In summary, we have identified HPV DNA in the majority of histologically-proven giant cell (temporal) arteritis specimens and validated these results by a completely independent outside laboratory assay.
Taiga Kasuya reexamined the type specimen and validated the species in a 2007 Mycoscience publication.
In addition, we assessed the measurement repeatability of the ESPI technique on an immersed rubber specimen, and validated the compensation technique proposed herein by comparing the displacement fields obtained between identical tests performed while the specimen was immersed in either air or phosphate-buffered saline (PBS).
Numerical simulations were carried out to design the test specimen geometry and validate data reduction procedures for the dynamic interface experiments.
The method is used to characterize eight impacted elastomeric specimens and is validated with comparisons between experimental and simulation results.
For meta-analyses, we chose ten data sets with pathological annotation of ER status based on IHC, EIA or both, incorporating a total of 1975 breast cancer specimens to derive and validate the classifiers for ER status (Table 1).
All cell lines were validated by demonstrating unique clonal cytogenetic aberrations within 10 passages of the present studies (MESO924, MESO257, MESO296, and MESO257 were validated by comparison with the corresponding surgical specimens, and JMN1B was validated by comparison with published cytogenetic aberrations).
The present work shows baseline concordant changes between PBMCs, plasma specimens, and brain, thus validating our human peripheral blood sample study with AD patients, pointing to circulating RNAs as an accessible and noninvasive biological source to detect changes in brain.
Firstly the monotonic and secondly the cyclic FE models of these specimens are discussed and validated.
The finite element (FE) models of test specimens were developed and validated against experimental results.
