<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(5)</volume><submitter>Mullin BH</submitter><pubmed_abstract>Osteoporosis is a common bone disease that has a strong genetic component. Genome-wide linkage studies have identified the chromosomal region 3p14-p22 as a quantitative trait locus for bone mineral density (BMD). We have previously identified associations between variation in two related genes located in 3p14-p22, ARHGEF3 and RHOA, and BMD in women. In this study we performed knockdown of these genes using small interfering RNA (siRNA) in human osteoblast-like and osteoclast-like cells in culture, with subsequent microarray analysis to identify genes differentially regulated from a list of 264 candidate genes. Validation of selected findings was then carried out in additional human cell lines/cultures using quantitative real-time PCR (qRT-PCR). The qRT-PCR results showed significant down-r</pubmed_abstract><journal>PloS one</journal><pagination>e98116</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4026532</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Influence of ARHGEF3 and RHOA knockdown on ACTA2 and other genes in osteoblasts and osteoclasts.</pubmed_title><pmcid>PMC4026532</pmcid><pubmed_authors>Mamotte C</pubmed_authors><pubmed_authors>Wilson SG</pubmed_authors><pubmed_authors>Mullin BH</pubmed_authors><pubmed_authors>Prince RL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Influence of ARHGEF3 and RHOA knockdown on ACTA2 and other genes in osteoblasts and osteoclasts.</name><description>Osteoporosis is a common bone disease that has a strong genetic component. Genome-wide linkage studies have identified the chromosomal region 3p14-p22 as a quantitative trait locus for bone mineral density (BMD). We have previously identified associations between variation in two related genes located in 3p14-p22, ARHGEF3 and RHOA, and BMD in women. In this study we performed knockdown of these genes using small interfering RNA (siRNA) in human osteoblast-like and osteoclast-like cells in culture, with subsequent microarray analysis to identify genes differentially regulated from a list of 264 candidate genes. Validation of selected findings was then carried out in additional human cell lines/cultures using quantitative real-time PCR (qRT-PCR). The qRT-PCR results showed significant down-r</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-04T08:42:21.988Z</modification><creation>2019-03-26T23:25:40Z</creation></dates><accession>S-EPMC4026532</accession><cross_references><pubmed>24840563</pubmed><doi>10.1371/journal.pone.0098116</doi></cross_references></HashMap>