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

Adhesion receptors of the immune system

Springer, T. A. (1990) · Nature · doi:10.1038/346425a0 · Cited by 6,477

Cell Adhesion: The Molecular Basis of Tissue Architecture and Morphogenesis

Gumbiner, B. M. (1996) · Cell · doi:10.1016/s0092-8674(00)81279-9 · Cited by 3,471

Annexins: From Structure to Function

Gerke, V., & Moss, S. E. (2002) · Physiological Reviews · doi:10.1152/physrev.00030.2001 · Cited by 2,029

A new class of membrane-bound chemokine with a CX3C motif

Bazan, J. F., Bacon, K. B., Hardiman, G., Wang, W., Soo, K., Rossi, D., Greaves, D. R., Zlotnik, A., & Schall, T. J. (1997) · Nature · doi:10.1038/385640a0 · Cited by 2,013

Monitoring of Blood Vessels and Tissues by a Population of Monocytes with Patrolling Behavior

Auffray, C., Fogg, D., Garfa, M., Elain, G., Join-Lambert, O., Kayal, S., Sarnacki, S., Cumano, A., Lauvau, G., & Geissmann, F. (2007) · Science · doi:10.1126/science.1142883 · Cited by 1,973

Human milk oligosaccharides: Every baby needs a sugar mama

Bode, L. (2012) · Glycobiology · doi:10.1093/glycob/cws074 · Cited by 1,809

International Union of Pharmacology. XXII. Nomenclature for Chemokine Receptors

Murphy, P. M., Baggiolini, M., Charo, I. F., Hébert, C. A., Horuk, R., Matsushima, K., Miller, L. H., Oppenheim, J. J., & Power, C. A. (2000) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01439-x · Cited by 1,817

Transected neurites, apoptotic neurons, and reduced inflammation in cortical multiple sclerosis lesions

Peterson, J. W., Bö, L., Mörk, S., Chang, A., & Trapp, B. D. (2001) · Annals of Neurology · doi:10.1002/ana.1123 · Cited by 1,403

The chemokine receptors CXCR3 and CCR5 mark subsets of T cells associated with certain inflammatory reactions.

Qin, S., Rottman, J. B., Myers, P., Kassam, N., Weinblatt, M., Loetscher, M., Koch, A. E., Moser, B., & Mackay, C. R. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1422 · Cited by 1,359

Immune cell migration in inflammation: present and future therapeutic targets

Luster, A. D., Alon, R., & von Andrian, U. H. (2005) · Nature Immunology · doi:10.1038/ni1275 · Cited by 1,313

Cutting edge: inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes

Bouchon, A., Dietrich, J., & Colonna, M. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.10.4991 · Cited by 1,284

Infiltration of CD4+ lymphocytes into the brain contributes to neurodegeneration in a mouse model of Parkinson disease

Brochard, V., Combadière, B., Prigent, A., Laouar, Y., Perrin, A., Beray-Berthat, V., Bonduelle, O., Alvarez-Fischer, D., Callebert, J., Launay, J.-M., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci36470 · Cited by 1,172

Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities

McKercher, S. R., Torbett, B. E., Anderson, K. L., Henkel, G. W., Vestal, D. J., Baribault, H., Klemsz, M., Feeney, A. J., Wu, G. E., Paige, C. J., et al. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00949.x · Cited by 1,130

The HIV coreceptors CXCR4 and CCR5 are differentially expressed and regulated on human T lymphocytes

Bleul, C. C., Wu, L., Hoxie, J. A., Springer, T. A., & Mackay, C. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.5.1925 · Cited by 1,134

Leukocyte Infiltration, Neuronal Degeneration, and Neurite Outgrowth after Ablation of Scar-Forming, Reactive Astrocytes in Adult Transgenic Mice

Bush, T. G., Puvanachandra, N., Horner, C. H., Polito, A., Ostenfeld, T., Svendsen, C. N., Mucke, L., Johnson, M. H., & Sofroniew, M. V. (1999) · Neuron · doi:10.1016/s0896-6273(00)80781-3 · Cited by 1,116

Three or more routes for leukocyte migration into the central nervous system

Ransohoff, R. M., Kivisäkk, P., & Kidd, G. (2003) · Nature Reviews Immunology · doi:10.1038/nri1130 · Cited by 1,052

IL-6: a regulator of the transition from neutrophil to monocyte recruitment during inflammation

Kaplanski, G. (2003) · Trends in Immunology · doi:10.1016/s1471-4906(02)00013-3 · Cited by 811

The α(1,3)Fucosyltransferase Fuc-TVII Controls Leukocyte Trafficking through an Essential Role in L-, E-, and P-selectin Ligand Biosynthesis

Malý, P., Thall, A. D., Petryniak, B., Rogers, C. E., Smith, P. L., Marks, R. M., Kelly, R. J., Gersten, K. M., Cheng, G., Saunders, T. L., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)80137-3 · Cited by 714

Structure, Function, and Inhibition of Chemokines

Fernandez, E. J., & Lolis, E. (2002) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.42.091901.115838 · Cited by 609

Tissue-Resident T Cells and Other Resident Leukocytes

Masopust, D., & Soerens, A. G. (2019) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042617-053214 · Cited by 608

Stress-induced redistribution of immune cells–from barracks to boulevards to battlefields: a tale of three hormones–Curt Richter Award winner

Dhabhar, F. S., Malarkey, W. B., Neri, E., & McEwen, B. S. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.05.008 · Cited by 589

Platelets in inflammation and thrombosis

Wagner, D. D., & Burger, P. C. (2003) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000095974.95122.ec · Cited by 570

A history of exploring cancer in context

Maman, S., & Witz, I. P. (2018) · Nature Reviews Cancer · doi:10.1038/s41568-018-0006-7 · Cited by 502

Calprotectin: from biomarker to biological function

Jukic, A., Bakiri, L., Wagner, E. F., Tilg, H., & Adolph, T. E. (2021) · Gut · doi:10.1136/gutjnl-2021-324855 · Cited by 500

Migratory properties of naive, effector, and memory CD8(+) T cells

Weninger, W., Crowley, M. A., Manjunath, N., & von Andrian, U. H. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.7.953 · Cited by 515

Leukocyte Trafficking Mediated by Selectin-Carbohydrate Interactions

McEver, R. P., Moore, K. L., & Cummings, R. D. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.19.11025 · Cited by 512

Lymphatic drainage of the brain and the pathophysiology of neurological disease

Weller, R. O., Djuanda, E., Yow, H.-Y., & Carare, R. O. (2009) · Acta Neuropathologica · doi:10.1007/s00401-008-0457-0 · Cited by 488

Decreased Atherosclerotic Lesion Formation in CX3CR1/Apolipoprotein E Double Knockout Mice

Combadière, C., Potteaux, S., Gao, J.-L., Esposito, B., Casanova, S., Lee, E. J., Debré, P., Tedgui, A., Murphy, P. M., & Mallat, Z. (2003) · Circulation · doi:10.1161/01.cir.0000057548.68243.42 · Cited by 476

Zoned Out: Functional Mapping of Stromal Signaling Microenvironments in the Thymus

Petrie, H. T., & Zúñiga-Pflücker, J. C. (2007) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115715 · Cited by 454

Leukocyte engagement of fibrin(ogen) via the integrin receptor αMβ2/Mac-1 is critical for host inflammatory response in vivo

Flick, M. J., Du, X., Witte, D. P., Jiroušková, M., Soloviev, D. A., Busuttil, S. J., Plow, E. F., & Degen, J. L. (2004) · Journal of Clinical Investigation · doi:10.1172/jci20741 · Cited by 450

Activated leukocyte cell adhesion molecule promotes leukocyte trafficking into the central nervous system

Cayrol, R., Wosik, K., Berard, J. L., Dodelet-Devillers, A., Ifergan, I., Kebir, H., Haqqani, A. S., Kreymborg, K., Krug, S., Moumdjian, R., et al. (2008) · Nature Immunology · doi:10.1038/ni1551 · Cited by 444

Endothelial heparan sulfate deficiency impairs L-selectin- and chemokine-mediated neutrophil trafficking during inflammatory responses

Wang, L., Fuster, M., Sriramarao, P., & Esko, J. D. (2005) · Nature Immunology · doi:10.1038/ni1233 · Cited by 413

Increased Atherosclerosis in Hyperlipidemic Mice With Inactivation of ABCA1 in Macrophages

Aiello, R. J., Brees, D., Bourassa, P.-A., Royer, L., Lindsey, S., Coskran, T., Haghpassand, M., & Francone, O. L. (2002) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000014804.35824.da · Cited by 390

p110δ, a novel phosphoinositide 3-kinase in leukocytes

Vanhaesebroeck, B., Welham, M. J., Kotani, K., Stein, R., Warne, P. H., Zvelebil, M. J., Higashi, K., Volinia, S., Downward, J., & Waterfield, M. D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.9.4330 · Cited by 376

Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

Gregg, A. R., Aarabi, M., Klugman, S., Leach, N. T., Bashford, M. T., Goldwaser, T., Chen, E., Sparks, T. N., Reddi, H. V., Rajkovic, A., et al. (2021) · Genetics in Medicine · doi:10.1038/s41436-021-01203-z · Cited by 367

Adhesion molecule expression and regulation on cells of the central nervous system

Lee, S. J., & Benveniste, E. N. (1999) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(99)00084-3 · Cited by 296

Role of β7 Integrins in Intestinal Lymphocyte Homing and Retention

Gorfu, G., Rivera-Nieves, J., & Ley, K. (2009) · Current Molecular Medicine · doi:10.2174/156652409789105525 · Cited by 292

Heparin’s anti-inflammatory effects require glucosamine 6-o-sulfation and are mediated by blockade of L- and P-selectins

Wang, L., Brown, J. R., Varki, A., & Esko, J. D. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0214996 · Cited by 288

Correction of leukocyte adhesion deficiency type II with oral fucose

Marquardt, T., Lühn, K., Srikrishna, G., Freeze, H. H., Harms, E., & Vestweber, D. (1999) · Blood · doi:10.1182/blood.v94.12.3976 · Cited by 280

The multifaceted profile of activated microglia

Lynch, M. A. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8077-9 · Cited by 268

Staphylococcus aureus extracellular adherence protein serves as anti-inflammatory factor by inhibiting the recruitment of host leukocytes

Chavakis, T., Hussain, M., Kanse, S. M., Peters, G., Bretzel, R. G., Flock, J.-I., Herrmann, M., & Preissner, K. T. (2002) · Nature Medicine · doi:10.1038/nm728 · Cited by 264

Cytokines and immunity to viral infections

Ramshaw, I. A., Ramsay, A. J., Karupiah, G., Rolph, M. S., Mahalingam, S., & Ruby, J. C. (1997) · Immunological Reviews · doi:10.1111/j.1600-065x.1997.tb01011.x · Cited by 257

Molecular Mechanisms Involved in Lymphocyte Recruitment in Inflamed Brain Microvessels: Critical Roles for P-Selectin Glycoprotein Ligand-1 and Heterotrimeric Gi-Linked Receptors

Piccio, L., Rossi, B., Scarpini, E., Laudanna, C., Giagulli, C., Issekutz, A. C., Vestweber, D., Butcher, E. C., & Constantin, G. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.4.1940 · Cited by 245

Integrin modulation and signaling in leukocyte adhesion and migration

Rose, D. M., Alon, R., & Ginsberg, M. H. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00536.x · Cited by 243

Integrin signalling in neutrophils and macrophages

Berton, G., & Lowell, C. A. (1999) · Cellular Signalling · doi:10.1016/s0898-6568(99)00003-0 · Cited by 224

Differential adhesion molecule requirements for immune surveillance and inflammatory recruitment

Carrithers, M. D., Visintin, I., Kang, S. J., & Janeway, C. A. (2000) · Brain · doi:10.1093/brain/123.6.1092 · Cited by 220

Untitled work

(1995) · PubMed · Cited by 215

The development of experimental autoimmune encephalomyelitis in the mouse requires alpha4-integrin but not alpha4beta7-integrin.

Engelhardt, B., Laschinger, M., Schulz, M., Samulowitz, U., Vestweber, D., & Hoch, G. (1998) · Journal of Clinical Investigation · doi:10.1172/jci4271 · Cited by 203

Endothelial focal adhesion kinase mediates cancer cell homing to discrete regions of the lungs via E-selectin up-regulation

Hiratsuka, S., Goel, S., Kamoun, W. S., Maru, Y., Fukumura, D., Duda, D. G., & Jain, R. K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100446108 · Cited by 196

Endothelial cell injury in cardiovascular surgery: ischemia-reperfusion.

Boyle, E. M., Pohlman, T. H., Cornejo, C. J., & Verrier, E. D. (1996) · The Annals of Thoracic Surgery · doi:10.1016/s0003-4975(96)00950-2 · Cited by 186

Antibodies against adhesion molecules reduce apoptosis after transient middle cerebral artery occlusion in rat brain

Chopp, M., Li, Y., Jiang, N., Zhang, R. L., & Prostak, J. (1996) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199607000-00007 · Cited by 185

VCAM-1-mediated Rac signaling controls endothelial cell-cell contacts and leukocyte transmigration

van Wetering, S., van den Berk, N., van Buul, J. D., Mul, F. P. J., Lommerse, I., Mous, R., Klooster, J.-P. T., Zwaginga, J.-J., & Hordijk, P. L. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00048.2003 · Cited by 185

Lymphocyte adhesion and transendothelial migration in the central nervous system: the role of LFA-1, ICAM-1, VLA-4 and VCAM-1. off.

(1995) · PubMed Central · Cited by 182

Toll-like Receptors in Defense and Damage of the Central Nervous System

Aravalli, R. N., Peterson, P. K., & Lokensgard, J. R. (2007) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-007-9071-5 · Cited by 173

Effects of cardiopulmonary bypass on leukocyte and endothelial adhesion molecules

Asimakopoulos, G., & Taylor, K. M. (1998) · The Annals of Thoracic Surgery · doi:10.1016/s0003-4975(98)00727-9 · Cited by 173

Antigen Presentation by Vascular Cells

Pober, J. S., Merola, J., Liu, R., & Manes, T. D. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01907 · Cited by 165

Endothelial heparan sulfate controls chemokine presentation in recruitment of lymphocytes and dendritic cells to lymph nodes

Bao, X., Moseman, E. A., Saito, H., Petryanik, B., Thiriot, A., Hatakeyama, S., Ito, Y., Kawashima, H., Yamaguchi, Y., Lowe, J. B., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.10.018 · Cited by 167

Heme Induces Neutrophil Migration and Reactive Oxygen Species Generation through Signaling Pathways Characteristic of Chemotactic Receptors

Porto, B. N., Alves, L. S., Fernández, P. L., Dutra, T. P., Figueiredo, R. T., Graça-Souza, A. V., & Bozza, M. T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703570200 · Cited by 161

ICAM-1-Induced Expression of Proinflammatory Cytokines in Astrocytes: Involvement of Extracellular Signal-Regulated Kinase and p38 Mitogen-Activated Protein Kinase Pathways

Lee, S. J., Drabik, K., Van Wagoner, N. J., Lee, S., Choi, C., Dong, Y., & Benveniste, E. N. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.8.4658 · Cited by 137

Mitochondrial damage-associated molecular patterns and vascular function

Wenceslau, C. F., McCarthy, C. G., Szasz, T., Spitler, K., Goulopoulou, S., Webb, R. C., & Working Group on DAMPs in Cardiovascular Disease (2014) · European Heart Journal · doi:10.1093/eurheartj/ehu047 · Cited by 135

A Role for the αvβ3 Integrin in the Transmigration of Monocytes

Weerasinghe, D., McHugh, K. P., Ross, F. P., Brown, E. J., Gisler, R. H., & Imhof, B. A. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.2.595 · Cited by 130

Synergy between proinflammatory ligands of G protein-coupled receptors in neutrophil activation and migration

Gouwy, M., Struyf, S., Catusse, J., Proost, P., & Van Damme, J. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.1003479 · Cited by 129

Monocyte Adhesion to Activated Aortic Endothelium: Role of L-Selectin and Heparan Sulfate Proteoglycans

Giuffrè, L., Cordey, A.-S., Monai, N., Tardy, Y., Schapira, M., & Spertini, O. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.136.4.945 · Cited by 122

Heparin inhibits the flow adhesion of sickle red blood cells to P-selectin

Matsui, N. M., Varki, A., & Embury, S. H. (2002) · Blood · doi:10.1182/blood-2002-02-0626 · Cited by 123

The extracellular matrix protein mindin serves as an integrin ligand and is critical for inflammatory cell recruitment

Jia, W., Li, H., & He, Y.-W. (2005) · Blood · doi:10.1182/blood-2005-04-1658 · Cited by 122

Tumor Necrosis Factor-α Induces Interleukin-6 Production and Integrin Ligand Expression by Distinct Transduction Pathways

De Cesaris, P., Starace, D., Riccioli, A., Padula, F., Filippini, A., & Ziparo, E. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.13.7566 · Cited by 116

Expression of the chemokine N51/KC in the thymus and epidermis of transgenic mice results in marked infiltration of a single class of inflammatory cells.

Lira, S. A., Zalamea, P., Heinrich, J. N., Fuentes, M. E., Carrasco, D., Lewin, A. C., Barton, D. S., Durham, S., & Bravo, R. (1994) · The Journal of experimental medicine · doi:10.1084/jem.180.6.2039 · Cited by 115

TNF-α-Induced Expression of Adhesion Molecules in the Liver Is Under the Control of TNFR1—Relevance for Concanavalin A-Induced Hepatitis

Wolf, D., Hallmann, R., Sass, G., Sixt, M., Küsters, S., Fregien, B., Trautwein, C., & Tiegs, G. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.2.1300 · Cited by 109

The extracellular adherence protein (Eap) of Staphylococcus aureus inhibits wound healing by interfering with host defense and repair mechanisms

Athanasopoulos, A. N. (2006) · Blood · doi:10.1182/blood-2005-08-3140 · Cited by 109

Sialoglycoproteins adsorbed by Pseudomonas aeruginosa facilitate their survival by impeding neutrophil extracellular trap through siglec-9

Khatua, B., Bhattacharya, K., & Mandal, C. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0511260 · Cited by 104

Lymphocyte homing to the gut: attraction, adhesion, and commitment

Salmi, M., & Jalkanen, S. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00285.x · Cited by 103

CCL‐11 or Eotaxin‐1: an immune marker for ageing and accelerated ageing in neuro‐psychiatric disorders

Ivanovska, M., Abdi, Z., Murdjeva, M., Macedo, D., Maes, A., & Maes, M. (2020) · Pharmaceuticals · doi:10.3390/ph13090230 · Cited by 83

In vivo expression of neutrophil inhibitory factor via gene transfer prevents lipopolysaccharide-induced lung neutrophil infiltration and injury by a beta2 integrin-dependent mechanism

Zhou, M. Y., Lo, S. K., Bergenfeldt, M., Tiruppathi, C., Jaffe, A., Xu, N., & Malik, A. B. (1998) · Journal of Clinical Investigation · doi:10.1172/jci407 · Cited by 81

Identification of a Novel Integrin αMβ2 Binding Site in CCN1 (CYR61), a Matricellular Protein Expressed in Healing Wounds and Atherosclerotic Lesions

Schober, J. M., Lau, L. F., Ugarova, T. P., & Lam, S. C.-T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301534200 · Cited by 76

A Role for Macrophage Inflammatory Protein-3α/CC Chemokine Ligand 20 in Immune Priming During T Cell-Mediated Inflammation of the Central Nervous System

Kohler, R. E., Caon, A. C., Willenborg, D. O., Clark-Lewis, I., & McColl, S. R. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.12.6298 · Cited by 79

Intestinal Barrier Interactions with Specialized CD8 T Cells

Konjar, Š., Ferreira, C., Blankenhaus, B., & Veldhoen, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01281 · Cited by 77

IFN-γ Inhibits Activation-Induced Expression of E- and P-Selectin on Endothelial Cells

Melrose, J., Tsurushita, N., Liu, G., & Berg, E. L. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.5.2457 · Cited by 75

Characterization of biodegradable drug delivery vehicles with the adhesive properties of leukocytes II: Effect of degradation on targeting activity

Eniola, A. O., & Hammer, D. A. (2005) · Biomaterials · doi:10.1016/j.biomaterials.2004.03.003 · Cited by 72

The role of osteopontin in foreign body giant cell formation

Tsai, A. T., Rice, J., Scatena, M., Liaw, L., Ratner, B. D., & Giachelli, C. M. (2005) · Biomaterials · doi:10.1016/j.biomaterials.2005.03.003 · Cited by 71

Prolactin stimulates integrin-mediated adhesion of circulating mononuclear cells to endothelial cells

Montes de Oca, P., Macotela, Y., Nava, G., López-Barrera, F., de la Escalera, G. M., & Clapp, C. (2005) · Laboratory Investigation · doi:10.1038/labinvest.3700256 · Cited by 71

Lymphocytes in the lung: an often neglected cell: Numbers, characterization and compartmentalization

Pabst, R., & Tschernig, T. (1995) · Anatomy and Embryology · doi:10.1007/bf00710098 · Cited by 71

Mechanisms of MAdCAM-1 gene expression in human intestinal microvascular endothelial cells

Ogawa, H., Binion, D. G., Heidemann, J., Theriot, M., Fisher, P. J., Johnson, N. A., Otterson, M. F., & Rafiee, P. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00406.2003 · Cited by 68

Synthetic Microvascular Networks for Quantitative Analysis of Particle Adhesion

Prabhakarpandian, B., Pant, K., Scott, R. C., Patillo, C. B., Irimia, D., Kiani, M. F., & Sundaram, S. (2008) · Biomedical Microdevices · doi:10.1007/s10544-008-9170-y · Cited by 68

Iron-dependent trafficking of 5-lipoxygenase and impact on human macrophage activation

Dufrusine, B., Di Francesco, A., Oddi, S., Scipioni, L., Angelucci, C. B., D'Addario, C., Serafini, M., Häfner, A.-K., Steinhilber, D., Maccarrone, M., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01347 · Cited by 63

Dexamethasone-induced effects on lymphocyte distribution and expression of adhesion molecules in treatment-resistant depression

Bauer, M. E., Papadopoulos, A., Poon, L., Perks, P., Lightman, S. L., Checkley, S., & Shanks, N. (2002) · Psychiatry Research · doi:10.1016/s0165-1781(02)00243-3 · Cited by 62

Mechanisms of Dendritic Cell Trafficking Across the Blood–brain Barrier

Sagar, D., Foss, C., El Baz, R., Pomper, M. G., Khan, Z. K., & Jain, P. (2012) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-011-9302-7 · Cited by 60

Negative Regulation of Myeloid Cell Proliferation and Function by the SH2 Domain-Containing Tyrosine Phosphatase-1

Dong, Q., Siminovitch, K. A., Fialkow, L., Fukushima, T., & Downey, G. P. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.6.3220 · Cited by 58

Rho GTPases and Regulation of Hematopoietic Stem Cell Localization

(2008) · Methods in Enzymology · doi:10.1016/s0076-6879(07)00427-2 · Cited by 54

RUNX/AML and C/EBP factors regulate CD11a integrin expression in myeloid cells through overlapping regulatory elements.

Puig-Kröger, A., Sánchez-Elsner, T., Ruiz, N., Andreu, E. J., Prosper, F., Jensen, U. B., Gil, J., Erickson, P., Drabkin, H., Groner, Y., et al. (2003) · Blood · doi:10.1182/blood-2003-02-0618 · Cited by 51

Understanding the molecular drivers of disease heterogeneity in Crohn's disease using multi-omic data integration and network analysis

Sudhakar, P., Verstockt, B., Cremer, J., Verstockt, S., Sabino, J., Ferrante, M., & Vermeire, S. (2021) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izaa281 · Cited by 49

Strength Endurance Training but Not Intensive Strength Training Reduces Senescence-Prone T Cells in Peripheral Blood in Community-Dwelling Elderly Women

Cao Dinh, H., Njemini, R., Onyema, O. O., Beyer, I., Liberman, K., De Dobbeleer, L., Renmans, W., Vander Meeren, S., Jochmans, K., Delaere, A., et al. (2019) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gly229 · Cited by 47

Neutrophil Gelatinase B and Chemokines in Leukocytosis and Stem Cell Mobilization

Starckx, S., Van den Steen, P. E., Wuyts, A., Van Damme, J., & Opdenakker, G. (2002) · Leukemia & Lymphoma · doi:10.1080/10428190290005982 · Cited by 49

Circulating adhesion molecules in obstructive sleep apnea and cardiovascular disease

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