Double Duty by CCL21 in Dendritic Cell Trafficking
Identifieur interne : 000C26 ( Pmc/Curation ); précédent : 000C25; suivant : 000C27Double Duty by CCL21 in Dendritic Cell Trafficking
Auteurs : Philip M. MurphySource :
- Immunity [ 1074-7613 ] ; 2010.
Abstract
Mechanisms controlling leukocyte adhesion, propulsion and directional migration are still not fully integrated. In this issue of
Url:
DOI: 10.1016/j.immuni.2010.05.004
PubMed: 20510869
PubMed Central: 3398834
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PMC:3398834Le document en format XML
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<author><name sortKey="Murphy, Philip M" sort="Murphy, Philip M" uniqKey="Murphy P" first="Philip M." last="Murphy">Philip M. Murphy</name>
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<series><title level="j">Immunity</title>
<idno type="ISSN">1074-7613</idno>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<p id="P1">Mechanisms controlling leukocyte adhesion, propulsion and directional migration are still not fully integrated. In this issue of <italic>Immunity</italic>
, <xref rid="R9" ref-type="bibr">Schumann et al (2010)</xref>
propose that DCs swarm to T cell zones by using immobilized CCL21 for adhesive random migration and soluble CCL21 for steering..</p>
</div>
</front>
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<pmc article-type="article-commentary"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-journal-id">9432918</journal-id>
<journal-id journal-id-type="pubmed-jr-id">8591</journal-id>
<journal-id journal-id-type="nlm-ta">Immunity</journal-id>
<journal-id journal-id-type="iso-abbrev">Immunity</journal-id>
<journal-title-group><journal-title>Immunity</journal-title>
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<issn pub-type="ppub">1074-7613</issn>
<issn pub-type="epub">1097-4180</issn>
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<article-meta><article-id pub-id-type="pmid">20510869</article-id>
<article-id pub-id-type="pmc">3398834</article-id>
<article-id pub-id-type="doi">10.1016/j.immuni.2010.05.004</article-id>
<article-id pub-id-type="manuscript">NIHMS390932</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
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<title-group><article-title>Double Duty by CCL21 in Dendritic Cell Trafficking</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Murphy</surname>
<given-names>Philip M.</given-names>
</name>
<aff id="A1">Laboratory of Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892</aff>
</contrib>
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<author-notes><corresp id="FN1">Contact Information: Philip M. Murphy, M. D., Bldg 10, Room 11N113, NIH, Bethesda, MD 20892, Tel: 301-496-8616, Fax: 301-401-4369, <email>pmm@nih.gov</email>
</corresp>
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<pub-date pub-type="nihms-submitted"><day>3</day>
<month>7</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="ppub"><day>28</day>
<month>5</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>17</day>
<month>7</month>
<year>2012</year>
</pub-date>
<volume>32</volume>
<issue>5</issue>
<fpage>590</fpage>
<lpage>592</lpage>
<abstract><title>Summary</title>
<p id="P1">Mechanisms controlling leukocyte adhesion, propulsion and directional migration are still not fully integrated. In this issue of <italic>Immunity</italic>
, <xref rid="R9" ref-type="bibr">Schumann et al (2010)</xref>
propose that DCs swarm to T cell zones by using immobilized CCL21 for adhesive random migration and soluble CCL21 for steering..</p>
</abstract>
<funding-group><award-group><funding-source country="United States">National Institute of Allergy and Infectious Diseases Extramural Activities : NIAID</funding-source>
<award-id>ZIA AI000615-21 || AI</award-id>
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