Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kristopher K. Short"'
Autor:
Kristopher K. Short, Stephanie K. Lathrop, Clara J. Davison, Haley A. Partlow, Johnathan A. Kaiser, Rebekah D. Tee, Elizabeth B. Lorentz, Jay T. Evans, David J. Burkhart
Publikováno v:
Pharmaceutics, Vol 14, Iss 7, p 1455 (2022)
A diversity of vaccines is necessary to reduce the mortality and morbidity of SARS-CoV-2. Vaccines must be efficacious, easy to manufacture, and stable within the existing cold chain to improve their availability around the world. Recombinant protein
Externí odkaz:
https://doaj.org/article/dc040770076e4fe8bccc69c38335ffb0
Autor:
Lois Walsh, Jay T. Evans, Hélène G. Bazin, Kristopher K. Short, Van Cybulski, David J. Burkhart, Shannon M. Miller
Publikováno v:
J Control Release
To increase vaccine immunogenicity, modern vaccines incorporate adjuvants, which serve to enhance immune cross-protection, improve humoral and cell-mediated immunity, and promote antigen dose sparing. Pattern recognition receptors (PRRs), including t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7830fbf3d75ac94c5fdc4faf68f0fa
https://doi.org/10.1016/j.jconrel.2019.10.025
https://doi.org/10.1016/j.jconrel.2019.10.025
Publikováno v:
J Cell Sci
Copper-responsive intracellular ATP7B trafficking is crucial for maintaining the copper balance in mammalian hepatocytes and thus copper levels in organs. The copper metabolism domain-containing protein 1 (COMMD1) binds both the ATP7B copper transpor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d3813ddd2e22b7efa1649fc0331976f
https://pubmed.ncbi.nlm.nih.gov/31515276
https://pubmed.ncbi.nlm.nih.gov/31515276
Publikováno v:
Journal of Cell Science.
Copper-responsive intracellular ATP7B trafficking is critical to maintain copper balance in mammalian hepatocytes and thus organismal copper levels. The COMMD1 protein binds both the ATP7B copper transporter and phosphatidylinositol (4,5)-bisphosphat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::343e832fc9f280127f622a75b79be295
https://doi.org/10.1242/jcs.231753
https://doi.org/10.1242/jcs.231753
Autor:
Oliver Fiehn, Jason L. Burkhead, Kristopher K. Short, Larry L. David, Phillip A. Wilmarth, Svetlana Lutsenko
Publikováno v:
Metallomics. 4:660
Wilson's disease (WD) is an inherited disorder of copper metabolism characterized by liver disease and/or neurologic and psychiatric pathology. The disease is a result of mutation in ATP7B, which encodes the ATP7B copper transporting ATPase. Loss of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b142d67eba0e7731dfe2ea28dd4368c9
https://doi.org/10.1039/c2mt20017a
https://doi.org/10.1039/c2mt20017a