| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5583988 | Seminars in Arthritis and Rheumatism | 2017 | 37 Pages |
Abstract
Murine models of SLE have proven useful for better comprehension of the multiple mechanisms involved in systemic autoimmunity that leads to LN. These critical tools should be considered when target therapies are designed to control this disorder.
Keywords
TNFαNZBAT1ATRPCPodocytesCD2-associated proteinH4RPDTCCD2APcGVHDCXCL10P3CNZWuPARIFNγSirt1LPRICAM-1MCP-1Pam3CysVCAM-1SOCS1MiR-26ainterferon-gammainterleukinforkhead box P3Immunosuppressive drugspyrrolidine dithiocarbamatesuppressor of cytokine signaling 1LymphoproliferationSystemic lupus erythematosusmacrophage inflammatory protein-1βRANTESSilent mating type information regulation 2 homolog 1intercellular adhesion molecule-1Vascular adhesion molecule-1lupus nephritisNew Zealand WhiteNew Zealand blacktransient receptor potential canonicalInterferon-inducible protein-10monocyte chemo-attractant protein-1Urokinase receptor
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Authors
Mariane MSc, Priscila Tamar Biology Student, PatrÃcia MSc, Odirlei André MD, PhD, Francisco VerÃssimo MD, PhD,