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The B-subdomain of the Xenopus laevis XFIN KRAB-AB domain is responsible for its weaker transcriptional repressor activity compared to human ZNF10/Kox1. , Born N., PLoS One. February 3, 2014; 9 (2): e87609.
NumbL is essential for Xenopus primary neurogenesis. , Nieber F., BMC Dev Biol. October 14, 2013; 13 36.
Multicilin promotes centriole assembly and ciliogenesis during multiciliate cell differentiation. , Stubbs JL., Nat Cell Biol. January 8, 2012; 14 (2): 140-7.
EBF proteins participate in transcriptional regulation of Xenopus muscle development. , Green YS., Dev Biol. October 1, 2011; 358 (1): 240-50.
Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus. , Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo. , Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
Macrophage Wnt7b is critical for kidney repair and regeneration. , Lin SL., Proc Natl Acad Sci U S A. March 2, 2010; 107 (9): 4194-9.
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.
Functional characterization of two CITED3 homologs (gcCITED3a and gcCITED3b) in the hypoxia-tolerant grass carp, Ctenopharyngodon idellus. , Ng PK., BMC Mol Biol. November 3, 2009; 10 101.
Notch activates Wnt-4 signalling to control medio- lateral patterning of the pronephros. , Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.
Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size. , Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
Coordinating the timing of cardiac precursor development during gastrulation: a new role for Notch signaling. , Miazga CM., Dev Biol. September 15, 2009; 333 (2): 285-96.
Involvement of an inner nuclear membrane protein, Nemp1, in Xenopus neural development through an interaction with the chromatin protein BAF. , Mamada H., Dev Biol. March 15, 2009; 327 (2): 497-507.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
Modulation of potassium channel function confers a hyperproliferative invasive phenotype on embryonic stem cells. , Morokuma J., Proc Natl Acad Sci U S A. October 28, 2008; 105 (43): 16608-13.
The lmx1b gene is pivotal in glomus development in Xenopus laevis. , Haldin CE ., Dev Biol. October 1, 2008; 322 (1): 74-85.
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.
A functional screen for genes involved in Xenopus pronephros development. , Kyuno J ., Mech Dev. July 1, 2008; 125 (7): 571-86.
Pleiotropic effects in Eya3 knockout mice. , Söker T., BMC Dev Biol. June 23, 2008; 8 118.
The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm. , Spagnoli FM ., Development. February 1, 2008; 135 (3): 451-61.
A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis. , Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
The prepattern transcription factor Irx3 directs nephron segment identity. , Reggiani L., Genes Dev. September 15, 2007; 21 (18): 2358-70.
Kidney development and gene expression in the HIF2alpha knockout mouse. , Steenhard BM., Dev Dyn. April 1, 2007; 236 (4): 1115-25.
Xenopus Dab2 is required for embryonic angiogenesis. , Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
Retinoic acid signalling is required for specification of pronephric cell fate. , Cartry J., Dev Biol. November 1, 2006; 299 (1): 35-51.
Kermit 2/ XGIPC, an IGF1 receptor interacting protein, is required for IGF signaling in Xenopus eye development. , Wu J ., Development. September 1, 2006; 133 (18): 3651-60.
The Notch-effector HRT1 gene plays a role in glomerular development and patterning of the Xenopus pronephros anlagen. , Taelman V., Development. August 1, 2006; 133 (15): 2961-71.
Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation. , Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
Novel insights regarding the operational characteristics and teleological purpose of the renal Na+-K+-Cl2 cotransporter (NKCC2s) splice variants. , Brunet GM., J Gen Physiol. October 1, 2005; 126 (4): 325-37.
Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus. , Chen JA ., Mech Dev. March 1, 2005; 122 (3): 307-31.
Selective degradation of excess Ldb1 by Rnf12/ RLIM confers proper Ldb1 expression levels and Xlim-1/ Ldb1 stoichiometry in Xenopus organizer functions. , Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
A trial for induction of supernumerary primordial germ cells in Xenopus tadpoles by injecting RNA of Xenopus vasa homologue into germline cells of 32-cell embryos. , Ikenishi K ., Dev Growth Differ. January 1, 2003; 45 (5-6): 417-26.
Adult and embryonic blood and endothelium derive from distinct precursor populations which are differentially programmed by BMP in Xenopus. , Walmsley M., Development. December 1, 2002; 129 (24): 5683-95.
Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney. , Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.
Smad10 is required for formation of the frog nervous system. , LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
Isolation and characterization of a Xenopus gene ( XMLP) encoding a MARCKS-like protein. , Zhao H ., Int J Dev Biol. October 1, 2001; 45 (7): 817-26.
Distinct origins of adult and embryonic blood in Xenopus. , Ciau-Uitz A ., Cell. September 15, 2000; 102 (6): 787-96.
The POU domain gene, XlPOU 2 is an essential downstream determinant of neural induction. , Matsuo-Takasaki M., Mech Dev. December 1, 1999; 89 (1-2): 75-85.
Distinct elements of the xsna promoter are required for mesodermal and ectodermal expression. , Mayor R ., Development. November 1, 1993; 119 (3): 661-71.
XlHbox 8: a novel Xenopus homeo protein restricted to a narrow band of endoderm. , Wright CV ., Development. April 1, 1989; 105 (4): 787-94.