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The length of each dendritic branch was determined using the measuring tool on the StereoInvestigator software (MicroBrightField) and following the dendrite through the Z-axis; the number of branches was tabulated at the same time.
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The stability of the phylogenetic branching was determined using bootstrap analyses.
The robustness of the branch support was determined using 1000 bootstrap replicates.
The thickening of the ductal branches in the mammary glands was determined using the measuring tool in Adobe Acrobat X Pro.
Equilibrium frequencies, topologies, and branch lengths were optimized, the starting tree was determined using BioNJ, and both nearest-neighbor interchange (NNI) and subtree pruning and regrafting (SPR) algorithms for tree searching were used.
The pore size distribution of the prepared samples (Fig. 9) was determined using BJH method applied to the desorption branch.
Bootstrapping was determined using 10,000 replicates, MULTREES option off, TBR branch swapping, and five random addition sequences.
The pore size distribution (PSD) was determined using the Barrett Joyner–Halenda (BJH) method applied to the adsorption branch of the isotherm.
ML bootstrap support was determined using 100 bootstrap replicates, each using 10 random taxon addition replicates with TBR branch swapping.
Proteasome activity was determined using fluorescence assays.
Survival was determined using Kaplan Meier test.
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