Using an initially isotropic sample, we demonstrate that the constitutive model can reproduce the various anisotropies that have been observed in experiments and simulations.
By using human umbilical cord blood-derived EPCs spiked into a buffer solution or a blood sample, we demonstrate a capture rate of more than 50% for a traveling length of only 1 cm, which is clearly advantageous in terms of cell trapping efficiency and image processing speed.
Based on the simulation data analysis and analysis with the Parkinson disease case and control sample, we demonstrate that the likelihood based approach outperforms the trend test and logistic regression methods for an increased statistical power and reduced false positive inference, which are popularly implemented in the GWAS literature.
Using primer-shift PCR analysis of human tissue samples we demonstrated that following ischemia there is a large mitochondrial DNA (mtDNA) deletion (approximately 7.3 kb) that encompasses the region encoding 11 electron transport protein subunits [13].
Using a group of well-characterized samples, we demonstrated that CNVplex® was an efficient, highly reliable method with high sensitivity and specificity.
Using an exceptional panel of human thymic samples, we demonstrated that medullary thymus epithelial cells (mTECs) promote the generation of tTreg cells and favor their function.
In our study, with reconstruction and with clinical samples, we demonstrated melting temperatures of 76 ± 2 °C in the JP2 positive samples, and 82 ± 2 °C in the 652 positive samples; a double melting peak was obtained with both genotype mixtures tested.
Because their expression profiles and genetic backgrounds were thought to vary across the samples, we demonstrated several approaches to integrating individual assemblies derived from all of the samples (Fig. 4).
By analysis of 28 DCIS patient samples, we demonstrated that DCIS lesions expressing higher nuclear BCL9 (percentage of cells expressing nuclear BCL9) were more likely to be ER-negative, PR-negative, high nuclear grade, and high in HER2 expression.
In a pilot study using 96FASP for analysis of eight soluble urine samples, we demonstrated that protein profiles of technical replicates invariably clustered; the protein profiles for distinct urine donors were very different from each other.
