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A number of research studies in academic settings have suggested that this method, called "sequential double blind", would lead to fewer witness errors than traditional line-ups.
It is suggested that this method may be applicable for tolerance induction to blood group antigens in patients receiving ABO incompatible allografts.
When we applied this improved method to Arabidopsis thaliana and Oryza sativa for validation, the results suggested that this method was sensitive and efficient, as it was capable of detecting as little as 1 to 5 μg of total RNA.
Nevertheless, follow-up researchers suggested that this method is of low reproducibility and laborious to screen for double-crossover integration events [34], [38].
However, Paris et al. showed that the UV fluorescence method produced a high rate of false positives and suggested that this method be abandoned as a LAMP read-out [15].
These advantageous features of sonoporation-based transformation suggested that this method can be readily adapted for high-throughput or remotely controlled screening and testing of genetic transformation schemes, where a large number of transformation experiments are performed in parallel, with or without robots.
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Our results suggest that this method is generally applicable to GPCRs.
The results suggest that this method is very efficient and effective.
Our findings suggest that this method could lay the foundation for treating severe degenerative brain disease.
This study suggests that this method might be a safe, easy, and effective management of paediatric condylar fractures.
These results suggest that this method may be a valuable tool in quantifying patellofemoral joint contact area in-vivo.
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