Cytokines and growth factors in airway remodeling in asthma

Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases

Wynn, T. A. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31487 · Cited by 1,487

A Critical Role for Eosinophils in Allergic Airways Remodeling

Humbles, A. A., Lloyd, C. M., McMillan, S. J., Friend, D. S., Xanthou, G., McKenna, E. E., Ghiran, S., Gerard, N. P., Yu, C., Orkin, S. H., et al. (2004) · Science · doi:10.1126/science.1100283 · Cited by 856

Anti-IL-5 treatment reduces deposition of ECM proteins in the bronchial subepithelial basement membrane of mild atopic asthmatics

Flood-Page, P. T., Menzies-Gow, A. N., Phipps, S., Sun, Y., Wangoo, A., Ludwig, M. S., Barnes, N. C., Robinson, D. S., & Kay, A. B. (2003) · Journal of Clinical Investigation · doi:10.1172/jci17974 · Cited by 843

Interleukin‐13 in asthma pathogenesis

Wills‐Karp, M. (2004) · Immunological Reviews · doi:10.1111/j.0105-2896.2004.00215.x · Cited by 683

Vascular endothelial growth factor (VEGF) induces remodeling and enhances TH2-mediated sensitization and inflammation in the lung

Lee, C. G., Link, H., Bałuk, P., Homer, R., Chapoval, S. P., Bhandari, V., Kang, M., Cohn, L. E., Kim, Y. K., McDonald, D. M., et al. (2004) · Nature Medicine · doi:10.1038/nm1105 · Cited by 586

The mechanisms, diagnosis, and management of severe asthma in adults

Holgate, S. T., & Polosa, R. (2006) · The Lancet · doi:10.1016/s0140-6736(06)69288-x · Cited by 407

Inhibition of airway remodeling in IL-5–deficient mice

Cho, J. Y., Miller, M., Baek, K. J., Han, J. W., Nayar, J., Lee, S. Y., McElwain, K., McElwain, S., Friedman, S., & Broide, D. H. (2004) · Journal of Clinical Investigation · doi:10.1172/jci19133 · Cited by 388

Airway remodeling contributes to the progressive loss of lung function in asthma: An overview

Pascual, R. M., & Peters, S. P. (2005) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2005.07.011 · Cited by 360

Mast cells can promote the development of multiple features of chronic asthma in mice

Yu, M. (2006) · Journal of Clinical Investigation · doi:10.1172/jci25702 · Cited by 281

Manipulation of Allergen-Induced Airway Remodeling by Treatment with Anti-TGF-β Antibody: Effect on the Smad Signaling Pathway

McMillan, S. J., Xanthou, G., & Lloyd, C. M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.9.5774 · Cited by 247

Emodin ameliorates ovalbumin-induced airway remodeling in mice by suppressing airway smooth muscle cells proliferation

Liu, Y., Li, X., He, C., Chen, R., Wei, L., Meng, L., & Zhang, W. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106855 · Cited by 23

Fungal Aeroallergens—The Impact of Climate Change

Sztandera−Tymoczek, M., & Szuster‐Ciesielska, A. (2023) · Journal of Fungi · doi:10.3390/jof9050544 · Cited by 23

The Role of Cytokines in Atopic Asthma

Finiasz, M. R., Otero, C., Bezrodnik, L., & Fink, S. B. (2011) · Current Medicinal Chemistry · doi:10.2174/092986711795328346 · Cited by 22

An imbalance in C/EBPs and increased mitochondrial activity in asthmatic airway smooth muscle cells: novel targets in asthma therapy?

Roth, M., & Black, J. L. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00188.x · Cited by 22

Integrative Roles of Pro‐Inflammatory Cytokines on Airway Smooth Muscle Structure and Function in Asthma

Ford, M. L., Reza, M. I., Ruwanpathirana, A., Sathish, V., & Britt, R. D. (2025) · Immunological Reviews · doi:10.1111/imr.70007 · Cited by 27

Lipoxin A4 inhibits ovalbumin-induced airway inflammation and airway remodeling in a mouse model of asthma

Liu, Y., Wei, L., He, C., Chen, R., & Meng, L. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109660 · Cited by 21

Down-regulation of secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related peptide-1 (SLURP-1), an endogenous allosteric α7 nicotinic acetylcholine receptor modulator, in murine and human asthmatic conditions

Narumoto, O., Horiguchi, K., Horiguchi, S., Moriwaki, Y., Takano‐Ohmuro, H., Shoji, S., Misawa, H., Yamashita, N., Nagase, T., Kawashima, K., et al. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.07.006 · Cited by 20

Effects of furosemide on allergic asthmatic responses in mice

Wang, S., Xiang, Y. ‐., Ellis, R., Wattie, J. N., Feng, M. M., Inman, M. D., & Lu, W. ‐. (2011) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2011.03811.x · Cited by 19

The Correlation between FSTL1 Expression and Airway Remodeling in Asthmatics

Liu, Y., Liu, T., Wu, J., Li, T., Jiao, X., Zhang, H., Zhao, J., Wang, J., Liu, L., Cao, L., et al. (2017) · Mediators of Inflammation · doi:10.1155/2017/7918472 · Cited by 20

Alcohol Primes the Airway for Increased Interleukin‐13 Signaling

Mitchell, P. O., Jensen, J. S., Ritzenthaler, J. D., Roman, J., Peláez, A., & Guidot, D. M. (2008) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2008.00863.x · Cited by 18

Uterine cervix as a fundamental part of the pathogenesis of pregnancy loss associated with ascending placentitis in mares

Fernandes, C. B., Ball, B. A., Loux, S. C., Boakari, Y. L., Scoggin, K. E. S., Ali, H. E., Cogliati, B., & Esteller‐Vico, A. (2019) · Theriogenology · doi:10.1016/j.theriogenology.2019.10.017 · Cited by 18

Ouabain modulates airway remodeling caused by Th2-high asthma in mice

Galvão, J. G. F. M., Silva, L. H. A. C., Lima, É. D. A., Carvalho, D. C. M., Alves, A. F., & Rodrigues‐Mascarenhas, S. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108808 · Cited by 17

Brevetoxin 2 alters expression of apoptotic, DNA damage, and cytokine genes in Jurkat cells

Murrell, R. N., & Gibson, J. E. (2010) · Human & Experimental Toxicology · doi:10.1177/0960327110372644 · Cited by 17

TLR3 activation increases chemokine expression in human fetal airway smooth muscle cells

Faksh, A., Britt, R. D., Vogel, E. R., Thompson, M. A., Pandya, H. C., Martin, R. J., Pabelick, C. M., & Prakash, Y. S. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00151.2015 · Cited by 17

Heterogeneity of Pulmonary Stem Cells

Lynch, T. J., Ievlev, V., & Parekh, K. R. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-24108-7_6 · Cited by 16

An orally active geranyl acetophenone attenuates airway remodeling in a murine model of chronic asthma

Lee, Y. Z., Shaari, K., Cheema, M. S., Tham, C. L., Sulaiman, M. R., & Israf, D. A. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.01.011 · Cited by 16

Exposure to diisononyl phthalate promotes atopic march by activating of NF-κB and p38 MAPK

Qin, W. D., Duan, J., Xie, X., Kang, J. M., Deng, T., & Chen, M. (2020) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2020.114981 · Cited by 16

Correlation between sestrin2 expression and airway remodeling in COPD

Zhang, D., Wei, Y., Ji, S., & Fei, G. (2020) · BMC Pulmonary Medicine · doi:10.1186/s12890-020-01329-x · Cited by 16

Cervix remodeling and parturition in the rat: lack of a role for hypogastric innervation

Boyd, J. W., Lechuga, T. J., Ebner, C. A., Kirby, M. A., & Yellon, S. M. (2009) · Reproduction · doi:10.1530/rep-08-0507 · Cited by 16

Arginase in Asthma – Recent Developments in Animal and Human Studies~!2009-11-12~!2010-03-23~!2010-05-04~!

North, M. L., Meurs, H., Zaagsma, J., Scott, J. A., & Maarsingh, H. (2010) · The Open Nitric Oxide Journal · doi:10.2174/1875042701002020020 · Cited by 15

Glucocorticoid dexamethasone regulates the differentiation of mouse conducting airway epithelial progenitor cells

Chen, H., Sun, X., Chi, R., Li, X., Feng, J., Wu, J., Ning, W., Liu, Z., & Wu, Q. (2013) · Steroids · doi:10.1016/j.steroids.2013.12.001 · Cited by 14

Inhibitory effects of Montelukast on mediator release by nasal epithelial cells from asthmatic subjects with or without allergic rhinitis

Scaife, A., Miller, D., Spiteri-Cornish, D., Turner, S., Devereux, G. S., & Walsh, G. M. (2013) · Respiratory Medicine · doi:10.1016/j.rmed.2013.09.006 · Cited by 14

Transforming growth factor-β1‑induced expression of connective tissue growth factor is enhanced in bronchial fibroblasts derived from asthmatic patients

Wójcik‐Pszczoła, K., Koczurkiewicz, P., Michalik, M., & Sanak, M. (2012) · Polskie Archiwum Medycyny Wewnętrznej · doi:10.20452/pamw.1343 · Cited by 14

The effects of antisense interleukin-4 gene transferred by recombinant adeno-associated virus vector on the airway remodeling in allergic rats

Cao, Y., Zeng, D., Song, Q., Cao, C., Xie, M., Liu, X., Xiong, S., Xu, Y., & Xiong, W. (2010) · Journal of Asthma · doi:10.1080/02770903.2010.514635 · Cited by 14

Research on the Mechanism and Application of Acupuncture Therapy for Asthma: A Review

Wang, F.-X., & Jin, L.-W. (2024) · Journal of Asthma and Allergy · doi:10.2147/jaa.s462262 · Cited by 13

Serum biomarkers of remodeling in severe asthma with fixed airway obstruction and the potential role of KL-6

Vianello, A., Guarnieri, G., Achille, A., Lionello, F., Lococo, S., Zaninotto, M., Caminati, M., & Senna, G. (2023) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2022-1323 · Cited by 13

The activation of M3 mAChR in airway epithelial cells promotes IL-8 and TGF-β1 secretion and airway smooth muscle cell migration

Lu, J., Xu, G.-N., Yu, P., Song, Y. J., Wang, X., Zhu, L., Chen, H., & Cui, Y. (2016) · Respiratory Research · doi:10.1186/s12931-016-0344-5 · Cited by 13

Neonatal Pulmonary Host Defense

Good, M. L., Kolls, J. K., & Empey, K. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00130-x · Cited by 13

Biologic therapies for asthma

Gruenberg, D. A., & Busse, W. W. (2009) · Current Opinion in Pulmonary Medicine · doi:10.1097/mcp.0b013e3283328398 · Cited by 12

Type 2 macrophages and Th2 CD4+ cells in interstitial lung diseases (ILDs): an overview.

Partida-Zavala, N., Ponce-Gallegos, M. A., Buendía-Roldán, I., & Falfán‐Valencia, R. (2018) · Sarcoidosis vasculitis and diffuse lung diseases · doi:10.36141/svdld.v35i2.6691 · Cited by 15

Novel Lung Growth Strategy with Biological Therapy Targeting Airway Remodeling in Childhood Bronchial Asthma

Tsuge, M., Ikeda, M., & Tsukahara, H. (2022) · Children · doi:10.3390/children9081253 · Cited by 16

Poly I:C Exacerbates Airway Inflammation and Remodeling in Cigarette Smoke-Exposed Mice

Mei, X., Lu, R., Cui, L., Tian, Y., Zhao, P., & Li, J. (2022) · Lung · doi:10.1007/s00408-022-00574-7 · Cited by 13

Moving toward consensus on diagnosis and management of severe asthma in adults

Colodenco, D., Palomares, Ó., Celis-Preciado, C. A., Kaplan, A. G., & Domingo, C. (2017) · Current Medical Research and Opinion · doi:10.1080/03007995.2017.1380617 · Cited by 12

Radical S-adenosyl methionine domain-containing 2, a potential target of D-tryptophan in asthma treatment, regulates T helper cell type 1/2 balance

Wang, F., & Shang, Y. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111581 · Cited by 11

The role of monoclonal antibodies in the treatment of severe asthma

Tourangeau, L. M., Kavanaugh, A., & Wasserman, S. I. (2011) · Therapeutic Advances in Respiratory Disease · doi:10.1177/1753465811400489 · Cited by 11

Study of gastric fluid induced cytokine and chemokine expression in airway smooth muscle cells and airway remodeling

Chiu, H. Y., Chen, C., Lin, H.-Y., Hsieh, C.-C., Lin, S. S., & Cheng, C.-M. (2011) · Cytokine · doi:10.1016/j.cyto.2011.09.024 · Cited by 11

The translational repressor T-cell intracellular antigen-1 (TIA-1) is a key modulator of Th2 and Th17 responses driving pulmonary inflammation induced by exposure to house dust mite

Simarro, M., Giannattasio, G., Xing, W., Lundequist, E. M., Stewart, S., Stevens, R. L., Orduña, A., Boyce, J. A., & Anderson, P. (2012) · Immunology Letters · doi:10.1016/j.imlet.2012.04.001 · Cited by 12

Mast Cell Tryptase Promotes Airway Remodeling by Inducing Anti-Apoptotic and Cell Growth Properties in Human Alveolar and Bronchial Epithelial Cells

Berlin, F., Mogren, S., Ly, C., Ramu, S., Hvidtfeldt, M. W., Uller, L., Porsbjerg, C. M., & Andersson, C. K. (2023) · Cells · doi:10.3390/cells12101439 · Cited by 10

Increased TGFβ1, VEGF and IFN-γ in the Sputum of Severe Asthma Patients With Bronchiectasis

Ma, D., Muñoz, X., Ojanguren, Í., Mesones, C. E. R., Soler-Segovia, D., Porres, D. V., & Cruz, M. J. (2024) · Archivos de Bronconeumología · doi:10.1016/j.arbres.2024.05.036 · Cited by 10

Pan-Phosphodiesterase Inhibitors Attenuate TGF-β-Induced Pro-Fibrotic Phenotype in Alveolar Epithelial Type II Cells by Downregulating Smad-2 Phosphorylation

Wójcik‐Pszczoła, K., Chłoń‐Rzepa, G., Jankowska, A., Ferreira, B., Koczurkiewicz, P., Pękala, E., Wyska, E., Pociecha, K., & Gosens, R. (2022) · Pharmaceuticals · doi:10.3390/ph15040423 · Cited by 10

The anti-asthmatic potential of Rho-kinase inhibitor hydroxyfasudil in the model of experimentally induced allergic airway inflammation

Fraňová, S., Molitorisová, M., Kalmanova, L., Palencarova, J., Jošková, M., Smieško, L., Mažerik, J., & Šútovská, M. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.175450 · Cited by 10

Czynnik Wzrostu śródbłonka Naczyniowego—Struktura, Funkcje oraz rola w Zapaleniu Oskrzeli i Przebiegu Klinicznym Astmy

Gomułka, K., & Liebhart, J. (2009) · Advances in respiratory medicine · doi:10.5603/arm.27770 · Cited by 10

Pharmacodynamic evaluation of dihydroxyflavone derivate chrysin in a guinea pig model of allergic asthma

Fraňová, S., Molitorisová, M., Kazimierová, I., Jošková, M., Forsberg, C. I. N., Nováková, E., & Šútovská, M. (2021) · Journal of Pharmacy and Pharmacology · doi:10.1093/jpp/rgaa008 · Cited by 9

Action of 1,25(OH)2D3 on Human Asthmatic Bronchial Fibroblasts: Implications for Airway Remodeling in Asthma

Plesa, M., Gaudet, M., Mogas, A. K., Olivenstein, R., Heialy, S. A., & Hamid, Q. A. (2020) · Journal of Asthma and Allergy · doi:10.2147/jaa.s261271 · Cited by 8

Effects of Inhalation of STIM-Orai Antagonist SKF 96365 on Ovalbumin-Induced Airway Remodeling in Guinea Pigs

Šútovská, M., Kočmálová, M., Kazimierová, I., Forsberg, C. I. N., Jošková, M., Adamkov, M., & Fraňová, S. (2021) · Advances in experimental medicine and biology · doi:10.1007/5584_2021_633 · Cited by 8

Effect of Benzo[a]pyrene on the Production of Vascular Endothelial Growth Factor by Human Eosinophilic Leukemia EoL-1 Cells

Gu, J., Chan, L., Wong, C. K. C., Wong, N.-S., Wong, C.-K., Leung, K.-N., & Mak, N. K. (2011) · Journal of Environmental Pathology Toxicology and Oncology · doi:10.1615/jenvironpatholtoxicoloncol.v30.i3.70 · Cited by 7

Moving toward consensus on diagnosis and management of severe asthma in children

Larenas‐Linnemann, D. E., Nieto, A., Palomares, Ó., Pitrez, P. M., & Cukier, G. (2017) · Current Medical Research and Opinion · doi:10.1080/03007995.2017.1400961 · Cited by 6

Low Dose Rate Radiation Regulates M2-like Macrophages in an Allergic Airway Inflammation Mouse Model

Jo, W. S., Kang, S., Jeong, S. K., Bae, M. J., Lee, C. G., Son, Y., Lee, H., Jeong, M. H., Kim, S. H., Moon, C., et al. (2022) · Dose-Response · doi:10.1177/15593258221117349 · Cited by 6

Proteomic identification of moesin upon exposure to acrolein

Lee, P., Kim, B., Lee, S., Leikauf, G. D., & Jang, A. (2018) · Proteome Science · doi:10.1186/s12953-017-0130-4 · Cited by 6

Kechuanning Gel Plaster Exerts Anti-inflammatory and Immunomodulatory Effects on Ovalbumin-induced Asthma Model Rats via ERK Pathway

Xie, M., Liu, T., Yin, J., Liu, J., Yang, L., Li, T., Chen, X., & Fan, Y. (2023) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207326666230503105935 · Cited by 5

Interferons as negative regulators of ILC2s in allergic lung inflammation and respiratory viral infections

Wang, C., Du, Z., Li, R., Luo, Y., Zhu, C., Ding, N., & Lei, A. (2023) · Journal of Molecular Medicine · doi:10.1007/s00109-023-02345-0 · Cited by 5

Effect of 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol on Immune Functions in Healthy Adults in a Randomized Controlled Trial

Hwang, H., Sohn, K., Han, Y., Chong, S., Yoon, S. Y., Kim, Y., Jeong, J., Kim, S.-H., & Kim, J. W. (2015) · Immune Network · doi:10.4110/in.2015.15.3.150 · Cited by 5

Microfungus Podosphaera fusca and the Fungus-like Organism Peronospora ficariae as Potential Inhalant Allergens in a Mouse Model of Asthma

Właź, P., Socała, K., Palusińska‐Szysz, M., Świderska-Burek, U., Szczypior, D., Krasowska, M., & Szuster‐Ciesielska, A. (2025) · Cells · doi:10.3390/cells14120914 · Cited by 4

Challenges in the Management of Severe Asthma: Role of Current and Future Therapies

Oliveinstein, R., Jahdali, H. A., Alkhamis, N., Halwani, R., Al‐Muhsen, S., & Hamid, Q. A. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211795428993 · Cited by 4

Therapeutic Applications

Tilley, S., Volmer, J., & Picher, M. (2011) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-1217-1_9 · Cited by 4

Bronchial asthma: novel therapeutic approaches

Chuchalin, A. G. (2011) · PULMONOLOGIYA · doi:10.18093/0869-0189-2011-0-4-5-12 · Cited by 4

Differential effects of dexamethasone and rosiglitazone in a sephadex-induced model of lung inflammation in rats: Possible role of tissue inhibitor of metalloproteinase-3

Soni, H., Nagar, J., Patel, P., Mohapatra, J., Sharma, M., Pandya, G., Umar, M., Chatterjee, A., Deshpande, S. S., & Jain, M. (2015) · Indian Journal of Pharmacology · doi:10.4103/0253-7613.153421 · Cited by 4

Airway Remodelling in Asthma

Pelaia, G., Vatrella, A., & Maselli, R. (2016) · Springer eBooks · doi:10.1007/978-3-319-46007-9_3 · Cited by 4

Plant Microfungi Tranzschelia pruni-spinosae and Phragmidium rubi-idaei Demonstrate Allergenic Capabilities in Mouse Models of Asthma

Właź, P., Socała, K., Krasowska-Kunach, M., Palusińska‐Szysz, M., Świderska-Burek, U., Szczypior, D., & Szuster‐Ciesielska, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27031507 · Cited by 3

Airway Wall Remodeling in Young and Adult Rats with Experimentally Provoked Bronchial Asthma

Uhlı́k, J., Šimůnková, P., Žaloudíková, M., Partlová, S., Jarkovský, J., & Vajner, L. (2014) · International Archives of Allergy and Immunology · doi:10.1159/000366278 · Cited by 3

An introduction to eosinophils and their biology

Ackerman, S. J. (2022) · European Respiratory Society eBooks · doi:10.1183/2312508x.10029020 · Cited by 3

A high-throughput 3D cantilever array to model airway smooth muscle hypercontractility in asthma

Beri, P., Plunkett, C. M., Barbara, J., Shih, C., Barnes, S. W., Ross, O., Choconta, P., Trinh, T., Gomez, D., Litvin, B., et al. (2023) · APL Bioengineering · doi:10.1063/5.0132516 · Cited by 3

Inhibiting or blocking LIGHT, a TNF superfamily member, for treating airway remodeling

Cazzola, M., & Matera, M. G. (2011) · Expert Review of Respiratory Medicine · doi:10.1586/ers.11.65 · Cited by 3

Ethyl p-methoxycinnamate isolated from Kaempferia galanga L. rhizome reduces airway remodeling in asthmatic rat models

Andarini, I., Salimo, H., Purwanto, B., Rahardjo, S. S., Wasita, B., & Widyaningsih, V. (2021) · Bali Medical Journal · doi:10.15562/bmj.v10i3.2701 · Cited by 3

Neonatal Pulmonary Host Defense

Empey, K. M., & Kolls, J. K. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-3479-7.10159-4 · Cited by 3

Small airway dysfunction in asthma: diagnostic, pathogenetic and therapeutic aspects

Валентиновна, Ю. А. (2025) · Bulletin physiology and pathology of respiration · doi:10.36604/1998-5029-2025-96-141-153 · Cited by 1

Estragole protects against ovalbumin-induced allergic asthma by amelioration of interleukin-4 and interleukin-5 expression in BALB/c mice

Asim, A., Shabbir, A., Alam, U., Mobashar, A., Parveen, S., Fatima, T., Haji, E. M., Almutairy, A. F., Alnasser, S. M., Alanazi, E. F., et al. (2025) · Journal of Molecular Histology · doi:10.1007/s10735-025-10655-5 · Cited by 1

Research on the molecular mechanism of Seretide treatment to asthma disease.

Liu, Z.-W., Yue, F., Gao, F.-Y., Qian, Y.-B., & Wang, R.-L. (2012) · PubMed · Cited by 1

Epithelial Cell-Mesenchymal Interaction, Epithelial-Leukocyte Interaction and Epithelial Immune-Response Genes in Allergic Disease

Holgate, S. T. (2009) · Springer eBooks · doi:10.1007/978-4-431-88315-9_15 · Cited by 1

Allergy and hypersensitivity — airway inflammation and remodeling

Saito, H. (2007) · Current Opinion in Immunology · doi:10.1016/j.coi.2007.09.001 · Cited by 1

Lung Injury Biomarkers

Kodavanti, U. P. (2010) · Biomarkers · doi:10.1002/9780470918562.ch8 · Cited by 1

Pathological Processes

Pearson, J. P., Aldhahrani, A., Chater, P. I., & Wilcox, M. D. (2018) · Springer eBooks · doi:10.1007/978-3-319-90525-9_4 · Cited by 1

Positional cloning and pathway analysis of the asthma susceptibility gene, NPSR1

Vendelin, J. (2007) · Työväentutkimus Vuosikirja

Regulatory T Cells

Corrigan, C. J., & Ryanna, K. (2011) · Wiley eBooks · doi:10.1002/9781444346688.ch4

Bronchiolitis obliterans syndrome after lung transplantation: biomarkers for inflammation and fibrogenesis

Kastelijn, E. A. (2012) · Utrecht University Repository (Utrecht University)

Standing Guard: Innate Lymphoid Cells Promote Immunity and Tissue Homeostasis at Barrier Surfaces

Monticelli, L. A., & Artis, D. (2013) · Else Kröner-Fresenius Symposia · doi:10.1159/000346504

Influência do montelucaste sobre o estado de ativação dos eosinófilos e função dos fagócitos em crianças asmáticas

Gonçalves, V. B. (2010) · Americanae (AECID Library)

Asma experimental em linhagens de camundongos selecionados para mínima (AIRmin) ou máxima (AIRmax) resposta inflamatória aguda.

Castro, J. M. D. A. (2010) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2010.tde-05102010-121444

Influência dos hormônios sexuais femininos sobre a inflamação alérgica pulmonar em modelo murino de asma crônica.

Soares, C. R. (2010) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2010.tde-06082010-135707

Detection and Clinical Significance of a Potential Mediator of Airway Remodelling in Preschool Wheezy Children

Zhang, Y., Bao, X., Wang, Y., & Chen, Y. (2014)

Efeito do derivado N-acilidrazônico LASSBio-897 sobre a resposta inflamatória pulmonar na asma e silicose experimentais

Viveiros, D. D. (2014) · Americanae (AECID Library)

Arginase in Asthma

North, M. L., Meurs, H., Zaagsma, J., Scott, J. A., & Maarsingh, H. (2010) · The Open Nitric Oxide Journal

Mast Cells

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Immunomodulatory Role of B Lymphocytes and Hyaluronic Acid in a Murine Model of Allergic Asthma

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Additional file 2 of Correlation between sestrin2 expression and airway remodeling in COPD

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Additional file 3 of Correlation between sestrin2 expression and airway remodeling in COPD

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