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Gene expression in notochord and nuclei pulposi: a study of gene families across the chordate phylum. , Raghavan R., BMC Ecol Evol. October 27, 2023; 23 (1): 63.
The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos. , Massé K ., Commun Biol. October 7, 2021; 4 (1): 1158.
Rab7 is required for mesoderm patterning and gastrulation in Xenopus. , Kreis J., Biol Open. July 15, 2021; 10 (7):
An Early Function of Polycystin-2 for Left- Right Organizer Induction in Xenopus. , Vick P ., iScience. April 27, 2018; 2 76-85.
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.
Expression pattern of bcar3, a downstream target of Gata2, and its binding partner, bcar1, during Xenopus development. , Green YS., Gene Expr Patterns. January 1, 2016; 20 (1): 55-62.
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.
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 alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform. , Dichmann DS ., Cell Rep. February 3, 2015; 10 (4): 527-36.
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.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y ., Development. October 1, 2014; 141 (19): 3740-51.
FAK transduces extracellular forces that orient the mitotic spindle and control tissue morphogenesis. , Petridou NI., Nat Commun. January 1, 2014; 5 5240.
Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning. , Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
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.
Regulation of primitive hematopoiesis by class I histone deacetylases. , Shah RR., Dev Dyn. February 1, 2013; 242 (2): 108-21.
Comparative Functional Analysis of ZFP36 Genes during Xenopus Development. , Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
sizzled function and secreted factor network dynamics. , Shi J., Biol Open. March 15, 2012; 1 (3): 286-94.
Identification and characterization of Xenopus kctd15, an ectodermal gene repressed by the FGF pathway. , Takahashi C ., Int J Dev Biol. January 1, 2012; 56 (5): 393-402.
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.
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.
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.
Xenopus Wntless and the retromer complex cooperate to regulate XWnt4 secretion. , Kim H ., Mol Cell Biol. April 1, 2009; 29 (8): 2118-28.
Xenopus ADAM19 is involved in neural, neural crest and muscle development. , Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
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.
Extracellular regulation of developmental cell signaling by XtSulf1. , Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.
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 crucial role of a high mobility group protein HMGA2 in cardiogenesis. , Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
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.
IRE1beta is required for mesoderm formation in Xenopus embryos. , Yuan L., Mech Dev. January 1, 2008; 125 (3-4): 207-22.
XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms. , van Grunsven LA., Dev Biol. June 1, 2007; 306 (1): 34-49.
Xenopus Dab2 is required for embryonic angiogenesis. , Cheong SM., BMC Dev Biol. December 19, 2006; 6 63.
ADMP2 is essential for primitive blood and heart development in Xenopus. , Kumano G ., Dev Biol. November 15, 2006; 299 (2): 411-23.
Heading in a new direction: implications of the revised fate map for understanding Xenopus laevis development. , Lane MC ., Dev Biol. August 1, 2006; 296 (1): 12-28.
Differential role of 14-3-3 family members in Xenopus development. , Lau JM., Dev Dyn. July 1, 2006; 235 (7): 1761-76.
Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity. , Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
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.
Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development. , Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
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.
Xenopus tropicalis peroxidasin gene is expressed within the developing neural tube and pronephric kidney. , Tindall AJ., Dev Dyn. February 1, 2005; 232 (2): 377-84.
A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system. , Saka Y ., Dev Biol. September 15, 2004; 273 (2): 210-25.
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.
Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway. , Zhao H ., Dev Biol. May 15, 2003; 257 (2): 278-91.
Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene. , Haldin CE ., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis. , Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
Xenopus frizzled 7 can act in canonical and non-canonical Wnt signaling pathways: implications on early patterning and morphogenesis. , Medina A., Mech Dev. April 1, 2000; 92 (2): 227-37.
XTIF2, a Xenopus homologue of the human transcription intermediary factor, is required for a nuclear receptor pathway that also interacts with CBP to suppress Brachyury and XMyoD. , de la Calle-Mustienes E ., Mech Dev. March 1, 2000; 91 (1-2): 119-29.
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.