Tissue Homeostasis and Inflammation

Cancer-related inflammation

Mantovani, A., Allavena, P., Sica, A., & Balkwill, F. (2008) · Nature · doi:10.1038/nature07205 · Cited by 11,399

Immunity, Inflammation, and Cancer

Grivennikov, S. I., Greten, F. R., & Karin, M. (2010) · Cell · doi:10.1016/j.cell.2010.01.025 · Cited by 10,755

Inflammation and metabolic disorders

Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199

Pattern Recognition Receptors and Inflammation

Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895

mTOR Signaling in Growth, Metabolism, and Disease

Saxton, R. A., & Sabatini, D. M. (2017) · Cell · doi:10.1016/j.cell.2017.02.004 · Cited by 7,555

Adipose Expression of Tumor Necrosis Factor-α: Direct Role in Obesity-Linked Insulin Resistance

Hotamisligil, G. S., Shargill, N. S., & Spiegelman, B. M. (1993) · Science · doi:10.1126/science.7678183 · Cited by 7,518

Origin and physiological roles of inflammation

Medzhitov, R. (2008) · Nature · doi:10.1038/nature07201 · Cited by 6,618

Astrocyte-endothelial interactions at the blood-brain barrier

Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595

Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis

Shweiki, D., Itin, A., Soffer, D., & Keshet, E. (1992) · Nature · doi:10.1038/359843a0 · Cited by 4,617

Release of chromatin protein HMGB1 by necrotic cells triggers inflammation

Scaffidi, P., Misteli, T., & Bianchi, M. E. (2002) · Nature · doi:10.1038/nature00858 · Cited by 4,221

Stalling of the endometrial decidual reaction determines the recurrence risk of miscarriage

Muter, J., Kong, C., Nebot, M. T., Tryfonos, M., Vrljicak, P., Brighton, P. J., Dimakou, D. B., Vickers, M., Yoshihara, H., Ott, S., et al. (2025) · Science Advances · doi:10.1126/sciadv.adv1988 · Cited by 21

Gatekeepers of the Gut: The Roles of Proteasomes at the Gastrointestinal Barrier

Mohapatra, G., Eisenberg‐Lerner, A., & Merbl, Y. (2021) · Biomolecules · doi:10.3390/biom11070989 · Cited by 23

The immunomodulatory effects of social isolation in mice are linked to temperature control

Hamilton, A., Rizzo, R., Brod, S., Ono, M., Perretti, M., Cooper, D., & D’Acquisto, F. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.02.022 · Cited by 22

Macrophage-Targeting and Hydrogen-Peroxide-Responsive Fluorescent Probe for Imaging of Inflammation In Vivo

Tao, M., Wang, M., Jiang, C., Liu, W., Zhu, W., Shi, X., & Hai, Z. (2023) · Chemical & Biomedical Imaging · doi:10.1021/cbmi.3c00113 · Cited by 20

Combined cerebrospinal fluid metabolomic and cytokine profiling in tuberculosis meningitis reveals robust and prolonged changes in immunometabolic networks

Tomalka, J. A., Sharma, A., Smith, A., Avaliani, T., Gujabidze, M., Bakuradze, T., Sabanadze, S., Jones, D. P., Avaliani, Z., Kipiani, M., et al. (2023) · Tuberculosis · doi:10.1016/j.tube.2023.102462 · Cited by 20

Acute response to pathogens in the early human placenta at single-cell resolution

Hoo, R., Ruiz-Morales, E. R., Kelava, I., Rawat, M., Icoresi-Mazzeo, C., Tuck, E. J., Sancho‐Serra, C., Chelaghma, S., Predeus, A. V., Murray, S., et al. (2024) · Cell Systems · doi:10.1016/j.cels.2024.04.002 · Cited by 23

Advances in hydrogels for capturing and neutralizing inflammatory cytokines

Qin, H., Li, Z., Li, S., Huang, J., Ren, J., & Wu, X. (2025) · Journal of Tissue Engineering · doi:10.1177/20417314251342175 · Cited by 21

Macrophage metabolic exhaustion and PANoptotic cell death drive chronic tissue inflammation in rheumatoid arthritis

Huang, T., Takashima, Y., Kumar, J., Morales, J., Le, K., Hu, Z., Rubino, S., Trousdale, R. T., Berry, G. J., Goronzy, J. J., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.01.019 · Cited by 24

Neuroinflammation: The Abused Concept

Galea, E., & Graeber, M. B. (2023) · ASN NEURO · doi:10.1177/17590914231197523 · Cited by 21

Inflammation in Posttraumatic Stress Disorder: Dysregulation or Recalibration?

Patas, K., Baker, D. G., Chrousos, G. P., & Agorastos, A. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230807152051 · Cited by 21

Distinct etiology of chronic inflammation – implications on degenerative diseases and cancer therapy

Maddipati, K. R. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460302 · Cited by 23

Infected wound repair correlates with collagen I induction and NOX2 activation by cold atmospheric plasma

Blaise, O., Duchesne, C., Capuzzo, E., Nahori, M., Fernandes, J., Connor, M. G., Hamon, M. A., Pizarro‐Cerdá, J., Lataillade, J., McGUCKIN, C. P., et al. (2024) · npj Regenerative Medicine · doi:10.1038/s41536-024-00372-0 · Cited by 18

Inflamm-aging as a diverse and context-dependent process: From species and population differences to individual trajectories

Franck, M., Daunizeau, C., Aronoff, J. E., Tanner, K., Trumble, B. C., Franceschi, C., Hertel, J., Fülöp, T., Lemoine, M., Gurven, M., et al. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102880 · Cited by 18

Ghost messages: cell death signals spread

Zhang, M., Lin, Y., Chen, R., Yu, H., Li, Y., Chen, M., Dou, C., Yin, P., Zhang, L., & Tang, P. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-022-01004-0 · Cited by 18

A new role for erythropoietin in the homeostasis of red blood cells

Arias, C. F., Valente-Leal, N., Bertocchini, F., Marques, S., Acosta, F. J., & Fernández-Arias, C. (2024) · Communications Biology · doi:10.1038/s42003-023-05758-2 · Cited by 18

Inflammation and depression: an evolutionary framework for the role of physical activity and exercise

Carrera‐Bastos, P., Silva, B. M. B. D. M., Stults‐Kolehmainen, M., Schuch, F. B., Ordóñez, F. M., Müller, P. D. T., Blanco, J. R., & Boullosa, D. A. (2025) · Frontiers in Psychology · doi:10.3389/fpsyg.2025.1554062 · Cited by 19

The role of the ferroptosis pathway in the regulation of polysaccharides for human health: A review

Niu, X., Yao, Y., Li, Y., Li, C., Pan, X., & Han, L. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.123349 · Cited by 16

Upregulation of NK cell activity, cytokine expression, and NF-κB pathway by ginsenoside concentrates from Panax ginseng berries in healthy mice and macrophage cell lines

Jang, J., He, Z., Huang, L., Hwang, J. Y., Kim, M., & Cho, J. Y. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.118681 · Cited by 16

Small-molecule fluorescent probes for bioactive species in inflammatory disease: arthritis, pneumonia and hepatitis

Zhang, X., Tang, F., Shu, W., Li, D., Liu, Y., Xiao, H., Zhou, J. P., & Li, P. (2023) · The Analyst · doi:10.1039/d3an01289a · Cited by 15

New Strategies for Macrophage Re-Education in Cancer: An Update

Lampiasi, N. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063414 · Cited by 15

Coumarin derivatives ameliorate the intestinal inflammation and pathogenic gut microbiome changes in the model of infectious colitis through antibacterial activity

Jung, H.-S., Park, Y., Gu, B., Han, G., Ji, W., Hwang, S. M., & Kim, M. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1362773 · Cited by 17

Immune Privilege Furnishes a Niche for Latent Infection

Forrester, J. V., Mölzer, C., & Kuffová, L. (2022) · Frontiers in Ophthalmology · doi:10.3389/fopht.2022.869046 · Cited by 14

Vitex trifolia L. modulates inflammatory mediators via down-regulation of the NF-κB signaling pathway in carrageenan-induced acute inflammation in experimental rats

Annamalai, P., & Thangam, E. B. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115583 · Cited by 14

The transcriptional control of the VEGFA-VEGFR1 (FLT1) axis in alternatively polarized murine and human macrophages

Domokos, A., Varga, Z., Jambrovics, K., Caballero-Sánchez, N., Szabó, E. V., Nagy, G., Scholtz, B., Halász, L., Váradi, E., Bene, K., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1168635 · Cited by 14

Orchestration of inflammation in contact allergy by innate immune and cellular stress responses

Martin, S. F., Rühl‐Muth, A., & Esser, P. R. (2023) · Allergo Journal International · doi:10.1007/s40629-023-00275-4 · Cited by 15

Transgenerational hormesis in healthy aging and antiaging medicine from bench to clinics: Role of food components

Calabrese, V., Osakabe, N., Siracusa, R., Modafferi, S., Paola, R. D., Cuzzocrea, S., Jacob, U. M., Fritsch, T., Abdelhameed, A. S., Rashan, L. J., et al. (2024) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2024.111960 · Cited by 15

Epigenetic silencing of interleukin-10 by host-derived oxidized phospholipids supports a lethal inflammatory response to infections

Gioia, M. D., Poli, V., Tan, P. J., Spreafico, R., Chu, A., Cuenca, A. G., Wu, Z., Benamar, M., Pandolfi, L., Meloni, F., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.06.017 · Cited by 13

Dickkopf1 Promotes Pulmonary Fibrosis upon Bleomycin-Induced Lung Injury

Sung, E., Park, M. H., Henegariu, O., Sime, P. J., & Chae, W. (2023) · American Journal Of Pathology · doi:10.1016/j.ajpath.2023.05.009 · Cited by 13

Organotypic heterogeneity in microvascular endothelial cell responses in sepsis—a molecular treasure trove and pharmacological Gordian knot

Cleuren, A. C. A., & Molema, G. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1252021 · Cited by 13

Synergistic effects of mesenchymal stem cell-derived extracellular vesicles and dexamethasone on macrophage polarization under inflammatory conditions

Mirsanei, Z., Jamshidi‐Adegani, F., Vakilian, S., Ahangari, F., Soufihasanabad, S., Al-Riyami, K. O., Soudi, S., Khaligh, S. G., Al‐Hashmi, S., & Hashemi, S. M. (2024) · Inflammopharmacology · doi:10.1007/s10787-024-01438-7 · Cited by 14

Alternative mRNA polyadenylation regulates macrophage hyperactivation via the autophagy pathway

Chen, Y., Chen, B., Li, J., Li, H., Wang, G., Cai, X., Zhang, Q., Liu, X., Chen, K., Wang, Z., et al. (2024) · Cellular and Molecular Immunology · doi:10.1038/s41423-024-01237-8 · Cited by 13

Fibroblastic reticular cells form reactive myeloid cell niches in human lymph nodes

Lütge, M., Kurz, L., Stanossek, Y., Meili, S., Cheng, H., Martin, A. D., Brandstadter, J. D., Maillard, I. P., Robinson, M. D., Stoeckli, S. J., et al. (2025) · Science Immunology · doi:10.1126/sciimmunol.ads6820 · Cited by 14

Adaptive biomimicry: design of neural interfaces with enhanced biointegration

Lara, R. P., Goding, J. A., & Green, R. A. (2021) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2021.10.004 · Cited by 13

Transcriptional and proteomic analysis of the innate immune response to microbial stimuli in a model invertebrate chordate

Liberti, A., Pollastro, C., Pinto, G., Illiano, A., Marino, R., Amoresano, A., Spagnuolo, A., & Sordino, P. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1217077 · Cited by 15

Extracellular Vesicles in Skin: Biological Function and Therapeutic Potential

Yuan, S., Jin, M., Zhang, Y., Zhang, M., Yuan, M., Ding, X., & Wang, J. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s548986 · Cited by 14

Frankincense preparation promotes formation of inflammation-resolving lipid mediators by manipulating lipoxygenases in human innate immune cells

Nischang, V., Witt, F., Börner, F., Gomez, M. F., Jordan, P. M., & Werz, O. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1332628 · Cited by 13

Bioactive microgel-coated electrospun membrane with cell-instructive interfaces and topology for abdominal wall defect repair

Xing, R., Gao, R., Huangfu, Y., Zhang, Y., Li, S., Zhang, C., Huang, P., Wang, W., Dong, A., & Feng, Z. (2024) · Biomaterials Science · doi:10.1039/d4bm00182f · Cited by 12

Assessment of acute toxicity, genotoxicity, and anti-inflammatory activity of SteLL, a lectin from Schinus terebinthifolia Raddi. Leaves, in mice

Marinho, A. D. O., da Costa, J. A., dos Santos, A. N. S., de Barros, M. C., Pimentel, C. D. N., da Silva, A. A., Paiva, P. M. G., Napoleão, T. H., & Patriota, L. L. D. S. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.118496 · Cited by 12

Nitrogen, Oxygen, and Sulphur Heterocycles as Potent Anti‐Inflammatory Agents: Insight Into the Synthetic Routes

Khadri, M. J. N., Shashikumar, U., Tsai, P., Manjappa, K. B., Ponnusamy, V. K., & Khanum, S. A. (2025) · ChemistrySelect · doi:10.1002/slct.202403824 · Cited by 12

Lung tumor immunity: redirecting macrophages through infection-induced inflammation

Aktay-Cetin, Ö., Pullamsetti, S. S., Herold, S., & Savai, R. (2025) · Trends in Immunology · doi:10.1016/j.it.2025.04.004 · Cited by 14

Dysambiol, an Anti-inflammatory Secomeroterpenoid from a Dysidea sp. Marine Sponge

Jiao, W., Li, J.-X., Liu, H., Luo, X., Hu, T., Shi, G., Xie, D.-D., Chen, H., Cheng, B., & Lin, H. (2023) · Organic Letters · doi:10.1021/acs.orglett.3c02409 · Cited by 12

Reciprocal regulation of fibroblast–macrophage equilibrium governs skin integrity

Vollmers, A. C., Wu, S. Z., Altieri, A., McCartney, E. E., Bender, H. S., Davidson, C. D., Lee, W. P., Zhang, J., Hu, C., Jeet, S., et al. (2026) · Nature Immunology · doi:10.1038/s41590-026-02434-5 · Cited by 16

Extracellular vesicle production: A bidirectional effect in the interplay between host and Candida fungi

Kulig, K., Rąpała‐Kozik, M., & Karkowska‐Kuleta, J. (2024) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2024.100255 · Cited by 11

The mRNA content of plasma extracellular vesicles provides a window into molecular processes in the brain during cerebral malaria

Mwikali, K., Mwangi, S., Pance, A., Ochola‐Oyier, L. I., Kariuki, S. M., Newton, C. R. J. C., Bejon, P., Rayner, J. C., & Abdi, A. I. (2024) · Science Advances · doi:10.1126/sciadv.adl2256 · Cited by 11

Regulatory T cells in the context: deciphering the dynamic interplay with the tissue environment

Huang, X. J., & Rudensky, A. Y. (2024) · Current Opinion in Immunology · doi:10.1016/j.coi.2024.102453 · Cited by 11

Emerging Role of NAT10 as ac4C Writer in Inflammatory Diseases: Mechanisms and Therapeutic Applications

Zhang, W., Lu, W., Wang, M., Yao, D., Ma, J., Hu, X., & Tao, M. (2024) · Current Drug Targets · doi:10.2174/0113894501346709241202110834 · Cited by 11

Spontaneous Inflammation Resolution Inspired Nanoparticles Promote Neutrophil Apoptosis and Macrophage Efferocytosis for Acute Respiratory Distress Syndrome Treatment

Wang, Y., Zhang, L., Zhang, J., Yu, S., Li, W., Zhou, T., Xing, L., Jeong, J., & Jiang, H. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202402421 · Cited by 11

Advances in plant-derived vesicle like nanoparticles-based therapies for inflammatory diseases

Cheng, Z., Lu, W., Shao, W., Zhang, C., She, Y., Song, R., Qi, R., Song, J., Zhang, W., Chang, X., et al. (2025) · Asian Journal of Pharmaceutical Sciences · doi:10.1016/j.ajps.2025.101052 · Cited by 11

Immune-related pathogenesis and therapeutic strategies of nonalcoholic steatohepatitis

Chung, K. W., Cho, Y. E., Kim, S.-J., & Hwang, S. (2022) · Archives of Pharmacal Research · doi:10.1007/s12272-022-01379-1 · Cited by 11

Immune Cell Ratios Are Higher in Bipolar Affective than Unipolar Depressive Disorder and Modulated by Mood Episode: A Retrospective, Cross-Sectional Study

Koureta, A., Asimakopoulos, L. O., Bozikas, V. P., & Agorastos, A. (2023) · Brain Sciences · doi:10.3390/brainsci13030448 · Cited by 12

Liver Progenitor Cells in Massive Hepatic Necrosis—How Can a Patient Survive Acute Liver Failure?

Lin, T., Feng, R., Liebe, R., & Weng, H. (2022) · Biomolecules · doi:10.3390/biom12010066 · Cited by 10

Design, Synthesis, in Vitro and in Silico Studies of Benzimidazole‐Linked Oxadiazole Derivatives as Anti‐inflammatory Agents

Çeli̇k, İ., Sarıaltın, S. Y., Çoban, T., & Ayhan‐Kılcıgil, G. (2022) · ChemistrySelect · doi:10.1002/slct.202201548 · Cited by 10

Itaconate inhibits corticosterone-induced necroptosis and neuroinflammation via up-regulating menin in HT22 cells

Liang, J.-Y., Gao, S., Jiang, J., Zhang, P., Zou, W., Tang, X., & Tang, Y. (2024) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-024-01012-3 · Cited by 10

Type 2 diabetes: a sacrifice program handling energy surplus

Ye, J., & Yin, J. (2024) · Life Metabolism · doi:10.1093/lifemeta/loae033 · Cited by 9

Abietic acid antagonizes the anti-inflammatory effects of celecoxib and ketoprofen: Preclinical assessment and molecular dynamic simulations

Hasan, R., Bhuia, M. S., Chowdhury, R., Saha, S., Khan, M. A., Afroz, M., Ansari, S. A., Ansari, I. A., Coutinho, H. D. M., & Islam, M. T. (2024) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2024.109298 · Cited by 9

Microbial metabolism of food allergens determines the severity of IgE-mediated anaphylaxis

Sánchez‐Martínez, E., Rondeau, L. E., Garrido‐Romero, M., da Luz, B. B., Haas, D. A., Yuen, G., Coppens, D., Hall, P., Dang, R., Wang, X.-Y., et al. (2026) · Cell Host & Microbe · doi:10.1016/j.chom.2026.02.013 · Cited by 9

The crosstalk between parenchymal cells and macrophages: A keeper of tissue homeostasis

Chen, Y., & Tang, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1050188 · Cited by 11

Embodied cognitive morphogenesis as a route to intelligent systems

Alicea, B., Gordon, R., & Parent, J. (2023) · Interface Focus · doi:10.1098/rsfs.2022.0067 · Cited by 9

Twist1–IRF9 Interaction Is Necessary for IFN-Stimulated Gene Anti-Zika Viral Infection

You, Y., Grasso, E., Alvero, A. B., Condon, J. C., Dimova, T., Hu, A., Ding, J., Alexandrova, M., Manchorova, D., Dimitrova, V., et al. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2300081 · Cited by 10

Down-Regulation of ABCA7 in Human Microglia, Astrocyte and THP-1 Cell Lines by Cholesterol Depletion, IL-1β and TNFα, or PMA

Wiener, J. P., Desire, S., Garliyev, V., Lyssenko, N. N., Praticò, D., & Lyssenko, N. N. (2023) · Cells · doi:10.3390/cells12172143 · Cited by 9

Actin Cytoskeleton Dynamics and Type I IFN-Mediated Immune Response: A Dangerous Liaison in Cancer?

Trono, P., Tocci, A., Musella, M., Sistigu, A., & Nisticò, P. (2021) · Biology · doi:10.3390/biology10090913 · Cited by 8

Anti-Inflammatory Activity of Cajanin, an Isoflavonoid Derivative Isolated from Canavalia lineata Pods

Hong, S.-J., Kwon, O., Hwang, D., Goo, S. H., Kim, D.-Y., Kim, M. H., Kim, S., Jang, H., & Oh, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169492 · Cited by 9

Development of synthetic lipoxin-A4 mimetics (sLXms): New avenues in the treatment of cardio-metabolic diseases

de Gaetano, M. (2022) · Seminars in Immunology · doi:10.1016/j.smim.2022.101699 · Cited by 9

50-color phenotyping of the human immune system with in-depth assessment of T cells and dendritic cellsPreprint

Konecny, A., Mage, P. L., Tyznik, A. J., Prlic, M., & Mair, F. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.14.571745 · Cited by 9

Type 2 neuroimmune circuits in the shaping of physiology

Pirzgalska, R. M., & Veiga‐Fernandes, H. (2023) · Immunity · doi:10.1016/j.immuni.2023.03.016 · Cited by 8

Thrombocyte-derived Dickkopf1 promotes macrophage polarization in the Bleomycin-induced lung injury model

Sung, E., Park, M. H., Song, S.-J., Alanya, H., Henegariu, O., Liu, J., Erson-Omay, Z., Sime, P. J., & Chae, W. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1247330 · Cited by 8

Analysis of SIKVAV’s receptor affinity, pharmacokinetics, and pharmacological characteristics: a matrikine with potent biological function

Filgueiras, L. A., de Andrade, F. D. C. P., Horita, S. I. M., Shirsat, S. D., Achal, V., Rai, M., Henriques‐Pons, A., & Mendes, A. N. (2024) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2024.2313709 · Cited by 8

Immune Regulation Patterns in Response to Environmental Pollutant Chromate Exposure-Related Genetic Damage: A Cross-Sectional Study Applying Machine Learning Methods

Su, Z., Zhang, Y., Hong, S., Zhang, Q., Ji, Z., Hu, G., Zhu, X., Yuan, F., Yu, S., Wang, T., et al. (2024) · Environmental Science & Technology · doi:10.1021/acs.est.4c00433 · Cited by 8

Palmitoleate protects against lipopolysaccharide-induced inflammation and inflammasome activity

Sahoo, P. K., Ravi, A., Liu, B., Yu, J., & Natarajan, S. K. (2024) · Journal of Lipid Research · doi:10.1016/j.jlr.2024.100672 · Cited by 9

Anti-inflammatory effects of cyclodextrin nanoparticles enable macrophage repolarization and reduce inflammation

Brettner, F. E. B., Gier, S., Haessler, A., Schreiner, J., Vogel‐Kindgen, S., & Windbergs, M. (2024) · Discover Nano · doi:10.1186/s11671-024-04175-6 · Cited by 9

Aging-dependent change in Th17 and cytokine response in multiple sclerosis

Zhu, W., Revu, S. K., Chen, C., Dahl, M., Ramkumar, A., Kelly, C. W., McGeachy, M. J., & Xia, Z. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03474-8 · Cited by 8

Threonine phosphorylation of STAT1 safeguards gut epithelial integrity and restricts interferon-mediated cytotoxicity

Metwally, H., Elbrashy, M. M., Kayama, H., Okuyama, K., Taniuchi, I., Takeda, K., & Kishimoto, T. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2511957122 · Cited by 8

Homeostatic control of energy metabolism by monocyte-derived macrophages

Martins, R., Blankehaus, B., Braza, F., Mesquita, M., Ventura, P., Singh, S., Weis, S., Pires, M. V., Pagnotta, S. E., Wu, Q., et al. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00622-x · Cited by 10

Rate thresholds in cell signaling have functional and phenotypic consequences in non-linear time-dependent environments

Thiemicke, A., & Neuert, G. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1124874 · Cited by 10

Macrophage Activity under Hyperglycemia: A Study of the Effect of Resveratrol and 3H-1,2-Dithiole-3-thione on Potential Polarization

Manríquez-Núñez, J., Mora, O., Villarroya, F., Reynoso‐Camacho, R., Pérez‐Ramírez, I. F., & Ramos‐Gómez, M. (2023) · Molecules · doi:10.3390/molecules28165998 · Cited by 8

Physiological trade-off of marine fish under Zn deficient and excess conditions

Ma, S., & Wang, W. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.166187 · Cited by 9

PMA-Zeolite: Chemistry and Diverse Medical Applications

Bulog, A., Pavelić, K., Šutić, I., & Pavelić, S. K. (2024) · Journal of Functional Biomaterials · doi:10.3390/jfb15100296 · Cited by 8

Selected Plant Extracts Regulating the Inflammatory Immune Response and Oxidative Stress: Focus on Quercus robur

Nehme, R., Chervet, A., Decombat, C., Habanjar, O., Longechamp, L., Rousset, A., Chalard, P., Gainche, M., Sénéjoux, F., Fraisse, D., et al. (2025) · Nutrients · doi:10.3390/nu17030510 · Cited by 8

Anti-Inflammatory Effect of Acetone Extracts from Microalgae Chlorella sp. WZ13 on RAW264.7 Cells and TPA-induced Ear Edema in Mice

Yang, L., Hu, F., Yan, Y., Yu, S., Chen, T., & Wang, Z. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.920082 · Cited by 8

Effect of animal venom toxins on the main links of the homeostasis of mammals (Review)

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