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The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains. , Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation. , Jourdeuil K., Front Cell Dev Biol. January 1, 2023; 11 1274788.
Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease. , Coppenrath K ., Genesis. December 1, 2021; 59 (12): e23453.
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development. , Shah AM., Dis Model Mech. March 3, 2020; 13 (3):
The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis. , Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.
Genomic integration of Wnt/ β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs. , Stevens ML ., Development. April 1, 2017; 144 (7): 1283-1295.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development. , Neilson KM ., Dev Biol. January 15, 2017; 421 (2): 171-182.
Crystal structure of the DNA binding domain of the transcription factor T-bet suggests simultaneous recognition of distant genome sites. , Liu CF., Proc Natl Acad Sci U S A. October 25, 2016; 113 (43): E6572-E6581.
Predicting Variabilities in Cardiac Gene Expression with a Boolean Network Incorporating Uncertainty. , Grieb M., PLoS One. July 16, 2015; 10 (7): e0131832.
The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development. , Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development. , Kolpakova A ., PLoS One. January 1, 2013; 8 (7): e69693.
Myogenic waves and myogenic programs during Xenopus embryonic myogenesis. , Della Gaspera B ., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm. , Janesick A ., Development. March 1, 2012; 139 (6): 1213-24.
PAPC and the Wnt5a/ Ror2 pathway control the invagination of the otic placode in Xenopus. , Jung B., BMC Dev Biol. June 10, 2011; 11 36.
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.
Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis. , Tazumi S., Dev Biol. October 15, 2010; 346 (2): 170-80.
The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors. , Hitachi K ., Int J Dev Biol. January 1, 2009; 53 (4): 631-9.
The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart. , Smith SJ ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.
Regulation of the early expression of the Xenopus nodal-related 1 gene, Xnr1. , Hyde CE ., Development. March 1, 2000; 127 (6): 1221-9.