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Genetic Polymorphism of CHRM2 in COPD: Clinical Significance and Therapeutic Implications
Journal article   Peer reviewed

Genetic Polymorphism of CHRM2 in COPD: Clinical Significance and Therapeutic Implications

Emanuela Cherubini, Maria Cristina Esposito, Davide Scozzi, Fabrizio Terzo, Giorgia Amira Osman, Salvatore Mariotta, Rita Mancini, Pierdonato Bruno and Alberto Ricci
Journal of Cellular Physiology, Vol.231(8)
2016

Abstract

Aged Aged, 80 and over Bronchodilator Agents Case-Control Studies Disease Progression Female Genetic Association Studies Genetic Predisposition to Disease Humans Lung Male Middle Aged Muscarinic Antagonists Phenotype Polymerase Chain Reaction Polymorphism, Single Nucleotide Pulmonary Disease, Chronic Obstructive Receptor, Muscarinic M2 Receptors, Adrenergic, beta-2 Receptors, Muscarinic Respiratory Function Tests Risk Factors Sequence Analysis, DNA Severity of Illness Index Treatment Outcome adrenergic receptor beta 2 adrenergic receptor muscarinic M2 receptor muscarinic M3 receptor muscarinic receptor salbutamol tiotropium bromide ADRB2 protein, human beta 2 adrenergic receptor bronchodilating agent CHRM2 protein, human CHRM3 protein, human muscarinic M2 receptor muscarinic receptor muscarinic receptor blocking agent aged Article chronic obstructive lung disease controlled study disease exacerbation disease severity female genetic polymorphism human lung function test major clinical study male priority journal receptor gene treatment response antagonists and inhibitors case control study disease course DNA sequence genetic association study genetic predisposition genetics lung middle aged pathophysiology phenotype polymerase chain reaction Pulmonary Disease, Chronic Obstructive risk factor severity of illness index single nucleotide polymorphism treatment outcome very elderly

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