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No significant difference between groups at baseline were detected using two-sample t-test Fig. 1 Mean plaque index (PI) score for each group throughout the study.
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Briefly, single peak sIPSCs with amplitudes greater than 2.1 times the SD of baseline noise were detected using a semiautomated sliding template detection procedure with AxoGraph X.
The blood samples of all individuals were detected using an Illumina HumanHap 550K v3.0 genotyping chip, and these data were quantile normalized to the same baseline for further analysis.
The proteins were detected using enhanced chemiluminescence.
Mendelian inconsistencies were detected using PedCheck (v.1.1) [35].
Then, putative TFBS were detected using Genomatix.
Protein bands were detected using ECL (Amersham).
Antigens were detected using standard protocols.
Protein bands were detected using SuperSignal Substrate (Pierce).
Bands were detected using ECL Western Blotting Detection Reagent (Amersham Biosciences).
Immunoreactive bands were detected using BCIP/NBT solution.
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