(Q47908242)

English

The interaction between DC and Plasmodium berghei/chabaudi-infected erythrocytes in mice involves direct cell-to-cell contact, internalization and TLR.

scientific article published in July 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

The interaction between DC and Plasmodium berghei/chabaudi-infected erythrocytes in mice involves direct cell-to-cell contact, internalization and TLR. (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

Plasmodium berghei

0 references

toll-like receptor

0 references

Plasmodium chabaudi

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

author name string

José F Moura Nunes

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

Inês Matos

3

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

António Coutinho

4

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

language of work or name

0 references

publication date

1 July 2009

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

European Journal of Immunology

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

39

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

7

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

1850-1863

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

Direct activation of dendritic cells by the malaria parasite, Plasmodium chabaudi chabaudi

1 reference

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Dendritic cells from malaria-infected mice are fully functional APC.

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Antigen presentation capacity and cytokine production by murine splenic dendritic cell subsets upon Salmonella encounter

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Candida albicans is phagocytosed, killed, and processed for antigen presentation by human dendritic cells

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Malaria blood stage parasites activate human plasmacytoid dendritic cells and murine dendritic cells through a Toll-like receptor 9-dependent pathway

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Toll-like receptor 9 mediates innate immune activation by the malaria pigment hemozoin

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Hemozoin (malarial pigment) inhibits differentiation and maturation of human monocyte-derived dendritic cells: a peroxisome proliferator-activated receptor-gamma-mediated effect

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Suppression of adaptive immunity to heterologous antigens during Plasmodium infection through hemozoin-induced failure of dendritic cell function

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Plasmodium strain determines dendritic cell function essential for survival from malaria

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TLR signalling and activation of IRFs: revisiting old friends from the NF-kappaB pathway

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Toll-like receptors in innate immunity

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Toll-like receptor signalling

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Dendritic cell survival and maturation are regulated by different signaling pathways.

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The NF-kappaB signaling pathway: immune evasion and immunoregulation during toxoplasmosis

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Plasmodium berghei infection in mice induces liver injury by an IL-12- and toll-like receptor/myeloid differentiation factor 88-dependent mechanism

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Chaperoning a cellular upheaval in malaria: heat shock proteins in Plasmodium falciparum.

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The toll-like receptor protein RP105 regulates lipopolysaccharide signaling in B cells

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Membrane sorting of toll-like receptor (TLR)-2/6 and TLR2/1 heterodimers at the cell surface determines heterotypic associations with CD36 and intracellular targeting

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Identifiers

10.1002/EJI.200838403

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/19585512

ResearchGate publication ID

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