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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Drug genetic associations with COVID-19 manifestations: a data mining and network biology approach

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Συγγραφέας
Charitou T., Kontou P.I., Tamposis I.A., Pavlopoulos G.A., Braliou G.G., Bagos P.G.
Ημερομηνία
2022
Γλώσσα
en
DOI
10.1038/s41397-022-00289-1
Λέξη-κλειδί
acetylsalicylic acid
alpha2 integrin
anakinra
apolipoprotein C1
apolipoprotein C3
apolipoprotein E
atazanavir
azithromycin
bamlanivimab
baricitinib
beta interferon
beta3 integrin
biological marker
canakinumab
casirivimab plus imdevimab
chloroquine
colchicine
cytochrome P450 2C19
cytochrome P450 2C9
cytochrome P450 2D6
cytochrome P450 3A4
cytochrome P450 3A5
dalteparin
dexamethasone
endothelial nitric oxide synthase
enoxaparin
favipiravir
glucuronosyltransferase 1A1
glucuronosyltransferase 1A3
glucuronosyltransferase 1A6
glucuronosyltransferase 1A7
glutathione peroxidase 1
HLA DQA1 antigen
HLA DRB1 antigen
hydrocortisone
hydroxychloroquine
insulin receptor substrate 1
ivermectin
lopinavir plus ritonavir
methylprednisolone
multidrug resistance associated protein 1
nitazoxanide
reduced folate carrier
remdesivir
ribavirin
ruxolitinib
sarilumab
SARS-CoV-2 vaccine
solute carrier organic anion transporter 1B1
tocilizumab
transporter associated with antigen processing 1
vasculotropin A
vitamin D receptor
Article
clinical decision making
clinical feature
clinical outcome
controlled study
coronavirus disease 2019
data mining
drug efficacy
drug repositioning
gene identification
gene interaction
genetic association
genetic variation
genome-wide association study
human
infection sensitivity
pandemic
pharmacogenetic testing
protein protein interaction
risk factor
systems biology
treatment response
drug therapy
genomics
pharmacogenetics
COVID-19
Data Mining
Genomics
Humans
Pharmacogenetics
Springer Nature
Εμφάνιση Μεταδεδομένων
Επιτομή
Available drugs have been used as an urgent attempt through clinical trials to minimize severe cases of hospitalizations with Coronavirus disease (COVID-19), however, there are limited data on common pharmacogenomics affecting concomitant medications response in patients with comorbidities. To identify the genomic determinants that influence COVID-19 susceptibility, we use a computational, statistical, and network biology approach to analyze relationships of ineffective concomitant medication with an adverse effect on patients. We statistically construct a pharmacogenetic/biomarker network with significant drug-gene interactions originating from gene-disease associations. Investigation of the predicted pharmacogenes encompassing the gene-disease-gene pharmacogenomics (PGx) network suggests that these genes could play a significant role in COVID-19 clinical manifestation due to their association with autoimmune, metabolic, neurological, cardiovascular, and degenerative disorders, some of which have been reported to be crucial comorbidities in a COVID-19 patient. © 2022, The Author(s), under exclusive licence to Springer Nature Limited.
URI
http://hdl.handle.net/11615/72544
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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