Autoimmune Disease and Impaired Uptake of Apoptotic Cells in MFG-E8-Deficient Mice

Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages

Fadok, V. A., Voelker, D. R., Campbell, P. A., Cohen, J., Bratton, D. L., & Henson, P. M. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.7.2207 · Cited by 3,321

Programmed Cell Death in Animal Development

Jacobson, M. D., Weil, M., & RAFF, M. C. (1997) · Cell · doi:10.1016/s0092-8674(00)81873-5 · Cited by 2,685

A blast from the past: clearance of apoptotic cells regulates immune responses

Savill, J., Dransfield, I., Gregory, C. D., & Haslett, C. (2002) · Nature reviews. Immunology · doi:10.1038/nri957 · Cited by 1,574

Corpse clearance defines the meaning of cell death

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

Identification of a factor that links apoptotic cells to phagocytes

Hanayama, R., Tanaka, M., Miwa, K., Shinohara, A., Iwamatsu, A., & Nagata, S. (2002) · Nature · doi:10.1038/417182a · Cited by 1,401

Phagocytosis and clearance of apoptotic cells is mediated by MER

Scott, R. S., McMahon, E. J., Pop, S. M., Reap, E. A., Caricchio, R., Cohen, P. L., Earp, H. S., & Matsushima, G. K. (2001) · Nature · doi:10.1038/35075603 · Cited by 1,215

T-cell apoptosis detected in situ during positive and negative selection in the thymus

Surh, C. D., & Sprent, J. (1994) · Nature · doi:10.1038/372100a0 · Cited by 1,082

Systemic Exposure to Irradiated Apoptotic Cells Induces Autoantibody Production

Mevorach, D., Zhou, J. L., Song, X., & Elkon, K. B. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.2.387 · Cited by 567

Phosphatidylserine (PS) induces PS receptor–mediated macropinocytosis and promotes clearance of apoptotic cells

Hoffmann, P. R., deCathelineau, A. M., Ogden, C. A., Leverrier, Y., Bratton, D. L., Daleke, D. L., Ridley, A. J., Fadok, V. A., & Henson, P. M. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200108080 · Cited by 541

cDNA cloning of a mouse mammary epithelial cell surface protein reveals the existence of epidermal growth factor-like domains linked to factor VIII-like sequences.

Stubbs, J. D., Lekutis, C., Singer, K. L., Bui, A., Yuzuki, D., Srinivasan, U., & Parry, G. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.21.8417 · Cited by 313

Role of apoptosis failure in etiopathogenesis of systemic lupus erythematosus and murine lupus

Sarter, K., Schulze, C., Voll, R. E., & i, M. H. (2007) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.4.1.33

Hepatitis A virus, TIM-1 and allergy

Umetsu, D. T., & DeKruyff, R. H. (2009) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8903-1_4

Lúpus Eritematoso sistémico: causas, mecanismos patológicos e alvos terapêuticos futuros

Fonseca, S. (2009) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/x97t-9941

Identification of genes and pathways involved in alveolar epithelial cell differentiation using DNA microarray

Chen, Z. (2005) · SHAREOK (University of Oklahoma; Oklahoma State University; Central Oklahoma University)

in Cellular Membranes

Leventis, P. A., & Grinstein, S. (2010)

Investigating The Impact of Multipurpose Solutions Released From Silicone Hydrogel Lenses on Corneal Epithelial Cells, in vitro

Tanti, N. C. (2010) · UWSpace (University of Waterloo)

Toll-like receptor 9 and systemic autoimmune diseases

Rothenfußer, S., & Latz, E. (2006) · Birkhäuser Basel eBooks · doi:10.1007/3-7643-7441-1_3

Autoimmune Consequences of Histone Deimination during Neutrophil Activation

Dwivedi, N. (2011) · doi:10.21007/etd.cghs.2011.0077

Self/Non-self Discrimination by Toll-like Receptor 9

Mouchess, M. L. (2011) · eScholarship (California Digital Library)

Novel Therapeutic for Systemic Inflammation: Role of MFG-E8

Jacob, A., & Wang, P. (2014) · Springer eBooks · doi:10.1007/978-94-017-8765-9_7

La lactadhérine, acteur de l'angiogenèse

Silvestre, J., Théry, C., Levy, B. I., Tedgui, A., Amigorena, S., & Mallat, Z. (2005)

The role of MerTK and BAFF in dendritic cell-B cell interactions

Gohlke, P. R. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/2zf1-z813

Pulmonary Macrophage-Targeted Therapies-The Way Forward in Chronic Inflammatory Lung Diseases?

Hodge, S. J. (2012) · Journal of Pulmonary & Respiratory Medicine · doi:10.4172/2161-105x.1000e105

Toll-Like Receptors in Development of Systemic Autoimmune Disease

Marshak‐Rothstein, A., & Shlomchik, M. J. (2008) · CRC Press eBooks · doi:10.1201/9781420068269.ch12

Dendritic Cells as Sensors for Foreign and Self Nucleic Acids

Reindl, W., & Krug, A. (2008) · CRC Press eBooks · doi:10.1201/9781420068269.ch5

The Subset of Tissue Macrophages and Their Development Pathway

Kohyama, M. (2015) · KAGAKU TO SEIBUTSU · doi:10.1271/kagakutoseibutsu.53.593

This information is current as ProductionLeading to Autoantibody Th Cell + Causes Elevated B Cell and CD4 Germinal Centers of Mer-Deficient Mice Prolonged Apoptotic Cell Accumulation in

Khan, T. N., Wong, E. B., Soni, C., & Ziaur, S. M. (2014)

Milk Fat Globule-EGF Factor 8 for Liver Fibrosis Therapy: Creaming Off the Beneficial Effects of Mesenchymal Stromal Cells

Forbes, S. J. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.02.032

Fc-Epsilon Receptor (CD23) Expressing Follicular Dendritic Cells as a Main Prognostic Factor in Follicular Lymphoma

Falaleeva, N. A., Osmanov, E. A., & Tupitsyn, N. N. (2017) · Advances in Biological Chemistry · doi:10.4236/abc.2017.72007

Contributions of the Bone Marrow Microenvironment to Bone and Skeletal Metastasis.

Soki, F. N. (2014) · Deep Blue (University of Michigan)

Action immunitaire de chimiothérapies anticancéreuses : un exemple à travers les modes d'actions des cellules "Interferon-producting Killer Dendritic Cells".

Mignot, G. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Exploring the role of CD248/endosialin/TEM-1 on lymphoid stromal cells in secondary lymphoid organs

Steinthal, N. (2017) · University of Birmingham Institutional Research Archive (University of Birmingham)

Functional Dissection of Lupus Susceptibility Loci on the New Zealand Black Mouse Chromosome 1

Cheung, Y. H. (2010) · TSpace (University of Toronto)

Identification of Genetic Loci that Contribute to the Immunopathogenesis of Systemic Lupus Erythematosus using Congenic Mouse Strains

Loh, C. (2011) · TSpace (University of Toronto)

Phagocytosis Assay for Apoptotic Cells in Drosophila Embryos

Nonaka, S., Hori, A., Nakanishi, Y., & Kuraishi, T. (2017) · Journal of Visualized Experiments · doi:10.3791/56352

Apoptotic Cell Clearance in Gut Tissue: Role of Intestinal Regeneration

Numata, Y., Hirayama, D., Wagatsuma, K., Iida, T., & Nakase, H. (2018) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-98146-8_6

The Contribution Of Metabolism To The Regulation Of Caspase Activity And Cell Death In T Lymphocytes

Secinaro, M. A. (2019) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont)

Regulation of innate immune responses by Mertk

Williams, J. C. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/c327-5x75

Implicación de los receptores LXR en trastornos autoinmunes, "cuando el propio cuerpo es el enemigo"

González, N. A. (2010) · Acceda (Universidad de Las Palmas de Gran Canaria)

The Role of Type I Interferons in TLR7-Mediated Lupus and UVB-Induced Immune Cell Responses

Wolf, S. (2019) · Deep Blue (University of Michigan)

Mechanisms of autoimmunity

Rosen, A. (2008) · Elsevier eBooks · doi:10.1016/b978-0-323-04404-2.10050-8

Down-regulation of MFG-E8 by RNA interference combined with doxorubicin triggers melanoma destruction

Wei, B.-L. Z.-Q., & Italia, S.-V. (2015)

The functionalization of single-walled carbon nanotubes with biomolecules to target professional phagocytes and promote biodegradation

Konduru, N. V. (2010) · D-Scholarship@Pitt (University of Pittsburgh)

Annexin A5: shifting from molecular imaging tool to therapeutic agent in cardiovascular diseases

Schutters, K. (2013) · Research Publications (Maastricht University) · doi:10.26481/dis.20131205ks

MFG-E8 in the Blood Cell Homeostasis and Coagulation

Dasgupta, S. K., & Thiagarajan, P. (2014) · Springer eBooks · doi:10.1007/978-94-017-8765-9_4

Hydroxychloroquine Enhances Efferocytosis and Modulates the Gut Microbiome in Mice With Pristane-induced LupusPreprint

Xue, T.-Y., Hsieh, F.-H., Tsay, J.-C. J., Peng, H.-Y., Tsao, Y.-C., Yin, M., Chao, C., Tsai, S.-Y., Lin, C.-P., Chen, J., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-1094062/v1

Faculty Opinions recommendation of Receptor for advanced glycation end products binds to phosphatidylserine and assists in the clearance of apoptotic cells.

Reddy, S. P. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.720681897.793583610

Immunogenic Catagen Initiates Alopecia AreataPreprint

Kim, J. Y., & Christiano, A. M. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3992677

Faculty Opinions recommendation of Follicular helper T cells are required for systemic autoimmunity.

Anderson, M. S., & DeVoss, J. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1157152.617265

Faculty Opinions recommendation of Class A scavenger receptors regulate tolerance against apoptotic cells, and autoantibodies against these receptors are predictive of systemic lupus.

Berton, G. (2007) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1091442.545904

Faculty Opinions recommendation of Engulfment of cerebral apoptotic bodies controls the course of prion disease in a mouse strain-dependent manner.

Saas, P., & Perruche, S. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.5559956.5527054

Apoptosis

Bánfalvi, G. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9561-0_4

Hydroxychloroquine enhances efferocytosis and modulates the gut microbiome in mice with pristane-induced lupusPreprint

Xue, T.-Y., Hsieh, F.-H., Tsay, J.-C. J., Peng, H., Tsao, Y.-C., Yin, M., Chao, C., Tsai, S.-Y., Lin, C.-P., Chen, J., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1094062/v2

NMR solution structure of C2 domain of MFG-E8 and insights into its recognition with phosphatidylserine

Li, B. (2013) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/54855

Faculty Opinions recommendation of The phosphatidylserine receptor has essential functions during embryogenesis but not in apoptotic cell removal.

Gordon, S. (2004) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1020707.236457

Faculty Opinions recommendation of Autocrine mfge8 signaling prevents developmental exhaustion of the adult neural stem cell pool.

Pardal, R. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733939109.793552964

Defining novel physiological roles for cardiac-residen Macrophages

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

抄録（マイスター賞表彰式・受賞講演，Distinguished Endocrinologist Award（最優秀指導者賞）表彰式・受賞講演，研究奨励賞受賞講演，教育講演，クリニカルアワー）

(2010) · Folia Endocrinologica Japonica · doi:10.1507/endocrine.86.1_73

Animal Models

Mizui, M., & Tsokos, G. C. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-384929-8.00030-7

Elevated MFG-E8 in CSF in the Early Stage Indicates Rapid Recovery of Mild Aneurysmal SAH Patients

Pang, C., Peng, Z., Li, X.-J., Gao, Y., Liu, X., Wang, H., Lu, Y., Zhuang, Z., Zhang, Q., Li, W., et al. (2022) · Disease Markers · doi:10.1155/2022/6731286

Defective apoptotic cell contractility provokes sterile inflammation, leading to liver damage and tumour suppression

Julian, L., Naylor, G. D., Wickman, G., Rath, N., Castino, G. F., Stevenson, D., Bryson, S., Munro, J., McGarry, L., Mullin, M., et al. (2023) · doi:10.32920/21985070

Defective apoptotic cell contractility provokes sterile inflammation, leading to liver damage and tumour suppression

Julian, L., Naylor, G. D., Wickman, G., Rath, N., Castino, G. F., Stevenson, D., Bryson, S., Munro, J., McGarry, L., Mullin, M., et al. (2023) · doi:10.32920/21985070.v1

Influência da interação de complexos tricarbonilrênio(I) com biomoléculas nos efeitos citotóxicos em células tumorais

de Lavor, T. S. (2023) · doi:10.14393/ufu.di.2023.129

Data from MFG-E8/Lactadherin Promotes Tumor Growth in an Angiogenesis-Dependent Transgenic Mouse Model of Multistage Carcinogenesis

Neutzner, M., Lopez, T., Xu, F., Bergmann‐Leitner, E. S., Leitner, W. W., & Udey, M. C. (2023) · doi:10.1158/0008-5472.c.6495663

Data from Phosphatidylserine-Targeting Antibody Induces M1 Macrophage Polarization and Promotes Myeloid-Derived Suppressor Cell Differentiation

Yin, Y., Huang, X., Lynn, K. D., & Thorpe, P. E. (2023) · doi:10.1158/2326-6066.c.6547999.v1

Development of human cell-expressed tag-free rhMFG-E8 as a radiation mitigator and a therapeutic for acute kidney injuryPreprint

Chaung, W. W., Zhang, F., Ma, G., Yen, H.-T., Jacob, A., Brenner, M., & Wang, P. (2023) · Research Square · doi:10.21203/rs.3.rs-2809755/v1

Opsonization of Early Apoptotic Cells by IgG from Lupus Nephritis Amplifies Activation of Early Complement Components and Promotes Inflammatory Phagocytosis

Yang, X., & Sun, J. (2022) · Journal on oncology · doi:10.52768/2692-563x/1054

Deciphering the role of MFGE8 in lactation biology using CRISPR- CAS9 based gene editing in Buffalo mammary epithelial cellsPreprint

Vats, P., Kumar, R. C., Kumar, R., Kaushik, J. K., Mohanty, A. K., & Kumar, S. (2023) · Research Square · doi:10.21203/rs.3.rs-2975964/v1

Comparative analysis of the occupancy of Histone H3 Lysine 4 methylation in the cells treated with TGFβ and Interferonγ

Naik, A., Dalpatraj, N., & Thakur, N. (2023) · Gene · doi:10.1016/j.gene.2023.147601

Ex Vivo Mfg-E8 Treatment Improves the Function of Lungs Harvested from Non-Heart-Beating Donors in Preclinical Porcine ModelPreprint

Li, P., Peng, K., Liu, L. G., Liu, Q. Y., Huang, Z. H., Ahmad, D. M. S., Wei, X., & Gao, S. H. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4651301

Homoeostatic Versus Pathogenic Autoantibodies: Origin, Structure and Effector Functions

Atisha‐Fregoso, Y., Pozovskiy, R., Haque, S., Watanabe, M., Zou, Y.-R., & Diamond, B. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95895-0.00006-4

ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosisPreprint

Guillet, S., Lazarov, T., Jordan, N., Boisson, B., Tello‐Lafoz, M., Craddock, B. P., Zhou, T., Nishi, C., Bareja, R., Yang, H., et al. (2024) · eLife · doi:10.7554/elife.96085.1

An investigation of cell turnover in the planarian epidermis

Lee, J.-R. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10443

Ex vivo MFG-E8 treatment improves the function of lungs procured from cardiac death donors in preclinical porcine model

Li, P., Peng, K., Liu, L. G., Liu, Q. Y., Huang, Z., Ahmad, D. M. S., Wei, X., & Gao, S. H. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e33614

Reviewer #1 (Public Review): ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis

Guillet, S., Lazarov, T., Jordan, N., et al. (2024) · eLife · doi:10.7554/elife.96085.2.sa2

Reviewer #2 (Public Review): ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis

Guillet, S., Lazarov, T., Jordan, N., et al. (2024) · eLife · doi:10.7554/elife.96085.2.sa1

eLife Assessment: ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis

Kurosaki, T. (2024) · eLife · doi:10.7554/elife.96085.2.sa3

ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosisPreprint

Guillet, S., Lazarov, T., Jordan, N., Boisson, B., Tello‐Lafoz, M., Craddock, B. P., Zhou, T., Nishi, C., Bareja, R., Yang, H., et al. (2024) · eLife · doi:10.7554/elife.96085.2

Sesquiterpene Lactone Lactucopicrin Boosts Apoptotic Cell Clearance by Colonic Epithelial Cells and Alleviates Colitis in Mice

Du, Y., Li, S., Chen, G., Mao, Y., Zhu, S., Zhang, W., Kang, M., Sui, Y., & Wang, D. (2025) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.70062

The Study on the Health Effects of Immune Responses Through Food Components

Chikazawa, M. (2024) · KAGAKU TO SEIBUTSU · doi:10.1271/kagakutoseibutsu.62.283

The role of Axl/Mertk/Tyro3 receptor tyrosine kinases in the clearance of apoptotic cells

Seitz, H. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/acdt-6997

Lupus nephritis : the role of renal DNase I in the progression of the disease

Seredkina, N. (2011)

Additional file 1 of MFG-E8 and HMGB1 Are Involved in the Mechanism Underlying Alcohol-Induced Impairment of Macrophage Efferocytosis

Wang, X., Bu, H.-F., Zhong, W., Asai, A., Zhou, Z., & Tan, X.-D. (2013) · Figshare · doi:10.6084/m9.figshare.7194260

3,3’-Diindolylmethane blocks the dissemination of gastric cancer cells in the peritoneal cavity through the MFGE8-MAPK/ERK signaling pathway

Liu, J., Zhang, Y., Yan, L., Li, F., Liu, A., Yang, Y., Yang, C., Li, Y., & Zhang, Y. (2025) · Cancer Cell International · doi:10.1186/s12935-025-04137-7

Serial assessment of the novel biomarker MFGE8 in comparison with GFAP for predicting severity and outcome after traumatic brain injury

Zou, M., Tang, Z., Luo, D., Zhong, J., Huang, Q., Jiang, Q., & Hong, T. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1750940

Rôle du stroma dans la progression de l'adénocarcinome pancréatique

Secq, V. (2014) · theses.fr (ABES) · doi:10.70675/3c4b7878z3e71z44fbza7f3zc5e1e99b02a2

Étude des mécanismes extracellulaires régulant la fonction du récepteur MerTK au cours de la phagocytose rétinienne

Parinot, C. (2015) · theses.fr (ABES) · doi:10.70675/d9dc4ed9zdf25z4c75z9e2ez4776a72bb628

Role of RANKL in the differentiation of B cell associated stroma in secondary lymphoid organs

Allouche, F. (2018) · doi:10.70675/5fe260caz36a6z4e78zb8e9z6f260a1978d0

Fonction des phagocytes de la plaque de Peyer dans la réponse immunitaire mucosale

Silva, C. D. (2017) · doi:10.70675/43b477f9z088dz4b9ezb4dcz2c6503728697

Étude du mécanisme de génération de forces mécaniques par les cellules apoptotiques et leur transmission au reste du tissu

Ambrosini, A. (2018) · theses.fr (ABES) · doi:10.70675/ac40f21bzaefbz4dc6zae8cz8b53a91128aa

Biominéralisation de la coquille d oeuf de poule : mise en évidence d'un transport vésiculaire du minéral impliquant les protéines EGF-like repeats and discoidin-like domains 3 (EDIL3) et Milk fat globule EGF-factor 8 (MFGE8)

Stapane, L. (2019) · doi:10.70675/327b5ab0zfdf1z4d16zbe93z7341bb2b96ea

Differentiation and activation of Peyer’s patch phagocytes in adulthood and upon weaning

Wagner, C. (2020) · theses.fr (ABES) · doi:10.70675/c0f7e7aazfdf6z474dz826bz26f9444d5035

Polarisation macrophagique au cours de la sclérodermie systémique : liens avec les mécanismes d'autoimmunité induite par la silice cristalline et perspectives thérapeutiques dans des modèles in vitro et in vivo

Lescoat, A. (2020) · theses.fr (ABES) · doi:10.70675/ee1dfaddz0ce3z4c69z97c8z154f8f565f3b

MFG-E8 inhibits AT1-AA production to alleviate preeclampsia

Xie, F., Shi, Z., Zhu, J., Lin, C., Zhou, Y., & Lin, F. (2026) · Cellular Immunology · doi:10.1016/j.cellimm.2026.105110

Phosphatidylserine exposure and cancer immune evasion

Beltrán‐Visiedo, M., Campbell, K. S., & Galluzzi, L. (2026) · Cell Research · doi:10.1038/s41422-026-01252-6

Integrated analyses of in vivo mouse models and liver organoids reveal MFG-E8-mediated protection against hepatocyte injury

Bu, H., Jiang, Q., Geng, H., Subramanian, S., Khan, N. H., Wang, X., & Tan, X. (2026) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00079.2026

Phosphatidylserine expression on the cell membrane surface triggers multiple physiological reactions in hemostasis, apoptosis, and immune system regulation

Moumaris, M., & Abuaf, N. (2026) · Journal of Biosciences · doi:10.1007/s12038-026-00620-z

Macrophage biology and immunoregulation in health and disease

Zhao, H., Chou, Y.-J., & Huang, S. C. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01486-9

Toll-Like Receptor 9 and Toll-Like Receptor 7 in the Development and Regulation of Systemic Autoimmune Disease

Marshak‐Rothstein, A., & Cancro, M. P. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-404732-7.00006-x

Dynamics of the phosphatidylserine-expressing cell surface during endocytosis of Annexin A5

van Genderen, H. (2007) · Research Publications (Maastricht University) · doi:10.26481/dis.20071018hg

HMGB1, RAGE, and the Myeloid Response to Pancreatic Cancer

Vernon, P. J. (2014) · D-Scholarship@Pitt (University of Pittsburgh)

MFG-E8-Dependent Clearance of Apoptotic Cells, and Autoimmunity Caused by Its Failure

Hanayama, R., Miyasaka, K., Nakaya, M., & Nagata, S. (2005) · KARGER eBooks · doi:10.1159/000090780 · Cited by 69

Cell Death and Autoimmune Disease

(2004) · Science s STKE · doi:10.1126/stke.2342004tw188

Autoimmune Diseases and the Role of MFG-E8

Hanayama, R. (2014) · Springer eBooks · doi:10.1007/978-94-017-8765-9_6 · Cited by 2

Apoptotic cell clearance by phagocytes

Tanaka, M. (2005) · International Congress Series · doi:10.1016/j.ics.2005.07.080 · Cited by 4

Autoimmunity in MFG-E8-deficient mice is associated with altered trafficking and enhanced cross-presentation of apoptotic cell antigens.

Peng, Y.-F., & Elkon, K. (2011) · Journal of Clinical Investigation · doi:10.1172/jci43254 · Cited by 96