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

Laitinen, L. A., Heino, M., Laitinen, A., Kava, T., & Haahtela, T. (1985) · American Review of Respiratory Disease · doi:10.1164/arrd.1985.131.4.599 · Cited by 1,278

Effect of chronic airway inflammation and exercise on pulmonary and systemic antioxidant status of healthy and heaves‐affected horses

Kirschvink, N. A., SMITH, N., Fiévez, L., Bougnet, V., Art, T., Degand, G., Marlin, D., ROBERTS, C., Genicot, B., Lindsey, P. J., et al. (2002) · Equine Veterinary Journal · doi:10.2746/042516402776180223 · Cited by 61

CD11b and Intercellular Adhesion Molecule-1 Are Involved in Pulmonary Neutrophil Recruitment in Lipopolysaccharide-Induced Airway Disease

Moreland, J. G., Fuhrman, R. M., Pruessner, J. A., & Schwartz, D. A. (2002) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.4694 · Cited by 61

Suppression of cytokine expression by roflumilast and dexamethasone in a model of chronic asthma

Herbert, C. A., Hettiaratchi, A., Webb, D. C., Thomas, P. S., Foster, P. S., & Kumar, R. K. (2008) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2008.02950.x · Cited by 61

Inflammation and remodeling in the adult and child with asthma

Jeffery, P. K. (2001) · Pediatric Pulmonology · doi:10.1002/ppul.2001 · Cited by 61

Opposite effect of corticosteroids and long‐acting β 2 ‐agonists on serum‐ and TGF‐β 1 ‐induced extracellular matrix deposition by primary human lung fibroblasts

Goulet, S., Bihl, M., Gambazzi, F., Tamm, M., & Roth, M. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20836 · Cited by 61

Effect of tiotropium bromide on airway remodeling in a chronic asthma model

Kang, J. Y., Rhee, C. K., Kim, J. S., Park, C. K., Kim, S. J., Lee, S. H., Yoon, H. K., Kwon, S. S., Kim, Y. K., & Lee, S. Y. (2012) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2012.05.005 · Cited by 60

Stress, asthma, and respiratory infections: Pathways involving airway immunology and microbial endocrinology

Trueba, A. F., & Ritz, T. (2012) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2012.09.012 · Cited by 63

A standardized methanol extract of Eclipta prostrata (L.) L. (Asteraceae) reduces bronchial hyperresponsiveness and production of Th2 cytokines in a murine model of asthma

Morel, L. J. D. F., de Azevedo, B. C., Carmona, F., Contini, S. H. T., Teles, A. M., Ramalho, F. S., Bertoni, B. W., França, S. D. C., Borges, M. D. C., & Pereira, A. M. S. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.12.008 · Cited by 60

CB 2 receptors regulate natural killer cells that limit allergic airway inflammation in a murine model of asthma

Ferrini, M. E., Hong, S., Stierle, A. A., Stierle, D. B., Stella, N., Roberts, K., & Jaffar, Z. H. (2016) · Allergy · doi:10.1111/all.13107 · Cited by 60

Regulatory effect of baicalin on the imbalance of Th17/Treg responses in mice with allergic asthma

Xu, L., Li, J., Zhang, Y., Zhao, P., & Zhang, X. (2017) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2017.07.013 · Cited by 60

Is Interleukin-13 Critical in Maintaining Airway Hyperresposiveness in Allergen-challenged Mice?

Leigh, R., Ellis, R., Wattie, J. N., Donaldson, D. D., & Inman, M. D. (2004) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200311-1488oc · Cited by 61

Therapeutic administration of Budesonide ameliorates allergen‐induced airway remodelling

McMillan, S. J., Xanthou, G., & Lloyd, C. M. (2005) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.02193.x · Cited by 60

Airway smooth muscle in asthma: Phenotype plasticity and function

Hirota, J. A., Nguyen, T. T. B., Schaafsma, D., Sharma, P. K., & Tran, T. (2008) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2008.12.004 · Cited by 59

Awara (Astrocaryum vulgare M.) pulp oil: Chemical characterization, and anti-inflammatory properties in a mice model of endotoxic shock and a rat model of pulmonary inflammation

Bony, E., Boudard, F., Brat, P., Dussossoy, E., Portet, K., Poucheret, P., Giaimis, J., & Michel, A. (2011) · Fitoterapia · doi:10.1016/j.fitote.2011.09.007 · Cited by 59

The inhaled Rho kinase inhibitor Y-27632 protects against allergen-induced acute bronchoconstriction, airway hyperresponsiveness, and inflammation

Schaafsma, D., Bos, I. S. T., Zuidhof, A. B., Zaagsma, J., & Meurs, H. (2008) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00498.2007 · Cited by 59

The Integrin-blocking Peptide RGDS Inhibits Airway Smooth Muscle Remodeling in a Guinea Pig Model of Allergic Asthma

Dekkers, B. G. J., Bos, I. S. T., Gosens, R., Halayko, A. J., Zaagsma, J., & Meurs, H. (2009) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200907-1065oc · Cited by 59

Is exhaled nitric oxide measurement a useful clinical test in asthma?

Smith, A. D., & Taylor, D. R. (2005) · Current Opinion in Allergy and Clinical Immunology · doi:10.1097/00130832-200502000-00010 · Cited by 59

Glucocorticoid-resistant asthma and novel anti-inflammatory drugs

Keenan, C. R., Salem, S., Fietz, E. R., Gualano, R. C., & Stewart, A. G. (2012) · Drug Discovery Today · doi:10.1016/j.drudis.2012.05.011 · Cited by 58

TGFβ1 induces IL‐6 and inhibits IL‐8 release in human bronchial epithelial cells: The role of Smad2/3

Ge, Q., Moir, L. M., Black, J. L., Oliver, B. G. G., & Burgess, J. K. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22295 · Cited by 58

Tryptase: potential role in airway inflammation and remodeling

Abraham, W. M. (2002) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00429.2001 · Cited by 58

Role of Transcription Factors in the Pathogenesis of Asthma and COPD

Caramori, G., Casolari, P., & Adcock, I. M. (2013) · Cell Communication & Adhesion · doi:10.3109/15419061.2013.775257 · Cited by 57

A TLR2 Agonist in German Cockroach Frass Activates MMP-9 Release and Is Protective against Allergic Inflammation in Mice

Page, K., Ledford, J. R., Zhou, P. H., & Wills-Karp, M. A. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900838 · Cited by 57

Asthma and pulmonary arterial hypertension: do they share a key mechanism of pathogenesis?

Said, S. I., Hamidi, S. A., & Bosc, L. V. G. (2010) · European Respiratory Journal · doi:10.1183/09031936.00097109 · Cited by 57

The effects of low dose leukotriene receptor antagonist therapy on airway remodeling and cysteinyl leukotriene expression in a mouse asthma model

Muz, M. H., Deveci, F., Bulut, Y., İlhan, N., Yekeler, H., & Turgut, T. (2006) · Experimental & Molecular Medicine · doi:10.1038/emm.2006.14 · Cited by 57

Mite avoidance can reduce air trapping and airway inflammation in allergic asthmatic children

Peroni, D. G., PIACENTINI, G. L., Costella, S., Pietrobelli, A., Bodini, A., Loiacono, A., Aralla, R., & Boner, A. L. (2002) · Clinical & Experimental Allergy · doi:10.1046/j.1365-2222.2002.01372.x · Cited by 57

FoxP3, GATA‐3 and T‐bet expression in elderly asthma

Pereira, S., Todo‐Bom, A. M., Geraldes, L., Schmidt‐Weber, C. B., Akdiş, C. A., & Mota‐Pinto, A. (2010) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2010.03640.x · Cited by 56

Down-regulation of Caveolin-1, an Inhibitor of Transforming Growth Factor-β Signaling, in Acute Allergen-induced Airway Remodeling

Saux, C. J. L., Teeters, K., Miyasato, S. K., Hoffmann, P. R., Bollt, O., Douet, V., Shohet, R. V., Broide, D. H., & Tam, E. K. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701572200 · Cited by 56

Exposure to multi-walled carbon nanotubes results in aggravation of airway inflammation and remodeling and in increased production of epithelium-derived innate cytokines in a mouse model of asthma

Ronzani, C., Casset, A., & Pons, F. (2013) · Archives of Toxicology · doi:10.1007/s00204-013-1116-3 · Cited by 56

Resolution of Inflammation in Asthma

Levy, B. D., Vachier, I., & Serhan, C. N. (2012) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2012.06.006 · Cited by 59

Profibrotic Effect of IL-9 Overexpression in a Model of Airway Remodeling

van den Brûle, S., Heymans, J., Havaux, X., Renauld, J., Lison, D., Huaux, F., & Denis, O. (2007) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0397oc · Cited by 60

Efficacy of Novel Highly Specific Bromodomain-Containing Protein 4 Inhibitors in Innate Inflammation–Driven Airway Remodeling

Tian, B., Liu, Z., Litvinov, J., Maroto, R., Jamaluddin, M., Rytting, E., Patrikeev, I., Ochoa, L., Vargas, G., Motamedi, M., et al. (2018) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2017-0445oc · Cited by 56

Airway Epithelial Dysfunction in Asthma: Relevant to Epidermal Growth Factor Receptors and Airway Epithelial Cells

Inoue, H., Akimoto, K., Homma, T., Tanaka, A., & Sagara, H. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9113698 · Cited by 56

Severe asthma: definition and mechanisms

Stirling, R. G., & Chung, K. F. (2001) · Allergy · doi:10.1034/j.1398-9995.2001.00143.x · Cited by 56

Lipoxins and lipoxin analogs in asthma

Levy, B. D. (2005) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2005.05.010 · Cited by 56

An inhalation model of airway allergic response to inhalation of environmentalAspergillus fumigatusconidia in sensitized BALB/c mice

Hoselton, S. A., Samarasinghe, A. E., Seydel, J. M., & Schuh, J. M. (2010) · Medical Mycology · doi:10.3109/13693786.2010.485582 · Cited by 56

Risk Factors for Near-Fatal Asthma

Gelb, A. F., Schein, A. J., Nussbaum, E., Shinar, C. M., Aelony, Y., Aharonian, H. S., & Zamel, N. (2004) · CHEST Journal · doi:10.1016/s0012-3692(15)31289-7 · Cited by 56

Lysophosphatidic acid in airway function and disease

Toews, M. L. (2002) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s1388-1981(02)00177-4 · Cited by 56

Severe asthma is an epithelial disease

Chanez, P. (2005) · European Respiratory Journal · doi:10.1183/09031936.05.00038605 · Cited by 56

Airway Endothelial Dysfunction in Asthma and Chronic Obstructive Pulmonary Disease: A Challenge for Future Research

Wanner, A., & Mendes, E. S. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201001-0038pp · Cited by 55

Ginsenoside Rh2 attenuates allergic airway inflammation by modulating nuclear factor-κB activation in a murine model of asthma

Li, L. C., Piao, H. M., Zheng, M. Y., LIN, Z. H., Choi, Y. H., & Yan, G. H. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4272 · Cited by 55

Adult attention deficit hyperactivity disorder is associated with asthma

Fasmer, O. B., Halmøy, A., Eagan, T., Oedegaard, K. J., & Haavik, J. (2011) · BMC Psychiatry · doi:10.1186/1471-244x-11-128 · Cited by 58

Eosinophils Induce Airway Smooth Muscle Cell Proliferation

Halwani, R., Vazquez‐Tello, A., Sumi, Y., Pureza, M. A., BaHammam, A. S., Al-Jahdali, H. H., GOUNNI, A. S., Mahboub, B., Al‐Muhsen, S., & Hamid, Q. A. (2012) · Journal of Clinical Immunology · doi:10.1007/s10875-012-9836-3 · Cited by 55

Functional relevance of NLRP3 inflammasome-mediated interleukin (IL)-1β during acute allergic airway inflammation

Ritter, M., Straubinger, K., Schmidt, S., Busch, D. H., Hagner, S., Garn, H., da Costa, C. P., & Layland, L. E. (2014) · Clinical & Experimental Immunology · doi:10.1111/cei.12400 · Cited by 56

Effects of Angelicin on Ovalbumin (OVA)-Induced Airway Inflammation in a Mouse Model of Asthma

Wei, D., Guo, X., Lin, L., Lin, M.-X., Gong, Y., Bin-yu, Y., & Huang, M. (2016) · Inflammation · doi:10.1007/s10753-016-0423-2 · Cited by 55

Bronchial Hyperresponsiveness, Airway Inflammation, and Airflow Limitation in Endurance Athletes

Vergès, S., Devouassoux, G., Flore, P., Rossini, E., Fior‐Gozlan, M., Levy, P. A., & Wuyam, B. (2005) · CHEST Journal · doi:10.1378/chest.127.6.1935 · Cited by 55

Gradual increase in priming of human eosinophils during extravasation from peripheral blood to the airways in response to allergen challenge

Luijk, B., Lindemans, C. A., Kanters, D. H. A. J., van der Heijde, R., Bertics, P. J., Lammers, J. J., Bates, M. E., & Koenderman, L. (2005) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.02.002 · Cited by 55

Spirometry in 3–5-year-old children with asthma

Nève, V., Edmé, J., Devos, P., Deschildre, A., Thumerelle, C., Santos, C., Methlin, C., Matran, M., & Matran, R. (2006) · Pediatric Pulmonology · doi:10.1002/ppul.20389 · Cited by 55

Airway inflammation in asthma and its consequences: Implications for treatment in children and adults

Djukanović, R. (2002) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2002.124568 · Cited by 55

BET Bromodomains Regulate Transforming Growth Factor-β-induced Proliferation and Cytokine Release in Asthmatic Airway Smooth Muscle

Perry, M. M., Durham, A. L., Austin, P. J., Adcock, I. M., & Chung, K. F. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.612671 · Cited by 54

The Other T Helper Cells in Asthma Pathogenesis

Vock, C., Hauber, H., & Wegmann, M. (2010) · Journal of Allergy · doi:10.1155/2010/519298 · Cited by 56

A Randomized Controlled Trial of the Effect of Broccoli Sprouts on Antioxidant Gene Expression and Airway Inflammation in Asthmatics

Sudini, K. R., Diette, G. B., Breysse, P. N., McCormack, M. C., Bull, D., Biswal, S. S., Zhai, S., Brereton, N. H., Peng, R. D., & Matsui, E. C. (2016) · The Journal of Allergy and Clinical Immunology In Practice · doi:10.1016/j.jaip.2016.03.012 · Cited by 56

Bronchial Epithelial IgA Secretion Is Impaired in Asthma. Role of IL-4/IL-13

Ladjemi, M. Z., Gras, D., Dupasquier, S., Detry, B. R., Lecocq, M., Garulli, C., Fregimilicka, C., Bouzin, C., Gohy, S. T., Chanez, P., et al. (2018) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201703-0561oc · Cited by 54

Th2-TRMs Maintain Life-Long Allergic Memory in Experimental Asthma in Mice

Bošnjak, B., Kazemi, S., Altenburger, L. M., Mokrović, G., & Epstein, M. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00840 · Cited by 54

Oxidative Imbalance as a Crucial Factor in Inflammatory Lung Diseases: Could Antioxidant Treatment Constitute a New Therapeutic Strategy?

Victoni, T., Barreto, E., Lagente, V., & Carvalho, V. F. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6646923 · Cited by 54

Treatment of Asthma and Food Allergy With Herbal Interventions From Traditional Chinese Medicine

Li, X.-M. (2011) · Mount Sinai Journal of Medicine A Journal of Translational and Personalized Medicine · doi:10.1002/msj.20294 · Cited by 54

Association between concentration of trace elements in serum and bronchial asthma among Japanese general population

Urushidate, S., Matsuzaka, M., Okubo, N., Iwasaki, H., Hasebe, T., Tsuya, R., Iwane, K., Inoüe, R., Yamai, K., Danjo, K., et al. (2010) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2010.06.001 · Cited by 53

Monitoring asthma therapy using indirect bronchial provocation tests*

Brannan, J. D., Koskela, H. O., & Anderson, S. D. (2007) · The Clinical Respiratory Journal · doi:10.1111/j.1752-699x.2007.00004.x · Cited by 53

Obstructive Lung Diseases: COPD, Asthma, and Many Imitators

Ryu, J. H., & Scanlon, P. D. (2001) · Mayo Clinic Proceedings · doi:10.4065/76.11.1144 · Cited by 53

Fluticasone and salmeterol downregulatein vitro, fibroblast proliferation and ICAM-1 or H-CAM expression

Silvestri, M., Fregonese, L., Sabatini, F., Dasic, G., & Rossi, G. A. (2001) · European Respiratory Journal · doi:10.1183/09031936.01.00067901 · Cited by 53

Citation classics: Top 50 cited articles in ‘respiratory system’

Tam, W., Wong, E. L., Wong, F. C. Y., & Hui, D. S. C. (2012) · Respirology · doi:10.1111/j.1440-1843.2012.02262.x · Cited by 52

Complement C3a Regulates Late Asthmatic Response and Airway Hyperresponsiveness in Mice

Mizutani, N., Nabe, T., & Yoshino, S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901468 · Cited by 52

Antioxidant Down-Regulates Interleukin-18 Expression in Asthma

Lee, K. S., Kim, S. R., Park, S. J., Min, K. H., Lee, K. Y., Jin, S. M., Yoo, W. H., & Lee, Y. C. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.024737 · Cited by 52

Oral exposure to cadmium and mercury alone and in combination causes damage to the lung tissue of Sprague-Dawley rats

Naidoo, S. V. K., Bester, M. J., Arbi, S., Venter, C., Dhanraj, P., & Oberholzer, H. M. (2019) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2019.03.021 · Cited by 52

Murine model of chronic human asthma

Kumar, R. K., & Foster, P. S. (2001) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2001.00981.x · Cited by 52

CD4+ T-Lymphocytes Regulate Airway Remodeling and Hyper-Reactivity in a Mouse Model of Chronic Asthma

Foster, P. S., Yang, M., Herbert, C. A., & Kumar, R. K. (2002) · Laboratory Investigation · doi:10.1038/labinvest.3780438 · Cited by 52

Effect ofMoringa oleiferaLam. Seed Extract on Toluene Diisocyanate-Induced Immune-Mediated Inflammatory Responses in Rats

Mahajan, S. G., Mali, R. G., & Mehta, A. A. (2007) · Journal of Immunotoxicology · doi:10.1080/15476910701337472 · Cited by 52

Relationship between exhaled air temperature and exhaled nitric oxide in childhood asthma

PIACENTINI, G. L., Bodini, A., Zerman, L., Costella, S., Zanolla, L., Peroni, D. G., & Boner, A. L. (2002) · European Respiratory Journal · doi:10.1183/09031936.02.00237702 · Cited by 52

Atypical development of the tracheal basement membrane zone of infant rhesus monkeys exposed to ozone and allergen

Evans, M. J., Fanucchi, M. V., Baker, G. L., Winkle, L. S. V., Pantle, L. M., Nishio, S. J., Schelegle, E. S., Gershwin, L. J., Miller, L. A., Hyde, D. M., et al. (2003) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00175.2003 · Cited by 52

Infection withStrongyloides venezuelensisInduces Transient Airway Eosinophilic Inflammation, an Increase in Immunoglobulin E, and Hyperresponsiveness in Rats

Silveira, M. R., Nunes, K. P., Cara, D. C., Souza, D. G., Corrêa, A., Teixeira, M. M., & Negrão‐Corrêa, D. A. (2002) · Infection and Immunity · doi:10.1128/iai.70.11.6263-6272.2002 · Cited by 52

Direct inhibition of arginase attenuated airway allergic reactions and inflammation in a Dermatophagoides farinae-induced NC/Nga mouse model

Takahashi, N., Ogino, K., Takemoto, K., Hamanishi, S., Wang, D.-H., Takigawa, T., Shibamori, M., Ishiyama, H., & Fujikura, Y. (2010) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00216.2009 · Cited by 52

Pheretima aspergillum decoction suppresses inflammation and relieves asthma in a mouse model of bronchial asthma by NF-κB inhibition

Huang, C., Li, W., Wu, B., Chen, W., Chen, L., Mo, G.-W., Zhang, Q., Gong, L., Li, J., Zhang, H., et al. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.05.028 · Cited by 51

Regulatory T cells mediated immunomodulation during asthma: a therapeutic standpoint

Khan, M. A. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02632-1 · Cited by 53

A guinea pig model of acute and chronic asthma using permanently instrumented and unrestrained animals

Meurs, H., Santing, R. E., Remie, R., van der Mark, T. W., Westerhof, F., Zuidhof, A. B., Bos, I. S. T., & Zaagsma, J. (2006) · Nature Protocols · doi:10.1038/nprot.2006.144 · Cited by 51

The Distinctive Effects of Acute and Chronic Psychological Stress on Airway Inflammation in a Murine Model of Allergic Asthma

Okuyama, K., Ohwada, K., Sakurada, S., Sato, N., Sora, I., Tamura, G., Takayanagi, M., & Ohno, I. (2007) · Allergology International · doi:10.2332/allergolint.o-06-435 · Cited by 52

The safety and quality of endobronchial biopsy in children under five years old

Saglani, S. (2003) · Thorax · doi:10.1136/thorax.58.12.1053 · Cited by 51

Hierarchical suppression of asthma-like responses by mucosal tolerance

Keller, A. C., Mucida, D., Gomes, E., Faquim-Mauro, E. L., Faria, A. M. C., Rodriguez, D., & Russo, M. (2006) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.10.019 · Cited by 51

IL-18 modulates chronic fungal asthma in a murine model; putative involvement of Toll-like receptor-2

Blease, K., Kunkel, S. L., & Hogaboam, C. M. (2001) · Inflammation Research · doi:10.1007/pl00000233 · Cited by 51

Inter‐relationships between airway inflammation, reticular basement membrane thickening and bronchial hyper‐reactivity to methacholine in asthma; a systematic bronchoalveolar lavage and airway biopsy analysis

Ward, C., Reid, D. W., Orsida, B., Feltis, B., Ryan, V. A., Johns, D. P., & Walters, E. H. (2005) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2005.02365.x · Cited by 51

Caveolins and Lung Function

Maniatis, N. A., Chernaya, O., Shinin, V., & Minshall, R. D. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-1222-9_11 · Cited by 50

Docosahexaenoic Acid Derivative Prevents Inflammation and Hyperreactivity in Lung

Morin, C., Fortin, S., Cantin, A. M., & Rousseau, É. (2010) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2010-0156oc · Cited by 50

Pharmacology of airway smooth muscle proliferation

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