<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Powell DA</submitter><funding>National Institutes of Health</funding><pagination>206</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5350118</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8</volume><pubmed_abstract>Natural resistance-associated macrophage protein (NRAMP) encoded by the &lt;i>Slc11a1&lt;/i> gene is a membrane-associated transporter of divalent metal ions. Murine &lt;i>Slc11a1&lt;/i> has two known alleles, a functional &lt;i>Slc11a1&lt;/i>&lt;sup>Gly169&lt;/sup>, which is found in DBA2/J, NOD/LtJ, and 129p3/J and related mouse strains, and a non-functional &lt;i>Slc11a1&lt;/i>&lt;sup>Asp169&lt;/sup>, that is found in C56Bl/6J (B6) and BALB/cJ mice. B6 mice congenic for &lt;i>Slc11a1&lt;/i>&lt;sup>Gly169&lt;/sup> (B6-&lt;i>Slc11a1&lt;sup>G169&lt;/sup>&lt;/i> ) are markedly resistant to the intracellular pathogens &lt;i>Salmonella, Leishmania&lt;/i>, and &lt;i>Mycobacterium tuberculosis&lt;/i>. We examined the host cell response and replication of &lt;i>Francisella&lt;/i> in B6-&lt;i>Slc11a1&lt;sup>G169&lt;/sup>&lt;/i> mice. Bone marrow-derived macrophages from either B6-&lt;i>S</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Efficacy of Resistance to &lt;i>Francisella&lt;/i> Imparted by ITY/NRAMP/SLC11A1 Depends on Route of Infection.</pubmed_title><pmcid>PMC5350118</pmcid><funding_grant_id>U54 AIO57157-06</funding_grant_id><pubmed_authors>Powell DA</pubmed_authors><pubmed_authors>Frelinger JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy of Resistance to &lt;i>Francisella&lt;/i> Imparted by ITY/NRAMP/SLC11A1 Depends on Route of Infection.</name><description>Natural resistance-associated macrophage protein (NRAMP) encoded by the &lt;i>Slc11a1&lt;/i> gene is a membrane-associated transporter of divalent metal ions. Murine &lt;i>Slc11a1&lt;/i> has two known alleles, a functional &lt;i>Slc11a1&lt;/i>&lt;sup>Gly169&lt;/sup>, which is found in DBA2/J, NOD/LtJ, and 129p3/J and related mouse strains, and a non-functional &lt;i>Slc11a1&lt;/i>&lt;sup>Asp169&lt;/sup>, that is found in C56Bl/6J (B6) and BALB/cJ mice. B6 mice congenic for &lt;i>Slc11a1&lt;/i>&lt;sup>Gly169&lt;/sup> (B6-&lt;i>Slc11a1&lt;sup>G169&lt;/sup>&lt;/i> ) are markedly resistant to the intracellular pathogens &lt;i>Salmonella, Leishmania&lt;/i>, and &lt;i>Mycobacterium tuberculosis&lt;/i>. We examined the host cell response and replication of &lt;i>Francisella&lt;/i> in B6-&lt;i>Slc11a1&lt;sup>G169&lt;/sup>&lt;/i> mice. Bone marrow-derived macrophages from either B6-&lt;i>S</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-04T09:00:24.63Z</modification><creation>2019-03-27T02:38:38Z</creation></dates><accession>S-EPMC5350118</accession><cross_references><pubmed>28360906</pubmed><doi>10.3389/fimmu.2017.00206</doi></cross_references></HashMap>