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In addition, the ability to maintain high-level expression of defined proteins in human cells for many days without genetic manipulation highlights the potential importance of long-RNA transfection in the development of reprogramming methods for therapeutic applications.
There are many potential methods for therapeutic monitoring.
Induction methods for therapeutic cooling are under investigated.
Induction methods for therapeutic cooling are underinvestigated [ 4].
Consequently, researchers are actively searching for cheaper and safer methods for therapeutic treatment.
Better methods for therapeutic gene correction and to promote iPSC differentiation into transplantable hematopoietic cells are also needed.
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However, consensus has not been achieved regarding the ideal method for therapeutic hypothermia (TH).
Our approach offers a paradigm for future use of network biology concept and method for therapeutic intervention in HCC.
Inhibition of MAOA might have potential in sepsis and so provide a novel method for therapeutic intervention.
However, whereas AAV vectors may provide a relatively safe in vivo delivery method for therapeutic genes, recombinant adenovirus may induce a severe immune response in patients.
The use of monoclonal antibodies as a drug delivery vehicles, or trigger for human immune response is already an accepted method for therapeutic treatment of patients in modern clinical oncology [ 2, 3].
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