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SiDMAP – Metabolomics for Drug Development

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← Combined genomics and targeted tracer fate association approach utilized in characterizing stress response in cancer
SiDMAP’s scientific advisor delivers talk showing single [1,2-13C2]-D-Glucose tracer cross-labels intracellular stearic acid and better traces mechanistic rosiglitazone response than what was obtained with extracellular [U-13C18]-stearate incubation in a separate study using HepG2 cells. →

Targeted tracer fate association study finds links among metformin, cholesterol, K-ras and pancreatic cancer growth-control

by admin Posted on July 12, 2013

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← Combined genomics and targeted tracer fate association approach utilized in characterizing stress response in cancer
SiDMAP’s scientific advisor delivers talk showing single [1,2-13C2]-D-Glucose tracer cross-labels intracellular stearic acid and better traces mechanistic rosiglitazone response than what was obtained with extracellular [U-13C18]-stearate incubation in a separate study using HepG2 cells. →

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  • News

    • SiDMAP’s scientific advisor delivers talk showing single [1,2-13C2]-D-Glucose tracer cross-labels intracellular stearic acid and better traces mechanistic rosiglitazone response than what was obtained with extracellular [U-13C18]-stearate incubation in a separate study using HepG2 cells.
    • Targeted tracer fate association study finds links among metformin, cholesterol, K-ras and pancreatic cancer growth-control
    • Combined genomics and targeted tracer fate association approach utilized in characterizing stress response in cancer
    • SiDMAP Collaboration with University of Utah School of Medicine Published in FASEB Journal
    • SiDMAP Collaboration With National Cancer Institute To Be Presented at The 2013 World Biotechnology Conference
    • Global Metabolomics Market to Reach $863.8 Million by 2017, According to a New Report by Global Industry Analysts, Inc.
    • SiDMAP studies of two Amgen anti-diabetic agents demonstrate mechanisms of glucose homeostatis regulation and energy metabolism.
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