Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jalia Dash"'
Autor:
Nneka Southwell, Onorina Manzo, Sandra Bacman, Dazhi Zhao, Nicole M Sayles, Jalia Dash, Keigo Fujita, Marilena D’Aurelio, Annarita Di Lorenzo, Giovanni Manfredi, Hibiki Kawamata
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 6, Pp 1352-1378 (2024)
Abstract Mutations in CHCHD10, a mitochondrial protein with undefined functions, are associated with autosomal dominant mitochondrial diseases. Chchd10 knock-in mice harboring a heterozygous S55L mutation (equivalent to human pathogenic S59L) develop
Externí odkaz:
https://doaj.org/article/06da78e884b74bbabfb6411ca3018288
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 10, Pp 1551-1564 (2022)
Abstract Objective ALS is a rapidly progressive, fatal disorder caused by motor neuron degeneration, for which there is a great unmet therapeutic need. AMX0035, a combination of sodium phenylbutyrate (PB) and taurursodiol (TUDCA, TURSO), has shown pr
Externí odkaz:
https://doaj.org/article/b328f1b530ff4aa19803c9324ea9f2a8
Publikováno v:
Annals of Clinical and Translational Neurology. 9:1551-1564
ALS is a rapidly progressive, fatal disorder caused by motor neuron degeneration, for which there is a great unmet therapeutic need. AMX0035, a combination of sodium phenylbutyrate (PB) and taurursodiol (TUDCA, TURSO), has shown promising results in
ALS is a rapidly progressive, fatal disorder caused by motor neuron degeneration, for which there is a great unmet therapeutic need. AMX0035, a combination of sodium phenylbutyrate (PB) and taurursodiol (TUDCA, Turso), has shown promising results in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77432788d9ace037c90bfff318ea3e52
https://doi.org/10.1101/2022.05.02.490306
https://doi.org/10.1101/2022.05.02.490306
Autor:
Samantha Meadows, Crystal Davis, Suzanne R. Burstein, Corey Anderson, Aamir Zuberi, Kirsten Bredvik, Teresa A. Milner, Jalia Dash, Alessandra Piersigilli, Giovanni Manfredi, Cathleen M. Lutz, Hibiki Kawamata, Laure Case
Publikováno v:
Acta Neuropathol
Mutations in coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10), a mitochondrial protein of unknown function, cause a disease spectrum with clinical features of motor neuron disease, dementia, myopathy and cardiomyopathy. To investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99e5af000f4c279f688e57bb9336a44
https://europepmc.org/articles/PMC6571048/
https://europepmc.org/articles/PMC6571048/