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Galectin-3 Facilitates Neutrophil Recruitment as an Innate Immune Response to a Parasitic Protozoa Cutaneous Infection
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470378076.ch7openalex-snapshot
Galectins as Danger Signals in Host–Pathogen and Host–Tumor Interactions: New Members of the Growing Group of “Alarmins”?
inferredcites →https://doi.org/10.1002/eji.200838651openalex-snapshot
Ischemia‐reperfusion injury is attenuated in VAP‐1‐deficient mice and by VAP‐1 inhibitors
inferredcites →https://doi.org/10.1002/jlb.52.2.135openalex-snapshot
Differences in the onset of the inflammatory response to cutaneous leishmaniasis in resistant and susceptible mice
inferredcites →https://doi.org/10.1002/jlb.53.5.511openalex-snapshot
Neutrophils contribute to hepatic ischemia- reperfusion injury by a CD18-independent mechanism
inferredcites →https://doi.org/10.1007/978-1-4614-0106-3_2openalex-snapshot
Galectins as Pattern Recognition Receptors: Structure, Function, and Evolution
inferredcites →https://doi.org/10.1016/0092-8674(94)90337-9openalex-snapshot
Traffic signals for lymphocyte recirculation and leukocyte emigration: The multistep paradigm
inferredcites →https://doi.org/10.1016/j.ceb.2011.05.001openalex-snapshot
Glycosylation, galectins and cellular signaling
inferredcites →https://doi.org/10.1016/j.cell.2004.10.009openalex-snapshot
A Role for Insect Galectins in Parasite Survival
inferredcites →https://doi.org/10.1016/j.immuni.2005.01.011openalex-snapshot
Phagocytosis of Apoptotic Neutrophils Regulates Granulopoiesis via IL-23 and IL-17
inferredcites →https://doi.org/10.1016/j.immuni.2008.01.011openalex-snapshot
Restoring the Association of the T Cell Receptor with CD8 Reverses Anergy in Human Tumor-Infiltrating Lymphocytes
inferredcites →https://doi.org/10.1016/j.immuni.2008.07.012openalex-snapshot
Dynamics of Neutrophil Migration in Lymph Nodes during Infection
inferredcites →https://doi.org/10.1016/j.it.2007.08.004openalex-snapshot
Inside, outside, upside down: damage-associated molecular-pattern molecules (DAMPs) and redox
inferredcites →https://doi.org/10.1016/j.it.2009.07.002openalex-snapshot
An elegant defense: how neutrophils shape the immune response
inferredcites →https://doi.org/10.1016/j.it.2009.07.011openalex-snapshot
NETs: a new strategy for using old weapons
inferredcites →https://doi.org/10.1016/j.pt.2009.08.003openalex-snapshot
Are neutrophils important host cells for Leishmania parasites?
inferredcites →https://doi.org/10.1016/s0002-9440(10)63255-5openalex-snapshot
Critical Role for Galectin-3 in Airway Inflammation and Bronchial Hyperresponsiveness in a Murine Model of Asthma
inferredcites →https://doi.org/10.1016/s0002-9440(10)64975-9openalex-snapshot
Targeted Disruption of the Galectin-3 Gene Results in Attenuated Peritoneal Inflammatory Responses
inferredcites →https://doi.org/10.1016/s0021-9258(17)41797-2openalex-snapshot
Regulation of secretion and surface expression of Mac-2, a galactoside-binding protein of macrophages.
inferredcites →https://doi.org/10.1016/s0076-6879(10)80013-8openalex-snapshot
Galectin-1 and HIV-1 Infection
inferredcites →https://doi.org/10.1016/s0165-2478(98)00099-6openalex-snapshot
The role of polymorphonuclear leukocytes in the resistance to cutaneous Leishmaniasis
inferredcites →https://doi.org/10.1016/s0304-4165(99)00177-4openalex-snapshot
Secretion of the galectin family of mammalian carbohydrate-binding proteins
inferredcites →https://doi.org/10.1023/b:glyc.0000014089.17121.ccopenalex-snapshot
Seeing strangers or announcing “danger”: Galectin-3 in two models of innate immunity
inferredcites →https://doi.org/10.1038/ki.1994.169openalex-snapshot
Leukocyte adhesion molecules and kidney diseases
inferredcites →https://doi.org/10.1038/nature05894openalex-snapshot
Macrophage-specific PPARγ controls alternative activation and improves insulin resistance
inferredcites →https://doi.org/10.1038/nri1785openalex-snapshot
Neutrophils and immunity: challenges and opportunities
inferredcites →https://doi.org/10.1038/nri2215openalex-snapshot
How dying cells alert the immune system to danger
inferredcites →https://doi.org/10.1038/nri2536openalex-snapshot
Turning 'sweet' on immunity: galectin–glycan interactions in immune tolerance and inflammation
inferredcites →https://doi.org/10.1038/nri2779openalex-snapshot
Phagocyte partnership during the onset and resolution of inflammation
inferredcites →https://doi.org/10.1038/nri2940openalex-snapshot
Tissue-based class control: the other side of tolerance
inferredcites →https://doi.org/10.1038/nri3024openalex-snapshot
Neutrophils in the activation and regulation of innate and adaptive immunity
inferredcites →https://doi.org/10.1038/nri933openalex-snapshot
The immunology of susceptibility and resistance to Leishmania major in mice
inferredcites →https://doi.org/10.1038/nrmicro2608openalex-snapshot
Leishmaniasis: complexity at the host–pathogen interface
inferredcites →https://doi.org/10.1038/oby.2007.526openalex-snapshot
Galectin‐3 Stimulates Preadipocyte Proliferation and Is Up‐regulated in Growing Adipose Tissue
inferredcites →https://doi.org/10.1046/j.1365-2567.1998.00517.xopenalex-snapshot
Maintenance of granulocyte numbers during acute peritonitis is defective in galectin‐3‐null mutant mice
inferredcites →https://doi.org/10.1056/nejm199505113321907openalex-snapshot
Pathogenesis of Pneumococcal Infection
inferredcites →https://doi.org/10.1073/pnas.0900226106openalex-snapshot
Leishmania amazonensis promastigotes induce and are killed by neutrophil extracellular traps
inferredcites →https://doi.org/10.1074/jbc.m201562200openalex-snapshot
Specific Recognition and Cleavage of Galectin-3 by Leishmania major through Species-specific Polygalactose Epitope
inferredcites →https://doi.org/10.1074/jbc.m302693200openalex-snapshot
Specific Recognition of Leishmania major Poly-β-galactosyl Epitopes by Galectin-9
inferredcites →https://doi.org/10.1074/jbc.m604506200openalex-snapshot
Visualization of Galectin-3 Oligomerization on the Surface of Neutrophils and Endothelial Cells Using Fluorescence Resonance Energy Transfer
inferredcites →https://doi.org/10.1080/019021490927060openalex-snapshot
CYSTIC FIBROSIS SPUTUM STIMULATES CD18-INDEPENDENT NEUTROPHIL MIGRATION ACROSS ENDOTHELIAL CELLS
inferredcites →https://doi.org/10.1083/jcb.200811059openalex-snapshot
Lattices, rafts, and scaffolds: domain regulation of receptor signaling at the plasma membrane
inferredcites →https://doi.org/10.1084/jem.170.6.1959openalex-snapshot
The Mac-2 antigen is a galactose-specific lectin that binds IgE.
inferredcites →https://doi.org/10.1084/jem.184.2.639openalex-snapshot
Selectins and neutrophil traffic: margination and Streptococcus pneumoniae-induced emigration in murine lungs.
inferredcites →https://doi.org/10.1084/jem.186.8.1357openalex-snapshot
Neutrophil Emigration in the Skin, Lungs, and Peritoneum: Different Requirements for CD11/CD18 Revealed by CD18-deficient Mice
inferredcites →https://doi.org/10.1086/339260openalex-snapshot
Leishmania‐Induced Cellular Recruitment during the Early Inflammatory Response: Modulation of Proinflammatory Mediators
inferredcites →https://doi.org/10.1093/cvr/28.9.1301openalex-snapshot
Postreperfusion inflammation: a model for reaction to injury in cardiovascular disease
inferredcites →https://doi.org/10.1096/fj.04-3416fjeopenalex-snapshot
Arginase and polyamine synthesis are key factors in the regulation of experimental leishmaniasis in vivo
inferredcites →https://doi.org/10.1097/01.ccm.0000057843.47705.e8openalex-snapshot
Neutrophils and acute lung injury
inferredcites →https://doi.org/10.1111/j.0105-2896.2004.00185.xopenalex-snapshot
Re‐examination of the immunosuppressive mechanisms mediating non‐cure of Leishmania infection in mice
inferredcites →https://doi.org/10.1111/j.1462-5822.2009.01348.xopenalex-snapshot
The impact of vector-mediated neutrophil recruitment on cutaneous leishmaniasis
inferredcites →https://doi.org/10.1111/j.1549-8719.2001.tb00159.xopenalex-snapshot
Mechanisms of Leukocyte Sequestration in Inflamed Lungs
inferredcites →https://doi.org/10.1111/j.1600-065x.2007.00579.xopenalex-snapshot
The grateful dead: damage‐associated molecular pattern molecules and reduction/oxidation regulate immunity
inferredcites →https://doi.org/10.1111/j.1600-065x.2009.00790.xopenalex-snapshot
Galectins in innate immunity: dual functions of host soluble β‐galactoside‐binding lectins as damage‐associated molecular patterns (DAMPs) and as receptors for pathogen‐associated molecular patterns (PAMPs)
inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00981.xopenalex-snapshot
Adaptive Regulation at the Cell Surface by N ‐Glycosylation
inferredcites →https://doi.org/10.1126/science.1159194openalex-snapshot
In Vivo Imaging Reveals an Essential Role for Neutrophils in Leishmaniasis Transmitted by Sand Flies
inferredcites →https://doi.org/10.1126/science.272.5258.60openalex-snapshot
Lymphocyte Homing and Homeostasis
inferredcites →https://doi.org/10.1128/iai.02006-06openalex-snapshot
Galectin-3 Modulates Immune and Inflammatory Responses during Helminthic Infection: Impact of Galectin-3 Deficiency on the Functions of Dendritic Cells
inferredcites →https://doi.org/10.1128/jvi.05351-11openalex-snapshot
Host-Soluble Galectin-1 Promotes HIV-1 Replication through a Direct Interaction with Glycans of Viral gp120 and Host CD4
inferredcites →https://doi.org/10.1146/annurev.immunol.23.021704.115653openalex-snapshot
HOW NEUTROPHILS KILL MICROBES
inferredcites →https://doi.org/10.1146/annurev.iy.12.040194.005015openalex-snapshot
Tolerance, Danger, and the Extended Family
inferredcites →https://doi.org/10.1146/annurev.ph.57.030195.000525openalex-snapshot
Leukocyte Traffic in the Lung
inferredcites →https://doi.org/10.1152/physiologyonline.2001.16.2.76openalex-snapshot
Leukocyte Recruitment in the Microcirculation: the Rolling Paradigm Revisited
inferredcites →https://doi.org/10.1152/physrev.00023.2002openalex-snapshot
Unique Structural Features That Influence Neutrophil Emigration Into the Lung
inferredcites →https://doi.org/10.1155/2010/719361openalex-snapshot
The Prominent Role of Neutrophils during the Initial Phase of Infection byLeishmaniaParasites
inferredcites →https://doi.org/10.1161/atvbaha.107.153130openalex-snapshot
VAP-1 and CD73, Endothelial Cell Surface Enzymes in Leukocyte Extravasation
inferredcites →https://doi.org/10.1164/rccm.2105034openalex-snapshot
Very Late Antigen-4 in CD18-Independent Neutrophil Emigration during Acute Bacterial Pneumonia in Mice
inferredcites →https://doi.org/10.1167/iovs.05-1193openalex-snapshot
Two Waves of Neutrophil Emigration in Response to Corneal Epithelial Abrasion: Distinct Adhesion Molecule Requirements
inferredcites →https://doi.org/10.1172/jci116686openalex-snapshot
CD18-independent neutrophil and mononuclear leukocyte emigration into the peritoneum of rabbits.
inferredcites →https://doi.org/10.1172/jci17592openalex-snapshot
Critical role of galectin-3 in phagocytosis by macrophages
inferredcites →https://doi.org/10.1182/blood-2009-11-254490openalex-snapshot
CCR7 is involved in the migration of neutrophils to lymph nodes
inferredcites →https://doi.org/10.1182/blood.v84.7.2068.bloodjournal8472068openalex-snapshot
Leukocyte-endothelial adhesion molecules
inferredcites →https://doi.org/10.1182/blood.v89.10.3503openalex-snapshot
Granules of the Human Neutrophilic Polymorphonuclear Leukocyte
inferredcites →https://doi.org/10.1182/blood.v91.9.3430openalex-snapshot
Galectin-3 Activates the NADPH-Oxidase in Exudated but not Peripheral Blood Neutrophils
inferredcites →https://doi.org/10.1189/jlb.0306164openalex-snapshot
DAMPs, PAMPs and alarmins: all we need to know about danger
inferredcites →https://doi.org/10.1189/jlb.0407247openalex-snapshot
Use of Ly6G-specific monoclonal antibody to deplete neutrophils in mice
inferredcites →https://doi.org/10.1189/jlb.1204702openalex-snapshot
Galectin-3 interacts with naïve and primed neutrophils, inducing innate immune responses
inferredcites →https://doi.org/10.1371/journal.ppat.1001185openalex-snapshot
Leishmania major Survival in Selective Phlebotomus papatasi Sand Fly Vector Requires a Specific SCG-Encoded Lipophosphoglycan Galactosylation Pattern
inferredcites →https://doi.org/10.14670/hh-26.247openalex-snapshot
Regulated expression of galectin-3, a multifunctional glycan-binding protein, in haematopoietic and non-haematopoietic tissues.
inferredcites →https://doi.org/10.2353/ajpath.2006.050636openalex-snapshot
Toxoplasma gondii Infection Reveals a Novel Regulatory Role for Galectin-3 in the Interface of Innate and Adaptive Immunity
inferredcites →https://doi.org/10.2353/ajpath.2008.070870openalex-snapshot
Galectin-3 Reduces the Severity of Pneumococcal Pneumonia by Augmenting Neutrophil Function
inferredcites →https://doi.org/10.2353/ajpath.2009.080500openalex-snapshot
Galectin-3 Is Critical for the Development of the Allergic Inflammatory Response in a Mouse Model of Atopic Dermatitis
inferredcites →https://doi.org/10.3389/fimmu.2012.00032openalex-snapshot
Does T Helper Differentiation Correlate with Resistance or Susceptibility to Infection with L. major? Some Insights From the Murine Model
inferredcites →https://doi.org/10.4049/jimmunol.0903273openalex-snapshot
Type I IFN Receptor Regulates Neutrophil Functions and Innate Immunity to Leishmania Parasites
inferredcites →https://doi.org/10.4049/jimmunol.1000893openalex-snapshot
Leishmania donovani Promastigotes Evade the Antimicrobial Activity of Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.4049/jimmunol.144.6.2327openalex-snapshot
CD18-dependent and -independent mechanisms of neutrophil emigration in the pulmonary and systemic microcirculation of rabbits.
inferredcites →https://doi.org/10.4049/jimmunol.153.7.3177openalex-snapshot
Quantitation of L-selectin and CD18 expression on rabbit neutrophils during CD18-independent and CD18-dependent emigration in the lung.
inferredcites →https://doi.org/10.4049/jimmunol.159.7.3595openalex-snapshot
Chemokine networks in vivo: involvement of C-X-C and C-C chemokines in neutrophil extravasation in vivo in response to TNF-alpha
inferredcites →https://doi.org/10.4049/jimmunol.163.2.995openalex-snapshot
Effects of CD18 Deficiency on the Emigration of Murine Neutrophils During Pneumonia
inferredcites →https://doi.org/10.4049/jimmunol.165.5.2628openalex-snapshot
An Immunomodulatory Function for Neutrophils During the Induction of a CD4+ Th2 Response in BALB/c Mice Infected with Leishmania major
inferredcites →https://doi.org/10.4049/jimmunol.166.12.7353openalex-snapshot
Role of Chemokines and Formyl Peptides in Pneumococcal Pneumonia-Induced Monocyte/Macrophage Recruitment
inferredcites →https://doi.org/10.4049/jimmunol.167.5.2839openalex-snapshot
CD18 Dependency of Transendothelial Neutrophil Migration Differs During Acute Pulmonary Inflammation
inferredcites →https://doi.org/10.4049/jimmunol.168.4.1813openalex-snapshot
Role of Galectin-3 as an Adhesion Molecule for Neutrophil Extravasation During Streptococcal Pneumonia
inferredcites →https://doi.org/10.4049/jimmunol.170.6.3233openalex-snapshot
Proinflammatory Activities of S100: Proteins S100A8, S100A9, and S100A8/A9 Induce Neutrophil Chemotaxis and Adhesion
inferredcites →https://doi.org/10.4049/jimmunol.172.7.4454openalex-snapshot
Macrophage Interactions with Neutrophils Regulate Leishmania major Infection
inferredcites →https://doi.org/10.4049/jimmunol.174.1.426openalex-snapshot
Morphine Impairs Host Innate Immune Response and Increases Susceptibility to Streptococcus pneumoniae Lung Infection
inferredcites →https://doi.org/10.4049/jimmunol.174.11.7160openalex-snapshot
Kinetoplastid Membrane Protein-11 DNA Vaccination Induces Complete Protection against Both Pentavalent Antimonial-Sensitive and -Resistant Strains of Leishmania donovani That Correlates with Inducible Nitric Oxide Synthase Activity and IL-4 Generation: Evidence for Mixed Th1- and Th2-Like…
inferredcites →https://doi.org/10.4049/jimmunol.180.4.2466openalex-snapshot
Role of Galectin-3 in Leukocyte Recruitment in a Murine Model of Lung Infection by Streptococcus pneumoniae
inferredcites →https://doi.org/10.4049/jimmunol.180.4.2650openalex-snapshot
Regulation of Alternative Macrophage Activation by Galectin-3
inferredcites →https://doi.org/10.4052/tigg.14.285openalex-snapshot
Galectins as Molecules of Danger Signal, which could Evoke an Immune Response to Infection.
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.3741239openalex-extracted
Mycobacterial Phthiocerol Dimycocerosate Induces Galectin-3 Upregulation to Impair Proinflammatory Responses and Favor Immune Evasion in vivo
inferred← citeshttps://doi.org/10.1002/9783527692156.ch2openalex-snapshot
Pathogen-associated Molecular Patterns
inferred← citeshttps://doi.org/10.1002/eji.201343381openalex-snapshot
Galectin‐3 negatively regulates the frequency and function of CD 4+ CD 25+ F oxp3+ regulatory T cells and influences the course of L eishmania major infection
inferred← citeshttps://doi.org/10.1007/978-981-15-1580-4_6openalex-snapshot
Galectins in Host Defense Against Microbial Infections
inferred← citeshttps://doi.org/10.1007/s00109-022-02207-1openalex-snapshot
Regulation of wound healing and fibrosis by galectins
inferred← citeshttps://doi.org/10.1007/s12035-019-1527-0openalex-snapshot
Delayed Galectin-3-Mediated Reprogramming of Microglia After Stroke is Protective
inferred← citeshttps://doi.org/10.1007/s12079-018-0453-7openalex-snapshot
Galectin-3 regulation of wound healing and fibrotic processes: insights for chronic skin wound therapeutics
inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00052-3openalex-snapshot
Mammalian Cytosolic Galectins Act as Damage-Associated Molecular Patterns, Resolution-Associated Molecular Patterns, and Pattern-Recognition Receptors in Innate Immunity
inferred← citeshttps://doi.org/10.1016/j.actatropica.2017.09.027openalex-snapshot
The roles of galectins in parasitic infections
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2025.108681openalex-snapshot
Dissecting the specificity of sugar code recognition - Unleashing the biomedical potential of galectins by protein engineering
inferred← citeshttps://doi.org/10.1016/j.carpath.2014.12.001openalex-snapshot
Galectin-3 is expressed in the myocardium very early post–myocardial infarction
inferred← citeshttps://doi.org/10.1016/j.cellimm.2016.08.004openalex-snapshot
Leishmania, the phagosome, and host responses: The journey of a parasite
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2026.02.002openalex-snapshot
The intricate relationship between cytokines and galectins in immune modulation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.146193openalex-snapshot
Mycobacterial phthiocerol dimycocerosate induces Galectin-3 upregulation to impair proinflammatory responses and favor immune evasion
inferred← citeshttps://doi.org/10.1016/j.smim.2024.101926openalex-snapshot
Decoding the multifaceted roles of galectins in self-defense
inferred← citeshttps://doi.org/10.1016/j.tibs.2016.11.003openalex-snapshot
Translating the ‘Sugar Code’ into Immune and Vascular Signaling Programs
inferred← citeshttps://doi.org/10.1021/acsinfecdis.4c01056openalex-snapshot
Galectins as Drivers of Host–Pathogen Dynamics in Mycobacterium tuberculosis Infection
inferred← citeshttps://doi.org/10.1038/mi.2013.77openalex-snapshot
DAMPs activating innate and adaptive immune responses in COPD
inferred← citeshttps://doi.org/10.1038/s41551-017-0094openalex-snapshot
Microscale arrays for the profiling of start and stop signals coordinating human-neutrophil swarming
inferred← citeshttps://doi.org/10.1038/s41565-025-01974-5openalex-snapshot
Limiting endosomal damage sensing reduces inflammation triggered by lipid nanoparticle endosomal escape
inferred← citeshttps://doi.org/10.1038/s41577-022-00829-7openalex-snapshot
The role of galectins in immunity and infection
inferred← citeshttps://doi.org/10.1038/s41598-018-21409-7openalex-snapshot
Lack of galectin-3 modifies differentially Notch ligands in bone marrow and spleen stromal cells interfering with B cell differentiation
inferred← citeshttps://doi.org/10.1074/jbc.m115.651497openalex-snapshot
Trichomonas vaginalis Lipophosphoglycan Exploits Binding to Galectin-1 and -3 to Modulate Epithelial Immunity
inferred← citeshttps://doi.org/10.1089/dna.2024.0134openalex-snapshot
Staphylococcus aureus Proteases: Orchestrators of Skin Inflammation
inferred← citeshttps://doi.org/10.1093/glycob/cwab062openalex-snapshot
Galectin-3 plays a protective role in Leishmania (Leishmania) amazonensis infection
inferred← citeshttps://doi.org/10.1093/glycob/cwad032openalex-snapshot
Novel inhibitory effect of galectin-3 on the respiratory burst induced by Staphylococcus aureus in human neutrophils
inferred← citeshttps://doi.org/10.1093/glycob/cwu101openalex-snapshot
Glycobiology of leukocyte trafficking in inflammation
inferred← citeshttps://doi.org/10.1096/fj.201900107ropenalex-snapshot
Galectin‐1 interacts with the human endogenous retroviral envelope protein syncytin‐2 and potentiates trophoblast fusion in humans
inferred← citeshttps://doi.org/10.1097/dad.0000000000001412openalex-snapshot
Dermatological Implications of Galectin-3 in Circulation: An Evaluation From the Perspective of Patients With Differential Manifestations of Post–Kala-Azar Dermal Leishmaniasis
inferred← citeshttps://doi.org/10.1099/mic.0.000322openalex-snapshot
Extracellular galectin-3 counteracts adhesion and exhibits chemoattraction in Helicobacter pylori-infected gastric cancer cells
inferred← citeshttps://doi.org/10.1101/2024.04.16.589801openalex-snapshot
Lipid Nanoparticle-Associated Inflammation is Triggered by Sensing of Endosomal Damage: Engineering Endosomal Escape Without Side Effects
inferred← citeshttps://doi.org/10.1101/2024.08.25.609576openalex-snapshot
N-Acetylglucosamine Facilitates Coordinated Myoblast Flow, Forming the Foundation for Efficient Myogenesis
inferred← citeshttps://doi.org/10.1111/apm.13502openalex-snapshot
Impact of extracellular enzymes on Staphylococcus aureus host tissue adaptation and infection
inferred← citeshttps://doi.org/10.1128/iai.00177-17openalex-snapshot
Galectin-3 Is a Target for Proteases Involved in the Virulence of Staphylococcus aureus
inferred← citeshttps://doi.org/10.1128/mbio.03708-21openalex-snapshot
Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
inferred← citeshttps://doi.org/10.1128/mcb.00064-16openalex-snapshot
New Regulatory Roles of Galectin-3 in High-Affinity IgE Receptor Signaling
inferred← citeshttps://doi.org/10.1155/2017/9247574openalex-snapshot
The Many Roles of Galectin-3, a Multifaceted Molecule, in Innate Immune Responses against Pathogens
inferred← citeshttps://doi.org/10.1155/2021/6687096openalex-snapshot
NETosis as a Pathogenic Factor for Heart Failure
inferred← citeshttps://doi.org/10.11606/d.17.2020.tde-23102019-165113openalex-snapshot
O papel das amastinas na ativação do inflamassoma e na manutenção da estabilidade dos vacúolos ocupados por Leishmania braziliensis
inferred← citeshttps://doi.org/10.11606/t.17.2014.tde-31072014-101629openalex-snapshot
Efeito da deficiência da molécula B2-integrina na produção de mediadores lipídicos e na resposta imune durante infecção experimental por Leishmania amazonensis
inferred← citeshttps://doi.org/10.11606/t.60.2020.tde-23052019-110350openalex-snapshot
Avaliação da participação de Gal-1 e Gal-4 na evolução da infecção experimental por Leishmania (Leishmania) amazonensis
inferred← citeshttps://doi.org/10.1186/s13071-015-0816-3openalex-snapshot
Transmembrane protein 63A is a partner protein of Haemonchus contortus galectin in the regulation of goat peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1186/s13395-025-00404-3openalex-snapshot
N-acetylglucosamine facilitates coordinated flow-like movement of myoblasts, forming a foundation for efficient myogenesis
inferred← citeshttps://doi.org/10.1189/jlb.3a0116-026rropenalex-snapshot
Galectin-3–null mice display defective neutrophil clearance during acute inflammation
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008741openalex-snapshot
Galectin-3 enhances neutrophil motility and extravasation into the airways during Aspergillus fumigatus infection
inferred← citeshttps://doi.org/10.14393/ufu.di.2021.188openalex-snapshot
Galectina-3 desempenha um papel protetivo na infecção por Leishmania (Leishmania) amazonensis
inferred← citeshttps://doi.org/10.2147/rrbc.s57407openalex-snapshot
Cell–matrix interactions governing skin repair: matricellular proteins as diverse modulators of cell function
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00751openalex-snapshot
Lactose Induces Phenotypic and Functional Changes of Neutrophils and Macrophages to Alleviate Acute Pancreatitis in Mice
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01762openalex-snapshot
The Sweet-Side of Leukocytes: Galectins as Master Regulators of Neutrophil Function
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1230266openalex-snapshot
Dynamic atlas of immune cells reveals multiple functional features of macrophages associated with progression of pulmonary fibrosis
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1946950openalex-snapshot
Adaptive resilience: agarikon mycelium modulates immune responses and provides oxidative stress buffering in human immune cells
inferred← citeshttps://doi.org/10.3389/fphar.2021.638258openalex-snapshot
Galectin-3, Possible Role in Pathogenesis of Periodontal Diseases and Potential Therapeutic Target
inferred← citeshttps://doi.org/10.3390/biology11030442openalex-snapshot
ATP Purinergic Receptor P2X1-Dependent Suicidal NETosis Induced by Cryptosporidium parvum under Physioxia Conditions
inferred← citeshttps://doi.org/10.3390/biom10050798openalex-snapshot
Galectin-3: Roles in Neurodevelopment, Neuroinflammation, and Behavior
inferred← citeshttps://doi.org/10.3390/cells12232671openalex-snapshot
Galectins in Protozoan Parasitic Diseases: Potential Applications in Diagnostics and Therapeutics
inferred← citeshttps://doi.org/10.4049/jimmunol.1600709openalex-snapshot
Galectin-3: A Positive Regulator of Leukocyte Recruitment in the Inflamed Microcirculation
inferred← citeshttps://doi.org/10.4052/tigg.1739.1seopenalex-snapshot
Cytosolic Galectins and Their Release and Roles as Carbohydrate-Binding Proteins in Host–Pathogen Interaction
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