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Analysis of knockout mice suggests a role for VGF in the control of fat storage and energy expenditure
Authors:Elizabeth Watson  Samira Fargali  Haruka Okamoto  Masato Sadahiro  Ronald E Gordon  Tandra Chakraborty  Mark W Sleeman  Stephen R Salton
Institution:(1) Department of Neuroscience, Mount Sinai School of Medicine, New York, NY, USA;(2) Regeneron Pharmaceuticals Inc., Tarrytown, NY, USA;(3) Department of Pathology, Mount Sinai School of Medicine, New York, NY, USA;(4) Biology Department, Adelphi University, Garden City, NY, USA;(5) Department of Geriatrics, Mount Sinai School of Medicine, New York, NY, USA
Abstract:

Background  

Previous studies of mixed background mice have demonstrated that targeted deletion of Vgf produces a lean, hypermetabolic mouse that is resistant to diet-, lesion-, and genetically-induced obesity. To investigate potential mechanism(s) and site(s) of action of VGF, a neuronal and endocrine secreted protein and neuropeptide precursor, we further analyzed the metabolic phenotypes of two independent VGF knockout lines on C57Bl6 backgrounds.
Keywords:
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