<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ortiz S</submitter><funding>NCI NIH HHS</funding><pagination>1450-63</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3247199</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>235(12)</volume><pubmed_abstract>Activation of T lymphoma cells expressing Syk, but not ZAP-70 tyrosine kinase, has been shown to negatively regulate cell activation and activation-induced cell death (AICD), perhaps due to differential induction of tyrosine phosphorylation modified proteins. To better understand the role of these proteins and their associated molecules/pathways, we studied a previously described model of T lymphoma cells expressing either a kinase-activated chimeric Syk or ZAP-70 genetically linked to T-cell receptor (TCR) ζ chain (Z/Syk or Z/ZAP cells, respectively). To help identify molecules and pathways linked to cell activation or AICD, a comparative semi-quantitative proteomics-based approach was utilized to analyze tyrosine-phosphorylated protein immunoprecipitates from two-minute short-term activa</pubmed_abstract><journal>Experimental biology and medicine (Maywood, N.J.)</journal><pubmed_title>Comparative analyses of differentially induced T-cell receptor-mediated phosphorylation pathways in T lymphoma cells.</pubmed_title><pmcid>PMC3247199</pmcid><funding_grant_id>P50 CA107399</funding_grant_id><funding_grant_id>P30 CA033572</funding_grant_id><funding_grant_id>P30 CA33572</funding_grant_id><funding_grant_id>F31 CA117055</funding_grant_id><pubmed_authors>Smith D</pubmed_authors><pubmed_authors>Liu CP</pubmed_authors><pubmed_authors>Lee TD</pubmed_authors><pubmed_authors>Ortiz S</pubmed_authors><pubmed_authors>Lee W</pubmed_authors><pubmed_authors>Forman SJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative analyses of differentially induced T-cell receptor-mediated phosphorylation pathways in T lymphoma cells.</name><description>Activation of T lymphoma cells expressing Syk, but not ZAP-70 tyrosine kinase, has been shown to negatively regulate cell activation and activation-induced cell death (AICD), perhaps due to differential induction of tyrosine phosphorylation modified proteins. To better understand the role of these proteins and their associated molecules/pathways, we studied a previously described model of T lymphoma cells expressing either a kinase-activated chimeric Syk or ZAP-70 genetically linked to T-cell receptor (TCR) ζ chain (Z/Syk or Z/ZAP cells, respectively). To help identify molecules and pathways linked to cell activation or AICD, a comparative semi-quantitative proteomics-based approach was utilized to analyze tyrosine-phosphorylated protein immunoprecipitates from two-minute short-term activa</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Dec</publication><modification>2026-04-20T03:13:51.075Z</modification><creation>2026-04-20T03:10:03.847Z</creation></dates><accession>S-EPMC3247199</accession><cross_references><pubmed>21127342</pubmed><doi>10.1258/ebm.2010.010056</doi></cross_references></HashMap>