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All of the predicted genes contained within the interval Os09g01690 (Os09g0104300)-Os09g38790 (Os09g0560900) were inspected for expression data, and there were nine genes with 4-fold changes, including a protein belonging to the Ulp1 protease family, an ethylene-responsive protein containing an AP2/ERF domain, an F-box-like protein, blight-associated protein p12, and a ribosomal protein.
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FlyAtlas data [ 23] was also inspected for unique expression in testis and predominant expression in testis for retrogenes and neighboring genes.
Progeny were dissected in PBS, and brains were immediately inspected for GFP expression using a fluorescence dissection scope (Olympus, model BX51W1).
Fifty-one cancerous and noncancerous pairs of frozen samples were inspected for high SIRT1 expression by western blot analysis (Fig. 1).
Express were inspected for regions suitable for intergenomic SNP assays.
Expression QTLs (eQTLs) were mapped and the PR interval QTL was inspected for the co-incidence of eQTLs.
Electropherograms were visually inspected for heterozygous SNPs.
Data were inspected for normality.
Scanned images were inspected for artefacts.
The alignment was visually inspected for optimality.
Before analysis, variables were inspected for normality.
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