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https://olympias.lib.uoi.gr/jspui/handle/123456789/19340Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Contopoulos-Ioannidis, D. G. | en |
| dc.contributor.author | Kouri, I. | en |
| dc.contributor.author | Ioannidis, J. P. | en |
| dc.date.accessioned | 2015-11-24T18:59:05Z | - |
| dc.date.available | 2015-11-24T18:59:05Z | - |
| dc.identifier.issn | 1744-8042 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/19340 | - |
| dc.rights | Default Licence | - |
| dc.subject | *Adrenergic beta-2 Receptor Agonists | en |
| dc.subject | *Adrenergic beta-Agonists/pharmacology | en |
| dc.subject | Animals | en |
| dc.subject | Humans | en |
| dc.subject | Pharmacogenetics/*methods | en |
| dc.subject | Polymorphism, Genetic/drug effects/genetics | en |
| dc.subject | Receptors, Adrenergic, beta-2/*genetics | en |
| dc.title | Pharmacogenetics of the response to beta 2 agonist drugs: a systematic overview of the field | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | 10.2217/14622416.8.8.933 | - |
| heal.identifier.secondary | http://www.ncbi.nlm.nih.gov/pubmed/17716228 | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής | el |
| heal.publicationDate | 2007 | - |
| heal.abstract | The response to beta2-agonist treatment shows large repeatability within individuals and may thus be determined by genetic influences. Here we present a systematic overview of the available genetic association and linkage data for beta2-agonist treatment response. Systematic searches identified 66 eligible articles, as of March 2007, pertaining either to B2AR gene polymorphisms and short-acting or long-acting beta2-agonists or to another 29 different genes. We systematize these study results according to gene, agent and type of outcomes addressed. The systematic review highlights major challenges in the field, including extreme multiplicity of analyses; lack of consensus for main phenotypes of interest; typically small sample sizes; and poor replicability of the proposed genetic variants. Future studies will benefit from standardization of analyses and outcomes, hypothesis-free genome-wide association testing platforms, potentially additional fine mapping around new discovered variants, and large-scale collaborative studies with prospective plans for replication among several teams, with transparent public recording of all data. | en |
| heal.journalName | Pharmacogenomics | en |
| heal.journalType | peer-reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ | |
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