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<art>
   <ui>1471-2105-9-S7-P10</ui>
   <ji>1471-2105</ji>
   <fm>
      <dochead>Poster presentation</dochead>
      <bibl>
         <title>
            <p>QTL mapping arthritis traits in CXB mice</p>
         </title>
         <aug>
            <au id="A1" ca="yes">
               <snm>Marshall</snm>
               <fnm>Dana</fnm>
               <insr iid="I1"/>
               <email>dmarshall@mmc.edu</email>
            </au>
            <au id="A2">
               <snm>Peirce</snm>
               <fnm>Jeremy</fnm>
               <insr iid="I2"/>
               <insr iid="I3"/>
            </au>
            <au id="A3">
               <snm>Zhou</snm>
               <fnm>Fang</fnm>
               <insr iid="I4"/>
            </au>
            <au id="A4">
               <snm>Lu</snm>
               <fnm>Lu</fnm>
               <insr iid="I3"/>
            </au>
            <au id="A5">
               <snm>Williams</snm>
               <fnm>Rob</fnm>
               <insr iid="I3"/>
            </au>
            <au id="A6">
               <snm>Manly</snm>
               <fnm>Ken</fnm>
               <insr iid="I3"/>
            </au>
            <au id="A7">
               <snm>Stuart</snm>
               <fnm>John</fnm>
               <insr iid="I4"/>
               <insr iid="I5"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Surgery, Meharry Medical College, Nashville, TN 37208, USA</p>
            </ins>
            <ins id="I2">
               <p>Illumina Inc., San Diego, CA, 92121, USA</p>
            </ins>
            <ins id="I3">
               <p>Department of Neuroscience, University of Tennessee Health Science Center, Memphis, TN 38104, USA</p>
            </ins>
            <ins id="I4">
               <p>Department of Rheumatology, University of Tennessee Health Science Center, Memphis, TN 38104, USA</p>
            </ins>
            <ins id="I5">
               <p>Research Division, Veterans Affairs Medical Center, Memphis, TN 38104, USA</p>
            </ins>
         </insg>
         <source>BMC Bioinformatics</source>
         <supplement>
            <title>
               <p>UT-ORNL-KBRIN Bioinformatics Summit 2008</p>
            </title>
            <editor>Eric C Rouchka and Julia Krushkal</editor>
            <note>Meeting abstracts &#8211; A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/pdf/1471-2105-9-S7-full.pdf">here</a>.</note>
         </supplement>
         <conference>
            <title>
               <p>UT-ORNL-KBRIN Bioinformatics Summit 2008</p>
            </title>
            <location>Cadiz, KY, USA</location>
            <date-range>28&#8211;30 March 2008</date-range>
            <url>http://www.kbrin.louisville.edu/summit/</url>
         </conference>
         <issn>1471-2105</issn>
         <pubdate>2008</pubdate>
         <volume>9</volume>
         <issue>Suppl 7</issue>
         <fpage>P10</fpage>
         <url>http://www.biomedcentral.com/1471-2105/9/S7/P10</url>
         <xrefbib>
            <pubid idtype="doi">10.1186/1471-2105-9-S7-P10</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>8</day>
               <month>7</month>
               <year>2008</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2008</year>
         <collab>Marshall et al; licensee BioMed Central Ltd.</collab>
      </cpyrt>
   </fm>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>B6 mice are of intermediate susceptibility to collagen-induced arthritis (CIA) while Balb/c mice are resistant, but are highly susceptible to proteoglycan-induced arthritis. Antigen presentation is H-2 directed but the disease that results is thought to be driven by regions outside of the MHC therefore, CXB mouse strains afford the opportunity to look at the influence of these regions on CIA. H2-b CXB strains are predicted to show variation in disease parameters relative to C57Bl/6, depending on which Balb/c chromosome regions is present. Nine of thirteen CXB strains are H-2b while one has a recombined H-2 region (CXB9). The four H-2d strains were crossed with C57Bl/6ByJ to generate F1 mice that could present collagen via the B6-contributed H-2b locus, while possibly identifying Balb/c loci that would have a dominant effect on disease progression. A number of disease and immunological parameters were collected and gene expression analysis was done on resting spleens. A range of incidence and severity of disease was seen and mice were assigned to susceptibility groups based on collected parameters. Preliminary QTL analysis has identified regions on chromosomes 13, 15 and 19 that correlate with susceptibility to CIA.</p>
      </sec>
   </bdy>
</art>
