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About:
Polymorphisms of interferon-inducible genes OAS-1 and MxA associated with SARS in the Vietnamese population
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Polymorphisms of interferon-inducible genes OAS-1 and MxA associated with SARS in the Vietnamese population
Creator
Hamano, Emi
Hijikata, Minako
Keicho, Naoto
Matsushita, Ikumi
Itoyama, Satoru
Kirikae, Teruo
Kuratsuji, Tadatoshi
Quy, Tran
Sasazuki, Takehiko
Yanai, Hideki
Kirikae, Fumiko
Dang Ha, Le
Long, Hoang
Phi, Nguyen
Van Ban, Vo
Source
Elsevier; Medline; PMC
abstract
Abstract We hypothesized that host antiviral genes induced by type I interferons might affect the natural course of severe acute respiratory syndrome (SARS). We analyzed single nucleotide polymorphisms (SNPs) of 2′,5′-oligoadenylate synthetase 1 (OAS-1), myxovirus resistance-A (MxA), and double-stranded RNA-dependent protein kinase in 44 Vietnamese SARS patients with 103 controls. The G-allele of non-synonymous A/G SNP in exon 3 of OAS-1 gene showed association with SARS (p =0.0090). The G-allele in exon 3 of OAS-1 and the one in exon 6 were in strong linkage disequilibrium and both of them were associated with SARS infection. The GG genotype and G-allele of G/T SNP at position −88 in the MxA gene promoter were found more frequently in hypoxemic group than in non-hypoxemic group of SARS (p =0.0195). Our findings suggest that polymorphisms of two IFN-inducible genes OAS-1 and MxA might affect susceptibility to the disease and progression of SARS at each level.
has issue date
2005-04-22
(
xsd:dateTime
)
bibo:doi
10.1016/j.bbrc.2005.02.101
bibo:pmid
15766558
has license
els-covid
sha1sum (hex)
09e8ffe2b970364e969a4b167ed6ecd1ff8f9554
schema:url
https://doi.org/10.1016/j.bbrc.2005.02.101
resource representing a document's title
Polymorphisms of interferon-inducible genes OAS-1 and MxA associated with SARS in the Vietnamese population
has PubMed Central identifier
PMC7092916
has PubMed identifier
15766558
schema:publication
Biochemical and Biophysical Research Communications
resource representing a document's body
covid:09e8ffe2b970364e969a4b167ed6ecd1ff8f9554#body_text
is
schema:about
of
named entity 'POPULATION'
named entity 'level'
named entity 'patients'
named entity 'susceptibility'
named entity 'induced'
named entity 'OAS'
named entity 'SARS'
named entity 'POLYMORPHISMS'
named entity 'PATIENTS'
named entity 'SUSCEPTIBILITY'
named entity 'SEVERE ACUTE RESPIRATORY SYNDROME'
named entity 'NON-'
named entity 'INFECTION'
named entity 'TYPE I INTERFERONS'
named entity 'FINDINGS'
named entity 'POSITION'
named entity 'ANALYZED'
named entity 'POLYMORPHISMS'
named entity 'GENES'
named entity '28P'
named entity '103'
named entity 'SARS'
named entity 'STRONG'
named entity 'INDUCED'
named entity 'ASSOCIATION'
named entity 'AFFECT'
named entity 'INTERFERON'
named entity 'OAS'
named entity 'VIETNAMESE'
named entity 'INDUCIBLE'
named entity 'ASSOCIATED WITH'
named entity 'GENE'
named entity 'SYNONYMOUS'
named entity 'NATURAL COURSE'
named entity 'SUGGEST'
named entity 'RESISTANCE'
named entity 'MXA'
named entity 'ALLELE'
named entity 'FOUND'
named entity 'GROUP'
named entity 'GENE PROMOTER'
named entity 'DISEASE'
named entity 'SYNTHETASE'
named entity 'LEVEL'
named entity 'MXA'
named entity 'MYXOVIRUS'
named entity 'VIETNAMESE'
named entity 'PROTEIN KINASE'
named entity 'SINGLE NUCLEOTIDE POLYMORPHISMS'
named entity 'LINKAGE DISEQUILIBRIUM'
named entity 'OLIGOADENYLATE'
named entity '2C5'
named entity 'FREQUENTLY'
named entity 'IFN'
named entity 'OAS'
named entity 'HOST'
named entity 'OUR'
named entity 'ASSOCIATED WITH'
named entity 'GENOTYPE'
named entity 'PROGRESSION'
named entity 'GENES'
named entity 'SNP'
named entity 'DEPENDENT'
named entity 'EXON'
named entity 'ANTIVIRAL'
named entity 'DOUBLE-STRANDED RNA'
covid:arg/09e8ffe2b970364e969a4b167ed6ecd1ff8f9554
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