cadherin7 and cadherin20 in the embryonic and adult rat central nervous system., Takahashi M., BMC Dev Biol. June 23, 2008; 8 87.
	Dystroglycan is required for proper retinal layering., Lunardi A., Dev Biol. February 15, 2006; 290 (2): 411-20.
	Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
	Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development., Takahashi N., Int J Dev Biol. January 1, 2005; 49 (8): 939-51.
	Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	XMeis3 protein activity is required for proper hindbrain patterning in Xenopus laevis embryos., Dibner C., Development. September 1, 2001; 128 (18): 3415-26.
	The circadian gene Clock is restricted to the anterior neural plate early in development and is regulated by the neural inducer noggin and the transcription factor Otx2., Green CB., Mech Dev. March 1, 2001; 101 (1-2): 105-10.
	Increased XRALDH2 activity has a posteriorizing effect on the central nervous system of Xenopus embryos., Chen Y., Mech Dev. March 1, 2001; 101 (1-2): 91-103.
	Cngsc, a homologue of goosecoid, participates in the patterning of the head, and is expressed in the organizer region of Hydra., Broun M., Development. December 1, 1999; 126 (23): 5245-54.
	Cytochalasin B inhibits morphogenetic movement and muscle differentiation of activin-treated ectoderm in Xenopus., Tamai K., Dev Growth Differ. February 1, 1999; 41 (1): 41-9.
	The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins., Latinkić BV., Genes Dev. December 1, 1997; 11 (23): 3265-76.
	XIPOU 2 is a potential regulator of Spemann's Organizer., Witta SE., Development. March 1, 1997; 124 (6): 1179-89.

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