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(D H) FRAP curves generated as described in Fig. 4. Bar graphs representing the recovered fraction for each fluorescent protein analysed are inlayed in respective curve plots.

The bar graphs representing the peak areas from triplicate runs for each protein are shown in Figure  4.

(B ) Bar graphs representing the average percentage of ER-mitochondria intersections associated with mitochondrial constriction for each construct used.

Eustachian tube width measurements were made using ImageJ, and were plotted as bar graphs representing the mean and s.e.m.m

(F – H ) Bar graphs representing the quantification of activity, RAP, and RAP stimulation (decay method) by wild-type POT1-TPP1.

Figure  2 shows stacked bar graphs representing the expression of MCT4, PDK1 and CAIX in more detail, since these proteins were the ones exhibiting a clear expression in fibroblasts surrounding both benign and malignant glands.

Bar graphs represent the average of at least 3 independent measurements ± SD, and are normalized on C1 response.

Bar graphs represent the combined 1H and 15N chemical shift perturbations of 15N-UbcH5a athesese molar ratios.

From all the obtained FRET ratios, the average was taken and the error bars on the bar graphs represent the standard error of the mean (SEM).

Bar graphs represent the average of at least 3 independent measurements ± SD, and are normalized on the untreated condition per cell line.

Bar graphs represent the average±s.e.m. fMRI signal across individual subjects in the corresponding regions (two-tailed paired t-test, **P<0.001).