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Aquatic models of human ciliary diseases. , Corkins ME, Krneta-Stankic V, Kloc M , Miller RK ., Genesis. February 1, 2021; 59 (1-2): e23410.
Xenopus to the rescue: A model to validate and characterize candidate ciliopathy genes. , Rao VG , Kulkarni SS ., Genesis. February 1, 2021; 59 (1-2): e23414.
CRISPR/Cas9 disease models in zebrafish and Xenopus: The genetic renaissance of fish and frogs. , Naert T, Vleminckx K , Vleminckx K ., Drug Discov Today Technol. August 1, 2018; 28 41-52.
Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy. , Duncan AR, Khokha MK ., 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, Marfo CA, Li D, Lane M, Khokha MK ., Dev Biol. December 15, 2015; 408 (2): 196-204.
The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality. , Boskovski MT, Yuan S, Pedersen NB, Goth CK, Makova S, Clausen H, Brueckner M , Khokha MK ., Nature. December 19, 2013; 504 (7480): 456-9.
Rare copy number variations in congenital heart disease patients identify unique genes in left- right patterning. , Fakhro KA, Choi M, Ware SM , Belmont JW, Towbin JA, Lifton RP, Khokha MK , Brueckner M ., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.