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Journal of Biological Chemistry, ISSN 0021-9258, 01/2013, Volume 288, Issue 3, pp. 2092 - 2102
Journal Article
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2013, Volume 288, Issue 3, pp. 2081 - 2091
Journal Article
Science, ISSN 0036-8075, 6/2003, Volume 300, Issue 5626, pp. 1763 - 1767
A novel coronavirus has been identified as the causative agent of severe acute respiratory syndrome (SARS). The viral main proteinase (M , also called ), which... 
Enzymes | Molecules | Coronavirus | Atoms | SARS | Reports | Dimers | Polyproteins | SARS virus | Monomers | Crystal structure | VIRUS-ENCODED PROTEINASES | 229E 3C-LIKE PROTEINASE | MULTIDISCIPLINARY SCIENCES | PROTEASES | Cysteine Endopeptidases - chemistry | Coronavirus 229E, Human - enzymology | Humans | Cysteine Proteinase Inhibitors - metabolism | Molecular Sequence Data | Crystallography, X-Ray | Cysteine Endopeptidases - metabolism | Pyrrolidinones - metabolism | Pyrrolidinones - pharmacology | Drug Design | Amino Acid Chloromethyl Ketones - metabolism | Cysteine Proteinase Inhibitors - chemistry | Binding Sites | Dimerization | Protein Structure, Tertiary | Recombinant Proteins - metabolism | Amino Acid Sequence | Transmissible gastroenteritis virus - enzymology | Catalytic Domain | Protein Structure, Secondary | Amino Acid Chloromethyl Ketones - chemistry | Isoxazoles - metabolism | Crystallization | Models, Molecular | Recombinant Proteins - chemistry | SARS Virus - drug effects | Antiviral Agents | Isoxazoles - chemistry | Severe Acute Respiratory Syndrome - drug therapy | Pyrrolidinones - chemistry | Isoxazoles - pharmacology | Sequence Homology, Amino Acid | Sequence Alignment | Protein Conformation | SARS Virus - enzymology | Severe acute respiratory syndrome | Research | Coronaviruses | Proteins | Viruses | Drug therapy
Journal Article
Current Opinion in Lipidology, ISSN 0957-9672, 10/2014, Volume 25, Issue 5, pp. 358 - 366
Purpose of review To review progress over the past 5 years in relating extracellular proteinases to plaque rupture, the cause of most myocardial infarctions,... 
Cathepsins | Plaque rupture | Metalloproteinases | Atherosclerosis | Serine proteinases | atherosclerosis | ATHEROSCLEROTIC LESIONS | MYOCARDIAL-INFARCTION | cathepsins | BIOCHEMISTRY & MOLECULAR BIOLOGY | metalloproteinases | plaque rupture | serine proteinases | NEUTROPHIL ELASTASE | MATRIX METALLOPROTEINASE-8 | REDUCES ATHEROSCLEROSIS | CYSTEINE PROTEASE CATHEPSINS | ENDOCRINOLOGY & METABOLISM | MUSCLE-CELL MIGRATION | TISSUE INHIBITOR | PERIPHERAL VASCULAR DISEASE | EXTRACELLULAR-MATRIX | CORONARY-ARTERY-DISEASE | ADAM17 Protein | Atherosclerosis - genetics | Humans | Molecular Targeted Therapy | Matrix Metalloproteinase Inhibitors - therapeutic use | Atherosclerosis - enzymology | Plaque, Atherosclerotic - enzymology | Myocardial Infarction - pathology | Membrane Proteins - metabolism | Plaque, Atherosclerotic - pathology | Myocardial Infarction - etiology | Cathepsin K - antagonists & inhibitors | Myocardial Infarction - enzymology | Atherosclerosis - pathology | Genome-Wide Association Study | ADAM Proteins - antagonists & inhibitors | Macrophages - pathology | ADAM10 Protein | Matrix Metalloproteinase Inhibitors - metabolism | Macrophages - enzymology | ADAM Proteins - metabolism | Amyloid Precursor Protein Secretases - metabolism | Cathepsin K - metabolism | Membrane Proteins - antagonists & inhibitors | Amyloid Precursor Protein Secretases - antagonists & inhibitors | Matrix Metalloproteinases - metabolism
Journal Article
Journal Article
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