Apoptotic Cells Induce Migration of Phagocytes via Caspase-3-Mediated Release of a Lipid Attraction Signal

Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF.

Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1112 · Cited by 3,166 · cited 1×

Caspase-3 Is Required for DNA Fragmentation and Morphological Changes Associated with Apoptosis

Jänicke, R. U., Sprengart, M. L., Wati, M. R., & Porter, A. G. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.16.9357 · Cited by 1,955

Natural adjuvants: Endogenous activators of dendritic cells

Gallucci, S., Lolkema, M. P., & Matzinger, P. (1999) · Nature Medicine · doi:10.1038/15200 · Cited by 1,601

Corpse clearance defines the meaning of cell death

Savill, J., & Fadok, V. A. (2000) · Nature · doi:10.1038/35037722 · Cited by 1,572

A receptor for phosphatidylserine-specific clearance of apoptotic cells

Fadok, V. A., Bratton, D. L., Rose, D. M., Pearson, A. M., Ezekowitz, R. A. B., & Henson, P. M. (2000) · Nature · doi:10.1038/35011084 · Cited by 1,491

Consequences of Cell Death

Sauter, B., Albert, M. L., Francisco, L. M., Larsson, M., Somersan, S., & Bhardwaj, N. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.3.423 · Cited by 1,357

Caspase-3-mediated cleavage of ROCK I induces MLC phosphorylation and apoptotic membrane blebbing

Sebbagh, M., Renvoizé, C., Hamelin, J., Riché, N., Bertoglio, J., & Bréard, J. (2001) · Nature Cell Biology · doi:10.1038/35070019 · Cited by 915

Sensing sterile injury: Opportunities for pharmacological control

Menezes, G. B., Mansur, D. S., McDonald, B., Kubes, P., & Teixeira, M. M. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.07.002 · Cited by 17

Lysophosphatidylcholine‐mediated functional inactivation of syndecan‐4 results in decreased adhesion and motility of dendritic cells

Bühligen, J., Himmel, M., Gebhardt, C., Simon, J. C., Ziegler, W. H., & Averbeck, M. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22301 · Cited by 16

Cells Exposed to Sublethal Oxidative Stress Selectively Attract Monocytes/Macrophages via Scavenger Receptors and MyD88-Mediated Signaling

Geiger-Maor, A., Levi, I., Even‐Ram, S., Smith, Y., Bowdish, D. M. E., Nussbaum, G., & Rachmilewitz, J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1101740 · Cited by 16

Host lipid sensing promotes invasion of cells with pathogenic Salmonella

Shivcharan, S., Yadav, J., & Qadri, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-33319-9 · Cited by 16

Phagocyte–myocyte interactions and consequences during hypoxic wound healing

Zhang, S., Dehn, S., DeBerge, M., Rhee, K., Hudson, B. I., & Thorp, E. B. (2014) · Cellular Immunology · doi:10.1016/j.cellimm.2014.04.006 · Cited by 16

Immunohistochemical analysis of the expression of TNF-alpha, TGF-beta, and caspase-3 in subcutaneous tissue of patients with HIV Lipodystrophy Syndrome

Oliveira, S. H. D. S. D., Aarão, T. L. D. S., Barbosa, L. D. S., Lisbôa, P. G. S., Dutra, C. D. T., Sousa, L. M., Quaresma, J. A. S., & Libonati, R. M. F. (2014) · Microbial Pathogenesis · doi:10.1016/j.micpath.2014.02.004 · Cited by 16

Elevated Serum Lysophosphatidylcholine in Patients with Systemic Lupus Erythematosus Impairs Phagocytosis of Necrotic Cells In Vitro

Grossmayer, G. E., Keppeler, H., Boeltz, S., Janko, C., Rech, J., i, M. H., Lauber, K., & Munoz, L. E. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01876 · Cited by 16

Untargeted Profiling of Bile Acids and Lysophospholipids Identifies the Lipid Signature Associated with Glycemic Outcome in an Obese Non-Diabetic Clinical Cohort

Christinat, N., Valsesia, A., & Masoodi, M. (2020) · Biomolecules · doi:10.3390/biom10071049 · Cited by 16

Macrophage Efferocytosis as a Therapeutic Strategy in Intervertebral Disc Degeneration

Chen, S., Zhang, H., Wang, Z., Zhu, D., Li, Y., Zhang, Y., Wang, D., Chen, S.-W., Liu, H., & Kang, X. (2025) · Cell Proliferation · doi:10.1111/cpr.70068 · Cited by 15

Boosting phototherapy efficacy of NIR-absorbing ruthenium (II) complex via supramolecular engineering

Wang, Z., Li, C., Huang, S., Ma, X., Sun, Y., Zhao, J., & Gou, S. (2022) · Materials Today Nano · doi:10.1016/j.mtnano.2022.100220 · Cited by 16

Imaging of cancer lipid metabolism in response to therapy

Arlauckas, S. P., Browning, E. A., Poptani, H., & Delikatny, E. J. (2019) · NMR in Biomedicine · doi:10.1002/nbm.4070 · Cited by 15

Perspective: Why and How Ubiquitously Distributed, Vascular-Associated, Pluripotent Stem Cells in the Adult Body (vaPS Cells) Are the Next Generation of Medicine

Alt, E., Schmitz, C., & Bai, X. (2021) · Cells · doi:10.3390/cells10092303 · Cited by 15

Lysophosphatidylcholine: A Novel Modulator ofTrypanosoma cruziTransmission

Silva-Neto, M. A. C., Carneiro, A. B., Silva-Cardoso, L., & Atella, G. C. (2011) · Journal of Parasitology Research · doi:10.1155/2012/625838 · Cited by 15

Differential effect of interleukin-10 on hepatocyte apoptosis

Santiago-Lomeli, M., Gómez-Quiroz, L. E., Ortíz-Ortega, V. M., Kershenobich, D., & Gutiérrez‐Ruíz, M. C. (2005) · Life Sciences · doi:10.1016/j.lfs.2004.10.048 · Cited by 15

O death where is thy sting? Immunologic tolerance to apoptotic self

Ravishankar, B., & McGaha, T. L. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1261-0 · Cited by 16

Infertility in the hyperplasic ovary of freshwater planarians: the role of programmed cell death

Harrath, A. H., Semlali, A., Mansour, L. A., Ahmed, M., Sirotkin, A. V., Alomar, S. Y., Arfah, M., Anazi, M. S. A., Alhazza, I. M., Nyengaard, J. R., et al. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1971-0 · Cited by 15

Deficiency of iPLA2β Primes Immune Cells for Proinflammation: Potential Involvement in Age-Related Mesenteric Lymph Node Lymphoma

Inhoffen, J., Tuma‐Kellner, S., Straub, B. K., Stremmel, W., & Chamulitrat, W. (2015) · Cancers · doi:10.3390/cancers7040901 · Cited by 15

Resident macrophages as potential therapeutic targets for cardiac ageing and injury

Zhang, S., Chen, R., Chakrabarti, S., & Su, Z. (2020) · Clinical & Translational Immunology · doi:10.1002/cti2.1167 · Cited by 15

Defects in Regulation of Local Immune Responses Resulting in Atherosclerosis

Ferencĭk, M., Štvrtinová, V., & Hulín, I. (2005) · Journal of Immunology Research · doi:10.1080/17402520500182295 · Cited by 15

Lymphocyte resistance to lysophosphatidylcholine mediated apoptosis in atherosclerosis

Zurgil, N., Afrimzon, E., Shafran, Y., Shovman, O., Gilburd, B., Brikman, H., Shoenfeld, Y., & Deutsch, M. (2006) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2006.02.013 · Cited by 15

The role of death-associated molecular patterns in the pathogenesis of systemic lupus erythematosus

Mevorach, D. (2004) · Rheumatic Disease Clinics of North America · doi:10.1016/j.rdc.2004.04.011 · Cited by 15

The Role of Phospholipases in Lipid Modification and Atherosclerosis

Ghesquiere, S. A. I., Hofker, M. H., & de Winther, M. P. J. (2005) · Cardiovascular Toxicology · doi:10.1385/ct:5:2:161 · Cited by 15

Biochemical alterations in the follicular fluid of bovine peri-ovulatory follicles and their association with final oocyte maturation

Alrabiah, N. A., Simintiras, C. A., Evans, A. C. O., Lonergan, P., & Fair, T. (2022) · Reproduction and Fertility · doi:10.1530/raf-22-0090 · Cited by 14

Intercellular contact and cargo transfer between Müller glia and to microglia precede apoptotic cell clearance in the developing retina

Morales, M., Findley, A. P., & Mitchell, D. M. (2024) · Development · doi:10.1242/dev.202407 · Cited by 14

Molecular Suicide Notes: Last Call from Apoptosing Cells

Peter, C., Wesselborg, S., & Lauber, K. (2009) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjp045 · Cited by 14

Tamoxifen induces apoptotic neutrophil efferocytosis in horses

Olave, C. J., Morales, N., Uberti, B., Henríquez, C., Sarmiento, J., Ortloff, A., Folch, H., & Morán, G. (2018) · Veterinary Research Communications · doi:10.1007/s11259-017-9709-6 · Cited by 14

Lipids and Membrane Microdomains: The Glycerolipid and Alkylphosphocholine Class of Cancer Chemotherapeutic Drugs

Zaremberg, V., Ganesan, S., & Mahadeo, M. (2019) · Handbook of experimental pharmacology · doi:10.1007/164_2019_222 · Cited by 14

Proliferation of Resident Macrophages Is Dispensable for Protection during Giardia duodenalis Infections

Fink, M. Y., Maloney, J. G., Keselman, A. M., Li, E., Menegas, S., Staniorski, C., & Singer, S. M. (2019) · ImmunoHorizons · doi:10.4049/immunohorizons.1900041 · Cited by 14

Heme Oxygenase-1 Contributes to Both the Engulfment and the Anti-Inflammatory Program of Macrophages during Efferocytosis

Fige, É., Szendrei, J., Sós, L., Kraszewska, I., Potor, L., Balla, J., & Szondy, Z. (2021) · Cells · doi:10.3390/cells10030652 · Cited by 14

Apoptosis in cancer cells induced by photodynamic treatment – a methodological approach

Kiesslich, T., Tortik, N., Pichler, M., Neureiter, D., & Plaetzer, K. (2013) · Journal of Porphyrins and Phthalocyanines · doi:10.1142/s1088424613300036 · Cited by 14

Signals, receptors, and cytokines involved in the immunomodulatory and anti‐inflammatory properties of apoptotic cells

Fürnrohr, B. G., Sheriff, A., Munoz, L. E., von Briesen, H., Urbonaviciute, V., Neubert, K., Kalden, J. R., i, M. H., & Voll, R. E. (2005) · Signal Transduction · doi:10.1002/sita.200500071 · Cited by 14

Role of macrophages in atherosclerosis

Chowdhury, A. S., Tamanna, S., & Kar, K. (2020) · Asian Journal of Medical and Biological Research · doi:10.3329/ajmbr.v6i3.49784 · Cited by 14

The cross‐talk between soluble “Find me” and “Keep out” signals as an initial step in regulating efferocytosis

Tajbakhsh, A., Yousefi, F., Abedi, S. M., Rezaee, M., Savardashtaki, A., Teng, Y., & Sahebkar, A. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30770 · Cited by 14

Will Modulation of Cell Death Increase PD Technique Survival?

Ortíz, A., & Catalan, M. P. (2004) · Peritoneal Dialysis International · doi:10.1177/089686080402400201 · Cited by 14

Efferocytosis in tissue engineering: A comprehensive review of emerging therapeutic strategies for enhanced tissue repair and regeneration

Zhang, Y., Nie, R., Feng, Z.-Y., Fan, M., Shen, Z., Zhang, X., Zhang, Q., Zou, C., Zhang, J., Huang, K., et al. (2025) · Bioactive Materials · doi:10.1016/j.bioactmat.2025.05.026 · Cited by 13

The small molecule fibroblast growth factor receptor inhibitor infigratinib exerts anti‐inflammatory effects and remyelination in a model of multiple sclerosis

Rajendran, R., Rajendran, V., Böttiger, G., Stadelmann, C., Shirvanchi, K., von Au, L., Bhushan, S., Wallendszus, N., Schunin, D., Westbrock, V., et al. (2023) · British Journal of Pharmacology · doi:10.1111/bph.16186 · Cited by 14

Endothelial Progenitor Cells Conditioned Medium Supports Number of GABAergic Neurons and Exerts Neuroprotection in Cultured Striatal Neuronal Progenitor Cells

Santo, S. D., Seiler, S., Andres, R. H., & Widmer, H. R. (2019) · Cell Transplantation · doi:10.1177/0963689719835192 · Cited by 13

The effect of reproductive toxicity induced by ZnO NPs in mice during early pregnancy through mitochondrial apoptotic pathway

Chen, L., Wu, H., Hong, W., Aguilar, Z. P., Fu, F., & Xu, H. (2021) · Environmental Toxicology · doi:10.1002/tox.23113 · Cited by 13

Transglutaminase 2 Dysfunctions in the Development of Autoimmune Disorders: Celiac Disease and TG2 − / − Mouse

Szondy, Z., Korponay-Szabo, I. R., Király, R., & Fésüs, L. (2011) · Advances in enzymology and related areas of molecular biology/Advances in enzymology and related subjects · doi:10.1002/9781118105771.ch7 · Cited by 13

Glycobiology of cellular expiry: Decrypting the role of glycan-lectin regulatory complex and therapeutic strategies focusing on cancer

Das, A. K., Ghosh, N., Mandal, A., & Sil, P. C. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115367 · Cited by 13

Role of transcription factors in apoptotic cells clearance

Gao, Y.-Q., Jiao, Y., Gong, X., Liu, J., Xiao, H., & Zheng, Q. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1110225 · Cited by 12

The efferocytosis process in aging: Supporting evidence, mechanisms, and therapeutic prospects for age-related diseases

Zhang, M., Wei, J., Sun, Y., He, C., Ma, S., Pan, X., & Zhu, X. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.03.008 · Cited by 15

Mechanism of efferocytosis in atherosclerosis

Shu, L.-X., Cao, L.-L., Guo, X., Wang, Z., & Wang, S. (2024) · Journal of Molecular Medicine · doi:10.1007/s00109-024-02439-3 · Cited by 16

Characterization of lysophosphatidylcholine-induced changes of intracellular calcium in Drosophila S2 cells

Wang, P., Wang, Q., Yang, L. C., Qin, Q., & Wu, Y. (2015) · Life Sciences · doi:10.1016/j.lfs.2015.02.014 · Cited by 12

A selective fluorescent chemosensor for phosphoserine

Cooley, C. M., Hettie, K. S., Klockow, J., Garrison, S. A., & Glass, T. E. (2013) · Organic & Biomolecular Chemistry · doi:10.1039/c3ob41677a · Cited by 12

‘This way please’: Apoptotic cells regulate phagocyte migration before and after engulfment

Ariel, A., & Ravichandran, K. S. (2016) · European Journal of Immunology · doi:10.1002/eji.201646505 · Cited by 12

Mechanisms of Vascular Disease

Manetti, M., & Kahaleh, B. (2016) · Springer eBooks · doi:10.1007/978-3-319-31407-5_16 · Cited by 12

Efferocytosis in lung mucosae: implications for health and disease

Pinto, K. G., Maia, E. P., Ferreira, J. R. M., & Filardy, A. A. (2022) · Immunology Letters · doi:10.1016/j.imlet.2022.07.005 · Cited by 12

Chemopreventive effect of a milk whey by-product derived from Buffalo (Bubalus bubalis) in protecting from colorectal carcinogenesis

Cacciola, N. A., Venneri, T., Salzano, A., D’Onofrio, N., Martano, M., Saggese, A., Vinale, F., Neglia, G., Campanile, C., Baccigalupi, L., et al. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01271-5 · Cited by 13

Lipid profiling of mammalian cells with in situ matrix-assisted laser desorption ionization-mass spectrometry

Zhang, Y., Li, H., Ma, Y., & Lin, J. (2013) · Science China Chemistry · doi:10.1007/s11426-013-4960-3 · Cited by 12

Microglia at the Centre of Brain Research: Accomplishments and Challenges for the Future

Soares, N. L., & Vieira, H. L. A. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03456-1 · Cited by 14

Serial Measurements of Apoptotic Cell Numbers Provide Better Acceptance Criterion for PBMC Quality than a Single Measurement Prior to the T Cell Assay

Wunsch, M., Caspell, R., Küerten, S., Lehmann, P., & Sundararaman, S. (2015) · Cells · doi:10.3390/cells4010040 · Cited by 13

The sirens' call

Fadok, V. A. (2003) · Nature Cell Biology · doi:10.1038/ncb0803-697 · Cited by 12

Deficiency of Group VIA Phospholipase A2 (iPLA2β) Renders Susceptibility for Chemical-Induced Colitis

Li, J., Inhoffen, J., Gan‐Schreier, H., Tuma‐Kellner, S., Stremmel, W., Sun, Z., & Chamulitrat, W. (2015) · Digestive Diseases and Sciences · doi:10.1007/s10620-015-3807-5 · Cited by 12

Microglial phagocytosis in epilepsy: Mechanisms and impact

Barath, A. S., & Wu, L. (2025) · The Journal of Physiology · doi:10.1113/jp288573 · Cited by 17

The constructive function of apoptosis: More than a dead-end job

Krasovec, G., Horkan, H. R., Quéinnec, É., & Chambon, J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1033645 · Cited by 11

The Yin–Yang arms of vaccines: disease-fighting power versus tissue-destructive inflammation

Tang, D.-C. C., & Nguyen, H. H. (2014) · Expert Review of Vaccines · doi:10.1586/14760584.2014.882775 · Cited by 11

Mechanisms of Vascular Disease

Kahaleh, B., & Mulligan‐Kehoe, M. J. (2011) · Springer eBooks · doi:10.1007/978-1-4419-5774-0_19 · Cited by 11

Immunomodulatory Actions of Lysophosphatidylcholine

Hong, C.-W., & Song, D. (2008) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2008.16.2.069 · Cited by 11

Chemokine Signaling Regulates Apoptosis as well as Immune Cell Traffic in Host Defense

Grayson, M. H., & Holtzman, M. J. (2006) · Cell Cycle · doi:10.4161/cc.5.4.2427 · Cited by 11

In vitro and in vivo clearance of Rose Bengal Acetate-PhotoDynamic Therapy-induced autophagic and apoptotic cells

Panzarini, E., Inguscio, V., Tenuzzo, B. A., & Dini, L. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370213494552 · Cited by 12

Serum metabolome profiling in patients with mild cognitive impairment reveals sex differences in lipid metabolism

Escarcega, R. D., J., V. K. M., Kyriakopoulos, V. E., Ortiz, G. J., Gusdon, A. M., Fan, H., Peesh, P., Conesa, M. P. B., Colpo, G. D., Ahnstedt, H. W., et al. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106747 · Cited by 11

Macrophages promote tumor growth by phagocytosis-mediated cytokine amplification in Drosophila

Hirooka, E., Hattori, R., Ikawa, K., Kobayashi, T., Matsuyama, M., Igaki, T., & Ohsawa, S. (2025) · Current Biology · doi:10.1016/j.cub.2025.05.068 · Cited by 10

Regulators of phagocytosis as pharmacologic targets for stroke treatment

Cheng, J. G., Wang, W., Xia, Y., Li, Y., Jia, J., & Xiao, G. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1122527 · Cited by 10

Lysophosphatidylcholine induces Ca2+ mobilization in Jurkat human T lymphocytes and CTLL-2 mouse T lymphocytes by different pathways

Wang, Q., & Wu, Y. (2011) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2011.10.007 · Cited by 10

Anion Transport or Nucleotide Binding by Ucp2 Is Indispensable for Ucp2-Mediated Efferocytosis

Lee, S., Moon, H., Kim, G., Cho, J. H., Dae-Hee, L., Ye, M. B., & Park, D. (2015) · Molecules and Cells · doi:10.14348/molcells.2015.0083 · Cited by 10

Changes in Gene Expression and Metabolism in the Testes of the Rat following Spinal Cord Injury

Fortune, R. D., Grill, R. J., Beeton, C., Tanner, M. R., Huq, R., & Loose, D. S. (2016) · Journal of Neurotrauma · doi:10.1089/neu.2016.4641 · Cited by 10

MALDI Mass Spectrometric Imaging of the Nematode Caenorhabditis elegans

Menger, R. F., Clendinen, C. S., Searcy, L. A., Edison, A. S., & Yost, R. A. (2015) · Current Metabolomics · doi:10.2174/2213235x03666150525223412 · Cited by 10

Responding to infection and apoptosis — a task for TH17 cells

Brereton, C. F., & Blander, J. M. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05747.x · Cited by 10

Heat shock protein 90 mediates the apoptosis and autophage in nicotinic-mycoepoxydiene-treated HeLa cells

Sun, Y., Xiao, S., Chen, J., Wang, M., Zheng, Z., Song, S., & Zhang, L. (2015) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmv034 · Cited by 10

Comparison of apoptosis detection markers combined with macrophage immunostaining to study phagocytosis of apoptotic cells in situ.

Schrijvers, D. M., Meyer, G. R. Y. D., Kockx, M. M., Herman, A. G., & Martinet, W. (2007) · PubMed Central · Cited by 10

Metabolic reprogramming of efferocytosis in the tumour microenvironment: From apoptotic‐cell clearance to therapeutic targeting

Yang, Q., Yan, J., & Yang, Q. (2026) · Clinical and Translational Medicine · doi:10.1002/ctm2.70601 · Cited by 10

Defective quorum sensing of acute lymphoblastic leukemic cells: evidence of collective behavior of leukemic populations as semi-autonomous aberrant ecosystems.

Patel, S. J., Dao, S., Darie, C. C., & Clarkson, B. D. (2016) · PubMed Central · Cited by 9

Otago Glaucoma Surgery Outcome Study: Further Histology and Immunohistochemistry of Molteno Implant Blebs

Molteno, A. C., Bevin, T. H., Dempster, A. G., & Devereux, F. J. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-16257 · Cited by 9

Extracellular nucleotides and adenosine regulate microglial motility and their role in cerebral ischemia

Li, Z., Li, W., Qin, L., & Tang, M. (2013) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2013.06.003 · Cited by 10

Lipidomic analysis of local inflammation models shows a specific systemic acute phase response to lipopolysaccharides

Hahnefeld, L., Kornstädt, L., Kratz, D., Ferreirós, N., Geißlinger, G., Pierre, S. C., & Scholich, K. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2020.158822 · Cited by 9

Radiation‐induced apoptosis in retinal progenitor cells is p53‐dependent with caspase‐independent DNA fragmentation

Herzog, K., Schulz, A., Buerkle, C., Gromoll, C., & Braun, J. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05381.x · Cited by 9

Alteration of lipid composition of rat thymus during thymic atrophy by whole-body X-irradiation

Park, H. S., Kim, S., Lee, Y., Choi, M. S., & Choi, M.-U. (2006) · International Journal of Radiation Biology · doi:10.1080/09553000600617189 · Cited by 9

Endogenous humoral autoreactive immune responses to apoptotic cells: Effects on phagocytic uptake, chemotactic migration and antigenic spread

Das, J., Arora, P., Gracias, D. T., Praveen, A., Raj, B. P. J., Martin, E., & Pal, R. (2008) · European Journal of Immunology · doi:10.1002/eji.200838624 · Cited by 9

Caspases – Key Players in Apoptosis

Cade, C. E., & Clark, A. C. (2015) · Springer eBooks · doi:10.1007/978-3-319-19497-4_2 · Cited by 10

A Common Pathway for All Autoimmune Diseases? The Unholy Alliance of Environment, Cell Death and Nucleic Acids

Hoffmann, M. H., & Steiner, G. E. (2009) · Current Immunology Reviews · doi:10.2174/157339509787314387 · Cited by 9

Supramolecular complex formation in cell signaling and disease: an update on a recurrent theme in cell life and death

Leyton, L., & Quest, A. F. G. (2004) · Biological Research · doi:10.4067/s0716-97602004000100004 · Cited by 9

Role of Attraction and Danger Signals in the Uptake of Apoptotic and Necrotic Cells and its Immunological Outcome

Peter, C., Wesselborg, S., & Lauber, K. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9293-0_3 · Cited by 9

When clearance fails: the role of efferocytosis in COPD

Tournoy, I. S., Geirnaert, S., Krysko, D. V., & Bracke, K. R. (2026) · European Respiratory Review · doi:10.1183/16000617.0177-2025 · Cited by 8

The dynamic inflammatory profile of pregnancy can be monitored using a novel lipid-based mass spectrometry technique

Rees, A., Edwards-I-Coll, Z., Richards, O., Raikes, M. E., Angelini, R., & Thornton, C. A. (2023) · Molecular Omics · doi:10.1039/d2mo00294a · Cited by 8

Development of a Murine model to dissect the CpG-oligonucleotide-enhancement of the killing of human B Cells by rituximab

Buhé, V., Pers, J., Marianowski, R., Berthou, C., Youinou, P., & Loisel, S. (2009) · Journal of Autoimmunity · doi:10.1016/j.jaut.2009.08.007 · Cited by 8

Inflammation and cancer revisited: An hypothesis on the oncogenic potential of the apoptotic tumor cell

Gregory, C. D. (2013) · Autoimmunity · doi:10.3109/08916934.2012.755961 · Cited by 8

Investigation into the role of phosphatidylserine in modifying the susceptibility of human lymphocytes to secretory phospholipase A2 using cells deficient in the expression of scramblase

Nelson, J. A., Francom, L., Anderson, L. M., Damm, K., Baker, R., Chen, J., Franklin, S., Hamaker, A., Izidoro, I., Moss, E., et al. (2012) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2012.01.005 · Cited by 8

Starry Sky Pattern in Hematopoietic Neoplasms: A Review of Pathophysiology and Differential Diagnosis

Dy-Ledesma, J. L., Khoury, J. D., Agbay, R. L. M. C., Garcia, M., Miranda, R. N., & Medeiros, L. J. (2016) · Advances in Anatomic Pathology · doi:10.1097/pap.0000000000000127 · Cited by 8

Another win for endothelial progenitor cells: Endothelial progenitor cell-derived conditioned medium promotes proliferation and exerts neuroprotection in cultured neuronal progenitor cells

Widmer, H.-R., Sadanandan, N., & Santo, S. D. (2019) · Brain Circulation · doi:10.4103/bc.bc_41_19 · Cited by 8

Efficacy of Lysophosphatidylcholine as Direct Treatment in Combination with Colistin against Acinetobacter baumannii in Murine Severe Infections Models

Miró-Canturri, A., Ayerbe-Algaba, R., Me, J.-M., Pachón, J., & Smani, Y. (2021) · Antibiotics · doi:10.3390/antibiotics10020194 · Cited by 8

Peripheral Blood Mononuclear Cell Secretome for Tissue Repair

Beer, L., Simader, E., Mildner, M., Gyöngyösi, M., & Ankersmit, H. J. (2018) · Springer eBooks · doi:10.1007/978-3-319-37076-7_61-2 · Cited by 8

Highly cited German research contributions to the fields of radiation oncology, biology, and physics: focus on collaboration and diversity

Nieder, C. (2012) · Strahlentherapie und Onkologie · doi:10.1007/s00066-012-0154-8 · Cited by 8

Genetic Control of Susceptibility to Candida albicans in SM/J Mice

Radovanovic, I., Leung, V., Iliescu, A., Bongfen, S. E., Mullick, A., Langlais, D., & Gros, P. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400783 · Cited by 9

Mistletoe extracts (Viscum album L.) iscador interact with the cell cycle machinery and target survival mechanisms in cancer cells

Ramaekers, F. C. S., Harmsma, M., Tusenius, K., Schütte, B., Werner, M. T., & Ramos, M. H. (2007) · Medicina-buenos Aires · Cited by 8

B cell biology, apoptosis, and autoantibodies to phospholipids

Cook, M. (2004) · Thrombosis Research · doi:10.1016/j.thromres.2004.06.037 · Cited by 8

Fundamentals of Stem Cells: Why and How Patients' Own Adult Stem Cells Are the Next Generation of MedicinePreprint

Alt, E., Schmitz, C., & Bai, X. (2019) · Preprints.org · doi:10.20944/preprints201904.0200.v1 · Cited by 7

Evaluation of Exploratory Fluid Biomarker Results from a Phase 1 Senolytic Trial in Mild Alzheimer’s DiseasePreprint

Orr, M. E., Garbarino, V. R., Palavicini, J., Melendez, J., Barthélemy, N. R., He, Y., Kautz, T. F., Lopez‐Cruzan, M., Mathews, J. J., Xu, P., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3994894/v1 · Cited by 8

Targeting Frequent Efferocytosis in Tumor Microenvironment is a New Direction for Cancer Treatment

Zhu, G., Wan, X., Wu, W., Jia, L., Yu, X., Mo, H., Wang, X., Zhou, Q., Tang, Q., & Wang, S. (2025) · Small Science · doi:10.1002/smsc.202400479 · Cited by 7

The role of efferocytosis in inflammatory bowel disease

Liu, Y., Li, Z.-Z., Han, Y., & Wang, Q. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1524058 · Cited by 7

Apoptotic cells induce migration of phagocytes via caspase-3-mediated release of a lipid attraction signal." Cell 113(6

Lauber, K., Bohn, E., Kröber, S. M., & Xiao, Y.-J. (2003)

Come and get it!

Bell, É. (2003) · Nature reviews. Immunology · doi:10.1038/nri1171

Attraction of phagocytes by apoptotic cells is mediated by lysophosphatidylcholine

Müeller, R. B., Sheriff, A., Gaipl, U. S., Wesselborg, S., & Lauber, K. (2007) · Autoimmunity · doi:10.1080/08916930701356911 · Cited by 62

Eliminierung apoptotischer Zellen durch professionelle Phagozyten: Generierung, Freisetzung und Erkennung des monozytären Attraktionssignals Lysophosphatidylcholin und Bedeutung von Annexin I als Brückenprotein in der phagozytotischen Synapse

Waibel, M. (2007) · University writing server of the University of Hohenheim (Universität Hohenheim)

Migration to Apoptotic “Find-me” Signals Is Mediated via the Phagocyte Receptor G2A

Peter, C., Waibel, M., Radu, C. G., Yang, L. V., Witte, O. N., Schulze-Osthoff, K., Wesselborg, S., & Lauber, K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m706586200 · Cited by 258