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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.
Quantitative analysis of transcriptome dynamics provides novel insights into developmental state transitions. , Johnson K., BMC Genomics. October 23, 2022; 23 (1): 723.
Evo-Devo of Urbilateria and its larval forms. , De Robertis EM ., Dev Biol. July 1, 2022; 487 10-20.
Retinoic Acid is Required for Normal Morphogenetic Movements During Gastrulation. , Gur M., Front Cell Dev Biol. January 1, 2022; 10 857230.
Rab7 is required for mesoderm patterning and gastrulation in Xenopus. , Kreis J., Biol Open. July 15, 2021; 10 (7):
Establishing embryonic territories in the context of Wnt signaling. , Velloso I., Int J Dev Biol. January 1, 2021; 65 (4-5-6): 227-233.
TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis. , Chen M., Elife. September 14, 2020; 9
Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin. , Vonica A ., Dev Biol. August 1, 2020; 464 (1): 71-87.
Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling. , Vacca B., Sci Rep. January 19, 2018; 8 (1): 1204.
Acetaldehyde inhibits retinoic acid biosynthesis to mediate alcohol teratogenicity. , Shabtai Y., Sci Rep. January 10, 2018; 8 (1): 347.
Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish. , Bisgrove BW., Elife. November 15, 2017; 6
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.
Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates. , Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula. , Ding Y ., Dev Biol. June 15, 2017; 426 (2): 176-187.
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.
Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals in Xenopus laevis. , Ding Y ., Proc Natl Acad Sci U S A. April 11, 2017; 114 (15): E3081-E3090.
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.
Sebox regulates mesoderm formation in early amphibian embryos. , Chen G., Dev Dyn. November 1, 2015; 244 (11): 1415-26.
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.
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 serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation. , Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites. , Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
Custos controls β-catenin to regulate head development during vertebrate embryogenesis. , Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.
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.
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.
Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus. , Lim CY., Development. February 1, 2013; 140 (4): 853-60.
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.
Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning. , Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins. , Callery EM ., Open Biol. April 1, 2012; 2 (4): 120060.
Waif1/5T4 inhibits Wnt/ β-catenin signaling and activates noncanonical Wnt pathways by modifying LRP6 subcellular localization. , Kagermeier-Schenk B., Dev Cell. December 13, 2011; 21 (6): 1129-43.
Novel functions of Noggin proteins: inhibition of Activin/ Nodal and Wnt signaling. , Bayramov AV., Development. December 1, 2011; 138 (24): 5345-56.
A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer. , Rankin SA , Rankin SA ., Dev Biol. March 15, 2011; 351 (2): 297-310.
Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos. , Schneider PN., Genesis. March 1, 2011; 49 (3): 117-23.
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.
Conservation and diversification of an ancestral chordate gene regulatory network for dorsoventral patterning. , Kozmikova I., PLoS One. February 3, 2011; 6 (2): e14650.
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.
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.
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.
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.
Xclaudin 1 is required for the proper gastrulation in Xenopus laevis. , Chang DJ., Biochem Biophys Res Commun. June 18, 2010; 397 (1): 75-81.
Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling. , Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
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.
DeltaNp63 antagonizes p53 to regulate mesoderm induction in Xenopus laevis. , Barton CE., Dev Biol. May 1, 2009; 329 (1): 130-9.
Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system. , Strate I., Development. February 1, 2009; 136 (3): 461-72.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos. , Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.