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Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus. , Gentsch GE ., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.
Rare copy number variations in congenital heart disease patients identify unique genes in left- right patterning. , Fakhro KA., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.
Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus. , Smith SJ ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.
Notch activates Wnt-4 signalling to control medio- lateral patterning of the pronephros. , Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.
Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size. , Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
In vitro organogenesis from undifferentiated cells in Xenopus. , Asashima M ., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
DM-GRASP/ ALCAM/ CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells. , Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.
Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1. , Movassagh M., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.
A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis. , Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
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.