AS
Amar Bahadur Singh or Amar B. Singh
Also known as: Amar Singh
PAVIR/Plastic and Reconstructive Surgery, Stanford University, Stanford University School of Medicine, Central Drug Research Institute, Banaras Hindu University, University of Allahabad
Employment
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PAVIR/Plastic and Reconstructive Surgery, Stanford University Senior Researcher/Lab Manager2021 - Present
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Stanford University School of Medicine Senior Research Associate2018 - 2021
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Palo Alto Veterans Institute for Research Research Associate I2014 - 2018
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Stanford University School of Medicine Post-Doctoral Fellow2012 - 2014
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Texas A&M University Post-Doctoral Fellow2009 - 2011
Education
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Central Drug Research Institute Ph.D.2004 - 2009
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Banaras Hindu University MS2001 - 2003
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University of Allahabad BS1998 - 2001
Projects & Funding
Projects & funding information is unavailable.
Publications (52)
- Establishing a Murine Model of Muscle Changes in Chronic Nerve Compression Save
- Role of aging in nerve and muscle changes after chronic nerve compression in mice Save
- Human-Derived collagen hydrogel as an antibiotic vehicle for topical treatment of bacterial biofilms Save
- Mice deficient in ER protein seipin have reduced adrenal cholesteryl ester lipid droplet formation and utilization. Save
- Identification of p115 as a novel ACSL4 interacting protein and its role in regulating ACSL4 degradation. Save
- FXR activation promotes intestinal cholesterol excretion and attenuates hyperlipidemia in SR‐B1‐deficient mice fed a high‐fat and high‐cholesterol diet Save
- Berberine decreases plasma triglyceride levels and upregulates hepatic TRIB1 in LDLR wild type mice and in LDLR deficient mice. Save
- Activation of FXR by obeticholic acid induces hepatic gene expression of SR-BI through a novel mechanism of transcriptional synergy with the nuclear receptor LXR. Save
- Liver-specific knockdown of long-chain acyl-CoA synthetase 4 reveals its key role in VLDL-TG metabolism and phospholipid synthesis in mice fed a high-fat diet. Save
- Identification of a novel function of hepatic long-chain acyl-CoA synthetase-1 (ACSL1) in bile acid synthesis and its regulation by bile acid-activated farnesoid X receptor. Save