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ARVCF catenin controls force production during vertebrate convergent extension. , Huebner RJ., Dev Cell. May 9, 2022; 57 (9): 1119-1131.e5.
Rab7 is required for mesoderm patterning and gastrulation in Xenopus. , Kreis J., Biol Open. July 15, 2021; 10 (7):
Pinhead antagonizes Admp to promote notochord formation. , Itoh K., iScience. June 25, 2021; 24 (6): 102520.
Furry is required for cell movements during gastrulation and functionally interacts with NDR1. , Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
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.
AKT signaling displays multifaceted functions in neural crest development. , Sittewelle M., Dev Biol. December 1, 2018; 444 Suppl 1 S144-S155.
Shared evolutionary origin of vertebrate neural crest and cranial placodes. , Horie R., Nature. August 1, 2018; 560 (7717): 228-232.
Transcriptomics of dorso- ventral axis determination in Xenopus tropicalis. , Monteiro RS ., Dev Biol. July 15, 2018; 439 (2): 69-79.
Intracellular calcium signal at the leading edge regulates mesodermal sheet migration during Xenopus gastrulation. , Hayashi K., Sci Rep. February 5, 2018; 8 (1): 2433.
RAPGEF5 Regulates Nuclear Translocation of β-Catenin. , Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates. , Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover. , Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
hmmr mediates anterior neural tube closure and morphogenesis in the frog Xenopus. , Prager A., Dev Biol. October 1, 2017; 430 (1): 188-201.
Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates. , Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo. , Blitz IL ., Dev Biol. June 15, 2017; 426 (2): 409-417.
RARβ2 is required for vertebrate somitogenesis. , Janesick A ., Development. June 1, 2017; 144 (11): 1997-2008.
sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis. , Exner CRT., Dev Biol. May 1, 2017; 425 (1): 33-43.
FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue. , Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
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.
PLD1 regulates Xenopus convergent extension movements by mediating Frizzled7 endocytosis for Wnt/PCP signal activation. , Lee H ., Dev Biol. March 1, 2016; 411 (1): 38-49.
Specification of anteroposterior axis by combinatorial signaling during Xenopus development. , Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1. , Liu C., Dev Biol. January 1, 2016; 409 (1): 26-38.
Early neural ectodermal genes are activated by Siamois and Twin during blastula stages. , Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
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.
The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus. , Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression. , Nelson AC., BMC Biol. October 3, 2014; 12 81.
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.
Active repression by RARγ signaling is required for vertebrate axial elongation. , Janesick A ., Development. June 1, 2014; 141 (11): 2260-70.
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.
A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. , Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning. , Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation. , Hara Y., Dev Biol. October 15, 2013; 382 (2): 482-95.
The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling. , Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Essential role of AWP1 in neural crest specification in Xenopus. , Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.
Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: similarities and dissimilarities between urodelean and anuran embryos. , Kaneda T., Dev Biol. September 1, 2012; 369 (1): 1-18.
Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation. , Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
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.
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.
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.
SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos. , Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
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.
Long-distance signals are required for morphogenesis of the regenerating Xenopus tadpole tail, as shown by femtosecond-laser ablation. , Mondia JP., PLoS One. January 1, 2011; 6 (9): e24953.
Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway. , Takai A., Development. October 1, 2010; 137 (19): 3293-302.
Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway. , Luxardi G ., Development. February 1, 2010; 137 (3): 417-26.
Comparison of Lim1 expression in embryos of frogs with different modes of reproduction. , Venegas-Ferrín M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.
Identification and gastrointestinal expression of Xenopus laevis FoxF2. , McLin VA ., Int J Dev Biol. January 1, 2010; 54 (5): 919-24.
Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus. , Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
Bestrophin genes are expressed in Xenopus development. , Onuma Y ., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.