Influenza A: Mechanism of Infection and Development of M2 Ion Channel Inhibitors
| dc.contributor.advisor | Krieg, Paul A. | en |
| dc.contributor.author | Sneyd, Hannah | |
| dc.creator | Sneyd, Hannah | en |
| dc.date.accessioned | 2018-01-19T20:32:01Z | |
| dc.date.available | 2018-01-19T20:32:01Z | |
| dc.date.issued | 2017 | |
| dc.identifier.uri | http://hdl.handle.net/10150/626385 | |
| dc.description.abstract | Influenza viral infection causes several hospitalizations and claims the lives of many people each year. The threat of epidemic and pandemic are more pressing than ever with newly mutated strains developing every year. Understanding the mechanism of infection of influenza can help identify new potential drug targets and help progress the development of antivirals. Currently there are two classes of FDA approved drugs, neuraminidase inhibitors and M2 ion channel inhibitors, to combat influenza infection. Unfortunately, viral resistance to M2 ion channel blockers has caused them to stop being used for treatment. This paper focuses on understanding influenzas ability to mutate and it mechanism of infection to develop new M2 ion channel blockers. | |
| dc.language.iso | en_US | en |
| dc.publisher | The University of Arizona. | en |
| dc.rights | Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. | en |
| dc.subject | Influenza A | en |
| dc.subject | M2 ion channel | en |
| dc.title | Influenza A: Mechanism of Infection and Development of M2 Ion Channel Inhibitors | en_US |
| dc.type | text | en |
| dc.type | Electronic Thesis | en |
| thesis.degree.grantor | University of Arizona | en |
| thesis.degree.level | masters | en |
| dc.contributor.committeemember | Krieg, Paul A. | en |
| dc.contributor.committeemember | Campos, Samuel K. | en |
| dc.contributor.committeemember | Ahmad, Nafees | en |
| thesis.degree.discipline | Graduate College | en |
| thesis.degree.discipline | Cellular and Molecular Medicine | en |
| thesis.degree.name | M.S. | en |
| refterms.dateFOA | 2018-09-12T01:03:51Z | |
| html.description.abstract | Influenza viral infection causes several hospitalizations and claims the lives of many people each year. The threat of epidemic and pandemic are more pressing than ever with newly mutated strains developing every year. Understanding the mechanism of infection of influenza can help identify new potential drug targets and help progress the development of antivirals. Currently there are two classes of FDA approved drugs, neuraminidase inhibitors and M2 ion channel inhibitors, to combat influenza infection. Unfortunately, viral resistance to M2 ion channel blockers has caused them to stop being used for treatment. This paper focuses on understanding influenzas ability to mutate and it mechanism of infection to develop new M2 ion channel blockers. |
