Associated Papers
The ALS-associated E425K mutation uncouples DNAJC7 from the Hsp70 chaperone cycle.
Elmaleh B et al.
The Febs Journal, 2026
Rare DNAJC7 Variants May Play a Minor Role in Chinese Patients with ALS.
Wang S et al.
Molecular Neurobiology, 2024
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
Mutations of DNAJC7 are rare in Chinese amyotrophic lateral sclerosis patients.
Sun X et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2021
Unraveling the multifaceted insights into amyotrophic lateral sclerosis: Genetic underpinnings, pathogenesis, and therapeutic horizons.
Sharma R et al.
Mutation Research. Reviews in Mutation Research, 0
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