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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.
JmjC Domain-containing Protein 6 ( Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 ( Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis. , Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.
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.
Genome-wide view of TGFβ/ Foxh1 regulation of the early mesendoderm program. , Chiu WT ., Development. December 1, 2014; 141 (23): 4537-47.
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.
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.
Left- right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions. , Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Xenopus furry contributes to release of microRNA gene silencing. , Goto T ., Proc Natl Acad Sci U S A. November 9, 2010; 107 (45): 19344-9.
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.
Identification of novel transcripts with differential dorso- ventral expression in Xenopus gastrula using serial analysis of gene expression. , Faunes F., Genome Biol. February 11, 2009; 10 (2): R15.
Early molecular effects of ethanol during vertebrate embryogenesis. , Yelin R ., Differentiation. June 1, 2007; 75 (5): 393-403.
Genomic analysis of Xenopus organizer function. , Hufton AL., BMC Dev Biol. June 6, 2006; 6 27.
Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos. , Reversade B ., Development. August 1, 2005; 132 (15): 3381-92.
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.
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.
Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays. , Wessely O ., Dev Biol. May 15, 2004; 269 (2): 552-66.
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.
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.
Neuroectodermal specification and regionalization of the Spemann organizer in Xenopus. , Fetka I., Mech Dev. May 1, 2000; 93 (1-2): 49-58.
Characterization of a subfamily of related winged helix genes, XFD-12/12'/12" (XFLIP), during Xenopus embryogenesis. , Sölter M., Mech Dev. December 1, 1999; 89 (1-2): 161-5.
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.
The Xcad-2 gene can provide a ventral signal independent of BMP-4. , Pillemer G., Mech Dev. June 1, 1998; 74 (1-2): 133-43.
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.
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.
Expression of the LIM class homeobox gene Xlim-1 in pronephros and CNS cell lineages of Xenopus embryos is affected by retinoic acid and exogastrulation. , Taira M ., Development. June 1, 1994; 120 (6): 1525-36.
Sequential expression of HNF-3 beta and HNF-3 alpha by embryonic organizing centers: the dorsal lip/node, notochord and floor plate. , Ruiz i Altaba A ., Mech Dev. December 1, 1993; 44 (2-3): 91-108.
Ectopic neural expression of a floor plate marker in frog embryos injected with the midline transcription factor Pintallavis. , Ruiz i Altaba A ., Proc Natl Acad Sci U S A. September 1, 1993; 90 (17): 8268-72.
Pintallavis, a gene expressed in the organizer and midline cells of frog embryos: involvement in the development of the neural axis. , Ruiz i Altaba A ., Development. September 1, 1992; 116 (1): 81-93.
A novel, activin-inducible, blastopore lip-specific gene of Xenopus laevis contains a fork head DNA-binding domain. , Dirksen ML., Genes Dev. April 1, 1992; 6 (4): 599-608.