Asthma: From Bronchoconstriction to Airways Inflammation and Remodeling

Nuclear Factor-κB — A Pivotal Transcription Factor in Chronic Inflammatory Diseases

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Transforming Growth Factor β in Tissue Fibrosis

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Predominant TH2-like Bronchoalveolar T-Lymphocyte Population in Atopic Asthma

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Eosinophilic Inflammation in Asthma

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Effect of Inhaled Formoterol and Budesonide on Exacerbations of Asthma

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Increased nitric oxide in exhaled air of asthmatic patients

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The matrix‐degrading metalloproteinases

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Life, death, and the pursuit of apoptosis.Preprint

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Collagen family of proteins

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Damage of the Airway Epithelium and Bronchial Reactivity in Patients with Asthma

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Inhibition of p38 MAPK Reduces Expression of Vascular Endothelial Growth Factor in Allergic Airway Disease

Kim, S. R., Lee, K. S., Park, S. J., Jeon, M. S., & Lee, Y. C. (2012) · Journal of Clinical Immunology · doi:10.1007/s10875-012-9672-5 · Cited by 20

Peroxidative Metabolism of β2-Agonists Salbutamol and Fenoterol and Their Analogues

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Responses and Limitations of the Respiratory System to Exercise

Lovering, A. T., Haverkamp, H. C., & Eldridge, M. W. (2005) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2005.05.005 · Cited by 20

Anti-asthmatic property and possible mode of activity of an ethanol leaf extract ofPolyscias fruticosa

Koffuor, G. A., Boye, A., Kyei, S., Ofori-Amoah, J., Asiamah, E. A., Barku, V. Y. A., Acheampong, J., Amegashie, E., & Awuku, A. K. (2015) · Pharmaceutical Biology · doi:10.3109/13880209.2015.1077465 · Cited by 20

Specific targeting and noninvasive magnetic resonance imaging of an asthma biomarker in the lung using polyethylene glycol functionalized magnetic nanocarriers

Faraj, A. A., Shaik, A. S., Afzal, S., Al‐Muhsen, S., & Halwani, R. (2015) · Contrast Media & Molecular Imaging · doi:10.1002/cmmi.1678 · Cited by 20

Volatile Anesthetics and Immunity

Sedghi, S., Kutscher, H. L., Davidson, B. A., & Knight, P. R. (2017) · Immunological Investigations · doi:10.1080/08820139.2017.1373905 · Cited by 20

CONTRACTILITY AND PHENOTYPE OF HUMAN BRONCHIOLE SMOOTH MUSCLE AFTER PROLONGED FETAL BOVINE SERUM EXPOSURE

Moir, L. M., Ward, J. P. T., & Hirst, S. J. (2003) · Experimental Lung Research · doi:10.1080/01902140303758 · Cited by 20

Extended freeze‐dried Mycobacterium bovis Bacillus Calmette–Guérin induces the release of interleukin‐12 but not tumour necrosis factor‐α by alveolar macrophages, both in vitro and in vivo

Hubeau, C., Singer, M., Lagranderie, M., Marchal, G., & Vargaftig, B. B. (2003) · Clinical & Experimental Allergy · doi:10.1046/j.1365-2222.2003.01612.x · Cited by 20

A Descriptive Study of Small Airway Reticular Basement Membrane Thickening in Clinically Stable Lung Transplant Recipients

Ward, C., Soyza, A. D., Fisher, A. J., Pritchard, G., Forrest, I., & Corris, P. A. (2005) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2004.02.018 · Cited by 20

Functional Effects of WNT1-Inducible Signaling Pathway Protein-1 on Bronchial Smooth Muscle Cell Migration and Proliferation in OVA-Induced Airway Remodeling

Yang, M., Du, Y., Xu, Z., & Jiang, Y. (2015) · Inflammation · doi:10.1007/s10753-015-0218-x · Cited by 19

Functional response to inhaled salbutamol and/or ipratropium bromide in Ascaris suum-sensitised cats with allergen-induced bronchospasms

Leemans, J., Kirschvink, N. A., Clercx, C., Cambier, C., & Gustin, P. G. (2009) · The Veterinary Journal · doi:10.1016/j.tvjl.2009.07.021 · Cited by 19

Gene-Metabolite Expression in Blood Can Discriminate Allergen-Induced Isolated Early from Dual Asthmatic Responses

Singh, A., Yamamoto, M., Kam, S. H. Y., Ruan, J., Gauvreau, G. M., O’Byrne, P. M., FitzGerald, J. M., Schellenberg, R. R., Boulet, L., Wojewodka, G., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067907 · Cited by 19

Combined budesonide/formoterol therapy in conjunction with allergen avoidance ameliorates house dust mite-induced airway remodeling and dysfunction

Johnson, J. R., Pacitto, S. R., Wong, J., Archer, E. W., Eirefelt, S., Miller‐Larsson, A., & Jordana, M. (2008) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.90229.2008 · Cited by 19

Bacterial DNA delays human eosinophil apoptosis

Ilmarinen, P., Hasala, H., Sareila, O., Moilanen, E., & Kankaanranta, H. (2008) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2008.11.012 · Cited by 19

Chemical-induced asthma and the role of clinical, toxicological, exposure and epidemiological research in regulatory and hazard characterization approaches

Vincent, M., Bernstein, J. A., Basketter, D. A., LaKind, J. S., Dotson, G. S., & Maier, A. (2017) · Regulatory Toxicology and Pharmacology · doi:10.1016/j.yrtph.2017.08.018 · Cited by 19

Nasal lavage cytology and mucosal histopathological alterations in patients with rhinitis

Kovalhuk, L. C. S., Telles, E. Q., Lima, M. N., & Filho, N. A. R. (2019) · Brazilian Journal of Otorhinolaryngology · doi:10.1016/j.bjorl.2019.01.005 · Cited by 19

Asthmatic Eosinophils Promote Contractility and Migration of Airway Smooth Muscle Cells and Pulmonary Fibroblasts In Vitro

Janulaitytė, I., Januškevičius, A., Kalinauskaitė-Žukauskė, V., Palačionytė, J., & Malakauskas, K. (2021) · Cells · doi:10.3390/cells10061389 · Cited by 21

Bronchodilator efficacy of the fixed combination of ipratropium and albuterol compared to albuterol alone in moderate-to-severe persistent asthma

Gelb, A. F., Karpel, J. P., Wise, R. A., Cassino, C., Johnson, P. A., & Conoscenti, C. (2008) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2008.02.005 · Cited by 19

Increased levels of angiopoietin‐2 in induced sputum from smoking asthmatic patients

Kanazawa, H., Asai, K., Tochino, Y., Kyoh, S., Kodama, T., & Hirata, K. (2009) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2009.03262.x · Cited by 19

Vasoactive peptides upregulate mRNA expression and secretion of vascular endothelial growth factor in human airway smooth muscle cells

Alagappan, V. K. T., Willems‐Widyastuti, A., Seynhaeve, A. L. B., Garrelds, I. M., ten Hagen, T. L. M., Saxena, P. R., & SHARMA, H. S. (2007) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:47:1:109 · Cited by 19

Cysteinyl leukotrienes regulate TGF-β1 and collagen production by bronchial fibroblasts obtained from asthmatic subjects

Eap, R., Jacques, E., Semlali, A., Plante, S., & Chakir, J. (2012) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2011.11.001 · Cited by 19

Site of inflammation influences site of hyperresponsiveness in experimental asthma

Collins, R. A., Sly, P. D., Turner, D. J., Herbert, C. A., & Kumar, R. K. (2003) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2003.09.003 · Cited by 19

The prevalence and identity of Chlamydia -specific IgE in children with asthma and other chronic respiratory symptoms

Patel, K., Anderson, E., Salva, P. S., & Webley, W. C. (2012) · Respiratory Research · doi:10.1186/1465-9921-13-32 · Cited by 19

Repeated Allergen Inhalation Induces Cytoskeletal Remodeling in Smooth Muscle from Rat Bronchioles

McVicker, C. G., Leung, S., Kanabar, V., Moir, L. M., Mahn, K., Chung, K. F., & Hirst, S. J. (2007) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0409oc · Cited by 19

Asthma 2008: Targeting Immunoglobulin E to Achieve Disease Control

Prenner, B. M. (2008) · Journal of Asthma · doi:10.1080/02770900802085485 · Cited by 19

In vitro wounding of airway smooth muscle cell monolayers increases expression of TGF-β receptors

Chen, G., & Khalil, N. (2002) · Respiratory Physiology & Neurobiology · doi:10.1016/s1569-9048(02)00111-8 · Cited by 19

Antigen challenge increases adherence of circulating neutrophils in horses with chronic obstructive pulmonary disease

Marr, K. A., Lees, P., & Cunningham, F. M. (2002) · Equine Veterinary Journal · doi:10.2746/042516402776181231 · Cited by 19

Angiopoietin-2 as a contributing factor of exercise-induced bronchoconstriction in asthmatic patients receiving inhaled corticosteroid therapy

Kanazawa, H., Tochino, Y., & Asai, K. (2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.09.026 · Cited by 20

Le remodelage bronchique dans l’asthme : mécanismes et enjeux thérapeutiques

Benayoun, L., & Pretolani, M. (2003) · médecine/sciences · doi:10.1051/medsci/2003193319 · Cited by 21

Monitoring response to treatment in asthma management: food for thought

Scichilone, N., Deykin, A., Pizzichini, E., Bellia, V., & Polosa, R. (2004) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2004.02020.x · Cited by 19

Inflammatory Diseases - A Modern Perspective

Nagal, A. (2011) · InTech eBooks · doi:10.5772/2437 · Cited by 19

Prevalence of Exercise-Induced Bronchoconstriction Measured by Standardized Testing in Healthy College Athletes

Burnett, D. M., Burns, S. P., Merritt, S., Wick, J., & Sharpe, M. R. (2016) · Respiratory Care · doi:10.4187/respcare.04493 · Cited by 19

Comprehensive review of Urtica dioica L. (Urticaceae) phytochemistry and anti-inflammatory properties

Parente, R., Paiva‐Santos, A. C., Cabral, C., & Costa, G. (2024) · Phytochemistry Reviews · doi:10.1007/s11101-024-09980-6 · Cited by 22

Genetic variation in immune signaling genes differentially expressed in asthmatic lung tissues

Tremblay, K., Daley, D., Chamberland, A., Lemire, M., Montpetit, A., Laviolette, M., Musk, A. W., James, A. L., Chan‐Yeung, M., Becker, A. B., et al. (2008) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2008.05.049 · Cited by 18

Inducible Nitric Oxide Synthase Inhibition Attenuates Physical Stress-Induced Lung Hyper-Responsiveness and Oxidative Stress in Animals with Lung Inflammation

Marques, R. H., Reis, F. G., Starling, C. M., Cabido, C., Almeida-Reis, R., Dohlnikoff, M., Prado, C. M., Leick, E. A., Martins, M. A., & Tibério, I. D. F. L. C. (2012) · NeuroImmunoModulation · doi:10.1159/000331264 · Cited by 18

Establishment and characterization of a murine model for allergic asthma using allergen-specific IgE monoclonal antibody to study pathological roles of IgE

Mizutani, N., Goshima, H., Nabe, T., & Yoshino, S. (2011) · Immunology Letters · doi:10.1016/j.imlet.2011.10.010 · Cited by 18

Prostaglandin modulation of airway inflammation and hyperresponsiveness in mice sensitized without adjuvant

Swedin, L., Ellis, R., Neimert-Andersson, T., Ryrfeldt, Å., Nilsson, G. P., Inman, M. D., Dahlén, S., & Mikael Adner, A. (2010) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2010.02.004 · Cited by 18

Effects of Inhaled Corticosteroids on Metalloproteinase-8 and Tissue Inhibitor of Metalloproteinase-1 in the Airways of Asthmatic Children

Obase, Y., Rytilä, P. H., Metso, T., Pelkonen, A. S., Tervahartiala, T. I., Turpeinen, M., Mäkelä, M., Saarialho‐Kere, U., Selroos, O., Sorsa, T. A., et al. (2009) · International Archives of Allergy and Immunology · doi:10.1159/000242362 · Cited by 18

Airway smooth muscle chemokine receptor expression and function in asthma

Saunders, R. M., Sutcliffe, A., Kaur, D., Siddiqui, S., Hollins, F., Wardlaw, A. J., Bradding, P. H., & Brightling, C. E. (2009) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2009.03310.x · Cited by 18

Potential roles of pentosidine in age-related and disease-related impairment of pulmonary functions in patients with asthma

Kanazawa, H., Tochino, Y., Kyoh, S., Ichimaru, Y., Asai, K., & Hirata, K. (2011) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.11.020 · Cited by 18

Signal peptide of eosinophil cationic protein upregulates transforming growth factor‐alpha expression in human cells

Chang, H., Kao, Y., Wu, C., Fan, T.-C., Lai, Y., Huang, K., Chang, Y., Tsai, J., & Chang, M. D. (2006) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21120 · Cited by 18

Effects of dynamic compression on lentiviral transduction in an in vitro airway wall model

Tomei, A. A., Choe, M. M., & Swartz, M. A. (2007) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00062.2007 · Cited by 18

Self-reported prenatal tobacco smoke exposure, AXL gene-body methylation, and childhood asthma phenotypes

Gao, L., Liu, X., Millstein, J., Siegmund, K. D., Dubeau, L., Maguire, R. L., Zhang, J. J., Fuemmeler, B. F., Kollins, S. H., Hoyo, C., et al. (2018) · Clinical Epigenetics · doi:10.1186/s13148-018-0532-x · Cited by 19

Mouse Models of Asthma: Characteristics, Limitations and Future Perspectives on Clinical Translation

Akkoç, T., O’Mahony, L., Ferstl, R., Akdiş, C. A., & Akkoç, T. (2021) · Advances in experimental medicine and biology · doi:10.1007/5584_2021_654 · Cited by 18

Effect of basic fibroblast growth factor on the proliferation, migration and phenotypic modulation of airway smooth muscle cells

Zou, H., Nie, X., Zhang, Y., Hu, M., & Alex, Z. Y. (2008) · Chinese Medical Journal · doi:10.1097/00029330-200803010-00011 · Cited by 18

Cytokines, structural cells of the lungs and airway inflammation

Laberge, S., & Bassam, S. E. (2004) · Paediatric Respiratory Reviews · doi:10.1016/s1526-0542(04)90009-7 · Cited by 18

A Locally Active Antiinflammatory Macrolide (MLD987) for Inhalation Therapy of Asthma

Hersperger, R., Buchheit, K., Cammisuli, S., Enz, A., Lohse, O., Ponelle, M., Schüler, W., Schweitzer, A., Walker, C., Zehender, H., et al. (2004) · Journal of Medicinal Chemistry · doi:10.1021/jm031101l · Cited by 18

Modulation of transcriptional responses by poly(I:C) and human rhinovirus: Effect of long-acting β2-adrenoceptor agonists

Rider, C. F., Miller‐Larsson, A., Proud, D., Giembycz, M. A., & Newton, R. C. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.02.056 · Cited by 18

Association ofCCR5-delta32 Mutation with Reduced Risk of Nonatopic Asthma in Slovenian Children

Berce, V., Repnik, K., & Potočnik, U. (2008) · Journal of Asthma · doi:10.1080/02770900802386024 · Cited by 18

Syk: A Novel Target for Treatment of Inflammation in Lung Disease

Sanderson, M. P., Lau, C., Schnapp, A., & Chow, C. (2009) · Inflammation & Allergy - Drug Targets · doi:10.2174/187152809788462626 · Cited by 18

CT Attenuation of the Bronchial Wall in Patients With Asthma: Comparison With Geometric Parameters and Correlation With Function and Histologic Characteristics

Léderlin, M., Laurent, F., Portron, Y., Ozier, A., Cochet, H., Berger, P., & Montaudon, M. (2012) · American Journal of Roentgenology · doi:10.2214/ajr.11.8396 · Cited by 18

Analysis of genomic responses in a rat lung model treated with a humidifier sterilizer containing polyhexamethyleneguanidine phosphate

Kim, M., Jeong, S. W., Choi, S., Han, J.-Y., Kim, S., Yoon, S., Oh, J., & Lee, K. (2016) · Toxicology Letters · doi:10.1016/j.toxlet.2016.11.005 · Cited by 18

Increased Expression of p22phox Mediates Airway Hyperresponsiveness in an Experimental Model of Asthma

Nagaraj, C., Haitchi, H. M., Heinemann, Á., Howarth, P. H., Olschewski, A., & Marsh, L. M. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6863 · Cited by 18

Summary of recommendations for the design of clinical trials and the registration of drugs used in the treatment of asthma

Holgate, S. T., Bousquet, J., Chung, K. F., Bisgaard, H. F., Pauwels, R., Fabbri, L. M., Rabe, K. F., Doherty, M., Snell, N. J. C., Cuss, F. M., et al. (2004) · Respiratory Medicine · doi:10.1016/j.rmed.2003.12.005 · Cited by 18

β-Adrenergic agonists inhibit corticosteroid-induced apoptosis of airway epithelial cells

Tse, R., Marroquin, B. A., Dorscheid, D. R., & White, S. R. (2003) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00030.2003 · Cited by 18

Use of the Mouse to Unravel Allergic Asthma: a Review of the Pathogenesis of Allergic Asthma in Mouse Models and Its Similarity to the Condition in Humans

Torres, R., Picado, C., & de Mora, F. (2005) · Archivos de Bronconeumología · doi:10.1016/s1579-2129(06)60415-1 · Cited by 18

Update on National Asthma Education and Prevention Program Pediatric Asthma Treatment Recommendations

Eid, N. S. (2004) · Clinical Pediatrics · doi:10.1177/000992280404300903 · Cited by 18

The effect of cyclodextrins on the aqueous solubility of a new MMP inhibitor: phase solubility, 1 H-NMR spectroscopy and molecular modeling studies, preparation and stability study of nebulizable solutions.

Bertholet, P., Gueders, M. M., Dive, G., Albert, A., Barillaro, V., Perly, B., Cataldo, D. D., Piel, G., Delattre, L., & Évrard, B. (2005) · PubMed · Cited by 18

Quantitative profiling of plasma peptides in asthmatic mice using liquid chromatography and mass spectrometry

Yeo, S., Roh, G. S., Kim, D., Lee, J. M., Seo, S., Cho, J. W., Kim, C., & Kwack, K. (2004) · PROTEOMICS · doi:10.1002/pmic.200400918 · Cited by 18

Differential Effects of Short-Acting β2-Agonists on Human Granulocyte Functions

Yasui, K., Kobayashi, N., Yamazaki, T., Agematsu, K., Matsuzaki, S., Nakata, S., & Baba, A. (2005) · International Archives of Allergy and Immunology · doi:10.1159/000089516 · Cited by 18

Physical Forces and Airway Remodeling in Asthma

Tschumperlin, D. J. (2011) · New England Journal of Medicine · doi:10.1056/nejme1103121 · Cited by 18

The geranyl acetophenone tHGA attenuates human bronchial smooth muscle proliferation via inhibition of AKT phosphorylation

Yap, H. M., Lee, Y. Z., Harith, H. H., Tham, C. L., Cheema, M. S., Shaari, K., & Israf, D. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-34847-0 · Cited by 17

The Wiser Strategy of Using Beta-Agonists in Asthma: Mechanisms and Rationales

Suh, D. I., & Johnston, S. L. (2024) · Allergy Asthma and Immunology Research · doi:10.4168/aair.2024.16.3.217 · Cited by 17

Synthetic double-stranded RNA enhances airway inflammation and remodelling in a rat model of asthma

Takayama, S., Tamaoka, M., Takayama, K., Okayasu, K., Tsuchiya, K., Miyazaki, Y., Sumi, Y., Martin, J. G., & Inase, N. (2011) · Immunology · doi:10.1111/j.1365-2567.2011.03473.x · Cited by 17

Genome-Wide Profiling of Antigen-Induced Time Course Expression Using Murine Models for Acute and Chronic Asthma

Park, S. G., Choi, J., Kim, H. J., Roh, G. S., Bok, J., Go, M. J., Kwack, K., Oh, B., & Kim, Y. (2007) · International Archives of Allergy and Immunology · doi:10.1159/000112502 · Cited by 17

The Targeted Oral, Once‐Daily Phosphodiesterase 4 Inhibitor Roflumilast and the Leukotriene Receptor Antagonist Montelukast Do Not Exhibit Significant Pharmacokinetic Interactions

Böhmer, G. M., Nassr, N., Wenger, M., Hünnemeyer, A., Lahu, G., Templin, S., Gleiter, C. H., & Hermann, R. (2009) · The Journal of Clinical Pharmacology · doi:10.1177/0091270008330980 · Cited by 17

Leukotriene B4 receptor 2 regulates the proliferation, migration, and barrier integrity of bronchial epithelial cells

Liu, M., Shen, J., Yuan, H., Chen, F., Song, H., Qin, H., Li, Y., Xu, J., Ye, Q., Li, S., et al. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26455 · Cited by 17

Transcriptomic Analysis Reveals a Link Between Hippo Signaling Pathway and Macrophages in Lungs of Mice with OVA-Induced Allergic Asthma

Xiao, H., Zhang, Q.-N., Sun, Q.-X., Li, L.-D., Xu, S.-Y., & Li, C.-Q. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s346505 · Cited by 17

Relationship Among Manganese, Arginase, and Nitric Oxide in Childhood Asthma

Koçyiğit, A., Zeyrek, D., Keles, H., & Köylü, A. (2004) · Biological Trace Element Research · doi:10.1385/bter:102:1-3:011 · Cited by 17

Relationship between Nasal and Bronchial Responsiveness in Perennial Allergic Rhinitic Patients with Asthma

Koh, Y., & Choi, I. S. (2002) · International Archives of Allergy and Immunology · doi:10.1159/000067593 · Cited by 17

Glucocorticoids Ameliorate Antigen-Induced Bronchial Smooth Muscle Hyperresponsiveness by Inhibiting Upregulation of RhoA in Rats

Chiba, Y., Goto, K., Hirahara, M., Sakai, H., & Misawa, M. (2008) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fp0071825 · Cited by 17

Regulation of asthmatic airway relaxation by estrogen and heat shock protein 90

Intapad, S., Dimitropoulou, C., Snead, C. M., Piyachaturawat, P., & Catravas, J. D. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.23045 · Cited by 17

Arginase 1 activity worsens lung‐protective immunity against Streptococcus pneumoniae infection

Knippenberg, S., Brumshagen, C., Aschenbrenner, F., Welte, T., & Maus, U. A. (2015) · European Journal of Immunology · doi:10.1002/eji.201445419 · Cited by 17

Mast Cell Mediators in Airway Remodeling

Oh, C. K. (2005) · KARGER eBooks · doi:10.1159/000087573 · Cited by 19

Resolution of allergic airways inflammation but persistence of airway smooth muscle proliferation after repeated allergen exposures

Leung, S. ‐., Eynott, P. R., Noble, A., Nath, P., & Chung, K. F. (2004) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2004.01870.x · Cited by 17

A subgroup analysis of the MONICA study: A 12-month, open-label study of add-on montelukast treatment in asthma patients

Virchow, J. C., Jr., Mehta, A., Ljungblad, L., & Mitfessel, H. (2010) · Journal of Asthma · doi:10.1080/02770903.2010.494753 · Cited by 17

Allergen inhalation decreases adenosine receptor expression in sputum and blood of asthma patients

Versluis, M., van den Berge, M., Timens, W., Luijk, B., Rutgers, B., Lammers, J. J., Postma, D. S., & Hylkema, M. N. (2008) · Allergy · doi:10.1111/j.1398-9995.2008.01735.x · Cited by 17

Increased expression of collagen receptors: α1β1 and α2β1 integrins on blood eosinophils in bronchial asthma

Bazan‐Socha, S., Bukiej, A., Pulka, G., Marcinkiewicz, C., & Musial, J. (2006) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2006.02540.x · Cited by 17

Measurement of airway inflammation in asthma

Wilson, N. (2002) · Current Opinion in Pulmonary Medicine · doi:10.1097/00063198-200201000-00005 · Cited by 17

A Review of Asthma and Scuba Diving

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Function of the Airway Epithelium in Asthma

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