Rezultati - Michael R Knowles

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  1. 1
    The Influence of Genetics on Cystic Fibrosis Phenotypes

    The Influence of Genetics on Cystic Fibrosis Phenotypes od Michael R. Knowles, M. Drumm

    Izdano 2012
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  2. 2
    Mucus clearance as a primary innate defense mechanism for mammalian airways

    Mucus clearance as a primary innate defense mechanism for mammalian airways od Michael R. Knowles, Richard C. Boucher

    Izdano 2002
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  3. 3
    'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations

    'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations od Peadar G. Noone, Michael R. Knowles

    Izdano 2001
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  4. 4
    Mucus clearance as a primary innate defense mechanism for mammalian airways

    Mucus clearance as a primary innate defense mechanism for mammalian airways od Michael R. Knowles, Richard C. Boucher

    Izdano 2002
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  5. 5
    Mucus clearance as a primary innate defense mechanism for mammalian airways

    Mucus clearance as a primary innate defense mechanism for mammalian airways od Michael R. Knowles, Richard C. Boucher

    Izdano 2002
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  6. 6
    Cystic Fibrosis Disease Modifiers: Complex Genetics Defines the Phenotypic Diversity in a Monogenic Disease

    Cystic Fibrosis Disease Modifiers: Complex Genetics Defines the Phenotypic Diversity in a Monogenic Disease od Wanda K. O’Neal, Michael R. Knowles

    Izdano 2018
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  7. 7
    Increased Bioelectric Potential Difference across Respiratory Epithelia in Cystic Fibrosis

    Increased Bioelectric Potential Difference across Respiratory Epithelia in Cystic Fibrosis od Michael R. Knowles, John T. Gatzy, Richard C. Boucher

    Izdano 1981
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  8. 8
    Primary ciliary dyskinesia: improving the diagnostic approach

    Primary ciliary dyskinesia: improving the diagnostic approach od Margaret W. Leigh, Maimoona A. Zariwala, Michael R. Knowles

    Izdano 2009
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  9. 9
    Activation by Extracellular Nucleotides of Chloride Secretion in the Airway Epithelia of Patients with Cystic Fibrosis

    Activation by Extracellular Nucleotides of Chloride Secretion in the Airway Epithelia of Patients with Cystic Fibrosis od Michael R. Knowles, Lane L. Clarke, Richard C. Boucher

    Izdano 1991
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  10. 10
    Primary Ciliary Dyskinesia

    Primary Ciliary Dyskinesia od Michael R. Knowles, Maimoona A. Zariwala, Margaret W. Leigh

    Izdano 2016
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  11. 11
    Improved recovery of mycobacteria from respiratory secretions of patients with cystic fibrosis

    Improved recovery of mycobacteria from respiratory secretions of patients with cystic fibrosis od Susan Whittier, Roy L. Hopfer, Michael R. Knowles, Peter H. Gilligan

    Izdano 1993
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  12. 12
    Oxygen Consumption and Ouabain Binding Sites in Cystic Fibrosis Nasal Epithelium

    Oxygen Consumption and Ouabain Binding Sites in Cystic Fibrosis Nasal Epithelium od M. Jackson Stutts, Michael R. Knowles, J. T. Gatzy, Richard C. Boucher

    Izdano 1986
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  13. 13
    Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: Association of the 5T allele with selected CFTR mutations and its incidence in atypical sinopulmonary disease

    Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: Association of the 5T allele with selected CFTR mutations and its incidence in... od Kenneth J. Friedman, Ruth A. Heim, Michael R. Knowles, Lawrence M. Silverman

    Izdano 1997
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  14. 14
    Environmental Risks for Nontuberculous Mycobacteria. Individual Exposures and Climatic Factors in the Cystic Fibrosis Population

    Environmental Risks for Nontuberculous Mycobacteria. Individual Exposures and Climatic Factors in the Cystic Fibrosis Population od D. Rebecca Prevots, Jennifer Adjemian, Aisling G. Fernandez, Michael R. Knowles, Kenneth N. Olivier

    Izdano 2014
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  15. 15
    Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.

    Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation. od Richard C. Boucher, M. Jackson Stutts, Michael R. Knowles, Lewis C. Cantley, J. T. Gatzy

    Izdano 1986
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  16. 16
    Classifying Severity of Cystic Fibrosis Lung Disease Using Longitudinal Pulmonary Function Data

    Classifying Severity of Cystic Fibrosis Lung Disease Using Longitudinal Pulmonary Function Data od Mark Schluchter, Michael W. Konstan, Mitchell L. Drumm, James R. Yankaskas, Michael R. Knowles

    Izdano 2006
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  17. 17
    Cystic fibrosis gene mutations and pancreatitis risk: Relation to epithelial ion transport and trypsin inhibitor gene mutations

    Cystic fibrosis gene mutations and pancreatitis risk: Relation to epithelial ion transport and trypsin inhibitor gene mutations od Peadar G. Noone, Zhaoqing Zhou, Lawrence M. Silverman, Paul S. Jowell, Michael R. Knowles, Jonathan Cohn

    Izdano 2001
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  18. 18
    Correction of Aberrant Splicing of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene by Antisense Oligonucleotides

    Correction of Aberrant Splicing of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene by Antisense Oligonucleotides od Kenneth J. Friedman, Jolanta Kole, Jonathan Cohn, Michael R. Knowles, Lawrence M. Silverman, Ryszard Kole

    Izdano 1999
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  19. 19
    Plasma TGF‐β<sub>1</sub> in pediatric cystic fibrosis: Potential biomarker of lung disease and response to therapy

    Plasma TGF‐β<sub>1</sub> in pediatric cystic fibrosis: Potential biomarker of lung disease and response to therapy od William T. Harris, Marianne S. Muhlebach, Robert A. Oster, Michael R. Knowles, John P. Clancy, Terry L. Noah

    Izdano 2011
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  20. 20
    Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease

    Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease od Michael R. Knowles, M. Leigh Anne Daniels, Stephanie D. Davis, Maimoona A. Zariwala, Margaret W. Leigh

    Izdano 2013
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