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Charles D. Smith

Researcher at University of Kentucky

Publications -  382
Citations -  19029

Charles D. Smith is an academic researcher from University of Kentucky. The author has contributed to research in topics: Kinase & Sphingosine. The author has an hindex of 75, co-authored 356 publications receiving 16915 citations. Previous affiliations of Charles D. Smith include University at Albany, SUNY & University of Washington.

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Early role of vascular dysregulation on late-onset Alzheimer’s disease based on multifactorial data-driven analysis

Yasser Iturria-Medina, +314 more
TL;DR: Imaging results suggest that intra-brain vascular dysregulation is an early pathological event during disease development, suggesting early memory deficit associated with the primary disease factors.
Journal Article

Discovery and evaluation of inhibitors of human sphingosine kinase.

TL;DR: These compounds are the first examples of nonlipid inhibitors of SK with in vivo antitumor activity and so provide leads for additional development of inhibitors of this important molecular target.
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Mutant V599EB-Raf regulates growth and vascular development of malignant melanoma tumors.

TL;DR: The mechanistic underpinnings by which mutant (V599E)B-RAF promotes melanoma development are identified and the effectiveness of targeting this protein to inhibit melanoma tumor growth is shown.
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Chemoattractant receptor-induced hydrolysis of phosphatidylinositol 4,5-bisphosphate in human polymorphonuclear leukocyte membranes. Requirement for a guanine nucleotide regulatory protein.

TL;DR: Results provide the first direct evidence that the fMet-Leu-Phe receptor in PMN membranes is coupled to polyphosphoinositide hydrolysis through an islet-activating protein-sensitive guanine nucleotide regulatory protein.
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Pharmacology and Antitumor Activity of ABC294640, a Selective Inhibitor of Sphingosine Kinase-2

TL;DR: Oral administration of ABC294640 to mice bearing mammary adenocarcinoma xenografts results in dose-dependent antitumor activity associated with depletion of S1P levels in the tumors and progressive tumor cell apoptosis, and this newly developed SK2 inhibitor provides an orally available drug candidate for the treatment of cancer and other diseases.