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Development of subdomains in the medial pallium of Xenopus laevis and Trachemys scripta: Insights into the anamniote-amniote transition. , Jiménez S., Front Neuroanat. 16 1039081.
Acute multidrug delivery via a wearable bioreactor facilitates long-term limb regeneration and functional recovery in adult Xenopus laevis. , Murugan NJ., Sci Adv. January 28, 2022; 8 (4): eabj2164.
Huntingtin CAG expansion impairs germ layer patterning in synthetic human 2D gastruloids through polarity defects. , Galgoczi S., Development. October 1, 2021; 148 (19):
Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1. , Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
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.
Id genes are essential for early heart formation. , Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT. , Gao L., Development. February 1, 2016; 143 (3): 492-503.
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.
A Molecular atlas of Xenopus respiratory system development. , Rankin SA , Rankin SA ., Dev Dyn. January 1, 2015; 244 (1): 69-85.
Myb promotes centriole amplification and later steps of the multiciliogenesis program. , Tan FE., Development. October 1, 2013; 140 (20): 4277-86.
Spinal cord regeneration in Xenopus tadpoles proceeds through activation of Sox2-positive cells. , Gaete M ., Neural Dev. April 26, 2012; 7 13.
Sonic hedgehog signaling is decoded by calcium spike activity in the developing spinal cord. , Belgacem YH., Proc Natl Acad Sci U S A. March 15, 2011; 108 (11): 4482-7.
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.
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.
Temporal regulation of Ath5 gene expression during eye development. , Willardsen MI., Dev Biol. February 15, 2009; 326 (2): 471-81.
Evolution of non-coding regulatory sequences involved in the developmental process: reflection of differential employment of paralogous genes as highlighted by Sox2 and group B1 Sox genes. , Kamachi Y., Proc Jpn Acad Ser B Phys Biol Sci. January 1, 2009; 85 (2): 55-68.
A dual requirement for Iroquois genes during Xenopus kidney development. , Alarcón P., Development. October 1, 2008; 135 (19): 3197-207.
Molecular links among the causative genes for ocular malformation: Otx2 and Sox2 coregulate Rax expression. , Danno H., Proc Natl Acad Sci U S A. April 8, 2008; 105 (14): 5408-13.
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.
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.
Tsukushi controls ectodermal patterning and neural crest specification in Xenopus by direct regulation of BMP4 and X-delta-1 activity. , Kuriyama S ., Development. January 1, 2006; 133 (1): 75-88.