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Dual origins of the mammalian accessory olfactory bulb revealed by an evolutionarily conserved migratory stream. , Huilgol D., Nat Neurosci. February 1, 2013; 16 (2): 157-65.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development. , Xu Y , Xu Y ., Cell. December 7, 2012; 151 (6): 1200-13.
Hes4 controls proliferative properties of neural stem cells during retinal ontogenesis. , El Yakoubi W., Stem Cells. December 1, 2012; 30 (12): 2784-95.
Characterization and expressional analysis of Dleu7 during Xenopus tropicalis embryogenesis. , Zhu X., Gene. November 1, 2012; 509 (1): 77-84.
Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/ β-catenin-mediated lung specification in Xenopus. , Rankin SA , Rankin SA ., Development. August 1, 2012; 139 (16): 3010-20.
Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning. , Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
Indian hedgehog signaling is required for proper formation, maintenance and migration of Xenopus neural crest. , Agüero TH., Dev Biol. April 15, 2012; 364 (2): 99-113.
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.
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.
RFX2 is broadly required for ciliogenesis during vertebrate development. , Chung MI ., Dev Biol. March 1, 2012; 363 (1): 155-65.
Transmembrane voltage potential controls embryonic eye patterning in Xenopus laevis. , Pai VP ., Development. January 1, 2012; 139 (2): 313-23.
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. , Barnett C., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left- Right Asymmetry. , Pai VP ., Stem Cells Int. January 1, 2012; 2012 353491.
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.
A novel mechanism for the transcriptional regulation of Wnt signaling in development. , Vacik T., Genes Dev. September 1, 2011; 25 (17): 1783-95.
Loss of Xenopus tropicalis EMSY causes impairment of gastrulation and upregulation of p53. , Rana AA., N Biotechnol. July 1, 2011; 28 (4): 334-41.
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.
Ontogenetic distribution of the transcription factor nkx2.2 in the developing forebrain of Xenopus laevis. , Domínguez L., Front Neuroanat. March 2, 2011; 5 11.
A conserved function of the chromatin ATPase Kismet in the regulation of hedgehog expression. , Terriente-Félix A., Dev Biol. February 15, 2011; 350 (2): 382-92.
Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation. , Juraver-Geslin HA ., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.
Retinoic acid is a key regulatory switch determining the difference between lung and thyroid fates in Xenopus laevis. , Wang JH ., BMC Dev Biol. January 26, 2011; 11 75.
Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns. , Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.
Xenopus sonic hedgehog guides retinal axons along the optic tract. , Gordon L., Dev Dyn. November 1, 2010; 239 (11): 2921-32.
Jiraiya attenuates BMP signaling by interfering with type II BMP receptors in neuroectodermal patterning. , Aramaki T., Dev Cell. October 19, 2010; 19 (4): 547-61.
Glyphosate-based herbicides produce teratogenic effects on vertebrates by impairing retinoic acid signaling. , Paganelli A., Chem Res Toxicol. October 18, 2010; 23 (10): 1586-95.
Sonic hedgehog expression during Xenopus laevis forebrain development. , Domínguez L., Dev Biol. August 6, 2010; 1347 19-32.
MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization. , Suzuki M ., Development. July 1, 2010; 137 (14): 2329-39.
B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo. , Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.
Lymph heart musculature is under distinct developmental control from lymphatic endothelium. , Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.
Sonic hedgehog is involved in formation of the ventral optic cup by limiting Bmp4 expression to the dorsal domain. , Zhao L., Mech Dev. January 1, 2010; 127 (1-2): 62-72.
Gene expression profiles of lens regeneration and development in Xenopus laevis. , Malloch EL., Dev Dyn. September 1, 2009; 238 (9): 2340-56.
Integration of telencephalic Wnt and hedgehog signaling center activities by Foxg1. , Danesin C., Dev Cell. April 1, 2009; 16 (4): 576-87.
Complementary expression of HSPG 6-O-endosulfatases and 6-O-sulfotransferase in the hindbrain of Xenopus laevis. , Winterbottom EF., Gene Expr Patterns. March 1, 2009; 9 (3): 166-72.
Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation. , Inomata H ., Cell. September 5, 2008; 134 (5): 854-65.
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.
Early molecular effects of ethanol during vertebrate embryogenesis. , Yelin R ., Differentiation. June 1, 2007; 75 (5): 393-403.
PP2A:B56epsilon is required for eye induction and eye field separation. , Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
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.
Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination. , Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.
The role of megalin ( LRP-2/ Gp330) during development. , Fisher CE., Dev Biol. August 15, 2006; 296 (2): 279-97.
Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase ( Xdhcr7) in neural development. , Tadjuidje E ., Dev Dyn. August 1, 2006; 235 (8): 2095-110.
Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase. , Koide T., Development. June 1, 2006; 133 (12): 2395-405.
Neural and eye-specific defects associated with loss of the imitation switch ( ISWI) chromatin remodeler in Xenopus laevis. , Dirscherl SS., Mech Dev. November 1, 2005; 122 (11): 1157-70.
Six3 functions in anterior neural plate specification by promoting cell proliferation and inhibiting Bmp4 expression. , Gestri G., Development. May 1, 2005; 132 (10): 2401-13.
The pro-apoptotic activity of a vertebrate Bar-like homeobox gene plays a key role in patterning the Xenopus neural plate by limiting the number of chordin- and shh-expressing cells. , Offner N., Development. April 1, 2005; 132 (8): 1807-18.
Dorsoventral patterning of the Xenopus eye: a collaboration of Retinoid, Hedgehog and FGF receptor signaling. , Lupo G., Development. April 1, 2005; 132 (7): 1737-48.
Regulated expression pattern of gremlin during zebrafish development. , Nicoli S., Gene Expr Patterns. April 1, 2005; 5 (4): 539-44.
Expression profile of Xenopus banded hedgehog, a homolog of mouse Indian hedgehog, is related to the late development of endochondral ossification in Xenopus laevis. , Moriishi T., Biochem Biophys Res Commun. March 25, 2005; 328 (4): 867-73.
Depletion of three BMP antagonists from Spemann's organizer leads to a catastrophic loss of dorsal structures. , Khokha MK ., Dev Cell. March 1, 2005; 8 (3): 401-11.