<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kochunov P</submitter><funding>NIBIB NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>65</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3340599</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3</volume><pubmed_abstract>&lt;h4>Background and purpose&lt;/h4>We hypothesized that the P-selectin (SELP) gene, localized to a region on chromosome 1q24, pleiotropically contributes to increased blood pressure and cerebral atrophy. We tested this hypothesis by performing genetic correlation analyses for 13 mRNA gene expression measures from P-selectin and 11 other genes located in 1q24 region and three magnetic resonance imaging derived indices of cerebral integrity.&lt;h4>Methods&lt;/h4>The subject pool consisted of 369 (219F; aged 28-85, average = 47.1 ± 12.7 years) normally aging, community-dwelling members of large extended Mexican-American families. Genetic correlation analysis decomposed phenotypic correlation coefficients into genetic and environmental components among 13 leukocyte-based mRNA gene expressions and three </pubmed_abstract><journal>Frontiers in genetics</journal><pubmed_title>P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans.</pubmed_title><pmcid>PMC3340599</pmcid><funding_grant_id>R01 MH078111</funding_grant_id><funding_grant_id>R01 MH083824</funding_grant_id><funding_grant_id>K01 EB006395</funding_grant_id><funding_grant_id>S10 RR029392</funding_grant_id><funding_grant_id>R37 MH059490</funding_grant_id><funding_grant_id>P01 HL045522</funding_grant_id><funding_grant_id>R01 DA027680</funding_grant_id><pubmed_authors>Cole SA</pubmed_authors><pubmed_authors>Johnson MP</pubmed_authors><pubmed_authors>Holcomb HH</pubmed_authors><pubmed_authors>Moses EK</pubmed_authors><pubmed_authors>Kochunov V</pubmed_authors><pubmed_authors>Blangero J</pubmed_authors><pubmed_authors>Goring H</pubmed_authors><pubmed_authors>Dyer TD</pubmed_authors><pubmed_authors>Almasy L</pubmed_authors><pubmed_authors>Kochunov P</pubmed_authors><pubmed_authors>Lancaster J</pubmed_authors><pubmed_authors>Winkler AM</pubmed_authors><pubmed_authors>Hong LE</pubmed_authors><pubmed_authors>Curran JE</pubmed_authors><pubmed_authors>Olvera RL</pubmed_authors><pubmed_authors>Mitchell B</pubmed_authors><pubmed_authors>Glahn DC</pubmed_authors><pubmed_authors>Duggirala R</pubmed_authors><pubmed_authors>Kent JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans.</name><description>&lt;h4>Background and purpose&lt;/h4>We hypothesized that the P-selectin (SELP) gene, localized to a region on chromosome 1q24, pleiotropically contributes to increased blood pressure and cerebral atrophy. We tested this hypothesis by performing genetic correlation analyses for 13 mRNA gene expression measures from P-selectin and 11 other genes located in 1q24 region and three magnetic resonance imaging derived indices of cerebral integrity.&lt;h4>Methods&lt;/h4>The subject pool consisted of 369 (219F; aged 28-85, average = 47.1 ± 12.7 years) normally aging, community-dwelling members of large extended Mexican-American families. Genetic correlation analysis decomposed phenotypic correlation coefficients into genetic and environmental components among 13 leukocyte-based mRNA gene expressions and three </description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2025-05-29T20:05:20.139Z</modification><creation>2019-06-05T17:16:02Z</creation></dates><accession>S-EPMC3340599</accession><cross_references><pubmed>22558002</pubmed><doi>10.3389/fgene.2012.00065</doi></cross_references></HashMap>