Ira Tabas

Ira Tabas

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Ira Tabas

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Inflammation and its resolution in atherosclerosis: mediators and therapeutic opportunities.

Nat Rev Cardiol 2019 Jul;16(7):389-406

Atherosclerosis Research Laboratory, Wihuri Research Institute, Helsinki, Finland.

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http://dx.doi.org/10.1038/s41569-019-0169-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727648PMC
July 2019

TAM receptors in cardiovascular disease.

Cardiovasc Res 2019 Jul;115(8):1286-1295

Centre for Immunobiology, Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Sir Graeme Davies Building, 120 University Place, Glasgow, UK.

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http://dx.doi.org/10.1093/cvr/cvz100DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587925PMC
July 2019

Dachshund Depletion Disrupts Mammary Gland Development and Diverts the Composition of the Mammary Gland Progenitor Pool.

Stem Cell Reports 2019 Jan 13;12(1):135-151. Epub 2018 Dec 13.

Pennsylvania Cancer and Regenerative Medicine Research Center, Baruch S. Blumberg Institute, 3805 Old Easton Road, Doylestown, PA 18902, USA; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 637551, Singapore. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22136711183047
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http://dx.doi.org/10.1016/j.stemcr.2018.11.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335505PMC
January 2019

Macrophage Inflammation, Erythrophagocytosis, and Accelerated Atherosclerosis in Jak2 Mice.

Circ Res 2018 11;123(11):e35-e47

From the Division of Molecular Medicine, Department of Medicine (W.W., W.L., T.F., Y.W., Y.T., C.W., B.C., I.T., A.R.T., N.W.), Columbia University Medical Center, New York, NY.

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http://dx.doi.org/10.1161/CIRCRESAHA.118.313283DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309796PMC
November 2018

Regulatory T Cells Promote Macrophage Efferocytosis during Inflammation Resolution.

Immunity 2018 10 2;49(4):666-677.e6. Epub 2018 Oct 2.

Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA; Department of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10747613183033
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http://dx.doi.org/10.1016/j.immuni.2018.07.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192849PMC
October 2018

Macrophage Trafficking, Inflammatory Resolution, and Genomics in Atherosclerosis: JACC Macrophage in CVD Series (Part 2).

J Am Coll Cardiol 2018 10;72(18):2181-2197

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York. Electronic address:

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http://dx.doi.org/10.1016/j.jacc.2018.08.2147DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522246PMC
October 2018

A New Activator of Hepatocyte CaMKII in Fasting and Type 2 Diabetes.

Diabetes 2018 09;67(9):1742-1744

Department of Medicine, Columbia University Irving Medical Center, New York, NY

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http://diabetes.diabetesjournals.org/lookup/doi/10.2337/dbi1
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http://dx.doi.org/10.2337/dbi18-0026DOI Listing
September 2018

MerTK signaling in macrophages promotes the synthesis of inflammation resolution mediators by suppressing CaMKII activity.

Sci Signal 2018 09 25;11(549). Epub 2018 Sep 25.

Departments of Medicine, Pathology and Cell Biology, and Physiology, Columbia University, New York, NY 10032, USA.

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http://stke.sciencemag.org/lookup/doi/10.1126/scisignal.aar3
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http://dx.doi.org/10.1126/scisignal.aar3721DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171110PMC
September 2018

The role of non-resolving inflammation in atherosclerosis.

J Clin Invest 2018 07 2;128(7):2713-2723. Epub 2018 Jul 2.

Department of Medicine.

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https://www.jci.org/articles/view/97950
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http://dx.doi.org/10.1172/JCI97950DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025992PMC
July 2018

Hepatocyte-secreted DPP4 in obesity promotes adipose inflammation and insulin resistance.

Nature 2018 03 21;555(7698):673-677. Epub 2018 Mar 21.

Department of Medicine, Columbia University Medical Center, New York, New York 10032, USA.

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http://dx.doi.org/10.1038/nature26138DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021131PMC
March 2018

Mechanisms and Consequences of Defective Efferocytosis in Atherosclerosis.

Front Cardiovasc Med 2017 8;4:86. Epub 2018 Jan 8.

Department of Medicine, Columbia University, New York, NY, United States.

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http://dx.doi.org/10.3389/fcvm.2017.00086DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770804PMC
January 2018

Mitochondrial Fission Promotes the Continued Clearance of Apoptotic Cells by Macrophages.

Cell 2017 Oct 21;171(2):331-345.e22. Epub 2017 Sep 21.

Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA; Department of Physiology, Columbia University, New York, NY 10032, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2017.08.041DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679712PMC
October 2017

Monocyte-Macrophages and T Cells in Atherosclerosis.

Immunity 2017 10;47(4):621-634

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA. Electronic address:

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http://dx.doi.org/10.1016/j.immuni.2017.09.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747297PMC
October 2017

MerTK Cleavage on Resident Cardiac Macrophages Compromises Repair After Myocardial Ischemia Reperfusion Injury.

Circ Res 2017 Sep 29;121(8):930-940. Epub 2017 Aug 29.

From the Department of Pathology and Feinberg Cardiovascular Research Institute, Feinberg School of Medicine, Northwestern University, Chicago, IL (M.D., X.Y.Y., S.D., S.Z., L.G., S.M., D.P., X.Z., D.C.Le., W.A.M., X.L., E.B.T.); Division of Molecular Medicine at Columbia University, New York (I.T.); and Department of Immunobiology, School of Medicine, Yale University (C.R.).

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http://dx.doi.org/10.1161/CIRCRESAHA.117.311327DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623080PMC
September 2017

Mitochondrial Oxidative Stress Promotes Atherosclerosis and Neutrophil Extracellular Traps in Aged Mice.

Arterioscler Thromb Vasc Biol 2017 08 8;37(8):e99-e107. Epub 2017 Jun 8.

From the Division of Cardiology (Y.W.), Division of Molecular Medicine (W.W, A.R.T., I.T.), Division of Molecular Medicine, Department of Medicine (N.W.), Columbia University Medical Center, New York, NY.

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http://dx.doi.org/10.1161/ATVBAHA.117.309580DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535797PMC
August 2017

microRNA-33 Regulates Macrophage Autophagy in Atherosclerosis.

Arterioscler Thromb Vasc Biol 2017 06 20;37(6):1058-1067. Epub 2017 Apr 20.

From the Marc and Ruti Bell Vascular Biology and Disease Program, Leon H. Charney Division of Cardiology, Department of Medicine (M.O., H.E., M.S.A., R.C.B., K.R., E.A.F., K.J.M.) and Division of Vascular Surgery, Department of Surgery (B.R.), New York University Medical Center; Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Canada (R.S., K.J.R., J.P.P.); National Research Council of Canada, Ottawa, Ontario (R.S., J.P.P.); Departments of Medicine, Pathology and Cell Biology, Columbia University, New York (X.L., I.T.); and University of Ottawa Heart Institute, Ontario, Canada (K.J.R.).

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http://dx.doi.org/10.1161/ATVBAHA.116.308916DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494696PMC
June 2017

Boosting Inflammation Resolution in Atherosclerosis: The Next Frontier for Therapy.

Am J Pathol 2017 Jun;187(6):1211-1221

Departments of Medicine, Pathology and Cell Biology, and Physiology, Columbia University Medical Center, New York, New York.

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http://dx.doi.org/10.1016/j.ajpath.2017.01.018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455064PMC
June 2017

2016 Russell Ross Memorial Lecture in Vascular Biology: Molecular-Cellular Mechanisms in the Progression of Atherosclerosis.

Authors:
Ira Tabas

Arterioscler Thromb Vasc Biol 2017 Feb 15;37(2):183-189. Epub 2016 Dec 15.

From the Departments of Medicine, Pathology and Cell Biology, and Physiology, Columbia University, New York.

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http://dx.doi.org/10.1161/ATVBAHA.116.308036DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269511PMC
February 2017

Deficiency of AXL in Bone Marrow-Derived Cells Does Not Affect Advanced Atherosclerotic Lesion Progression.

Sci Rep 2016 12 13;6:39111. Epub 2016 Dec 13.

Department of Medicine, Columbia University Medical Center, New York, USA.

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http://dx.doi.org/10.1038/srep39111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153620PMC
December 2016

Hepatocyte TAZ/WWTR1 Promotes Inflammation and Fibrosis in Nonalcoholic Steatohepatitis.

Cell Metab 2016 12 27;24(6):848-862. Epub 2016 Oct 27.

Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA; Department of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cmet.2016.09.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226184PMC
December 2016

An imbalance between specialized pro-resolving lipid mediators and pro-inflammatory leukotrienes promotes instability of atherosclerotic plaques.

Nat Commun 2016 Sep 23;7:12859. Epub 2016 Sep 23.

Department of Anesthesiology, Perioperative and Pain Medicine, Departments of Medicine, Pathology &Cell Biology, and Physiology, Columbia University Medical Center, 630 West 168th Street, New York, New York 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036151PMC
http://dx.doi.org/10.1038/ncomms12859DOI Listing
September 2016

Heart disease: Death-defying plaque cells.

Authors:
Ira Tabas

Nature 2016 08 20;536(7614):32-3. Epub 2016 Jul 20.

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http://dx.doi.org/10.1038/nature18916DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103697PMC
August 2016

Suppression of Adaptive Immune Cell Activation Does Not Alter Innate Immune Adipose Inflammation or Insulin Resistance in Obesity.

PLoS One 2015 28;10(8):e0135842. Epub 2015 Aug 28.

Department of Medicine, Columbia University, New York, NY, 10032, United States of America; Department of Pathology & Cell Biology, Columbia University, New York, NY, 10032, United States of America; Department of Physiology & Cellular Biophysics, Columbia University, New York, NY, 10032, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0135842PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552860PMC
June 2016

MerTK cleavage limits proresolving mediator biosynthesis and exacerbates tissue inflammation.

Proc Natl Acad Sci U S A 2016 Jun 19;113(23):6526-31. Epub 2016 May 19.

Department of Medicine, Columbia University, New York, NY 10032; Department of Pathology and Cell Biology, Columbia University, New York, NY 10032; Department of Physiology, Columbia University, New York, NY 10032;

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http://dx.doi.org/10.1073/pnas.1524292113DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988577PMC
June 2016

Hepatocyte DACH1 Is Increased in Obesity via Nuclear Exclusion of HDAC4 and Promotes Hepatic Insulin Resistance.

Cell Rep 2016 06 26;15(10):2214-2225. Epub 2016 May 26.

Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA; Department of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22111247163055
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068925PMC
http://dx.doi.org/10.1016/j.celrep.2016.05.006DOI Listing
June 2016

Macrophage Phenotype and Function in Different Stages of Atherosclerosis.

Circ Res 2016 Feb;118(4):653-67

From the Departments of Medicine (I.T.), Anatomy and Cell Biology (I.T.), and Physiology and Cellular Biophysics (I.T.), Columbia University, New York; and the Department of Medicine, Division of Metabolism, Endocrinology, and Nutrition (K.E.B.) and Department of Pathology (K.E.B.), UW Diabetes Institute, University of Washington School of Medicine, Seattle.

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http://circres.ahajournals.org/content/circresaha/118/4/653.
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http://dx.doi.org/10.1161/CIRCRESAHA.115.306256DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762068PMC
February 2016

How an artery heals.

Circ Res 2015 Nov;117(11):909-13

From the Section of Endocrinology, Diabetes, & Metabolism, Temple University School of Medicine, Philadelphia, PA (K.J.W.); Department of Molecular and Clinical Medicine, Sahlgrenska Academy of the University of Gothenburg, Göteborg, Sweden (K.J.W.); Departments of Medicine, Pathology & Cell Biology, and Physiology, Columbia University Medical Center, New York, NY (I.T.); and Department of Medicine (Cardiology), the Marc and Ruti Bell Program in Vascular Biology and The Center for the Prevention of Cardiovascular Disease, NYU School of Medicine, New York, NY (E.A.F.).

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http://dx.doi.org/10.1161/CIRCRESAHA.115.307609DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663458PMC
November 2015

Treatment of Obese Insulin-Resistant Mice With an Allosteric MAPKAPK2/3 Inhibitor Lowers Blood Glucose and Improves Insulin Sensitivity.

Diabetes 2015 Oct 11;64(10):3396-405. Epub 2015 Jun 11.

Department of Medicine, Columbia University, New York, NY Department of Pathology and Cell Biology, Columbia University, New York, NY Department of Physiology and Cellular Biophysics, Columbia University, New York, NY

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http://diabetes.diabetesjournals.org/content/early/2015/06/0
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http://diabetes.diabetesjournals.org/lookup/doi/10.2337/db14
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http://dx.doi.org/10.2337/db14-1945DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587644PMC
October 2015

C/EBP-Homologous Protein (CHOP) in Vascular Smooth Muscle Cells Regulates Their Proliferation in Aortic Explants and Atherosclerotic Lesions.

Circ Res 2015 May 14;116(11):1736-43. Epub 2015 Apr 14.

From the Departments of Medicine (A.-X.Z., X.W., M.J.N., I.T.), Pathology and Cell Biology (C.S.L., I.T.), and Physiology and Cellular Biophysics (I.T.), Columbia University, New York, NY; Department of Molecular and Clinical Medicine/Wallenberg Laboratory, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden (A.-X.Z., J.B.); CVMD iMed Translational Science, AstraZeneca R and D, Mölndal, Sweden (A.-X.Z.); Soonchunhyang Institute of Med-Bio Science, Soonchunhyang University, Cheon-an, South Korea (J.H.); and Degenerative Disease Program, Sanford-Burnham Medical Research Institute, La Jolla, CA (J.H., J.Y., R.J.K.).

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http://dx.doi.org/10.1161/CIRCRESAHA.116.305602DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441876PMC
May 2015

Recent insights into the cellular biology of atherosclerosis.

J Cell Biol 2015 Apr;209(1):13-22

Robert M. Berne Cardiovascular Research Center, University of Virginia School of Medicine, Charlottesville, VA 22908.

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http://dx.doi.org/10.1083/jcb.201412052DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395483PMC
April 2015

Emerging roles of mitochondria ROS in atherosclerotic lesions: causation or association?

Authors:
Ying Wang Ira Tabas

J Atheroscler Thromb 2014 8;21(5):381-90. Epub 2014 Apr 8.

Columbia University Medical Center.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174275PMC
http://dx.doi.org/10.5551/jat.23929DOI Listing
January 2015

Identification of a non-growth factor role for GM-CSF in advanced atherosclerosis: promotion of macrophage apoptosis and plaque necrosis through IL-23 signaling.

Circ Res 2015 Jan 27;116(2):e13-24. Epub 2014 Oct 27.

From the Departments of Medicine (M.S., I.T.), Pathology and Cell Biology (I.T.), and Physiology and Cellular Biophysics (I.T.), Columbia University, New York, NY; and Department of Pathology, Feinberg Cardiovascular Research Institute, Northwestern University, Chicago, IL (E.T.).

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http://circres.ahajournals.org/content/early/2014/10/27/CIRC
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http://circres.ahajournals.org/cgi/doi/10.1161/CIRCRESAHA.11
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http://dx.doi.org/10.1161/CIRCRESAHA.116.304794DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297527PMC
January 2015

Accelerating the pace of atherosclerosis research.

Arterioscler Thromb Vasc Biol 2015 Jan;35(1):11-2

From the Saha Cardiovascular Research Center, University of Kentucky, Lexington (A.D.); Department of Medicine, Columbia University Medical Center, New York, NY (I.T.); and Departments of Medicine and Genetics, Institute for Translational Medicine and Therapeutics, and Cardiovascular Institute, Perelman School of Medicine of the University of Pennsylvania, Philadelphia (D.J.R.).

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http://dx.doi.org/10.1161/ATVBAHA.114.304833DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840438PMC
January 2015

A solvent-free thermosponge nanoparticle platform for efficient delivery of labile proteins.

Nano Lett 2014 Nov 21;14(11):6449-55. Epub 2014 Oct 21.

Laboratory of Nanomedicine and Biomaterials, Department of Anesthesiology, Brigham and Women's Hospital and ‡Department of Microbiology and Immunobiology, Division of Immunology, Harvard Medical School , Boston, Massachusetts 02115, United States.

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http://dx.doi.org/10.1021/nl502994yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245989PMC
November 2014

Resolvin D1 limits 5-lipoxygenase nuclear localization and leukotriene B4 synthesis by inhibiting a calcium-activated kinase pathway.

Proc Natl Acad Sci U S A 2014 Oct 22;111(40):14530-5. Epub 2014 Sep 22.

Department of Medicine, Department of Pathology and Cell Biology, and Department of Physiology, Columbia University, New York, NY 10032;

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http://www.pnas.org/lookup/doi/10.1073/pnas.1410851111
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http://dx.doi.org/10.1073/pnas.1410851111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210018PMC
October 2014

Common therapeutic targets in cardiometabolic disease.

Sci Transl Med 2014 Jun;6(239):239ps5

Department of Medicine, Department of Pathology and Cell Biology, and Department of Physiology, Columbia University, New York, NY 10032-3725, USA.

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http://dx.doi.org/10.1126/scitranslmed.3008908DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176709PMC
June 2014

Inflammation and its resolution as determinants of acute coronary syndromes.

Circ Res 2014 Jun;114(12):1867-79

From the Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (P.L.); Department of Medicine, Columbia University Medical Center, New York, NY (I.T.); and Division of Cardiology, Department of Medicine, New York University School of Medicine (E.A.F.).

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https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.114.30269
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http://dx.doi.org/10.1161/CIRCRESAHA.114.302699DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078767PMC
June 2014

CaMKII in cardiometabolic disease.

Aging (Albany NY) 2014 Jun;6(6):430-1

Department of Medicine, Columbia University, New York, NY 10032.

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http://www.aging-us.com/article/100675
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100805PMC
http://dx.doi.org/10.18632/aging.100675DOI Listing
June 2014

Interleukin-3/granulocyte macrophage colony-stimulating factor receptor promotes stem cell expansion, monocytosis, and atheroma macrophage burden in mice with hematopoietic ApoE deficiency.

Arterioscler Thromb Vasc Biol 2014 May 20;34(5):976-84. Epub 2014 Mar 20.

From the Division of Molecular Medicine, Department of Medicine (M. Wang, M.S., S.A., A.J.M., C.W., I.T., M. Westerterp, A.R.T.) and Department of Pharmacology (M. Wang), Columbia University, New York, NY; Department of Medicine, University of California San Diego, La Jolla (A.G., J.W.); and Department of Medical Biochemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands (M. Westerterp).

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http://dx.doi.org/10.1161/ATVBAHA.113.303097DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091799PMC
May 2014

A new RIDDle in DC-mediated cross-presentation.

Nat Immunol 2014 Mar;15(3):213-5

Department of Medicine, the Department of Pathology & Cell Biology, and the Department of Physiology & Cellular Biophysics, Columbia University Medical Center, New York, New York, USA.

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http://dx.doi.org/10.1038/ni.2826DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174447PMC
March 2014

Dendritic cells in atherosclerosis.

Semin Immunopathol 2014 Jan 6;36(1):93-102. Epub 2013 Nov 6.

Department of Medicine, Columbia University, 630 West 168th Street PH9-406, New York, NY, 10032, USA,

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http://dx.doi.org/10.1007/s00281-013-0400-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946524PMC
January 2014

Macrophage mitochondrial oxidative stress promotes atherosclerosis and nuclear factor-κB-mediated inflammation in macrophages.

Circ Res 2014 Jan 2;114(3):421-33. Epub 2013 Dec 2.

From the Departments of Medicine, Physiology, and Cellular Biophysics, and Pathology and Cell Biology (Y.W., I.T.), and Medical Scientist Training Program (G.Z.W.), Columbia University, New York, NY; and Department of Pathology, University of Washington, Seattle, WA (P.S.R.).

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http://dx.doi.org/10.1161/CIRCRESAHA.114.302153DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946745PMC
January 2014

Activation of calcium/calmodulin-dependent protein kinase II in obesity mediates suppression of hepatic insulin signaling.

Cell Metab 2013 Dec 21;18(6):803-15. Epub 2013 Nov 21.

Department of Medicine, Columbia University, New York, NY 10032, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cmet.2013.10.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863383PMC
December 2013

The UPR in atherosclerosis.

Semin Immunopathol 2013 May 4;35(3):321-32. Epub 2013 Apr 4.

Department of Medicine, Columbia University, New York, NY, USA.

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http://dx.doi.org/10.1007/s00281-013-0372-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967405PMC
May 2013

Development and in vivo efficacy of targeted polymeric inflammation-resolving nanoparticles.

Proc Natl Acad Sci U S A 2013 Apr 26;110(16):6506-11. Epub 2013 Mar 26.

Laboratory of Nanomedicine and Biomaterials, Department of Anesthesiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.1073/pnas.1303377110DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631648PMC
April 2013

Making things stick in the fight against atherosclerosis.

Authors:
Ira Tabas

Circ Res 2013 Apr;112(8):1094-6

Departments of Medicine, Anatomy & Cell Biology, and Physiology & Cellular Biophysics, Columbia University, New York, NY 10032, USA.

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http://dx.doi.org/10.1161/CIRCRESAHA.113.301227DOI Listing
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April 2013

ACAT inhibition reduces the progression of preexisting, advanced atherosclerotic mouse lesions without plaque or systemic toxicity.

Arterioscler Thromb Vasc Biol 2013 Jan 8;33(1):4-12. Epub 2012 Nov 8.

Marc and Ruti Bell Vascular Biology and Disease Research Program of the Leon H. Charney Division of Cardiology and the Department of Medicine (Cardiology), New York University School of Medicine, Smilow 7, 522 First Ave, New York, NY 10029, USA.

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January 2013

Treg-mediated suppression of atherosclerosis requires MYD88 signaling in DCs.

J Clin Invest 2013 Jan 21;123(1):179-88. Epub 2012 Dec 21.

Columbia University, Department of Medicine, New York, New York 10032, USA.

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January 2013

Anti-inflammatory therapy in chronic disease: challenges and opportunities.

Science 2013 Jan;339(6116):166-72

Department of Medicine, Columbia University, New York, NY 10032, USA.

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January 2013

Cardiology: Bad matters made worse.

Authors:
Ira Tabas

Nature 2012 Jul 18;487(7407):306-8. Epub 2012 Jul 18.

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July 2012

Role of endoplasmic reticulum stress in metabolic disease and other disorders.

Annu Rev Med 2012 ;63:317-28

Department of Medicine, Columbia University, New York, New York 10032, USA.

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May 2012

Inositol-1,4,5-trisphosphate receptor regulates hepatic gluconeogenesis in fasting and diabetes.

Nature 2012 Apr 8;485(7396):128-32. Epub 2012 Apr 8.

Clayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.

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April 2012

Guidelines for the use and interpretation of assays for monitoring autophagy.

Authors:
Daniel J Klionsky Fabio C Abdalla Hagai Abeliovich Robert T Abraham Abraham Acevedo-Arozena Khosrow Adeli Lotta Agholme Maria Agnello Patrizia Agostinis Julio A Aguirre-Ghiso Hyung Jun Ahn Ouardia Ait-Mohamed Slimane Ait-Si-Ali Takahiko Akematsu Shizuo Akira Hesham M Al-Younes Munir A Al-Zeer Matthew L Albert Roger L Albin Javier Alegre-Abarrategui Maria Francesca Aleo Mehrdad Alirezaei Alexandru Almasan Maylin Almonte-Becerril Atsuo Amano Ravi Amaravadi Shoba Amarnath Amal O Amer Nathalie Andrieu-Abadie Vellareddy Anantharam David K Ann Shailendra Anoopkumar-Dukie Hiroshi Aoki Nadezda Apostolova Giuseppe Arancia John P Aris Katsuhiko Asanuma Nana Y O Asare Hisashi Ashida Valerie Askanas David S Askew Patrick Auberger Misuzu Baba Steven K Backues Eric H Baehrecke Ben A Bahr Xue-Yuan Bai Yannick Bailly Robert Baiocchi Giulia Baldini Walter Balduini Andrea Ballabio Bruce A Bamber Edward T W Bampton Gábor Bánhegyi Clinton R Bartholomew Diane C Bassham Robert C Bast Henri Batoko Boon-Huat Bay Isabelle Beau Daniel M Béchet Thomas J Begley Christian Behl Christian Behrends Soumeya Bekri Bryan Bellaire Linda J Bendall Luca Benetti Laura Berliocchi Henri Bernardi Francesca Bernassola Sébastien Besteiro Ingrid Bhatia-Kissova Xiaoning Bi Martine Biard-Piechaczyk Janice S Blum Lawrence H Boise Paolo Bonaldo David L Boone Beat C Bornhauser Karina R Bortoluci Ioannis Bossis Frédéric Bost Jean-Pierre Bourquin Patricia Boya Michaël Boyer-Guittaut Peter V Bozhkov Nathan R Brady Claudio Brancolini Andreas Brech Jay E Brenman Ana Brennand Emery H Bresnick Patrick Brest Dave Bridges Molly L Bristol Paul S Brookes Eric J Brown John H Brumell Nicola Brunetti-Pierri Ulf T Brunk Dennis E Bulman Scott J Bultman Geert Bultynck Lena F Burbulla Wilfried Bursch Jonathan P Butchar Wanda Buzgariu Sergio P Bydlowski Ken Cadwell Monika Cahová Dongsheng Cai Jiyang Cai Qian Cai Bruno Calabretta Javier Calvo-Garrido Nadine Camougrand Michelangelo Campanella Jenny Campos-Salinas Eleonora Candi Lizhi Cao Allan B Caplan Simon R Carding Sandra M Cardoso Jennifer S Carew Cathleen R Carlin Virginie Carmignac Leticia A M Carneiro Serena Carra Rosario A Caruso Giorgio Casari Caty Casas Roberta Castino Eduardo Cebollero Francesco Cecconi Jean Celli Hassan Chaachouay Han-Jung Chae Chee-Yin Chai David C Chan Edmond Y Chan Raymond Chuen-Chung Chang Chi-Ming Che Ching-Chow Chen Guang-Chao Chen Guo-Qiang Chen Min Chen Quan Chen Steve S-L Chen WenLi Chen Xi Chen Xiangmei Chen Xiequn Chen Ye-Guang Chen Yingyu Chen Yongqiang Chen Yu-Jen Chen Zhixiang Chen Alan Cheng Christopher H K Cheng Yan Cheng Heesun Cheong Jae-Ho Cheong Sara Cherry Russ Chess-Williams Zelda H Cheung Eric Chevet Hui-Ling Chiang Roberto Chiarelli Tomoki Chiba Lih-Shen Chin Shih-Hwa Chiou Francis V Chisari Chi Hin Cho Dong-Hyung Cho Augustine M K Choi DooSeok Choi Kyeong Sook Choi Mary E Choi Salem Chouaib Divaker Choubey Vinay Choubey Charleen T Chu Tsung-Hsien Chuang Sheau-Huei Chueh Taehoon Chun Yong-Joon Chwae Mee-Len Chye Roberto Ciarcia Maria R Ciriolo Michael J Clague Robert S B Clark Peter G H Clarke Robert Clarke Patrice Codogno Hilary A Coller María I Colombo Sergio Comincini Maria Condello Fabrizio Condorelli Mark R Cookson Graham H Coombs Isabelle Coppens Ramon Corbalan Pascale Cossart Paola Costelli Safia Costes Ana Coto-Montes Eduardo Couve Fraser P Coxon James M Cregg José L Crespo Marianne J Cronjé Ana Maria Cuervo Joseph J Cullen Mark J Czaja Marcello D'Amelio Arlette Darfeuille-Michaud Lester M Davids Faith E Davies Massimo De Felici John F de Groot Cornelis A M de Haan Luisa De Martino Angelo De Milito Vincenzo De Tata Jayanta Debnath Alexei Degterev Benjamin Dehay Lea M D Delbridge Francesca Demarchi Yi Zhen Deng Jörn Dengjel Paul Dent Donna Denton Vojo Deretic Shyamal D Desai Rodney J Devenish Mario Di Gioacchino Gilbert Di Paolo Chiara Di Pietro Guillermo Díaz-Araya Inés Díaz-Laviada Maria T Diaz-Meco Javier Diaz-Nido Ivan Dikic Savithramma P Dinesh-Kumar Wen-Xing Ding Clark W Distelhorst Abhinav Diwan Mojgan Djavaheri-Mergny Svetlana Dokudovskaya Zheng Dong Frank C Dorsey Victor Dosenko James J Dowling Stephen Doxsey Marlène Dreux Mark E Drew Qiuhong Duan Michel A Duchosal Karen Duff Isabelle Dugail Madeleine Durbeej Michael Duszenko Charles L Edelstein Aimee L Edinger Gustavo Egea Ludwig Eichinger N Tony Eissa Suhendan Ekmekcioglu Wafik S El-Deiry Zvulun Elazar Mohamed Elgendy Lisa M Ellerby Kai Er Eng Anna-Mart Engelbrecht Simone Engelender Jekaterina Erenpreisa Ricardo Escalante Audrey Esclatine Eeva-Liisa Eskelinen Lucile Espert Virginia Espina Huizhou Fan Jia Fan Qi-Wen Fan Zhen Fan Shengyun Fang Yongqi Fang Manolis Fanto Alessandro Fanzani Thomas Farkas Jean-Claude Farré Mathias Faure Marcus Fechheimer Carl G Feng Jian Feng Qili Feng Youji Feng László Fésüs Ralph Feuer Maria E Figueiredo-Pereira Gian Maria Fimia Diane C Fingar Steven Finkbeiner Toren Finkel Kim D Finley Filomena Fiorito Edward A Fisher Paul B Fisher Marc Flajolet Maria L Florez-McClure Salvatore Florio Edward A Fon Francesco Fornai Franco Fortunato Rati Fotedar Daniel H Fowler Howard S Fox Rodrigo Franco Lisa B Frankel Marc Fransen José M Fuentes Juan Fueyo Jun Fujii Kozo Fujisaki Eriko Fujita Mitsunori Fukuda Ruth H Furukawa Matthias Gaestel Philippe Gailly Malgorzata Gajewska Brigitte Galliot Vincent Galy Subramaniam Ganesh Barry Ganetzky Ian G Ganley Fen-Biao Gao George F Gao Jinming Gao Lorena Garcia Guillermo Garcia-Manero Mikel Garcia-Marcos Marjan Garmyn Andrei L Gartel Evelina Gatti Mathias Gautel Thomas R Gawriluk Matthew E Gegg Jiefei Geng Marc Germain Jason E Gestwicki David A Gewirtz Saeid Ghavami Pradipta Ghosh Anna M Giammarioli Alexandra N Giatromanolaki Spencer B Gibson Robert W Gilkerson Michael L Ginger Henry N Ginsberg Jakub Golab Michael S Goligorsky Pierre Golstein Candelaria Gomez-Manzano Ebru Goncu Céline Gongora Claudio D Gonzalez Ramon Gonzalez Cristina González-Estévez Rosa Ana González-Polo Elena Gonzalez-Rey Nikolai V Gorbunov Sharon Gorski Sandro Goruppi Roberta A Gottlieb Devrim Gozuacik Giovanna Elvira Granato Gary D Grant Kim N Green Aleš Gregorc Frédéric Gros Charles Grose Thomas W Grunt Philippe Gual Jun-Lin Guan Kun-Liang Guan Sylvie M Guichard Anna S Gukovskaya Ilya Gukovsky Jan Gunst Asa B Gustafsson Andrew J Halayko Amber N Hale Sandra K Halonen Maho Hamasaki Feng Han Ting Han Michael K Hancock Malene Hansen Hisashi Harada Masaru Harada Stefan E Hardt J Wade Harper Adrian L Harris James Harris Steven D Harris Makoto Hashimoto Jeffrey A Haspel Shin-ichiro Hayashi Lori A Hazelhurst Congcong He You-Wen He Marie-Joseé Hébert Kim A Heidenreich Miep H Helfrich Gudmundur V Helgason Elizabeth P Henske Brian Herman Paul K Herman Claudio Hetz Sabine Hilfiker Joseph A Hill Lynne J Hocking Paul Hofman Thomas G Hofmann Jörg Höhfeld Tessa L Holyoake Ming-Huang Hong David A Hood Gökhan S Hotamisligil Ewout J Houwerzijl Maria Høyer-Hansen Bingren Hu Chien-An A Hu Hong-Ming Hu Ya Hua Canhua Huang Ju Huang Shengbing Huang Wei-Pang Huang Tobias B Huber Won-Ki Huh Tai-Ho Hung Ted R Hupp Gang Min Hur James B Hurley Sabah N A Hussain Patrick J Hussey Jung Jin Hwang Seungmin Hwang Atsuhiro Ichihara Shirin Ilkhanizadeh Ken Inoki Takeshi Into Valentina Iovane Juan L Iovanna Nancy Y Ip Yoshitaka Isaka Hiroyuki Ishida Ciro Isidoro Ken-ichi Isobe Akiko Iwasaki Marta Izquierdo Yotaro Izumi Panu M Jaakkola Marja Jäättelä George R Jackson William T Jackson Bassam Janji Marina Jendrach Ju-Hong Jeon Eui-Bae Jeung Hong Jiang Hongchi Jiang Jean X Jiang Ming Jiang Qing Jiang Xuejun Jiang Xuejun Jiang Alberto Jiménez Meiyan Jin Shengkan Jin Cheol O Joe Terje Johansen Daniel E Johnson Gail V W Johnson Nicola L Jones Bertrand Joseph Suresh K Joseph Annie M Joubert Gábor Juhász Lucienne Juillerat-Jeanneret Chang Hwa Jung Yong-Keun Jung Kai Kaarniranta Allen Kaasik Tomohiro Kabuta Motoni Kadowaki Katarina Kagedal Yoshiaki Kamada Vitaliy O Kaminskyy Harm H Kampinga Hiromitsu Kanamori Chanhee Kang Khong Bee Kang Kwang Il Kang Rui Kang Yoon-A Kang Tomotake Kanki Thirumala-Devi Kanneganti Haruo Kanno Anumantha G Kanthasamy Arthi Kanthasamy Vassiliki Karantza Gur P Kaushal Susmita Kaushik Yoshinori Kawazoe Po-Yuan Ke John H Kehrl Ameeta Kelekar Claus Kerkhoff David H Kessel Hany Khalil Jan A K W Kiel Amy A Kiger Akio Kihara Deok Ryong Kim Do-Hyung Kim Dong-Hou Kim Eun-Kyoung Kim Hyung-Ryong Kim Jae-Sung Kim Jeong Hun Kim Jin Cheon Kim John K Kim Peter K Kim Seong Who Kim Yong-Sun Kim Yonghyun Kim Adi Kimchi Alec C Kimmelman Jason S King Timothy J Kinsella Vladimir Kirkin Lorrie A Kirshenbaum Katsuhiko Kitamoto Kaio Kitazato Ludger Klein Walter T Klimecki Jochen Klucken Erwin Knecht Ben C B Ko Jan C Koch Hiroshi Koga Jae-Young Koh Young Ho Koh Masato Koike Masaaki Komatsu Eiki Kominami Hee Jeong Kong Wei-Jia Kong Viktor I Korolchuk Yaichiro Kotake Michael I Koukourakis Juan B Kouri Flores Attila L Kovács Claudine Kraft Dimitri Krainc Helmut Krämer Carole Kretz-Remy Anna M Krichevsky Guido Kroemer Rejko Krüger Oleg Krut Nicholas T Ktistakis Chia-Yi Kuan Roza Kucharczyk Ashok Kumar Raj Kumar Sharad Kumar Mondira Kundu Hsing-Jien Kung Tino Kurz Ho Jeong Kwon Albert R La Spada Frank Lafont Trond Lamark Jacques Landry Jon D Lane Pierre Lapaquette Jocelyn F Laporte Lajos László Sergio Lavandero Josée N Lavoie Robert Layfield Pedro A Lazo Weidong Le Laurent Le Cam Daniel J Ledbetter Alvin J X Lee Byung-Wan Lee Gyun Min Lee Jongdae Lee Ju-Hyun Lee Michael Lee Myung-Shik Lee Sug Hyung Lee Christiaan Leeuwenburgh Patrick Legembre Renaud Legouis Michael Lehmann Huan-Yao Lei Qun-Ying Lei David A Leib José Leiro John J Lemasters Antoinette Lemoine Maciej S Lesniak Dina Lev Victor V Levenson Beth Levine Efrat Levy Faqiang Li Jun-Lin Li Lian Li Sheng Li Weijie Li Xue-Jun Li Yan-bo Li Yi-Ping Li Chengyu Liang Qiangrong Liang Yung-Feng Liao Pawel P Liberski Andrew Lieberman Hyunjung J Lim Kah-Leong Lim Kyu Lim Chiou-Feng Lin Fu-Cheng Lin Jian Lin Jiandie D Lin Kui Lin Wan-Wan Lin Weei-Chin Lin Yi-Ling Lin Rafael Linden Paul Lingor Jennifer Lippincott-Schwartz Michael P Lisanti Paloma B Liton Bo Liu Chun-Feng Liu Kaiyu Liu Leyuan Liu Qiong A Liu Wei Liu Young-Chau Liu Yule Liu Richard A Lockshin Chun-Nam Lok Sagar Lonial Benjamin Loos Gabriel Lopez-Berestein Carlos López-Otín Laura Lossi Michael T Lotze Peter Lőw Binfeng Lu Bingwei Lu Bo Lu Zhen Lu Frédéric Luciano Nicholas W Lukacs Anders H Lund Melinda A Lynch-Day Yong Ma Fernando Macian Jeff P MacKeigan Kay F Macleod Frank Madeo Luigi Maiuri Maria Chiara Maiuri Davide Malagoli May Christine V Malicdan Walter Malorni Na Man Eva-Maria Mandelkow Stéphen Manon Irena Manov Kai Mao Xiang Mao Zixu Mao Philippe Marambaud Daniela Marazziti Yves L Marcel Katie Marchbank Piero Marchetti Stefan J Marciniak Mateus Marcondes Mohsen Mardi Gabriella Marfe Guillermo Mariño Maria Markaki Mark R Marten Seamus J Martin Camille Martinand-Mari Wim Martinet Marta Martinez-Vicente Matilde Masini Paola Matarrese Saburo Matsuo Raffaele Matteoni Andreas Mayer Nathalie M Mazure David J McConkey Melanie J McConnell Catherine McDermott Christine McDonald Gerald M McInerney Sharon L McKenna BethAnn McLaughlin Pamela J McLean Christopher R McMaster G Angus McQuibban Alfred J Meijer Miriam H Meisler Alicia Meléndez Thomas J Melia Gerry Melino Maria A Mena Javier A Menendez Rubem F S Menna-Barreto Manoj B Menon Fiona M Menzies Carol A Mercer Adalberto Merighi Diane E Merry Stefania Meschini Christian G Meyer Thomas F Meyer Chao-Yu Miao Jun-Ying Miao Paul A M Michels Carine Michiels Dalibor Mijaljica Ana Milojkovic Saverio Minucci Clelia Miracco Cindy K Miranti Ioannis Mitroulis Keisuke Miyazawa Noboru Mizushima Baharia Mograbi Simin Mohseni Xavier Molero Bertrand Mollereau Faustino Mollinedo Takashi Momoi Iryna Monastyrska Martha M Monick Mervyn J Monteiro Michael N Moore Rodrigo Mora Kevin Moreau Paula I Moreira Yuji Moriyasu Jorge Moscat Serge Mostowy Jeremy C Mottram Tomasz Motyl Charbel E-H Moussa Sylke Müller Sylviane Muller Karl Münger Christian Münz Leon O Murphy Maureen E Murphy Antonio Musarò Indira Mysorekar Eiichiro Nagata Kazuhiro Nagata Aimable Nahimana Usha Nair Toshiyuki Nakagawa Kiichi Nakahira Hiroyasu Nakano Hitoshi Nakatogawa Meera Nanjundan Naweed I Naqvi Derek P Narendra Masashi Narita Miguel Navarro Steffan T Nawrocki Taras Y Nazarko Andriy Nemchenko Mihai G Netea Thomas P Neufeld Paul A Ney Ioannis P Nezis Huu Phuc Nguyen Daotai Nie Ichizo Nishino Corey Nislow Ralph A Nixon Takeshi Noda Angelika A Noegel Anna Nogalska Satoru Noguchi Lucia Notterpek Ivana Novak Tomoyoshi Nozaki Nobuyuki Nukina Thorsten Nürnberger Beat Nyfeler Keisuke Obara Terry D Oberley Salvatore Oddo Michinaga Ogawa Toya Ohashi Koji Okamoto Nancy L Oleinick F Javier Oliver Laura J Olsen Stefan Olsson Onya Opota Timothy F Osborne Gary K Ostrander Kinya Otsu Jing-hsiung James Ou Mireille Ouimet Michael Overholtzer Bulent Ozpolat Paolo Paganetti Ugo Pagnini Nicolas Pallet Glen E Palmer Camilla Palumbo Tianhong Pan Theocharis Panaretakis Udai Bhan Pandey Zuzana Papackova Issidora Papassideri Irmgard Paris Junsoo Park Ohkmae K Park Jan B Parys Katherine R Parzych Susann Patschan Cam Patterson Sophie Pattingre John M Pawelek Jianxin Peng David H Perlmutter Ida Perrotta George Perry Shazib Pervaiz Matthias Peter Godefridus J Peters Morten Petersen Goran Petrovski James M Phang Mauro Piacentini Philippe Pierre Valérie Pierrefite-Carle Gérard Pierron Ronit Pinkas-Kramarski Antonio Piras Natik Piri Leonidas C Platanias Stefanie Pöggeler Marc Poirot Angelo Poletti Christian Poüs Mercedes Pozuelo-Rubio Mette Prætorius-Ibba Anil Prasad Mark Prescott Muriel Priault Nathalie Produit-Zengaffinen Ann Progulske-Fox Tassula Proikas-Cezanne Serge Przedborski Karin Przyklenk Rosa Puertollano Julien Puyal Shu-Bing Qian Liang Qin Zheng-Hong Qin Susan E Quaggin Nina Raben Hannah Rabinowich Simon W Rabkin Irfan Rahman Abdelhaq Rami Georg Ramm Glenn Randall Felix Randow V Ashutosh Rao Jeffrey C Rathmell Brinda Ravikumar Swapan K Ray Bruce H Reed John C Reed Fulvio Reggiori Anne Régnier-Vigouroux Andreas S Reichert John J Reiners Russel J Reiter Jun Ren José L Revuelta Christopher J Rhodes Konstantinos Ritis Elizete Rizzo Jeffrey Robbins Michel Roberge Hernan Roca Maria C Roccheri Stephane Rocchi H Peter Rodemann Santiago Rodríguez de Córdoba Bärbel Rohrer Igor B Roninson Kirill Rosen Magdalena M Rost-Roszkowska Mustapha Rouis Kasper M A Rouschop Francesca Rovetta Brian P Rubin David C Rubinsztein Klaus Ruckdeschel Edmund B Rucker Assaf Rudich Emil Rudolf Nelson Ruiz-Opazo Rossella Russo Tor Erik Rusten Kevin M Ryan Stefan W Ryter David M Sabatini Junichi Sadoshima Tapas Saha Tatsuya Saitoh Hiroshi Sakagami Yasuyoshi Sakai Ghasem Hoseini Salekdeh Paolo Salomoni Paul M Salvaterra Guy Salvesen Rosa Salvioli Anthony M J Sanchez José A Sánchez-Alcázar Ricardo Sánchez-Prieto Marco Sandri Uma Sankar Poonam Sansanwal Laura Santambrogio Shweta Saran Sovan Sarkar Minnie Sarwal Chihiro Sasakawa Ausra 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Efthimios Sivridis Vojtech Skop Vladimir P Skulachev Ruth S Slack Soraya S Smaili Duncan R Smith Maria S Soengas Thierry Soldati Xueqin Song Anil K Sood Tuck Wah Soong Federica Sotgia Stephen A Spector Claudia D Spies Wolfdieter Springer Srinivasa M Srinivasula Leonidas Stefanis Joan S Steffan Ruediger Stendel Harald Stenmark Anastasis Stephanou Stephan T Stern Cinthya Sternberg Björn Stork Peter Strålfors Carlos S Subauste Xinbing Sui David Sulzer Jiaren Sun Shi-Yong Sun Zhi-Jun Sun Joseph J Y Sung Kuninori Suzuki Toshihiko Suzuki Michele S Swanson Charles Swanton Sean T Sweeney Lai-King Sy Gyorgy Szabadkai Ira Tabas Heinrich Taegtmeyer Marco Tafani Krisztina Takács-Vellai Yoshitaka Takano Kaoru Takegawa Genzou Takemura Fumihiko Takeshita Nicholas J Talbot Kevin S W Tan Keiji Tanaka Kozo Tanaka Daolin Tang Dingzhong Tang Isei Tanida Bakhos A Tannous Nektarios Tavernarakis Graham S Taylor Gregory A Taylor J Paul Taylor Lance S Terada Alexei Terman Gianluca Tettamanti Karin Thevissen Craig B Thompson Andrew Thorburn Michael Thumm FengFeng Tian Yuan Tian Glauco Tocchini-Valentini Aviva M Tolkovsky Yasuhiko Tomino Lars Tönges Sharon A Tooze Cathy Tournier John Tower Roberto Towns Vladimir Trajkovic Leonardo H Travassos Ting-Fen Tsai Mario P Tschan Takeshi Tsubata Allan Tsung Boris Turk Lorianne S Turner Suresh C Tyagi Yasuo Uchiyama Takashi Ueno Midori Umekawa Rika Umemiya-Shirafuji Vivek K Unni Maria I Vaccaro Enza Maria Valente Greet Van den Berghe Ida J van der Klei Wouter van Doorn Linda F van Dyk Marjolein van Egmond Leo A van Grunsven Peter Vandenabeele Wim P Vandenberghe Ilse Vanhorebeek Eva C Vaquero Guillermo Velasco Tibor Vellai Jose Miguel Vicencio Richard D Vierstra Miquel Vila Cécile Vindis Giampietro Viola Maria Teresa Viscomi Olga V Voitsekhovskaja Clarissa von Haefen Marcela Votruba Keiji Wada Richard Wade-Martins Cheryl L Walker Craig M Walsh Jochen Walter Xiang-Bo Wan Aimin Wang Chenguang Wang Dawei Wang Fan Wang Fen Wang Guanghui Wang Haichao Wang Hong-Gang Wang Horng-Dar Wang Jin Wang Ke Wang Mei Wang Richard C Wang Xinglong Wang Xuejun Wang Ying-Jan Wang Yipeng Wang Zhen Wang Zhigang Charles Wang Zhinong Wang Derick G Wansink Diane M Ward Hirotaka Watada Sarah L Waters Paul Webster Lixin Wei Conrad C Weihl William A Weiss Scott M Welford Long-Ping Wen Caroline A Whitehouse J Lindsay Whitton Alexander J Whitworth Tom Wileman John W Wiley Simon Wilkinson Dieter Willbold Roger L Williams Peter R Williamson Bradly G Wouters Chenghan Wu Dao-Cheng Wu William K K Wu Andreas Wyttenbach Ramnik J Xavier Zhijun Xi Pu Xia Gengfu Xiao Zhiping Xie Zhonglin Xie Da-zhi Xu Jianzhen Xu Liang Xu Xiaolei Xu Ai Yamamoto Akitsugu Yamamoto Shunhei Yamashina Michiaki Yamashita Xianghua Yan Mitsuhiro Yanagida Dun-Sheng Yang Elizabeth Yang Jin-Ming Yang Shi Yu Yang Wannian Yang Wei Yuan Yang Zhifen Yang Meng-Chao Yao Tso-Pang Yao Behzad Yeganeh Wei-Lien Yen Jia-jing Yin Xiao-Ming Yin Ook-Joon Yoo Gyesoon Yoon Seung-Yong Yoon Tomohiro Yorimitsu Yuko Yoshikawa Tamotsu Yoshimori Kohki Yoshimoto Ho Jin You Richard J Youle Anas Younes Li Yu Long Yu Seong-Woon Yu Wai Haung Yu Zhi-Min Yuan Zhenyu Yue Cheol-Heui Yun Michisuke Yuzaki Olga Zabirnyk Elaine Silva-Zacarin David Zacks Eldad Zacksenhaus Nadia Zaffaroni Zahra Zakeri Herbert J Zeh Scott O Zeitlin Hong Zhang Hui-Ling Zhang Jianhua Zhang Jing-Pu Zhang Lin Zhang Long Zhang Ming-Yong Zhang Xu Dong Zhang Mantong Zhao Yi-Fang Zhao Ying Zhao Zhizhuang J Zhao Xiaoxiang Zheng Boris Zhivotovsky Qing Zhong Cong-Zhao Zhou Changlian Zhu Wei-Guo Zhu Xiao-Feng Zhu Xiongwei Zhu Yuangang Zhu Teresa Zoladek Wei-Xing Zong Antonio Zorzano Jürgen Zschocke Brian Zuckerbraun

Autophagy 2012 Apr;8(4):445-544

Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.

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April 2012

Toll-like receptor activation suppresses ER stress factor CHOP and translation inhibition through activation of eIF2B.

Nat Cell Biol 2012 Jan 8;14(2):192-200. Epub 2012 Jan 8.

Department of Medicine, Columbia University, New York 10032, USA.

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January 2012

Homozygosity for an allele encoding deacetylated FoxO1 protects macrophages from cholesterol-induced inflammation without increasing apoptosis.

Arterioscler Thromb Vasc Biol 2011 Dec 22;31(12):2920-8. Epub 2011 Sep 22.

Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, NY, USA.

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December 2011

Mechanisms of ER stress-induced apoptosis in atherosclerosis.

Arterioscler Thromb Vasc Biol 2011 Dec;31(12):2792-7

Department of Medicine, Columbia University-PH 9-405, 630 W. 168th St., New York, NY 10032, USA.

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December 2011

Insulin resistance, hyperglycemia, and atherosclerosis.

Cell Metab 2011 Nov;14(5):575-85

Department of Pathology, Diabetes and Obesity Center of Excellence, 815 Mercer Street, University of Washington, Seattle, WA 98109, USA.

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November 2011

Shedding of the Mer tyrosine kinase receptor is mediated by ADAM17 protein through a pathway involving reactive oxygen species, protein kinase Cδ, and p38 mitogen-activated protein kinase (MAPK).

J Biol Chem 2011 Sep 2;286(38):33335-44. Epub 2011 Aug 2.

Departments of Medicine, Pathology and Cell Biology, and Physiology, and Cellular Biophysics, Columbia University, New York, New York 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190938PMC
September 2011

The role of macrophages and dendritic cells in the clearance of apoptotic cells in advanced atherosclerosis.

Eur J Immunol 2011 Sep;41(9):2515-8

Department of Medicine, Division of Molecular Medicine, Columbia University, New York, NY 10032, USA.

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http://dx.doi.org/10.1002/eji.201141719DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289088PMC
September 2011

Pulling down the plug on atherosclerosis: finding the culprit in your heart.

Authors:
Ira Tabas

Nat Med 2011 Jul 7;17(7):791-3. Epub 2011 Jul 7.

Department of Medicine, Columbia University, New York, New York, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254051PMC
July 2011

A reporter for tracking the UPR in vivo reveals patterns of temporal and cellular stress during atherosclerotic progression.

J Lipid Res 2011 May 25;52(5):1033-8. Epub 2011 Feb 25.

Department of Medicine and Anatomy, Columbia University, New York, NY 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3073465PMC
May 2011

Macrophages in the pathogenesis of atherosclerosis.

Cell 2011 Apr;145(3):341-55

Department of Medicine, New York University Medical Center, NY 10016, USA.

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http://dx.doi.org/10.1016/j.cell.2011.04.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111065PMC
April 2011

Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress.

Authors:
Ira Tabas David Ron

Nat Cell Biol 2011 Mar;13(3):184-90

Department of Medicine, Anatomy & Cell Biology, Columbia University, New York, NY 10032, USA.

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http://www.nature.com/doifinder/10.1038/ncb0311-184
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107571PMC
March 2011

NADPH oxidase links endoplasmic reticulum stress, oxidative stress, and PKR activation to induce apoptosis.

J Cell Biol 2010 Dec 6;191(6):1113-25. Epub 2010 Dec 6.

Department of Medicine, Columbia University, New York, NY 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002036PMC
December 2010

The role of endoplasmic reticulum stress in the progression of atherosclerosis.

Authors:
Ira Tabas

Circ Res 2010 Oct;107(7):839-50

Department of Medicine, Columbia University, New York, NY 10032, USA.

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http://dx.doi.org/10.1161/CIRCRESAHA.110.224766DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951143PMC
October 2010

Induction of ER stress in macrophages of tuberculosis granulomas.

PLoS One 2010 Sep 15;5(9):e12772. Epub 2010 Sep 15.

Division of Molecular Medicine, Department of Medicine, Columbia University, New York, New York, United States of America.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939897PMC
September 2010

ABCA1 and ABCG1 protect against oxidative stress-induced macrophage apoptosis during efferocytosis.

Circ Res 2010 Jun 29;106(12):1861-9. Epub 2010 Apr 29.

Division of Molecular Medicine, Department of Medicine, 630 W 168th St, Columbia University, New York, NY 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2995809PMC
June 2010

Association of plasma sphingomyelin levels and incident coronary heart disease events in an adult population: Multi-Ethnic Study of Atherosclerosis.

Arterioscler Thromb Vasc Biol 2010 Mar 23;30(3):628-33. Epub 2009 Dec 23.

Department of Internal Medicine/Cardiology, University of Virginia Medical Center, Charlottesville, VA 22908, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862629PMC
March 2010

Macrophage death and defective inflammation resolution in atherosclerosis.

Authors:
Ira Tabas

Nat Rev Immunol 2010 Jan 4;10(1):36-46. Epub 2009 Dec 4.

Department of Medicine, Physiology and Cellular Biophysics, Columbia University, New York, New York 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854623PMC
January 2010

The impact of macrophage insulin resistance on advanced atherosclerotic plaque progression.

Circ Res 2010 Jan;106(1):58-67

Department of Medicine, Columbia University, 630 West 168th St, New York, NY 10032, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805467PMC
January 2010

Macrophage apoptosis in advanced atherosclerosis.

Ann N Y Acad Sci 2009 Sep;1173 Suppl 1:E40-5

Department of Medicine, Columbia University Medical Center, New York, New York, USA.

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http://dx.doi.org/10.1111/j.1749-6632.2009.04957.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762639PMC
September 2009