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- W2100453417 abstract "Because the activity of mitochondrial glycerol phosphate dehydrogenase (mGPD) in the pancreatic β-cell is normally among the highest of the body, but is low in the pancreatic islets of numerous rodent models of NIDDM and is reported to be low in the islets of the few humans studied with NIDDM (1,2), it has been questioned whether mGPD might be a diabetes candidate gene. Linkage studies have failed to find an association between mGPD and NIDDM in Caucasians (3) and Mexican Americans (4), which suggests that mutations in mGPD are not a common cause of NIDDM. Since NIDDM is a multifactorial and heterogeneous disorder, it is possible that abnormalities in many individual genes influencing reactions that are important for the maintenance of normal glucose homeostasis in the β-cell will be found in a low percentage of individuals with NIDDM. With this idea in mind, conditions for using single-stranded conformational polymorphism (SSCP) analysis of the mGPD gene were developed to use this method to screen for mutations in this gene." @default.
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- W2100453417 date "1997-10-01" @default.
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- W2100453417 title "Single-Stranded Conformational Polymorphism Analysis of the Mitochondria! Glycerol Phosphate Dehydrogenase Gene in NIDDM" @default.
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- W2100453417 doi "https://doi.org/10.2337/diacare.46.10.1660" @default.
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