Associated Papers
A multiscale approach reveals the molecular architecture of the autoinhibited kinesin KIF5A.
Carrington G et al.
The Journal of Biological Chemistry, 2024
38309508 (PubMed )
Supplement: mmc1.pdf
A stop or go switch: glycogen synthase kinase 3β phosphorylation of the kinesin 1 motor domain at Ser314 halts motility without detaching from microtubules.
Banerjee R et al.
Development (cambridge, England), 2021
Tubulin mutations in neurodevelopmental disorders as a tool to decipher microtubule function.
Fourel G et al.
Febs Letters, 2020
Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series.
Andréasson M et al.
Neurology. Genetics, 2019
Structural consequences of hereditary spastic paraplegia disease-related mutations in kinesin.
Dutta M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2018
Role of kinesin-1 in the pathogenesis of SPG10, a rare form of hereditary spastic paraplegia.
Kawaguchi K
The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry, 2013
Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity.
Ebbing B et al.
Human Molecular Genetics, 2008
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