{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Petyuk VA"],"funding":["National Center for Research Resources","NIA NIH HHS","Medical Research Council","NIMH NIH HHS","National Institute for Health Research (NIHR)","NINDS NIH HHS","National Institutes of Health","NIH","National Institute of General Medical Sciences","NIGMS NIH HHS"],"pagination":["2721-2739"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6136080"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["141(9)"],"pubmed_abstract":["Our hypothesis is that changes in gene and protein expression are crucial to the development of late-onset Alzheimer&rsquo;s disease. Previously we examined how DNA alleles control downstream expression of RNA transcripts and how those relationships are changed in late-onset Alzheimer&rsquo;s disease. We have now examined how proteins are incorporated into networks in two separate series and evaluated our outputs in two different cell lines. Our pipeline included the following steps: (i) predicting expression quantitative trait loci; (ii) determining differential expression; (iii) analysing networks of transcript and peptide relationships; and (iv) validating effects in two separate cell lines. We performed all our analysis in two separate brain series to validate effects. Our two series i"],"journal":["Brain : a journal of neurology"],"pubmed_title":["The human brainome: network analysis identifies HSPA2 as a novel Alzheimer&rsquo;s disease target."],"pmcid":["PMC6136080"],"funding_grant_id":["P30 AG013846","P50 AG005128","P41GM103493","P30 AG053760","P50 AG005146","AG041232","P50 AG005681","P50 AG005144","G0502157","P41 GM103493","P30 AG019610","P41RR018522","G0900652","R01 AG041232","R01 AG034504","P50 AG005134","U01 AG016976","P50 AG005136","NF-SI-0611-10048","P30 AG010161","RF1 AG057457","P50-AG08671","RF1 AG015819","P50 MH060451","G1100540","G0400074","P50 NS039764","R01 AG017917","P50 AG016570"],"pubmed_authors":["Lieberman AP","Beckmann ND","Smith RD","Andreev V","Lovestone S","Myers AJ","Navarro L","Xie F","Ferrer I","Piehowski PD","Wang S","Schadt E","Engel A","De Jager P","Sue LI","Hardy JA","Morris CM","Reiman EM","Henrion MYR","Ervin JF","Chang R","Ramirez-Restrepo M","McKeith IG","Perry RH","Serrano GE","Hulette CM","Clarke J","Petyuk VA","Schneider JA","Bennett DA","Zhu K","Guettoche T","Woltjer RL","Beach TG","Albin RL","Mash DC","Huentelman MJ"],"additional_accession":[]},"is_claimable":false,"name":"The human brainome: network analysis identifies HSPA2 as a novel Alzheimer&rsquo;s disease target.","description":"Our hypothesis is that changes in gene and protein expression are crucial to the development of late-onset Alzheimer&rsquo;s disease. Previously we examined how DNA alleles control downstream expression of RNA transcripts and how those relationships are changed in late-onset Alzheimer&rsquo;s disease. We have now examined how proteins are incorporated into networks in two separate series and evaluated our outputs in two different cell lines. Our pipeline included the following steps: (i) predicting expression quantitative trait loci; (ii) determining differential expression; (iii) analysing networks of transcript and peptide relationships; and (iv) validating effects in two separate cell lines. We performed all our analysis in two separate brain series to validate effects. Our two series i","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Sep","modification":"2025-04-18T13:29:14.2Z","creation":"2019-03-26T23:56:53Z"},"accession":"S-EPMC6136080","cross_references":{"pubmed":["30137212"],"doi":["10.1093/brain/awy215"]}}