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Cdx1 and Gsc distinctly regulate the transcription of BMP4 target gene ventx3.2 by directly binding to the proximal promoter region in Xenopus gastrulae. , Goutam RS., Mol Cells. March 23, 2024; 47 (4): 100058.
R-Spondin 2 governs Xenopus left- right body axis formation by establishing an FGF signaling gradient. , Lee H , Lee H ., Nat Commun. February 2, 2024; 15 (1): 1003.
ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation. , Wang C ., EMBO Rep. February 1, 2024; 25 (2): 646-671.
The early dorsal signal in vertebrate embryos requires endolysosomal membrane trafficking. , Azbazdar Y., Bioessays. January 1, 2024; 46 (1): e2300179.
Transmembrane protein 150b attenuates BMP signaling in the Xenopus organizer. , Keum BR., J Cell Physiol. August 1, 2023; 238 (8): 1850-1866.
Two Homeobox Transcription Factors, Goosecoid and Ventx1.1, Oppositely Regulate Chordin Transcription in Xenopus Gastrula Embryos. , Kumar V ., Cells. March 11, 2023; 12 (6):
Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR. , Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
Targeted search for scaling genes reveals matrixmetalloproteinase 3 as a scaler of the dorsal- ventral pattern in Xenopus laevis embryos. , Orlov EE., Dev Cell. January 10, 2022; 57 (1): 95-111.e12.
Reduced Retinoic Acid Signaling During Gastrulation Induces Developmental Microcephaly. , Gur M., Front Cell Dev Biol. January 1, 2022; 10 844619.
Goosecoid Controls Neuroectoderm Specification via Dual Circuits of Direct Repression and Indirect Stimulation in Xenopus Embryos. , Umair Z., Mol Cells. October 31, 2021; 44 (10): 723-735.
Foxd4l1.1 Negatively Regulates Chordin Transcription in Neuroectoderm of Xenopus Gastrula. , Kumar V ., Cells. October 17, 2021; 10 (10):
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.
Pinhead antagonizes Admp to promote notochord formation. , Itoh K., iScience. May 7, 2021; 24 (6): 102520.
Dusp1 modulates activin/smad2 mediated germ layer specification via FGF signal inhibition in Xenopus embryos. , Umair Z., Anim Cells Syst (Seoul). November 27, 2020; 24 (6): 359-370.
TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis. , Chen M., Elife. September 14, 2020; 9
Natural size variation among embryos leads to the corresponding scaling in gene expression. , Leibovich A., Dev Biol. June 15, 2020; 462 (2): 165-179.
Role of dipeptidyl peptidase-4 as a potentiator of activin/nodal signaling pathway. , Park DS., BMB Rep. December 1, 2018; 51 (12): 636-641.
Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis. , Ding Y ., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.
Notch1 is asymmetrically distributed from the beginning of embryogenesis and controls the ventral center. , Castro Colabianchi AM., Development. July 17, 2018; 145 (14):
ADMP controls the size of Spemann's organizer through a network of self-regulating expansion-restriction signals. , Leibovich A., BMC Biol. January 22, 2018; 16 (1): 13.
Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates. , Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
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.
Ubiquitin C-terminal hydrolase37 regulates Tcf7 DNA binding for the activation of Wnt signalling. , Han W., Sci Rep. February 15, 2017; 7 42590.
Expression of the ALK1 family of type I BMP/ADMP receptors during gastrula stages in Xenopus embryos. , Leibovich A., Int J Dev Biol. January 1, 2017; 61 (6-7): 465-470.
The MLL/Setd1b methyltransferase is required for the Spemann's organizer gene activation in Xenopus. , Lin H., Mech Dev. November 1, 2016; 142 1-9.
Activation of a T-box- Otx2- Gsc gene network independent of TBP and TBP-related factors. , Gazdag E., Development. April 15, 2016; 143 (8): 1340-50.
Differential requirement of bone morphogenetic protein receptors Ia (ALK3) and Ib (ALK6) in early embryonic patterning and neural crest development. , Schille C., BMC Dev Biol. January 19, 2016; 16 1.
Specification of anteroposterior axis by combinatorial signaling during Xenopus development. , Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
The prodomain of BMP4 is necessary and sufficient to generate stable BMP4/7 heterodimers with enhanced bioactivity in vivo. , Neugebauer JM., Proc Natl Acad Sci U S A. May 5, 2015; 112 (18): E2307-16.
Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation. , Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo. , Li HY., Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y ., Development. October 1, 2014; 141 (19): 3740-51.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
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.
Setting appropriate boundaries: fate, patterning and competence at the neural plate border. , Groves AK., Dev Biol. May 1, 2014; 389 (1): 2-12.
Zygotic expression of Exostosin1 ( Ext1) is required for BMP signaling and establishment of dorsal- ventral pattern in Xenopus. , Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
Scaling of dorsal-ventral patterning by embryo size-dependent degradation of Spemann's organizer signals. , Inomata H ., Cell. June 6, 2013; 153 (6): 1296-311.
Current perspectives of the signaling pathways directing neural crest induction. , Stuhlmiller TJ., Cell Mol Life Sci. November 1, 2012; 69 (22): 3715-37.
Self-regulation of the head-inducing properties of the Spemann organizer. , Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
Sizzled- tolloid interactions maintain foregut progenitors by regulating fibronectin-dependent BMP signaling. , Kenny AP ., Dev Cell. August 14, 2012; 23 (2): 292-304.
TAK1 promotes BMP4/ Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network. , Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus. , Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/ nodal signaling in Xenopus ectodermal cells. , Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos. , Lee SY., Differentiation. September 1, 2011; 82 (2): 99-107.
xCITED2 Induces Neural Genes in Animal Cap Explants of Xenopus Embryos. , Yoon J., Exp Neurobiol. September 1, 2011; 20 (3): 123-9.
Role of BMP, FGF, calcium signaling, and Zic proteins in vertebrate neuroectodermal differentiation. , Aruga J ., Neurochem Res. July 1, 2011; 36 (7): 1286-92.
The function of heterodimeric AP-1 comprised of c- Jun and c- Fos in activin mediated Spemann organizer gene expression. , Lee SY., PLoS One. January 1, 2011; 6 (7): e21796.
Direct response elements of BMP within the PV.1A promoter are essential for its transcriptional regulation during early Xenopus development. , Lee HS , Lee HS ., PLoS One. January 1, 2011; 6 (8): e22621.
Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo. , Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
Xclaudin 1 is required for the proper gastrulation in Xenopus laevis. , Chang DJ., Biochem Biophys Res Commun. June 18, 2010; 397 (1): 75-81.