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The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells

Detalles Bibliográficos
Autores principales: Vittecoq, O, Corrigall, V, Bodman-Smith, M, Panayi, G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833680/
http://dx.doi.org/10.1186/ar743
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author Vittecoq, O
Corrigall, V
Bodman-Smith, M
Panayi, G
author_facet Vittecoq, O
Corrigall, V
Bodman-Smith, M
Panayi, G
author_sort Vittecoq, O
collection PubMed
description
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institution National Center for Biotechnology Information
language English
publishDate 2003
publisher BioMed Central
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spelling pubmed-28336802010-03-08 The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells Vittecoq, O Corrigall, V Bodman-Smith, M Panayi, G Arthritis Res Ther Meeting Abstract BioMed Central 2003 2003-02-24 /pmc/articles/PMC2833680/ http://dx.doi.org/10.1186/ar743 Text en
spellingShingle Meeting Abstract
Vittecoq, O
Corrigall, V
Bodman-Smith, M
Panayi, G
The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
title The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
title_full The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
title_fullStr The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
title_full_unstemmed The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
title_short The molecular chaperone BiP (GRP 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
title_sort molecular chaperone bip (grp 78) inhibits the differentiation of normal human monocytes into immature dendritic cells
topic Meeting Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833680/
http://dx.doi.org/10.1186/ar743
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