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Alpha 1-antitrypsin (1AT) deficiency is a common hereditary disorder characterized by a reduction of serum levels of 1AT, emphysema, and liver disease (1-8).
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Key Phrases - Statistically Improbable Phrases (SIPs):
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intravenous augmentation therapy, nonindex cases, peptidyl carbamates, beta ribbon, bone marrow cell differentiation, unrecognized inherited disorder, human leukocyte elastase, turkey ovomucoid inhibitor, destructive lung disease, hepatic cell lines, neutrophil elastase gene, severe alpha, bilateral lung transplantation, canonical conformation, other serpins, porcine pancreatic elastase, human neutrophil elastase, deficient variant, intermediate alpha, peptide chloromethyl ketones, obstructive impairment, protein proteinase inhibitors, trifluoromethyl ketones, inhibitor phenotypes, biochemical efficacy
Key Phrases - Capitalized Phrases (CAPs):
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Respir Dis, Biol Chem, Clin Invest, New York, Hum Genet, Principal Investigator, Proc Natl Acad Sci, Mol Biol, Med Chem, United States, Biochem Biophys Res Commun, Physiol Chem, Mol Cell Biol, Van Thiel, Exp Med, Genes Dev, Acta Med Scand, Clin Lab Invest, Academic Press, Hoppe Seylers, National Institutes of Health, Nucleic Acids Res, Ann Intern Med, Biochim Biophys Acta, National Heart
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