(Q45863504)

17 December 2017

title

High-mobility group box 1 (HMGB1) as a master regulator of innate immunity (English)

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17 December 2017

author

Patrizia Rovere-Querini

3

object named as

Patrizia Rovere-Querini

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17 December 2017

Alessandra Castiglioni

1

1 reference

17 December 2017

Valentina Canti

2

1 reference

17 December 2017

Angelo A Manfredi

4

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17 December 2017

publication date

11 September 2010

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17 December 2017

published in

Cell and Tissue Research

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17 December 2017

volume

343

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17 December 2017

issue

1

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17 December 2017

page(s)

189-199

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17 December 2017

https://scigraph.springernature.com/pub.10.1007/s00441-010-1033-1

exact match

0 references

cites work

The N-terminal domain of thrombomodulin sequesters high-mobility group-B1 protein, a novel antiinflammatory mechanism

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

The role of HMGB1 in the pathogenesis of rheumatic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

21 January 2018

Chromatin and cell death

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

Release of high mobility group box 1 by dendritic cells controls T cell activation via the receptor for advanced glycation end products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

The relationship between apoptosis and high-mobility group protein 1 release from murine macrophages stimulated with lipopolysaccharide or polyinosinic-polycytidylic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

HMGB1: endogenous danger signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

Regulation of dendritic- and T-cell fate by injury-associated endogenous signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

High mobility group box protein 1: an endogenous signal for dendritic cell maturation and Th1 polarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

Physiological and pathophysiological outcomes of the interactions of HMGB1 with cell surface receptors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

HMGB1 develops enhanced proinflammatory activity by binding to cytokines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

HMGB proteins: interactions with DNA and chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

The alarmin functions of high-mobility group proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

Nucleocytoplasmic shuttling of HMGB1 is regulated by phosphorylation that redirects it toward secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

High mobility group box 1 protein binding to lipopolysaccharide facilitates transfer of lipopolysaccharide to CD14 and enhances lipopolysaccharide-mediated TNF-alpha production in human monocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-010-1033-1

TLR9 signals after translocating from the ER to CpG DNA in the lysosome

21 January 2018

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NI1028

Identifiers

DOI

10.1007/S00441-010-1033-1

1 reference

17 December 2017

Dimensions Publication ID

0 references

1 reference

17 December 2017