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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.
ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis. , Janesick A ., Development. August 1, 2013; 140 (15): 3095-106.
Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes. , Kennedy AE ., Dev Biol. May 1, 2012; 365 (1): 229-40.
Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development. , Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.
Fgf is required to regulate anterior- posterior patterning in the Xenopus lateral plate mesoderm. , Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation. , Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.
Retinoic acid regulates anterior- posterior patterning within the lateral plate mesoderm of Xenopus. , Deimling SJ., Mech Dev. October 1, 2009; 126 (10): 913-23.
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.
Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays. , Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.