2015 ACR/ARHP Annual Meeting

November 6-11, 2015. San Francisco, CA.

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Abstract Number: 2084

Dendritic Cell-Specific Transmembrane Protein (DC-STAMP) Modulates Bone Resorption in Inflammatory Arthritis and Fracture Repair
Abstract Number: 2085

DC-STAMP Regulates Osteoclastogenesis through the Ca2+ /NFATc1 Axis
Abstract Number: 2086

Inhibition of Macrophage Inflammatory Protein 1-Alpha (CCL3) Significantly Reduced Bone Resorption in Vitro and the Development of Erosive Joint Pathology in Collagen-Induced Arthritis
Abstract Number: 2087

Defective Circadian Control in Mesenchymal Cells Reduces Adult Bone Mass
Abstract Number: 2088

Immature Dendritic Are Potent OC Precursors in RA and Are Targeted By RA-Specific Antibodies
Abstract Number: 2089

Netrin-1 and Its Receptors Unc5b and DCC May be Useful Targets for Preventing Multiple Myeloma Bone Lesions
Abstract Number: 2090

Gender-Specific Pathways Linking Arthritis, Activity Limitation and Incident Heart Disease: A Causal Mediation Analysis of the Canadian Longitudinal National Population Health Survey
Abstract Number: 2091

Influence of Increasing Physical Activity on Longitudinal Changes in Disability Status Among Inactive Older Adults
Abstract Number: 2092

Knee Pain Burden Is Associated with Decreased Moderate to Vigorous Physical Activity: Data from the Osteoarthritis Initiative
Abstract Number: 2093

Are General and Central Adiposity Associated with MRI-Assessed Structural Changes in the Knees of Older Adults?
Abstract Number: 2094

Identification of Gout Flare Using an Administrative Claims Based Algorithm
Abstract Number: 2095

Dietary Patterns (DASH, Prudent, Western Diets) and the Risk of Gout in US Women – the Nurses Health Study
Abstract Number: 2096

Immune Dysregulation in Patients with TRNT1 Deficiency
Abstract Number: 2097

HLA-B27 Expression Profoundly Shapes the Host-Microbiota Metabolome
Abstract Number: 2098

Prioritizing Likely Causative Genes in Genome-Wide Association Studies (GWAS) Identified Risk Loci for Immune-Mediated Inflammatory Disorders Using Cell-Type Specific Expression Quantitative Loci (eQTL) Information

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].