ACR Meeting Abstracts

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Abstracts tagged "Cell Migration"

  • Abstract Number: 1853 • 2013 ACR/ARHP Annual Meeting

    Functions Of Aminopeptidase N/CD13 In Vitro On Rheumatoid Arthritis Synovial Cells

    Rachel Morgan1, Nilofar Behbahani-Nejad2, Judith Endres3 and David A. Fox4, 1Immunology, University of Michigan, Ann Arbor, MI, 2University of Michigan, Ann Arbor, MI, 3Rheumatology/Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, 4Internal Medicine, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose: Aminopeptidase N (CD13, EC 3.4.11.2) is a metalloproteinase expressed on the surface of fibroblast like synoviocytes (FLS) that is also found in soluble form…
  • Abstract Number: 1152 • 2013 ACR/ARHP Annual Meeting

    Ligation Of TLR5 Promotes Myeloid Cell Infiltration and Differentiation Into Mature Osteoclasts In RA Patients and Experimental Arthritis

    Seung-jae Kim1, Zhenlong Chen1, Nathan D. Chamberlain1, Michael V. Volin2, Suncica Volkov1, William Swedler3, Shiva Arami4, Anjali Mehta5, Nadera J. Sweiss6 and Shiva Shahrara1, 1Medicine/Rheumatology, University of Illinois at Chicago, Chicago, IL, 2Department of Microbiology and Immunology, Chicago College of Osteopathic Medicine Midwestern University, Downers Grove, IL, 3Section of Rheumatology, University of Illinois at Chicago, Chicago, IL, 4Medicine - Rheumatology, University of Illinois at Chicago, Chicago, IL, 5University of Illinois at Chicago, Chicago, IL, 6internal medicine section of rheumatology, University of Illinois at Chicago, Chicago, IL

    Background/Purpose: The aim of this study was to examine the importance of TLR5 ligation in the pathogenesis of rheumatoid arthritis (RA) and experimental arthritis. Methods:…
  • Abstract Number: 933 • 2013 ACR/ARHP Annual Meeting

    Characterizing The Expression and Function Of CCL28 and Its Corresponding Receptor CCR10 In The Pathogenesis Of RA

    Zhenlong Chen1, Seung-jae Kim1, Michael V. Volin2, Suncica Volkov1, William Swedler3, Nadera J. Sweiss4 and Shiva Shahrara1, 1Medicine/Rheumatology, University of Illinois at Chicago, Chicago, IL, 2Department of Microbiology and Immunology, Chicago College of Osteopathic Medicine Midwestern University, Downers Grove, IL, 3Section of Rheumatology, University of Illinois at Chicago, Chicago, IL, 4internal medicine section of rheumatology, University of Illinois at Chicago, Chicago, IL

    Background/Purpose: This study was conducted to determine the expression pattern and function of CCL28 and its corresponding receptor CCR10 in the pathogenesis of rheumatoid arthritis…
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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.).

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