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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.
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.
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.
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.
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.
Concentrations of TATA box-binding protein ( TBP)-type genes affect chordamesodermal gene expression. , Goto T ., Int J Dev Biol. January 1, 2008; 52 (4): 371-5.
Early molecular effects of ethanol during vertebrate embryogenesis. , Yelin R ., Differentiation. June 1, 2007; 75 (5): 393-403.
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.
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.
Patterning the forebrain: FoxA4a/ Pintallavis and Xvent2 determine the posterior limit of Xanf1 expression in the neural plate. , Martynova N., Development. May 1, 2004; 131 (10): 2329-38.
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.
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.
Gli1 is a target of Sonic hedgehog that induces ventral neural tube development. , Lee J ., Development. July 1, 1997; 124 (13): 2537-52.
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.
Differential expression of fork head genes during early Xenopus and zebrafish development. , Dirksen ML., Dev Genet. January 1, 1995; 17 (2): 107-16.
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.
Identification of nine tissue-specific transcription factors of the hepatocyte nuclear factor 3/forkhead DNA-binding-domain family. , Clevidence DE., Proc Natl Acad Sci U S A. May 1, 1993; 90 (9): 3948-52.
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.