Genetic compensation for cilia defects in <i>cep290</i> mutants by upregulation of cilia-associated small GTPases
Magdalena Cárdenas-Rodríguez(Massachusetts General Hospital), Iain A. Drummond(Mount Desert Island Biological Laboratory)
Cited by 28
Related Papers
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
|Nature Genetics|2003|643
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
|Nature Genetics|2006|573
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
|Nature Genetics|2006|565
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
|Cell|2012|392
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
|The American Journal of Human Genetics|2013|201