We also discuss recent work on tissue engineering for DSAEK grafts using cultured HCECs and HCEC precursor cell isolation method (the sphere-forming assay).
In a large number of measuring and characterization methods, the sphere size distribution of particles embedded in a medium has to be estimated from profile radii observed in cross sections or thin slices.
Here we redirect attention to a fast pseudospectral method on the sphere developed by Merilees in 1973, recently revived by Fornberg.
The incorporation of NAS functionality into acrylic microspheres for DNA microbiosensor application provides advantages of a simple preparation method where the spheres can be synthesised and functionalised via a one-step procedure using photopolymerisation in a short duration (several minutes).
In this contribution we propose a method for unfolding the sphere size distribution given a sample of profile radii which combines the advantages of kernel estimators with those of regularization methods.
An alternative method is called the sphere decoder (SD), and this has attracted significant attention in the last decade, due to the considerable complexity reduction it achieves [1, 2].
A variable resolution global spectral method is created on the sphere using High resolution Tropical Belt Transformation (HTBT).
Parameters measured in trabecular bone consisted of bone volume/tissue volume (BV/TV, %), direct trabecular thickness and trabecular spacing (Tb.Th⁎ and Tb.Sp⁎, µm) using the sphere method, bone surface/bone volume (BS/BV, mm− 1), trabecular number (Tb.N, mm− 1), structure model index (SMI), trabecular pattern factor (Tb.Pf), and degree of anisotropy (DA).
To our knowledge, there have been few reports on the isolation and long-term propagation of liver CSCs by the method of sphere culture.
Next, we propose a method for estimating the spheres on which source signals exist by using ICA solution and the near-field model.
It is different from our previous system based on the sphere fitting method.
