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Comparative analysis of the promoter and intragenic regions of BoFLC paralogues with Arabidopsis FLC revealed extensive differences in overall structure and organisation but showed high conservation within those segments known to be essential in regulating FLC expression. We show that these two spectroscopies complement each other in such a way that a comparative study allows one to extract quantitative and unambiguous information about the underlying pairing structure and the phase of the SC gap. The required spatio-temporal resolution makes description of calcium signals difficult because of the low signal-to-noise ratio. Fasting insulin and lipid profile were measured and insulin resistance was determined using the homeostasis model assessment insulin resistance index (HOMA-R) and the quantitative insulin sensitivity check index.
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