Stretch-induced Activation of Transforming Growth Factor-β1 in Pulmonary Fibrosis

Making sense of latent TGFβ activation

Annes, J. P., Munger, J. S., & Rifkin, D. B. (2002) · Journal of Cell Science · doi:10.1242/jcs.00229 · Cited by 1,624

Myofibroblast contraction activates latent TGF-β1 from the extracellular matrix

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Adenovector-mediated gene transfer of active transforming growth factor-beta1 induces prolonged severe fibrosis in rat lung.

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Latent TGF-β structure and activation

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Allosteric inhibition of lysyl oxidase–like-2 impedes the development of a pathologic microenvironment

Barry-Hamilton, V., Spangler, R., Marshall, D., McCauley, S., Rodriguez, H. M., Oyasu, M., Mikels, A., Vaysberg, M., Ghermazien, H., Wai, C., et al. (2010) · Nature Medicine · doi:10.1038/nm.2208 · Cited by 870

Targeting of αv integrin identifies a core molecular pathway that regulates fibrosis in several organs

Henderson, N. C., Arnold, T. D., Katamura, Y., Giacomini, M. M., Rodriguez, J. D., McCarty, J. H., Pellicoro, A., Raschperger, E., Betsholtz, C., Ruminski, P. G., et al. (2013) · Nature Medicine · doi:10.1038/nm.3282 · Cited by 866

Feedback amplification of fibrosis through matrix stiffening and COX-2 suppression

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Increased stiffness of the rat liver precedes matrix deposition: implications for fibrosis

Georges, P. C., Hui, J.-J., Gombos, Z., McCormick, M. E., Wang, A. Y., Uemura, M., Mick, R., Janmey, P. A., Furth, E. E., & Wells, R. G. (2007) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00032.2007 · Cited by 577

Matrix stiffness-induced myofibroblast differentiation is mediated by intrinsic mechanotransduction

Huang, X., Yang, N., Fiore, V. F., Barker, T. H., Sun, Y., Morris, S. W., Ding, Q., Thannickal, V. J., & Zhou, Y. (2012) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2012-0050oc · Cited by 530

TGF-β – an excellent servant but a bad master

Kubiczkova, L., Sedlarikova, L., Hajek, R., & Sevcikova, S. (2012) · Journal of Translational Medicine · doi:10.1186/1479-5876-10-183 · Cited by 511

Specific epigenetic regulators serve as potential therapeutic targets in idiopathic pulmonary fibrosis

Sehgal, M., Jakhete, S. M., Manekar, A. G., & Sasikumar, S. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e09773 · Cited by 23

Jiawei Maxing Shigan Tang alleviates radiation-induced lung injury via TGF-β1/Smad signaling pathway mediated by regulatory T cells

Wang, M., Feng, Y., Zhang, P., Shen, K., Su, J., Zhong, Y., Yang, X., Lin, S., & Lu, J. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.117389 · Cited by 23

Clevudine attenuates bleomycin-induced early pulmonary fibrosis via regulating M2 macrophage polarization

Li, S., Gao, S., Jiang, Q., Liang, Q. L., Luan, J., Zhang, R., Zhang, F., Ruan, H., Li, X., Li, X., et al. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.108271 · Cited by 23

Novedades diagnósticas y terapéuticas en fibrosis pulmonar progresiva

Molina‐Molina, M., Buendía-Roldán, I., Castillo, D., Caro, F. M., Valenzuela, C., & Selman, M. (2022) · Archivos de Bronconeumología · doi:10.1016/j.arbres.2021.12.006 · Cited by 22

The novel role of ER protein TXNDC5 in the pathogenesis of organ fibrosis: mechanistic insights and therapeutic implications

Hung, C., Tsai, Y.-W., Wu, Y., Yeh, C., & Yang, K. (2022) · Journal of Biomedical Science · doi:10.1186/s12929-022-00850-x · Cited by 21

Theophylline Attenuates BLM-Induced Pulmonary Fibrosis by Inhibiting Th17 Differentiation

Park, S.-J., Hahn, H.-J., Oh, S., & Lee, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021019 · Cited by 23

Serum Levels of Surfactant Proteins in Patients with Combined Pulmonary Fibrosis and Emphysema (CPFE)

Papaioannou, A. Ι., Κostikas, Κ., Manali, E. D., Papadaki, G. F., Roussou, A., Spathis, A., Mazioti, A., Tomos, I. P., Papanikolaou, I. C., Loukides, S., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157789 · Cited by 23

Asiaticoside attenuates bleomycin-induced pulmonary fibrosis in A2aR−/− mice by promoting the BMP7/Smad1/5 signaling pathway

Zhang, T., Dai, J., Ye, W., Cai, L., Wei, J., Chen, M., Huang, X., & Wang, X. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.04.156 · Cited by 21

Therapeutic targets and early stage clinical trials for pulmonary fibrosis

Sato, S., Yanagihara, T., & Kolb, M. R. J. (2018) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2019.1554054 · Cited by 20

Protective Role of Nuclear Factor Erythroid-2-Related Factor 2 against Mechanical Trauma-Induced Apoptosis in a Vaginal Distension-Induced Stress Urinary Incontinence Mouse Model

Tang, J., Liu, C., Li, B., Hong, S., Li, Q., Wang, L., Min, J., Hu, M., Li, Y., He, S., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/2039856 · Cited by 20

Biomechanical Properties and Cellular Responses in Pulmonary Fibrosis

He, A., He, L., Chen, T., Li, X., & Cao, C. (2024) · Bioengineering · doi:10.3390/bioengineering11080747 · Cited by 22

The Myofibroblast: TGFβ-1, A Conductor which Plays a Key Role in Fibrosis by Regulating the Balance between PPARγ and the Canonical WNT Pathway

Lecarpentier, Y., Schussler, O., CLAES, V. A., & Vallée, A. (2017) · Nuclear Receptor Research · doi:10.11131/2017/101299 · Cited by 19

Epithelial damage and ageing: the perfect storm

Hewitt, R. J., Pearmain, L., Lyka, E., & Dickens, J. A. (2025) · Thorax · doi:10.1136/thorax-2024-222060 · Cited by 20

Mitochondrial Dysfunction-Associated Arrhythmogenic Substrates in Diabetes Mellitus

Song, J., Yang, R., Yang, J., & Zhou, L. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01670 · Cited by 18

High amplitude stretching of ATII cells and fibroblasts results in profibrotic effects

Kühn, H., Zobel, C., Vollert, G., Gurcke, M., Jenszöwski, C., Barina, C., Frille, A., & Wirtz, H. R. W. (2019) · Experimental Lung Research · doi:10.1080/01902148.2019.1636424 · Cited by 18

Cell-Based Therapies for Tissue Fibrosis

Lim, R., Ricardo, S. D., & Sievert, W. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00633 · Cited by 17

Controlled Growth Factor Delivery and Cyclic Stretch Induces a Smooth Muscle Cell-like Phenotype in Adipose-Derived Stem Cells

Walters, B., Turner, P. A., Rolauffs, B., Hart, M. L., & Stegemann, J. P. (2021) · Cells · doi:10.3390/cells10113123 · Cited by 17

Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective

Papiris, S. A., Kannengiesser, C., Borie, R., Kolilekas, L., Kallieri, M., Apollonatou, V., Ba, I., Nathan, N., Bush, A., Griese, M., et al. (2022) · Diagnostics · doi:10.3390/diagnostics12122928 · Cited by 18

Cough, an unresolved problem in interstitial lung diseases

van Manen, M. J. G., & Wijsenbeek, M. S. (2019) · Current Opinion in Supportive and Palliative Care · doi:10.1097/spc.0000000000000447 · Cited by 17

Intermittent CPAP limits hyperoxia-induced lung damage in a rabbit model of bronchopulmonary dysplasia

Gie, A. G., Salaets, T., Vignero, J., Regin, Y., Vanoirbeek, J. A., Deprest, J. A., & Toelen, J. (2020) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00465.2019 · Cited by 17

Mechanical Stretch Induces Senescence of Lung Epithelial Cells and Drives Fibroblast Activation by Paracrine Mechanisms

Martín-Vicente, P., López‐Martínez, C., López-Alonso, I., Exojo-Ramírez, S. M., Duarte-Herrera, I. D., Amado‐Rodríguez, L., Ordoñez, I., Cuesta‐Llavona, E., Gómez, J., Campo, N., et al. (2024) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2023-0449oc · Cited by 16

The role of mechanical stretch and TGF-β2 in epithelial-mesenchymal transition of retinal pigment epithelial cells

Cao, Q. (2019) · International Journal of Ophthalmology · doi:10.18240/ijo.2019.12.03 · Cited by 15

The Cellular and Molecular Effects of Fetoscopic Endoluminal Tracheal Occlusion in Congenital Diaphragmatic Hernia

Olutoye, O. O., Short, W. D., Gilley, J., Hammond, J. D., Belfort, M. A., Lee, T. C., King, A., Espinoza, J., Joyeux, L., Lingappan, K., et al. (2022) · Frontiers in Pediatrics · doi:10.3389/fped.2022.925106 · Cited by 16

Clinical significance of self-reported cough intensity and frequency in patients with interstitial lung disease: a cross-sectional study

Sato, R., Handa, T., Matsumoto, H., Kubo, T., & Hirai, T. (2019) · BMC Pulmonary Medicine · doi:10.1186/s12890-019-1012-6 · Cited by 15

Improved Alveolar Dynamics and Structure After Alveolar Epithelial Type II Cell Transplantation in Bleomycin Induced Lung Fibrosis

López-Rodríguez, E., Gay-Jordi, G., Knudsen, L., Ochs, M., & Serrano‐Mollar, A. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.640020 · Cited by 15

Heat shock protein: a hot topic in idiopathic pulmonary fibrosis

Bonniaud, P., Bellaye, P., Burgy, O., & Kolb, M. R. J. (2017) · European Respiratory Journal · doi:10.1183/13993003.02152-2016 · Cited by 15

Piezo1 Activation Improves NSCLC Liver Metastasis Immunotherapy by Overriding Matrix Stiffness‐Mediated Bimodal PD‐L1/CXCL10 Regulation

Zhang, T., Li, Y., Cheng, B., Zhao, X., Liu, M., Feng, J., Bai, Y., Yu, Y., Jiang, P., Geng, L., et al. (2025) · Advanced Science · doi:10.1002/advs.202501335 · Cited by 18

Gramine protects against pressure overload-induced pathological cardiac hypertrophy through Runx1-TGFBR1 signaling

Xu, L., Su, Y., Yang, X., Bai, X., Wang, Y., Zhuo, C., & Meng, Z. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154779 · Cited by 14

Neutrophil Activity and Extracellular Matrix Degradation: Drivers of Lung Tissue Destruction in Fatal COVID-19 Cases and Implications for Long COVID

Narasaraju, T., Neeli, I., Criswell, S. L., Amita, K., Meng, W., Silva, V., Bila, G., Vovk, V., Serhiy, Z., Bowlin, G. L., et al. (2024) · Biomolecules · doi:10.3390/biom14020236 · Cited by 15

Inhibition of mmp13a during zebrafish fin regeneration disrupts fin growth, osteoblasts differentiation, and Laminin organization

Li, L., Zhang, J., & Akimenko, M. (2019) · Developmental Dynamics · doi:10.1002/dvdy.112 · Cited by 14

A phycocyanin derived eicosapeptide attenuates lung fibrosis development

Li, Q., Wen, P., Zhang, Z., Pei, X., Sun, Z., & Ou, Y. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174356 · Cited by 15

Catch your breath: The protective role of the angiotensin AT2 receptor for the treatment of idiopathic pulmonary fibrosis

Young, O. N., Bourke, J. E., & Widdop, R. E. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115839 · Cited by 16

The dawn of the omics era in human precision-cut lung slices

Stegmayr, J., & Wagner, D. E. (2021) · European Respiratory Journal · doi:10.1183/13993003.00203-2021 · Cited by 12

BMP3 inhibits TGFβ2-mediated myofibroblast differentiation during wound healing of the embryonic cornea

Spurlin, J. W., Garis, M. R., & Lwigale, P. Y. (2022) · npj Regenerative Medicine · doi:10.1038/s41536-022-00232-9 · Cited by 13

Allyl Methyl Sulfide Preserved Pressure Overload-Induced Heart Failure Via Modulation of Mitochondrial Function

Mohammed, S. A., Bugga, P., Meghwani, H., Reddy, M. P. K., Arava, S. K., & Banerjee, S. K. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111316 · Cited by 13

Ginsenoside Rg1 protects against cigarette smoke-induced airway remodeling by suppressing the TGF-β1/Smad3 signaling pathway.

Guan, S., Yu, P., Cao, J., Xi, X., Zhang, Q., Zhu, C., Hu, H., Gong, X., & Fan, H. (2020) · PubMed Central · Cited by 13

Emerging roles of noncoding RNAs in idiopathic pulmonary fibrosis

Wang, H., Sun, K., Peng, H. F., Wang, Y., & Zhang, L. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-02170-5 · Cited by 14

Stretch regulates alveologenesis and homeostasis via mesenchymal Gαq/11-mediated TGFβ2 activation

Goodwin, A. T., John, A. E., Joseph, C., Habgood, A., Tatler, A. L., Suszták, K., Palmer, M., Offermanns, S., Henderson, N. C., & Jenkins, G. R. (2023) · Development · doi:10.1242/dev.201046 · Cited by 12

Adipokines in interstitial lung diseases

Zieliński, M., Chwalba, A., Jastrzębski, D., & Ziora, D. I. (2023) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2023.104109 · Cited by 13

MicroRNA-26a inhibits hyperplastic scar formation by targeting Smad2

Qi, J., Liu, Y., Hu, K., Zhang, Y., Wu, Y., & Zhang, X. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.5984 · Cited by 11

The CaT stretcher: An open-source system for delivering uniaxial strain to cells and tissues (CaT)

Wang, Y., Singer, R., Liu, X., Inman, S. J., Cao, Q., Zhou, Q., Noble, A., Li, L., Tafoya, A. A., Babi, M., et al. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.959335 · Cited by 10

Another piece in the pirfenidone puzzle

Lehmann, M., & Kolb, M. R. J. (2023) · European Respiratory Journal · doi:10.1183/13993003.00240-2023 · Cited by 10

Peptide PD29 treats bleomycin-induced pulmonary fibrosis by inhibiting the TGF-β/smad signaling pathway

Sun, Q., Hu, J., Yu, P., Zhu, Z., Yu, R., Ge, C., Li, C., Wu, G., Lin, B., Liu, G., et al. (2019) · Experimental Lung Research · doi:10.1080/01902148.2019.1614696 · Cited by 9

Mechanisms of mechanical stimulation in the development of respiratory system diseases

Xia, T. D., Pan, Z., Wan, H., Li, Y., Mao, G., Zhao, J., Zhang, F., & Pan, S. (2024) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00122.2024 · Cited by 8

Basement membrane structure and function: Relating biology to mechanics

Page, A. W., & Ferrell, N. J. (2025) · Matrix Biology · doi:10.1016/j.matbio.2025.08.004 · Cited by 9

SPECT Imaging of Lysyl Oxidase-like 2 in a Model of Idiopathic Pulmonary Fibrosis

Vizier, R., Garnier, A.-R., Dias, A. M. M., Moreau, M., Claron, M., Collin, B., Denat, F., Bellaye, P., & Gonçalves, V. (2023) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.3c00232 · Cited by 8

The myofibroblast and Giulio Gabbiani: An inseparable couple celebrates their 50 years golden wedding anniversary

Desmoulière, A., & Hinz, B. (2021) · Wound Repair and Regeneration · doi:10.1111/wrr.12942 · Cited by 9

Mechanobiology and Resolution of Lung Fibrosis

Link, P. A., & Tschumperlin, D. J. (2025) · Annual Review of Physiology · doi:10.1146/annurev-physiol-031725-021041 · Cited by 11

The importance of mechanical forces in chronic respiratory diseases

Burgess, J. K., Nawroth, J. C., Ibáñez‐Fonseca, A., & Gavara, N. (2026) · European Respiratory Review · doi:10.1183/16000617.0155-2025 · Cited by 9

The role of heat shock protein 90 in idiopathic pulmonary fibrosis: state of the art

Monteleone, G., Cameli, P., & Bonella, F. (2025) · European Respiratory Review · doi:10.1183/16000617.0147-2024 · Cited by 9

A roadmap for developing and engineering in vitro pulmonary fibrosis models

Dabaghi, M., Carpio, M. B., Saraei, N., Moran-Mirabal, J. M., Kolb, M. R. J., & Hirota, J. A. (2023) · Biophysics Reviews · doi:10.1063/5.0134177 · Cited by 7

Breathing-induced stretch enhances the efficacy of an inhaled and orally delivered anti-fibrosis drug in vitro

Doryab, A., Heydarian, M., Yildirim, A. Ö., Hilgendorff, A., Behr, J., & Schmid, O. (2023) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2023.104316 · Cited by 5

Update in Interstitial Lung Disease 2016

Wells, A. U., & Maher, T. M. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201702-0351up · Cited by 8

Cough and dyspnea management in pulmonary fibrosis

van Veelen, A., Wijsenbeek, M. S., & Koudstaal, T. (2025) · Current Opinion in Supportive and Palliative Care · doi:10.1097/spc.0000000000000753 · Cited by 5

Updates on the Prevalence, Quality of Life, and Management of Chronic Cough in Interstitial Lung Diseases

Трушенко, Н. В., Suvorova, O., Shmidt, A. E., Chikina, S. Y., Levina, I. A., Lavginova, B. B., & Avdeev, S. N. (2025) · Diagnostics · doi:10.3390/diagnostics15091139 · Cited by 5

Mechanotransduction in fibrosis: Mechanisms and treatment targets

Yeh, C., Chou, C. E. N., & Yang, K. (2021) · Current topics in membranes · doi:10.1016/bs.ctm.2021.07.004 · Cited by 4

Lysophosphatidic Acid Regulates Rho Family of GTPases in Lungs

Tran, K. C., & Zhao, J. (2021) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-021-00993-y · Cited by 5

Complications of Chronic Cough

Jacobs, S. S. (2020) · CHEST Journal · doi:10.1016/j.chest.2020.08.005 · Cited by 5

Cicatrisation normale et hypertrophique, influence de l’environnement mécanique

Girard, D., & Desmoulière, A. (2018) · Revue Francophone de Cicatrisation · doi:10.1016/j.refrac.2018.07.004 · Cited by 4

Antitussive Effect of a Chest Band in Patients with Interstitial Lung Disease: The Preliminary Results from a Pre-post Intervention Study

Sato, R., Handa, T., Matsumoto, H., Hirai, K., Ohkura, N., Kubo, T., & Hirai, T. (2021) · Internal Medicine · doi:10.2169/internalmedicine.6716-20 · Cited by 4

Transforming growth factor-beta and liver injury in an arginine vasopressin-induced pregnant rat model

Govender, N., Ramdin, S., Reddy, R., & Naicker, T. (2021) · Daehan saengsik uihak hoeji/Clinical and experimental reproductive medicine · doi:10.5653/cerm.2020.04035 · Cited by 4

Insight into the pathogenesis of interstitial lung diseases and near-to-native lung fibrosis models

Štefániková, M., Sedláková, V., Portakal, T., Hampl, A., Vaňhara, P., & Doubková, M. (2025) · European journal of medical research · doi:10.1186/s40001-025-03504-4 · Cited by 3

Mechanopharmacology of cellular microenvironment stiffness: Therapeutic strategies for age‐related diseases

Wang, H., Juan, C. D. H., Lee, Z.-Y., & Thai, T. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70236 · Cited by 4

Worldwide productivity and research trend of publications concerning extracellular vesicles role in fibrosis: A bibliometric study from 2013 to 2022

Peng, Y., Tang, R. N., Xu, Q., Mei, S., Zhou, Y., Feng, J., Zhang, S., & He, Z. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24357 · Cited by 3

Dysregulated microRNAs and long non-coding RNAs associated with extracellular matrix stiffness

Qiu, H., Fu, Y., Guo, Z., Zhang, X., Wang, X., & Wu, H. (2024) · Experimental Cell Research · doi:10.1016/j.yexcr.2024.114014 · Cited by 3

IL-11 Drives Dermal Fibroblast Activation in Mechanical Stretch-Mediated Skin Expansion

Liu, Y., Khoong, Y., Xia, W., Xu, R., Widjaja, A. A., Liang, H., Luo, S., Yang, E., Huang, X., & Zan, T. (2025) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2025.07.023 · Cited by 3

Cell–matrix interactions in lung disease and regeneration: ERS Lung Science Conference 2018 report

Meiners, S., Lloyd, C. M., & Chambers, R. C. (2018) · European Respiratory Review · doi:10.1183/16000617.0040-2018 · Cited by 3

Mechanotransduction: A Master Regulator of Alveolar Cell Fate Determination

Devi, K., & Parekh, K. R. (2025) · Bioengineering · doi:10.3390/bioengineering12070760 · Cited by 2

Idiopathic pulmonary fibrosis from a multiscale mechanobiology perspective: Mechanisms and future therapeutic prospects

Xia, T., Wang, X., Yang, Z., & Zhao, R. (2026) · iScience · doi:10.1016/j.isci.2026.115335 · Cited by 4

Mechanobiologically dynamic biomaterials for tissue healing and disease treatment

Lee, J., Yun, Y. G., Shenoy, V. B., Leong, K. W., & Kim, H. (2026) · Cell Biomaterials · doi:10.1016/j.celbio.2026.100536 · Cited by 4

Anti-MDA5 Antibody-positive Clinically Amyopathic Dermatomyositis Complicated by Unilateral Right-sided Interstitial Lung Disease

Kori, M., Awano, N., Inomata, M., Kuse, N., Tone, M., Yoshimura, H., Jo, T., Takada, K., Kumasaka, T., Takemura, T., et al. (2020) · Internal Medicine · doi:10.2169/internalmedicine.3604-19 · Cited by 2

Objective measurement of cough in pulmonary fibrosis: a cohort study – ImpaCT

Kebbe, J., Hart, S. P., Kaner, R. J., Kulkarni, T., Wollin, L., Coeck, C., Vinisko, R., Patel, N., & Wijsenbeek, M. S. (2024) · ERJ Open Research · doi:10.1183/23120541.00310-2024 · Cited by 2

Cardio‐Respiratory Complications in Adult Monozygotic Twins With Myhre Syndrome

Sim, H., Wilke, F., Hamburger, E., Sang, C. J., & Hildebrandt, C. C. (2025) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.32150 · Cited by 2

The Importance of Cutaneous Innervation in Wound Healing: From Animal Studies to Clinical Applications

Ge, S. X., & Khachemoune, A. (2021) · The International Journal of Lower Extremity Wounds · doi:10.1177/15347346211045022 · Cited by 2

Hsp90 and Its Role in Heme-Maturation of Client Proteins: Implications for Human Diseases

Ghosh, A., & Stuehr, D. J. (2019) · Heat shock proteins · doi:10.1007/978-3-030-23158-3_12 · Cited by 2

The Extracellular Matrix-Cell Interaction in ILD

Upagupta, C., Yanagihara, T., & Kolb, M. R. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-08-102723-3.00021-4 · Cited by 3

CD98 is critical for a conserved inflammatory response to diverse injury stimuli relevant to IPF exacerbations and COVID pneumonitisPreprint

Stylianou, P., Rushwan, S., Wang, W., Miah, M. A., Darweesh, O., MacKinnon, A. C., Roach, K. M., Hitchman, C. J., Gonchar, O., Thorpe, S. D., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.12.503154 · Cited by 2

The Curious Case of Cough in Interstitial Lung Diseases

van Manen, M. J. G., & Hart, S. P. (2022) · CHEST Journal · doi:10.1016/j.chest.2022.04.139 · Cited by 2

Serotonin and Fibrosis

Distler, O., Neidhart, M., & Błyszczuk, P. (2021) · The Receptors · doi:10.1007/978-3-030-55920-5_13 · Cited by 1

Pulmonary Fibrosis

Suki, B., & Bates, J. H. T. (2025) · Springer eBooks · doi:10.1007/978-3-031-95322-4_8 · Cited by 1

Regulation of inflammatory lung injury and repair by transforming growth factors

Chakrabarti, M., Phillips, M., Dhar, R., Herron, A., Kubinak, J. L., Wilson, K. M., Murphy, E. A., Azhar, M., & Evans, C. E. (2025) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00154.2025 · Cited by 1

Mechanical stretch reduces fibroblast activation in heart failure with reduced ejection fraction

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Cancer-associated and non-neoplastic fibrosis: Comparative mechanisms and emerging antifibrotic strategies

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