Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Chloe Nagasawa"'
Autor:
Minato Hirano, Gaddiel Galarza-Muñoz, Chloe Nagasawa, Geraldine Schott, Liuyang Wang, Alejandro L Antonia, Vaibhav Jain, Xiaoying Yu, Steven G Widen, Farren BS Briggs, Simon G Gregory, Dennis C Ko, William S Fagg, Shelton Bradrick, Mariano A Garcia-Blanco
Publikováno v:
eLife, Vol 12 (2023)
Genes associated with increased susceptibility to multiple sclerosis (MS) have been identified, but their functions are incompletely understood. One of these genes codes for the RNA helicase DExD/H-Box Polypeptide 39B (DDX39B), which shows genetic an
Externí odkaz:
https://doaj.org/article/c38f1aa37a0a4f6ba7bae9127557c87f
Autor:
Chloe Nagasawa, Allison Ogren, Nataliya Kibiryeva, Jennifer Marshall, James E. O’Brien, Naoya Kenmochi, Douglas C. Bittel
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 5, Iss 2, p 26 (2018)
Congenital heart disease (CHD) is a leading cause of death in children
Externí odkaz:
https://doaj.org/article/f80b0f18d3444076bdb08d6e123a7e78
Autor:
Minato Hirano, Gaddiel Galarza-Muñoz, Geraldine Schott, Liuyang Wang, Chloe Nagasawa, Alejandro L. Antonia, Vaibhav Jain, Xiaoying Yu, Steven G. Widen, Farren B.S. Briggs, Simon G. Gregory, Dennis C. Ko, W. Samuel Fagg, Shelton S. Bradrick, Mariano A. Garcia-Blanco
SummaryGenes associated with increased susceptibility to multiple sclerosis (MS) have been identified, but their functions are incompletely understood. One of these genes codes for the RNA helicase DExD/H-Box Polypeptide 39B (DDX39B), which shows gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58b2e9db8e6b695cb8caf4a9a811cecc
https://doi.org/10.1101/2022.01.25.477795
https://doi.org/10.1101/2022.01.25.477795