Pharmacology of histone deacetylase inhibitors
| dc.contributor.advisor | Pórszász, Róbert | |
| dc.contributor.advisordept | Debreceni Egyetem::Általános Orvostudományi Kar::Farmakológiai és Farmakoterápiai Intézet | hu_HU |
| dc.contributor.author | Farahnoosh, Hanna | |
| dc.contributor.department | DE--Általános Orvostudományi Kar | hu_HU |
| dc.contributor.opponent | Szentmiklósi, József András | |
| dc.contributor.opponent | Drimba, László | |
| dc.contributor.opponentdept | Debreceni Egyetem::Általános Orvostudományi Kar::Farmakológiai és Farmakoterápiai Intézet | hu_HU |
| dc.contributor.opponentdept | Kenézy Kórház Aneszteziológiai és Intenziv Therápiás Osztály | hu_HU |
| dc.date.accessioned | 2017-08-04T09:50:24Z | |
| dc.date.available | 2017-08-04T09:50:24Z | |
| dc.date.created | 2015-06-12 | |
| dc.description.abstract | Currently three HDAC inhibitors have been approved by the FDA where the use of vorinostat and romidepsin against refractory cutaneous and peripheral T cell lymphoma has been the most successful clinical applications of HDACis. Better understanding of the functioning of the HDACs has led to the development of new therapies that exert their effects through inhibiting it. These drugs have the potential to offer great advantages to other treatments currently in use. | hu_HU |
| dc.description.course | általános orvos | hu_HU |
| dc.description.courselang | angol | hu_HU |
| dc.description.degree | egységes, osztatlan | hu_HU |
| dc.format.extent | 38 | hu_HU |
| dc.identifier.uri | http://hdl.handle.net/2437/242876 | |
| dc.language.iso | en | hu_HU |
| dc.subject | HDAC | hu_HU |
| dc.subject.dspace | Pharmacology | hu_HU |
| dc.title | Pharmacology of histone deacetylase inhibitors | hu_HU |