Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hannah S. Seo"'
Autor:
Catherine A. A. Lee, Hannah S. Seo, Anibal G. Armien, Frank S. Bates, Jakub Tolar, Samira M. Azarin
Publikováno v:
Fluids and Barriers of the CNS, Vol 15, Iss 1, Pp 1-15 (2018)
Abstract Background X-linked adrenoleukodystrophy (X-ALD) is caused by mutations in the ABCD1 gene. 40% of X-ALD patients will convert to the deadly childhood cerebral form (ccALD) characterized by increased permeability of the brain endothelium that
Externí odkaz:
https://doaj.org/article/a7a44b92acd24c39ad97941c4eca7c2a
Publikováno v:
Current Opinion in Chemical Engineering. 30:1-8
As the interface between the vasculature and the central nervous system (CNS), the blood-brain barrier (BBB), composed of brain microvascular endothelial cells (BMECs), plays a crucial role in maintaining the health of the CNS but hinders drug delive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dec5e762088e06dee5e0bd11ddf9262
https://doi.org/10.1016/j.coche.2020.05.006
https://doi.org/10.1016/j.coche.2020.05.006
Autor:
Hannah S. Seo, Greg Haugstad, Benjamin J. Hackel, Timothy P. Lodge, Guangcui Yuan, Joseph M. Metzger, Frank Heinrich, Sushil K. Satija, Samira M. Azarin, Guichuan Yu, Mihee Kim, Wenjia Zhang, Frank S. Bates
Publikováno v:
Langmuir
Maintaining the integrity of cell membranes is indispensable for cellular viability. Poloxamer 188 (P188), a poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) (PEO–PPO–PEO) triblock copolymer with a number-average molecular weig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e430f97e700b21b8d547513683ab31d2
https://doi.org/10.1021/acs.langmuir.9b03208
https://doi.org/10.1021/acs.langmuir.9b03208
Autor:
Hannah S. Seo, Catherine A. Lee, Frank S. Bates, Samira M. Azarin, Jakub Tolar, Aníbal G. Armién
Publikováno v:
Fluids and Barriers of the CNS, Vol 15, Iss 1, Pp 1-15 (2018)
Fluids and Barriers of the CNS
Fluids and Barriers of the CNS
Background X-linked adrenoleukodystrophy (X-ALD) is caused by mutations in the ABCD1 gene. 40% of X-ALD patients will convert to the deadly childhood cerebral form (ccALD) characterized by increased permeability of the brain endothelium that constitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4522912c90d5b28d01f6afd4fc31937a
http://link.springer.com/article/10.1186/s12987-018-0094-5
http://link.springer.com/article/10.1186/s12987-018-0094-5