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Temporal transcriptomic profiling reveals dynamic changes in gene expression of Xenopus animal cap upon activin treatment. , Satou-Kobayashi Y., Sci Rep. July 15, 2021; 11 (1): 14537.
RARγ is required for mesodermal gene expression prior to gastrulation in Xenopus. , Janesick A ., Development. September 17, 2018; 145 (18):
Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition. , Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.
Specification of anteroposterior axis by combinatorial signaling during Xenopus development. , Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning. , Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
Early neural ectodermal genes are activated by Siamois and Twin during blastula stages. , Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
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.
Variable combinations of specific ephrin ligand/Eph receptor pairs control embryonic tissue separation. , Rohani N ., PLoS Biol. September 23, 2014; 12 (9): e1001955.
Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification. , Yasuoka Y ., Nat Commun. July 9, 2014; 5 4322.
Inference of the Xenopus tropicalis embryonic regulatory network and spatial gene expression patterns. , Zheng Z., BMC Syst Biol. January 8, 2014; 8 3.
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.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo. , Ninomiya H., J Cell Sci. April 15, 2012; 125 (Pt 8): 1877-83.
Indian hedgehog signaling is required for proper formation, maintenance and migration of Xenopus neural crest. , Agüero TH., Dev Biol. April 15, 2012; 364 (2): 99-113.
Transient expression of Ngn3 in Xenopus endoderm promotes early and ectopic development of pancreatic beta and delta cells. , Oropeza D., Genesis. March 1, 2012; 50 (3): 271-85.
A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling. , Peyrot SM., Dev Biol. April 15, 2011; 352 (2): 254-66.
MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization. , Suzuki M ., Development. July 1, 2010; 137 (14): 2329-39.
Evolutionary origin of the Otx2 enhancer for its expression in visceral endoderm. , Kurokawa D., Dev Biol. June 1, 2010; 342 (1): 110-20.
Highly conserved functions of the Brachyury gene on morphogenetic movements: insight from the early-diverging phylum Ctenophora. , Yamada A., Dev Biol. March 1, 2010; 339 (1): 212-22.
Early molecular effects of ethanol during vertebrate embryogenesis. , Yelin R ., Differentiation. June 1, 2007; 75 (5): 393-403.
Kinesin-mediated transport of Smad2 is required for signaling in response to TGF-beta ligands. , Batut J., Dev Cell. February 1, 2007; 12 (2): 261-74.
beta-Catenin controls cell sorting at the notochord- somite boundary independently of cadherin-mediated adhesion. , Reintsch WE., J Cell Biol. August 15, 2005; 170 (4): 675-86.
Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus. , Chen JA ., Mech Dev. March 1, 2005; 122 (3): 307-31.
The Notch-target gene hairy2a impedes the involution of notochordal cells by promoting floor plate fates in Xenopus embryos. , López SL ., Development. March 1, 2005; 132 (5): 1035-46.
The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos. , Callery EM ., Dev Biol. February 15, 2005; 278 (2): 542-59.
Of Fox and Frogs: Fox (fork head/winged helix) transcription factors in Xenopus development. , Pohl BS., Gene. January 3, 2005; 344 21-32.
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.
Inhibition of mesodermal fate by Xenopus HNF3beta/ FoxA2. , Suri C., Dev Biol. January 1, 2004; 265 (1): 90-104.
Selective degradation of excess Ldb1 by Rnf12/ RLIM confers proper Ldb1 expression levels and Xlim-1/ Ldb1 stoichiometry in Xenopus organizer functions. , Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
Notch activates sonic hedgehog and both are involved in the specification of dorsal midline cell-fates in Xenopus. , López SL ., Development. May 1, 2003; 130 (10): 2225-38.
A novel Xenopus Smad-interacting forkhead transcription factor ( XFast-3) cooperates with XFast-1 in regulating gastrulation movements. , Howell M., Development. June 1, 2002; 129 (12): 2823-34.
Antisense inhibition of Xbrachyury impairs mesoderm formation in Xenopus embryos. , Giovannini N., Dev Growth Differ. April 1, 2002; 44 (2): 147-59.
Role of Goosecoid, Xnot and Wnt antagonists in the maintenance of the notochord genetic programme in Xenopus gastrulae. , Yasuo H., Development. October 1, 2001; 128 (19): 3783-93.
Determinants of T box protein specificity. , Conlon FL ., Development. October 1, 2001; 128 (19): 3749-58.
Fox (forkhead) genes are involved in the dorso- ventral patterning of the Xenopus mesoderm. , El-Hodiri H ., Int J Dev Biol. January 1, 2001; 45 (1): 265-71.
A screen for targets of the Xenopus T-box gene Xbra. , Saka Y ., Mech Dev. May 1, 2000; 93 (1-2): 27-39.
Functions for Drosophila brachyenteron and forkhead in mesoderm specification and cell signalling. , Kusch T., Development. September 1, 1999; 126 (18): 3991-4003.
derrière: a TGF-beta family member required for posterior development in Xenopus. , Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
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.
XSmad2 directly activates the activin-inducible, dorsal mesoderm gene XFKH1 in Xenopus embryos. , Howell M., EMBO J. December 15, 1997; 16 (24): 7411-21.
Markers of vertebrate mesoderm induction. , Stennard F ., Curr Opin Genet Dev. October 1, 1997; 7 (5): 620-7.
The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds. , Armes NA., Development. October 1, 1997; 124 (19): 3797-804.
Gli1 is a target of Sonic hedgehog that induces ventral neural tube development. , Lee J ., Development. July 1, 1997; 124 (13): 2537-52.
Expression pattern of an axolotl floor plate-specific fork head gene reflects early developmental differences between frogs and salamanders. , Whiteley M., Dev Genet. January 1, 1997; 20 (2): 145-51.
Regulated expression of the retinoblastoma gene product by fibroblast growth factor but not by activin during mesoderm induction in Xenopus. , Greenland J., Dev Genes Evol. December 1, 1996; 206 (5): 333-6.
Inhibition of Xbra transcription activation causes defects in mesodermal patterning and reveals autoregulation of Xbra in dorsal mesoderm. , Conlon FL ., Development. August 1, 1996; 122 (8): 2427-35.
Bone morphogenetic protein-4 ( BMP-4) acts during gastrula stages to cause ventralization of Xenopus embryos. , Jones CM ., Development. May 1, 1996; 122 (5): 1545-54.
Overexpression of the homeobox gene Xnot-2 leads to notochord formation in Xenopus. , Gont LK., Dev Biol. February 25, 1996; 174 (1): 174-8.
A fork head related multigene family is transcribed in Xenopus laevis embryos. , Lef J., Int J Dev Biol. February 1, 1996; 40 (1): 245-53.
Bone morphogenetic protein 2 in the early development of Xenopus laevis. , Clement JH., Mech Dev. August 1, 1995; 52 (2-3): 357-70.