<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liao W</submitter><funding>Science and Technology Projects of Jiangxi Provincial Education Department</funding><funding>the Leading Talents Project of Jiangxi Provincial Science and the Technology Department’s Training Plan for Major Disciplines and Technical Leaders</funding><funding>the Leading Talents Project of Jiangxi Provincial Science and the Technology Department's Training Plan for Major Disciplines and Technical Leaders</funding><funding>the National Natural Science Foundation of China</funding><funding>General science and technology projects of Jiangxi Provincial Health Commission</funding><pagination>300</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10239159</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>There is a mutual hemodynamic and pathophysiological basis between the heart and brain. Glutamate (GLU) signaling plays an important role in the process of myocardial ischemia (MI) and ischemic stroke (IS). To further explore the common protective mechanism after cardiac and cerebral ischemic injuries, the relationship between GLU receptor-related genes and MI and IS were analyzed.&lt;h4>Results&lt;/h4>A total of 25 crosstalk genes were identified, which were mainly enriched in the Toll-like receptor signaling pathway, Th17 cell differentiation, and other signaling pathways. Protein-protein interaction analysis suggested that the top six genes with the most interactions with shared genes were IL6, TLR4, IL1B, SRC, TLR2, and CCL2. Immune infiltration analysis suggested that imm</pubmed_abstract><journal>BMC genomics</journal><pubmed_title>Bioinformatics and experimental analyses of glutamate receptor and its targets genes in myocardial and cerebral ischemia.</pubmed_title><pmcid>PMC10239159</pmcid><funding_grant_id>No. 81960326</funding_grant_id><funding_grant_id>GJ2201436</funding_grant_id><funding_grant_id>No. 202210884</funding_grant_id><funding_grant_id>No. 20213BCJ0001</funding_grant_id><pubmed_authors>Zhou M</pubmed_authors><pubmed_authors>Zeng C</pubmed_authors><pubmed_authors>He C</pubmed_authors><pubmed_authors>Hu S</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Luo M</pubmed_authors><pubmed_authors>Liao W</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Duan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bioinformatics and experimental analyses of glutamate receptor and its targets genes in myocardial and cerebral ischemia.</name><description>&lt;h4>Background&lt;/h4>There is a mutual hemodynamic and pathophysiological basis between the heart and brain. Glutamate (GLU) signaling plays an important role in the process of myocardial ischemia (MI) and ischemic stroke (IS). To further explore the common protective mechanism after cardiac and cerebral ischemic injuries, the relationship between GLU receptor-related genes and MI and IS were analyzed.&lt;h4>Results&lt;/h4>A total of 25 crosstalk genes were identified, which were mainly enriched in the Toll-like receptor signaling pathway, Th17 cell differentiation, and other signaling pathways. Protein-protein interaction analysis suggested that the top six genes with the most interactions with shared genes were IL6, TLR4, IL1B, SRC, TLR2, and CCL2. Immune infiltration analysis suggested that imm</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-05-29T19:22:50.139Z</modification><creation>2025-04-06T11:13:35.098Z</creation></dates><accession>S-EPMC10239159</accession><cross_references><pubmed>37268894</pubmed><doi>10.1186/s12864-023-09408-z</doi></cross_references></HashMap>