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To the best of our knowledge no population based screening method for ADPKD has yet been devised.
As an alternative to bisulphite sequencing, we present a restriction enzyme based screening method for the identification of committed Tregs and apply this method to evaluate the effect of various culturing conditions.
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This reflects the general deficiency of HPV DNA based screening methods, and need for complementary cytology.
Current methods for detecting MCs range from simple biological based screening methods to more complex analytical techniques such as mass spectrometry [ 16].
A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.
The restriction enzyme based screening method we describe provides a helpful tool for determination of Treg commitment as well as optimization of culturing conditions for Treg generation.
However, in a recent study we have developed a new microtiter plate-based screening method that is far more suitable for the study of xylanase action on complex biomass [ 24].
The objective is to provide a quantitative EEG-based screening method for the alcohol abuser.
Presented data is promising to design a gene panel and develop a blood-based screening method for breast cancer which relies on pathologic methylation changes.
Taken together, we developed an efficient FACS-based screening method for high antibody-producing CHO cells with the benefits of the split GFP system.
This putrescine oxidase was discovered by using a plate-based screening method for oxidase activity, which has been used before to screen for improved mutants during directed evolution experiments (Alexeeva et al. 2002).
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