(Q28214380)

1

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Joshua Eastvold

2

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Peter Elsbach

3

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Theresa Lee Gioannini

Journal of Biological Chemistry

5

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language of work or name

English

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publication date

8 March 2002

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published in

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volume

277

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issue

10

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page(s)

7970-8

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cites work

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CD14, a receptor for complexes of lipopolysaccharide (LPS) and LPS binding protein

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Toll, a new piece in the puzzle of innate immunity

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CD14 is a pattern recognition receptor

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The genomic organization of the genes for human lipopolysaccharide binding protein (LBP) and bactericidal permeability increasing protein (BPI) is highly conserved

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Human bactericidal/permeability-increasing protein and a recombinant NH2-terminal fragment cause killing of serum-resistant gram-negative bacteria in whole blood and inhibit tumor necrosis factor release induced by the bacteria

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Structural and functional organization of the human neutrophil 60 kDa bactericidal/permeability-increasing protein

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Oct-1 and CCAAT/enhancer-binding protein (C/EBP) bind to overlapping elements within the interleukin-8 promoter. The role of Oct-1 as a transcriptional repressor

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Identification of a lipopolysaccharide binding domain in CD14 between amino acids 57 and 64.

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Lipopolysaccharide (LPS)-binding proteins BPI and LBP form different types of complexes with LPS.

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Catalytic properties of lipopolysaccharide (LPS) binding protein. Transfer of LPS to soluble CD14.

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A hydrophobic cluster at the surface of the human plasma phospholipid transfer protein is critical for activity on high density lipoproteins

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Mononuclear cell line THP-1 internalizes bactericidal/permeability-increasing protein by a non-receptor-mediated mechanism consistent with pinocytosis

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Toll-like receptor-2 mediates lipopolysaccharide-induced cellular signalling

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The involvement of CD14 in stimulation of cytokine production by uronic acid polymers

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Soluble CD14 enhances membrane CD14-mediated responses to peptidoglycan: structural requirements differ from those for responses to lipopolysaccharide

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Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction

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21 January 2018

Identifiers

DOI

10.1074/JBC.M109622200

1 reference

Consolidated OpenCitations Corpus – April 2017

2146638

2146638

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference