Syndecan-3 is selectively pro-inflammatory in the joint and contributes to antigen-induced arthritis in mice
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1478-6354
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Syndecan-3 is selectively pro-inflammatory in the joint and contributes to antigen-induced arthritis in mice ; volume:16 ; number:4 ; day:11 ; month:7 ; year:2014 ; pages:1-14 ; date:8.2014
Arthritis Research & Therapy ; 16, Heft 4 (11.7.2014), 1-14, 8.2014
- Creator
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Kehoe, Oksana
- Contributor
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Kalia, Neena
King, Sophie
Eustace, Andrew
Boyes, Charlotte
Reizes, Ofer
Williams, Anwen
Patterson, Angela
Middleton, Jim
SpringerLink (Online service)
- DOI
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10.1186/ar4610
- URN
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urn:nbn:de:1111-20160519879
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kehoe, Oksana
- Kalia, Neena
- King, Sophie
- Eustace, Andrew
- Boyes, Charlotte
- Reizes, Ofer
- Williams, Anwen
- Patterson, Angela
- Middleton, Jim
- SpringerLink (Online service)
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Explicit contextual information selectively contributes to predictive switching of internal models
A reduction of Syndecan-4 in macrophages promotes atherosclerosis by aggravating the proinflammatory capacity of macrophages
N-terminal syndecan-2 domain selectively enhances 6-O heparan sulfate chains sulfation and promotes VEGFA165-dependent neovascularization
Desensitized chimeric antigen receptor T cells selectively recognize target cells with enhanced antigen expression
Syndecan-3 and syndecan-4 are enriched in Schwann cell perinodal processes
Die Bedeutung der Proteoglykane Syndecan-1 und Syndecan-4 während der Frakturheilung
Publisher Correction: N-terminal syndecan-2 domain selectively enhances 6-O heparan sulfate chains sulfation and promotes VEGFA165-dependent neovascularization
A chronic pro-inflammatory environment contributes to the physiopathology of actinic lentigines
Syndecan-1 in Liver Diseases
The pro-inflammatory effect of Staphylokinase contributes to community-associated Staphylococcus aureus pneumonia
Dynamic interplay between sortilin and syndecan-1 contributes to prostate cancer progression
Lokalisation und Regulierung von Syndecan-2, Syndecan-3 und Syndecan-4 im humanen Endometrium
Explicit contextual information selectively contributes to predictive switching of internal models
A reduction of Syndecan-4 in macrophages promotes atherosclerosis by aggravating the proinflammatory capacity of macrophages
N-terminal syndecan-2 domain selectively enhances 6-O heparan sulfate chains sulfation and promotes VEGFA165-dependent neovascularization
Desensitized chimeric antigen receptor T cells selectively recognize target cells with enhanced antigen expression
Syndecan-3 and syndecan-4 are enriched in Schwann cell perinodal processes
Die Bedeutung der Proteoglykane Syndecan-1 und Syndecan-4 während der Frakturheilung
Publisher Correction: N-terminal syndecan-2 domain selectively enhances 6-O heparan sulfate chains sulfation and promotes VEGFA165-dependent neovascularization
A chronic pro-inflammatory environment contributes to the physiopathology of actinic lentigines
Syndecan-1 in Liver Diseases