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231225s2022 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2021.108911
|2 doi
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|a pubmed24n1115.xml
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|a (DE-627)NLM334654513
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|a (NLM)34929414
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|a (PII)S1521-6616(21)00248-5
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Hajeer, Ali
|e verfasserin
|4 aut
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|a Association of KIR gene polymorphisms with COVID-19 disease
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 21.01.2022
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|a Date Revised 21.12.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2021 Elsevier Inc. All rights reserved.
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|a BACKGROUND: Natural killer (NK) cells play an essential role against viruses. NK cells express killer cell immunoglobulin-like receptors (KIRs) which regulate their activity and function. The polymorphisms in KIR haplotypes confer differential viral susceptibility and disease severity caused by infections. We investigated the association between KIR genes and COVID-19 disease severity
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|a METHODS: 424 COVID-19 positive patients were divided according to their disease severity into mild, moderate and severe. KIR genes were genotyped using next generation sequencing (NGS). Association between KIR genes and COVID-19 disease severity was conducted and significant correlations were reported
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|a RESULTS: In the COVID-19 patients, KIR Bx genotype was more common than AA genotype. The Bx genotype was found more frequently in patients with mild disease, while in severe disease the AA genotype was more common than the Bx genotype. The KIR2DS4 gene carried the highest risk for severe COVID-19 infection (OR 8.48, pc= 0.0084) followed by KIR3DL1 (OR 7.61, pc= 0.0192)
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|a CONCLUSIONS: Our findings suggest that KIR2DS4 and KIR3DL1 genes carry risk for severe COVID-19 disease
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|a Journal Article
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|a COVID-19
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|a KIR
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|a Natural killer
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|a Risk
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|a SARS CoV-2
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|a Saudi Arabia
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|a Virus
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|a Receptors, KIR
|2 NLM
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1 |
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|a Jawdat, Dunia
|e verfasserin
|4 aut
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1 |
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|a Massadeh, Salam
|e verfasserin
|4 aut
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1 |
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|a Aljawini, Nora
|e verfasserin
|4 aut
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1 |
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|a Abedalthagafi, Malak S
|e verfasserin
|4 aut
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1 |
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|a Arabi, Yaseen M
|e verfasserin
|4 aut
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700 |
1 |
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|a Alaamery, Manal
|e verfasserin
|4 aut
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773 |
0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 234(2022) vom: 01. Jan., Seite 108911
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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773 |
1 |
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|g volume:234
|g year:2022
|g day:01
|g month:01
|g pages:108911
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|u http://dx.doi.org/10.1016/j.clim.2021.108911
|3 Volltext
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|a GBV_ILN_350
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|a AR
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|d 234
|j 2022
|b 01
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|h 108911
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