On the public citation graph

Apoptotic Cells Promote Their Own Clearance and Immune Tolerance through Activation of the Nuclear Receptor LXR

https://doi.org/10.1016/j.immuni.2009.06.018
0 signed · 730 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1529-0131(199807)41:7<1241::aid-art15>3.0.co;2-hopenalex-snapshot
Impaired phagocytosis of apoptotic cell material by monocyte-derived macrophages from patients with systemic lupus erythematosus
inferredcites →https://doi.org/10.1002/ar.1092290412openalex-snapshot
Kinetics of the tingible body macrophage response in mouse germinal center development and its depression with age
inferredcites →https://doi.org/10.1002/jnr.21038openalex-snapshot
Liver X receptor activation decreases the severity of experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1016/j.cell.2004.09.032openalex-snapshot
LXR-Dependent Gene Expression Is Important for Macrophage Survival and the Innate Immune Response
inferredcites →https://doi.org/10.1016/j.cell.2007.10.034openalex-snapshot
TAM Receptors Are Pleiotropic Inhibitors of the Innate Immune Response
inferredcites →https://doi.org/10.1016/j.cell.2008.04.052openalex-snapshot
LXR Signaling Couples Sterol Metabolism to Proliferation in the Acquired Immune Response
inferredcites →https://doi.org/10.1016/j.cmet.2005.01.002openalex-snapshot
ABCG1 has a critical role in mediating cholesterol efflux to HDL and preventing cellular lipid accumulation
inferredcites →https://doi.org/10.1016/j.febslet.2006.07.074openalex-snapshot
Phosphorylation of the liver X receptors
inferredcites →https://doi.org/10.1016/j.immuni.2008.03.003openalex-snapshot
Contextual Regulation of Inflammation: A Duet by Transforming Growth Factor-β and Interleukin-10
inferredcites →https://doi.org/10.1016/j.it.2006.03.005openalex-snapshot
Apoptotic cell removal in development and tissue homeostasis
inferredcites →https://doi.org/10.1016/j.jaut.2003.11.003openalex-snapshot
Decreased phagocytosis of apoptotic cells in diseased SLE mice
inferredcites →https://doi.org/10.1016/j.molcel.2006.11.022openalex-snapshot
Parallel SUMOylation-Dependent Pathways Mediate Gene- and Signal-Specific Transrepression by LXRs and PPARγ
inferredcites →https://doi.org/10.1016/j.tcb.2003.10.004openalex-snapshot
Cues for apoptotic cell engulfment: eat-me, don't eat-me and come-get-me signals
inferredcites →https://doi.org/10.1016/s0076-6879(99)04024-0openalex-snapshot
Mapping DNA interaction sites of chromosomal proteins using immunoprecipitation and polymerase chain reaction
inferredcites →https://doi.org/10.1016/s0092-8674(00)81432-4openalex-snapshot
Cholesterol and Bile Acid Metabolism Are Impaired in Mice Lacking the Nuclear Oxysterol Receptor LXRα
inferredcites →https://doi.org/10.1016/s0092-8674(03)00422-7openalex-snapshot
Apoptotic Cells Induce Migration of Phagocytes via Caspase-3-Mediated Release of a Lipid Attraction Signal
inferredcites →https://doi.org/10.1016/s0952-7915(00)00168-0openalex-snapshot
Apoptosis genes and autoimmunity
inferredcites →https://doi.org/10.1016/s0960-9822(01)00474-2openalex-snapshot
Apoptotic cell removal
inferredcites →https://doi.org/10.1016/s1074-7613(02)00302-3openalex-snapshot
Mice Lacking the p53-Effector Gene Gadd45a Develop a Lupus-Like Syndrome
inferredcites →https://doi.org/10.1016/s1097-2765(03)00384-8openalex-snapshot
Crosstalk between LXR and Toll-like Receptor Signaling Mediates Bacterial and Viral Antagonism of Cholesterol Metabolism
inferredcites →https://doi.org/10.1016/s1097-2765(04)00237-0openalex-snapshot
Clearance of Apoptotic Cells
inferredcites →https://doi.org/10.1021/jm0255116openalex-snapshot
Identification of a Nonsteroidal Liver X Receptor Agonist through Parallel Array Synthesis of Tertiary Amines
inferredcites →https://doi.org/10.1034/j.1600-065x.2003.00045.xopenalex-snapshot
Overview: apoptotic signaling pathways in the immune system
inferredcites →https://doi.org/10.1038/35017029openalex-snapshot
ABC1 promotes engulfment of apoptotic cells and transbilayer redistribution of phosphatidylserine.
inferredcites →https://doi.org/10.1038/35037722openalex-snapshot
Corpse clearance defines the meaning of cell death
inferredcites →https://doi.org/10.1038/35075603openalex-snapshot
Phagocytosis and clearance of apoptotic cells is mediated by MER
inferredcites →https://doi.org/10.1038/37022openalex-snapshot
Immunosuppressive effects of apoptotic cells
inferredcites →https://doi.org/10.1038/417182aopenalex-snapshot
Identification of a factor that links apoptotic cells to phagocytes
inferredcites →https://doi.org/10.1038/nature06307openalex-snapshot
Identification of Tim4 as a phosphatidylserine receptor
inferredcites →https://doi.org/10.1038/ng0598-56openalex-snapshot
Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies
inferredcites →https://doi.org/10.1038/nm1102-1243openalex-snapshot
The liver X receptor gene team: Potential new players in atherosclerosis
inferredcites →https://doi.org/10.1038/nm1724openalex-snapshot
Molecular imaging of lymphoid organs and immune activation by positron emission tomography with a new [18F]-labeled 2′-deoxycytidine analog
inferredcites →https://doi.org/10.1038/nm820openalex-snapshot
Reciprocal regulation of inflammation and lipid metabolism by liver X receptors
inferredcites →https://doi.org/10.1038/nri2214openalex-snapshot
Engulfment of apoptotic cells: signals for a good meal
inferredcites →https://doi.org/10.1038/nri2303openalex-snapshot
Immunobiology of the TAM receptors
inferredcites →https://doi.org/10.1038/nri702openalex-snapshot
Cytokines and autoimmunity
inferredcites →https://doi.org/10.1038/nri957openalex-snapshot
A blast from the past: clearance of apoptotic cells regulates immune responses
inferredcites →https://doi.org/10.1038/sj.cdd.4401900openalex-snapshot
Macrophages use different internalization mechanisms to clear apoptotic and necrotic cells
inferredcites →https://doi.org/10.1073/pnas.0701096104openalex-snapshot
Attenuation of neuroinflammation and Alzheimer's disease pathology by liver x receptors
inferredcites →https://doi.org/10.1073/pnas.182199799openalex-snapshot
Identification of macrophage liver X receptors as inhibitors of atherosclerosis
inferredcites →https://doi.org/10.1073/pnas.200367697openalex-snapshot
Control of cellular cholesterol efflux by the nuclear oxysterol receptor LXRα
inferredcites →https://doi.org/10.1074/jbc.m100474200openalex-snapshot
ATP-binding Cassette Transporter A1 Contains an NH2-terminal Signal Anchor Sequence That Translocates the Protein's First Hydrophilic Domain to the Exoplasmic Space
inferredcites →https://doi.org/10.1074/jbc.m213071200openalex-snapshot
Liver X Receptor-dependent Repression of Matrix Metalloproteinase-9 Expression in Macrophages
inferredcites →https://doi.org/10.1084/jem.174.4.827openalex-snapshot
Macrosialin, a macrophage-restricted membrane sialoprotein differentially glycosylated in response to inflammatory stimuli.
inferredcites →https://doi.org/10.1084/jem.20012094openalex-snapshot
Delayed Apoptotic Cell Clearance and Lupus-like Autoimmunity in Mice Lacking the c-mer Membrane Tyrosine Kinase
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a022622openalex-snapshot
Promotion of the Uptake of PS Liposomes and Apoptotic Cells by a Product of Growth Arrest-Specific Gene, gas6
inferredcites →https://doi.org/10.1126/science.1094359openalex-snapshot
Autoimmune Disease and Impaired Uptake of Apoptotic Cells in MFG-E8-Deficient Mice
inferredcites →https://doi.org/10.1128/mcb.21.22.7558-7568.2001openalex-snapshot
Autoregulation of the Human Liver X Receptor α Promoter
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.012103.134432openalex-snapshot
NUCLEAR RECEPTORS IN MACROPHAGE BIOLOGY: At the Crossroads of Lipid Metabolism and Inflammation
inferredcites →https://doi.org/10.1146/annurev.immunol.23.021704.115816openalex-snapshot
MACROPHAGE RECEPTORS AND IMMUNE RECOGNITION
inferredcites →https://doi.org/10.1159/000350152openalex-snapshot
Renal and Extrarenal Effects of Gum Arabic (Acacia Senegal) - What Can be Learned from Animal Experiments?
inferredcites →https://doi.org/10.1161/atvbaha.108.167197openalex-snapshot
Mertk Receptor Mutation Reduces Efferocytosis Efficiency and Promotes Apoptotic Cell Accumulation and Plaque Necrosis in Atherosclerotic Lesions of Apoe −/− Mice
inferredcites →https://doi.org/10.1161/atvbaha.108.169078openalex-snapshot
Defective Mer Receptor Tyrosine Kinase Signaling in Bone Marrow Cells Promotes Apoptotic Cell Accumulation and Accelerates Atherosclerosis
inferredcites →https://doi.org/10.1172/jci1112openalex-snapshot
Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF.
inferredcites →https://doi.org/10.1172/jci200523915openalex-snapshot
Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I
inferredcites →https://doi.org/10.1172/jci23915openalex-snapshot
Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I
inferredcites →https://doi.org/10.1177/096120339700600326openalex-snapshot
Defective Phagocytosis of Apoptotic Cells: Possible Explanation for the Induction of Autoantibodies in SLE
inferredcites →https://doi.org/10.1182/blood-2005-12-006858openalex-snapshot
Autoreactive MZ and B-1 B-cell activation by Faslpr is coincident with an increased frequency of apoptotic lymphocytes and a defect in macrophage clearance
inferredcites →https://doi.org/10.1182/blood-2006-04-017368openalex-snapshot
Apoptotic cells induce Mer tyrosine kinase–dependent blockade of NF-κB activation in dendritic cells
inferredcites →https://doi.org/10.1210/me.2003-0061openalex-snapshot
Liver X Receptor Signaling Pathways in Cardiovascular Disease
inferredcites →https://doi.org/10.4049/jimmunol.161.11.6250openalex-snapshot
CD36 Is Required for Phagocytosis of Apoptotic Cells by Human Macrophages That Use Either a Phosphatidylserine Receptor or the Vitronectin Receptor (αvβ3)
inferredcites →https://doi.org/10.4049/jimmunol.162.6.3498openalex-snapshot
A Novel Receptor Tyrosine Kinase, Mer, Inhibits TNF-α Production and Lipopolysaccharide-Induced Endotoxic Shock
inferredcites →https://doi.org/10.4049/jimmunol.170.6.3223openalex-snapshot
Lupus-Prone Mice Have an Abnormal Response to Thioglycolate and an Impaired Clearance of Apoptotic Cells
inferredcites →https://doi.org/10.4049/jimmunol.173.10.5971openalex-snapshot
Rac2-Deficient Murine Macrophages Have Selective Defects in Superoxide Production and Phagocytosis of Opsonized Particles
inferredcites →https://doi.org/10.4049/jimmunol.173.10.6366openalex-snapshot
Apolipoprotein E Modulates Clearance of Apoptotic Bodies In Vitro and In Vivo, Resulting in a Systemic Proinflammatory State in Apolipoprotein E-Deficient Mice

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4624957openalex-extracted
inferred← citeshttps://doi.org/10.1002/1873-3468.12702openalex-snapshot
Liver X receptors link lipid metabolism and inflammation
inferred← citeshttps://doi.org/10.1002/9781118105771.ch7openalex-snapshot
Transglutaminase 2 Dysfunctions in the Development of Autoimmune Disorders: Celiac Disease and TG2 − / − Mouse
inferred← citeshttps://doi.org/10.1002/adma.202308377openalex-snapshot
Enhancing CAR Macrophage Efferocytosis Via Surface Engineered Lipid Nanoparticles Targeting LXR Signaling
inferred← citeshttps://doi.org/10.1002/adtp.202100056openalex-snapshot
Targeting Lymphoid Tissues to Promote Immune Tolerance
inferred← citeshttps://doi.org/10.1002/advs.202307201openalex-snapshot
Reprogramming of the LXRα Transcriptome Sustains Macrophage Secondary Inflammatory Responses
inferred← citeshttps://doi.org/10.1002/advs.202513474openalex-snapshot
A Conjugation Delivery System of Macrophages and Platelet Pharmacytes Promotes Regeneration After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1002/art.30507openalex-snapshot
Increased synovial expression of nuclear receptors correlates with protection in pristane-induced arthritis: A possible novel genetically regulated homeostatic mechanism
inferred← citeshttps://doi.org/10.1002/art.43268openalex-snapshot
Efferocytosis and Its Role in Rheumatic Diseases
inferred← citeshttps://doi.org/10.1002/eji.201344292openalex-snapshot
LXR‐dependent and ‐independent effects of oxysterols on immunity and tumor growth
inferred← citeshttps://doi.org/10.1002/glia.22423openalex-snapshot
Regulation of microglia activation and deactivation by nuclear receptors
inferred← citeshttps://doi.org/10.1002/glia.24295openalex-snapshot
Microglia and astrocyte activation is region‐dependent in the α‐synuclein mouse model of Parkinson's disease
inferred← citeshttps://doi.org/10.1002/hep4.1078openalex-snapshot
Role of gp91phox in hepatic macrophage programming and alcoholic liver disease
inferred← citeshttps://doi.org/10.1002/hep4.1584openalex-snapshot
Activation of Liver X Receptor α Sensitizes Mice to T‐Cell Mediated Hepatitis
inferred← citeshttps://doi.org/10.1002/hep4.1880openalex-snapshot
Chronic Activation of LXRα Sensitizes Mice to Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.1002/iid3.779openalex-snapshot
Progranulin deficiency suppresses allergic asthma and enhances efferocytosis via PPAR‐γ/MFG‐E8 regulation in macrophages
inferred← citeshttps://doi.org/10.1002/jlb.2a0817-341rropenalex-snapshot
Apoptotic cells trigger the ABCA1/STAT6 pathway leading to PPAR-γ expression and activation in macrophages
inferred← citeshttps://doi.org/10.1002/jlb.5hi0420-648ropenalex-snapshot
Frontline Science: Activation of metabolic nuclear receptors restores periodontal tissue homeostasis in mice with leukocyte adhesion deficiency-1
inferred← citeshttps://doi.org/10.1002/mco2.70764openalex-snapshot
Efferocytosis: Signaling Pathways and New Therapeutic Strategies for Diseases
inferred← citeshttps://doi.org/10.1002/path.2792openalex-snapshot
Cell death in the neighbourhood: direct microenvironmental effects of apoptosis in normal and neoplastic tissues
inferred← citeshttps://doi.org/10.1002/path.4108openalex-snapshot
Hanging in the balance: endogenous anti‐inflammatory mechanisms in tissue repair and fibrosis
inferred← citeshttps://doi.org/10.1002/path.6138openalex-snapshot
Extracellular vesicles arising from apoptosis: forms, functions, and applications
inferred← citeshttps://doi.org/10.1002/stem.2361openalex-snapshot
Concise Review: Apoptotic Cell-Based Therapies–Rationale, Preclinical Results and Future Clinical Developments
inferred← citeshttps://doi.org/10.1007/82_2015_467openalex-snapshot
Prix Fixe: Efferocytosis as a Four-Course Meal
inferred← citeshttps://doi.org/10.1007/978-1-4419-9371-7_5openalex-snapshot
Apoptosis and TH17 Cell Differentiation
inferred← citeshttps://doi.org/10.1007/978-1-4419-9461-5_18openalex-snapshot
Signaling in Atherosclerosis
inferred← citeshttps://doi.org/10.1007/978-1-4614-0106-3_19openalex-snapshot
Nutritional Immunity: Homology Modeling of Nramp Metal Import
inferred← citeshttps://doi.org/10.1007/978-1-4939-1311-4_18openalex-snapshot
Macrophages Govern the Progression and Termination of Inflammation in Atherosclerosis and Metabolic Diseases
inferred← citeshttps://doi.org/10.1007/978-1-4939-3338-9_5openalex-snapshot
Detection and Functional Analysis of Tumor-Derived LXR Ligands
inferred← citeshttps://doi.org/10.1007/978-1-4939-9130-3_11openalex-snapshot
Measuring Apoptotic Cell Engulfment (Efferocytosis) Efficiency
inferred← citeshttps://doi.org/10.1007/978-1-4939-9130-3_6openalex-snapshot
Bone Marrow-Derived Macrophage Immortalization of LXR Nuclear Receptor-Deficient Cells
inferred← citeshttps://doi.org/10.1007/978-1-60761-720-4_7openalex-snapshot
Experimental Use of Mouse Models of Systemic Lupus Erythematosus
inferred← citeshttps://doi.org/10.1007/978-3-030-50480-9_10openalex-snapshot
Practical Approaches in M2 Macrophage Biology: Analysis, Pharmacology, and Didactical Interpretation of M2 Macrophage Functions
inferred← citeshttps://doi.org/10.1007/978-3-030-50480-9_4openalex-snapshot
Signal Mechanisms of M2 Macrophage Activation
inferred← citeshttps://doi.org/10.1007/978-3-030-50480-9_6openalex-snapshot
Immune Functions of the M2 Macrophages: Host Defense, Self-tolerance, and Autoimmunity
inferred← citeshttps://doi.org/10.1007/978-3-031-43883-7_7openalex-snapshot
Oxysterols in Infectious Diseases
inferred← citeshttps://doi.org/10.1007/978-3-031-92785-0_4openalex-snapshot
Metabolic Implications of Efferocytosis During Inflammation
inferred← citeshttps://doi.org/10.1007/978-3-0348-0620-6_207-1openalex-snapshot
Nuclear Receptor Signaling in the Control of Inflammation
inferred← citeshttps://doi.org/10.1007/978-3-319-11888-8_2openalex-snapshot
The TAM Receptor Family
inferred← citeshttps://doi.org/10.1007/978-3-319-39406-0_2openalex-snapshot
Clearance of Dying Cells by Phagocytes: Mechanisms and Implications for Disease Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-39406-0_3openalex-snapshot
Microenvironmental Effects of Cell Death in Malignant Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-39406-0_5openalex-snapshot
Axl and Mer Receptor Tyrosine Kinases: Distinct and Nonoverlapping Roles in Inflammation and Cancer?
inferred← citeshttps://doi.org/10.1007/978-3-7643-8550-7_207openalex-snapshot
Nuclear Receptor Signaling in the Control of Inflammation
inferred← citeshttps://doi.org/10.1007/978-981-96-3675-4_8openalex-snapshot
Cell Death in Atherosclerosis: Apoptosis? Or Necrosis? Or More?
inferred← citeshttps://doi.org/10.1007/s00005-010-0093-yopenalex-snapshot
Monocyte and Macrophage Abnormalities in Systemic Lupus Erythematosus
inferred← citeshttps://doi.org/10.1007/s00005-012-0179-9openalex-snapshot
Biological Roles of Liver X Receptors in Immune Cells
inferred← citeshttps://doi.org/10.1007/s00011-023-01811-2openalex-snapshot
Effects of neutrophil fate on inflammation
inferred← citeshttps://doi.org/10.1007/s00018-013-1261-0openalex-snapshot
O death where is thy sting? Immunologic tolerance to apoptotic self
inferred← citeshttps://doi.org/10.1007/s00018-026-06314-xopenalex-snapshot
FADS1-mediated Efferocytosis in Tumor-Associated Macrophages Shapes an Immunosuppressive Microenvironment in Gastric Cancer
inferred← citeshttps://doi.org/10.1007/s00109-010-0673-7openalex-snapshot
The role of nucleotides in apoptotic cell clearance: implications for disease pathogenesis
inferred← citeshttps://doi.org/10.1007/s00262-015-1779-0openalex-snapshot
Cholesterol metabolites and tumor microenvironment: the road towards clinical translation
inferred← citeshttps://doi.org/10.1007/s00281-018-0698-5openalex-snapshot
Efferocytosis in the tumor microenvironment
inferred← citeshttps://doi.org/10.1007/s00281-018-0699-4openalex-snapshot
Acute and chronic phagocyte determinants of cardiac allograft vasculopathy
inferred← citeshttps://doi.org/10.1007/s00395-015-0520-7openalex-snapshot
Emerging role of liver X receptors in cardiac pathophysiology and heart failure
inferred← citeshttps://doi.org/10.1007/s00401-014-1310-2openalex-snapshot
Macrophage subsets and microglia in multiple sclerosis
inferred← citeshttps://doi.org/10.1007/s00424-017-1941-yopenalex-snapshot
Macrophages in vascular inflammation and atherosclerosis
inferred← citeshttps://doi.org/10.1007/s00726-011-1119-4openalex-snapshot
Retinoids produced by macrophages engulfing apoptotic cells contribute to the appearance of transglutaminase 2 in apoptotic thymocytes
inferred← citeshttps://doi.org/10.1007/s10067-012-2033-1openalex-snapshot
The beneficial role of vitamin D in systemic lupus erythematosus (SLE)
inferred← citeshttps://doi.org/10.1007/s10456-018-9604-yopenalex-snapshot
Time-dependent LXR/RXR pathway modulation characterizes capillary remodeling in inflammatory corneal neovascularization
inferred← citeshttps://doi.org/10.1007/s10495-010-0509-5openalex-snapshot
A model to die for: signaling to apoptotic cell removal in worm, fly and mouse
inferred← citeshttps://doi.org/10.1007/s10495-010-0516-6openalex-snapshot
Mechanisms of failed apoptotic cell clearance by phagocyte subsets in cardiovascular disease
inferred← citeshttps://doi.org/10.1007/s10495-010-0530-8openalex-snapshot
Clearance of dying cells and systemic lupus erythematosus: the role of C1q and the complement system
inferred← citeshttps://doi.org/10.1007/s10495-013-0873-zopenalex-snapshot
Novel role of ICAM3 and LFA-1 in the clearance of apoptotic neutrophils by human macrophages
inferred← citeshttps://doi.org/10.1007/s10495-016-1310-xopenalex-snapshot
Transcriptional control of apoptotic cell clearance by macrophage nuclear receptors
inferred← citeshttps://doi.org/10.1007/s10555-011-9283-2openalex-snapshot
How to improve the immunogenicity of chemotherapy and radiotherapy
inferred← citeshttps://doi.org/10.1007/s10620-014-3284-2openalex-snapshot
Targeting Apoptosis in Autoimmune Hepatitis
inferred← citeshttps://doi.org/10.1007/s10620-015-3708-7openalex-snapshot
Transitioning from Idiopathic to Explainable Autoimmune Hepatitis
inferred← citeshttps://doi.org/10.1007/s11882-015-0548-7openalex-snapshot
Regulation of Adaptive Immunity in Health and Disease by Cholesterol Metabolism
inferred← citeshttps://doi.org/10.1007/s11883-012-0239-yopenalex-snapshot
Liver X Receptors, Atherosclerosis and Inflammation
inferred← citeshttps://doi.org/10.1007/s11883-025-01294-yopenalex-snapshot
The Atherosclerotic Plaque Microenvironment as a Therapeutic Target
inferred← citeshttps://doi.org/10.1007/s11892-021-01376-6openalex-snapshot
Auto-antigen and Immunomodulatory Agent–Based Approaches for Antigen-Specific Tolerance in NOD Mice
inferred← citeshttps://doi.org/10.1007/s12016-013-8403-xopenalex-snapshot
Photosensitivity, Apoptosis, and Cytokines in the Pathogenesis of Lupus Erythematosus: a Critical Review
inferred← citeshttps://doi.org/10.1007/s12016-025-09023-8openalex-snapshot
Lipid Metabolism: An Emerging Player in Sjögren’s Syndrome
inferred← citeshttps://doi.org/10.1007/s12032-023-02153-zopenalex-snapshot
Targeting MerTK decreases efferocytosis and increases anti-tumor immune infiltrate in prostate cancer
inferred← citeshttps://doi.org/10.1007/s12185-014-1561-7openalex-snapshot
Innate immune cells as homeostatic regulators of the hematopoietic niche
inferred← citeshttps://doi.org/10.1007/s12264-026-01693-4openalex-snapshot
An ApoE-Associated Low-Inflammatory Microglial State Emerges After Inflammatory Challenge in Alzheimer’s Disease Mice
inferred← citeshttps://doi.org/10.1007/s13311-014-0316-8openalex-snapshot
The Evolving Biology of Microglia in Alzheimer's Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.11012-4openalex-snapshot
Nuclear Receptors in Immune Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-380995-7.00001-xopenalex-snapshot
Macrophage Proinflammatory Activation and Deactivation
inferred← citeshttps://doi.org/10.1016/b978-0-12-404599-6.00006-8openalex-snapshot
Molecular Determinants of Atherosclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-804274-8.00004-7openalex-snapshot
Autoimmune Hepatitis
inferred← citeshttps://doi.org/10.1016/b978-0-12-813753-6.00003-2openalex-snapshot
Roles for AXL and MERTK in Resistance to Cytotoxic and Targeted Therapies
inferred← citeshttps://doi.org/10.1016/b978-0-12-821385-8.00001-9openalex-snapshot
Spleen, lymph nodes, and lymphoid tissues—Inflammatory system
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2019.02.004openalex-snapshot
Voices from the dead: The complex vocabulary and intricate grammar of dead cells
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2018.08.006openalex-snapshot
Activating the Nucleic Acid-Sensing Machinery for Anticancer Immunity
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2020.09.011openalex-snapshot
Immunological role of TAM receptors in the cancer microenvironment
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2014.10.011openalex-snapshot
EBV, the Human Host, and the 7TM Receptors
inferred← citeshttps://doi.org/10.1016/j.addr.2019.05.007openalex-snapshot
Intrinsic cancer vaccination
inferred← citeshttps://doi.org/10.1016/j.alit.2015.03.001openalex-snapshot
Activation of LXRs using the synthetic agonist GW3965 represses the production of pro-inflammatory cytokines by murine mast cells
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102757openalex-snapshot
Intercellular communication after myocardial infarction: Macrophage as the centerpiece
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102967openalex-snapshot
Liver X receptors and the hallmarks of aging: From molecular mechanisms to therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2010.01.011openalex-snapshot
ABC transporters, atherosclerosis and inflammation
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2015.06.042openalex-snapshot
Liver X receptors at the intersection of lipid metabolism and atherogenesis
inferred← citeshttps://doi.org/10.1016/j.autrev.2017.04.006openalex-snapshot
Dysregulated homeostasis of target tissues or autoantigens - A novel principle in autoimmunity
inferred← citeshttps://doi.org/10.1016/j.autrev.2024.103578openalex-snapshot
Efferocytosis: Unveiling its potential in autoimmune disease and treatment strategies
inferred← citeshttps://doi.org/10.1016/j.bbadis.2010.12.015openalex-snapshot
Liver X receptors as regulators of macrophage inflammatory and metabolic pathways
inferred← citeshttps://doi.org/10.1016/j.bbadis.2018.10.005openalex-snapshot
The deficiency of macrophage erythropoietin signaling contributes to delayed acute inflammation resolution in diet-induced obese mice
inferred← citeshttps://doi.org/10.1016/j.bbalip.2011.06.003openalex-snapshot
n−3 Fatty acids ameliorate hepatic steatosis and dysfunction after LXR agonist ingestion in mice
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.12.014openalex-snapshot
Glucocorticoids enhance prolonged clearance of apoptotic cells by upregulating liver X receptor, peroxisome proliferator-activated receptor-δ and UCP2
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119434openalex-snapshot
Cytoskeletal orchestration of glucose uptake in Sertoli cell to support efferocytosis of apoptotic germ cells
inferred← citeshttps://doi.org/10.1016/j.bbi.2025.106089openalex-snapshot
LXR-β regulates microglial efferocytosis and neuroinflammation in CPSP via STAT6 activation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.11.005openalex-snapshot
Elimination of the unnecessary: Intra- and extracellular signaling by anionic phospholipids
inferred← citeshttps://doi.org/10.1016/j.bbrep.2025.102161openalex-snapshot
The potential of efferocytosis for the treatment of bronchial asthma: A review of current trends, mechanisms and prospects
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2022.07.026openalex-snapshot
Apoptotic vesicles ameliorate lupus and arthritis via phosphatidylserine-mediated modulation of T cell receptor signaling
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.05.026openalex-snapshot
Efferocytosis in tissue engineering: A comprehensive review of emerging therapeutic strategies for enhanced tissue repair and regeneration
inferred← citeshttps://doi.org/10.1016/j.biocel.2012.04.024openalex-snapshot
From tumor cell metabolism to tumor immune escape
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.01.034openalex-snapshot
Apoptotic cell-mimicking gold nanocages loaded with LXR agonist for attenuating the progression of murine systemic lupus erythematosus
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115540openalex-snapshot
Efferocytosis: An accomplice of cancer immune escape
inferred← citeshttps://doi.org/10.1016/j.bone.2020.115807openalex-snapshot
Liver X receptors and skeleton: Current state-of-knowledge
inferred← citeshttps://doi.org/10.1016/j.carbpol.2022.119632openalex-snapshot
Cyclodextrin boostered-high density lipoprotein for antiatherosclerosis by regulating cholesterol efflux and efferocytosis
inferred← citeshttps://doi.org/10.1016/j.cell.2011.04.005openalex-snapshot
Macrophages in the Pathogenesis of Atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.cell.2011.12.006openalex-snapshot
Metabolic Connections during Apoptotic Cell Engulfment
inferred← citeshttps://doi.org/10.1016/j.cell.2012.06.054openalex-snapshot
Regulated Accumulation of Desmosterol Integrates Macrophage Lipid Metabolism and Inflammatory Responses
inferred← citeshttps://doi.org/10.1016/j.cell.2013.04.040openalex-snapshot
Rhythmic Modulation of the Hematopoietic Niche through Neutrophil Clearance
inferred← citeshttps://doi.org/10.1016/j.cell.2018.09.025openalex-snapshot
Aster: A New Star in Cholesterol Trafficking
inferred← citeshttps://doi.org/10.1016/j.cell.2020.05.003openalex-snapshot
The Physiology, Pathology, and Potential Therapeutic Applications of the TREM2 Signaling Pathway
inferred← citeshttps://doi.org/10.1016/j.cellimm.2018.05.005openalex-snapshot
Origin and specialization of splenic macrophages
inferred← citeshttps://doi.org/10.1016/j.cellimm.2025.104957openalex-snapshot
Potential therapeutic strategies targeting efferocytosis for inflammation resolution and tissue repair in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.01.007openalex-snapshot
The Nuclear Receptor LXR Limits Bacterial Infection of Host Macrophages through a Mechanism that Impacts Cellular NAD Metabolism
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.11.100openalex-snapshot
LXR Suppresses Inflammatory Gene Expression and Neutrophil Migration through cis-Repression and Cholesterol Efflux
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.101openalex-snapshot
Dead Cells Induce Innate Anergy Via Mertk after Acute Viral Infection
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110222openalex-snapshot
Polyamine import and accumulation causes immunomodulation in macrophages engulfing apoptotic cells
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2011.06.004openalex-snapshot
Liver X Receptor: an oxysterol sensor and a major player in the control of lipogenesis
inferred← citeshttps://doi.org/10.1016/j.clim.2019.06.009openalex-snapshot
The contribution of macrophages to systemic lupus erythematosus
inferred← citeshttps://doi.org/10.1016/j.clim.2020.108361openalex-snapshot
Common innate pathways to autoimmune disease
inferred← citeshttps://doi.org/10.1016/j.clim.2021.108764openalex-snapshot
Myxomavirus serpin alters macrophage function and prevents diffuse alveolar hemorrhage in pristane-induced lupus
inferred← citeshttps://doi.org/10.1016/j.cmet.2013.04.021openalex-snapshot
Reciprocal Regulation of Hepatic and Adipose Lipogenesis by Liver X Receptors in Obesity and Insulin Resistance
inferred← citeshttps://doi.org/10.1016/j.cmet.2016.07.016openalex-snapshot
Beneficial and Adverse Effects of an LXR Agonist on Human Lipid and Lipoprotein Metabolism and Circulating Neutrophils
inferred← citeshttps://doi.org/10.1016/j.cmet.2016.11.009openalex-snapshot
SREBP1 Contributes to Resolution of Pro-inflammatory TLR4 Signaling by Reprogramming Fatty Acid Metabolism
inferred← citeshttps://doi.org/10.1016/j.cmet.2017.04.005openalex-snapshot
Cholesterol Accumulation in Dendritic Cells Links the Inflammasome to Acquired Immunity
inferred← citeshttps://doi.org/10.1016/j.cmet.2018.12.004openalex-snapshot
Efferocytosis Fuels Requirements of Fatty Acid Oxidation and the Electron Transport Chain to Polarize Macrophages for Tissue Repair
inferred← citeshttps://doi.org/10.1016/j.cmet.2020.01.001openalex-snapshot
Macrophage Metabolism of Apoptotic Cell-Derived Arginine Promotes Continual Efferocytosis and Resolution of Injury
inferred← citeshttps://doi.org/10.1016/j.cmet.2021.08.001openalex-snapshot
First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis
inferred← citeshttps://doi.org/10.1016/j.cmet.2021.10.015openalex-snapshot
Efferocytosis induces macrophage proliferation to help resolve tissue injury
inferred← citeshttps://doi.org/10.1016/j.coi.2010.01.003openalex-snapshot
Infection and apoptosis as a combined inflammatory trigger
inferred← citeshttps://doi.org/10.1016/j.coi.2010.09.008openalex-snapshot
The dendritic cell–tumor cross-talk in cancer
inferred← citeshttps://doi.org/10.1016/j.coi.2010.10.001openalex-snapshot
TAM receptor signaling and autoimmune disease
inferred← citeshttps://doi.org/10.1016/j.coph.2012.07.003openalex-snapshot
Control of the immune system by oxysterols and cancer development
inferred← citeshttps://doi.org/10.1016/j.coph.2020.02.003openalex-snapshot
Lipid metabolism as a mechanism of immunomodulation in macrophages: the role of liver X receptors
inferred← citeshttps://doi.org/10.1016/j.coph.2020.05.001openalex-snapshot
Integrating the roles of liver X receptors in inflammation and infection: mechanisms and outcomes
inferred← citeshttps://doi.org/10.1016/j.cyto.2016.12.003openalex-snapshot
Liver X receptors agonists suppress NLRP3 inflammasome activation
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2017.06.005openalex-snapshot
Tumor-derived factors affecting immune cells
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2023.06.008openalex-snapshot
Lipid metabolism in regulation of B cell development and autoimmunity
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2025.05.002openalex-snapshot
Efferocytosis at the frontline of homeostasis: Shaping the bone microenvironment and therapeutic implications in related diseases
inferred← citeshttps://doi.org/10.1016/j.dci.2016.08.007openalex-snapshot
Molecular and functional characterization of liver X receptor in ayu, Plecoglossus altivelis: Regulator of inflammation and efferocytosis
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.173873openalex-snapshot
Apoptotic neurons and amyloid-beta clearance by phagocytosis in Alzheimer's disease: Pathological mechanisms and therapeutic outlooks
inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.175953openalex-snapshot
Liver X receptors: From pharmacology to nanoparticle-based drug delivery
inferred← citeshttps://doi.org/10.1016/j.expneurol.2015.12.003openalex-snapshot
Rescuing effects of RXR agonist bexarotene on aging-related synapse loss depend on neuronal LRP1
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.105498openalex-snapshot
Modulation of efferocytosis and inflammation resolution by live and non-live probiotics through gut microbiota interactions in preclinical and clinical studies
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.06.027openalex-snapshot
Nuclear receptors: TH17 cell control from within
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.08.010openalex-snapshot
Mitochondrial regulation of macrophage cholesterol homeostasis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.02.010openalex-snapshot
Macrophage polarization by potential nutraceutical compounds: A strategic approach to counteract inflammation in atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.05.004openalex-snapshot
TREM2 protects against inflammation by regulating the release of mito-DAMPs from hepatocytes during liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.06.002openalex-snapshot
Biological functions and biomedical applications of extracellular vesicles derived from blood cells
inferred← citeshttps://doi.org/10.1016/j.healun.2021.11.011openalex-snapshot
Plasma proteome of brain-dead organ donors predicts heart transplant outcome
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e28399openalex-snapshot
Efferocytosis: Current status and future prospects in the treatment of autoimmune diseases
inferred← citeshttps://doi.org/10.1016/j.ijrobp.2019.03.028openalex-snapshot
LXR Signaling Regulates Macrophage Survival and Inflammation in Response to Ionizing Radiation
inferred← citeshttps://doi.org/10.1016/j.imbio.2013.06.009openalex-snapshot
Macrophages engulfing apoptotic thymocytes produce retinoids to promote selection, differentiation, removal and replacement of double positive thymocytes
inferred← citeshttps://doi.org/10.1016/j.imlet.2023.02.001openalex-snapshot
Cellular mechanisms underlying the impairment of macrophage efferocytosis
inferred← citeshttps://doi.org/10.1016/j.immuni.2013.10.010openalex-snapshot
The Spleen in Local and Systemic Regulation of Immunity
inferred← citeshttps://doi.org/10.1016/j.immuni.2016.01.002openalex-snapshot
Erythropoeitin Signaling in Macrophages Promotes Dying Cell Clearance and Immune Tolerance
inferred← citeshttps://doi.org/10.1016/j.immuni.2016.11.008openalex-snapshot
Cholesterol Accumulation in CD11c+ Immune Cells Is a Causal and Targetable Factor in Autoimmune Disease
inferred← citeshttps://doi.org/10.1016/j.immuni.2016.12.006openalex-snapshot
Immune Cell Intolerance for Excess Cholesterol
inferred← citeshttps://doi.org/10.1016/j.immuni.2017.10.006openalex-snapshot
Tissue-Resident Macrophages Are Locally Programmed for Silent Clearance of Apoptotic Cells
inferred← citeshttps://doi.org/10.1016/j.immuni.2019.02.001openalex-snapshot
Dysregulated Lung Commensal Bacteria Drive Interleukin-17B Production to Promote Pulmonary Fibrosis through Their Outer Membrane Vesicles
inferred← citeshttps://doi.org/10.1016/j.immuni.2022.12.003openalex-snapshot
Control of tumor-associated macrophage responses by nutrient acquisition and metabolism
inferred← citeshttps://doi.org/10.1016/j.immuni.2023.03.018openalex-snapshot
Age-dependent differences in efferocytosis determine the outcome of opsonophagocytic protection from invasive pathogens
inferred← citeshttps://doi.org/10.1016/j.intimp.2011.09.002openalex-snapshot
Synthetic LXR agonist T0901317 attenuates lipopolysaccharide-induced acute lung injury in rats
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.106134openalex-snapshot
The role of nuclear factors as “Find-Me”/alarmin signals and immunostimulation in defective efferocytosis and related disorders
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.107177openalex-snapshot
Autoantigen-specific immune tolerance in pathological and physiological cell death: Nanotechnology comes into view
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.107240openalex-snapshot
Regulation of cytochrome P450 4F11 expression by liver X receptor alpha
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.111692openalex-snapshot
Indoleamine 2, 3-dioxygenase 1 activation in macrophage exacerbates hepatic ischemia-reperfusion injury by triggering hepatocyte ferroptosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112042openalex-snapshot
Current understanding on TREM-2 molecular biology and physiopathological functions
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112343openalex-snapshot
IL-17A/IL-17RA interaction blockade sensitizes synovial macrophages to efferocytosis and PD-L1 signaling via rewiring STAT-3/ADAM17/MERTK axis in rheumatoid arthritis animal model
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115088openalex-snapshot
Macrophages Atp6v0d2 regulates XBP1-mediated cholesterol metabolism to suppress metabolic dysfunction-associated steatohepatitis progression
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115990openalex-snapshot
Interplay between lipid metabolism and macrophage dynamics in ischemic stroke: From mechanistic insights to therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.isci.2024.109454openalex-snapshot
Disease phenotypic screening in neuron-glia cocultures identifies blockers of inflammatory neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115307openalex-snapshot
Deletion of miR-130b/301b cluster promotes macrophage efferocytosis and resolution of adipose tissue inflammation
inferred← citeshttps://doi.org/10.1016/j.isci.2026.117238openalex-snapshot
BOLD-100 treatment induces systemic lipid crosstalk in metastatic colorectal carcinoma patients in a combination treatment with FOLFOX
inferred← citeshttps://doi.org/10.1016/j.it.2011.04.009openalex-snapshot
Neutrophil clearance: when the party is over, clean-up begins
inferred← citeshttps://doi.org/10.1016/j.it.2016.09.001openalex-snapshot
The Intracellular Cholesterol Landscape: Dynamic Integrator of the Immune Response
inferred← citeshttps://doi.org/10.1016/j.it.2017.06.009openalex-snapshot
Programmed Cell Death and Inflammation: Winter Is Coming
inferred← citeshttps://doi.org/10.1016/j.it.2021.08.004openalex-snapshot
What’s the deal with efferocytosis and asthma?
inferred← citeshttps://doi.org/10.1016/j.it.2023.10.004openalex-snapshot
Macrophage phenotypes and functions: resolving inflammation and restoring homeostasis
inferred← citeshttps://doi.org/10.1016/j.jaci.2013.05.044openalex-snapshot
The role of lipid-activated nuclear receptors in shaping macrophage and dendritic cell function: From physiology to pathology
inferred← citeshttps://doi.org/10.1016/j.jaut.2021.102723openalex-snapshot
Liver X receptor beta deficiency attenuates autoimmune-associated neuroinflammation in a T cell-dependent manner
inferred← citeshttps://doi.org/10.1016/j.jbspin.2015.01.008openalex-snapshot
The association of Tyro3/Axl/Mer signaling with inflammatory response, disease activity in patients with primary Sjögren's syndrome
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2022.01.002openalex-snapshot
Macrophage COX2 Mediates Efferocytosis, Resolution Reprogramming, and Intestinal Epithelial Repair
inferred← citeshttps://doi.org/10.1016/j.jconrel.2017.12.023openalex-snapshot
Liposome-induced immunosuppression and tumor growth is mediated by macrophages and mitigated by liposome-encapsulated alendronate
inferred← citeshttps://doi.org/10.1016/j.jep.2025.119741openalex-snapshot
Xin-shu-bao tablets ameliorates ventricular remodeling against HFrEF via PPARγ/MFGE8 pathway based on MALDI-MSI and lipidomics
inferred← citeshttps://doi.org/10.1016/j.jgr.2023.10.001openalex-snapshot
Ginsenoside F2 Restrains Hepatic Steatosis and Inflammation by Altering the Binding Affinity of Liver X Receptor Coregulators
inferred← citeshttps://doi.org/10.1016/j.jmb.2017.08.012openalex-snapshot
LC3-Associated Phagocytosis and Inflammation
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2013.11.010openalex-snapshot
7-Dehydrocholesterol metabolites produced by sterol 27-hydroxylase (CYP27A1) modulate liver X receptor activity
inferred← citeshttps://doi.org/10.1016/j.jtcme.2024.10.003openalex-snapshot
Electroacupuncture improves cardiac function in hyperlipidemic rats by enhancing efferocytosis in myocardial macrophages via the PPARγ-LXRα-MerTK pathway
inferred← citeshttps://doi.org/10.1016/j.kint.2023.03.030openalex-snapshot
Macrophage transcription factor TonEBP promotes systemic lupus erythematosus and kidney injury via damage-induced signaling pathways
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119287openalex-snapshot
Molecular mechanism of liver X receptors in cancer therapeutics
inferred← citeshttps://doi.org/10.1016/j.lfs.2024.123204openalex-snapshot
Defective macrophage efferocytosis in advanced atherosclerotic plaque and mitochondrial therapy
inferred← citeshttps://doi.org/10.1016/j.mam.2021.100942openalex-snapshot
Nuclear receptors, the aryl hydrocarbon receptor, and macrophage function
inferred← citeshttps://doi.org/10.1016/j.molimm.2011.07.022openalex-snapshot
Apoptotic cells enhance IL-10 and reduce IL-23 production in human dendritic cells treated with zymosan
inferred← citeshttps://doi.org/10.1016/j.molimm.2025.10.003openalex-snapshot
Role of efferocytosis in liver transplantation via hepatic macrophage
showing the first 200 of 665
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.