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    Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis. 

    Connelly, Jessica J; Crosslin, DR; Crossman, DC; Freedman, NJ; Ginsburg, Geoffrey Steven; Goldschmidt-Clermont, PJ; Granger, CB; ... (22 authors) (PLoS Genet, 2009-01)
    Neuropeptide Y (NPY) is a strong candidate gene for coronary artery disease (CAD). We have previously identified genetic linkage to familial CAD in the genomic region of NPY. We performed follow-up genetic, biostatistical, ...
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    Hybrid transgenic mice reveal in vivo specificity of G protein-coupled receptor kinases in the heart. 

    Benovic, JL; Duncan, SJ; Eckhart, AD; Koch, Walter J; Lefkowitz, Robert J; Penn, RB (Circ Res, 2000-01-07)
    G protein-coupled receptor kinases (GRKs) phosphorylate activated G protein-coupled receptors, including alpha(1B)-adrenergic receptors (ARs), resulting in desensitization. In vivo analysis of GRK substrate selectivity has ...
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    The CO/HO system reverses inhibition of mitochondrial biogenesis and prevents murine doxorubicin cardiomyopathy. 

    Ali, AS; Carraway, MS; Piantadosi, Claude Anthony; Reynolds, CM; Suliman, Hagir B; Welty-Wolf, KE (J Clin Invest, 2007-12)
    The clinical utility of anthracycline anticancer agents, especially doxorubicin, is limited by a progressive toxic cardiomyopathy linked to mitochondrial damage and cardiomyocyte apoptosis. Here we demonstrate that ...
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    Treatment with Imatinib in NSCLC is associated with decrease of phosphorylated PDGFR-beta and VEGF expression, decrease in interstitial fluid pressure and improvement of oxygenation. 

    Dewhirst, Mark Wesley; Herndon, James Emmett II; Rabbani, ZN; Vlahovic, G; Vujaskovic, Z (Br J Cancer, 2006-10-23)
    Elevated intratumoral interstitial fluid pressure (IFP) and tumour hypoxia are independent predictive factors for poor survival and poor treatment response in cancer patients. However, the relationship between IFP and tumour ...
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    Augmentation of cardiac contractility mediated by the human beta(3)-adrenergic receptor overexpressed in the hearts of transgenic mice. 

    Kohout, TA; Lefkowitz, Robert J; Mao, L; McDonald, Patricia H; Perry, SJ; Rockman, Howard A; Takaoka, H (Circulation, 2001-11-13)
    BACKGROUND: Stimulation of beta(1)- and beta(2)-adrenergic receptors (ARs) in the heart results in positive inotropy. In contrast, it has been reported that the beta(3)AR is also expressed in the human heart and that its ...
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    Gene expression signatures that predict radiation exposure in mice and humans. 

    Chao, Nelson J; Chute, JP; Dressman, HK; Ginsburg, Geoffrey Steven; Marshall, D; Meadows, Sarah K; Muramoto, Garrett G; ... (8 authors) (PLoS Med, 2007-04)
    BACKGROUND: The capacity to assess environmental inputs to biological phenotypes is limited by methods that can accurately and quantitatively measure these contributions. One such example can be seen in the context of exposure ...
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    Gene expression signatures of radiation response are specific, durable and accurate in mice and humans. 

    Chao, Nelson J; Chute, JP; Dressman, HK; Ginsburg, Geoffrey Steven; Himburg, Heather; Meadows, Sarah K; Muramoto, Garrett G; ... (10 authors) (PLoS One, 2008-04-02)
    BACKGROUND: Previous work has demonstrated the potential for peripheral blood (PB) gene expression profiling for the detection of disease or environmental exposures. METHODS AND FINDINGS: We have sought to determine the ...
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    beta-Arrestin1 mediates nicotinic acid-induced flushing, but not its antilipolytic effect, in mice. 

    Chen, JR; DeWire, SM; Kovacs, JJ; Lam, CM; Lefkowitz, Robert J; Muehlbauer, Michael J; Shukla, Arun Kumar; ... (10 authors) (J Clin Invest, 2009-05)
    Nicotinic acid is one of the most effective agents for both lowering triglycerides and raising HDL. However, the side effect of cutaneous flushing severely limits patient compliance. As nicotinic acid stimulates the GPCR ...
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    Differential mechanisms of morphine antinociceptive tolerance revealed in (beta)arrestin-2 knock-out mice. 

    Bohn, LM; Caron, MG; Lefkowitz, Robert J (J Neurosci, 2002-12-01)
    Morphine induces antinociception by activating mu opioid receptors (muORs) in spinal and supraspinal regions of the CNS. (Beta)arrestin-2 (beta)arr2), a G-protein-coupled receptor-regulating protein, regulates the muOR in ...
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    Enhanced rewarding properties of morphine, but not cocaine, in beta(arrestin)-2 knock-out mice. 

    Bohn, LM; Caron, MG; Dykstra, LA; Gainetdinov, RR; Lefkowitz, Robert J; Medvedev, IO; Sotnikova, TD (J Neurosci, 2003-11-12)
    The reinforcing and psychomotor effects of morphine involve opiate stimulation of the dopaminergic system via activation of mu-opioid receptors (muOR). Both mu-opioid and dopamine receptors are members of the G-protein-coupled ...
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    AuthorLefkowitz, Robert J (20)Koch, Walter J (6)Rockman, Howard A (5)Caron, MG (4)Ginsburg, Geoffrey Steven (4)Chao, Nelson J (3)Chute, JP (3)Dressman, HK (3)Meadows, Sarah K (3)Muramoto, Garrett G (3)... View MoreDate Issued2001 (6)2005 (3)2007 (3)2008 (3)2000 (2)2002 (2)2003 (2)2004 (2)2006 (2)2009 (2)TypeJournal article (27)SubjectAnimals (27)
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    Humans (12)Arrestins (10)beta-Arrestins (10)Male (9)Mice, Knockout (9)Mice, Transgenic (9)Myocardium (9)Female (7)... View MoreAffiliation of Duke Author(s)
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