How neutrophils meet their end

Neutrophil Extracellular Traps Kill Bacteria

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Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders

Hsiao, E. Y., McBride, S. W., Hsien, S., Sharon, G., Hyde, E. R., McCue, T., Codelli, J. A., Chow, J., Reisman, S. E., Petrosino, J. F., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.024 · Cited by 3,283 · see citing works

Pore-forming activity and structural autoinhibition of the gasdermin family

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In Vivo Analysis of Autophagy in Response to Nutrient Starvation Using Transgenic Mice Expressing a Fluorescent Autophagosome Marker

Mizushima, N., Yamamoto, A., Matsui, M., Yoshimori, T., & Ohsumi, Y. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-09-0704 · Cited by 2,323 · see citing works

Immunosuppressive effects of apoptotic cells

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Macrophage phagocytosis of aging neutrophils in inflammation. Programmed cell death in the neutrophil leads to its recognition by macrophages.

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Neutrophil extracellular traps license macrophages for cytokine production in atherosclerosis

Warnatsch, A., Ιωάννου, Μ., Wang, Q., & Papayannopoulos, V. (2015) · Science · doi:10.1126/science.aaa8064 · Cited by 1,280 · see citing works

Netting Neutrophils Induce Endothelial Damage, Infiltrate Tissues, and Expose Immunostimulatory Molecules in Systemic Lupus Erythematosus

Villanueva, E. C., Yalavarthi, S., Berthier, C. C., Hodgin, J. B., Khandpur, R., Lin, A. M., Rubin, C. J., Zhao, W., Olsen, S. H., Klinker, M. W., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100450 · Cited by 1,246 · see citing works

The microbiome in early life: Implications for health outcomes

Tamburini, S., Shen, N., Wu, H. C., & Clemente, J. C. (2016) · Nature Medicine · doi:10.1038/nm.4142 · Cited by 1,213 · see citing works

Infection-induced NETosis is a dynamic process involving neutrophil multitasking in vivo

Yipp, B. G., Petri, B., Salina, D., Jenne, C. N., Scott, B. N. V., Zbytnuik, L. D., Pittman, K., Asaduzzaman, M., Wu, K., Meijndert, H. C., et al. (2012) · Nature Medicine · doi:10.1038/nm.2847 · Cited by 1,169 · see citing works

A Novel Mechanism of Rapid Nuclear Neutrophil Extracellular Trap Formation in Response to <i>Staphylococcus aureus</i>

Pilsczek, F. H., Salina, D., Poon, K. K. H., Fahey, C., Yipp, B. G., Sibley, C. D., Robbins, S. M., Green, F. H. Y., Surette, M. G., Sugai, M., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000675 · Cited by 1,114 · see citing works

Phagocytosis of Apoptotic Neutrophils Regulates Granulopoiesis via IL-23 and IL-17

Stark, M. A., Huo, Y., Burcin, T. L., MORRIS, M. A., Olson, T. S., & Ley, K. F. (2005) · Immunity · doi:10.1016/j.immuni.2005.01.011 · Cited by 945 · see citing works

Neutrophil ageing is regulated by the microbiome

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Neutrophils and NETS in modulating acute and chronic inflammation

Castanheira, F. V. S., & Kubes, P. (2019) · Blood · doi:10.1182/blood-2018-11-844530 · Cited by 792 · see citing works

Chemokines Acting via CXCR2 and CXCR4 Control the Release of Neutrophils from the Bone Marrow and Their Return following Senescence

Martin, C., Burdon, P. C. E., Bridger, G. J., Gutierrez-Ramos, J.-C., Williams, T. J., & Rankin, S. M. (2003) · Immunity · doi:10.1016/s1074-7613(03)00263-2 · Cited by 770 · see citing works

Gasdermin D plays a vital role in the generation of neutrophil extracellular traps

Sollberger, G., Choidas, A., Burn, G. L., Habenberger, P., Lucrezia, R. D., Kordes, S., Menninger, S., Eickhoff, J., Nußbaumer, P., Klebl, B., et al. (2018) · Science Immunology · doi:10.1126/sciimmunol.aar6689 · Cited by 761 · see citing works

Developmental Analysis of Bone Marrow Neutrophils Reveals Populations Specialized in Expansion, Trafficking, and Effector Functions

Evrard, M., Kwok, I., Chong, S. Z., Teng, K. W. W., Becht, É., Chen, J., Sieow, J. L., Penny, H. L., Ching, G. C., Devi, S., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.02.002 · Cited by 704 · see citing works

Platelets and neutrophil extracellular traps collaborate to promote intravascular coagulation during sepsis in mice

McDonald, B., Davis, R. P., Kim, S., Tse, M., Esmon, C. T., Kołaczkowska, E., & Jenne, C. N. (2017) · Blood · doi:10.1182/blood-2016-09-741298 · Cited by 666 · see citing works

The autophagy protein Atg7 is essential for hematopoietic stem cell maintenance

Mortensen, M., Soilleux, E. J., Djordjevic, G., Tripp, R., Lutteropp, M., Sadighi-Akha, E., Stranks, A. J., Glanville, J., Knight, S., W. Jacobsen, S.-E., et al. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20101145 · Cited by 657 · see citing works

Noncanonical inflammasome signaling elicits gasdermin D–dependent neutrophil extracellular traps

Chen, K. W., Monteleone, M. M., Boucher, D., Sollberger, G., Ramnath, D., Condon, N. D., von Pein, J. B., Brož, P., Sweet, M. J., & Schroder, K. (2018) · Science Immunology · doi:10.1126/sciimmunol.aar6676 · Cited by 640 · see citing works

Host DNases prevent vascular occlusion by neutrophil extracellular traps

Jiménez-Alcázar, M., Rangaswamy, C., Panda, R., Bitterling, J., Simsek, Y., Long, A. T., Bilyy, R. O., Krenn, V., Renné, C., Renné, T., et al. (2017) · Science · doi:10.1126/science.aam8897 · Cited by 597 · see citing works

The multifactorial role of neutrophils in rheumatoid arthritis

Wright, H. L., Moots, R. J., & Edwards, S. W. (2014) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2014.80 · Cited by 591 · see citing works

The microbiota regulates neutrophil homeostasis and host resistance to Escherichia coli K1 sepsis in neonatal mice

Deshmukh, H. S., Liu, Y., Menkiti, O. R., Mei, J., Dai, N., O'Leary, C. E., Oliver, P. M., Kolls, J. K., Weiser, J. N., & Worthen, G. S. (2014) · Nature Medicine · doi:10.1038/nm.3542 · Cited by 579 · see citing works

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Klein, C., Grudzien, M., Appaswamy, G., Germeshausen, M., Sandrock, I., Schäffer, A. A., Rathinam, C., Boztuǧ, K., Schwinzer, B., Rezaei, N., et al. (2006) · Nature Genetics · doi:10.1038/ng1940 · Cited by 501 · see citing works

Maladaptive role of neutrophil extracellular traps in pathogen-induced lung injury

Lefrançais, E., Mallavia, B., Zhuo, H., Calfee, C. S., & Looney, M. R. (2018) · JCI Insight · doi:10.1172/jci.insight.98178 · Cited by 472 · see citing works

A Neutrophil Timer Coordinates Immune Defense and Vascular Protection

Adrover, J. M., del Fresno, C., Crainiciuc, G., Cuartero, M. I., Casanova-Acebes, M., Weiss, L. A., Encabo, H. H., Silvestre-Roig, C., Rossaint, J., Cossío, I., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.01.002 · Cited by 449 · see citing works

Neutrophil secretion products pave the way for inflammatory monocytes

Soehnlein, O., Zernecke, A., Eriksson, E. E., Rothfuchs, A. G., Pham, C. T. N., Herwald, H., Bidzhekov, K., Rottenberg, M. E., Weber, C., & Lindbom, L. (2008) · Blood · doi:10.1182/blood-2008-02-139634 · Cited by 437 · see citing works

Externalized histone H4 orchestrates chronic inflammation by inducing lytic cell death

Silvestre-Roig, C., Braster, Q., Wichapong, K., Lee, E. Y., Teulon, J., Berrebeh, N., Winter, J., Adrover, J. M., Santos, G. S., Froese, A., et al. (2019) · Nature · doi:10.1038/s41586-019-1167-6 · Cited by 431 · see citing works

Gasdermin D Exerts Anti-inflammatory Effects by Promoting Neutrophil Death

Kambara, H., Liu, F., Zhang, X., Liu, P., Bajrami, B., Teng, Y., Zhao, L., Zhou, S., Yu, H., Zhou, W., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.02.067 · Cited by 418 · see citing works

Akt inhibition promotes autophagy and sensitizes PTEN-null tumors to lysosomotropic agents

Degtyarev, M. Y., Mazière, A. M. G. L. D., Orr, C., Lin, J. M., Lee, B. B., Tien, J., Prior, W. W., van Dijk, S., Wu, H., Gray, D. C., et al. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200801099 · Cited by 411 · see citing works

Pyroptosis triggers pore-induced intracellular traps (PITs) that capture bacteria and lead to their clearance by efferocytosis

Jorgensen, I., Zhang, Y., Krantz, B. A., & Miao, E. A. (2016) · Journal of Experimental Medicine · doi:10.1084/jem.20151613 · Cited by 403 · see citing works

Living on the Edge: Efferocytosis at the Interface of Homeostasis and Pathology

Morioka, S., Maueröder, C., & Ravichandran, K. S. (2019) · Immunity · doi:10.1016/j.immuni.2019.04.018 · Cited by 391 · see citing works

Resident Macrophages Cloak Tissue Microlesions to Prevent Neutrophil-Driven Inflammatory Damage

Uderhardt, S., Martins, A. J., Tsang, J. S., Lämmermann, T., & Germain, R. N. (2019) · Cell · doi:10.1016/j.cell.2019.02.028 · Cited by 383 · see citing works

Immunity around the clock

Man, K., Loudon, A., & Chawla, A. (2016) · Science · doi:10.1126/science.aah4966 · Cited by 325 · see citing works

Autophagy-Dependent Generation of Free Fatty Acids Is Critical for Normal Neutrophil Differentiation

Riffelmacher, T., Clarke, A. J., Richter, F. C., Stranks, A. J., Pandey, S., Danielli, S., Hublitz, P., Yu, Z., Johnson, E., Schwerd, T., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.08.005 · Cited by 301 · see citing works

Human neutrophil kinetics: modeling of stable isotope labeling data supports short blood neutrophil half-lives

Lahoz-Beneytez, J., Elemans, M., Zhang, Y., Ahmed, R., Salam, A., Block, M., Niederalt, C., Asquith, B., & Macallan, D. C. (2016) · Blood · doi:10.1182/blood-2016-03-700336 · Cited by 294 · see citing works

Annexin-1 and Peptide Derivatives Are Released by Apoptotic Cells and Stimulate Phagocytosis of Apoptotic Neutrophils by Macrophages

Scannell, M., Flanagan, M. B., deStefani, A., Wynne, K. J., Cagney, G., Godson, C., & MADERNA, P. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.7.4595 · Cited by 282 · see citing works

Cathepsin G Inhibition by Serpinb1 and Serpinb6 Prevents Programmed Necrosis in Neutrophils and Monocytes and Reduces GSDMD-Driven Inflammation

Burgener, S. S., Leborgne, N. G. F., Snipas, S. J., Salvesen, G. S., Bird, P. I., & Benarafa, C. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.065 · Cited by 276 · see citing works

REDD1/autophagy pathway promotes thromboinflammation and fibrosis in human systemic lupus erythematosus (SLE) through NETs decorated with tissue factor (TF) and interleukin-17A (IL-17A)

Frangou, E. A., Chrysanthopoulou, A., Mitsios, A., Kambas, K., Arelaki, S., Angelidou, I., Αραμπατζιόγλου, Α., Gakiopoulou, H., Bertsias, G. K., Verginis, P., et al. (2018) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2018-213181 · Cited by 272 · see citing works

Interferon-gamma inhibits scavenger receptor expression and foam cell formation in human monocyte-derived macrophages.

Geng, Y., & Hansson, G. K. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115718 · Cited by 265 · see citing works

MerTK receptor cleavage promotes plaque necrosis and defective resolution in atherosclerosis

Cai, B., Thorp, E. B., Doran, A. C., Sansbury, B. E., Daemen, M. J. A. P., Dorweiler, B., Spite, M., Fredman, G., & Tabas, I. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90520 · Cited by 262 · see citing works

Aged neutrophils contribute to the first line of defense in the acute inflammatory response

Uhl, B., Vadlau, Y., Zuchtriegel, G., Nekolla, K., Sharaf, K., Gaertner, F. C., Maßberg, S., Krombach, F., & Reichel, C. A. (2016) · Blood · doi:10.1182/blood-2016-05-718999 · Cited by 242 · see citing works

Neutrophil IL-1β Processing Induced by Pneumolysin Is Mediated by the NLRP3/ASC Inflammasome and Caspase-1 Activation and Is Dependent on K+ Efflux

Karmakar, M., Katsnelson, M. J., Malak, H. A., Greene, N. G., Howell, S. J., Hise, A. G., Camilli, A., Kadioglu, A., Dubyak, G., & Pearlman, E. M. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1401624 · Cited by 231 · see citing works

Neutrophils in Rheumatoid Arthritis: Breaking Immune Tolerance and Fueling Disease

O’Neil, L. J., & Kaplan, M. J. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.12.008 · Cited by 228 · see citing works

Neutrophils Discriminate between Lipopolysaccharides of Different Bacterial Sources and Selectively Release Neutrophil Extracellular Traps

Pieterse, E., Rother, N., Yanginlar, C., Hilbrands, L. B., & van der Vlag, J. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00484 · Cited by 217 · see citing works

Inflammasome-dependent Pyroptosis and IL-18 Protect against Burkholderia pseudomallei Lung Infection while IL-1β Is Deleterious

Ceballos‐Olvera, I., Sahoo, M., Miller, M. A., del Barrio, L., & Re, F. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002452 · Cited by 208 · see citing works

Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis

Grenda, D. S., Murakami, M. A., Ghatak, J., Xia, J., Boxer, L. A., Dale, D. C., Dinauer, M. C., & Link, D. C. (2007) · Blood · doi:10.1182/blood-2006-11-057299 · Cited by 202 · see citing works

The role of the bone marrow in neutrophil clearance under homeostatic conditions in the mouse

Furze, R. C., & Rankin, S. M. (2008) · The FASEB Journal · doi:10.1096/fj.08-109876 · Cited by 202 · see citing works

Chrono-pharmacological Targeting of the CCL2-CCR2 Axis Ameliorates Atherosclerosis

Winter, C., Silvestre-Roig, C., Ortega‐Gómez, A., Lemnitzer, P., Poelman, H., Schumski, A., Winter, J., Drechsler, M. D., de Jong, R., Immler, R., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.05.002 · Cited by 198 · see citing works

Neutrophil pyroptosis: new perspectives on sepsis

Liu, L., & Sun, B. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03060-1 · Cited by 197 · see citing works

Prolyl hydroxylase 3 (PHD3) is essential for hypoxic regulation of neutrophilic inflammation in humans and mice

Walmsley, S. R., Chilvers, E. R., Thompson, A. A., Vaughan, K., Marriott, H. M., Parker, L. C., Shaw, G., Parmar, S., Schneider, M., Sabroe, I., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci43273 · Cited by 191 · see citing works

Phagocytosis of Staphylococcus aureus by Human Neutrophils Prevents Macrophage Efferocytosis and Induces Programmed Necrosis

Greenlee‐Wacker, M. C., Rigby, K. M., Kobayashi, S. D., Porter, A. R., DeLeo, F. R., & Nauseef, W. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302692 · Cited by 185 · see citing works

Role of the liver in regulating numbers of circulating neutrophils

Shi, J., Gilbert, G. E., Kokubo, Y., & Ohashi, T. (2001) · Blood · doi:10.1182/blood.v98.4.1226 · Cited by 178 · see citing works

Gene Expression Profiling Provides Insight into the Pathophysiology of Chronic Granulomatous Disease

Kobayashi, S. D., Voyich, J. M., Braughton, K. R., Whitney, A. R., Nauseef, W. M., Malech, H. L., & DeLeo, F. R. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.1.636 · Cited by 177 · see citing works

RIPK3 Restricts Viral Pathogenesis via Cell Death-Independent Neuroinflammation

Daniels, B. P., Snyder, A. G., Olsen, T. M., Orozco, S. L., Oguin, T. H., Tait, S. W. G., Martinez, J., Gale, M., Loo, Y., & Oberst, A. (2017) · Cell · doi:10.1016/j.cell.2017.03.011 · Cited by 177 · see citing works

Sirt3 promotes antimycobacterial defenses by coordinating mitochondrial and autophagic functions

Kim, T. S., Jin, Y. B., Kim, Y. S., Kim, S., Kim, J. K., Lee, H.-M., Suh, H.-W., Choe, J. H., Kim, Y. J., Koo, B.-S., et al. (2019) · Autophagy · doi:10.1080/15548627.2019.1582743 · Cited by 172 · see citing works

Autophagy Is Required for Neutrophil-Mediated Inflammation

Bhattacharya, A., Wei, Q., Shin, J. N., Fattah, E. A., Bonilla, D. L., Xiang, Q., & Eissa, N. T. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.08.019 · Cited by 169 · see citing works

Nuclear RIPK3 and MLKL contribute to cytosolic necrosome formation and necroptosis

Weber, K., Roelandt, R., Bruggeman, I., Estornes, Y., & Vandenabeele, P. (2018) · Communications Biology · doi:10.1038/s42003-017-0007-1 · Cited by 169 · see citing works

Cigarette smoke-induced necroptosis and DAMP release trigger neutrophilic airway inflammation in mice

Pouwels, S. D., Zijlstra, G. J., van der Toorn, M., Hesse, L., Gras, R., ten Hacken, N. H. T., Krysko, D. V., Vandenabeele, P., de Vries, M., van Oosterhout, A. J. M., et al. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00174.2015 · Cited by 168 · see citing works

NETosing Neutrophils Activate Complement Both on Their Own NETs and Bacteria via Alternative and Non-alternative Pathways

Yuen, J., Pluthero, F. G., Douda, D. N., Riedl, M., Cherry, A., Ulanova, M., Kahr, W. H. A., Palaniyar, N., & Licht, C. P. B. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00137 · Cited by 165 · see citing works

Opposite Effects of Rho Family GTPases on Engulfment of Apoptotic Cells by Macrophages

Nakaya, M., Tanaka, M., Okabe, Y., Hanayama, R., & Nagata, S. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m510972200 · Cited by 155 · see citing works

Targeting of proteins to granule subsets is determined by timing and not by sorting: The specific granule protein NGAL is localized to azurophil granules when expressed in HL-60 cells.

Cabec, V. L., Cowland, J. B., Calafat, J., & Borregaard, N. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6454 · Cited by 154 · see citing works

The antimicrobial peptide LL-37 facilitates the formation of neutrophil extracellular traps

Neumann, A., Berends, E. T. M., Nerlich, A. G., Molhoek, E. M., Gallo, R. L., Meerloo, T., Nizet, V., Naim, H. Y., & von Köckritz‐Blickwede, M. (2014) · Biochemical Journal · doi:10.1042/bj20140778 · Cited by 145 · see citing works

Circadian-Regulated Cell Death in Cardiovascular Diseases

Rabinovich-Nikitin, I., Lieberman, B., Martino, T. A., & Kirshenbaum, L. A. (2019) · Circulation · doi:10.1161/circulationaha.118.036550 · Cited by 138 · see citing works

Histone Acetylation Promotes Neutrophil Extracellular Trap Formation

Hamam, H. J., Khan, M. A., & Palaniyar, N. (2019) · Biomolecules · doi:10.3390/biom9010032 · Cited by 133 · see citing works

Necroptosis suppresses inflammation via termination of TNF- or LPS-induced cytokine and chemokine production

Kearney, C. J., Cullen, S. P., Tynan, G. A., Henry, C. M., Clancy, D. M., Lavelle, E. C., & Martin, S. J. (2015) · Cell Death and Differentiation · doi:10.1038/cdd.2014.222 · Cited by 132 · see citing works

Class IA PI3K p110β Subunit Promotes Autophagy through Rab5 Small GTPase in Response to Growth Factor Limitation

Dou, Z., Pan, J.-A., Dbouk, H. A., Ballou, L. M., DeLeon, J. L., Fan, Y., Chen, J.-S., Liang, Z., Li, G., Backer, J., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.01.022 · Cited by 130 · see citing works

Matters of life and death. How neutrophils die or survive along NET release and is “NETosis” = necroptosis?

Desai, J., Mulay, S. R., Nakazawa, D., & Anders, H. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2195-0 · Cited by 115 · see citing works

The Involvement of the Apoptosis-Modulating Proteins ERK 1/2, Bcl-xL and Bax in the Resolution of Acute Inflammation in Vivo

Sawatzky, D. A., Willoughby, D. A., Colville‐Nash, P., & Rossi, A. G. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.050058 · Cited by 113 · see citing works

Regulation of the innate immune system by autophagy: neutrophils, eosinophils, mast cells, NK cells

Germič, N., Frangež, Ž., Yousefi, S., & Simon, H. (2019) · Cell Death and Differentiation · doi:10.1038/s41418-019-0295-8 · Cited by 111 · see citing works

The generation of neutrophils in the bone marrow is controlled by autophagy

Rožman, S., Yousefi, S., Oberson, K., Kaufmann, T., Benarafa, C., & Simon, H. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.169 · Cited by 110 · see citing works

Klebsiella pneumoniae infection of murine neutrophils impairs their efferocytic clearance by modulating cell death machinery

Jondle, C. N., Gupta, K., Mishra, B. B., & Sharma, J. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007338 · Cited by 101 · see citing works

Swimming Motility Mediates the Formation of Neutrophil Extracellular Traps Induced by Flagellated Pseudomonas aeruginosa

Floyd, M., Winn, M., Cullen, C., Sil, P., Chassaing, B., Yoo, D., Gewirtz, A. T., Goldberg, J. B., McCarter, L. L., & Rada, B. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005987 · Cited by 96 · see citing works

Granulocytopoiesis

Cronkite, E. P., & Fliedner, T. M. (1964) · New England Journal of Medicine · doi:10.1056/nejm196406182702506 · Cited by 91 · see citing works

Necroptosis and neutrophil-associated disorders

Wang, X., Yousefi, S., & Simon, H. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0058-8 · Cited by 88 · see citing works

NADPH oxidase activation regulates apoptotic neutrophil clearance by murine macrophages

Bagaitkar, J., Huang, J., Zeng, M. Y., Pech, N. K., Monlish, D. A., Perez‐Zapata, L. J., Miralda, I., Schuettpelz, L. G., & Dinauer, M. C. (2018) · Blood · doi:10.1182/blood-2017-09-809004 · Cited by 82 · see citing works

Neutrophil Necroptosis Is Triggered by Ligation of Adhesion Molecules following GM-CSF Priming

Wang, X.-L., He, Z.-Y., Liu, H., Yousefi, S., & Simon, H. (2016) · Journal of Immunology · doi:10.4049/jimmunol.1600051 · Cited by 80 · see citing works

Oxidized LDL induces FAK-dependent RSK signaling to drive NF-κB activation and VCAM-1 expression

Yurdagul, A., Sulzmaier, F. J., Chen, X. L., Pattillo, C. B., Schlaepfer, D. D., & Orr, A. W. (2016) · Journal of Cell Science · doi:10.1242/jcs.182097 · Cited by 78 · see citing works

Anoxia and glucose supplementation preserve neutrophil viability and function

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