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Individual specimens were independently analysed by two of us (M.P and F.S), without knowledge of mice genotype.
The histopathologic characteristics of all tumor specimens were independently reviewed by experienced hematopathologists.
The immunostained specimens were independently evaluated by two blinded investigators (HB and HO).
In each case, histopathologic specimens were independently reviewed by two pathologists.
The specimens were independently examined by an experienced pathologist (SI) and a resident (OB).
The histological specimens were independently assessed by two gastroenterologists with no knowledge of the clinical findings of the patients.
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Circumferentially deep-notched tensile specimens are independently employed to measure the cohesive strength of the adhesive as a function of constraint.
The evaluation of the specimens was independently performed by two investigators, who had no access to either the clinical data or the laboratory information for the patients of the study.
Trypsin-digested, fractionated peptides from each clinical specimen were independently identified and quantified using a MudPIT approach using HPLC-Chip nano ESI-MS/MS analysis.
The total number of spectra from either benign or PDAC specimen were independently normalized, and the normalized cumulative spectral counts of all the peptides for each protein were used as a measure of protein abundance.
All specimens were reviewed independently by two pathologists.
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