Philip M. Bauer, Ph.D. - Publications

Affiliations: 
University of California, Los Angeles, Los Angeles, CA 
Area:
regulation and modulation of nitric oxide (NO) production and cytotoxicity in macrophages, vascular cells, and tumor cells

18 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
2015 Song GJ, Leslie KL, Barrick S, Mamonova T, Fitzpatrick JM, Drombosky KW, Peyser N, Wang B, Pellegrini M, Bauer PM, Friedman PA, Mierke DF, Bisello A. Phosphorylation of ezrin-radixin-moesin-binding phosphoprotein 50 (EBP50) by Akt promotes stability and mitogenic function of S-phase kinase-associated protein-2 (Skp2). The Journal of Biological Chemistry. 290: 2879-87. PMID 25492869 DOI: 10.1074/Jbc.M114.609768  0.347
2013 Bauer EM, Shapiro R, Billiar TR, Bauer PM. High mobility group Box 1 inhibits human pulmonary artery endothelial cell migration via a Toll-like receptor 4- and interferon response factor 3-dependent mechanism(s). The Journal of Biological Chemistry. 288: 1365-73. PMID 23148224 DOI: 10.1074/Jbc.M112.434142  0.347
2012 Yu J, Zhang Y, Zhang X, Rudic RD, Bauer PM, Altieri DC, Sessa WC. Endothelium derived nitric oxide synthase negatively regulates the PDGF-survivin pathway during flow-dependent vascular remodeling. Plos One. 7: e31495. PMID 22355372 DOI: 10.1371/Journal.Pone.0031495  0.418
2012 Song GJ, Barrick S, Leslie KL, Bauer PM, Alonso V, Friedman PA, Fiaschi-Taesch NM, Bisello A. The scaffolding protein EBP50 promotes vascular smooth muscle cell proliferation and neointima formation by regulating Skp2 and p21(cip1). Arteriosclerosis, Thrombosis, and Vascular Biology. 32: 33-41. PMID 22034511 DOI: 10.1161/Atvbaha.111.235200  0.345
2011 Gangopahyay A, Oran M, Bauer EM, Wertz JW, Comhair SA, Erzurum SC, Bauer PM. Bone morphogenetic protein receptor II is a novel mediator of endothelial nitric-oxide synthase activation. The Journal of Biological Chemistry. 286: 33134-40. PMID 21808054 DOI: 10.1074/Jbc.M111.274100  0.362
2011 Bernatchez P, Sharma A, Bauer PM, Marin E, Sessa WC. A noninhibitory mutant of the caveolin-1 scaffolding domain enhances eNOS-derived NO synthesis and vasodilation in mice. The Journal of Clinical Investigation. 121: 3747-55. PMID 21804187 DOI: 10.1172/Jci44778  0.386
2010 Bauer EM, Qin Y, Miller TW, Bandle RW, Csanyi G, Pagano PJ, Bauer PM, Schnermann J, Roberts DD, Isenberg JS. Thrombospondin-1 supports blood pressure by limiting eNOS activation and endothelial-dependent vasorelaxation. Cardiovascular Research. 88: 471-81. PMID 20610415 DOI: 10.1093/Cvr/Cvq218  0.318
2010 Rodriguez AI, Gangopadhyay A, Kelley EE, Pagano PJ, Zuckerbraun BS, Bauer PM. HO-1 and CO decrease platelet-derived growth factor-induced vascular smooth muscle cell migration via inhibition of Nox1. Arteriosclerosis, Thrombosis, and Vascular Biology. 30: 98-104. PMID 19875720 DOI: 10.1161/ATVBAHA.109.197822  0.392
2007 Li L, Hisamoto K, Kim KH, Haynes MP, Bauer PM, Sanjay A, Collinge M, Baron R, Sessa WC, Bender JR. Variant estrogen receptor-c-Src molecular interdependence and c-Src structural requirements for endothelial NO synthase activation. Proceedings of the National Academy of Sciences of the United States of America. 104: 16468-73. PMID 17921256 DOI: 10.1073/Pnas.0704315104  0.331
2005 Bernatchez PN, Bauer PM, Yu J, Prendergast JS, He P, Sessa WC. Dissecting the molecular control of endothelial NO synthase by caveolin-1 using cell-permeable peptides. Proceedings of the National Academy of Sciences of the United States of America. 102: 761-6. PMID 15637154 DOI: 10.1073/Pnas.0407224102  0.369
2005 Bauer PM, Yu J, Chen Y, Hickey R, Bernatchez PN, Looft-Wilson R, Huang Y, Giordano F, Stan RV, Sessa WC. Endothelial-specific expression of caveolin-1 impairs microvascular permeability and angiogenesis. Proceedings of the National Academy of Sciences of the United States of America. 102: 204-9. PMID 15615855 DOI: 10.1073/Pnas.0406092102  0.43
2003 Boo YC, Sorescu GP, Bauer PM, Fulton D, Kemp BE, Harrison DG, Sessa WC, Jo H. Endothelial NO synthase phosphorylated at SER635 produces NO without requiring intracellular calcium increase. Free Radical Biology & Medicine. 35: 729-41. PMID 14583337 DOI: 10.1016/S0891-5849(03)00397-6  0.411
2003 Bauer PM, Fulton D, Boo YC, Sorescu GP, Kemp BE, Jo H, Sessa WC. Compensatory phosphorylation and protein-protein interactions revealed by loss of function and gain of function mutants of multiple serine phosphorylation sites in endothelial nitric-oxide synthase. The Journal of Biological Chemistry. 278: 14841-9. PMID 12591925 DOI: 10.1074/Jbc.M211926200  0.339
2001 Bauer PM, Buga GM, Ignarro LJ. Role of p42/p44 mitogen-activated-protein kinase and p21waf1/cip1 in the regulation of vascular smooth muscle cell proliferation by nitric oxide. Proceedings of the National Academy of Sciences of the United States of America. 98: 12802-7. PMID 11592976 DOI: 10.1073/Pnas.211443198  0.529
2001 Bauer PM, Buga GM, Fukuto JM, Pegg AE, Ignarro LJ. Nitric oxide inhibits ornithine decarboxylase via S-nitrosylation of cysteine 360 in the active site of the enzyme. The Journal of Biological Chemistry. 276: 34458-64. PMID 11461922 DOI: 10.1074/Jbc.M105219200  0.557
2001 Ignarro LJ, Buga GM, Wei LH, Bauer PM, Wu G, del Soldato P. Role of the arginine-nitric oxide pathway in the regulation of vascular smooth muscle cell proliferation. Proceedings of the National Academy of Sciences of the United States of America. 98: 4202-8. PMID 11259671 DOI: 10.1073/Pnas.071054698  0.603
1999 Bauer PM, Fukuto JM, Buga GM, Pegg AE, Ignarro LJ. Nitric oxide inhibits ornithine decarboxylase by S-nitrosylation. Biochemical and Biophysical Research Communications. 262: 355-8. PMID 10462479 DOI: 10.1006/Bbrc.1999.1210  0.577
1998 Buga GM, Wei LH, Bauer PM, Fukuto JM, Ignarro LJ. NG-hydroxy-L-arginine and nitric oxide inhibit Caco-2 tumor cell proliferation by distinct mechanisms. The American Journal of Physiology. 275: R1256-64. PMID 9756558 DOI: 10.1152/Ajpregu.1998.275.4.R1256  0.595
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