Authors have analysed the reporting of positive results in acupuncture [19] and low accessibility of studies [20] from foreign countries but there are few specific data available on the relative quality and quality of reporting of acupuncture trials in non-English language journals.
This could be a consequence of low accessibility of pores or, possibly, shielding of the bead surface by microscopic fragments of cryogelated PVA or agarose.
However, due to low accessibility of drinking water within study area several types of water borne diseases were observed as in Table 4 below.
It is shown that both the methods fail to preserve the activity of short ABD binders to hIFNγ due to either low accessibility of the binding site of the scaffold, or disruption of its tertiary structure.
Despite a widespread application of zeolites in catalysis, these microporous materials still suffer from a low accessibility of active sites located deep in crystals due to limited size of channels (< 1 nm).
In the context of contact rates, several authors (e.g., Baykara-Krumme 2010; Blohm and Diehl 2001; Koch 1997; Feskens et al. 2006) have reported a low accessibility of migrants (operationalized by the criterion citizenship) in Germany because of higher mobility (e.g., longer visits to the country of origin) or due to specific work schedules (e.g., shift work) or self-employment.
This is probably due to the relative low accessibility of pIX from capsid surface [20] [22] and spatial hindrance effect of antibody-conjugated gold particles against each other during staining.
One problem that remains to be resolved for this type of drug screening, however, is the low accessibility of compounds because the worm cuticle acts as a barrier to small molecule diffusion [30].
Interestingly, H1 staining was not observed in intact nuclei due to the low accessibility of the histones within condensed chromatin to the antibody, under the experimental conditions used for immunofluorescence staining (performed without permeabilization).
Two main factors could explain the reduction in xylanase activity: i) the low accessibility of the substrate to the enzyme and ii) disruptions in the structure of the enzyme that would result in the presence of inactive forms of xylanase in PBs.
