Papers associated with cell part (and twist1)

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	Paracrine regulation of neural crest EMT by placodal MMP28., Gouignard N., PLoS Biol. August 1, 2023; 21 (8): e3002261.
	Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease., Mishra-Gorur K., Proc Natl Acad Sci U S A. April 18, 2023; 120 (16): e2214997120.
	OTUD3: A Lys6 and Lys63 specific deubiquitinase in early vertebrate development., Job F., Biochim Biophys Acta Gene Regul Mech. March 1, 2023; 1866 (1): 194901.
	Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
	BMP signaling is enhanced intracellularly by FHL3 controlling WNT-dependent spatiotemporal emergence of the neural crest., Alkobtawi M., Cell Rep. June 22, 2021; 35 (12): 109289.
	Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J., Genesis. February 1, 2021; 59 (1-2): e23404.
	Paired Box 9 (PAX9), the RNA polymerase II transcription factor, regulates human ribosome biogenesis and craniofacial development., Farley-Barnes KI., PLoS Genet. August 19, 2020; 16 (8): e1008967.
	A doublecortin-domain protein of Toxoplasma and its orthologues bind to and modify the structure and organization of tubulin polymers., Leung JM., BMC Mol Cell Biol. February 28, 2020; 21 (1): 8.
	The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration., Schwenty-Lara J., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.
	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
	Lineage tracing of sclerotome cells in amphibian reveals that multipotent somitic cells originate from lateral somitic frontier., Della Gaspera B., Dev Biol. September 1, 2019; 453 (1): 11-18.
	The Ric-8A/Gα13/FAK signalling cascade controls focal adhesion formation during neural crest cell migration in Xenopus., Toro-Tapia G., Development. November 21, 2018; 145 (22):
	Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo., Kotini M., Nat Commun. September 21, 2018; 9 (1): 3846.
	Redistribution of Adhesive Forces through Src/FAK Drives Contact Inhibition of Locomotion in Neural Crest., Roycroft A., Dev Cell. June 4, 2018; 45 (5): 565-579.e3.
	Glycogen synthase kinase 3 controls migration of the neural crest lineage in mouse and Xenopus., Gonzalez Malagon SG., Nat Commun. March 19, 2018; 9 (1): 1126.
	no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development., Nakayama T., Dev Biol. June 15, 2017; 426 (2): 472-486.
	Controlled levels of canonical Wnt signaling are required for neural crest migration., Maj E., Dev Biol. September 1, 2016; 417 (1): 77-90.
	Delamination of neural crest cells requires transient and reversible Wnt inhibition mediated by Dact1/2., Rabadán MA., Development. June 15, 2016; 143 (12): 2194-205.
	Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.
	Formin Is Associated with Left-Right Asymmetry in the Pond Snail and the Frog., Davison A., Curr Biol. March 7, 2016; 26 (5): 654-60.
	A PTK7/Ror2 Co-Receptor Complex Affects Xenopus Neural Crest Migration., Podleschny M., PLoS One. December 16, 2015; 10 (12): e0145169.
	Cadherin Switch during EMT in Neural Crest Cells Leads to Contact Inhibition of Locomotion via Repolarization of Forces., Scarpa E., Dev Cell. August 24, 2015; 34 (4): 421-34.
	GSK3 and Polo-like kinase regulate ADAM13 function during cranial neural crest cell migration., Abbruzzese G., Mol Biol Cell. December 15, 2014; 25 (25): 4072-82.
	Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.
	In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity., Kuriyama S., J Cell Biol. July 7, 2014; 206 (1): 113-27.
	Plakophilin-3 catenin associates with the ETV1/ER81 transcription factor to positively modulate gene activity., Munoz WA., PLoS One. January 1, 2014; 9 (1): e86784.
	Par3 controls neural crest migration by promoting microtubule catastrophe during contact inhibition of locomotion., Moore R., Development. December 1, 2013; 140 (23): 4763-75.
	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.
	Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.
	Calponin 2 acts as an effector of noncanonical Wnt-mediated cell polarization during neural crest cell migration., Ulmer B., Cell Rep. March 28, 2013; 3 (3): 615-21.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Plakophilin-3 is required for late embryonic amphibian development, exhibiting roles in ectodermal and neural tissues., Munoz WA., PLoS One. January 1, 2012; 7 (4): e34342.
	Neural crest specification by noncanonical Wnt signaling and PAR-1., Ossipova O., Development. December 1, 2011; 138 (24): 5441-50.
	Caldesmon regulates actin dynamics to influence cranial neural crest migration in Xenopus., Nie S., Mol Biol Cell. September 1, 2011; 22 (18): 3355-65.
	Peter Pan functions independently of its role in ribosome biogenesis during early eye and craniofacial cartilage development in Xenopus laevis., Bugner V., Development. June 1, 2011; 138 (11): 2369-78.
	Prohibitin1 acts as a neural crest specifier in Xenopus development by repressing the transcription factor E2F1., Schneider M., Development. December 1, 2010; 137 (23): 4073-81.
	PlexinA1 interacts with PTK7 and is required for neural crest migration., Wagner G., Biochem Biophys Res Commun. November 12, 2010; 402 (2): 402-7.
	Collective chemotaxis requires contact-dependent cell polarity., Theveneau E., Dev Cell. July 20, 2010; 19 (1): 39-53.
	Cadherin-11 regulates protrusive activity in Xenopus cranial neural crest cells upstream of Trio and the small GTPases., Kashef J., Genes Dev. June 15, 2009; 23 (12): 1393-8.
	Modeling and analysis of MH1 domain of Smads and their interaction with promoter DNA sequence motif., Makkar P., J Mol Graph Model. April 1, 2009; 27 (7): 803-12.
	PTK7 recruits dsh to regulate neural crest migration., Shnitsar I., Development. December 1, 2008; 135 (24): 4015-24.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Ajuba LIM proteins are snail/slug corepressors required for neural crest development in Xenopus., Langer EM., Dev Cell. March 1, 2008; 14 (3): 424-36.
	The tektin family of microtubule-stabilizing proteins., Amos LA., Genome Biol. January 1, 2008; 9 (7): 229.
	The small GTPase RhoV is an essential regulator of neural crest induction in Xenopus., Guémar L., Dev Biol. October 1, 2007; 310 (1): 113-28.
	Expression of RhoB in the developing Xenopus laevis embryo., Vignal E., Gene Expr Patterns. January 1, 2007; 7 (3): 282-8.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y., Dev Biol. September 15, 2004; 273 (2): 210-25.
	Xpbx1b and Xmeis1b play a collaborative role in hindbrain and neural crest gene expression in Xenopus embryos., Maeda R., Proc Natl Acad Sci U S A. April 16, 2002; 99 (8): 5448-53.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.

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