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140122 ||| eng |
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|a 9781461507413
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|a Abraham, Nader G.
|e [editor]
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|a Heme Oxygenase in Biology and Medicine
|h Elektronische Ressource
|c edited by Nader G. Abraham
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|a 1st ed. 2002
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|a New York, NY
|b Springer US
|c 2002, 2002
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|a XIX, 515 p
|b online resource
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|a Role of Distinct Transcription Factors and Reactive Oxygen Intermediates -- 37. Doppel Protein Expression Correlates with Heme Oxygenase 1 and Nitric Oxide Synthase Induction -- 38. Generation of Nitric Oxide and Carbon Monoxide Provide Protection Against Cardiac Anaphylaxis -- Section VI. The Network of Heme Oxygenase and Program cell Growth and Death -- 39. Heme Oxygenase-1 Inhibits Vascular Smooth Muscle Cell Proliferation -- 40. Induction of Apoptosis in Vascular Smooth Muscle Cells by Heme Oxygenase-1-Derived Carbon Monoxide -- 41. Role of Heme Oxygenase in Angiogenesis and Renal Carcinoma -- 42. On the Promoting Action of Tamoxifen In the p-Dimethylaminoazobenzene Induced Hepatocarcinogenesis CF1 Mice Model and the Cytoprotective Role of Heme Oxygenase --
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|a 43. Human Heme Oxygenase Gene Transfer Promotes Body Growth and Normalizes Blood Pressure in Spontaneously Hypertensive Rats Without Affecting Sprague-Dawley Rats
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|a Studies from Laboratory Bench to New Nursery -- 2. Carbon Monoxide: A Potential Antiinflammatory Agent and Mediator of Lung Anti-Oxidant Defenses -- 3. Correlation of the Altered Vascular Effects of Carbon Monoxide and the Cardiovascular Complications of Diabetes -- 4. Endogenous Carbon Monoxide Has Protective Roles in Neointimal Development Elicited by Arterial Injury -- 5. End Tidal Breath Carbon Monoxide (ETCO) Levels in Pregnant Women -- 6. The Role of Heme Oxygenase in Pregnancy -- 7. Increased Carbon Monoxide in Exhaled Air in Patients with Inflammatory Respiratory Diseases -- 8. Carbon Monoxide and Iron, by Products of Heme Oxygenase, Modulate Vasular Endothelial Growth Factor Synthesis in Vascular Smooth Muscle Cells --
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|a Role in Septic Diaphragmatic Failure -- 18. Heme Oxygenase-1 (HO-1): Multiple Effects of a Protective Gene That Prevents Graft Rejection --
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|a Studies in Microsomal and Cellular Systems -- 32. Molecular Mechanism of Heme Oxygenase-1 Gene Induction by Activation of the Protein Kinase A-Dependent Signaling Pathway -- 33. Regulation of Heme Oxygenase-1 Gene Transcription Via the Stress-Response Element -- 34. Heme Oxygenase-1: A Major Player in the Defense Against the Oxidative Tissue Injury -- 35. Heme Oxygenase, Ginkgo Biloba Extract and its Terpenoids Protect Myocytes Against Oxidative Injury --
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|a A Possible Consequence of its Interaction with Plasma Lipoproteins -- 25. Anti-Atherogenic Properties of Heme Oxygenase -- 26. Heme Oxygenase and the Novel Tumour-Specific Anti-Vascular Compound Combretastatin A4-Phosphate -- 27. The Heme Oxygenase/Carbon Monoxide System In Hepatobiliary Pathophysiology -- Section V. Heme Oxygenase System and Oxidative Stress Response --
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|a Human anatomy
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|a Cancer research
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|a Human Genetics
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|a Oncology
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|a Anatomy
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|a Oncology
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|a Human genetics
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|a Cancer Research
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|a eng
|2 ISO 639-2
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|b SBA
|a Springer Book Archives -2004
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|u https://doi.org/10.1007/978-1-4615-0741-3?nosfx=y
|x Verlag
|3 Volltext
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|a 616.994
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|a Heme oxygenase is rapidly taking its place as the centerpiece of multiple inter acting metabolic systems. Only 25 years ago heme oxygenase and its metabolic prod ucts appeared to be merely a simple metabolic system-one substrate, heme; one enzyme, heme oxygenase; and one set of products, iron to be recycled, and bilirubin and carbon monoxide to be disposed. From a group of about 25 people in 1974, as judged by attendance at various Gordon conferences, heme oxygenase has, in the year 2000, attracted working scientists-and clinicians I might add-by the hundreds and has produced referenced publications by the thousands. It is well-deserved attention. Heme oxygenase system is now similar to the metabolic networks surrounding glucose in those complex maps of glycolytic and non-glycolytic metabolic pathways, which we had to memorize as students. The relevance of heme oxygenase to regulatory biology was recognized many years ago, but the work conducted over the past five years has created a new wave of emphasis focusing on genetic manipulation to alter heme oxygenase gene expression, the regulatory actions of heme oxygenase products including carbon monoxide, and the significance of changes in the heme oxygenase system. The physiological and pathological relevance of heme oxygenase in the brain, heart, liver, bone marrow, organ transplant, lung and kidney, opens many areas of investigation in various dis ciplines. Advances in the pharmacology of bilirubin and its ability as an antioxidant have provided a new avenue in clinical research
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