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It is worth noting that approximately half of the genes in our microarray study were down-regulated by Cobra1 knockdown.
Protein lysates (20 µg of total protein) from the same skeletal muscle samples used for the microarray study were separated on 10% BIS-TRIS gels and proteins were transferred to nitrocellulose membranes (all from Invitrogen).
Data from each microarray study were normalised by global normalisation.
Data from each microarray study were subjected to global normalisation.
Data from each microarray study were normalised by the global normalisation method.
A total of 14 mature miRNAs from the microarray study were selected for qRT-PCR.
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A GeneChip microarray study was designed to compare gene expression profiles of BZA to that of other SERMs, raloxifene (RAL) and lasofoxifene (LAS).
In order to gain insights into MPP+-induced neurotoxicity, a gene expression microarray study was performed using a midbrain-derived dopaminergic neuronal cell line, MN9D.
A microarray study was performed to identify the sdiA regulon of E. coli.
Raw data of this microarray study are available at the GEO website (GSE2259).
A microarray study was undertaken to define the gene expression profile in response to exosome treatment on a global scale.
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