Associated Papers
The ALS-associated E425K mutation uncouples DNAJC7 from the Hsp70 chaperone cycle.
Elmaleh B et al.
The Febs Journal, 2026
Harnessing deep learning into hidden mutations of neurological disorders for therapeutic challenges.
Yang S et al.
Archives of Pharmacal Research, 2023
DnaJC7 in Amyotrophic Lateral Sclerosis.
Dilliott AA et al.
International Journal of Molecular Sciences, 2022
Validation of the pathogenic role of rare DNAJC7 variants in Chinese patients with amyotrophic lateral sclerosis.
He J et al.
Neurobiology of Aging, 2021
Mutations of DNAJC7 are rare in Chinese amyotrophic lateral sclerosis patients.
Sun X et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2021
Mutation Analysis of DNAJC Family for Early-Onset Parkinson's Disease in a Chinese Cohort.
Li C et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2020
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