{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zhou A"],"funding":["NEI NIH HHS","NIMHD NIH HHS","NINDS NIH HHS"],"pagination":["40-55"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3249392"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["4(1)"],"pubmed_abstract":["In a recent study on ischemic rodent brains, we quantitatively characterised and compared brain proteomes under ischemic-preconditioned or injured or tolerant conditions. We discovered an enriched presence of repressive transcriptional regulator proteins with essential roles as epigenetic regulators in ischemic-tolerant brains (Stapels et al., 2010). We further showed their robust, dynamic and differential changes under different ischemic conditions in brains and in cultured neuronal cells. In the present work, using neuronal cell cultures, we aimed to characterise the nascent proteome, the proteome that presents early when the cells receive an ischemic insult. These would be the proteomic changes of newly synthesised proteins. Identification of effectors of this phase of response to ische"],"journal":["International journal of computational biology and drug design"],"pubmed_title":["Nascent proteomes of ischemic-injured and ischemic-tolerant neuronal cells."],"pmcid":["PMC3249392"],"funding_grant_id":["S21 MD000101","R01 NS057484","R01 NS057484-02","R01 NS057484-03","R01 NS057484-04","R01 NS057484-05","R01 NS024728","EY10572","NS24728-19","P30 EY010572","R01 NS057484-01A1"],"pubmed_authors":["Zhou A","Simon RP","David L"],"additional_accession":[]},"is_claimable":false,"name":"Nascent proteomes of ischemic-injured and ischemic-tolerant neuronal cells.","description":"In a recent study on ischemic rodent brains, we quantitatively characterised and compared brain proteomes under ischemic-preconditioned or injured or tolerant conditions. We discovered an enriched presence of repressive transcriptional regulator proteins with essential roles as epigenetic regulators in ischemic-tolerant brains (Stapels et al., 2010). We further showed their robust, dynamic and differential changes under different ischemic conditions in brains and in cultured neuronal cells. In the present work, using neuronal cell cultures, we aimed to characterise the nascent proteome, the proteome that presents early when the cells receive an ischemic insult. These would be the proteomic changes of newly synthesised proteins. Identification of effectors of this phase of response to ische","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011","modification":"2025-04-05T14:43:14.762Z","creation":"2019-10-26T13:34:46Z"},"accession":"S-EPMC3249392","cross_references":{"pubmed":["21330693"],"doi":["10.1504/IJCBDD.2011.038656","10.1504/ijcbdd.2011.038656"]}}