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In 2008, the NT Department of Health commissioned an evaluation to identify enabling factors and barriers to successful implementation of the Program, and to identify potential pathways for future development.
To identify the pharmacological network with a broad coverage of biological pathways for future development of a useful predictive tool, we extended the base pharmacological network to include intermediators that interacted with the known targets of DIPN drugs.
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The discovery of this signaling pathway lays the foundation for future development of GPR30-based therapies for PCa.
Our work has identified potentially new molecular targets for future development of therapeutic strategies in redirecting metabolic pathways of human cancer.
Needs for future development are also discussed.
General ideas for future development are discussed.
Both produced recommendations for future development.
Model for future development.
Implications for future development are discussed.
There are several issues for future development.
Framed as challenges for future development, these include the notion that dementia is a broad clinical outcome produced by underlying but heterogeneous neuropathological pathways.
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CEO of Professional Science Editing for Scientists @ prosciediting.com