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Summary Anatomy Item Literature (2919) Expression Attributions Wiki
XB-ANAT-23

Papers associated with skin (and nodal1)

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The early dorsal signal in vertebrate embryos requires endolysosomal membrane trafficking., Azbazdar Y., Bioessays. January 1, 2024; 46 (1): e2300179.                            

Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.          

TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9                                                                                           

A Conserved Role of the Unconventional Myosin 1d in Laterality Determination., Tingler M., Curr Biol. March 5, 2018; 28 (5): 810-816.e3.                

Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish., Bisgrove BW., Elife. November 15, 2017; 6                 

c21orf59/kurly Controls Both Cilia Motility and Polarization., Jaffe KM., Cell Rep. March 1, 2016; 14 (8): 1841-9.                  

Myocyte enhancer factor 2D regulates ectoderm specification and adhesion properties of animal cap cells in the early Xenopus embryo., Katz Imberman S., FEBS J. August 1, 2015; 282 (15): 2930-47.

TGF-β Signaling Regulates the Differentiation of Motile Cilia., Tözser J., Cell Rep. May 19, 2015; 11 (7): 1000-7.                

Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral-right blastomere., Tingler M., Genesis. June 1, 2014; 52 (6): 588-99.            

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.                                  

Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.                      

Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus., Lim CY., Development. February 1, 2013; 140 (4): 853-60.                                              

Whole-genome microRNA screening identifies let-7 and mir-18 as regulators of germ layer formation during early embryogenesis., Colas AR., Genes Dev. December 1, 2012; 26 (23): 2567-79.      

Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left-Right Asymmetry., Pai VP., Stem Cells Int. January 1, 2012; 2012 353491.          

Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos., Lee SY., Differentiation. September 1, 2011; 82 (2): 99-107.                    

Flow on the right side of the gastrocoel roof plate is dispensable for symmetry breakage in the frog Xenopus laevis., Vick P., Dev Biol. July 15, 2009; 331 (2): 281-91.                                        

Molecular determinants of multiple effects of nickel on NMDA receptor channels., Gavazzo P., Neurotox Res. January 1, 2009; 15 (1): 38-48.

Long- and short-range signals control the dynamic expression of an animal hemisphere-specific gene in Xenopus., Mir A., Dev Biol. March 1, 2008; 315 (1): 161-72.            

Unexpected activities of Smad7 in Xenopus mesodermal and neural induction., de Almeida I., Mech Dev. January 1, 2008; 125 (5-6): 421-31.              

The role of FoxC1 in early Xenopus development., Cha JY., Dev Dyn. October 1, 2007; 236 (10): 2731-41.        

Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination., Hilton EN., Hum Mol Genet. July 15, 2007; 16 (14): 1773-82.              

The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.              

FoxI1e activates ectoderm formation and controls cell position in the Xenopus blastula., Mir A., Development. February 1, 2007; 134 (4): 779-88.                  

Cyclophane and acyclic cyclophane: novel channel blockers of N-methyl-D-aspartate receptor., Masuko T., Neurochem Int. January 1, 2007; 50 (2): 443-9.

FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    

Xenopus POU factors of subclass V inhibit activin/nodal signaling during gastrulation., Cao Y., Mech Dev. August 1, 2006; 123 (8): 614-25.            

Formation of the ascidian epidermal sensory neurons: insights into the origin of the chordate peripheral nervous system., Pasini A., PLoS Biol. July 1, 2006; 4 (7): e225.              

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.              

Anthraquinone polyamines: novel channel blockers to study N-methyl-D-aspartate receptors., Kashiwagi K., J Pharmacol Exp Ther. June 1, 2004; 309 (3): 884-93.

Regulation of vertebrate eye development by Rx genes., Bailey TJ., Int J Dev Biol. January 1, 2004; 48 (8-9): 761-70.    

Pharmacology of delta2 glutamate receptors: effects of pentamidine and protons., Williams K., J Pharmacol Exp Ther. May 1, 2003; 305 (2): 740-8.

The orphan receptor ALK7 and the Activin receptor ALK4 mediate signaling by Nodal proteins during vertebrate development., Reissmann E., Genes Dev. August 1, 2001; 15 (15): 2010-22.                

Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus., Wessely O., Dev Biol. June 1, 2001; 234 (1): 161-73.              

An N-methyl-D-aspartate receptor channel blocker with neuroprotective activity., Tai KK., Proc Natl Acad Sci U S A. March 13, 2001; 98 (6): 3519-24.

Effects of volatile solvents on recombinant N-methyl-D-aspartate receptors expressed in Xenopus oocytes., Cruz SL., Br J Pharmacol. December 1, 2000; 131 (7): 1303-8.

Molecular determinants of coordinated proton and zinc inhibition of N-methyl-D-aspartate NR1/NR2A receptors., Low CM., Proc Natl Acad Sci U S A. September 26, 2000; 97 (20): 11062-7.

More than 95% reversal of left-right axis induced by right-sided hypodermic microinjection of activin into Xenopus neurula embryos., Toyoizumi R., Dev Biol. May 15, 2000; 221 (2): 321-36.                

Primary structure requirements for Xenopus nodal-related 3 and a comparison with regions required by Xenopus nodal-related 2., Ezal CH., J Biol Chem. May 12, 2000; 275 (19): 14124-31.

Endodermal Nodal-related signals and mesoderm induction in Xenopus., Agius E., Development. March 1, 2000; 127 (6): 1173-83.          

In vitro and in vivo characterization of conantokin-R, a selective NMDA receptor antagonist isolated from the venom of the fish-hunting snail Conus radiatus., White HS., J Pharmacol Exp Ther. January 1, 2000; 292 (1): 425-32.

4-Hydroxy-1-[2-(4-hydroxyphenoxy)ethyl]-4-(4-methylbenzyl)piperidine: a novel, potent, and selective NR1/2B NMDA receptor antagonist., Zhou ZL., J Med Chem. July 29, 1999; 42 (15): 2993-3000.

Direct neural induction and selective inhibition of mesoderm and epidermis inducers by Xnr3., Hansen CS., Development. January 1, 1997; 124 (2): 483-92.

Nodal-related signals induce axial mesoderm and dorsalize mesoderm during gastrulation., Jones CM., Development. November 1, 1995; 121 (11): 3651-62.                

On the capacity current in myelinated nerve fibres., Wiese H., Gen Physiol Biophys. August 1, 1983; 2 (4): 297-312.

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