Cited by 1,702Asthma and respiratory diseasesChronic Obstructive Pulmonary Disease (COPD) ResearchOccupational exposure and asthma

The DOI matches its Crossref record; 550 of the 552 references it cites were found in a registry or an index.

Asthma: From Bronchoconstriction to Airways Inflammation and Remodeling

BOUSQUET, JEAN, JEFFERY, PETER K., BUSSE, WILLIAM W., JOHNSON, MALCOLM, VIGNOLA, ANTONIO M.·2000·American Journal of Respiratory and Critical Care Medicine

DOI 10.1164/ajrccm.161.5.9903102

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1164/ajrccm.161.5.9903102

Cites

550 of 550 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Nuclear Factor-κB — A Pivotal Transcription Factor in Chronic Inflammatory Diseases
Barnes, P. J., & Karin, M. (1997) · New England Journal of Medicine · doi:10.1056/nejm199704103361506 · Cited by 4,622
Transforming Growth Factor β in Tissue Fibrosis
Epstein, F. H., Border, W. A., & Noble, N. A. (1994) · New England Journal of Medicine · doi:10.1056/nejm199411103311907 · Cited by 3,044
Predominant TH2-like Bronchoalveolar T-Lymphocyte Population in Atopic Asthma
Robinson, D. S., Hamid, Q. A., Ying, S., Tsicopoulos, A., Barkans, J. R., Bentley, A. M., Corrigan, C. J., Durham, S. R., & Kay, A. B. (1992) · New England Journal of Medicine · doi:10.1056/nejm199201303260504 · Cited by 2,769
Eosinophilic Inflammation in Asthma
Bousquet, J., Chanez, P., Lacoste, J. Y., Barneon, G., Ghavanian, N., Enander, I., Venge, P., Ahlstedt, S., Simony-Lafontaine, J., Godard, P., et al. (1990) · New England Journal of Medicine · doi:10.1056/nejm199010113231505 · Cited by 2,499
Self-citation
Effect of Inhaled Formoterol and Budesonide on Exacerbations of Asthma
PAUWELS, R. A., Löfdahl, C., Postma, D. S., Tattersfield, A. E., O’Byrne, P. M., Barnes, P. J., & Ullman, A. (1997) · New England Journal of Medicine · doi:10.1056/nejm199711133372001 · Cited by 1,518
Increased nitric oxide in exhaled air of asthmatic patients
Kharitonov, S. A., Yates, D. H., Robbins, R. A., Barnes, P. J., Logan-Sinclair, R., & Shinebourne, E. A. (1994) · The Lancet · doi:10.1016/s0140-6736(94)90931-8 · Cited by 1,432
The matrix‐degrading metalloproteinases
Matrisian, L. M. (1992) · BioEssays · doi:10.1002/bies.950140705 · Cited by 1,362
Life, death, and the pursuit of apoptosis.Preprint
White, E. (1996) · Genes & Development · doi:10.1101/gad.10.1.1 · Cited by 1,306
Collagen family of proteins
REST, M. V. D., & Garrone, R. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.13.1916105 · Cited by 1,302
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

Show all 552 references

Research works printed but not linked: 9

Management of Pediatric Asthma, 1997, Symposium proceedings. London, England, November 18, 1996., Pediatr. Pulmonol. Suppl., 15, 1
Nakamura, 1995, Bronchial epithelial cells regulate fibroblast proliferation., Am. J. Physiol., 269, L377
Schlick, 1993, Current issues in the assessment of interstitial lung disease., Monaldi Arch. Chest Dis., 48, 237
International Asthma Management Project, 1992, International Consensus Report on Diagnosis and Management of Asthma., Allergy, 47, 1
Gerber, 1985, Effets des gluco-corticostéroids dans l'asthme à dyspnée continue: étude histologique et immuno-histochimique de la muqueuse bronchique., Rev. Mal. Respir., 2, 313
Corrigan, 1993, Peripheral blood T-lymphocyte activation in asthma is accompanied by elevated serum concentrations of IL-5: effect of glucocorticoid therapy., Am. Rev. Respir. Dis., 147, 540, 10.1164/ajrccm/147.3.540 · DOI
Freedman, 1972, The functional geometry of the bronchi., Bull. Physiopath. Respir., 8, 545
Messner, 1960, Causes of death and pathologic findings ion 304 cases of bronchial asthma., Dis. Chest, 38, 616, 10.1378/chest.38.6.616 · DOI
Woolcock, 1968, The static elastic properties of the lung in asthma., Am. Rev. Respir. Dis., 98, 788

Sorted by citations

Items 501–600 of 1,000

Protein tyrosine phosphatase SHP 2 regulates TGF ‐β1 production in airway epithelia and asthmatic airway remodeling in mice
Qin, X., Zhang, G., Zhang, X., Qiu, Z. ‐., Wang, P. ‐., Li, Y. ‐., Li, W., Xie, Q.-M., Ke, Y., Lee, J. J., et al. (2012) · Allergy · doi:10.1111/all.12048 · Cited by 48
Mucosal Remodeling in Chronic Rhinosinusitis
Rehl, R. M., Balla, A. A., Cabay, R. J., Hearp, M. L., Pytynia, K. B., & Joe, S. A. (2007) · American Journal of Rhinology · doi:10.2500/ajr.2007.21.3096 · Cited by 48
Viruses and asthma: the role of common respiratory viruses in asthma and its potential meaning for SARS‐CoV‐2
Novak, N., & Cabanillas, B. (2020) · Immunology · doi:10.1111/imm.13240 · Cited by 47
Novel non-canonical TGF-β signaling networks: Emerging roles in airway smooth muscle phenotype and function
Yeganeh, B., Mukherjee, S., Moir, L. M., Kumawat, K., Kashani, H. H., Bagchi, R. A., Baarsma, H. A., Gosens, R., & Ghavami, S. (2012) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2012.07.006 · Cited by 49
Unconventional therapy use among asthma patients in a tertiary care center in Riyadh, Saudi Arabia
Moamary, M. S. A. (2008) · Annals of Thoracic Medicine · doi:10.4103/1817-1737.39636 · Cited by 47
Inducible nitric oxide synthase inhibition attenuates lung tissue responsiveness and remodeling in a model of chronic pulmonary inflammation in guinea pigs
Starling, C. M., Prado, C. M., Leick-Maldonado, E. A., Lanças, T., Reis, F. G., Aristóteles, L. R. C. R. B., Dolhnikoff, M., Martins, M. A., & Tibério, I. D. F. L. C. (2008) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2008.11.011 · Cited by 47
Augmented epithelial endothelin-1 expression in refractory asthma
Pégorier, S., Arouche, N., Dombret, M.-C., Aubier, M., & Pretolani, M. (2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.09.023 · Cited by 47
Comparisons of effects of intravenous and inhaled methacholine on airway physiology in a murine asthma model
Jonasson, S., Hedenstierna, G., Hedenström, H., & Hjoberg, J. (2008) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2008.12.005 · Cited by 47
Add-on montelukast in inadequately controlled asthma patients in a 6-month open-label study: The MONtelukast In Chronic Asthma (MONICA) study
Virchow, J. C., Jr., Mehta, A., Ljungblad, L., & Mitfessel, H. (2009) · Respiratory Medicine · doi:10.1016/j.rmed.2009.11.022 · Cited by 47
TGF-β, Eosinophils and IL-13 in Allergic Airway Remodeling: A Critical Appraisal with Therapeutic Considerations
Fattouh, R., & Jordana, M. (2008) · Inflammation & Allergy - Drug Targets · doi:10.2174/187152808786848388 · Cited by 48
Inhaled corticosteroids and growth of airway function in asthmatic children
Merkus, P. J. F. M., van Pelt, W., van Houwelingen, H. C., van Essen‐Zandvliet, L. E. M., Duiverman, E. J., Kerrebijn, K. F., & Quanjer, P. H. (2004) · European Respiratory Journal · doi:10.1183/09031936.04.00031504 · Cited by 47
Sensitization of isolated rat vagal pulmonary sensory neurons by eosinophil-derived cationic proteins
Gu, Q., Wiggers, M. E., Gleich, G. J., & Lee, L. (2008) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00271.2007 · Cited by 47
Eotaxin and RANTES enhance 5-oxo-6,8,11,14-eicosatetraenoic acid–induced eosinophil chemotaxis
Powell, W. S., Ahmed, S., Gravel, S., & Rokach, J. (2001) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2001.112847 · Cited by 47
IL-13 Augments Compressive Stress–Induced Tissue Factor Expression in Human Airway Epithelial Cells
Mitchel, J. A., Antoniak, S., Lee, J., Kim, S., McGill, M., Kasahara, D. I., Randell, S. H., Israel, E., Shore, S. A., Mackman, N., et al. (2015) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2015-0252oc · Cited by 46
Children and adolescents’ health-related quality of life in relation to eczema, asthma and hay fever: results from a population-based cross-sectional study
Matterne, U., Schmitt, J. M., Diepgen, T. L., & Apfelbacher, C. (2011) · Quality of Life Research · doi:10.1007/s11136-011-9868-9 · Cited by 49
Asthma in Older Adults
Braman, S. S., & Hanania, N. A. (2007) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2007.08.007 · Cited by 46
Chronic IL9 and IL-13 Exposure Leads to an Altered Differentiation of Ciliated Cells in a Well-Differentiated Paediatric Bronchial Epithelial Cell Model
Parker, J. C., Thavagnanam, S., Skibiński, G., Lyons, J. D., Bell, J., Heaney, L. G., & Shields, M. D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061023 · Cited by 46
Neuronal Modulation of Airway and Vascular Tone and Their Influence on Nonspecific Airways Responsiveness in Asthma
Canning, B. J., Woo, A., & Mazzone, S. B. (2012) · Journal of Allergy · doi:10.1155/2012/108149 · Cited by 46
Emerging role of non-coding RNAs in allergic disorders
Ghafouri‐Fard, S., Shoorei, H., Taheri, M. N., & Sanak, M. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110615 · Cited by 46
Inflammatory markers in childhood asthma
Dodig, S., Richter, D., & Zrinski-Topić, R. (2011) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.2011.094 · Cited by 46
Corticosteroid-Induced Apoptosis of Airway Epithelium*
White, S. R., & Dorscheid, D. R. (2002) · CHEST Journal · doi:10.1378/chest.122.6_suppl.278s · Cited by 46
Chemokine Receptor 2 Blockade Prevents Asthma in a Cynomolgus Monkey Model
Mellado, M., de Ana, A. M., Gómez, L., Martínez-A, C., & Rodrı́guez-Frade, J. M. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.128538 · Cited by 46
Anti-inflammatory modulation of chronic airway inflammation in the murine house dust mite model
Ulrich, K., Hincks, J. S., Walsh, R., Wetterstrand, E. M. C., Fidock, M. D., Sreckovic, S., Lamb, D. J., Douglas, G. J., Yeadon, M., Huguet, C., et al. (2008) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2008.02.006 · Cited by 46
Fritillaria cirrhosa, Anemarrhena asphodeloides, Lee‐Mo‐Tang and Cyclosporine a Inhibit Ovalbumin‐Induced Eosinophil Accumulation and Th2‐Mediated Bronchial Hyperresponsiveness in a Murine Model of Asthma
Yeum, H., Lee, Y., Kim, S., Roh, S., Lee, J., & Seo, Y.-B. (2007) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/j.1742-7843.2007.00043.x · Cited by 45
Mannitol and exercise challenge tests in asthmatic children
Kersten, E. T. G., Driessen, J. M. M., van der Berg, J. D., & Thio, B. J. (2009) · Pediatric Pulmonology · doi:10.1002/ppul.21034 · Cited by 45
The Roles of Phytochemicals in Bronchial Asthma
Park, H. S., Kim, S. R., Kim, J. O., & Lee, Y. C. (2010) · Molecules · doi:10.3390/molecules15106810 · Cited by 48
Ras homolog family member A/Rho-associated protein kinase 1 signaling modulates lineage commitment of mesenchymal stem cells in asthmatic patients through lymphoid enhancer–binding factor 1
Xia, K., Do, D. C., Li, C., Zhao, Y., Kollárik, M., Fu, Q., Wan, M., & Gao, P. (2018) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.08.023 · Cited by 47
Cordyceps polysaccharide ameliorates airway inflammation in an ovalbumin-induced mouse model of asthma via TGF-β1/Smad signaling pathway
Ya, Z., Li, L., & Cai, T. (2020) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2020.103412 · Cited by 45
Synthesis and Structure−Activity Relationships of Long-acting β2Adrenergic Receptor Agonists Incorporating Arylsulfonamide Groups
Procopiou, P. A., Barrett, V. J., Bevan, N., Biggadike, K., Butchers, P. R., Coe, D. M., Conroy, R., Edney, D. D., Field, R. N., Ford, A. J., et al. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm801016j · Cited by 45
Comparison of intranasal and transcutaneous immunization for induction of protective immunity against Chlamydia muridarum respiratory tract infection
Skelding, K. A., Hickey, D. K., Horvat, J. C., Bao, S., Roberts, K. G., Finnie, J. M., Hansbro, P. M., & Beagley, K. W. (2005) · Vaccine · doi:10.1016/j.vaccine.2005.07.104 · Cited by 45
Early and late bronchoconstrictions, airway hyper‐reactivity, leucocyte influx and lung histamine and nitric oxide after inhaled antigen: effects of dexamethasone and rolipram
Toward, T. J., & Broadley, K. J. (2004) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2004.01833.x · Cited by 45
Effects of Inhaled Corticosteroids on Pathology in Asthma and Chronic Obstructive Pulmonary Disease
Chanez, P., BOURDIN, A. A., Vachier, I., Godard, P., Bousquet, J., & Vignola, A. M. (2004) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200402-006ms · Cited by 45
Self-citation
Eosinophils enhance WNT-5a and TGF-β1 genes expression in airway smooth muscle cells and promote their proliferation by increased extracellular matrix proteins production in asthma
Januškevičius, A., Vaitkienė, S., Gosens, R., Janulaitytė, I., Hoppenot, D., Sakalauskas, R., & Malakauskas, K. (2016) · BMC Pulmonary Medicine · doi:10.1186/s12890-016-0254-9 · Cited by 45
Intranasal Curcumin Inhibits Pulmonary Fibrosis by Modulating Matrix Metalloproteinase-9 (MMP-9) in Ovalbumin-Induced Chronic Asthma
Chauhan, P., Dash, D., & Singh, R. (2016) · Inflammation · doi:10.1007/s10753-016-0475-3 · Cited by 45
Airway remodeling in the pathogenesis of asthma
Vignola, A. M., Gagliardo, R. P., Siena, A., Chiappara, G., Bonsignore, M. R., Bousquet, J., & Bonsignore, G. (2001) · Current Allergy and Asthma Reports · doi:10.1007/s11882-001-0077-4 · Cited by 45
Self-citation
Airway Remodeling: Lessons From Animal Models
Ramos‐Barbón, D., Ludwig, M. S., & Martin, J. G. (2004) · Clinical Reviews in Allergy & Immunology · doi:10.1385/criai:27:1:003 · Cited by 46
Synergistic effects of fluticasone propionate and salmeterol on inhibiting rhinovirus‐induced epithelial production of remodelling‐associated growth factors
Volonaki, E., Psarras, S., Xepapadaki, P., Psomali, D., Gourgiotis, D., & Papadopoulos, N. G. (2006) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2006.02566.x · Cited by 44
On the Role of Mechanics in Chronic Lung Disease
Eskandari, M., Pfaller, M. R., & Ellen Kuhl, A. (2013) · Materials · doi:10.3390/ma6125639 · Cited by 44
Airway acidification in childhood asthma exacerbations
Caffarelli, C., Dascola, C. P., Peroni, D. G., Ricò, S., Stringari, G., Varini, M., Folesani, G., & Corradi, M. (2014) · Allergy and Asthma Proceedings · doi:10.2500/aap.2014.35.3740 · Cited by 44
Feature analysis of hyperpolarized helium‐3 pulmonary MRI: A study of asthmatics versus nonasthmatics
Tustison, N. J., Altes, T. A., Song, G., de Lange, E. E., Mugler, J. P., & Gee, J. C. (2010) · Magnetic Resonance in Medicine · doi:10.1002/mrm.22390 · Cited by 44
Quercetin: a flavonoid with the potential to treat asthma
Fortunato, L. R., Alves, C. D. F., Teixeira, M. M., & Rogério, A. D. P. (2012) · Brazilian Journal of Pharmaceutical Sciences · doi:10.1590/s1984-82502012000400002 · Cited by 46
Diagnosis and management of asthma in the elderly
Scichilone, N., Pedone, C., Battaglia, S. L., Sorino, C., & Bellia, V. (2014) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2014.01.004 · Cited by 44
Mitochondrial Dysfunction in Metabolic Syndrome and Asthma
Mabalirajan, U., & Ghosh, B. (2013) · Journal of Allergy · doi:10.1155/2013/340476 · Cited by 44
2-Methoxyestradiol (2-ME) reduces the airway inflammation and remodeling in an experimental mouse model
Huerta‐Yépez, S., Baay-Guzman, G. J., Garcia-Zepeda, R., Hernández‐Pando, R., Vega, M. I., González-Bonilla, C. R., & Bonavida, B. (2008) · Clinical Immunology · doi:10.1016/j.clim.2008.07.023 · Cited by 44
Preformulation and Evaluation of Tofacitinib as a Therapeutic Treatment for Asthma
Younis, U. S., Vallorz, E. L., Addison, K. J., Ledford, J. G., & Myrdal, P. B. (2019) · AAPS PharmSciTech · doi:10.1208/s12249-019-1377-0 · Cited by 44
The therapeutic potential of drugs targeting the arginase pathway in asthma
Ricciardolo, F. L. M., Zaagsma, J., & Meurs, H. (2005) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.14.10.1221 · Cited by 44
Effect of an inhaled adenosine A2A agonist on the allergen‐induced late asthmatic response
Luijk, B., van den Berge, M., Kerstjens, H. A. M., Postma, D. S., Cass, L., Sabin, A. T., & Lammers, J. J. (2007) · Allergy · doi:10.1111/j.1398-9995.2007.01557.x · Cited by 44
TGF‐β effects on airway smooth muscle cell proliferation, VEGF release and signal transduction pathways
Shin, J. H., Shim, J. W., Kim, D. S., & Shim, J. Y. (2009) · Respirology · doi:10.1111/j.1440-1843.2008.01469.x · Cited by 44
Therapeutic effect of surfactant protein D in allergic inflammation of mite‐sensitized mice
Liu, C.-F., Chen, Y. ‐., Shieh, C. ‐., Yu, C., Reid, K. B. M., & Wang, J. (2005) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2005.02205.x · Cited by 44
Stem Cells and Chronic Lung Disease
Gomperts, B. N., & Strieter, R. M. (2006) · Annual Review of Medicine · doi:10.1146/annurev.med.58.081905.134954 · Cited by 44
The pattern of methacholine responsiveness in mice is dependent on antigen challenge dose
Zosky, G. R., von Garnier, C., Stumbles, P. A., Holt, P. G., Sly, P. D., & Turner, D. J. (2004) · Respiratory Research · doi:10.1186/1465-9921-5-15 · Cited by 44
Validation of IKKβ as therapeutic target in airway inflammatory disease by adenoviral‐mediated delivery of dominant‐negative IKKβ to pulmonary epithelial cells
Catley, M. C., Chivers, J. E., Holden, N. S., Barnes, P. J., & Newton, R. C. (2005) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706170 · Cited by 43
Insights into mast cell functions in asthma using mouse models
Lei, Y., Gregory, J. A., Nilsson, G. P., & Mikael Adner, A. (2013) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2013.03.019 · Cited by 43
Complement mediators: key regulators of airway tissue remodeling in asthma
Khan, M. A., Assiri, A. M., & Broering, D. C. (2015) · Journal of Translational Medicine · doi:10.1186/s12967-015-0565-2 · Cited by 43
Induced Trefoil Factor Family 1 Expression by Trans-Differentiating Clara Cells in a Murine Asthma Model
Kouznetsova, I., Chwieralski, C. E., Bälder, R., Hinz, M., Braun, A. C., Krug, N., & Hoffmann, W. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0008oc · Cited by 43
Is the neutrophil a worthy target in severe asthma and chronic obstructive pulmonary disease?
Louis, R., & Djukanović, R. (2006) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2006.02493.x · Cited by 43
Angiopoietin-1 Protects against Airway Inflammation and Hyperreactivity in Asthma
Simoes, D. C. M., Vassilakopoulos, T., Toumpanakis, D., Petrochilou, K., Roussos, C., & Papapetropoulos, A. (2008) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200708-1141oc · Cited by 43
TGFB1 promoter polymorphism C-509T and pathophysiology of asthma
Ueda, T., Niimi, A., Matsumoto, H., Takemura, M., Yamaguchi, M., Matsuoka, H., Jinnai, M., Chin, K., Minakuchi, M., Cheng, L., et al. (2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.10.005 · Cited by 43
Airway lipoxin A4/formyl peptide receptor 2–lipoxin receptor levels in pediatric patients with severe asthma
Gagliardo, R. P., Gras, D., Grutta, S. L., Chanez, P., Sano, C. D., Albano, G. D., Vachier, I., Montalbano, A. M., Anzalone, G., Bonanno, A., et al. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.11.045 · Cited by 43
Lung proteome alterations in a mouse model for nonallergic asthma
Houtman, R., Krijgsveld, J., Kool, M., Romijn, E. P., Redegeld, F. A., Nijkamp, F. P., Heck, A. J. R., & Humphery‐Smith, I. (2003) · PROTEOMICS · doi:10.1002/pmic.200300469 · Cited by 43
Tumor Necrosis Factor-α Increases Airway Smooth Muscle Oxidants Production through a NADPH Oxidase-like System to Enhance Myosin Light Chain Phosphorylation and Contractility
Thabut, G., Benna, J. E., Samb, A., Corda, S., Megret, J., Lesèche, G., Vicaut, É., Aubier, M., & Boczkowski, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200315200 · Cited by 43
Stress-Activated Protein Kinases Mediate Cell Migration in Human Airway Epithelial Cells
White, S. R., Tse, R., & Marroquin, B. A. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2004-0118oc · Cited by 43
Impact of Smoking on Asthma Therapy
Livingston, E., Thomson, N. C., & Chalmers, G. W. (2005) · Drugs · doi:10.2165/00003495-200565110-00005 · Cited by 43
γ‐Secretase Inhibitor Alleviates Acute Airway Inflammation of Allergic Asthma in Mice by Downregulating Th17 Cell Differentiation
Zhang, W., Zhang, X., Sheng, A., Weng, C., Zhu, T., Zhao, W., & Li, C. (2015) · Mediators of Inflammation · doi:10.1155/2015/258168 · Cited by 42
Caerulomycin A inhibits Th2 cell activity: a possible role in the management of asthma
Kujur, W., Gurram, R. K., Haleem, N., Maurya, S. K., & Agrewala, J. N. (2015) · Scientific Reports · doi:10.1038/srep15396 · Cited by 42
Patient-Specific Airway Wall Remodeling in Chronic Lung Disease
Eskandari, M., Kuschner, W. G., & Ellen Kuhl, A. (2015) · Annals of Biomedical Engineering · doi:10.1007/s10439-015-1306-7 · Cited by 42
Up-Regulation of Thrombin Activity Induced by Vascular Endothelial Growth Factor in Asthmatic Airways
Kanazawa, H., & Yoshikawa, T. (2007) · CHEST Journal · doi:10.1378/chest.07-0945 · Cited by 42
The importance of the airway microvasculature in asthma
Wilson, J. W., & Hii, S.-I. (2006) · Current Opinion in Allergy and Clinical Immunology · doi:10.1097/01.all.0000200505.54425.47 · Cited by 42
Molecular cloning and functional characterization of murine cysteinyl-leukotriene 1 (CysLT1) receptors11Abbreviations: LT, leukotriene; hCysLT1R, human cysteinyl-leukotriene receptor (subtype 1); mCysLT1R, mouse cysteinyl-leukotriene receptor (subtype 1); CysLT2R, cysteinyl-leukotriene receptor (subtype 2); HEK, human embryonic kidney; ORF, open reading frame; RT-PCR, reverse transcription-polymerase chain reaction; and RACE, rapid amplification of cDNA ends.
Martin, V., Sawyer, N., Stocco, R., Unett, D. J., Lerner, M. R., Abramovitz, M., & Funk, C. D. (2001) · Biochemical Pharmacology · doi:10.1016/s0006-2952(01)00774-2 · Cited by 42
A Centennial History of Research on Asthma Pathogenesis
Walter, M. J., & Holtzman, M. J. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.f300 · Cited by 42
Type I IL-1 Receptor (IL-1RI) as Potential New Therapeutic Target for Bronchial Asthma
Lee, J., Wang, L., Yu, H., Lin, Y., Yang, Y., & Chiang, B. (2010) · Mediators of Inflammation · doi:10.1155/2010/567351 · Cited by 42
A comparison between intratracheal and inhalation delivery of Aspergillus fumigatus conidia in the development of fungal allergic asthma in C57BL/6 mice
Samarasinghe, A. E., Hoselton, S. A., & Schuh, J. M. (2010) · Fungal Biology · doi:10.1016/j.funbio.2010.09.013 · Cited by 42
Airway Remodeling: A Comparison Between Fatal and Nonfatal Asthma
Chen, F. H., Samson, K. T. R., Miura, K., Ueno, K., Odajima, Y., Shougo, T., Yamaguchi, Y., & Shioda, S. (2004) · Journal of Asthma · doi:10.1081/jas-200026405 · Cited by 42
Effect ofMoringa oleiferaLam. Seed Extract on Ovalbumin-Induced Airway Inflammation in Guinea Pigs
Mahajan, S. G., & Mehta, A. A. (2008) · Inhalation Toxicology · doi:10.1080/08958370802027443 · Cited by 42
Eulophia macrobulbon – an orchid with significant anti-inflammatory and antioxidant effect and anticancerogenic potential exerted by its root extract
Schuster, R., Zeindl, L. T., Hölzer, W., Khumpirapang, N., Okonogi, S., Viernstein, H., & Mueller, M. (2016) · Phytomedicine · doi:10.1016/j.phymed.2016.11.018 · Cited by 42
Clinical practice guidelines: Medical follow-up of patients with asthma—Adults and adolescents
Roche, N., Morel, H., Martel, P., & Godard, P. (2005) · Respiratory Medicine · doi:10.1016/j.rmed.2005.03.011 · Cited by 42
Induction of Human Airway Smooth Muscle Apoptosis by Neutrophils and Neutrophil Elastase
Oltmanns, U., Sukkar, M. B., Xie, S., John, M., & Chung, K. F. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2004-0321oc · Cited by 42
Treatment of Experimental Asthma by Decoy-mediated Local Inhibition of Activator Protein-1
Desmet, C. J., Gosset, P., Henry, E., Garzé, V., Faísca, P., Vos, N., Jaspar, F., Melotte, D., Lambrecht, B. N., Desmecht, D. J.-M., et al. (2005) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200410-1431oc · Cited by 42
Building a better mouse model: experimental models of chronic asthma
Fulkerson, P. C., Rothenberg, M. E., & Hogan, S. P. (2005) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2005.02354.x · Cited by 44
Elastosis during airway wall remodeling explains multiple co-existing instability patterns
Eskandari, M., Javili, A., & Ellen Kuhl, A. (2016) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2016.05.022 · Cited by 41
Protection of Plasminogen Activator Inhibitor-1-Deficient Mice from Nasal Allergy
Sejima, T., Madoiwa, S., Mimuro, J., Sugo, T., Okada, K., Ueshima, S., Matsuo, O., Ishida, T., Ichimura, K., & Sakata, Y. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.12.8135 · Cited by 41
Antigen sensitization modulates alveolar macrophage functions in an asthma model
Careau, É., Proulx, L.-I., Pouliot, P., Spahr, A., Turmel, V., & Bissonnette, É. Y. (2006) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00219.2005 · Cited by 41
The Impact of Allergic Rhinitis and Asthma on Human Nasal and Bronchial Epithelial Gene Expression
Wagener, A. H., Zwinderman, A. H., Luiten, S., Fokkens, W. J., Bel, E. H., Sterk, P. J., & van Drunen, C. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080257 · Cited by 42
Complement components as potential therapeutic targets for asthma treatment
Khan, M. A., Nicolls, M. R., Surguladze, B., & Saadoun, I. M. K. (2014) · Respiratory Medicine · doi:10.1016/j.rmed.2014.01.005 · Cited by 41
The effects of inhaled budesonide and formoterol in combination and alone when given directly after allergen challenge
Duong, M. T., Gauvreau, G. M., Watson, R. M., Obminski, G., Strinich, T. X., Evans, M., Howie, K. J., Killian, K. J., & O’Byrne, P. M. (2006) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2006.10.018 · Cited by 40
Effect of aging on airway remodeling and muscarinic receptors in a murine acute asthma model
Kang, J. Y., Rhee, C. K., Kim, S. J., Kwon, S. S., Kim, J.-Y., & Lee, S. (2013) · Clinical Interventions in Aging · doi:10.2147/cia.s50496 · Cited by 40
Distinctive characteristics of bronchial reticular basement membrane and vessel remodelling in chronic obstructive pulmonary disease (COPD) and in asthma: they are not the same disease
Soltani, A., Muller, H. K., Sohal, S. S., Reid, D. W., Weston, S., Wood-Baker, R. R., & Walters, E. H. (2012) · Histopathology · doi:10.1111/j.1365-2559.2011.04147.x · Cited by 40
Reversible airway obstruction in cystic fibrosis: Common, but not associated with characteristics of asthma
Levine, H., Cohen‐Cymberknoh, M., Klein, N., Hoshen, M. B., Mussaffi, H., Stafler, P., Breuer, O., Kerem, E., & Blau, H. (2016) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2016.01.003 · Cited by 40
Putting the Squeeze on Airway Epithelia
Park, J., Fredberg, J. J., & Drazen, J. M. (2015) · Physiology · doi:10.1152/physiol.00004.2015 · Cited by 40
Targeting Chromatin Remodeling in Inflammation and Fibrosis
Yang, J., Tian, B., & Brasier, A. R. (2016) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2016.11.001 · Cited by 40
hsa-miR-20a-5p attenuates allergic inflammation in HMC-1 cells by targeting HDAC4
Lu, Y. C., Li, Z., Xie, B., Song, Y., Ye, X., & Liu, P. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.01.010 · Cited by 40
Anti-Inflammatory and Anti-Oxidative Effects of Myrtenol in the Rats with Allergic Asthma.
Rajizadeh, M. A., Najafipour, H., Fekri, M. S., Rostamzadeh, F., Jafari, E., Bejeshk, M. A., & Masoumi‐Ardakani, Y. (2019) · PubMed Central · doi:10.22037/ijpr.2019.1100749 · Cited by 42
Molecular Mechanisms of Allergic Disease
Venarske, D., & deShazo, R. D. (2003) · Southern Medical Journal · doi:10.1097/01.smj.0000097887.04639.39 · Cited by 40
Redox regulation of mast cell histamine release in thioredoxin-1 (TRX) transgenic mice
Son, A., Nakamura, H., Kondo, N., Matsuo, Y., Liu, W., Oka, S., Ishii, Y., & Yodoi, J. (2006) · Cell Research · doi:10.1038/sj.cr.7310031 · Cited by 41
Interleukin-1β mediates human airway epithelial cell migration via NF-κB
White, S. R., Fischer, B. M., Marroquin, B. A., & Stern, R. K. (2008) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00065.2008 · Cited by 40
IMIQUIMOD, A TOLL‐LIKE RECEPTOR 7 LIGAND, INHIBITS AIRWAY REMODELLING IN A MURINE MODEL OF CHRONIC ASTHMA
Du, Q., Zhou, L., Chen, Z., Gu, X., Huang, M., & Yin, K. (2008) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2008.05027.x · Cited by 40
Tumstatin regulates the angiogenic and inflammatory potential of airway smooth muscle extracellular matrix
Harkness, L. M., Weckmann, M., Kopp, M., Becker, T., Ashton, A. W., & Burgess, J. K. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13232 · Cited by 40
The 100 most influential publications in asthma from 1960 to 2017: A bibliometric analysis
Qu, Y., Zhang, C., Hu, Z., Li, S., Chen, K., Ning, Y., Shang, Y., & Bai, C. (2018) · Respiratory Medicine · doi:10.1016/j.rmed.2018.03.014 · Cited by 41
Gas exchange during exercise in habitually active asthmatic subjects
Haverkamp, H. C., Dempsey, J. A., Miller, J. D., Romer, L. M., Pegelow, D. F., Rodman, J. R., & Eldridge, M. W. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00041.2005 · Cited by 40
Differences in radiological/HRCT findings in eosinophilic bronchitis and asthma: implication for bronchial responsiveness
Park, S. (2005) · Thorax · doi:10.1136/thx.2005.044420 · Cited by 40

Authors: BOUSQUET, J., JEFFERY, P. K., BUSSE, W. W., JOHNSON, M., & VIGNOLA, A. M.
Affiliations: University of Wisconsin–Madison (US)
ORCID: BOUSQUET, JEAN
Venue: American Journal of Respiratory and Critical Care Medicine
Publisher: Oxford University Press (OUP)
Published: 2000-05-01
Volume: 161
Issue: 5
Pages: 1720-1745
ISSN: 1073-449X (ISSN-L)
1535-4970
DOI: 10.1164/ajrccm.161.5.9903102
OpenAlex: W2121464855
Cited by: 1,702
References: 552
Citations by year: 2026: 8 · 2025: 19 · 2024: 28 · 2023: 27 · 2022: 33 · 2021: 53 · 2020: 39 · 2019: 37 · 2018: 41 · 2017: 36 · 2016: 61 · 2015: 61 · 2014: 65 · 2013: 72 · 2012: 78
FWCI: 10.56
Type: journal article
Language: en
Open access: closed
Licence: academic.oup.com/pages/standard-publication-reuse-rights (vor)
Locations: American Journal of Respiratory and Critical Care Medicine (publishedVersion)
PubMed (publishedVersion)
Topics: Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Asthma and respiratory diseases
Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Occupational exposure and asthma
Keywords: asthma, bronchoconstriction, airway inflammation, airway remodeling
MeSH terms: Animals, Asthma, Bronchi, Humans, Inflammation, Bronchoconstriction

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Asthma: From Bronchoconstriction to Airways Inflammation and Remodeling

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks