Annexin A1 and glucocorticoids as effectors of the resolution of inflammation

How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions

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Antiinflammatory Action of Glucocorticoids — New Mechanisms for Old Drugs

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Resolution of inflammation: the beginning programs the end

Serhan, C. N., & Savill, J. (2005) · Nature Immunology · doi:10.1038/ni1276 · Cited by 2,552

Annexins: linking Ca2+ signalling to membrane dynamics

Gerke, V., Creutz, C. E., & Moss, S. E. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1661 · Cited by 1,412

Resolution of in flammation: state of the art, definitions and terms

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Promotion of Tissue Inflammation by the Immune Receptor Tim-3 Expressed on Innate Immune Cells

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Histone deacetylase 2–mediated deacetylation of the glucocorticoid receptor enables NF-κB suppression

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Glucocorticoids and the Th1/Th2 Balance

Elenkov, I. J. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1321.010 · Cited by 618

Glucocorticoids promote a TH2 cytokine response by CD4+ T cells in vitro

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The Lipoxin Receptor ALX: Potent Ligand-Specific and Stereoselective Actions in Vivo

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Annexin-A1 Regulates TLR-Mediated IFN-β Production through an Interaction with TANK-Binding Kinase 1

Bist, P., Shu, S., Lee, H., Arora, S., Nair, S., Lim, J. Y., Dayalan, J., Gasser, S., Biswas, S. K., Fairhurst, A., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301504 · Cited by 48

An emphasis on molecular mechanisms of anti-inflammatory effects and glucocorticoid resistance

Ingawale, D. K., Mandlik, S. K., & Patel, S. S. (2014) · Journal of Complementary and Integrative Medicine · doi:10.1515/jcim-2014-0051 · Cited by 49

Increased Adiposity in Annexin A1-Deficient Mice

Akasheh, R. T., Pini, M., Pang, J., & Fantuzzi, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082608 · Cited by 47

Adapting to environmental stresses: the role of the microbiota in controlling innate immunity and behavioral responses

Fagundes, C. T., Amaral, F. A., Teixeira, A. L., Souza, D. G., & Teixeira, M. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01077.x · Cited by 48

Immunoresolving actions of oral resolvin D1 include selective regulation of the transcription machinery in resolution‐phase mouse macrophages

Recchiuti, A., Codagnone, M., Pierdomenico, A. M., Rossi, C., Mari, V. C., Cianci, E., Simiele, F., Gatta, V., & Romano, M. (2014) · The FASEB Journal · doi:10.1096/fj.13-248393 · Cited by 50

Annexin A1 translocates to nucleus and promotes the expression of pro-inflammatory cytokines in a PKC-dependent manner after OGD/R

Zhao, B., Wang, J., Liu, L., Li, X., Liu, S., Xia, Q., & Shi, J. (2016) · Scientific Reports · doi:10.1038/srep27028 · Cited by 49

Annexin A1 Contained in Extracellular Vesicles Promotes the Activation of Keratinocytes by Mesoglycan Effects: An Autocrine Loop Through FPRs

Pessolano, E., Belvedere, R., Bizzarro, V., Franco, P., Marco, I. D., Petrella, F., Porta, A., Tosco, A., Parente, L., Perretti, M., et al. (2019) · Cells · doi:10.3390/cells8070753 · Cited by 47

Glioma-derived ANXA1 suppresses the immune response to TLR3 ligands by promoting an anti-inflammatory tumor microenvironment

Zheng, Y., Jiang, H., Yang, N., Shen, S., Huang, D., Jia, L., Ling, J., Xu, L., Li, M., Yu, K., et al. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01110-0 · Cited by 46

Annexin A1: Novel roles in skeletal muscle biology

Bizzarro, V., Petrella, A., & Parente, L. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.24032 · Cited by 46

miR-146a and miR-196a2 Polymorphisms in Patients with Ischemic Stroke in the Northern Chinese Han Population

Zhu, R., Liu, X., He, Z., & Li, Q. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1364-5 · Cited by 46

Formyl Peptide Receptor 2 Plays a Deleterious Role During Influenza A Virus Infections

Tcherniuk, S. O., Cénac, N., Comte, M., Frouard, J., Errazuriz-Cerda, E., Galabov, A. G., Morange, P., Vergnolle, N., Si‐Tahar, M., Alessi, M., et al. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw127 · Cited by 47

Resolution of inflammation in neuromyelitis optica spectrum disorders

Wang, X., Jiao, W., Lin, M., Lu, C., Liu, C., Wang, Y., Ma, D., Wang, X., Yin, P., Feng, J., et al. (2018) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2018.09.040 · Cited by 47

Annexins in Adipose Tissue: Novel Players in Obesity

Grewal, T., Enrich, C., Rentero, C., & Buechler, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20143449 · Cited by 46

Emerging Role of Exosomes in Diagnosis and Treatment of Infectious and Inflammatory Bowel Diseases

Larabi, A. B., Barnich, N., & Nguyen, H. T. T. (2020) · Cells · doi:10.3390/cells9051111 · Cited by 47

Colonization by Enterobacteriaceae is crucial for acute inflammatory responses in murine small intestine via regulation of corticosterone production

Garcia, Z. M., Arifa, R. D. D. N., Acúrcio, L. B., de Brito, C. B., Gouvea, J. O., Lima, R. L., Bastos, R. W., Dias, A. C. F., Dourado, L. P. A., Bastos, L. F. S., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1765946 · Cited by 46

The effect of galectins on leukocyte trafficking in inflammation: sweet or sour?

Cooper, D., Iqbal, A. J., Gittens, B. R., Cervone, C., & Perretti, M. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06291.x · Cited by 46

Attenuation of plasma annexin A1 in human obesity

Kosicka, A., Cunliffe, A., Mackenzie, R., Zariwala, M. G., Perretti, M., Flower, R. J., & Renshaw, D. W. (2012) · The FASEB Journal · doi:10.1096/fj.12-213728 · Cited by 45

A comparison of the bovine uterine and plasma proteome using i TRAQ proteomics

Faulkner, S., Elia, G., Mullen, M. P., O’Boyle, P., Dunn, M. J., & Morris, D. G. (2012) · PROTEOMICS · doi:10.1002/pmic.201100609 · Cited by 45

Annexin A1 and specialized proresolving lipid mediators: promoting resolution as a therapeutic strategy in human inflammatory diseases

Perucci, L. O., Sugimoto, M. A., Gomes, K. B., Dusse, L. M. S., Teixeira, M. M., & Sousa, L. P. (2017) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2017.1364363 · Cited by 45

Conserved aging-related signatures of senescence and inflammation in different tissues and species

Barth, E., Srivastava, A., Stojiljkovic, M. R., Frahm, C., Axer, H., Witte, O. W., & Marz, M. (2019) · Aging · doi:10.18632/aging.102345 · Cited by 47

Extra-adrenal glucocorticoid synthesis in the intestinal epithelium: more than a drop in the ocean

Noti, M., Sidler, D., & Brunner, T. (2009) · Seminars in Immunopathology · doi:10.1007/s00281-009-0159-2 · Cited by 44

Exposure to chemical cocktails before or after conception – The effect of timing on ovarian development

Bellingham, M., Amezaga, M. R., Mandon‐Pepin, B., Speers, C., Kyle, C., Evans, N. P., Sharpe, R. M., Cotinot, C., Rhind, S. M., & Fowler, P. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.06.016 · Cited by 44

Development of novel treatment strategies for inflammatory diseases—similarities and divergence between glucocorticoids and GILZ

Cheng, Q., Morand, E. F., & Yang, Y. H. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00169 · Cited by 45

Inhibition of Phosphodiesterase-4 during Pneumococcal Pneumonia Reduces Inflammation and Lung Injury in Mice

Tavares, L. P., Garcia, C. C., Vago, J. P., Queiroz‐Junior, C. M., Galvão, I., David, B. A., Rachid, M. A., Silva, P., Russo, R. C., Teixeira, M. M., et al. (2015) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2015-0083oc · Cited by 44

Role of the glucocorticoid‐induced leucine zipper gene in dexamethasone‐induced inhibition of mouse neutrophil migration via control of annexin A1 expression

Ricci, E., Ronchetti, S., Pericolini, E., Gabrielli, E., Cari, L., Gentili, M., Roselletti, E., Migliorati, G., Vecchiarelli, A., & Riccardi, C. (2017) · The FASEB Journal · doi:10.1096/fj.201601315r · Cited by 44

Annexin A1 N-Terminal Derived Peptide Ac2-26 Exerts Chemokinetic Effects on Human Neutrophils

Dalli, J., Montero‐Melendez, T., McArthur, S., & Perretti, M. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2012.00028 · Cited by 44

Ginsenoside Rh1 potentiates dexamethasone’s anti-inflammatory effects for chronic inflammatory disease by reversing dexamethasone-induced resistance

Li, J., Du, J., Liu, D., Cheng, B., Fang, F., Weng, L., Wang, C., & Ling, C. (2014) · Arthritis Research & Therapy · doi:10.1186/ar4556 · Cited by 43

The glucocorticoid budesonide has protective and deleterious effects in experimental colitis in mice

Ocón, B., Aranda, C. J., Gámez‐Belmonte, R., Suárez, M. D., Zarzuelo, A., Martínez‐Augustin, O., & de Medina, F. S. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.07.010 · Cited by 43

Annexins and plasma membrane repair

Koerdt, S. N., Ashraf, A. P. K., & Gerke, V. (2019) · Current topics in membranes · doi:10.1016/bs.ctm.2019.07.006 · Cited by 43

Disease Resolution in Chikungunya—What Decides the Outcome?

Srivastava, P., Kumar, A., Hasan, A., Mehta, D., Kumar, R., Sharma, C., & Sunil, S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00695 · Cited by 44

Airway lipoxin A4/formyl peptide receptor 2–lipoxin receptor levels in pediatric patients with severe asthma

Gagliardo, R. P., Gras, D., Grutta, S. L., Chanez, P., Sano, C. D., Albano, G. D., Vachier, I., Montalbano, A. M., Anzalone, G., Bonanno, A., et al. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.11.045 · Cited by 43

Humanized Mouse Models of Systemic Lupus Erythematosus: Opportunities and Challenges

Chen, J., Liao, S., Zhou, H., Yang, L., Guo, F., Chen, S., Li, A., Pan, Q., Yang, C., Liu, J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.816956 · Cited by 42

Glucocorticoids regulate lipid mediator networks by reciprocal modulation of 15-lipoxygenase isoforms affecting inflammation resolution

Rao, Z., Brunner, E., Giszas, B., Iyer-Bierhoff, A., Gerstmeier, J., Börner, F., Jordan, P. M., Pace, S., Meyer, K. P. L., Hofstetter, R. K., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2302070120 · Cited by 42

Acute Stress Elicited by Bungee Jumping Suppresses Human Innate Immunity

van Westerloo, D. J., Choi, G., Löwenberg, E. C., Truijen, J., de Vos, A. F., Endert, E., Meijers, J. C. M., Zhou, L., Pereira, M. P., Queiroz, K. C. S., et al. (2010) · Molecular Medicine · doi:10.2119/molmed.2010.00204 · Cited by 43

PPARγ Ligand–induced Annexin A1 Expression Determines Chemotherapy Response via Deubiquitination of Death Domain Kinase RIP in Triple-negative Breast Cancers

Chen, L., Yuan, Y., Kar, S., Kanchi, M. M., Arora, S., Kim, J. E., Koh, P. F., Yousef, E. M., Samy, R. P., Shanmugam, M. K., et al. (2017) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-16-0739 · Cited by 42

Specialized Pro-resolving Mediators Regulate Alveolar Fluid Clearance during Acute Respiratory Distress Syndrome

Wang, Q., Yan, S.-F., Yu, H., & Jin, S. (2018) · Chinese Medical Journal · doi:10.4103/0366-6999.229890 · Cited by 42

Endogenous Galectin-1 and Acute Inflammation

Iqbal, A. J., Sampaio, A. L. F., Μaione, F., Greco, K. V., Niki, T., Hirashima, M., Perretti, M., & Cooper, D. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2010.11.073 · Cited by 42

Targeting the Annexin A1-FPR2/ALX pathway for host-directed therapy in dengue disease

Costa, V. V., Sugimoto, M. A., Hubner, J., Bonilha, C. S., Queiroz‐Junior, C. M., Gonçalves-Pereira, M. H., Chen, J., Gobbetti, T., Rodrigues, G. O. L., Bambirra, J. L., et al. (2022) · eLife · doi:10.7554/elife.73853 · Cited by 42

Regulation of the CCL2 Gene in Pancreatic β-Cells by IL-1β and Glucocorticoids: Role of MKP-1

Burke, S. J., Goff, M. R., Updegraff, B. L., Lu, D., Brown, P. L., Minkin, S. C., Biggerstaff, J., Zhao, L., Karlstad, M. D., & Collier, J. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046986 · Cited by 43

Ginsenoside Rg1 attenuates ultraviolet B-induced glucocortisides resistance in keratinocytes via Nrf2/HDAC2 signalling

Li, J., Liu, D., Wu, J., Zhang, D., Cheng, B., Zhang, Y., Yin, Z., Wang, Y., Du, J., & Ling, C. (2016) · Scientific Reports · doi:10.1038/srep39336 · Cited by 41

An engineered cyclic peptide alleviates symptoms of inflammation in a murine model of inflammatory bowel disease

Caceres, C. C., Bansal, P. S., Navarro, S., Wilson, D. T. R., Don, L., Giacomin, P., Loukas, A. C., & Daly, N. L. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.779215 · Cited by 41

Extracellular Vesicles in Inflammatory Bowel Disease: Small Particles, Big Players

Valter, M., Verstockt, S., Ferreiro, J. A. F., & Cleynen, I. (2020) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjaa179 · Cited by 42

A Prognostic Microenvironment-Related Immune Signature via ESTIMATE (PROMISE Model) Predicts Overall Survival of Patients With Glioma

Qiu, H., Li, Y., Cheng, S., Li, J., He, C. H., & Li, J. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.580263 · Cited by 43

Apoptotic neurons and amyloid-beta clearance by phagocytosis in Alzheimer's disease: Pathological mechanisms and therapeutic outlooks

Tajbakhsh, A., Read, M. I., Barreto, G. E., Ávila-Rodriguez, M., Hayat, S. M. G., & Sahebkar, A. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.173873 · Cited by 41

Efferocytosis during Skeletal Muscle Regeneration

Juban, G., & Chazaud, B. (2021) · Cells · doi:10.3390/cells10123267 · Cited by 41

Annexin-1 regulated by HAUSP is essential for UV-induced damage response

Park, J.-J., Lim, K.-H., & Baek, K.-H. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.32 · Cited by 41

Implications for eicosapentaenoic acid- and docosahexaenoic acid-derived resolvins as therapeutics for arthritis

Souza, P. R., & Norling, L. V. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.05.072 · Cited by 42

Ten years of proteomics in multiple sclerosis

Farias, A. S., Pradella, F., Schmitt, A., Santos, L. M. B., & Martins‐de‐Souza, D. (2014) · PROTEOMICS · doi:10.1002/pmic.201300268 · Cited by 40

Quantitative Proteomics Profiling of Murine Mammary Gland Cells Unravels Impact of Annexin-1 on DNA Damage Response, Cell Adhesion, and Migration

Swa, H. L. F., Blackstock, W. P., Lim, L. H. K., & Gunaratne, J. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m111.011205 · Cited by 40

Targeting pro-resolution pathways to combat chronic inflammation in COPD.

Bozinovski, S., Anthony, D., & Vlahos, R. (2014) · PubMed Central · doi:10.3978/j.issn.2072-1439.2014.08.08 · Cited by 40

The hidden role of NLRP3 inflammasome in obesity‐related COVID‐19 exacerbations: Lessons for drug repurposing

Bertocchi, I., Foglietta, F., Collotta, D., Eva, C. E., Brancaleone, V., Thiemermann, C., & Collino, M. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15229 · Cited by 40

Chronic Hyperglycemia Drives Functional Impairment of Lymphocytes in Diabetic INSC94Y Transgenic Pigs

Giese, I.-M., Schilloks, M.-C., Degroote, R. L., Weigand, M., Renner, S., Wolf, E., Hauck, S. M., & Deeg, C. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.607473 · Cited by 40

Neuroprotective Effects of Annexin A1 Tripeptide after Deep Hypothermic Circulatory Arrest in Rats

Zhang, Z., Ma, Q., Shah, B., Mackensen, G. B., Lo, D. C., Mathew, J. P., Podgoreanu, M. V., & Terrando, N. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01050 · Cited by 39

Proresolving protein Annexin A1: The role in type 2 diabetes mellitus and obesity

Pietrani, N. T., Ferreira, C. N., Rodrigues, K. F., Perucci, L. O., Carneiro, F. S., Bosco, A., Oliveira, M. C., Pereira, S. S., Teixeira, A. L., Alvarez-Leite, J. I., et al. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.04.024 · Cited by 40

Molecular regulators of resolution of inflammation: potential therapeutic targets in the reproductive system

Hutchinson, J. L., Rajagopal, S. P., Sales, K. J., & Jabbour, H. N. (2011) · Reproduction · doi:10.1530/rep-11-0069 · Cited by 39

Absence of Annexin A1 impairs host adaptive immunity against Mycobacterium tuberculosis in vivo

Koh, V. H. Q., Julia, M. G., Lin, W., Michelle, A. L. T., Zarina, Z. R. S., Lina, L. H. K., & Alonso, S. (2014) · Immunobiology · doi:10.1016/j.imbio.2014.12.001 · Cited by 38

Annexin-A1 restricts Th17 cells and attenuates the severity of autoimmune disease

Yazid, S., Gardner, P. J., Carvalho, L. S., Chu, C. J., Flower, R. J., Solito, E., Lee, R., Ali, R. R., & Dick, A. D. (2015) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.12.004 · Cited by 39

TNFR1/Phox Interaction and TNFR1 Mitochondrial Translocation Thwart Silica-Induced Pulmonary Fibrosis

Fazzi, F., Njah, J., Giuseppe, M. D., Winnica, D., Go, K. L., Sala, E., Croix, C. M. S., Watkins, S. C., Tyurin, V. A., Phinney, D. G., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1103516 · Cited by 37

Antiallergic Cromones Inhibit Neutrophil Recruitment Onto Vascular Endothelium via Annexin-A1 Mobilization

Yazid, S., Leoni, G., Getting, S. J., Cooper, D., Solito, E., Perretti, M., & Flower, R. J. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.209536 · Cited by 37

FPR2: A Novel Promising Target for the Treatment of Influenza

Alessi, M., Cénac, N., Si‐Tahar, M., & Riteau, B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01719 · Cited by 37

CFTR Inhibition Provokes an Inflammatory Response Associated with an Imbalance of the Annexin A1 Pathway

Dalli, J., Rosignoli, G., Hayhoe, R. P. G., Edelman, A., & Perretti, M. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.091149 · Cited by 36

Dexamethasone for Severe COVID-19: How Does It Work at Cellular and Molecular Levels?

Kino, T., Burd, I. D., & Segars, J. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136764 · Cited by 36

Anti‐annexin 1 antibodies: A new diagnostic marker in the serum of patients with discoid lupus erythematosus

Kretz, C. C., Norpo, M., Abeler‐Dörner, L., Linke, B., Haust, M., Edler, L., Krammer, P. H., & Kuhn, A. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2010.01145.x · Cited by 36

Induction of an anti-inflammatory human monocyte subtype is a unique property of glucocorticoids, but can be modified by IL-6 and IL-10

Tsianakas, A., Varga, G., Barczyk, K., Bode, G., Nippe, N., Kran, N., Roth, J., Luger, T. A., Ehrchen, J. M., & Sunderkötter, C. H. (2011) · Immunobiology · doi:10.1016/j.imbio.2011.10.002 · Cited by 36

Natural selection in bats with historical exposure to white-nose syndrome

Harazim, M., Horáček, I., Jakešová, L., Luermann, K., Moravec, J., Morgan, S., Pikula, J., Sosı́k, P., Vavrušová, Z., Zahradníková, A., et al. (2018) · BMC Zoology · doi:10.1186/s40850-018-0035-4 · Cited by 36

A therapeutic antibody targeting annexin-A1 inhibits cancer cell growth in vitro and in vivo

Al‐Ali, H., Crichton, S. J., Fabian, C., Pepper, C. J., Butcher, D. R., Dempsey, F. C., & Parris, C. N. (2024) · Oncogene · doi:10.1038/s41388-023-02919-9 · Cited by 35

Annexin 1: A glucocorticoid‐inducible protein that modulates inflammatory pain

Chen, L., Lv, F., & Pei, L. (2013) · European Journal of Pain · doi:10.1002/j.1532-2149.2013.00373.x · Cited by 35

Targeting formyl peptide receptors to facilitate the resolution of inflammation

Filep, J. G., Sekheri, M., & Kebir, D. E. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.06.025 · Cited by 35

Sex-dependent differences in the secretome of human endothelial cells

Cattaneo, M. G., Banfi, C., Brioschi, M., Lattuada, D., & Vicentini, L. M. (2021) · Biology of Sex Differences · doi:10.1186/s13293-020-00350-3 · Cited by 35

Annexin A protein family in atherosclerosis

Li, Y., Wang, Y., Huang, L., Zhao, Y.-Y., Chen, L.-H., & Zhang, C. (2022) · Clinica Chimica Acta · doi:10.1016/j.cca.2022.05.009 · Cited by 37

Formyl Peptide Receptor as a Novel Therapeutic Target for Anxiety-Related Disorders

Irene, G., Rattazzi, L., Piras, G., Gobbetti, T., Panza, E., Perretti, M., Dalley, J. W., & D’Acquisto, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0114626 · Cited by 35

Efficient Reovirus- and Measles Virus-Mediated Pore Expansion during Syncytium Formation Is Dependent on Annexin A1 and Intracellular Calcium

Ciechonska, M., Key, T. A., & Duncan, R. (2014) · Journal of Virology · doi:10.1128/jvi.00121-14 · Cited by 35

Emerging Nanotechnologies and Microbiome Engineering for the Treatment of Inflammatory Bowel Disease

Abed, O. A., Attlassy, Y., Xu, J., Han, K., & Moon, J. J. (2022) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.2c00222 · Cited by 34

Switching Off Key Signaling Survival Molecules to Switch On the Resolution of Inflammation

Perez, D., Vago, J. P., Athayde, R. M., Reis, A. C., Teixeira, M. M., Sousa, L. P., & Pinho, V. (2014) · Mediators of Inflammation · doi:10.1155/2014/829851 · Cited by 34

Caffeine modulates glucocorticoid-induced expression of CTGF in lung epithelial cells and fibroblasts

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Mast cells mediate early neutrophil recruitment and exhibit anti‐inflammatory propertiesviathe formyl peptide receptor 2/lipoxin A4receptor

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MC-12, an Annexin A1-Based Peptide, Is Effective in the Treatment of Experimental Colitis

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Gene expression signature-based approach identifies a pro-resolving mechanism of action for histone deacetylase inhibitors

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H 2 S-induced thiol-based redox switches: Biochemistry and functional relevance for inflammatory diseases

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Combined Transcriptomics, Proteomics and Bioinformatics Identify Drug Targets in Spinal Cord Injury

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Heterogeneity in mechanisms influencing glucocorticoid sensitivity: The need for a systems biology approach to treatment of glucocorticoid-resistant inflammation

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ANXA1 directs Schwann cells proliferation and migration to accelerate nerve regeneration through the FPR2/AMPK pathway

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Inhibition of STAT6 Activation by AS1517499 Inhibits Expression and Activity of PPARγ in Macrophages to Resolve Acute Inflammation in Mice

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