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Aquatic models of human ciliary diseases. , Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.
Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy. , Duncan AR., Semin Cell Dev Biol. March 1, 2016; 51 73-9.
CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus. , Bhattacharya D., Dev Biol. December 15, 2015; 408 (2): 196-204.
The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality. , Boskovski MT., Nature. December 19, 2013; 504 (7480): 456-9.
A lectin-based glycomic approach to identify characteristic features of Xenopus embryogenesis. , Onuma Y ., PLoS One. January 1, 2013; 8 (2): e56581.
A large scale screen for neural stem cell markers in Xenopus retina. , Parain K ., Dev Neurobiol. April 1, 2012; 72 (4): 491-506.
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.