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Functional analysis of an individual IFT protein: IFT46 is required for transport of outer dynein arms into flagella.
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Assembly of IFT trains at the ciliary base depends on IFT74.
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice.
Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone.