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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.
Purine Biosynthesis Pathways Are Required for Myogenesis in Xenopus laevis. , Duperray M., Cells. September 28, 2023; 12 (19):
The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos. , Massé K ., Commun Biol. October 7, 2021; 4 (1): 1158.
Bicc1 and Dicer regulate left- right patterning through post-transcriptional control of the Nodal inhibitor Dand5. , Maerker M., Nat Commun. September 16, 2021; 12 (1): 5482.
Wnt-inducible Lrp6- APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway. , Colozza G ., Sci Rep. December 9, 2020; 10 (1): 21555.
The SNPs in myoD gene from normal muscle developing individuals have no effect on muscle mass. , Ding S., BMC Genet. September 2, 2019; 20 (1): 72.
Id genes are essential for early heart formation. , Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
Hspa9 is required for pronephros specification and formation in Xenopus laevis. , Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
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.
Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus. , Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
The Wnt/ JNK signaling target gene alcam is required for embryonic kidney development. , Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.
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.
Interrogating transcriptional regulatory sequences in Tol2-mediated Xenopus transgenics. , Loots GG ., PLoS One. July 1, 2013; 8 (7): e68548.
Comparative Functional Analysis of ZFP36 Genes during Xenopus Development. , Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development. , Kolpakova A ., PLoS One. January 1, 2013; 8 (7): e69693.
Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae. , Rodrigues AM., BMC Dev Biol. February 27, 2012; 12 9.
Involvement of the eukaryotic initiation factor 6 and kermit2/ gipc2 in Xenopus laevis pronephros formation. , Tussellino M., Int J Dev Biol. January 1, 2012; 56 (5): 357-62.
Cardiac neural crest is dispensable for outflow tract septation in Xenopus. , Lee YH ., Development. May 1, 2011; 138 (10): 2025-34.
Lhx1 is required for specification of the renal progenitor cell field. , Cirio MC ., PLoS One. April 15, 2011; 6 (4): e18858.
Role of Tbx2 in defining the territory of the pronephric nephron. , Cho GS., Development. February 1, 2011; 138 (3): 465-74.
Tissue-specific expression of Sarcoplasmic/Endoplasmic Reticulum Calcium ATPases ( ATP2A/SERCA) 1, 2, 3 during Xenopus laevis development. , Pegoraro C., Gene Expr Patterns. January 1, 2011; 11 (1-2): 122-8.
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.
Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size. , Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
Mad is required for wingless signaling in wing development and segment patterning in Drosophila. , Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis. , Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.
Coordination of cell polarity during Xenopus gastrulation. , Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.
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.
FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development. , Urban AE ., Dev Biol. September 1, 2006; 297 (1): 103-17.
Limb regeneration in Xenopus laevis froglet. , Suzuki M , Suzuki M ., ScientificWorldJournal. May 12, 2006; 6 Suppl 1 26-37.
Cooperative non-cell and cell autonomous regulation of Nodal gene expression and signaling by Lefty/ Antivin and Brachyury in Xenopus. , Cha YR., Dev Biol. February 15, 2006; 290 (2): 246-64.
Spatio-temporal expression of MRF4 transcripts and protein during Xenopus laevis embryogenesis. , Della Gaspera B ., Dev Dyn. February 1, 2006; 235 (2): 524-9.
Characteristics of initiation and early events for muscle development in the Xenopus limb bud. , Satoh A ., Dev Dyn. December 1, 2005; 234 (4): 846-57.
XIC is required for Siamois activity and dorsoanterior development. , Snider L ., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
Muscle formation in regenerating Xenopus froglet limb. , Satoh A ., Dev Dyn. June 1, 2005; 233 (2): 337-46.
neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia. , Ma Q., Neuron. March 1, 1998; 20 (3): 469-82.
Activation of the cardiac alpha-actin promoter depends upon serum response factor, Tinman homologue, Nkx-2.5, and intact serum response elements. , Chen CY ., Dev Genet. January 1, 1996; 19 (2): 119-30.
The regulation of MyoD gene expression: conserved elements mediate expression in embryonic axial muscle. , Asakura A., Dev Biol. October 1, 1995; 171 (2): 386-98.