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Abstract Number: 104
Novel, Selective, Orally Active PAD4 Inhibitors for the Treatment of Autoimmune Disorders
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Abstract Number: 105
The DLEU2/miR-15a/16-1 Cluster Inhibit Foxp3+ Treg Cells in Salivary Glands of pSS via Targeting Foxp3
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Abstract Number: 106
Increased T Cell Polyreactivity with Marked Accumulation of TNF-α DP (CD4+CD8+) in the Synovial Tissue of pre-RA, Arthralgia Subjects
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Abstract Number: 107
Expanded Peripheral T Helper Cells Characterize the Early Rheumatoid Arthritis Synovium
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Abstract Number: 108
Mucosal Associated Invariant T Cells in Giant Cell Arteritis
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Abstract Number: 109
Targeting CD6 Expression Attenuates T Cell Activity in Murine Collagen Induced Arthritis
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Abstract Number: 110
Bioinformatics Analysis of Transcriptomics Data Reveals That SRSF1 Is a Novel Molecular Brake for the T Cell Activation Program and Controls Key Cytokine Signaling Genes Implicated in Systemic Lupus Erythematosus
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Abstract Number: 111
The Transcription Factor STAT3 Regulates Pathogenic Th17 Responses in Autoimmune Disease via Noncanonical Roles
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Abstract Number: 112
Impact of Interleukin-9 on the Immune Suppressive Functions of Regulatory T Cells in Rheumatoid Arthritis
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Abstract Number: 113
In Vitro Characterization of the Effect of Cenerimod, a Potent and Selective Sphingosine 1-Phosphate Receptor 1 (S1P1) Modulator, on S1P1 Receptor Expression, Receptor Internalization, and Migration of Primary Human T Cells in the Presence or Absence of Glucocorticoids
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Abstract Number: 114
Persistent Synovial Resident Memory T Cells Mediate Arthritis Flares
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Abstract Number: 115
CD8+ Cytotoxic T Lymphocytes Are Clonally-expanded in IgG4-related Disease and Home to Affected Tissues
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Abstract Number: 116
Defective EZH2 Expression Attenuates Treg Differentiation in Rheumatoid Arthritis
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Abstract Number: 117
The Indole Derivative NecroX Blocks Th17 Cell Differentiation and Fibroblast-like Synoviocytes-mediated Th1/Th17 Responses in Rheumatoid Arthritis
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Abstract Number: 118
Polymorphonuclear Neutrophils and Regulatory T Lymphocytes (Treg) Cooperate to Sustain Treg Activity but This Interaction Is Altered in Rheumatoid Arthritis Patients
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