<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nagy Z</submitter><funding>British Heart Foundation</funding><funding>Medical Research Council</funding><pagination>331-343</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6484457</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>133(4)</volume><pubmed_abstract>Conditional knockout (KO) mouse models are invaluable for elucidating the physiological roles of platelets. The &lt;i>Platelet factor 4-Cre recombinase&lt;/i> (&lt;i>Pf4-Cre&lt;/i>) transgenic mouse is the current model of choice for generating megakaryocyte/platelet-specific KO mice. Platelets and leukocytes work closely together in a wide range of disease settings, yet the specific contribution of platelets to these processes remains unclear. This is partially a result of the &lt;i>Pf4-Cre&lt;/i> transgene being expressed in a variety of leukocyte populations. To overcome this issue, we developed a &lt;i>Gp1ba-Cre&lt;/i> transgenic mouse strain in which &lt;i>Cre&lt;/i> expression is driven by the endogenous &lt;i>Gp1ba&lt;/i> locus. By crossing &lt;i>Gp1ba-Cre&lt;/i> and &lt;i>Pf4-Cre&lt;/i> mice to the &lt;i>mT/mG&lt;/i> dual-fluorescence</pubmed_abstract><journal>Blood</journal><pubmed_title>The &lt;i>Gp1ba-Cre&lt;/i> transgenic mouse: a new model to delineate platelet and leukocyte functions.</pubmed_title><pmcid>PMC6484457</pmcid><funding_grant_id>FS/13/1/29894</funding_grant_id><funding_grant_id>RG/15/13/31673</funding_grant_id><funding_grant_id>GBT1564</funding_grant_id><funding_grant_id>FS/15/58/31784</funding_grant_id><pubmed_authors>Vogtle T</pubmed_authors><pubmed_authors>Gareus R</pubmed_authors><pubmed_authors>Di Nunzio G</pubmed_authors><pubmed_authors>Geer MJ</pubmed_authors><pubmed_authors>Tarakhovsky A</pubmed_authors><pubmed_authors>Neel BG</pubmed_authors><pubmed_authors>Desanti GE</pubmed_authors><pubmed_authors>Weiss A</pubmed_authors><pubmed_authors>Senis YA</pubmed_authors><pubmed_authors>Mazharian A</pubmed_authors><pubmed_authors>Heising S</pubmed_authors><pubmed_authors>Mori J</pubmed_authors><pubmed_authors>Nagy Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>The &lt;i>Gp1ba-Cre&lt;/i> transgenic mouse: a new model to delineate platelet and leukocyte functions.</name><description>Conditional knockout (KO) mouse models are invaluable for elucidating the physiological roles of platelets. The &lt;i>Platelet factor 4-Cre recombinase&lt;/i> (&lt;i>Pf4-Cre&lt;/i>) transgenic mouse is the current model of choice for generating megakaryocyte/platelet-specific KO mice. Platelets and leukocytes work closely together in a wide range of disease settings, yet the specific contribution of platelets to these processes remains unclear. This is partially a result of the &lt;i>Pf4-Cre&lt;/i> transgene being expressed in a variety of leukocyte populations. To overcome this issue, we developed a &lt;i>Gp1ba-Cre&lt;/i> transgenic mouse strain in which &lt;i>Cre&lt;/i> expression is driven by the endogenous &lt;i>Gp1ba&lt;/i> locus. By crossing &lt;i>Gp1ba-Cre&lt;/i> and &lt;i>Pf4-Cre&lt;/i> mice to the &lt;i>mT/mG&lt;/i> dual-fluorescence</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2026-04-29T01:16:59.046Z</modification><creation>2025-05-29T19:47:28.977Z</creation></dates><accession>S-EPMC6484457</accession><cross_references><pubmed>30429161</pubmed><doi>10.1182/blood-2018-09-877787</doi></cross_references></HashMap>