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CXCL5 protein, human

Known as: ENA-78 protein, human, Epithelial-Derived Neutrophil-Activating Protein 78, epithelial-cell-derived neutrophil attractant-78 protein, human 
C-X-C motif chemokine 5 (114 aa, ~12 kDa) is encoded by the human CXCL5 gene. This protein is involved in both chemotaxis and activation of… Expand
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Chemokines are small proteins that control several tissue functions, including cell recruitment and activation under homeostatic… Expand
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Highly Cited
2012
Highly Cited
2012
CXCL5 (epithelial neutrophil‐activating peptide‐78) is a member of a proangiogenic subgroup of the CXC‐type chemokine family of… Expand
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Highly Cited
2012
Highly Cited
2012
PURPOSE To determine cytokine and chemokine concentrations in the tears of patients with dry eye disease (DED) and analyze the… Expand
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Highly Cited
2012
Highly Cited
2012
Neutrophils are essential for maintaining innate immune surveillance under normal conditions, but also represent a major… Expand
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Highly Cited
2011
Highly Cited
2011
Epithelial neutrophil-activating peptide-78 (CXCL5), a member of the CXC chemokine family, has been shown to be involved in… Expand
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Highly Cited
2010
Highly Cited
2010
The chemokine sink hypothesis pertaining to erythrocyte Duffy Antigen Receptor for Chemokines (DARC) during inflammation has… Expand
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Highly Cited
2008
Highly Cited
2008
CXCL5 is a proangiogenic CXC-type chemokine that is an inflammatory mediator and a powerful attractant for granulocytic immune… Expand
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Highly Cited
2004
Highly Cited
2004
Interleukin (IL)‐17 is the founding member of an emerging family of inflammatory cytokines whose functions remain poorly defined… Expand
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Highly Cited
2002
Highly Cited
2002
Lysophosphatidylcholines (lyso-PCs), generated during blood storage, are etiologic in a two-insult, sepsis-based model of… Expand
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Highly Cited
1991
Highly Cited
1991
A new neutrophil-activating peptide, termed ENA-78, was identified in the conditioned media of stimulated human type II… Expand
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