Associated Papers
Molecular basis for the activation of outer dynein arms in cilia.
Issa KHB et al.
Nature Structural & Molecular Biology, 2025
Mitochondrial functional impairment in ARL3-mutation related rod-cone dystrophy.
Zhang X et al.
Faseb Bioadvances, 2024
ARL3 GTPases facilitate ODA16 unloading from IFT in motile cilia.
Huang Y et al.
Science Advances, 2024
Mechanisms underlying morphological and functional changes of cilia in fibroblasts derived from patients bearing ARL3T31A and ARL3T31A/C118F mutations.
Zhang X et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2024
Interactions between TULP3 tubby domain and ARL13B amphipathic helix promote lipidated protein transport to cilia.
Palicharla VR et al.
Molecular Biology of the Cell, 2023
36652335 (PubMed )
Supplement: mbc-34-ar18-s002.pdf
Autosomal Recessive Rod-Cone Dystrophy Associated With Compound Heterozygous Variants in ARL3 Gene.
Fu L et al.
Frontiers in Cell and Developmental Biology, 2021
A New STAT3-binding Partner, ARL3, Enhances the Phosphorylation and Nuclear Accumulation of STAT3.
Togi S et al.
The Journal of Biological Chemistry, 2016
Arl3 and LC8 regulate dissociation of dynactin from dynein.
Jin M et al.
Nature Communications, 2014
The ARL2 GTPase is required for mitochondrial morphology, motility, and maintenance of ATP levels.
Newman LE et al.
Plos One, 2014
Targeting of the Arf-like GTPase Arl3p to the Golgi requires N-terminal acetylation and the membrane protein Sys1p.
Behnia R et al.
Nature Cell Biology, 2004
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