Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Natsuko, Macabuag"'
Autor:
Blanca, Torroba, Natsuko, Macabuag, Elisabeth M, Haisma, Amy, O'Neill, Maria E, Herva, Roxana S, Redis, Michael V, Templin, Lauren E, Black, David F, Fischer
Publikováno v:
Expert Opinion on Drug Discovery. 18:181-192
Spinal Muscular Atrophy (SMA), the second most prevalent autosomal genetic disease affecting infants, is caused by the lack ofThis manuscript will cover two of the three mechanistically distinct available treatment options for SMA, both targeting the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba36e48f54cbb6e977d3802f85514c4b
https://doi.org/10.1080/17460441.2022.2149733
https://doi.org/10.1080/17460441.2022.2149733
Autor:
Natsuko Macabuag, William Esmieu, Perla Breccia, Rebecca Jarvis, Wesley Blackaby, Ovadia Lazari, Liudvikas Urbonas, Maria Eznarriaga, Rachel Williams, Annelieke Strijbosch, Rhea Van de Bospoort, Kim Matthews, Cole Clissold, Tammy Ladduwahetty, Huw Vater, Patrick Heaphy, Douglas G. Stafford, Hong-Jun Wang, John E. Mangette, George McAllister, Vahri Beaumont, Thomas F. Vogt, Hilary A. Wilkinson, Elizabeth M. Doherty, Celia Dominguez
Publikováno v:
Journal of medicinal chemistry. 65(18)
Huntington's disease (HD) is a lethal autosomal dominant neurodegenerative disorder resulting from a CAG repeat expansion in the huntingtin (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf9b7293f23145d9276a05495bc08822
https://pubmed.ncbi.nlm.nih.gov/36098485
https://pubmed.ncbi.nlm.nih.gov/36098485