Each placenta was inspected (morphology, weight, and cord position, calcification, etc).
Because of rapid neurodegeneration and accumulation of intracellular autofluorescent material are characteristic features of INCL pathology, we evaluated the morphology, weight, and the accumulation of autofluorescent material in the brain and in the spleen of WT, heterozygous, and Ppt1-KI mice.
The deposition mechanism has been correlated with the sol gel transition in sc-CO2 conditions and the impact of the deposition temperature, sol formulation and sc-CO2 flow rate on the membrane characteristics (morphology, weight increase and single gas permeance) have been discussed.
They developed without obvious alteration in gross morphology, weight, size, and fecundity compared to wild-type mice.
The degradation profile for foams of neat PDLLA and the influence of Bioglass® addition were comprehensively assessed in terms of changes in dimensional stability, pore morphology, weight loss, molecular weight and mechanical properties (dry and wet states).
Accordingly, we investigated the spleens from WT, heterozygous, and Ppt1-KI mice to determine the morphology, weight, the presence or absence of autofluorescence, and GRODs.
Various changes during degradation in vitro, which included changes in acidity of the degradation medium, morphology, weight, composition, molecular weight of the PLGA component and mechanical properties of the scaffold, were investigated.
The characteristics of scaffolds explored as a function of degradation time include crystalline structure, pore morphology, molecular weight, and wet/dry weight.
Direct synthesis from the vapor phase allows for in situ control of film morphology, molecular weight and crosslinking, and the combinatorial system decreases the time required to find the relationship between these interrelated properties.
The three sterilization techniques, ETO, γ and RFGD plasma, were compared in terms of their immediate and long-term effects on the dimensions, morphology, molecular weight and degradation profile of the scaffolds.
We found that both Lck-Cre/IFT20 f/f and CD4-Cre/IFT20 f/f mice were indistinguishable from their wild-type littermates in body size, as well as in the morphology and weight of the spleen and thymus.
