المؤلفون: McDonald, Merry-Lynn N, Cho, Michael H, Sørheim, Inga-Cecilie, Lutz, Sharon M, Castaldi, Peter J, Lomas, David A, Coxson, Harvey O, Edwards, Lisa D, MacNee, William, Vestbo, Jørgen, Yates, Julie C, Agusti, Alvar, Calverley, Peter MA, Celli, Bartolome, Crim, Courtney, Rennard, Stephen I, Wouters, Emiel FM, Bakke, Per, Tal-Singer, Ruth, Miller, Bruce E, Gulsvik, Amund, Casaburi, Richard, Wells, J Michael, Regan, Elizabeth A, Make, Barry J, Hokanson, John E, Lange, Christoph, Crapo, James D, Beaty, Terri H, Silverman, Edwin K, Hersh, Craig P

المصدر: American Journal of Respiratory Cell and Molecular Biology. 51(5)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Lung, Prevention, Clinical Research, Chronic Obstructive Pulmonary Disease, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Respiratory, Black or African American, Aged, Aged, 80 and over, Chromosomes, Human, Pair 15, Female, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Humans, Hypoxia, Male, Middle Aged, Oximetry, Oxygen, Polymorphism, Single Nucleotide, Prognosis, Pulmonary Disease, Chronic Obstructive, Rest, White People, chronic obstructive pulmonary disease, hypoxemia, pulse oximetry, genome-wide association study, oxygen saturation, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators, Cardiorespiratory Medicine and Haematology, Respiratory System, Biochemistry and cell biology, Cardiovascular medicine and haematology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5zx1p9rsTest

المؤلفون: McDonald, M.L.N., Cho, M.H., Sorheim, I.C., Lutz, S.M., Castaldi, P.J., Lomas, D.A., Coxson, H.O., Edwards, L.D., MacNee, W., Vestbo, J., Yates, J.C., Agusti, A., Calverley, P.M.A., Celli, B., Crim, C., Rennard, S.I., Wouters, E.F.M., Bakke, P., Tal-Singer, R., Miller, B.E., Gulsvik, A., Casaburi, R., Wells, J.M., Regan, E.A., Make, B.J., Hokanson, J.E., Lange, C., Crapo, J.D., Beaty, T.H., Silverman, E.K., Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints, the, COPDGene Investigators, the, Hersh, C.P.

المساهمون: Pulmonologie, RS: CAPHRI School for Public Health and Primary Care, RS: NUTRIM - R3 - Chronic inflammatory disease and wasting, RS: CAPHRI - Asthma and COPD

المصدر: American Journal of Respiratory Cell and Molecular Biology, 51(5), 678-687. American Thoracic Society
McDonald, M-L N, Cho, M H, Sørheim, I-C, Lutz, S M, Castaldi, P J, Lomas, D A, Coxson, H O, Edwards, L D, MacNee, W, Vestbo, J, Yates, J C, Agusti, A, Calverley, P M A, Celli, B, Crim, C, Rennard, S I, Wouters, E F M, Bakke, P, Tal-Singer, R, Miller, B E, Gulsvik, A, Casaburi, R, Wells, J M, Regan, E A, Make, B J, Hokanson, J E, Lange, C, Crapo, J D, Beaty, T H, Silverman, E K, Hersh, C P, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators & Mattheisen, M 2014, ' Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease ' American Journal of Respiratory Cell and Molecular Biology (Online), vol. 51, no. 5, pp. 678-87 . https://doi.org/10.1165/rcmb.2014-0135OCTest
American journal of respiratory cell and molecular biology, vol 51, iss 5

مصطلحات موضوعية: Male, Candidate gene, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators, Respiratory System, Clinical Biochemistry, Genome-wide association study, Cardiorespiratory Medicine and Haematology, Gastroenterology, Hypoxemia, Pulmonary Disease, Chronic Obstructive, Anoxia, 80 and over, 2.1 Biological and endogenous factors, Oximetry, Aetiology, Hypoxia, Lung, Original Research, Genetics, African Americans, Aged, 80 and over, COPD, education.field_of_study, Single Nucleotide, Middle Aged, Prognosis, pulse oximetry, Respiratory, Female, medicine.symptom, Human, Pulmonary and Respiratory Medicine, Chronic Obstructive, medicine.medical_specialty, Chronic Obstructive Pulmonary Disease, Rest, Population, European Continental Ancestry Group, Biology, Polymorphism, Single Nucleotide, Chromosomes, White People, Pulmonary Disease, Chromosome 15, Clinical Research, Internal medicine, Genetic variation, medicine, Humans, Genetic Predisposition to Disease, Polymorphism, education, Molecular Biology, Aged, Chromosomes, Human, Pair 15, hypoxemia, Whites, Prevention, Human Genome, Pair 15, Genetic Variation, Cell Biology, Hypoxia (medical), medicine.disease, oxygen saturation, Black or African American, Oxygen, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a6b85c0cf42a2fe921db7675dd59c4dTest
https://cris.maastrichtuniversity.nl/en/publications/4927b6a8-a84b-4d93-9586-839cf22b3a20Test