Circulating Fibrocytes Define a New Leukocyte Subpopulation That Mediates Tissue Repair

Antibodies, a laboratory manual

(1989) · Biomedicine & Pharmacotherapy · doi:10.1016/0753-3322(89)90130-3 · Cited by 12,366

The Pathogenesis of Atherosclerosis — An Update

Ross, R. (1986) · New England Journal of Medicine · doi:10.1056/nejm198602203140806 · Cited by 4,877

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

Sinclair, A. H., Berta, P., Palmer, M. S., Hawkins, J. R., Griffiths, B. L., Smith, M. J., Foster, J. W., Frischauf, A.-M., Lovell-Badge, R., & Goodfellow, P. N. (1990) · Nature · doi:10.1038/346240a0 · Cited by 3,236

Antigenic analysis of hematopoiesis. III. A hematopoietic progenitor cell surface antigen defined by a monoclonal antibody raised against KG-1a cells.

Civin, C. I., Strauss, L. C., Brovall, C., Fackler, M. J., Schwartz, J. F., & Shaper, J. H. (1984) · The Journal of Immunology · doi:10.4049/jimmunol.133.1.157 · Cited by 1,202

Expression of the CD34 gene in vascular endothelial cells

Fina, L., Molgaard, H., Robertson, D., Bradley, N., Monaghan, P., Delia, D., Sutherland, D., Baker, M., & Greaves, M. (1990) · Blood · doi:10.1182/blood.v75.12.2417.2417 · Cited by 886

Comparison of three actin-coding sequences in the mouse; Evolutionary relationships between the actin genes of warm-blooded vertebrates

Alonso, S., Minty, A., Bourlet, Y., & Buckingham, M. (1986) · Journal of Molecular Evolution · doi:10.1007/bf02100994 · Cited by 643

Widespread occurrence of intermediate-sized filaments of the vimentin-type in cultured cells from diverse vertebrates

Franke, W. W., Schmid, E., Winter, S., Osborn, M., & Weber, K. (1979) · Experimental Cell Research · doi:10.1016/0014-4827(79)90418-x · Cited by 633

Current protocols in immunology: edited by J.E. Coligan, A.M. Kruisbeek, D.H. Margulies, E.M. Shevach and W. Strober, Greene Publishing Associates and Wiley‐Interscience; New York, 1991; 900 pages approx. + 200 pages approx. (Supplement 1) $245.00 (USA), $270.00 (elsewhere). ISBN 0‐471‐52276‐7

Wisdom, G. B. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)80333-p · Cited by 579

Antigen CD34+ marrow cells engraft lethally irradiated baboons.

Berenson, R. J., Andrews, R. G., Bensinger, W. I., Kalamasz, D., Knitter, G., Buckner, C. D., & Bernstein, I. D. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113409 · Cited by 574

Wound Healing: Biochemical and Clinical Aspects

Clay, R. P. (1993) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)60711-3 · Cited by 534

Multilineage potential of adult human mesenchymal stem cells

Pittenger, M. F., Mackay, A. M., Beck, S. C., Jaiswal, R. K., Douglas, R., Mosca, J. D., Moorman, M. A., Simonetti, D. W., Craig, S., & Marshak, D. R. (1999) · Science · doi:10.1126/science.284.5411.143 · Cited by 21,052

Marrow Stromal Cells as Stem Cells for Nonhematopoietic Tissues

Prockop, D. J. (1997) · Science · doi:10.1126/science.276.5309.71 · Cited by 4,629

Cellular and molecular mechanisms of fibrosis

Wynn, T. (2008) · The Journal of Pathology · doi:10.1002/path.2277 · Cited by 4,495

TGF-β: the master regulator of fibrosis

Meng, X.-M., Nikolic-Paterson, D. J., & Lan, H. Y. (2016) · Nature Reviews Nephrology · doi:10.1038/nrneph.2016.48 · Cited by 3,528

Molecular and cellular mechanisms of liver fibrosis and its regression

Kisseleva, T., & Brenner, D. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00372-7 · Cited by 2,024

Cardiac Fibrosis: The Fibroblast Awakens

Travers, J. G., Kamal, F. A., Robbins, J., Yutzey, K. E., & Blaxall, B. C. (2016) · Circulation Research · doi:10.1161/circresaha.115.306565 · Cited by 1,596

Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases

Wynn, T. A. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31487 · Cited by 1,456

Suppression of Antitumor Immunity by Stromal Cells Expressing Fibroblast Activation Protein–α

Kraman, M., Bambrough, P. J., Arnold, J. N., Roberts, E. W., Magiera, L., Jones, J. O., Gopinathan, A., Tuveson, D. A., & Fearon, D. T. (2010) · Science · doi:10.1126/science.1195300 · Cited by 1,134

Acute Exacerbations of Idiopathic Pulmonary Fibrosis

Collard, H. R., Moore, B. B., Flaherty, K. R., Brown, K. K., Kaner, R. J., King, T. E., Lasky, J. A., Loyd, J. E., Noth, I., Olman, M. A., et al. (2007) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200703-463pp · Cited by 1,130

Fibroblasts in fibrosis: novel roles and mediators

Kendall, R. T., & Feghali-Bostwick, C. A. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00123 · Cited by 1,082

Circulating fibrocytes traffic to the lungs in response to CXCL12 and mediate fibrosis

Phillips, R. J., Burdick, M. D., Hong, K., Lutz, M. A., Murray, L. A., Xue, Y. Y., Belperio, J. A., Keane, M. P., & Strieter, R. M. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200420997 · Cited by 1,079

Macrophages: versatile players in renal inflammation and fibrosis

Tang, P. M.-K., Nikolic-Paterson, D. J., & Lan, H.-Y. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-019-0110-2 · Cited by 1,033

Cardiac Fibroblast: The Renaissance Cell

Souders, C. A., Bowers, S. L. K., & Baudino, T. A. (2009) · Circulation Research · doi:10.1161/circresaha.109.209809 · Cited by 984

Peripheral Blood Fibrocytes: Differentiation Pathway and Migration to Wound Sites

Abe, R., Donnelly, S. C., Peng, T., Bucala, R., & Metz, C. N. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.12.7556 · Cited by 967

Perspective Article: Tissue repair, contraction, and the myofibroblast

Desmoulière, A., Chaponnier, C., & Gabbiani, G. (2005) · Wound Repair and Regeneration · doi:10.1111/j.1067-1927.2005.130102.x · Cited by 892

The lysophosphatidic acid receptor LPA1 links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leak

Tager, A. M., LaCamera, P., Shea, B. S., Campanella, G. S., Selman, M., Zhao, Z., Polosukhin, V., Wain, J., Karimi-Shah, B. A., Kim, N. D., et al. (2008) · Nature Medicine · doi:10.1038/nm1685 · Cited by 823

Tissue engineering of replacement skin: the crossroads of biomaterials, wound healing, embryonic development, stem cells and regeneration

Metcalfe, A. D., & Ferguson, M. W. J. (2007) · Journal of The Royal Society Interface · doi:10.1098/rsif.2006.0179 · Cited by 785

Mesenchymal Stem Cells as Therapeutics

Parekkadan, B., & Milwid, J. M. (2010) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-070909-105309 · Cited by 759

Failed Tubule Recovery, AKI-CKD Transition, and Kidney Disease Progression

Venkatachalam, M. A., Weinberg, J. M., Kriz, W., & Bidani, A. K. (2015) · Journal of the American Society of Nephrology · doi:10.1681/asn.2015010006 · Cited by 744

Resident fibroblast lineages mediate pressure overload–induced cardiac fibrosis

Moore-Morris, T., Guimarães-Camboa, N., Banerjee, I., Zambon, A. C., Kisseleva, T., Velayoudon, A., Stallcup, W. B., Gu, Y., Dalton, N. D., Cedenilla, M., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci74783 · Cited by 630

Host Responses in Tissue Repair and Fibrosis

Duffield, J. S., Lupher, M., Thannickal, V. J., & Wynn, T. A. (2013) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-020712-163930 · Cited by 624

Fibroblast Differentiation in Wound Healing and Fibrosis

Darby, I. A., & Hewitson, T. D. (2007) · International Review of Cytology · doi:10.1016/s0074-7696(07)57004-x · Cited by 600

Molecular Targets in Pulmonary Fibrosis

Scotton, C. J., & Chambers, R. C. (2007) · Chest · doi:10.1378/chest.06-2568 · Cited by 538

Organ and tissue fibrosis: Molecular signals, cellular mechanisms and translational implications

Weiskirchen, R., Weiskirchen, S., & Tacke, F. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.06.003 · Cited by 538

Inflammation and immunity in IPF pathogenesis and treatment

Heukels, P., Moor, C. C., von der Thüsen, J. H., Wijsenbeek, M. S., & Kool, M. (2019) · Respiratory Medicine · doi:10.1016/j.rmed.2018.12.015 · Cited by 517

Regulation of Transforming Growth Factor-β1–driven Lung Fibrosis by Galectin-3

MacKinnon, A. C., Gibbons, M. A., Farnworth, S. L., Leffler, H., Nilsson, U. J., Delaine, T., Simpson, A. J., Forbes, S. J., Hirani, N., Gauldie, J., et al. (2012) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201106-0965oc · Cited by 516

Mechanisms of Fibrogenesis

Kisseleva, T., & Brenner, D. A. (2008) · Experimental Biology and Medicine · doi:10.3181/0707-mr-190 · Cited by 503

Contribution of Bone Marrow–Derived Cells to Skin: Collagen Deposition and Wound Repair

Fathke, C., Wilson, L., Hutter, J., Kapoor, V., Smith, A., Hocking, A., & Isik, F. (2004) · STEM CELLS · doi:10.1634/stemcells.22-5-812 · Cited by 490

Bone marrow-derived fibrocytes participate in pathogenesis of liver fibrosis

Kisseleva, T., Uchinami, H., Feirt, N., Quintana-Bustamante, O., Segovia, J. C., Schwabe, R. F., & Brenner, D. A. (2006) · Journal of Hepatology · doi:10.1016/j.jhep.2006.04.014 · Cited by 469

Cellular Mechanisms of Tissue Fibrosis. 1. Common and organ-specific mechanisms associated with tissue fibrosis

Zeisberg, M., & Kalluri, R. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00328.2012 · Cited by 462

Transforming Growth Factor-β1 Induces the Differentiation of Myogenic Cells into Fibrotic Cells in Injured Skeletal Muscle

Li, Y., Foster, W., Deasy, B. M., Chan, Y., Prisk, V., Tang, Y., Cummins, J., & Huard, J. (2004) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63188-4 · Cited by 451

CCR2-Mediated Recruitment of Fibrocytes to the Alveolar Space after Fibrotic Injury

Moore, B. B., Kolodsick, J. E., Thannickal, V. J., Cooke, K., Moore, T. A., Hogaboam, C., Wilke, C. A., & Toews, G. B. (2005) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)62289-4 · Cited by 441

Identification of Markers that Distinguish Monocyte-Derived Fibrocytes from Monocytes, Macrophages, and Fibroblasts

Pilling, D., Fan, T., Huang, D., Kaul, B., & Gomer, R. H. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007475 · Cited by 433

Mechanisms of liver fibrosis and its role in liver cancer

Dhar, D., Baglieri, J., Kisseleva, T., & Brenner, D. A. (2020) · Experimental Biology and Medicine · doi:10.1177/1535370219898141 · Cited by 429

Normal Cutaneous Wound Healing: Clinical Correlation with Cellular and Molecular Events

Baum, C. L., & Arpey, C. J. (2005) · Dermatologic Surgery · doi:10.1097/00042728-200506000-00011 · Cited by 404

Regulation of angiogenesis: Wound healing as a model

EMING, S., BRACHVOGEL, B., ODORISIO, T., & KOCH, M. (2007) · Progress in Histochemistry and Cytochemistry · doi:10.1016/j.proghi.2007.06.001 · Cited by 392

Idiopathic Pulmonary Fibrosis (IPF): An Overview

Barratt, S., Creamer, A., Hayton, C., & Chaudhuri, N. (2018) · Journal of Clinical Medicine · doi:10.3390/jcm7080201 · Cited by 382

Cytokine mediated tissue fibrosis

Borthwick, L. A., Wynn, T. A., & Fisher, A. J. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.09.014 · Cited by 375

Epithelial to Mesenchymal Transition and Peritoneal Membrane Failure in Peritoneal Dialysis Patients: Pathologic Significance and Potential Therapeutic Interventions

Aroeira, L. S., Aguilera, A., Sánchez-Tomero, J. A., Bajo, M. A., del Peso, G., Jiménez-Heffernan, J. A., Selgas, R., & López-Cabrera, M. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006111292 · Cited by 358

Potential cellular and molecular causes of hypertrophic scar formation

van der Veer, W. M., Bloemen, M. C. T., Ulrich, M. M. W., Molema, G., van Zuijlen, P. P., Middelkoop, E., & Niessen, F. B. (2009) · Burns · doi:10.1016/j.burns.2008.06.020 · Cited by 353

Origin of myofibroblasts and cellular events triggering fibrosis

Mack, M., & Yanagita, M. (2015) · Kidney International · doi:10.1038/ki.2014.287 · Cited by 342

The Role of Fibrosis and Liver-Associated Fibroblasts in the Pathogenesis of Hepatocellular Carcinoma

Baglieri, J., Brenner, D. A., & Kisseleva, T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20071723 · Cited by 341

The reactive stroma microenvironment and prostate cancer progression

Barron, D. A., & Rowley, D. R. (2012) · Endocrine-Related Cancer · doi:10.1530/erc-12-0085 · Cited by 329

Bone Marrow Ly6Chigh Monocytes Are Selectively Recruited to Injured Kidney and Differentiate into Functionally Distinct Populations

Lin, S. L., Castaño, A. P., Nowlin, B. T., Lupher, M. L., & Duffield, J. S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901473 · Cited by 326

Reactive oxygen species and fibrosis: further evidence of a significant liaison

Richter, K., & Kietzmann, T. (2016) · Cell and Tissue Research · doi:10.1007/s00441-016-2445-3 · Cited by 322

Intradermal adipocytes mediate fibroblast recruitment during skin wound healing

Schmidt, B. A., & Horsley, V. (2013) · Development · doi:10.1242/dev.087593 · Cited by 318

Evidence for tissue-resident mesenchymal stem cells in human adult lung from studies of transplanted allografts

Lama, V. N., Smith, L., Badri, L., Flint, A., Andrei, A.-C., Murray, S., Wang, Z., Liao, H., Toews, G. B., Krebsbach, P. H., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29713 · Cited by 318

Stem Cells and Cell Therapies in Lung Biology and Lung Diseases

Weiss, D. J., Kolls, J. K., Ortiz, L. A., Panoskaltsis-Mortari, A., & Prockop, D. J. (2008) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200804-037dw · Cited by 309

Platelet‐rich plasma enhances the initial mobilization of circulation‐derived cells for tendon healing

Kajikawa, Y., Morihara, T., Sakamoto, H., Matsuda, K., Oshima, Y., Yoshida, A., Nagae, M., Arai, Y., Kawata, M., & Kubo, T. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21368 · Cited by 300

A stromal address code defined by fibroblasts

Parsonage, G., Filer, A. D., Haworth, O., Nash, G. B., Rainger, G. E., Salmon, M., & Buckley, C. D. (2005) · Trends in Immunology · doi:10.1016/j.it.2004.11.014 · Cited by 297

Bone marrow‐derived stem cells in wound healing: a review

Wu, Y., Wang, J., Scott, P. G., & Tredget, E. E. (2007) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2007.00221.x · Cited by 288

The Mechanistic Basis of Infarct Healing

Frangogiannis, N. G. (2006) · Antioxidants & Redox Signaling · doi:10.1089/ars.2006.8.1907 · Cited by 288

New Mechanisms of Pulmonary Fibrosis

Strieter, R. M., & Mehrad, B. (2009) · Chest · doi:10.1378/chest.09-0510 · Cited by 284

Type-1 pericytes accumulate after tissue injury and produce collagen in an organ-dependent manner

Birbrair, A., Zhang, T., Files, D. C., Mannava, S., Smith, T., Wang, Z.-M., Messi, M. L., Mintz, A., & Delbono, O. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt512 · Cited by 282

Bone-marrow-derived myofibroblasts contribute to the cancer-induced stromal reaction

Ishii, G., Sangai, T., Oda, T., Aoyagi, Y., Hasebe, T., Kanomata, N., Endoh, Y., Okumura, C., Okuhara, Y., Magae, J., et al. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)01544-4 · Cited by 281

Exploring the role of stem cells in cutaneous wound healing

Lau, K., Paus, R., Tiede, S., Day, P., & Bayat, A. (2009) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.00942.x · Cited by 279

Pulmonary Fibrosis as a Result of Acute Lung Inflammation: Molecular Mechanisms, Relevant In Vivo Models, Prognostic and Therapeutic Approaches

Savin, I. A., Zenkova, M. A., & Sen’kova, A. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232314959 · Cited by 279

Macrophages promote renal fibrosis through direct and indirect mechanisms

Nikolic-Paterson, D. J., Wang, S., & Lan, H. Y. (2014) · Kidney International Supplements · doi:10.1038/kisup.2014.7 · Cited by 279

Secondary lymphoid tissue chemokine (SLC/CCL21)/CCR7 signaling regulates fibrocytes in renal fibrosis

Sakai, N., Wada, T., Yokoyama, H., Lipp, M., Ueha, S., Matsushima, K., & Kaneko, S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511200103 · Cited by 278

Isolation and Characterization of Size‐Sieved Stem Cells from Human Bone Marrow

Hung, S., Chen, N., Hsieh, S., Li, H., Ma, H., & Lo, W. (2002) · STEM CELLS · doi:10.1634/stemcells.20-3-249 · Cited by 276

The role of CXC chemokines in pulmonary fibrosis

Strieter, R. M., Gomperts, B. N., & Keane, M. P. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30562 · Cited by 273

Pivotal Advance: Th-1 cytokines inhibit, and Th-2 cytokines promote fibrocyte differentiation

Shao, D. D., Suresh, R., Vakil, V., Gomer, R. H., & Pilling, D. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.1107782 · Cited by 272

The pathogenesis of idiopathic pulmonary fibrosis

Coward, W. R., Saini, G., & Jenkins, G. (2010) · Therapeutic Advances in Respiratory Disease · doi:10.1177/1753465810379801 · Cited by 272

Liver fibrosis: cellular mechanisms of progression and resolution

Henderson, N. C., & Iredale, J. P. (2007) · Clinical Science · doi:10.1042/cs20060242 · Cited by 270

Connective tissue growth factor: a fibrogenic master switch in fibrotic liver diseases

Gressner, O. A., & Gressner, A. M. (2008) · Liver International · doi:10.1111/j.1478-3231.2008.01826.x · Cited by 270

Comparative analysis of lesion development and intraspinal inflammation in four strains of mice following spinal contusion injury

Kigerl, K. A., McGaughy, V. M., & Popovich, P. G. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20827 · Cited by 270

Chemokines and chemokine receptors are involved in the resolution or progression of renal disease

Anders, H.-J., Vielhauer, V., & Schlöndorff, D. (2003) · Kidney International · doi:10.1046/j.1523-1755.2003.00750.x · Cited by 270

Tumor-associated fibroblasts predominantly come from local and not circulating precursors

Arina, A., Idel, C., Hyjek, E. M., Alegre, M.-L., Wang, Y., Bindokas, V. P., Weichselbaum, R. R., & Schreiber, H. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1600363113 · Cited by 238

Reduction of Bleomycin-Induced Pulmonary Fibrosis by Serum Amyloid P

Pilling, D., Roife, D., Wang, M., Ronkainen, S. D., Crawford, J. R., Travis, E. L., & Gomer, R. H. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.6.4035 · Cited by 230

Living Beyond Our Physiological Means: Small Vessel Disease of the Brain Is an Expression of a Systemic Failure in Arteriolar Function: A Unifying Hypothesis

Thompson, C. S., & Hakim, A. M. (2009) · Stroke · doi:10.1161/strokeaha.108.542266 · Cited by 208

Cell-matrix interactions in dermal repair and scarring

Eckes, B., Nischt, R., & Krieg, T. (2010) · Fibrogenesis & Tissue Repair · doi:10.1186/1755-1536-3-4 · Cited by 205

Scleroderma pathogenesis: a pivotal role for fibroblasts as effector cells

Gilbane, A. J., Denton, C. P., & Holmes, A. M. (2013) · Arthritis Research & Therapy · doi:10.1186/ar4230 · Cited by 196

Human skin stem cells and the ageing process

Zouboulis, C. C., Adjaye, J., Akamatsu, H., Moe-Behrens, G., & Niemann, C. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.09.001 · Cited by 176

Biomarkers in idiopathic pulmonary fibrosis

Drakopanagiotakis, F., Wujak, L., Wygrecka, M., & Markart, P. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.01.023 · Cited by 132

Cellular and extracellular matrix modulation of corneal stromal opacity

Torricelli, A. A. M., & Wilson, S. E. (2014) · Experimental Eye Research · doi:10.1016/j.exer.2014.09.013 · Cited by 124

Altered monocyte and fibrocyte phenotype and function in scleroderma interstitial lung disease: reversal by caveolin-1 scaffolding domain peptide

Tourkina, E., Bonner, M., Oates, J., Hofbauer, A., Richard, M., Znoyko, S., Visconti, R. P., Zhang, J., Hatfield, C. M., Silver, R. M., et al. (2011) · Fibrogenesis & Tissue Repair · doi:10.1186/1755-1536-4-15 · Cited by 104

The Development of Serum Amyloid P as a Possible Therapeutic

Pilling, D., & Gomer, R. H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02328 · Cited by 92

Sca‐1 + cardiac fibroblasts promote development of heart failure

Chen, G., Bracamonte‐Baran, W., Diny, N. L., Hou, X., Talor, M. V., Fu, K., Liu, Y., Davogustto, G., Vasquez, H., Taegtmeyer, H., et al. (2018) · European Journal of Immunology · doi:10.1002/eji.201847583 · Cited by 53

Targeting the stromal microenvironment in chronic inflammation

FILER, A., PITZALIS, C., & BUCKLEY, C. (2006) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2006.03.007 · Cited by 45

Fibrocytes in health and disease

Blakaj, A., & Bucala, R. (2012) · Fibrogenesis & Tissue Repair · doi:10.1186/1755-1536-5-s1-s6 · Cited by 44

Gene expression study of monocytes/macrophages during early foreign body reaction and identification of potential precursors of myofibroblasts

Mesure, L., De Visscher, G., Vranken, I., Lebacq, A., & Flameng, W. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012949 · Cited by 40

Levels of circulating endothelial cells are low in idiopathic pulmonary fibrosis and are further reduced by anti-fibrotic treatments

De Biasi, S., Cerri, S., Bianchini, E., Gibellini, L., Persiani, E., Montanari, G., Luppi, F., Carbonelli, C. M., Zucchi, L., Bocchino, M., et al. (2015) · BMC Medicine · doi:10.1186/s12916-015-0515-0 · Cited by 28

Candidate rejuvenating factor GDF11 and tissue fibrosis: friend or foe?

Frohlich, J., & Vinciguerra, M. (2020) · GeroScience · doi:10.1007/s11357-020-00279-w · Cited by 28

The Role of Fibrocytes in Sickle Cell Lung Disease

Field, J. J., Burdick, M. D., DeBaun, M. R., Strieter, B. A., Liu, L., Mehrad, B., Rose, C. E., Linden, J., & Strieter, R. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033702 · Cited by 23

GLI1 activates pro-fibrotic pathways in myelofibrosis fibrocytes

Manshouri, T., Veletic, I., Li, P., Yin, C. C., Post, S. M., Verstovsek, S., & Estrov, Z. (2022) · Cell Death & Disease · doi:10.1038/s41419-022-04932-4 · Cited by 19

Circulating fibrocytes as biomarkers of impaired lung function in adults with sickle cell disease

Mehrad, B., Burdick, M. D., Wandersee, N. J., Shahir, K. S., Zhang, L., Simpson, P. M., Strieter, R. M., & Field, J. J. (2017) · Blood Advances · doi:10.1182/bloodadvances.2017010777 · Cited by 11

Monocytes/macrophages as one of the sources of myofibroblasts in the development of tissue fibrosis: the role of noncoding RNAs

Balan, O. V., Malysheva, I. E., & Fedorenko, O. M. (2025) · Russian Journal of Genetics · doi:10.1134/s1022795424701643 · Cited by 1