Immune cell migration in inflammation: present and future therapeutic targets

Traffic signals for lymphocyte recirculation and leukocyte emigration: The multistep paradigm

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Immunobiology of Dendritic Cells

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Chemokines — Chemotactic Cytokines That Mediate Inflammation

Luster, A. D. (1998) · New England Journal of Medicine · doi:10.1056/nejm199802123380706 · Cited by 3,633

Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties

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Central Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance

Sallusto, F., Geginat, J., & Lanzavecchia, A. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104702 · Cited by 3,067

Leukocyte-endothelial cell recognition: Three (or more) steps to specificity and diversity

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Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1

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Decreased lesion formation in CCR2−/− mice reveals a role for chemokines in the initiation of atherosclerosis

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In vivo depletion of CD11c+ dendritic cells abrogates priming of CD8+ T cells by exogenous cell-associated antigens.

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Lineage relationship and protective immunity of memory CD8 T cell subsets

Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni889 · Cited by 1,864

A microphysiological assay for studying T-cell chemotaxis, trafficking and tumor killing

Grandhi, T. S. P., Mebrahtu, M., Musso, R., Fullman, A., Nifong, B., Wisdom, K. M., Roh, T. T., Sender, M., Poore, D., Macdougall, C. E., et al. (2024) · Biofabrication · doi:10.1088/1758-5090/ad847f · Cited by 7

Low-Intensity Pulsed Ultrasound Dynamically Modulates the Migration of BV2 Microglia

Li, D., Yong, Y., Qiao, C., Jiang, H., Lin, J., Wei, J., Zhou, Y., & Li, F. (2024) · Ultrasound in Medicine & Biology · doi:10.1016/j.ultrasmedbio.2024.11.010 · Cited by 8

Immune disease dialogue of chemokine-based cell communications as revealed by single-cell RNA sequencing meta-analysis

Rahman, M. F., Kurlovs, A. H., Vodnala, M., Meibalan, E., Means, T. K., Nouri, N., de Rinaldis, E., & Savova, V. (2024) · Frontiers in Systems Biology · doi:10.3389/fsysb.2024.1466368 · Cited by 8

PIP5K-Ras bistability triggers plasma membrane symmetry breaking to define cellular polarity and regulate migration

Deng, Y., Banerjee, T., Matsuoka, S., Biswas, D., Kurtz, L. A., Borleis, J. A., Long, Y., Banerjee, P., Zhan, H., Pal, D. S., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-77894-2 · Cited by 8

6-Amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis

Cesarini, S., Spallarossa, A., Ranise, A., Bruno, O., Arduino, N., Bertolotto, M. B., Dallegri, F., Tognolini, M., Gobbetti, T., & Barocelli, E. (2009) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2009.04.006 · Cited by 7

Co-administration of L-Ascorbic Acid and α-Tocopherol Alleviates Arsenic-Induced Immunotoxicities in the Thymus and Spleen by Dwindling Oxidative Stress-Induced Inflammation

Maity, J., Pal, P., Pal, R., & Mukhopadhyay, P. K. (2023) · Biological Trace Element Research · doi:10.1007/s12011-023-03841-7 · Cited by 7

Effects of the Oral Administration of Viable and Heat-Killed Streptococcus bovis HC5 Cells to Pre-Sensitized BALB/c Mice

Paiva, A. D., Fernandes, K. M., Dias, R. S., Rocha, A. D. S., de Oliveira, L. L., Neves, C. A., de Paula, S. O., & Mantovani, H. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048313 · Cited by 7

Beyond Pattern Recognition: TLR2 Promotes Chemotaxis, Cell Adhesion, and Migration in THP-1 Cells

Colleselli, K., Ebeyer-Masotta, M., Neuditschko, B., Stierschneider, A., Pollhammer, C., Potočnjak, M., Hundsberger, H., Herzog, F., & Wiesner, C. (2023) · Cells · doi:10.3390/cells12101425 · Cited by 8

Adult Stem Cel Diferentiation and Trafficking And Their Implications in Disease

Zhuge, Y., Liu, Z., & Velazquez, O. C. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7037-4_12 · Cited by 7

Cloning and functional characterization of recombinant equine P-selectin

Xu, J. Y., Cai, J., Anderson, B., Wagner, B., Albrecht, R. M., Peek, S. F., Suresh, M., & Darien, B. J. (2007) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2007.01.004 · Cited by 7

Large-scale single-cell phylogenetic mapping of clonal evolution in the human aging esophagusPreprint

Prieto, T., Yuan, D. J., Zinno, J., Hughes, C., Midler, N., Kao, S., Huuhtanen, J., Raviram, R., Fotopoulou, F., Ruthen, N. G., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.11.681805 · Cited by 9

Dysregulation of cell migration by matrix metalloproteinases in geleophysic dysplasia

Morales, A. A., Camarena, V., Peart, L., Smithson, S., Shaw, L., Webber, L., Negron, J. M., Sola, J. E., Brady, A., Walz, K., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-04666-1 · Cited by 6

The roles of tissue-resident memory T cells (TRMs) in diseases and vaccine development: A comprehensive review

Wei, H., Wang, Y., Jiang, S., Zhang, X., & Zhang, J. (2025) · Vaccine · doi:10.1016/j.vaccine.2025.127605 · Cited by 6

Immunocyte reprogramming empowers live-cell drug delivery: Mechanistic insights, delivery strategies, and clinical perspectives

Sun, Z., Ge, J., Fu, H., Chen, Z., Zhao, C., Li, X., Sun, Y., Gao, Z., Li, Y., & Li, Y. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.10.019 · Cited by 6

A Review of Fabrication and Applications of Confined Microchannels for Cell Migration Assay

Mazalan, M., Toyohara, R., & OHASHI, T. (2024) · International Journal of Precision Engineering and Manufacturing · doi:10.1007/s12541-024-01045-0 · Cited by 6

Unraveling the interplay between inflammation and stem cell mobilization or homing: Implications for tissue repair and therapeutics

Chang, H., Liou, Y.-S., & Sun, D. (2024) · Tzu Chi Medical Journal · doi:10.4103/tcmj.tcmj_100_24 · Cited by 7

Fast-crosslinking, shape-adaptable, conductive, and dual-antibacterial hydrogels based on oxidized dextran and polyvinyl alcohol-ε-polylysine for infected skeletal muscle healing

Guo, Y. F., Wang, S., Wang, H., Zhang, D., Shen, L., Han, X., Zhao, X., Guo, B., & Deng, Z. (2025) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2025.124382 · Cited by 6

EGCG induces G-CSF expression and neutrophilia in experimental sepsis

Li, W., Wu, A. H., Zhu, S., Li, J., Wu, R., D’Angelo, J. K., & Wang, H. (2015) · Immunologic Research · doi:10.1007/s12026-015-8681-x · Cited by 6

Beneficial effects of the n-3 long-chain polyunsaturated fatty acids in surgical patients: Updating the evidence

Bernabé-García, M., López‐Alarcón, M., Blanco-Favela, F. A., Mancilla-Ramı́rez, J., Mansilla‐Olivares, A., & Arredondo-Garcı́a, J. L. (2011) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2011.04.012 · Cited by 6

Autoselective transport of mammalian cells with a chemotactic droplet

Holler, S., & Hanczyc, M. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-62325-z · Cited by 6

Modelling how curved active proteins and shear flow pattern cellular shape and motility

Sadhukhan, S., Penič, S., Iglič, A., & Gov, N. S. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1193793 · Cited by 6

Chapter 18 A Chemokine‐Mediated In Vivo T‐Cell Recruitment Assay

Campanella, G. S. V., & Luster, A. D. (2009) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(09)05418-4 · Cited by 6

Blood-Brain Barrier Disruption and Encephalitis in Animal Models of AIDS

Nicole, A., Andrew, A. J., & Andrew, G. D. B. (2011) · InTech eBooks · doi:10.5772/20366 · Cited by 6

Three-Dimensional Migration of Neutrophils Through an Electrospun Nanofibrous Membrane

Jin, S., Park, T.-M., Kim, C.-H., Kim, J.-S., Le, B. D., Jeong, Y. H., Kwak, J.-Y., & Yoon, S. (2015) · BioTechniques · doi:10.2144/000114297 · Cited by 6

Stepwise inhibition of T cell recruitment at post-capillary venules by orally active desulfated heparins in inflammatory arthritis

Faruque, H. A., Kang, J. H., Hwang, S. R., Sung, S., Alam, M. M., Sa, K. H., Nam, E. J., Byun, Y. R., & Kang, Y. M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0176110 · Cited by 6

Time to Develop Therapeutic Antibodies Against Harmless Proteins Colluding with Sepsis Mediators?

Li, J., Bao, G., & Wang, H. (2020) · ImmunoTargets and Therapy · doi:10.2147/itt.s262605 · Cited by 6

Cellular Adhesion in Inflammation

Broide, D. H., & Sriramarao, P. (2009) · Elsevier eBooks · doi:10.1016/b978-0-323-05659-5.00009-7 · Cited by 6

Structural and Phylogenetic Analysis of CXCR4 Protein Reveals New Insights into Its Role in Emerging and Re-Emerging Diseases in Mammals

Naheed, F., Mumtaz, R., Shabbir, S., Jamil, A., Asif, A. R., Rahman, A., Ahmad, H. I., Essa, M., Akhtar, H., Mahmoud, S. F., et al. (2023) · Vaccines · doi:10.3390/vaccines11030671 · Cited by 6

Harnessing T-Cell Immunity to Target Brain Tumors

Walker, P. R., Prins, R. M., Dietrich, P., & Liau, L. M. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-553-8_48 · Cited by 7

The parasite-derived rOv-ASP-1 is an effective antigen-sparing CD4 + T cell-dependent adjuvant for the trivalent inactivated influenza vaccine, and functions in the absence of MyD88 pathway

Jain, S., George, P. J., Deng, W., Koussa, J., Parkhouse, K., Hensley, S. E., Jiang, J. K., Lu, J. L., Liu, Z., Wei, J., et al. (2018) · Vaccine · doi:10.1016/j.vaccine.2018.05.029 · Cited by 6

Collective migrations in an epithelial–cancerous cell monolayer

Lv, J.-Q., Chen, P., Guan, L., Góźdź, W. T., Feng, X., & Li, B. (2021) · Acta Mechanica Sinica · doi:10.1007/s10409-021-01083-1 · Cited by 6

Two-photon microscopy analysis of leukocyte trafficking and motility

Okada, T. (2010) · Seminars in Immunopathology · doi:10.1007/s00281-010-0210-3 · Cited by 7

Correction: Overhauser-Enhanced MRI of Elastase Activity from In Vitro Human Neutrophil Degranulation

Parzy, E., Bouchaud, V., Massot, P., Voisin, P. J., Koonjoo, N., Moncelet, D., Franconi, J., Thiaudière, E., & Mellet, P. (2013) · PLoS ONE · doi:10.1371/annotation/47f8c256-07a4-44a1-88cb-8c461e0d45e4 · Cited by 6

Cryo-ET of actin cytoskeleton and membrane structure in lamellipodia formation using optogenetics

Inaba, H., Imasaki, T., Aoyama, K., Yoshihara, S., Takazaki, H., Kato, T., Goto, H., Mitsuoka, K., Nitta, R., & Nakata, T. (2025) · iScience · doi:10.1016/j.isci.2025.112529 · Cited by 5

Immune and Immune‐Integrated Organoids as NextGeneration Platforms for Disease Modeling

Rashidan, K., Ayadilord, M., Hazrati, A., Nazerian, A., Shafiee, A., & Hashemi, S. M. (2025) · MedComm · doi:10.1002/mco2.70531 · Cited by 6

Injected extracellular vesicles and other nanoparticles hitchhike on erythrocytes and platelets from circulation towards organ clearance

Pavlova, S., Mamand, D. R., Hagey, D. W., Liang, X., Estupiñan, H. Y., Zheng, W., Zhou, G., Amin, R., Zickler, A. M., Bonner-Harris, S., et al. (2025) · Extracellular Vesicle · doi:10.1016/j.vesic.2025.100103 · Cited by 5

Cells function as a ternary logic gate to decide migration direction under integrated chemical and fluidic cues

Moon, H., Saha, S., Mugler, A., & Han, B. (2022) · Lab on a Chip · doi:10.1039/d2lc00807f · Cited by 5

Diarylidene‐ N ‐Methyl‐4‐Piperidones and Spirobibenzopyrans as Antioxidant and Anti‐Inflammatory Agents

Rokkam, S. K., Mas‐Rosario, J. A., Joshi, B. P., Joshi, M., Choudhury, A. R., Kar, S., Golakoti, N. R., & Farkas, M. E. (2023) · Chemistry & Biodiversity · doi:10.1002/cbdv.202300822 · Cited by 5

Neutrophils exhibit flexible migration strategies and trail formation mechanisms on varying adhesive substrates

Gao, W., Zhang, X., Hu, W., Han, J., Liu, X., Zhang, Y., & Long, M. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.122881 · Cited by 5

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Mak, J. K. L., Qin, C., Krüger, M., Kuukka, A., FinnGen, Palotie, A. V., Daly, M. J., Riley-Gillis, B., Jacob, H. J., Paul, D. S., et al. (2025) · Nature Aging · doi:10.1038/s43587-025-00925-y · Cited by 5

Autonomous Cell Migration to CSF1 Sources via a Synthetic Protein-Based System

Qudrat, A., & Truong, K. (2017) · ACS Synthetic Biology · doi:10.1021/acssynbio.7b00076 · Cited by 5

Opportunities to Target T Cell Trafficking in Pediatric Inflammatory Bowel Disease

Giannoudaki, E., Gargan, S., Hussey, S., Long, A., & Walsh, P. T. (2021) · Frontiers in Pediatrics · doi:10.3389/fped.2021.640497 · Cited by 5

Investigation of the clinical utility of adhesion molecules in the management of thyroid nodules

Rabi, L. T., Peres, K. C., Nascimento, M. H., Teixeira, E. D. S., de Freitas, L. L. L., Barreto, I. S., Geraldo, M. V., da Assumpção, L. V. M., Máximo, V., Tincani, Á. J., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-31302-7 · Cited by 5

Effects of grape juice intake on the cell migration properties in overweight women: Modulation mechanisms of cell migration in vitro by delphinidin-3-O-glucoside

Casagrande, J. G., Rogero, M. M., de Oliveira, D. C., Quintanilha, B. J., Capetini, V. C., Makiyama, E. N., Neves, B. R. O., Gonçalves, C. E. D. S., de Freitas, S., Hassimotto, N. M. A., et al. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113873 · Cited by 5

In vivo tracking of mesenchymal stem cell dynamics and therapeutics in LPS-induced acute lung injury models

Wang, C., Hezam, K., Fu, E., Pan, K., Liu, Y., & Li, Z. (2024) · Experimental Cell Research · doi:10.1016/j.yexcr.2024.114013 · Cited by 5

Spatial distribution-based progression of spinal cord injury pathology: a key role for neuroimmune cells

Li, J., Zhai, X.-L., & Yu, C. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1505755 · Cited by 5

SLPI controls neutrophil migration abilities and impacts neutrophil skin infiltration in experimental psoriasis

Kwiecińska, P., Santocki, M., Skrzeczyńska-Moncznik, J., Sinkevich, I., Piwowarczyk, K., Majewski, P., Grygier, B., Majchrzak-Gorecka, M., Czyż, J., Kołaczkowska, E., et al. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05606-y · Cited by 5

Blood transcriptome bridges orthogonal immunotypes and gut microbiome enterotypes in humans

Affaticati, F., Hà, M., Gehrmann, T., Boeck, I. D., Kuznetsova, M., Vandoren, R., Deuren, V. M. L. V., Alcedo, S., Jansens, H., Reu, H. D., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117752 · Cited by 5

Recombinant Herpesvirus Glycoprotein G Improves the Protective Immune Response to Helicobacter pylori Vaccination in a Mouse Model of Disease

Baker, L., Chitas, A. M. L., Hartley, C. A., Coppo, M. J. C., Vaz, P. K., Stent, A. W., Gilkerson, J. R., Devlin, J. M., & Every, A. L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096563 · Cited by 5

Genetic Variation Is the Major Determinant of Individual Differences in Leukocyte Endothelial Adhesion

Grassi, M. A., Rao, V. R., Winkler, K. P., Zhang, W., Bogaard, J. D., Chen, S., LaCroix, B. L., Lenkala, D., Rehman, J., Malik, A. B., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087883 · Cited by 5

Bioactive Carbohydrate: Dietary Fibers and Colorectal Cancer

Raman, M., Ambalam, P. S., & Doble, M. (2015) · Springer eBooks · doi:10.1007/978-81-322-2586-7_3 · Cited by 5

Acoustics of porous-elastic fluid saturated medium (an overview of the Biot theory)

Knyaz’kov, N. N., & Sharfarets, B. P. (2016) · NAUCHNOE PRIBOROSTROENIE · doi:10.18358/np-26-1-i7784 · Cited by 5

Microfluidic Devices for Studying the Effect of Netrin‐1 on Neutrophil and Breast Cancer Cell Migration

Hipolito, J., Peretz‐Soroka, H., Moya, A., Booy, E. P., Yang, K., Gupta, M., Meier, M., McKenna, S. A., Koch, M., Santos, S. C., et al. (2018) · Advanced Biosystems · doi:10.1002/adbi.201700178 · Cited by 5

Endothelial cell monolayer-based microfluidic systems mimicking complex in vivo microenvironments for the study of leukocyte dynamics in inflamed blood vessels

Lee, J., Huh, H. K., Park, S. H., Lee, S. J., & Doh, J. (2018) · Methods in cell biology · doi:10.1016/bs.mcb.2018.05.002 · Cited by 5

Early warning for inactive ovaries based on liver function index, serum MDA, IL-6, FGF21 and ANGPTL8 in dairy cows

Wang, Z., Song, Y., Zhang, F., Zhao, C., Fu, S., Xia, C., & Bai, Y. (2021) · Italian Journal of Animal Science · doi:10.1080/1828051x.2021.2020177 · Cited by 5

Enhanced motility and interaction of nasopharyngeal carcinoma with epithelial cells in confined microwells

Xiao, H., Xu, Y., & Pang, S. W. (2023) · Lab on a Chip · doi:10.1039/d2lc00616b · Cited by 5

Persistent random walks: a unified theory for durotaxis and negative durotaxis

Yang, Y., & Jiang, H. (2023) · The European Physical Journal Special Topics · doi:10.1140/epjs/s11734-023-00963-w · Cited by 5

An Experimental Model for Simultaneous Study of Migration of Cell Fragments, Single Cells, and Cell Sheets

Sun, Y., Sun, Y., Zhu, K., Draper, B. W., Zeng, Q., Mogilner, A., & Zhao, M. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3480-5_19 · Cited by 5

Foxo in T Cells Regulates Thermogenic Program through Ccr4/Ccl22 Axis

Kikuchi, T., Nakae, J., Kawano, Y., Watanabe, N., Onodera, M., & Itoh, H. (2019) · iScience · doi:10.1016/j.isci.2019.11.006 · Cited by 5

AAAPT Diagnostic Criteria for Acute Knee Arthroplasty Pain

Abdallah, F. W., Gilron, I., Fillingim, R. B., Tighe, P. J., Parvataneni, H. K., Ghasemlou, N., Sawhney, M., & McCartney, C. J. L. (2019) · Pain Medicine · doi:10.1093/pm/pnz355 · Cited by 5

Limitations of cell-lineage-specific non-dynamic gene recombination in CD11c.Cre+ITGA4fl/fl mice

Manouchehri, N., Hussain, R. Z., Cravens, P. D., Doelger, R., Greenberg, B. M., Okuda, D. T., Forsthuber, T. G., Eagar, T. N., & Stüve, O. (2020) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2020.577245 · Cited by 5

Detecting Effects of Low Levels of FCCP on Stem Cell Micromotion and Wound-Healing Migration by Time-Series Capacitance Measurement

Wang, S.-H., Tung, T.-H., Chiu, S.-P., Chou, H.-Y., Hung, Y.-H., Lai, Y.-T., Lee, Y.-W., Lee, S., & Lo, C. (2021) · Sensors · doi:10.3390/s21093017 · Cited by 5

The Role of Hyperglycemia in CD4 T-Cell Survival and Differentiation

Iwai, N., Steib, C., Marzo, A. L., & Lerret, N. M. (2018) · American Society for Clinical Laboratory Science · doi:10.29074/ascls.2018000331 · Cited by 5

Chapter 15 Methods to Study Myeloid Cell Roles in Angiogenesis

Schmid, M. C., & Varner, J. A. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(08)03015-2 · Cited by 5

Differential Expression of Alpha 4 Integrins on Effector Memory T Helper Cells during Bordetella Infections. Delayed Responses in Bordetella pertussis

Nguyen, T. M., Ravindra, D., Kwong, B., Waheed, S., Ferguson, R., Tarlton, N. J., Wu, V., Sequeira, C. S., Bremer, M., & Abramson, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052903 · Cited by 5

Influence of myosin activity and mechanical impact on keratocyte polarization

Moure, A., & Gómez, H. (2020) · Soft Matter · doi:10.1039/d0sm00473a · Cited by 5

Firategrast—natalizumab in a pill?

Prat, A., & Stüve, O. (2012) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70306-4 · Cited by 5

Role of Short-Chain Fatty Acids from Gut Microbiota in Neuroendocrine Pathogenesis Management

Sahu, N., Upadhyay, P., & Mishra, S. K. (2022) · Nutritional neurosciences · doi:10.1007/978-981-19-4530-4_9 · Cited by 4

Anti-inflammatory and anti-cancer potential of pterostilbene: A review

Surien, O., Masre, S. F., Basri, D. F., & Ghazali, A. R. (2023) · Asian Pacific Journal of Tropical Biomedicine · doi:10.4103/2221-1691.391155 · Cited by 4

Infection in Diabetes: Epidemiology, Immune Dysfunctions, and Therapeutics

Roy, R., Singh, R. K., & Shafikhani, S. H. (2024) · Contemporary diabetes · doi:10.1007/978-3-031-55715-6_17 · Cited by 4

Neutrophil Migration Is Mediated by VLA-6 in the Inflamed Adipose Tissue

Lim, H., Choe, Y. H., Lee, J., Kim, G. E., Hyun, J. W., & Hyun, Y. (2024) · Immune Network · doi:10.4110/in.2024.24.e23 · Cited by 4

Perfluoropentane-based oxygen-loaded nanodroplets reduce microglial activation through metabolic reprogramming

Luo, W., Xu, C., Li, L., Ji, Y., Wang, Y., Li, Y., & Ye, Y. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01299 · Cited by 4

Decoding physical principles of cell migration under controlled environment using microfluidics

Suh, Y. J., Li, A. T., Pandey, M., Nordmann, C. S., Huang, Y., & Wu, M. (2024) · Biophysics Reviews · doi:10.1063/5.0199161 · Cited by 4

Hyphal penetration is the major pathway of translocation of Candida albicans across the blood-cerebrospinal fluid barrier

Schmidt, S., Schwerk, C., Schroten, H., Ishikawa, H., Schubert, R., Lehrnbecher, T., & Rudolph, H. (2025) · Fluids and Barriers of the CNS · doi:10.1186/s12987-025-00644-x · Cited by 4

Galanin-Mediated Inflammatory Responses in Zebrafish Spinal Cord Regeneration

Okitsu-Sakurayama, S., Kasica, N., Potoczna, M., Szczepanek, J. D., Wa̧sowicz, K., & Podlasz, P. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05228-2 · Cited by 4

Curved Microfluidic Confinement Reveals Cell-Shape-Dependent Nuclear Mechanotransduction in Adaptive Migration

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