Conditional macrophage ablation in transgenic mice expressing a Fas-based suicide gene

Death Receptors: Signaling and Modulation

Ashkenazi, A., & Dixit, V. M. (1998) · Science · doi:10.1126/science.281.5381.1305 · Cited by 5,866

Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages

Scott, E. W., Simon, M. C., Anastasi, J., & Singh, H. (1994) · Science · doi:10.1126/science.8079170 · Cited by 1,532

Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects

Dai, X.-M., Ryan, G. R., Hapel, A. J., Dominguez, M. G., Russell, R. G., Kapp, S., Sylvestre, V., & Stanley, E. R. (2002) · Blood · doi:10.1182/blood.v99.1.111 · Cited by 1,184

Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities

McKercher, S. R., Torbett, B. E., Anderson, K. L., Henkel, G. W., Vestal, D. J., Baribault, H., Klemsz, M., Feeney, A. J., Wu, G. E., Paige, C. J., et al. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00949.x · Cited by 1,130

IL-6 switches the differentiation of monocytes from dendritic cells to macrophages

Chomarat, P., Banchereau, J., Davoust, J. M., & Palucka, K. (2000) · Nature Immunology · doi:10.1038/82763 · Cited by 906

Peritoneal Adhesions: Etiology, Pathophysiology, and Clinical Significance

Liakakos, T., Thomakos, N., Fine, P. M., Dervenis, C., & Young, R. L. (2001) · Digestive Surgery · doi:10.1159/000050149 · Cited by 687

A macrophage colony-stimulating factor receptor–green fluorescent protein transgene is expressed throughout the mononuclear phagocyte system of the mouse

Sasmono, R. T., Oceandy, D., Pollard, J. W., Tong, W., Pavli, P., Wainwright, B. J., Ostrowski, M. C., Himes, S. R., & Hume, D. A. (2003) · Blood · doi:10.1182/blood-2002-02-0569 · Cited by 662

Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse

Cecchini, M. G., Dominguez, M. G., Mocci, S., Wetterwald, A., Felix, R., Fleisch, H. A., Chisholm, O., Hofstetter, W., Pollard, J. W., & Stanley, E. R. (1994) · Development · doi:10.1242/dev.120.6.1357 · Cited by 557

Developmental kinetics and lifespan of dendritic cells in mouse lymphoid organs

Kamath, A. T., Henri, S., Battye, F. L., Tough, D. F., & Shortman, K. (2002) · Blood · doi:10.1182/blood.v100.5.1734.h81702001734_1734_1741 · Cited by 454

Mesothelial cells: Their structure, function and role in serosal repair

Mutsaers, S. E. (2002) · Respirology · doi:10.1046/j.1440-1843.2002.00404.x · Cited by 436

Genetic Cell Ablation

Grégoire, D., & Kmita, M. (2013) · Methods in molecular biology · doi:10.1007/978-1-60327-292-6_25 · Cited by 16

Targeting Lymphoma-associated Macrophage Expansion via CSF1R/JAK Inhibition is a Therapeutic Vulnerability in Peripheral T-cell Lymphomas

Gao, X., Kady, N., Wang, C., Abdelrahman, S., Gann, P. H., Sverdlov, M. S., Wolfe, A., Brown, N. A., Reneau, J. C., Robida, A. M., et al. (2022) · Cancer Research Communications · doi:10.1158/2767-9764.crc-22-0336 · Cited by 14

Minimally invasive longitudinal intravital imaging of cellular dynamics in intact long bone

Bhattacharyya, N. D., Kyaw, W., McDonald, M. M., Dhenni, R., Grootveld, A. K., Xiao, Y., Chai, R. C. C., Khoo, W. H., Dansereau, L. C., Sergio, C. M., et al. (2023) · Nature Protocols · doi:10.1038/s41596-023-00894-9 · Cited by 13

Effect of LysM+ macrophage depletion on lung pathology in mice with chronic bronchitis

Saini, Y., Lewis, B. W., Yu, D., Dang, H., Livraghi-Butrico, A., Piero, F. D., O’Neal, W. K., & Boucher, R. C. (2018) · Physiological Reports · doi:10.14814/phy2.13677 · Cited by 14

CD45 expression discriminates waves of embryonic megakaryocytes in the mouse

Cortegano, I., Serrano, N., Ruíz, C., Rodríguez, M., Prado, C., Alía, M., Hidalgo, A., Cano, E., de Andrés, B., & Gaspar, M.-L. (2018) · Haematologica · doi:10.3324/haematol.2018.192559 · Cited by 14

A survey of neurological decompression illness in commercial breath-hold divers (Ama) of Japan.

Tamaki, H., Kohshi, K., Ishitake, T., & Wong, R. M. S. (2010) · PubMed · Cited by 14

Peripheral macrophages contribute to nociceptor priming in mice with chronic intermittent hypoxia

Chivers, S. B., Andrade, M. A., Hammack, R. J., Shannonhouse, J. L., Gómez, R. S., Zhang, Y., Nguyen, B. T., Shah, P., Kim, Y. S., Toney, G. M., et al. (2024) · Science Signaling · doi:10.1126/scisignal.adn8936 · Cited by 13

Acute systemic macrophage depletion in osteoarthritic mice alleviates pain-related behaviors and does not affect joint damage

Geraghty, T., Ishihara, S., Obeidat, A. M., Adamczyk, N. S., Hunter, R. S., Li, J., Wang, L., Lee, H., Ko, F. C., Malfait, A., et al. (2024) · Arthritis Research & Therapy · doi:10.1186/s13075-024-03457-9 · Cited by 13

Loss of p27 phosphorylation at Ser10 accelerates early atherogenesis by promoting leukocyte recruitment via RhoA/ROCK

Molina-Sánchez, P., Chèvre, R., Rius, C., Fuster, J. J., & Andrés, V. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.04.013 · Cited by 13

Visualization of Immune Responses in the Cornea

Perez, V. L. (2017) · Cornea · doi:10.1097/ico.0000000000001354 · Cited by 13

Electrostatic Accumulation and Release of DNA Using a Micromachined Lance

Aten, Q. T., Jensen, B. D., Burnett, S. H., & Howell, L. L. (2011) · Journal of Microelectromechanical Systems · doi:10.1109/jmems.2011.2167658 · Cited by 12

Investigating the role of macrophages in tumor formation using a MaFIA mouse model

Clifford, A., El‐Naggar, A. M., Robison, R. A., & O'Neill, K. L. (2013) · Oncology Reports · doi:10.3892/or.2013.2508 · Cited by 12

Aspartic protease and caspase 3/7 activation are central for macrophage apoptosis following infection withEscherichia coli

Albee, L. D., Shi, B., & Perlman, H. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0506358 · Cited by 12

Analysis of Thymocyte Migration, Cellular Interactions, and Activation by Multiphoton Fluorescence Microscopy of Live Thymic Slices

Lancaster, J. N., & Ehrlich, L. I. R. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6931-9_2 · Cited by 12

Macrophages Switch to an Osteo‐Modulatory Profile Upon RANKL Induction in a Medaka ( Oryzias latipes ) Osteoporosis Model

Phan, Q. T., Liu, R., Tan, W. H., Imangali, N., Cheong, B., Schartl, M., & Winkler, C. (2020) · JBMR Plus · doi:10.1002/jbm4.10409 · Cited by 11

Transient depletion of macrophages alters local inflammatory response at the site of disc herniation in a transgenic mouse model

Xiao, L., Matharoo, J., Chi, J. A., Ma, J., Chen, M., Manley, B. J., Xu, P., Shi, W., Felder, R. A., Sung, S.-S. J., et al. (2023) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2023.01.574 · Cited by 11

Disruption of hyaluronic acid in skeletal muscle induces decreased voluntary activity via chemosensitive muscle afferent sensitization in male mice

Queme, L. F., Dourson, A. J., Hofmann, M. C., Butterfield, A., Paladini, R. D., & Jankowski, M. P. (2022) · eNeuro · doi:10.1523/eneuro.0522-21.2022 · Cited by 11

Modeling Dendritic Cell Vaccination for Influenza Prophylaxis: Potential Applications for Niche Populations

Konduri, V., Decker, W. K., Halpert, M. M., Gilbert, B. E., & Safdar, A. (2013) · The Journal of Infectious Diseases · doi:10.1093/infdis/jit087 · Cited by 11

OsteoMac: A new player on the bone biology scene

Iglesias‐Velázquez, Ó., Tresguerres, F. G. F., Tresguerres, I. F., Berrocal, M. I. L., López‐Pintor, R. M., Baca, L., & Torres, J. (2024) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2024.152244 · Cited by 13

Cancer fitness genes: emerging therapeutic targets for metastasis

Shen, M., & Kang, Y. (2022) · Trends in cancer · doi:10.1016/j.trecan.2022.08.007 · Cited by 10

IL-1R Type 1–Deficient Mice Demonstrate an Impaired Host Immune Response against Cutaneous Vaccinia Virus Infection

Tian, T., Jin, M. Q., Dubin, K. A., King, S. L., Hoetzenecker, W., Murphy, G. F., Chen, C. A., Kupper, T. S., & Fuhlbrigge, R. C. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1500106 · Cited by 10

Controlling Protein–Protein Interactions Using Chemical Inducers and Disrupters of Dimerization

Clackson, T. (2007) · Chemical biology · doi:10.1002/9783527619375.ch4b · Cited by 10

Towards in vivo amplification: Overcoming hurdles in the use of hematopoietic stem cells in transplantation and gene therapy.

Nagree, M. S., López-Vásquez, L., & Medin, J. A. (2015) · PubMed · doi:10.4252/wjsc.v7.i11.1233 · Cited by 11

Characterising Pre-pubertal Resistance to Death from Endotoxemia

Joachim, R. B., Suber, F., & Kobzik, L. (2017) · Scientific Reports · doi:10.1038/s41598-017-16743-1 · Cited by 9

Generation of a novel mouse model for the inducible depletion of macrophages in vivo

Gheryani, N. A., Coffelt, S. B., Gartland, A., Rumney, R. M. H., Kiss‐Toth, E., Lewis, C. E., Tozer, G. M., Greaves, D. R., Dear, T. N., & Miller, G. (2012) · genesis · doi:10.1002/dvg.22343 · Cited by 9

Depletion of Microglia from Primary Cellular Cultures

Pont‐Lezica, L., Colasse, S., & Bessis, A. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-520-0_7 · Cited by 9

Apoptosis and Clearance of the Secretory Mammary Epithelium

Jamie, C. B., & Rebecca, S. (2013) · InTech eBooks · doi:10.5772/52160 · Cited by 8

Characterisation of periorbital mechanical allodynia in the reserpine-induced fibromyalgia model in mice: The role of the Schwann cell TRPA1/NOX1 signalling pathway

Brum, E. S., Landini, L., Souza Monteiro de Araújo, D., Marini, M., Geppetti, P., Nassini, R., De Logu, F., & Oliveira, S. M. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.01.040 · Cited by 8

Macrophage repolarization by immune checkpoint blockade drives T cell engagement in the tumor microenvironment

Kwok, T., Silva, I., Korpe, S., Dong, H., & Lancaster, J. N. (2025) · iScience · doi:10.1016/j.isci.2025.113538 · Cited by 10

In vivo depletion and genetic targeting of mouse intestinal CX3CR1+ mononuclear phagocytes

Koscsó, B., Gowda, K., & Bogunovic, M. (2015) · Journal of Immunological Methods · doi:10.1016/j.jim.2015.12.009 · Cited by 8

Targeted clearance of senescent cells alleviates alcohol-associated liver disease by restoring cellular function and immune balance

Tian, T., Xue, Y., Song, Z., Jin-Smith, B., Barkin, J., Ottallah, M., Mannan, M., Zhirkova, A. M., Zhou, D., & Pi, L. (2025) · GeroScience · doi:10.1007/s11357-025-01952-8 · Cited by 7

Invasion-Block and S-MARVEL: A high-content screening and image analysis platform identifies ATM kinase as a modulator of melanoma invasion and metastasis

Guo, D., Jurek, R. J., Beaumont, K. A., Sharp, D. M., Tan, S., Mariana, A., Failes, T. W., Grootveld, A. K., Bhattacharyya, N. D., Phan, T. G., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2303978120 · Cited by 7

Pleiotropic role for monocyte C-fms protein in response to vascular injury: Potential therapeutic target

Metharom, P., Martin, K., Kumar, A. H. S., Sawhney, N., Cronin, M. F., McCarthy, D. G., Maguire, A. R., & Caplice, N. M. (2011) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2011.01.037 · Cited by 7

Rapid Isolation of Dorsal Root Ganglion Macrophages

Yu, X., Leff, J., & Guan, Z. (2019) · Journal of Visualized Experiments · doi:10.3791/60023 · Cited by 8

Macrophage Epigenetic Memories of Early Life Injury Drive Neonatal Nociceptive PrimingPreprint

Dourson, A. J., Fadaka, A. O., Warshak, A. M., Paranjpe, A., Weinhaus, B., Queme, L. F., Hofmann, M. C., Evans, H. M., Donmez, O. A., Forney, C. R., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.13.528015 · Cited by 7

Conditional Loss of MEF2C Expression in Osteoclasts Leads to a Sex-Specific Osteopenic Phenotype

Maisuria, R., Norton, A., Shao, C., Bradley, E. W., & Mansky, K. C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612686 · Cited by 6

Intravital multiphoton microscopy as a novel tool in the field of immunopharmacology

Morimoto, A., Kikuta, J., & Ishii, M. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.107429 · Cited by 6

AP20187-Mediated Activation of A Chimeric Insulin Receptor Results in Insulin-Like Actions in Skeletal Muscle And Liver of Diabetic Mice

Cotugno, G., Formisano, P., Giacco, F., Colella, P., Bèguinot, F., & Auricchio, A. (2007) · Human Gene Therapy · doi:10.1089/hum.2006.116 · Cited by 6

A Monocytic Barrier to the Humanization of Immunodeficient Mice

Du, E. J., & Muench, M. O. (2023) · Current Stem Cell Research & Therapy · doi:10.2174/011574888x263597231001164351 · Cited by 5

Macrophages Modulate Optic Nerve Crush Injury Scar Formation and Retinal Ganglion Cell Function

Liu, Y., Liu, X., Dorizas, C. A., Hao, Z., & Lee, R. K. (2024) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.65.10.22 · Cited by 5

Skeletal muscle macrophage ablation in mice

Krall, J., Gibbs, K. W., Belfield, L. T., Liu, C., Purcell, L. D., Bivona, J. J., Poynter, M. E., Stapleton, R. D., Toth, M. J., & Files, D. C. (2022) · Journal of Immunological Methods · doi:10.1016/j.jim.2022.113329 · Cited by 5

Macrophages of multiple hematopoietic origins reside in the developing prostate

Feng, S., North, T. M., Wivell, P., Pletcher, A., Popratiloff, A. S., & Shibata, M. (2024) · Development · doi:10.1242/dev.203070 · Cited by 5

Intravital imaging of immune cells and their interactions with other cell types in the spinal cord: Experiments with multicolored moving cells

Evans, T. A., Barkauskas, D. S., & Silver, J. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.112972 · Cited by 5

Modulation of tumor inflammatory signaling and drug sensitivity by CMTM4

Xu, Y., Kang, K., Coakley, B. A., Eisenstein, S. G., Parveen, A., Mai, S., Wang, Y. S., Zheng, J., Boral, D., Mai, J., et al. (2025) · The EMBO Journal · doi:10.1038/s44318-024-00330-y · Cited by 6

Pro-inflammatory macrophages suppress HIV replication in humanized mice and ex vivo co-cultures

Baroncini, L., Muller, C. K. S., Kadzioch, N. P., Wolfensberger, R., Russenberger, D., Bredl, S., Mlambo, T., & Speck, R. F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1439328 · Cited by 4

Membrane tethering of CreER decreases uninduced cell labeling and cytotoxicity while maintaining recombination efficiency

Chen, M., Tian, X., Xu, L., Wu, R., He, H., Zhu, H., Xu, W., & Wei, C. (2022) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2022.01.022 · Cited by 2

Cirsium setidens Nakai extract and pectolinarin as active compounds promote innate immunity in RAW 264.7 cells and splenocytes

Kim, S. J., Kim, S., Fauziah, A. N., Park, J. M., Ryu, J. A., Yoon, S. R., Han, C., & Jung, S. K. (2025) · Applied Food Research · doi:10.1016/j.afres.2025.101243 · Cited by 3

Acinetobacter quorum sensing contributes to inflammation-induced inhibition of orthopaedic implant osseointegration

Choe, H., Hausman, B. S., Hujer, K., Akkuş, O., Rather, P. N., Lee, Z., Bonomo, R., & Greenfield, E. M. (2022) · European Cells and Materials · doi:10.22203/ecm.v043a18 · Cited by 3

Colony stimulating factor 1 receptor ( Csf1r ) expressing cell ablation in mafia (macrophage‐specific Fas‐induced apoptosis) mice alters monocyte landscape and atherosclerotic lesion characteristics

Medina, I., Wieland, E. B., Temmerman, L., Otten, J. J. T., Bermúdez, B., Bot, I., Rademakers, T., Wijnands, E., Schurgers, L. J., Mees, B., et al. (2024) · European Journal of Immunology · doi:10.1002/eji.202350943 · Cited by 3

Use of Intravital Microscopy and In Vitro Chemotaxis Assays to Study the Roles of Sphingosine-1-Phosphate in Bone Homeostasis

Ishii, T., Kawamura, S., Nishiyama, I., Kikuta, J., & Ishii, M. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-800-9_10 · Cited by 3

Microglial reactivity in brainstem chemosensory nuclei in response to hypercapnia

Eugenín, J. L., Beltrán-Castillo, S., Irribarra, E., Pulgar‐Sepúlveda, R., Abarca, N., & Rommy von Bernhardi, M. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1332355 · Cited by 3

Neuromuscular Polytrauma Pain is Resolved by Macrophage COX-2 Nanoimmunomodulation

Cortez, I., Gaffney, C. M., Vichare, R., Crelli, C. V., Liu, L., Lee, E. F., Edralin, J. D., Nichols, J. M., Pham, H. V., Mehdi, S., et al. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s460418 · Cited by 3

Larger is stealthier

Bank, R. A. (2015) · Nature Materials · doi:10.1038/nmat4304 · Cited by 2

The role of dendritic cells in the cornea in the adaptive immune response following Herpes Simplex Virus-1 ocular infection

Buela, K.-A. G. (2015) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 2

Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption

McDonald, M. M., Khoo, W. H., Ng, P. Y., Xiao, Y., Zamerli, J., Thatcher, P., Kyaw, W., Pathmanandavel, K., Grootveld, A. K., Moran, I., et al. (2021) · Yearbook of pediatric endocrinology · doi:10.1530/ey.18.5.12 · Cited by 2

Attenuation of Immune Suppression to Complement Glioma Immunotherapy

Field, C. S. (2016) · doi:10.26686/wgtn.17013761.v1 · Cited by 2

Mechanical Stabilization of Mouse Carotid Artery for In Vivo Intravital Microscopy Imaging of Atherogenesis

Chèvre, R. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2929-0_25 · Cited by 1

Monocyte-Derived Macrophages Expressing Dopamine D2-Subtype Receptors Drive Alcohol Effects on Mesolimbic Neurons and Microglia

Nelson, C. A., Obray, J. D., Clarke, T. J., Brundage, J., Folsom, R. J., Moreno, C. M., Williams, P. E., Ford, L. H., Hope, S. I., Weber, K. S., et al. (2025) · Biomedicines · doi:10.3390/biomedicines13102327 · Cited by 1

Development of an immunodeficient mouse that allows for conditional ablation of monocytic cells

Hui, A. J., Lai, K., Doyle, E. H., Rivera-Torruco, G., Gutierrez, A. G., Du, E. J., Meijer, Y. B. M., Smith, G., Gilfanova, R., Chung, K. G., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1699385 · Cited by 1

YopM and Plague

Straley, S. C. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-3561-7_31 · Cited by 1

Macrophages and pathophysiology of bone cancers

Sousa, S., & Määttä, J. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-416721-6.00009-1 · Cited by 1

Effects of immune cells on mesenchymal stem cells during fracture healing

Ehnert, S., Relja, B., Schmidt‐Bleek, K., Fischer, V., Ignatius, A. A., Linnemann, C., Rinderknecht, H., Huber-Lang, M. S., Kalbitz, M., Histing, T., et al. (2021) · World Journal of Stem Cells · doi:10.4252/wjsc.v13.i11.1670 · Cited by 1

Intravital Confocal Microscopy of Dermal Innate Immune Responses to Flea-Transmitted Yersinia pestis

Shannon, J. G., & Hinnebusch, B. J. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9541-7_5 · Cited by 1

Editorial: Systemic autoimmunity caused by Fas deficiency in macrophages: A new perspective on the first identified autoimmunity gene

Mountz, J. D., Li, J., & Hsu, H. (2011) · Arthritis & Rheumatism · doi:10.1002/art.34321 · Cited by 1

Tissue-Resident CD169+ macrophages as a frontline of host defense in Plasmodium infection

Gupta, P. (2017) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/70327

Kupffer cells

Kiyani, A., & Seki, E. (2015) · Wiley eBooks · doi:10.1002/9781118663387.ch4 · Cited by 1

Caspase-1 activates gasdermin A in non-mammals

Billman, Z. P., Kovacs, S. B., Wei, B., Kang, K., Cissé, O. H., & Miao, E. A. (2023) · doi:10.1101/2023.09.28.559989 · Cited by 1

Caspase-1 activates gasdermin A in all non-mammalsPreprint

Billman, Z. P., Kovacs, S. B., Wei, B., Kang, K., Cissé, O. H., & Miao, E. A. (2023) · eLife · doi:10.7554/elife.92362.1 · Cited by 1

Caspase-1 activates gasdermin A in non-mammals

Billman, Z. P., Kovacs, S. B., Wei, B., Kang, K., Cissé, O. H., & Miao, E. A. (2024) · doi:10.7554/elife.92362.3 · Cited by 1

Yersinia pestis VIRULENCE FACTOR YopM UNDERMINES THE FUNCTION OF DISTINCT CCR2 + Gr1 + CELLS IN SPLEEN AND LIVER DURING SYSTEMIC PLAGUE

Ye, Z. (2010) · UKnowledge (University of Kentucky)

THE EFFECT OF POLYCHLORINATED BIPHENYLS ON LIVER TUMOR PROMOTION: A ROLE FOR KUPFFER CELLS?

Bunaciu, R. P. (2005) · UKnowledge (University of Kentucky)

The Hematopoietic Compartment Regulates Osteoblast Differentiation And Apoptosis During Cytokine Treatment

Christopher, M. J. (2010) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k76m34tv

Heterogeneity and Pliability of Tumor-educated Macrophages

Roberts, R. D. (2008) · The Knowledge Bank (The Ohio State University)

EUROPEAN SCHOOL OF MOLECULAR MEDICINE

Napoli, S. D. (2010)

The individual and unique roles for eosinophils and interleukin-5 in the innate immune response to sepsis

Linch, S. N. (2014) · doi:10.6083/m4c24tf6

The Paradoxical Roles of Cell Death Pathways in Immune Cells

McComb, S. (2013) · uO Research (University of Ottawa) · doi:10.20381/ruor-3097

Attenuation of Immune Suppression to Complement Glioma Immunotherapy

Field, C. S. (2016) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17013761 · Cited by 1

Regulation of T Cell Death in Alloimmune-Mediated Vascular Rejection

von Rossum, A. (2015) · Summit (Simon Fraser University)

Regulation of a multipotent spinal cord progenitor population

Briona, L. K. (2014) · doi:10.33525/0t-5j4p-6cpv

The role of alveolar macrophages in Influenza A infection

Purnama, C. (2013) · doi:10.32657/10356/53722

Establishing a new rodent model of partial bladder outlet obstruction and the role of macrophages in bladder obstruction

Sidler, M. (2017) · TSpace (University of Toronto)

Modulation of adaptive and innate immune responses by myeloid cells during malaria

Lai, S. M. (2019) · doi:10.32657/10220/48099

Macrophage ablation significantly reduces uptake of imaging probe into organs of the reticuloendothelial system

Sabel, B. O., Brand, K., Rueckel, J., Hoppe, B. F., Fink, N., & Bartling, S. H. (2020) · Acta Radiologica · doi:10.1177/0284185120943048

Atrophie, croissance et fonction musculaire : l'impact des leucocytes et de la triade RANK/RANKL/OPG

Dumont, N. A. (2013) · Corpus Université Laval (Université Laval)

Faculty Opinions recommendation of KIT oncogene inhibition drives intratumoral macrophage M2 polarization.

Mantovani, A. (2014) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718203579.793489606

Faculty Opinions recommendation of Sphingosine-1-phosphate mobilizes osteoclast precursors and regulates bone homeostasis.

Zaidi, M., & Iqbal, J. Z. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1148895.605983

Faculty Opinions recommendation of Erythro-myeloid progenitors contribute endothelial cells to blood vessels.

Hirschi, K. K. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734075201.793562733

Defining novel physiological roles for cardiac-residen Macrophages

Ávila, J. Á. N. (2020) · doi:10.4321/repisalud.10674

Faculty Opinions recommendation of Dorsal root ganglion macrophages contribute to both the initiation and persistence of neuropathic pain.

Vetter, I. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737216984.793578085

Inducible and Repressible Systems for Transgene Expression

Schetelig, M. F., Lees, R. S., D'Amato, R., & Benedict, M. Q. (2022) · CABI eBooks · doi:10.1079/9781800621176.0002

1130 Investigating macrophage modulation in a murine model of soft tissue sarcoma

Hildebrand, K., Hildebrand, K. M., Zemp, F. J., Arcila, C. S., & Monument, M. J. (2022) · Regular and Young Investigator Award Abstracts · doi:10.1136/jitc-2022-sitc2022.1130

Immunomodulation under the lens of real‐time in vivo imaging

Bousso, P., & Grandjean, C. L. (2023) · European Journal of Immunology · doi:10.1002/eji.202249921

Caspase-1 activates gasdermin A in non-mammalsPreprint

Billman, Z. P., Kovacs, S. B., Wei, B., Kang, K., Cissé, O. H., & Miao, E. A. (2024) · eLife · doi:10.7554/elife.92362.2

Reviewer #2 (Public Review): Caspase-1 activates gasdermin A in non-mammals

Billman, Z. P., Kovacs, S. B., Wei, B., et al. (2024) · eLife · doi:10.7554/elife.92362.3.sa0

Author Response: Caspase-1 activates gasdermin A in non-mammals

Billman, Z. P., Kovacs, S. B., Wei, B., Kang, K., Cissé, O. H., & Miao, E. A. (2024) · eLife · doi:10.7554/elife.92362.3.sa3

Heterogeneity and ontogeny of mouse thymic macrophages reveal a requirement for Csf1r-expressing myeloid cells during early T cell development

Wang, H. H., Rajan, V., Wong, A., Epelman, S., & Zúñiga‐Pflücker, J. C. (2026) · eLife · doi:10.7554/elife.109219

Two axolotl-adapted cell-ablation platforms reveal macrophage-dependent processes essential for spinal-cord and skeletal regenerationPreprint

Johnson, G., Hart, A., Sujansky, M., Graber, J. H., & Godwin, J. W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.10.705144

A macrophage-induced subpopulation of mesenchymal cells expressing Fcer1g contributes to wound-induced fibrosis

Ma, X., Wang, E., Puviindran, V., Su, Z., Liu, X., Shimada, E., Yan, C., Liu, Y., Li, Z., Nadesan, P., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69449-2

A Csf1r lineage gives rise to dermal lymphatic endothelial cellsPreprint

Canu, G., Correra, R., Plein, A., Denti, L., Fantin, A., & Ruhrberg, C. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.17.712362

Rôle des neutrophiles dans le contrôle des mammites chez l'animal cible et modèle

Rambault, M. (2022) · theses.fr (ABES) · doi:10.70675/e394badezaa07z46b4zb1fezf0f6c1ac3052

Conditional macrophage ablation in transgenic mice expressing a Fas-based suicide

Burnett, R. H., Kershen, E. J., Zhang, J., Zeng, L., Straley, S. C., Kaplan, A. M., & Cohen, D. A. (2004)

Generation of a novel mouse model for the inducible depletion of macrophages in vivo

Gheryani, N. A., Coffelt, S. B., Gartland, A., Rumney, R. M. H., Kiss‐Toth, E., Lewis, C. E., Tozer, G. M., Greaves, D. R., Dear, T. N., & Miller, G. (2012) · genesis · doi:10.1002/dvg.22343 · Cited by 9

Inducible transgenes under the control of the hCD68 promoter identifies mouse macrophages with a distribution that differs from the F4/80 - and CSF-1R–expressing populations

Pillai, M. M., Hayes, B. J., & Torok‐Storb, B. (2009) · Experimental Hematology · doi:10.1016/j.exphem.2009.09.003 · Cited by 29

Transgenic mice expressing a hemopoietic growth factor gene (GM-CSF) develop accumulations of macrophages, blindness, and a fatal syndrome of tissue damage

Lang, R. A., Metcalf, D., Cuthbertson, R. A., Lyons, I. G., Stanley, E. G., Kelso, A., Kannourakis, G., Williamson, D. J., Klintworth, G. K., Gonda, T. J., et al. (1987) · Cell · doi:10.1016/0092-8674(87)90136-x · Cited by 366

Autocrine Deactivation of Macrophages in Transgenic Mice

Promoter, H. C., Lang, R., Erlangen, U., Profile, S., Greaves, D. R., Murray, P. J., & Promoter, H. C. (2002)