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The New England Journal of Medicine
|
May 24, 1973
Initiation of globin synthesis in beta-thalassemia
R G Crystal, N A Elson, A Nienhuis, et al.
The Journal of Clinical Investigation
|
September 1, 1991
Neutrophil accumulation in the lung in alpha 1-antitrypsin deficiency. Spontaneous release of leukotriene B4 by alveolar macrophages
R C Hubbard, G Fells, J Gadek, et al.
The American Journal of Pathology
|
March 1, 1985
Patterns of pulmonary structural remodeling after experimental paraquat toxicity. The morphogenesis of intraalveolar fibrosis
Y Fukuda, V J Ferrans, C I Schoenberger, et al.
Nature Genetics
|
February 1, 1993
Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA
C S Chu, B C Trapnell, S Curristin, et al.
The American Review of Respiratory Disease
|
January 1, 1988
Colchicine suppresses the release of fibroblast growth factors from alveolar macrophages in vitro. The basis of a possible therapeutic approach ot the fibrotic disorders
S I Rennard, P B Bitterman, T Ozaki, et al.
The American Journal of Pathology
|
March 1, 1986
Intraluminal fibrosis in interstitial lung disorders
F Basset, V J Ferrans, P Soler, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
January 1, 1985
Characterization of mononuclear phagocyte subpopulations in the human lung by using monoclonal antibodies: changes in alveolar macrophage phenotype associated with pulmonary sarcoidosis
A J Hance, S Douches, R J Winchester, et al.
The American Review of Respiratory Disease
|
January 1, 1985
Experimental polymyxin B-induced interstitial lung disease characterized by an accumulation of cytotoxic eosinophils in the alveolar structures
X H Sun, W B Davis, Y Fukuda, et al.
The American Journal of Pathology
|
August 1, 1990
Intraluminal fibrosis and elastic fiber degradation lead to lung remodeling in pulmonary Langerhans cell granulomatosis (histiocytosis X)
Y Fukuda, F Basset, P Soler, et al.
American Journal of Human Genetics
|
April 1, 1990
Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern
M D Holmes, M L Brantly, D T Curiel, et al.
Page
of 51
Search research articles
Search
Showing results (261-270 of 509) with videos related to
Sort By:
Page
of 51
The New England Journal of Medicine
|
May 24, 1973
Initiation of globin synthesis in beta-thalassemia
R G Crystal, N A Elson, A Nienhuis, et al.
The Journal of Clinical Investigation
|
September 1, 1991
Neutrophil accumulation in the lung in alpha 1-antitrypsin deficiency. Spontaneous release of leukotriene B4 by alveolar macrophages
R C Hubbard, G Fells, J Gadek, et al.
The American Journal of Pathology
|
March 1, 1985
Patterns of pulmonary structural remodeling after experimental paraquat toxicity. The morphogenesis of intraalveolar fibrosis
Y Fukuda, V J Ferrans, C I Schoenberger, et al.
Nature Genetics
|
February 1, 1993
Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA
C S Chu, B C Trapnell, S Curristin, et al.
The American Review of Respiratory Disease
|
January 1, 1988
Colchicine suppresses the release of fibroblast growth factors from alveolar macrophages in vitro. The basis of a possible therapeutic approach ot the fibrotic disorders
S I Rennard, P B Bitterman, T Ozaki, et al.
The American Journal of Pathology
|
March 1, 1986
Intraluminal fibrosis in interstitial lung disorders
F Basset, V J Ferrans, P Soler, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
January 1, 1985
Characterization of mononuclear phagocyte subpopulations in the human lung by using monoclonal antibodies: changes in alveolar macrophage phenotype associated with pulmonary sarcoidosis
A J Hance, S Douches, R J Winchester, et al.
The American Review of Respiratory Disease
|
January 1, 1985
Experimental polymyxin B-induced interstitial lung disease characterized by an accumulation of cytotoxic eosinophils in the alveolar structures
X H Sun, W B Davis, Y Fukuda, et al.
The American Journal of Pathology
|
August 1, 1990
Intraluminal fibrosis and elastic fiber degradation lead to lung remodeling in pulmonary Langerhans cell granulomatosis (histiocytosis X)
Y Fukuda, F Basset, P Soler, et al.
American Journal of Human Genetics
|
April 1, 1990
Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern
M D Holmes, M L Brantly, D T Curiel, et al.
Page
of 51