???pagination.result.count???
???pagination.result.page???
1
Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution. , Hossain N., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.
Adaptive correction of craniofacial defects in pre-metamorphic Xenopus laevis tadpoles involves thyroid hormone-independent tissue remodeling. , Pinet K., Development. July 22, 2019; 146 (14):
E-cigarette aerosol exposure can cause craniofacial defects in Xenopus laevis embryos and mammalian neural crest cells. , Kennedy AE ., PLoS One. September 8, 2017; 12 (9): e0185729.
Formation of a "Pre- mouth Array" from the Extreme Anterior Domain Is Directed by Neural Crest and Wnt/PCP Signaling. , Jacox L., Cell Rep. August 2, 2016; 16 (5): 1445-1455.
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome. , Devotta A., Dev Biol. July 15, 2016; 415 (2): 371-382.
A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements. , Square T ., Dev Biol. January 15, 2015; 397 (2): 293-304.
The extreme anterior domain is an essential craniofacial organizer acting through Kinin- Kallikrein signaling. , Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.
Sox9 function in craniofacial development and disease. , Lee YH , Lee YH ., Genesis. April 1, 2011; 49 (4): 200-8.
Serotonin 2B receptor signaling is required for craniofacial morphogenesis and jaw joint formation in Xenopus. , Reisoli E., Development. September 1, 2010; 137 (17): 2927-37.