Delayed Wound Healing in CXCR2 Knockout Mice

Wound Healing--Aiming for Perfect Skin Regeneration

Martin, P. B. (1997) · Science · doi:10.1126/science.276.5309.75 · Cited by 4,842

Actin-Based Cell Motility and Cell Locomotion

Mitchison, T. J., & Cramer, L. P. (1996) · Cell · doi:10.1016/s0092-8674(00)81281-7 · Cited by 1,538

The role of the macrophage in wound repair. A study with hydrocortisone and antimacrophage serum.

(1975) · PubMed Central · Cited by 1,437

Selective attraction of monocytes and T lymphocytes of the memory phenotype by cytokine RANTES

Schall, T. J., Bacon, K. B., Toy, K. J., & Goeddel, D. V. (1990) · Nature · doi:10.1038/347669a0 · Cited by 1,378

Neutralisation of TGF-β1 and TGF-β2 or exogenous addition of TGF-β3 to cutaneous rat wounds reduces scarring

Shah, M., Foreman, D. M., & Ferguson, M. W. J. (1995) · Journal of Cell Science · doi:10.1242/jcs.108.3.985 · Cited by 1,168

Wound Macrophages Express TGF-α and Other Growth Factors in Vivo: Analysis by mRNA Phenotyping

Rappolee, D. A., Mark, D., Banda, M. J., & Werb, Z. (1988) · Science · doi:10.1126/science.3041594 · Cited by 1,105

Expression of vascular permeability factor (vascular endothelial growth factor) by epidermal keratinocytes during wound healing.

Brown, L. F., Yeo, K. T., Berse, B., Yeo, T. K., Senger, D. R., Dvorak, H. F., & van de Water, L. (1992) · The Journal of experimental medicine · doi:10.1084/jem.176.5.1375 · Cited by 878

Preferential Migration of Activated CD4 + and CD8 + T Cells in Response to MIP-1α and MIP-1β

Taub, D. D., Conlon, K., Lloyd, A. R., Oppenheim, J. J., & Kelvin, D. J. (1993) · Science · doi:10.1126/science.7682337 · Cited by 730

Neutrophil and B Cell Expansion in Mice That Lack the Murine IL-8 Receptor Homolog

Cacalano, G., Lee, J., Kikly, K. K., Ryan, A. M., Pitts-Meek, S., Hultgren, B., Wood, W. I., & Moore, M. W. (1994) · Science · doi:10.1126/science.8036519 · Cited by 663

Human monocyte chemoattractant protein‐1 (MCP‐1) Full‐length cDNA cloning, expression in mitogen‐stimulated blood mononuclear leukocytes, and sequence similarity to mouse competence gene JE

Yoshimura, T., Yuhki, N., Moore, S. K., Appella, E., Lerman, M. I., & Leonard, E. J. (1989) · FEBS Letters · doi:10.1016/0014-5793(89)80590-3 · Cited by 589

Analysis of the Influence of Jaw Periosteal Cells on Macrophages Phenotype Using an Innovative Horizontal Coculture System

He, F., Umrath, F., OHLE, C. V., Reinert, S., & Alexander, D. (2021) · Biomedicines · doi:10.3390/biomedicines9121753 · Cited by 10

The lysosomal trafficking regulator is necessary for normal wound healing

Zbinden, J. C., Mirhaidari, G. J. M., Blum, K. M., Musgrave, A., Reinhardt, J. W., Breuer, C. K., & Barker, J. C. (2021) · Wound Repair and Regeneration · doi:10.1111/wrr.12984 · Cited by 9

Single cell transcriptomic analysis of Graves’ disease thyroid glands reveals the broad immunoregulatory potential of thyroid follicular and stromal cells and implies a major re-interpretation of the role of aberrant HLA class II expression in autoimmunity

Álvarez‐Sierra, D., Rodríguez-Grande, J., Gómez, A., Bello, I., Caubet, E., González, Ó., Zafón, C., Iglesias, C., Moreno, P., Ruíz, N., et al. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103072 · Cited by 11

Role of CXCR2 in the Ac-PGP-Induced Mobilization of Circulating Angiogenic Cells and its Therapeutic Implications

Kwon, Y. W., Lee, S.-J., Heo, S. C., Lee, T. W., Park, G. T., Yoon, J. W., Kim, S. C., Shin, H. J., Lee, S. C., & Kim, J. H. (2018) · Stem Cells Translational Medicine · doi:10.1002/sctm.18-0035 · Cited by 9

IL-8 receptor signaling as a novel target for angiogenic retinopathies

Garcia, M. J., Beall, A. L., Morales, M. S., Beatty, N. J., Palmer, S. A., Jhala, M. G., Drmanovic, A., Priest, S. O., Zhang, Y., Yang, R., et al. (2025) · Angiogenesis · doi:10.1007/s10456-025-10015-7 · Cited by 10

Serine protease from Tricosanthus tricuspidata accelerates healing of Echis carinatus venom-induced necrotic wound

Rudresha, G. V., Manjuprasanna, V. N., Urs, A. P., Choudhury, M., Rajaiah, R., & Vishwanath, B. S. (2020) · Toxicon · doi:10.1016/j.toxicon.2020.05.009 · Cited by 8

Peritoneal and Systemic Responses of Obese Type II Diabetic Rats to Chronic Exposure to a Hyperbranched Polyglycerol‐Based Dialysis Solution

Han, B. L., Guan, Q., Chafeeva, I., Mendelson, A. A., da Roza, G., Liggins, R., Kizhakkedathu, J. N., & Du, C. (2018) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13038 · Cited by 8

Response of chemokine receptors CXCR2 and integrin β2 after Streptococcus agalactiae and Aeromonas hydrophila challenge in GIFT strain of Nile tilapia Oreochromis niloticus

Hu, Q., Ao, Q., & Zhu, J. (2020) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2020.103897 · Cited by 8

Angiogenesis

Gerritsen, M. E. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374530-9.00008-5 · Cited by 8

Topical application of lectin Artin M improves wound healing in defects created in the palatal mucosa: an in vivo study in dogs

Kim, Y. J., de Molon, R. S., da Silva, V. C., Conrado, M., Spolidório, L. C., Roque-Barreira, M. C. A., & Cirelli, J. A. (2020) · Odontology · doi:10.1007/s10266-020-00495-y · Cited by 7

Transcriptomic Analysis of Human Mesenchymal Stem Cell Therapy in Incontinent Rat Injured Urethra

Sadeghi, Z., Kenyon, J. D., Richardson, B., Khalifa, A., Cartwright, M. J., Conroy, B., Caplan, A. I., Cameron, M. J., & Hijaz, A. (2020) · Tissue Engineering Part A · doi:10.1089/ten.tea.2020.0033 · Cited by 7

What good can neutrophils do in UC?

Salas, A. (2022) · Gut · doi:10.1136/gutjnl-2021-326484 · Cited by 7

Scratch wound-induced CXCL8 upregulation is EGFR-dependent in keratinocytes

Furue, K., Ito, T., Tsuji, G., Nakahara, T., & Furue, M. (2020) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2020.07.002 · Cited by 7

Effectiveness of Amniotic Fluid Injection in the Treatment of Trigger Finger: A Pilot Study

Quinet, M. T., Raghavan, M., Morris, E. C., Smith, T. B., Cook, H., Walter, N., & Shuler, M. S. (2020) · Journal of Hand Surgery Global Online · doi:10.1016/j.jhsg.2020.06.004 · Cited by 7

The CXC Chemokine Receptors in Four-Eyed Sleeper (Bostrychus sinensis) and Their Involvement in Responding to Skin Injury

Dong, M., Zhang, H., Mo, C., Li, W., Zhang, W., Jia, K., Liu, W., & Yi, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810022 · Cited by 7

Dysfunctional wound healing in chronic wounds

Stephens, P. (2011) · Elsevier eBooks · doi:10.1533/9780857093301.1.3 · Cited by 7

Inflammation in Wound Repair: Role and Function of Inflammation in Wound Repair

MacLeod, A. S., & Kwock, J. T. (2017) · Wiley eBooks · doi:10.1002/9781119282518.ch14 · Cited by 7

Mammalian musculoskeletal regeneration is associated with reduced inflammatory cytokines and an influx of T cellsPreprint

Gawriluk, T. R., Simkin, J., Hacker, C. K., Kimani, J., Kiama, S., Ezenwa, V., & Seifert, A. (2019) · bioRxiv · doi:10.1101/723783 · Cited by 8

HEALS-A and GRADES: Novel Histological and Clinical Scales for Assessing Skin Regeneration in Murine Wound Healing Models

Muñoz-Torres, J. R., Veloz, I. G., Velasco-Elizondo, P., & Martínez‐Fierro, M. L. (2025) · Diagnostics · doi:10.3390/diagnostics15030387 · Cited by 10

Modulating the CXCR2 Signaling Axis Using Engineered Chemokine Fusion Proteins to Disrupt Myeloid Cell Infiltration in Pancreatic Cancer

Christopher, B. N., Golick, L., Basar, A., Reyes, L., Robinson, R. M., Angerstein, A. O., Krieg, C., Hobbs, G. A., D, D. C. G., O’Bryan, J. P., et al. (2025) · Biomolecules · doi:10.3390/biom15050645 · Cited by 6

Apoptosis and Cell Clearance in Skin Wound Healing

Cleene, H. K. L. D., Keçeli, B. N., & Maschalidi, S. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-92785-0_5 · Cited by 6

G Protein–Coupled Receptors in Skin Aging

Cheung, S. T., Do, Y., Kim, E., Rella, A., Goyarts, E. C., Pernodet, N., & Wong, Y. H. (2024) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2024.06.1288 · Cited by 6

Absence of Langerhans cells resulted in over-influx of neutrophils and increased bacterial burden in skin wounds

Wang, Z., Hu, Y., Shen, X. Z., & Tan, W. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-07143-1 · Cited by 6

Wound Healing Effects of a Lipocalin-Derived Peptide

Tavassi, A. M. C. (2014) · Journal of Clinical Toxicology · doi:10.4172/2161-0495.1000187 · Cited by 6

Experimental models and high-throughput diagnostics for tissue regeneration

Andreadis, S. T. (2006) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.6.11.1071 · Cited by 6

CXC Chemokines in Angiogenesis Related to Pulmonary Fibrosis

Strieter, R. M., Belperio, J. A., & Keane, M. P. (2003) · Lung biology in health and disease · doi:10.1201/b14211-13 · Cited by 6

Zinc-Based Nanoparticles Reduce the Bacterial Burden and Protect Collagen in a Mouse Cutaneous Wound Model

Fulindi, R. B., Barbosa, T. W. L., Enriquez, V., Charles‐Niño, C., de Freitas, N. G., Salto, M. P., Chiavacci, L. A., Pratavieira, S., Araújo, J. P., COSTA, P. I. D., et al. (2026) · ACS Omega · doi:10.1021/acsomega.5c06287 · Cited by 5

Vascular Microarchitecture of Murine Colitis‐Associated Lymphoid Angiogenesis

Turhan, A., Lin, M., Lee, G. S., Miele, L. F., Tsuda, A., Konerding, M. A., & Mentzer, S. J. (2009) · The Anatomical Record · doi:10.1002/ar.20902 · Cited by 5

Local Angioneogenetic Effect of Intramuscular Interleukin-8 Injection

Bozok, Ş., Kestellı, M., Yurekli, I. I., Güzeloğlu, M., Aksun, M., Ortaç, R., Tulukoğlu, E., & Şahin, A. (2012) · Turkiye Klinikleri Journal of Medical Sciences · doi:10.5336/medsci.2011-26065 · Cited by 5

CXC‐ receptor 2 promotes extracellular matrix production and attenuates migration in peripapillary human scleral fibroblasts under mechanical strain

Qiu, C., Wang, C., Sun, X., Xu, J., Wu, J., Zhang, R., Li, G., Xue, K., Zhang, X., & Qian, S. (2022) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17609 · Cited by 5

The Role of Thrombin in Tumor Biology

Kobrinsky, B. A., & Karpatkin, S. (2008) · Springer eBooks · doi:10.1007/978-0-387-09637-7_9 · Cited by 5

CXC Chemokines in Angiogenesis

Strieter, R. M., Belperio, J. A., Arenberg, D. A., Smith, M. I., Burdick, M. D., & Keane, M. P. (2002) · Elsevier eBooks · doi:10.1016/b978-044451002-0/50010-5 · Cited by 5

Toward Understanding Wound Immunology for High-Fidelity Skin RegenerationPreprint

Xue, Y., Reddy, S., & Garza, L. A. (2022) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041241 · Cited by 5

Evaluating the Effects of BSA-Coated Gold Nanorods on Cell Migration Potential and Inflammatory Mediators in Human Dermal Fibroblasts

Mahmoud, N. N., Hammad, A. S., Kaabi, A., Alawi, H. H., Khatoon, S., & Al‐Asmakh, M. (2024) · Journal of Functional Biomaterials · doi:10.3390/jfb15100284 · Cited by 4

Adverse effects of CXCR2 deficiency in mice reared under non-gnotobiotic conditions

Garcia, M. J., Morales, M. S., Yang, T. S., Holden, J., Bossardet, O. L., Palmer, S. A., Jhala, M. G., Priest, S. O., Namburu, N. S., Beatty, N. J., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-75532-9 · Cited by 4

Skin Stretching Techniques: A Review of Clinical Application in Wound Repair

Yang, T., Tan, Z., Chen, X., Wang, F., Tao, R., Tong, Y., Wang, X., Fan, H., Yu, M., & Zhu, Z. (2024) · Plastic & Reconstructive Surgery Global Open · doi:10.1097/gox.0000000000006405 · Cited by 4

Fermitin family homolog 2 (Kindlin-2) affects vascularization during the wound healing process by regulating the Wnt/β-catenin signaling pathway in vascular endothelial cells

Ying, J., Wang, Q., Lu, L., Liu, J., Guo, R., Hu, H., Jiang, H., & Qi, F. (2021) · Bioengineered · doi:10.1080/21655979.2021.1957526 · Cited by 4

Arntl deficiency in myeloid cells reduces neutrophil recruitment and delays skeletal muscle repair

Watanabe, A., Koike, H., Kumagami, N., Shimba, S., Manabe, I., & Oishi, Y. (2023) · Scientific Reports · doi:10.1038/s41598-023-33830-8 · Cited by 3

Radiation‐induced sensitivity of tissue‐resident mesenchymal stem cells in the head and neck region

Spiegel, J. L., Hambrecht, M., Kohlbauer, V., Haubner, F., Ihler, F., Canis, M., Schilling, A. F., Böker, K. O., Dressel, R., Streckfuß‐Bömeke, K., et al. (2019) · Head & Neck · doi:10.1002/hed.25768 · Cited by 4

Immune-dysregulated neutrophils characterized by upregulation of CXCL1 may be a potential factor in the pathogenesis of abdominal aortic aneurysm and systemic lupus erythematosus

Zhang, L., Li, Q., Zhou, C., Zhang, Z., Zhang, J., & Qin, X. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e18037 · Cited by 4

c-Jun NH2-TERMINAL KINASE REGULATES LIPOPOLYSACCHARIDE-INDUCED PULMONARY MONONUCLEAR CELL RECRUITMENT VIA CCL2

Young, S. K., & Arndt, P. G. (2009) · Experimental Lung Research · doi:10.3109/01902140902853168 · Cited by 4

Guidance molecules and chemokines in angiogenesis and vascular remodeling

Rubina, K. A., Semina, E. V., & Va, T. (2017) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093017050015 · Cited by 4

Inflammation

Steinhoff, M., Griffiths, C. E. M., Church, M. K., & Luger, T. A. (2004) · Wiley eBooks · doi:10.1002/9780470750520.ch9 · Cited by 4

Spatiotemporal Single-Cell Roadmap of Human Skin Wound HealingPreprint

Liu, Z., Li, D., Bian, X., Luo, L., Björklund, Å. K., Li, L., Zhang, L., Chen, Y., Guo, L. M., Gao, J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.30.609923 · Cited by 4

Chemokine receptors in vascular biology: a review of current evidence, implications, and therapeutic targets for hypertension

de Moraes, L. H. O., Beling, T., Pimenta, G. F., & Bruder-Nascimento, T. (2025) · Clinical science · doi:10.1042/cs20257214 · Cited by 4

Sirolimus diminishes the expression of GRO-α (CXCL-1) /CXCR2 axis in human keratinocytes and cutaneous squamous cell carcinoma cells

Schaper‐Gerhardt, K., Hansel, A., Walter, A., Grimmelmann, I., & Gutzmer, R. (2021) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2021.08.007 · Cited by 3

Chemokines Effective on Platelet Functions

Fırat, A. A. (2022) · Biochemistry · doi:10.5772/intechopen.107183 · Cited by 3

Safety and pharmacology of AMY109, a long-acting anti–interleukin-8 antibody, for endometriosis: a double-blind, randomized phase 1 trial

Wang, P., Hsiao, S., Matsuki, S., Hanada, R., Chen, C., Nishimoto-Kakiuchi, A., Sekiya, M., Nakai, K., Matsushima, J., & Sawada, M. (2025) · F&S Reports · doi:10.1016/j.xfre.2025.04.009 · Cited by 3

Cell and Gene Transfer Strategies for Vascularization During Skin Wound Healing

Hendrickx, B., Hondt, M. D., Verdonck, K., Vranckx, J. J., & Luttun, A. (2013) · Humana Press eBooks · doi:10.1007/978-1-62703-417-3_26 · Cited by 3

Mice Knockouts for Chemokines and Chemokine Receptors

Schuh, J. M., Kunkel, S. L., & Hogaboam, C. M. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-405-4_19 · Cited by 3

Wound Healing

McGrath, J. A., & BREATHNACH, S. M. (2004) · Wiley eBooks · doi:10.1002/9780470750520.ch11 · Cited by 3

Manuka honey and its component, methyl syringate, shift neutrophil release profiles from pro-inflammatory while preserving pro-regenerative growth factor release in vitro

Main, E. N., Hall, S. C., & Bowlin, G. L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1760968 · Cited by 2

Beyond first responders: neutrophils shape biomaterial-guided regeneration

Pereira, M. M., Sousa, A. L., & Barbosa, J. N. (2026) · Biomaterials Science · doi:10.1039/d6bm00277c · Cited by 3

Chemokine receptors in tissue cells and angiogenesis

Romagnani, P., Lasagni, L., & Romagnani, S. (2006) · Birkhäuser-Verlag eBooks · doi:10.1007/3-7643-7423-3_12 · Cited by 2

The Role of CXCR2 in Pancreatic Cancer Development and Progression

Purohit, A. (2015) · DigitalCommons@UNMC · Cited by 2

The Contribution of Immune Cells to Angiogenesis in Inflammation and Tumor Growth

Ribatti, D. (2017) · Springer eBooks · doi:10.1007/978-3-319-68448-2_7 · Cited by 3

Vascular Stem Cells in Regulation of Angiogenesis

Lu, J., Pompili, V. J., & Das, H. (2013) · Springer eBooks · doi:10.1007/978-1-4614-5857-9_8 · Cited by 2

The Angiogenic Switch: Role of Immune Cells

Noonan, D. M., Ventura, A., Bruno, A., Pagani, A., & Albini, A. (2010) · Springer eBooks · doi:10.1007/978-1-4419-7219-4_5 · Cited by 2

Head-out immersion in hot water does not increase serum CXCL1 in healthy men

Sakurai, Y., Umemoto, Y., Kawasaki, T., Kojima, D., Kinoshita, T., Yamashiro, M., Banno, M., Arakawa, H., & Tajima, F. (2017) · Trends in Immunotherapy · doi:10.24294/ti.v1.i1.37 · Cited by 2

Chemokine receptors (version 2019.5) in the IUPHAR/BPS Guide to Pharmacology Database

Bachelerie, F., Ben‐Baruch, A., Charo, I. F., Combadière, C., Förster, R., Farber, J. M., Graham, G. J., Hills, R., Horuk, R., Locati, M., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f14/2019.5 · Cited by 2

Inflammation, Immunology and Allergy

Steinhoff, M. S. (2016) · Wiley eBooks · doi:10.1002/9781118441213.rtd0008 · Cited by 2

Angiogenic response in wound healing

Chan, Y. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816413-6.00006-x · Cited by 1

Epigenetic integration of signaling from the regenerative environment

Geara, P., & Dilworth, F. J. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.02.003 · Cited by 1

Traumatic Brain Injury Induces Early Barrier Protective Responses in Incisional Skin Wounds Accelerating Cutaneous Wound Healing

Aghapour, M., Heuvel, F. O., Fröhlich, A., Heinzl, A., Maity, P., Singh, K., Wang, Y., Cheng, J., Roselli, F., & Scharffetter‐­Kochanek, K. (2025) · Wound Repair and Regeneration · doi:10.1111/wrr.70079 · Cited by 1

Interleukin‐8 Overexpressing Collagen Microgel‐Based Cellular Microtissue Accelerates the Healing of Diabetic Foot Ulcers

Chung, H., Jang, W. Y., Choi, J., & Kim, S. (2025) · Small · doi:10.1002/smll.202511027 · Cited by 1

Cxcr2 is Required for Osteoclast Regulation, Bone Structure, and Hematological Response During Bone (Re)modeling

Flatt, C. L., Fick, A., James, B., Hester, F., Nano, S., Steinke, A. M., Li, J., Niebur, G. L., & Littlepage, L. E. (2026) · Calcified Tissue International · doi:10.1007/s00223-025-01470-x · Cited by 1

IL-8 contributes to postoperative adhesion formation through the crosstalk of neutrophils and mesothelial cells

Nakagawa, K., Tanimura, H., Yamazaki, M., Sato, I., Kobayashi, S., Kohara, M., Sakamoto, Y., Sakaguchi, N., Kato, A., AZUMA, M., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-42159-x · Cited by 1

β-arrestin 1 and integrin-linked kinase interact in epidermal keratinocytes and regulate cell motility

Murphy‐Marshman, H., Ivanova, I. A., Bhattacharya, M. M., & Dagnino, L. (2025) · Tissue Barriers · doi:10.1080/21688370.2025.2465048 · Cited by 1

Bradykinin’s carbamylation as a mechanistic link to impaired wound healing in patients with kidney dysfunction

Kamińska, M., Kałucka, U., Bábíčková, J., Benedyk‐Machaczka, M., Skandalou, E., Grant, M. M., Marti, H.-P., & Mydel, P. M. (2025) · BMC Biology · doi:10.1186/s12915-025-02187-x · Cited by 1

CXC Chemokines in Cancer Angiogenesis

Mehrad, B., & Strieter, R. M. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-267-4_8 · Cited by 2

Chemokines in Angiogenesis

Keane, M. P., Belperio, J. A., & Strieter, R. M. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-184-0_9 · Cited by 1

Chemokines: Role as Immunomodulators and Potential as Adjuvants for DNA Vaccines

Murphy, P. M. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0105-3_17 · Cited by 1

Schistosomula

Gobert, G. N., & Nawaratna, S. S. K. (2016) · CRC Press eBooks · doi:10.1201/9781315368900-10 · Cited by 1

Angiogenesis

Gerritsen, M. E. (1984) · Comprehensive physiology · doi:10.1002/j.2040-4603.1984.tb01017.x · Cited by 1

Low Molecular Weight CXCR2 Antagonists as Promising Therapeutics

Mihara, K., & Wijkmans, J. C. H. M. (2010) · Methods and principles in medicinal chemistry · doi:10.1002/9783527631995.ch12 · Cited by 1

MECHANISMS BY WHICH HYPERBARIC OXYGEN THERAPY MAY RESOLVE INFLAMMATION IN CHRONIC WOUNDS

Almzaiel, A. J. (2013) · PEARL (University of Plymouth) · doi:10.24382/1451 · Cited by 1

Short tail with skin lesion phenotype occurs in transgenic mice with keratin-14 promoter-directed expression of mutant CXCR2

Yu, Y., Su, Y., Opalenik, S. R., Sobolik-Delmaire, T., Neel, N. F., Zaja‐Milatovic, S., Short, S. P., Sai, J., & Richmond, A. J. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0807544 · Cited by 1

Cell-Cell Interaction | Chemokine Receptors

Raman, D., Howard, C. M., Tilley, A. M. C., & Sridharan, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00083-9 · Cited by 1

Inflammation

Steinhoff, M. S., Groves, R. W., LeBoit, P. E., & Luger, T. A. (2010) · Wiley eBooks · doi:10.1002/9781444317633.ch12 · Cited by 1

Angiogenesis

Gerritsen, M. E. (2008) · Comprehensive physiology · doi:10.1002/cphy.cp020408 · Cited by 1

CXC Chemokines in Cancer

(2005) · Current topics in membranes · doi:10.1016/s1063-5823(04)55010-x

Dynamics of cell-cell junctions in keratinocytes

Chavez, M. G. (2009) · UNM’s Digital Repository (University of New Mexico)

Estudo dos mecanismos genéticos e celulares durante a fase inflamatória do processo de regeneração tecidual em animais selecionados geneticamente para a máxima resposta inflamatória aguda homozigotos para os alelos R ou S do gene Slc11a1.

Gasparelo, T. A. C. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2009.tde-03022010-093331

An investigation into the role of chemokines in haemopoietic stem cell quiescence

Sinclair, A. (2015) · Enlighten: Theses (The University of Glasgow)

Avaliação do efeito da Artin M no processo de repação em mucosa mastigatória

Kim, Y. J. (2011) · Americanae (AECID Library)

Effect of Advanced Age on the Innate Immune Response to Cutaneous Wound Infection

Brubaker, A. L. (2013) · Loyola eCommons (Loyola University of Chicago)

Terapia angiogénica en el tratamiento de la cardiopatía isquémica

Inclán, A. V. (2007) · Revista cubana de cirugía

Immunomodulation in Perioperative Medicine

Peltz, G. (2011) · Pain Management · doi:10.2217/pmt.11.5

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