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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The role of caveolae in the pathophysiology of lung diseases

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YAP is up-regulated in the bronchial airway smooth muscle of the chronic asthma mouse model.

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Focal Adhesion Kinase Regulates Collagen I–Induced Airway Smooth Muscle Phenotype Switching

Dekkers, B. G. J., Spanjer, A. I. R., van der Schuyt, R. D., Kuik, W.-J., Zaagsma, J., & Meurs, H. (2013) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.113.203042 · Cited by 25

EVALUATION OF ANTI-ASTHMATIC PROPERTY OF SOLANUM XANTHOCARPUM FLOWER EXTRACTS.

Vadnere, G. P., & Singhai, A. K. (2008) · Cited by 25

Association between reduced bronchodilatory effect of deep inspiration and loss of alveolar attachments

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Markers of Vascular Perturbation Correlate with Airway Structural Change in Asthma

Johansson, M. W., Kruger, S. J., Schiebler, M. L., Evans, M. D., Sorkness, R. L., Denlinger, L. C., Busse, W. W., Jarjour, N. N., Montgomery, R. R., Mosher, D. F., et al. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201301-0185oc · Cited by 24

SETD7 promotes TNF-α-induced proliferation and migration of airway smooth muscle cells in vitro through enhancing NF-κB/CD38 signaling

Wu, Y., Zou, F., Lu, Y., Li, X. J., Li, F., Feng, X.-L., Sun, X., & Liu, Y. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.04.043 · Cited by 24

MicroRNA-744 Inhibits Proliferation of Bronchial Epithelial Cells by Regulating Smad3 Pathway via Targeting Transforming Growth Factor-β1 (TGF-β1) in Severe Asthma

Huang, H., Lu, H., Liang, L., Zhi, Y., Huo, B., Wu, L., Xu, L., & Shen, Z.-B. (2019) · Medical Science Monitor · doi:10.12659/msm.912412 · Cited by 24

Salton Sea aerosol exposure in mice induces a pulmonary response distinct from allergic inflammation

Biddle, T. A., Li, Q., Maltz, M. R., Tandel, P. N., Chakraborty, R., Yisrael, K., Drover, R. W., Cocker, D. R., & Lo, D. D. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.148450 · Cited by 24

Long-term exposure to ambient temperature and mortality risk in China: A nationwide study using the difference-in-differences design

Hu, J., Zhou, M., Qin, M., Tong, S., Hou, Z., Xu, Y., Zhou, C., Xiao, Y., Yu, M., Huang, B., et al. (2021) · Environmental Pollution · doi:10.1016/j.envpol.2021.118392 · Cited by 24

Unraveling the Link between Ιnsulin Resistance and Bronchial Asthma

Bartziokas, Κ., Papaioannou, A. Ι., Drakopanagiotakis, F., Gouveri, E., Παπάνας, Ν., & Steiropoulos, P. (2024) · Biomedicines · doi:10.3390/biomedicines12020437 · Cited by 26

Cellular network in airways inflammation and remodelling

Vignola, A. M., Grutta, S. L., Chiappara, G., Benkeder, A., Bellia, V., & Bonsignore, G. (2002) · Paediatric Respiratory Reviews · doi:10.1053/prrv.2001.0166 · Cited by 24

Flunisolide Decreases Exhaled Nitric Oxide and Nitrotyrosine Levels in Asthmatic Children

Bodini, A., Peroni, D. G., Zardini, F., Corradi, M., Alinovi, R., Boner, A. L., & PIACENTINI, G. L. (2006) · Mediators of Inflammation · doi:10.1155/mi/2006/31919 · Cited by 24

Clinical Significance of Plasma and Serum Vascular Endothelial Growth Factor in Asthma

Lee, K. Y., Lee, K. S., Park, S. J., Kim, S. R., Min, K. H., Choe, Y. H., & Lee, Y. C. (2008) · Journal of Asthma · doi:10.1080/02770900802216775 · Cited by 24

The importance of airway remodelling in the natural course of asthma

Janson, C. (2010) · The Clinical Respiratory Journal · doi:10.1111/j.1752-699x.2010.00194.x · Cited by 24

Gene Expression Profiling in Lungs of Chronic Asthmatic Mice Treated with Galectin-3: Downregulation of Inflammatory and Regulatory Genes

López, E., Zafra, M. P., Sastre, B., Gámez, C., Lahoz, C., & del Pozo, V. (2011) · Mediators of Inflammation · doi:10.1155/2011/823279 · Cited by 26

In Vivo Micro-CT Assessment of Airway Remodeling in a Flexible OVA-Sensitized Murine Model of Asthma

Léderlin, M., Ozier, A., Dournes, G., Ousova, O., Girodet, P., Bégueret, H., Marthan, R., Montaudon, M., Laurent, F., & Berger, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048493 · Cited by 24

The effect of cannabinoids on dinitrofluorobenzene-induced experimental asthma in mice

Bozkurt, T. E., Yaşar, Y. K., Durlu‐Kandilci, N. T., Onder, S. C., & Şahin-Erdemli, İ. (2016) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2016.05.012 · Cited by 24

Nocturnal Heart Rate Variability Spectrum Characterization in Preschool Children With Asthmatic Symptoms

Milagro, J., Gil, E., Lázaro, J. M., Seppä, V., Malmberg, L. P., Pelkonen, A. S., Kotaniemi‐Syrjänen, A., Mäkelä, M. J., Viik, J., & Bailón, R. (2017) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2017.2775059 · Cited by 24

Epigenetic Aspects of Chronic Diseases

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Endothelial cells in the innate response to allergens and initiation of atopic asthma

Asosingh, K., Weiss, K., Queisser, K. A., Wanner, N., Yin, M., Aronica, M. A., & ERZURUM, S. C. (2018) · Journal of Clinical Investigation · doi:10.1172/jci97720 · Cited by 24

Immunomodulation in Cystic Fibrosis: Why and How?

Giacalone, V. D., Dobosh, B. S., Gaggar, A., Tirouvanziam, R. M., & Margaroli, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093331 · Cited by 24

Cell permeable NFAT inhibitory peptide Sim-2-VIVIT inhibits T-cell activation and alleviates allergic airway inflammation and hyper-responsiveness

Choi, J., Sohn, J.-H., Park, T. Y., Park, J., & Lee, S. (2012) · Immunology Letters · doi:10.1016/j.imlet.2012.01.016 · Cited by 25

Isosteric ramatroban analogs: selective and potent CRTH-2 antagonists

Robarge, M. J., Bom, D. C., Tumey, L. N., Varga, N., Gleason, E., Silver, D., Song, J., Murphy, S. M., Ekema, G., Doucette, C., et al. (2005) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2004.12.055 · Cited by 24

Is allergic asthma associated with delayed fetal maturation or the persistence of conserved fetal genes?

Bousquet, J., Vignola, A. M., & Yssel, H. (2000) · Allergy · doi:10.1034/j.1398-9995.2000.00923.x · Cited by 24

Toll-Like Receptor Signaling: Emerging Opportunities in Human Diseases and Medicine

Bhattacharjee, R. N., & Akira, S. (2005) · Current Immunology Reviews · doi:10.2174/1573395052952897 · Cited by 24

Regular treatment with formoterol for chronic asthma: serious adverse events

Cates, C. J., Cates, M. J., & Lasserson, T. J. (2008) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006923.pub2 · Cited by 24

Respiratory syncytial virus augments production of fibroblast growth factor basic in vitro: Implications for a possible mechanism of prolonged wheezing after infection

Dosanjh, A., Rednam, S., & Martin, M. (2003) · Pediatric Allergy and Immunology · doi:10.1046/j.0905-6157.2003.00090.x · Cited by 23

Targeting CXCR2 signaling in inflammatory lung diseases: neutrophil-driven inflammation and emerging therapies

Hussain, M. S., Goyal, A., Goyal, K., Renuka Jyothi, S., Nellore, J., Shahwan, M. J., Rekha, A., Ali, H., Dhanasekaran, M., MacLoughlin, R. J., et al. (2025) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-025-03970-x · Cited by 24

An overview of the biology of a long-acting inhaled treprostinil prodrug

Chapman, R. W., Corboz, M. R., Malinin, V., Plaunt, A. J., Konicek, D. M., Li, Z., & Perkins, W. R. (2020) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2021.102002 · Cited by 23

Recent advances of eosinophils and its correlated diseases

Zhang, T., Zhu, H., Zhang, J., Huang, Z., Xiang, Z., & Hong, T. (2022) · Frontiers in Public Health · doi:10.3389/fpubh.2022.954721 · Cited by 23

Asthma in cystic fibrosis.

Balfour-Lynn, I. M. (2003) · Europe PMC (PubMed Central) · Cited by 23

Clarithromycin suppresses airway hyperresponsiveness and inflammation in mouse models of asthma

Hrvačić, B., Bošnjak, B., Bosnar, M., Ferenčić, Ž., Glojnarić, I., & Haber, V. E. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.06.032 · Cited by 23

Activation of protease-activated receptors (PARs)-1 and -2 promotes alpha-smooth muscle actin expression and release of cytokines from human lung fibroblasts

Asokananthan, N., Lan, R. S., Graham, P. T., Bakker, A. J., Tokanovic, A., & Stewart, G. A. (2015) · Physiological Reports · doi:10.14814/phy2.12295 · Cited by 23

Leukotriene D4 and Interleukin-13 Cooperate to Increase the Release of Eotaxin-3 by Airway Epithelial Cells

Provost, V., Langlois, A., Chouinard, F., Rola‐Pleszczynski, M., Chakir, J., Flamand, N., & Laviolette, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043544 · Cited by 23

The synergistic anti-asthmatic effects of glycyrrhizin and salbutamol

Yang, Y., Shi, Q., Liu, Z., Li, R.-J., Pan, P., Hou, Y., Lu, W., & Bai, G. (2010) · Acta Pharmacologica Sinica · doi:10.1038/aps.2009.207 · Cited by 23

L-Arginine administration attenuates airway inflammation by altering L-arginine metabolism in an NC/Nga mouse model of asthma

Zhang, R., Kubo, M., Murakami, I., Setiawan, H., Takemoto, K., Inoue, K., Fujikura, Y., & Ogino, K. (2015) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.14-140 · Cited by 23

Smoking Affects Eotaxin Levels in Asthma Patients

Krisiukėnienė, A., Babušytė, A., Stravinskaitė, K., Lötvall, J. O., Sakalauskas, R., & Šitkauskienė, B. (2009) · Journal of Asthma · doi:10.1080/02770900902846349 · Cited by 23

Effect of formoterol with or without budesonide in repeated low-dose allergen challenge

Dahlén, B., Lantz, A.-S., IHRE, E., Skedinger, M., Henriksson, E. W., Jörgensen, L., Ekström, T., Se, D., & Larsson, K. (2009) · European Respiratory Journal · doi:10.1183/09031936.00095508 · Cited by 23

Surfactant protein SP-D modulates activity of immune cells: proteomic profiling of its interaction with eosinophilic cells

Mahajan, L., Gautam, P., Dodagatta-Marri, E., Madan, T., & Kishore, U. (2014) · Expert Review of Proteomics · doi:10.1586/14789450.2014.897612 · Cited by 23

Airway hyperresponsiveness is associated with activated CD4+ T cells in the airways

Zosky, G. R., Larcombe, A. N., White, O. J., Burchell, J. T., von Garnier, C., Holt, P. G., Turner, D. J., Wikström, M. E., Sly, P. D., & Stumbles, P. A. (2009) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00053.2009 · Cited by 23

Barrier Housing and Gender Effects on Allergic Airway Disease in a Murine House Dust Mite Model

Weiss, K., Wanner, N., Queisser, K. A., Frimel, M., Nunn, T., Myshrall, T., Sangwan, N., ERZURUM, S. C., & Asosingh, K. (2021) · ImmunoHorizons · doi:10.4049/immunohorizons.2000096 · Cited by 23

Exhaled breath temperature as a marker of airway remodelling in asthma: a preliminary study

PIACENTINI, G. L., Peroni, D. G., Bodini, A., Corradi, M., & Boner, A. L. (2008) · Allergy · doi:10.1111/j.1398-9995.2007.01622.x · Cited by 23

GSTA1, GSTO1 and GSTO2 gene polymorphisms in Italian asthma patients

Polimanti, R. A., Piacentini, S., Moscatelli, B., Pellicciotti, L., Manfellotto, D., & Fuciarelli, M. (2010) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2010.05385.x · Cited by 23

Δ9-Tetrahydrocannabinol reverses TNFα-induced increase in airway epithelial cell permeability through CB2 receptors

Shang, V., Kendall, D. A., & Roberts, R. E. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.09.008 · Cited by 23

The involvement of matrix metalloproteinases in basement membrane injury in a murine model of acute allergic airway inflammation

Kumagai, K., Ohno, I., Imai, K., Nawata, J., Hayashi, K., Okada, S., Senoo, H., Hattori, T., & Shirato, K. (2002) · Clinical & Experimental Allergy · doi:10.1046/j.1365-2745.2002.01491.x · Cited by 23

The disease management approach to controlling asthma

Haahtela, T. (2002) · Respiratory Medicine · doi:10.1053/rmed.2001.1231 · Cited by 23

Cytokine production from sputum cells in eosinophilic versus non-eosinophilic asthmatics

Quaedvlieg, V., Henket, M., Sele, J., & Louis, R. E. (2005) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2005.02968.x · Cited by 23

Challenges in pulmonary fibrosis: 7 {middle dot} Novel therapies and lung transplantation

Williams, T. J., & Wilson, J. W. (2008) · Thorax · doi:10.1136/thx.2004.031054 · Cited by 23

Short-term variability in respiratory impedance and effect of deep breath in asthmatic and healthy subjects with airway smooth muscle activation and unloading

Gobbi, A., Pellegrino, R., Gulotta, C., Antonelli, A., Pompilio, P. P., Crimi, C., Torchio, R., Dutto, L., Parola, P., Dellacà, R. L., et al. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00013.2013 · Cited by 22

A short history from Karelia study to biodiversity and public health interventions

Haahtela, T., Alenius, H. T., Auvinen, P., Fyhrquist, N., von Hertzen, L., Jousilahti, P., Karisola, P., Laatikainen, T. K., Lehtimäki, J., Paalanen, L., et al. (2023) · Frontiers in Allergy · doi:10.3389/falgy.2023.1152927 · Cited by 24

Association of sleep disorders with asthma: a meta-analysis

Liu, X., Hong, C., Liu, Z., Fan, L., Yin, M., Yunhu, C., Ren, X., & Gu, X. (2023) · BMJ Open Respiratory Research · doi:10.1136/bmjresp-2023-001661 · Cited by 22

Deciphering the Interplay between the Epithelial Barrier, Immune Cells, and Metabolic Mediators in Allergic Disease

Kan, L. L., Li, P., Hon, S. S.-M., Lai, A. Y.-T., Li, A., Wong, K. C., Huang, D., & Wong, C. K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25136913 · Cited by 22

Relaxant effects of a hydroalcoholic extract of Ruta graveolens on isolated rat tracheal rings

Águila, L., Jenny Ruedlinger, S., Mansilla, K., Ordenes, J., Salvatici, R. P., Campos, R. R., & Romero, F. (2015) · Biological Research · doi:10.1186/s40659-015-0017-8 · Cited by 22

Postnatal Development of the Lamina Reticularis in Primate Airways

Evans, M. J., Fanucchi, M. V., Plopper, C. G., & Hyde, D. M. (2010) · The Anatomical Record · doi:10.1002/ar.20824 · Cited by 22

Blocking of Akt/NF-κB Signaling by Pentoxifylline Inhibits Platelet-Derived Growth Factor–Stimulated Proliferation in Brown Norway Rat Airway Smooth Muscle Cells

Chiou, Y., Shieh, J., & Lin, C. (2006) · Pediatric Research · doi:10.1203/01.pdr.0000246105.56278.98 · Cited by 22

High sensitivity C-reactive protein: Its correlation with sputum cell counts in bronchial asthma

Allam, M. H., Said, A. F., Omran, A., El‐Rehim, D. M. A., & Kasem, A. (2009) · Respiratory Medicine · doi:10.1016/j.rmed.2009.06.020 · Cited by 22

Mast cell engraftment of the peripheral lung enhances airway hyperresponsiveness in a mouse asthma model

Fuchs, B., Sjöberg, L., Westerberg, C. M., Ekoff, M., Swedin, L., Dahlén, S., Mikael Adner, A., & Nilsson, G. P. (2012) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00227.2012 · Cited by 22

Protective effects of phosphodiesterase inhibitors on lung function and remodeling in a murine model of chronic asthma

CAMPOS, H. S., Xisto, D. G., Oliveira, M. B., Teixeira, I., Negri, E., Mauad, T., Carnielli, D., Lima, L. M., Barreiro, E. J., Faffe, D. S., et al. (2006) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2006000200016 · Cited by 22

The laminin β1-competing peptide YIGSR induces a hypercontractile, hypoproliferative airway smooth muscle phenotype in an animal model of allergic asthma

Dekkers, B. G. J., Bos, I. S. T., Halayko, A. J., Zaagsma, J., & Meurs, H. (2010) · Respiratory Research · doi:10.1186/1465-9921-11-170 · Cited by 22

The Effect of House Dust Mite Immunotherapy, Probiotic and Nigella sativa in The Number of Th17 Cell and Asthma Control Test Score

Kardani, A. K. (2013) · IOSR Journal of Dental and Medical Sciences · doi:10.9790/0853-0643747 · Cited by 22

Caveolae, caveolin-1 and lung diseases of aging

Wicher, S. A., Prakash, Y. S., & Pabelick, C. M. (2019) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2019.1575733 · Cited by 22

Thyme oil alleviates Ova-induced bronchial asthma through modulating Th2 cytokines, IgE, TSLP and ROS

Mousa, A., Almatroudi, A., Alwashmi, A. S. S., Abdulmonem, W. A., Aljohani, A. S. M., Alhumaydhi, F. A., Alsahli, M. A., Alrumaihi, F., Allemailem, K. S., Abdellatif, A. A. H., et al. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111726 · Cited by 22

Tracheal relaxation of five Ivorian anti-asthmatic plants: Role of epithelium and K+ channels in the effect of the aqueous-alcoholic extract of Dichrostachys cinerea root bark

Irie-N’guessan, G., Champy, P., Kouakou-Siransy, G., Koffi, A., Kablan, B. J., & Leblais, V. (2011) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2011.09.016 · Cited by 22

Mycobacterium bovis BCG killed by extended freeze-drying reduces airway hyperresponsiveness in 2 animal models

Lagranderie, M., Abolhassani, M., Vanoirbeek, J. A., Lefort, J., Nahori, M., Silva, J. R. L. E., Huerre, M., Vargaftig, B. B., & Marchal, G. (2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.09.033 · Cited by 22

Flavones derived from nature attenuate the immediate and late-phase asthmatic responses to aerosolized-ovalbumin exposure in conscious guinea pigs

Lee, J.-Y., Kim, J. M., & Kim, C. J. (2013) · Inflammation Research · doi:10.1007/s00011-013-0670-8 · Cited by 22

Review: Pharmacological treatment of airway remodeling: inhaled corticosteroids or antileukotrienes?

Riccioni, G., Ilio, C. D., & D’Orazio, N. (2004) · PubMed · Cited by 22

Effect of early versus late intervention with inhaled corticosteroids on airway wall thickness in patients with asthma

Kurashima, K., Kanauchi, T., Hoshi, T., Takaku, Y., Ishiguro, T., Takayanagi, N., Ubukata, M., & Sugita, Y. (2008) · Respirology · doi:10.1111/j.1440-1843.2008.01384.x · Cited by 22

Chromosome 14 linkage analysis and mutation study of 2 serpin genes in allergic asthmatic families

Malerba, G., Patuzzo, C., Trabetti, E., Lauciello, M. C., Galavotti, R., Pescollderungg, L., Whalen, M. B., Zanoni, G., Martinati, L. C., Boner, A. L., et al. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.113865 · Cited by 22

Intranasal steroid reduces exhaled bronchial cysteinyl leukotrienes in allergic patients

Failla, M., Biondi, G., Pistorio, M. P., Gili, E., Mastruzzo, C., Vancheri, C., & Crimi, N. (2006) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2006.02449.x · Cited by 22

Descubriendo el asma de origen alérgico a través del ratón. Un repaso a la patogenia de los modelos de asma alérgica en el ratón y su similitud con el asma alérgica humana

Torres, R., Picado, C., & de Mora, F. (2005) · Archivos de Bronconeumología · doi:10.1016/s0300-2896(05)70605-0 · Cited by 22

Combination Therapy with Inhaled Long‐Acting β2‐Agonists and Inhaled Corticosteroids: A Paradigm Shift in Asthma Management

Stoloff, S. W., Poinsett-Holmes, K., & Dorinsky, P. (2002) · Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy · doi:10.1592/phco.22.3.212.33550 · Cited by 22

Aerosolized aqueous dust extracts collected near a drying lake trigger acute neutrophilic pulmonary inflammation reminiscent of microbial innate immune ligands

Biddle, T. A., Yisrael, K., Drover, R. W., Li, Q., Maltz, M. R., Topacio, T. M., Yu, J., Castillo, D. D., Gonzales, D., Freund, H. L., et al. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.159882 · Cited by 26

Association between Cystic Fibrosis exacerbations, lung function, T2 inflammation and microbiological colonization

Albon, D. P., Zhang, L., Patrie, J. T., Jones, M., Li, Z. G., Noonan, E., & Borish, L. (2023) · Allergy Asthma and Clinical Immunology · doi:10.1186/s13223-023-00760-z · Cited by 21

P2X7 signaling influences the production of pro-resolving and pro-inflammatory lipid mediators in alveolar macrophages derived from individuals with asthma

Townsend, E. A., Guadarrama, A. G., Shi, L., Roti, E. C. R., & Denlinger, L. C. (2023) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00070.2023 · Cited by 21

Azithromycin Inhibits IL-5 Production of T Helper Type 2 Cells from Asthmatic Children

Lin, S., Lee, W.-J., Liang, Y.-W., Yan, D., Cheng, P., & Kuo, M. (2011) · International Archives of Allergy and Immunology · doi:10.1159/000322872 · Cited by 21

Identifying a biomarker network for corticosteroid resistance in asthma from bronchoalveolar lavage samples

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Repeated allergic asthma in early versus late pregnancy differentially impacts offspring brain and behavior development

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Inhaled steroids and airway remodelling in asthma.

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Ablation of Arg1 in hematopoietic cells improves respiratory function of lung parenchyma, but not that of larger airways or inflammation in asthmatic mice

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Role of matrix metalloproteinases in chronic rhinosinusitis

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In vitro sensitization of human bronchus by β2-adrenergic agonists

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Priming of Eosinophil Migration Across Lung Epithelial Cell Monolayers and Upregulation of CD11b/CD18 Are Elicited by Extracellular Ca2+

Liu, L., Håkansson, L., Ridefelt, P., Garcia, R. C., & Venge, P. (2003) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.4771 · Cited by 21

Effects of Inhaled Corticosteroids, Leukotriene Receptor Antagonists, or Both, Plus Long-Acting ??2-Agonists on Asthma Pathophysiology

Vignola, A. M. (2003) · Drugs · doi:10.2165/00003495-200363002-00004 · Cited by 21

Airway Remodeling from Bench to Bedside: Current Perspectives

Slade, D., & Kraft, M. (2006) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2005.11.001 · Cited by 21

Combination therapy with relaxin and methylprednisolone augments the effects of either treatment alone in inhibiting subepithelial fibrosis in an experimental model of allergic airways disease

Royce, S. G., Sedjahtera, A., Samuel, C. S., & Tang, M. L. K. (2012) · Clinical Science · doi:10.1042/cs20120024 · Cited by 20

Asthma: role of the angiotensin‐(1‐7)/Mas (MAS1) pathway in pathophysiology and therapy

Gregório, J. F., Rodrigues‐Machado, M. D. G., Santos, R. A. S., Carvalho-Ribeiro, I. A., Nunes, O. M., Oliveira, I. F. A., Vasconcellos, A. V. D. O., Campagnole‐Santos, M. J., & Magalhães, G. S. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15619 · Cited by 21

Airway irritation and cough evoked by acid: from human to ion channel

Gu, Q., & Lee, L. (2011) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2011.04.005 · Cited by 20

Peroxisome Proliferator-Activated Receptor γ as a Novel Therapeutic Target in Asthma

Park, S. J., & Lee, Y. C. (2008) · Journal of Asthma · doi:10.1080/02770900701247319 · Cited by 20

Bronchodilatory effect of ethanolic extract of the leaves of Nyctanthes arbortristis

Khan, M. H., & Sopi, R. (2013) · Pharmacognosy Research · doi:10.4103/0974-8490.112422 · Cited by 20

Leukotriene pathway polymorphisms are associated with altered cysteinyl leukotriene production in children with acute asthma

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Alveolar macrophages reduce airway hyperresponsiveness and modulate cytokine levels

Careau, É., Turmel, V., Lauzon‐Joset, J., & Bissonnette, É. Y. (2010) · Experimental Lung Research · doi:10.3109/01902140903410757 · Cited by 20

MODELING THE AIRWAY EPITHELIUM IN ALLERGIC ASTHMA: INTERLEUKIN-13– INDUCED EFFECTS IN DIFFERENTIATED MURINE TRACHEAL EPITHELIAL CELLS

Lankford, S. M., Macchione, M., Crews, A. L., McKANE, S. A., Akley, N. J., & Martin, L. D. (2005) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1290/0502012 · Cited by 20

Effects of budesonide/formoterol combination therapy versus budesonide alone on airway dimensions in asthma

Hoshino, M., & Ohtawa, J. (2012) · Respirology · doi:10.1111/j.1440-1843.2012.02130.x · Cited by 20

Monitoring sputum eosinophils in mucosal inflammation and remodelling: a pilot study

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Semaphorin 7A plays a critical role in IgE-mediated airway inflammation in mice

Mizutani, N., Nabe, T., & Yoshino, S. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.07.004 · Cited by 20

Sesamin attenuates allergic airway inflammation through the suppression of nuclear factor-kappa B activation

Li, L., Piao, H., Zheng, M., Jin, Z., Zhao, L., & Yan, G. (2016) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2016.3903 · Cited by 20

Effect of Angelica glauca essential oil on allergic airway changes induced by histamine and ovalbumin in experimental animals

Sharma, S., Rasal, V. P., Patil, P. A., & Joshi, R. K. (2017) · Indian Journal of Pharmacology · doi:10.4103/0253-7613.201019 · Cited by 20

High prevalence of bronchiectasis on chest CT in a selected cohort of children with severe Asthma

Lo, D. K. H., Maniyar, A., Gupta, S., & Gaillard, E. A. (2019) · BMC Pulmonary Medicine · doi:10.1186/s12890-019-0900-0 · Cited by 20

Effect of Bronchoconstriction on Airway Remodeling in Asthma

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Airway Remodeling in Asthma: An Introduction

Nakagawa, T., & Hoshino, M. (2004) · Clinical Reviews in Allergy & Immunology · doi:10.1385/criai:27:1:001 · Cited by 7

Bronchoconstriction and Airway Remodeling

Brashier, B. B., Iyer, N., & Salvi, S. S. (2011) · New England Journal of Medicine · doi:10.1056/nejmc1107353 · Cited by 2

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Update on Airway Inflammation and Remodeling in Asthma

Hashimoto, S., Matsumoto, K., Gon, Y., Takahashi, N., Ichiwata, T., & Pawankar, R. (2007) · Allergy & Clinical Immunology International - Journal of the World Allergy Organization · doi:10.1027/0838-1925.19.5.178 · Cited by 8