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Eph/ephrin signaling controls cell contacts and formation of a structurally asymmetrical tissue boundary in the Xenopus gastrula. , Barua D., Dev Biol. October 1, 2022; 490 73-85.
Retinoic Acid is Required for Normal Morphogenetic Movements During Gastrulation. , Gur M., Front Cell Dev Biol. January 1, 2022; 10 857230.
Sorting at embryonic boundaries requires high heterotypic interfacial tension. , Canty L., Nat Commun. July 31, 2017; 8 (1): 157.
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.
EphA4-dependent Brachyury expression is required for dorsal mesoderm involution in the Xenopus gastrula. , Evren S., Development. October 1, 2014; 141 (19): 3649-61.
Variable combinations of specific ephrin ligand/Eph receptor pairs control embryonic tissue separation. , Rohani N ., PLoS Biol. September 23, 2014; 12 (9): e1001955.
Ephrin-Eph signaling in embryonic tissue separation. , Fagotto F ., Cell Adh Migr. January 1, 2014; 8 (4): 308-26.
A molecular base for cell sorting at embryonic boundaries: contact inhibition of cadherin adhesion by ephrin/ Eph-dependent contractility. , Fagotto F ., Dev Cell. October 14, 2013; 27 (1): 72-87.
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. , Barnett C., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
Caldesmon regulates actin dynamics to influence cranial neural crest migration in Xenopus. , Nie S ., Mol Biol Cell. September 1, 2011; 22 (18): 3355-65.
The involvement of Eph-Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements. , Park EC ., Dev Biol. February 15, 2011; 350 (2): 441-50.
Sox9 is required for invagination of the otic placode in mice. , Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
Xenopus Teashirt1 regulates posterior identity in brain and cranial neural crest. , Koebernick K., Dev Biol. October 1, 2006; 298 (1): 312-26.
Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation. , Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus. , Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
Microarray-based identification of VegT targets in Xenopus. , Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.
Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning. , Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
Neural induction in whole chick embryo cultures by FGF. , Alvarez IS., Dev Biol. July 1, 1998; 199 (1): 42-54.
The EphA4 and EphB1 receptor tyrosine kinases and ephrin-B2 ligand regulate targeted migration of branchial neural crest cells. , Smith A., Curr Biol. August 1, 1997; 7 (8): 561-70.
Embryonic expression of eph signalling factors in Xenopus. , Weinstein DC ., Mech Dev. July 1, 1996; 57 (2): 133-44.
Novel members of the eph receptor tyrosine kinase subfamily expressed during Xenopus development. , Scales JB ., Oncogene. November 2, 1995; 11 (9): 1745-52.
Pagliaccio, a member of the Eph family of receptor tyrosine kinase genes, has localized expression in a subset of neural crest and neural tissues in Xenopus laevis embryos. , Winning RS., Mech Dev. June 1, 1994; 46 (3): 219-29.
Regional specificity of RAR gamma isoforms in Xenopus development. , Pfeffer PL., Mech Dev. February 1, 1994; 45 (2): 147-53.
Tail formation as a continuation of gastrulation: the multiple cell populations of the Xenopus tailbud derive from the late blastopore lip. , Gont LK., Development. December 1, 1993; 119 (4): 991-1004.