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Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs. , Bredeson JV., Nat Commun. January 17, 2024; 15 (1): 579.
Evolution of Somite Compartmentalization: A View From Xenopus. , Della Gaspera B ., Front Cell Dev Biol. January 1, 2021; 9 790847.
The extraordinary biology and development of marsupial frogs (Hemiphractidae) in comparison with fish, mammals, birds, amphibians and other animals. , Del Pino EM ., Mech Dev. December 1, 2018; 154 2-11.
Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus. , Gentsch GE ., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.
The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development. , Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
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.
Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos. , Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
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.
Lin28 proteins are required for germ layer specification in Xenopus. , Faas L., Development. March 1, 2013; 140 (5): 976-86.
Regulation of primitive hematopoiesis by class I histone deacetylases. , Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis. , Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
A developmental requirement for HIRA-dependent H3.3 deposition revealed at gastrulation in Xenopus. , Szenker E., Cell Rep. June 28, 2012; 1 (6): 730-40.
Cardiac neural crest is dispensable for outflow tract septation in Xenopus. , Lee YH ., Development. May 1, 2011; 138 (10): 2025-34.
XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis. , Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
Genetic control of hematopoietic development in Xenopus and zebrafish. , Ciau-Uitz A ., Int J Dev Biol. January 1, 2010; 54 (6-7): 1139-49.
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.
A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds. , Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.
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.
Fli1 acts at the top of the transcriptional network driving blood and endothelial development. , Liu F., Curr Biol. August 26, 2008; 18 (16): 1234-40.
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.
Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1. , Herr P., Development. May 1, 2008; 135 (10): 1813-22.
The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros. , Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
ADMP2 is essential for primitive blood and heart development in Xenopus. , Kumano G ., Dev Biol. November 15, 2006; 299 (2): 411-23.
Function of the two Xenopus smad4s in early frog development. , Chang C ., J Biol Chem. October 13, 2006; 281 (41): 30794-803.
Emilin1 links TGF-beta maturation to blood pressure homeostasis. , Zacchigna L., Cell. March 10, 2006; 124 (5): 929-42.
XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development. , Ori M ., Development. February 1, 2006; 133 (4): 631-40.
Cloning and characterization of Xenopus Id4 reveals differing roles for Id genes. , Liu KJ , Liu KJ ., Dev Biol. December 15, 2003; 264 (2): 339-51.
Cloning and characterization of Xenopus laevis drg2, a member of the developmentally regulated GTP-binding protein subfamily. , Ishikawa K., Gene. December 11, 2003; 322 105-12.
Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants. , Latinkić BV., Development. August 1, 2003; 130 (16): 3865-76.
The secreted Frizzled-related protein Sizzled functions as a negative feedback regulator of extreme ventral mesoderm. , Collavin L., Development. February 1, 2003; 130 (4): 805-16.
Isolation, characterization, and expression analysis of zebrafish large Mafs. , Kajihara M., J Biochem. January 1, 2001; 129 (1): 139-46.
FGF signaling restricts the primary blood islands to ventral mesoderm. , Kumano G ., Dev Biol. December 15, 2000; 228 (2): 304-14.
Use of large-scale expression cloning screens in the Xenopus laevis tadpole to identify gene function. , Grammer TC ., Dev Biol. December 15, 2000; 228 (2): 197-210.
Spatial and temporal properties of ventral blood island induction in Xenopus laevis. , Kumano G ., Development. December 1, 1999; 126 (23): 5327-37.
SCL specifies hematopoietic mesoderm in Xenopus embryos. , Mead PE ., Development. July 1, 1998; 125 (14): 2611-20.
A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation. , Horb ME ., Development. May 1, 1997; 124 (9): 1689-98.
Ventral expression of GATA-1 and GATA-2 in the Xenopus embryo defines induction of hematopoietic mesoderm. , Kelley C ., Dev Biol. September 1, 1994; 165 (1): 193-205.
An inhibitory effect of Xenopus gastrula ectoderm on muscle cell differentiation and its role for dorsoventral patterning of mesoderm. , Kato K., Dev Biol. May 1, 1994; 163 (1): 222-9.
Expression of GATA-binding proteins during embryonic development in Xenopus laevis. , Zon LI ., Proc Natl Acad Sci U S A. December 1, 1991; 88 (23): 10642-6.