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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2006-9-11
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pubmed:abstractText |
To elucidate the molecular consequences of hereditary protein S (PS) deficiency, we investigated the in vitro synthesis of the PS missense mutants in COS-1 cells and their activated protein C (APC) cofactor activities.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1538-7933
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pubmed:author |
pubmed-author:HamaguchiMM,
pubmed-author:KojimaTT,
pubmed-author:KunishimaSS,
pubmed-author:MatsushitaTT,
pubmed-author:MurateTT,
pubmed-author:NaoeTT,
pubmed-author:OkadaHH,
pubmed-author:SaitoHH,
pubmed-author:TakagiAA,
pubmed-author:TakamatsuJJ,
pubmed-author:YamamotoKK,
pubmed-author:YamazakiTT
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pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2003-9
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:16961607-Adult,
pubmed-meshheading:16961607-DNA Mutational Analysis,
pubmed-meshheading:16961607-Female,
pubmed-meshheading:16961607-Gene Expression Regulation,
pubmed-meshheading:16961607-Genetic Linkage,
pubmed-meshheading:16961607-Half-Life,
pubmed-meshheading:16961607-Humans,
pubmed-meshheading:16961607-Male,
pubmed-meshheading:16961607-Middle Aged,
pubmed-meshheading:16961607-Mutation, Missense,
pubmed-meshheading:16961607-Protein S,
pubmed-meshheading:16961607-Protein S Deficiency
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pubmed:year |
2006
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pubmed:articleTitle |
In vitro characterization of missense mutations associated with quantitative protein S deficiency.
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pubmed:affiliation |
Department of Pathophysiological Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan. okadahir@nnh.hosp.go.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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