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American Journal of Respiratory Cell and Molecular Biology
|
May 15, 2014
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease
Merry-Lynn N McDonald, Michael H Cho, Inga-Cecilie Sørheim, et al.
Human Molecular Genetics
|
July 31, 2018
Whole exome sequencing analysis in severe chronic obstructive pulmonary disease
Dandi Qiao, Asher Ameli, Dmitry Prokopenko, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 16, 2016
Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease
Brian D Hobbs, Margaret M Parker, Han Chen, et al.
Gut
|
February 26, 2021
Hepatobiliary phenotypes of adults with alpha-1 antitrypsin deficiency
Malin Fromme, Carolin V Schneider, Vitor Pereira, et al.
Human Genetics
|
September 19, 2012
Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD
Nadia N Hansel, Ingo Ruczinski, Nicholas Rafaels, et al.
Human Molecular Genetics
|
November 15, 2011
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13
Michael H Cho, Peter J Castaldi, Emily S Wan, et al.
COPD
|
April 19, 2011
Opportunities and challenges in the genetics of COPD 2010: an International COPD Genetics Conference report
Edwin K Silverman, Jørgen Vestbo, Alvar Agusti, et al.
Plos One
|
May 30, 2015
Correction: Susceptibility to chronic mucus hypersecretion, a genome wide association study
Akkelies E Dijkstra, Joanna Smolonska, Maarten van den Berge, et al.
Plos One
|
April 10, 2014
Susceptibility to chronic mucus hypersecretion, a genome wide association study
Akkelies E Dijkstra, Joanna Smolonska, Maarten van den Berge, et al.
Nature Genetics
|
February 27, 2019
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Phuwanat Sakornsakolpat, Dmitry Prokopenko, Maxime Lamontagne, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 282) with videos related to
Sort By:
Page
of 29
American Journal of Respiratory Cell and Molecular Biology
|
May 15, 2014
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease
Merry-Lynn N McDonald, Michael H Cho, Inga-Cecilie Sørheim, et al.
Human Molecular Genetics
|
July 31, 2018
Whole exome sequencing analysis in severe chronic obstructive pulmonary disease
Dandi Qiao, Asher Ameli, Dmitry Prokopenko, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 16, 2016
Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease
Brian D Hobbs, Margaret M Parker, Han Chen, et al.
Gut
|
February 26, 2021
Hepatobiliary phenotypes of adults with alpha-1 antitrypsin deficiency
Malin Fromme, Carolin V Schneider, Vitor Pereira, et al.
Human Genetics
|
September 19, 2012
Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD
Nadia N Hansel, Ingo Ruczinski, Nicholas Rafaels, et al.
Human Molecular Genetics
|
November 15, 2011
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13
Michael H Cho, Peter J Castaldi, Emily S Wan, et al.
COPD
|
April 19, 2011
Opportunities and challenges in the genetics of COPD 2010: an International COPD Genetics Conference report
Edwin K Silverman, Jørgen Vestbo, Alvar Agusti, et al.
Plos One
|
May 30, 2015
Correction: Susceptibility to chronic mucus hypersecretion, a genome wide association study
Akkelies E Dijkstra, Joanna Smolonska, Maarten van den Berge, et al.
Plos One
|
April 10, 2014
Susceptibility to chronic mucus hypersecretion, a genome wide association study
Akkelies E Dijkstra, Joanna Smolonska, Maarten van den Berge, et al.
Nature Genetics
|
February 27, 2019
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Phuwanat Sakornsakolpat, Dmitry Prokopenko, Maxime Lamontagne, et al.
Page
of 29