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Bo Deng, Ph.D. - Publications

Affiliations: 
2011 University of California, Los Angeles, Los Angeles, CA 
Area:
Physiology Biology, Cell Biology
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Men XM, Xu ZW, Tao X, Deng B, Qi KK. expression closely correlates with muscle fiber types in porcine muscle and regulates myosin heavy chains mRNA expression in C2C12 cells. Peerj. 9: e11065. PMID 33976958 DOI: 10.7717/peerj.11065  0.461
2012 Deng B, Wehling-Henricks M, Villalta SA, Wang Y, Tidball JG. IL-10 triggers changes in macrophage phenotype that promote muscle growth and regeneration. Journal of Immunology (Baltimore, Md. : 1950). 189: 3669-80. PMID 22933625 DOI: 10.4049/Jimmunol.1103180  0.756
2011 Villalta SA, Deng B, Rinaldi C, Wehling-Henricks M, Tidball JG. IFN-γ promotes muscle damage in the mdx mouse model of Duchenne muscular dystrophy by suppressing M2 macrophage activation and inhibiting muscle cell proliferation. Journal of Immunology (Baltimore, Md. : 1950). 187: 5419-28. PMID 22013114 DOI: 10.4049/Jimmunol.1101267  0.758
2011 Villalta SA, Rinaldi C, Deng B, Liu G, Fedor B, Tidball JG. Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype. Human Molecular Genetics. 20: 790-805. PMID 21118895 DOI: 10.1093/Hmg/Ddq523  0.77
2009 Deng B, Glanzman D, Tidball JG. Nitric oxide generated by muscle corrects defects in hippocampal neurogenesis and neural differentiation caused by muscular dystrophy. The Journal of Physiology. 587: 1769-78. PMID 19237426 DOI: 10.1113/Jphysiol.2008.166256  0.714
2009 Villalta SA, Nguyen HX, Deng B, Gotoh T, Tidball JG. Shifts in macrophage phenotypes and macrophage competition for arginine metabolism affect the severity of muscle pathology in muscular dystrophy. Human Molecular Genetics. 18: 482-96. PMID 18996917 DOI: 10.1093/Hmg/Ddn376  0.671
2005 Wehling-Henricks M, Jordan MC, Roos KP, Deng B, Tidball JG. Cardiomyopathy in dystrophin-deficient hearts is prevented by expression of a neuronal nitric oxide synthase transgene in the myocardium. Human Molecular Genetics. 14: 1921-33. PMID 15917272 DOI: 10.1093/Hmg/Ddi197  0.6
2004 Shiao T, Fond A, Deng B, Wehling-Henricks M, Adams ME, Froehner SC, Tidball JG. Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking alpha- and beta1-syntrophins. Human Molecular Genetics. 13: 1873-84. PMID 15238508 DOI: 10.1093/Hmg/Ddh204  0.684
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