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Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
On the origin of vertebrate somites. , Onai T., Zoological Lett. June 15, 2015; 1 33.
Apoptosis and differentiation of Xenopus tail-derived myoblasts by thyroid hormone. , Tamura K ., J Mol Endocrinol. June 1, 2015; 54 (3): 185-92.
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus. , Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
An essential role for LPA signalling in telencephalon development. , Geach TJ ., Development. February 1, 2014; 141 (4): 940-9.
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.
In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency. , Gentsch GE ., Cell Rep. September 26, 2013; 4 (6): 1185-96.
Differential muscle regulatory factor gene expression between larval and adult myogenesis in the frog Xenopus laevis: adult myogenic cell-specific myf5 upregulation and its relation to the notochord suppression of adult muscle differentiation. , Yamane H., In Vitro Cell Dev Biol Anim. August 1, 2013; 49 (7): 524-36.
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.
Kcnh1 voltage-gated potassium channels are essential for early zebrafish development. , Stengel R., J Biol Chem. October 12, 2012; 287 (42): 35565-35575.
Sim2 prevents entry into the myogenic program by repressing MyoD transcription during limb embryonic myogenesis. , Havis E., Development. June 1, 2012; 139 (11): 1910-20.
Thyroid hormone-dependent development in Xenopus laevis: a sensitive screen of thyroid hormone signaling disruption by municipal wastewater treatment plant effluent. , Searcy BT., Gen Comp Endocrinol. May 1, 2012; 176 (3): 481-92.
Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development. , Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.
Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae. , Rodrigues AM., BMC Dev Biol. February 27, 2012; 12 9.
The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo. , Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
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.
Lymph heart musculature is under distinct developmental control from lymphatic endothelium. , Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.
The RNA-binding protein Seb4/ RBM24 is a direct target of MyoD and is required for myogenesis during Xenopus early development. , Li HY., Mech Dev. January 1, 2010; 127 (5-6): 281-91.
Genetic control of hematopoietic development in Xenopus and zebrafish. , Ciau-Uitz A ., Int J Dev Biol. January 1, 2010; 54 (6-7): 1139-49.
Functional dissection of XDppa2/4 structural domains in Xenopus development. , Siegel D ., Mech Dev. December 1, 2009; 126 (11-12): 974-89.
Xenopus Rnd1 and Rnd3 GTP-binding proteins are expressed under the control of segmentation clock and required for somite formation. , Goda T., Dev Dyn. November 1, 2009; 238 (11): 2867-76.
Myosin-X is required for cranial neural crest cell migration in Xenopus laevis. , Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.
Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size. , Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats. , Bosnakovski D., PLoS One. September 16, 2009; 4 (9): e7003.
Mad is required for wingless signaling in wing development and segment patterning in Drosophila. , Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis. , Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.
Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis. , Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.
Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1. , Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
Xenopus BTBD6 and its Drosophila homologue lute are required for neuronal development. , Bury FJ., Dev Dyn. November 1, 2008; 237 (11): 3352-60.
Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development. , Dichmann DS ., Dev Dyn. July 1, 2008; 237 (7): 1755-66.
Binding of sFRP-3 to EGF in the extra-cellular space affects proliferation, differentiation and morphogenetic events regulated by the two molecules. , Scardigli R., PLoS One. June 18, 2008; 3 (6): e2471.
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.
Hes6 is required for MyoD induction during gastrulation. , Murai K., Dev Biol. December 1, 2007; 312 (1): 61-76.
The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo. , Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
Hedgehog signaling regulates the amount of hypaxial muscle development during Xenopus myogenesis. , Martin BL., Dev Biol. April 15, 2007; 304 (2): 722-34.
The role of the Spemann organizer in anterior- posterior patterning of the trunk. , Jansen HJ ., Mech Dev. January 1, 2007; 124 (9-10): 668-81.
PCNS: a novel protocadherin required for cranial neural crest migration and somite morphogenesis in Xenopus. , Rangarajan J., Dev Biol. July 1, 2006; 295 (1): 206-18.
FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus. , Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
Emilin1 links TGF-beta maturation to blood pressure homeostasis. , Zacchigna L., Cell. March 10, 2006; 124 (5): 929-42.
A novel role for lbx1 in Xenopus hypaxial myogenesis. , Martin BL., Development. January 1, 2006; 133 (2): 195-208.
Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity. , Yabe S., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.
Distinct roles for Xenopus Tcf/Lef genes in mediating specific responses to Wnt/beta-catenin signalling in mesoderm development. , Liu F., Development. December 1, 2005; 132 (24): 5375-85.
Characteristics of initiation and early events for muscle development in the Xenopus limb bud. , Satoh A ., Dev Dyn. December 1, 2005; 234 (4): 846-57.
The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis. , Huot ME., Mol Biol Cell. September 1, 2005; 16 (9): 4350-61.
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.
Sirenomelia in Bmp7 and Tsg compound mutant mice: requirement for Bmp signaling in the development of ventral posterior mesoderm. , Zakin L., Development. May 1, 2005; 132 (10): 2489-99.
JNK and ROKalpha function in the noncanonical Wnt/ RhoA signaling pathway to regulate Xenopus convergent extension movements. , Kim GH ., Dev Dyn. April 1, 2005; 232 (4): 958-68.