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Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral- right blastomere. , Tingler M., Genesis. June 1, 2014; 52 (6): 588-99.
Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein. , Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
NumbL is essential for Xenopus primary neurogenesis. , Nieber F., BMC Dev Biol. October 14, 2013; 13 36.
Coco regulates dorsoventral specification of germ layers via inhibition of TGFβ signalling. , Bates TJ., Development. October 1, 2013; 140 (20): 4177-81.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
Polycomb repressive complex PRC2 regulates Xenopus retina development downstream of Wnt/ β-catenin signaling. , Aldiri I ., Development. July 1, 2013; 140 (14): 2867-78.
sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling. , Gibb N ., Development. April 1, 2013; 140 (7): 1537-49.
Rab GTPases are required for early orientation of the left- right axis in Xenopus. , Vandenberg LN., Mech Dev. January 1, 2013; 130 (4-5): 254-71.
Specific domains of FoxD4/5 activate and repress neural transcription factor genes to control the progression of immature neural ectoderm to differentiating neural plate. , Neilson KM ., Dev Biol. May 15, 2012; 365 (2): 363-75.
The RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus. , Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.
Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/ β-catenin signaling pathway. , Fujimi TJ ., Dev Biol. January 15, 2012; 361 (2): 220-31.
Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus. , Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.
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.
Geminin is required for zygotic gene expression at the Xenopus mid- blastula transition. , Kerns SL., PLoS One. January 1, 2012; 7 (5): e38009.
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.
HEB and E2A function as SMAD/FOXH1 cofactors. , Yoon SJ ., Genes Dev. August 1, 2011; 25 (15): 1654-61.
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.
Transmembrane potential of GlyCl-expressing instructor cells induces a neoplastic-like conversion of melanocytes via a serotonergic pathway. , Blackiston D ., Dis Model Mech. January 1, 2011; 4 (1): 67-85.
Antagonistic role of XESR1 and XESR5 in mesoderm formation in Xenopus laevis. , Kinoshita T., Int J Dev Biol. January 1, 2011; 55 (1): 25-31.
Yes-associated protein 65 ( YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone. , Gee ST ., PLoS One. January 1, 2011; 6 (6): e20309.
Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus. , Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
The RNA-binding protein Xp54nrb isolated from a Ca²+-dependent screen is expressed in neural structures during Xenopus laevis development. , Neant I ., Int J Dev Biol. January 1, 2011; 55 (10-12): 923-31.
Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network. , Yan B ., Dev Dyn. December 1, 2010; 239 (12): 3467-80.
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.
Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin. , Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.
Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/ CREB pathway. , Keren-Politansky A., Dev Biol. November 15, 2009; 335 (2): 374-84.
Coordinating the timing of cardiac precursor development during gastrulation: a new role for Notch signaling. , Miazga CM., Dev Biol. September 15, 2009; 333 (2): 285-96.
CDK9/cyclin complexes modulate endoderm induction by direct interaction with Mix.3/ mixer. , Zhu H., Dev Dyn. June 1, 2009; 238 (6): 1346-57.
foxD5 plays a critical upstream role in regulating neural ectodermal fate and the onset of neural differentiation. , Yan B ., Dev Biol. May 1, 2009; 329 (1): 80-95.
A role for Syndecan-4 in neural induction involving ERK- and PKC-dependent pathways. , Kuriyama S ., Development. February 1, 2009; 136 (4): 575-84.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
PMesogenin1 and 2 function directly downstream of Xtbx6 in Xenopus somitogenesis and myogenesis. , Tazumi S., Dev Dyn. December 1, 2008; 237 (12): 3749-61.
A p38 MAPK- CREB pathway functions to pattern mesoderm in Xenopus. , Keren A., Dev Biol. October 1, 2008; 322 (1): 86-94.
Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus. , Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.
A functional screen for genes involved in Xenopus pronephros development. , Kyuno J ., Mech Dev. July 1, 2008; 125 (7): 571-86.
PACSIN2 regulates cell adhesion during gastrulation in Xenopus laevis. , Cousin H ., Dev Biol. July 1, 2008; 319 (1): 86-99.
The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus. , Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.
The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm. , Spagnoli FM ., Development. February 1, 2008; 135 (3): 451-61.
Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis. , Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.
Hes6 is required for MyoD induction during gastrulation. , Murai K., Dev Biol. December 1, 2007; 312 (1): 61-76.
Tsukushi modulates Xnr2, FGF and BMP signaling: regulation of Xenopus germ layer formation. , Morris SA., PLoS One. October 10, 2007; 2 (10): e1004.
The small GTPase RhoV is an essential regulator of neural crest induction in Xenopus. , Guémar L., Dev Biol. October 1, 2007; 310 (1): 113-28.
Xenopus Lefty requires proprotein cleavage but not N-linked glycosylation to inhibit nodal signaling. , Westmoreland JJ., Dev Dyn. August 1, 2007; 236 (8): 2050-61.
Retinoic acid-mediated patterning of the pre-pancreatic endoderm in Xenopus operates via direct and indirect mechanisms. , Pan FC., Mech Dev. August 1, 2007; 124 (7-8): 518-31.
Vertebrate Ctr1 coordinates morphogenesis and progenitor cell fate and regulates embryonic stem cell differentiation. , Haremaki T ., Proc Natl Acad Sci U S A. July 17, 2007; 104 (29): 12029-34.
Alterations of rx1 and pax6 expression levels at neural plate stages differentially affect the production of retinal cell types and maintenance of retinal stem cell qualities. , Zaghloul NA ., Dev Biol. June 1, 2007; 306 (1): 222-40.
Wnt-5A/ Ror2 regulate expression of XPAPC through an alternative noncanonical signaling pathway. , Schambony A ., Dev Cell. May 1, 2007; 12 (5): 779-92.
Wnt/beta-catenin signaling controls Mespo expression to regulate segmentation during Xenopus somitogenesis. , Wang J ., Dev Biol. April 15, 2007; 304 (2): 836-47.
Xenopus glucose transporter 1 (xGLUT1) is required for gastrulation movement in Xenopus laevis. , Suzawa K ., Int J Dev Biol. January 1, 2007; 51 (3): 183-90.
Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/ Smad1 pathway. , Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.