Semaphorins and their receptors in immune cell interactions

Untitled work

Hynes (2002) · doi:10.1016/s0092-8674(02)00971-6 · Cited by 8,606

Getting to the site of inflammation: the leukocyte adhesion cascade updated

Ley, K., Laudanna, C., Cybulsky, M. I., & Nourshargh, S. (2007) · Nature Reviews Immunology · doi:10.1038/nri2156 · Cited by 4,354

Immunobiology: the immune system in health and disease

(1995) · Choice Reviews Online · doi:10.5860/choice.32-3876 · Cited by 4,110

A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment

Szabo, S. J., Kim, S. T., Costa, G. L., Zhang, X., Fathman, C. G., & Glimcher, L. H. (2000) · Cell · doi:10.1016/s0092-8674(00)80702-3 · Cited by 3,589

VLA Proteins in the Integrin Family: Structures, Functions, and Their Role on Leukocytes

Hemler, M. E. (1990) · Annual Review of Immunology · doi:10.1146/annurev.iy.08.040190.002053 · Cited by 1,561

Neuropilin is a semaphorin III receptor.

Kolodkin, A., Levengood, D. V., Rowe, E. G., Tai, Y.-T., Giger, R., & Ginty, D. (1997) · Cell · doi:10.1016/s0092-8674(00)80535-8 · Cited by 1,262

Plexins Are a Large Family of Receptors for Transmembrane, Secreted, and GPI-Anchored Semaphorins in Vertebrates

Tamagnone, L., Artigiani, S., Chen, H., He, Z., Ming, G., Song, H., Chédotal, A., Winberg, M. L., Goodman, C. S., Poo, M.-M., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80063-x · Cited by 1,163

Neuropilin Is a Receptor for the Axonal Chemorepellent Semaphorin III

He, Z., & Tessier‐Lavigne, M. (1997) · Cell · doi:10.1016/s0092-8674(00)80534-6 · Cited by 1,137

Germinal-Center Organization and Cellular Dynamics

Allen, C. D. C., Okada, T., & Cyster, J. G. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.009 · Cited by 1,025

The semaphorin genes encode a family of transmembrane and secreted growth cone guidance molecules

Kolodkin, A. L., Matthes, D., & Goodman, C. S. (1993) · Cell · doi:10.1016/0092-8674(93)90625-z · Cited by 957

Soluble Semaphorin 4D Serum Concentrations Are Elevated in Critically Ill Patients with Liver Cirrhosis and Correlate with Aminotransferases

Jhaisha, S. A., Hohlstein, P., Yagmur, E., Köller, V., Pollmanns, M. R., Adams, J. K., Wirtz, T. H., Brozat, J. F., Bündgens, L., Hamesch, K., et al. (2024) · Diagnostics · doi:10.3390/diagnostics14040370 · Cited by 2

PTEN in antigen presenting cells is a master regulator for Th17-mediated autoimmune pathology

Blüml, S., Schabbauer, G., Hainzl, E., Niederreiter, B., Hladik, A., Lohmeyer, T., Bonelli, M. M., Zinser, E., Koenders, M. I., van den Berg, W., et al. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3610 · Cited by 2

IL-17-producing ©™T cells are important for the development of arthritis in a rheumatoid arthritis model

Akitsu, A., Ishigame, H., Kakuta, S., Saijo, S., & Iwakura, Y. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3604 · Cited by 2

Neurotrophins and neuropeptides as inflammatory mediators in case of chronic dermatosis

Kubanova, A. A., Smolyannikova, V. A., Chikin, V. V., & Karamova, A. Е. (2014) · Vestnik dermatologii i venerologii · doi:10.25208/0042-4609-2014-90-6-57-61 · Cited by 2

Research Advances in the Immunomodulatory Functions of CD100/SEMA4D and Their Roles in Viral Infectious Diseases

Zhao, M., Chen, L., Chen, Y., Yang, X., Feng, X., Yang, D., Zheng, X., & Liu, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094341 · Cited by 1

Plasma Semaphorin 3A as a Potential Biomarker for Cognitive Impairment in Cerebral Small Vessel Disease

Ma, H., Li, H., Fu, X., Li, X., Wei, C., & Ma, A. (2025) · International Journal of General Medicine · doi:10.2147/ijgm.s554075 · Cited by 1

Single-cell RNA sequencing reveals aberrant airway epithelial–immune cell cross-talk in pulmonary fibrosis

Hewitt, R. J., Chakravarty, P., Perez-Lloret, J., Banchero, M., Berg, M., van den Berge, M., Traves, W. J., Yates, L. L., Walker, S. A., Gaboriau, D. C. A., et al. (2025) · ERJ Open Research · doi:10.1183/23120541.01273-2025 · Cited by 2

Semaphorins: from CD8⁺ T cells to cancer immunotherapy

Liu, Z., Wu, Y., Xu, P., Xu, H., Yin, K., & Wang, S. (2026) · Biomarker Research · doi:10.1186/s40364-026-00903-5 · Cited by 1

Quantitative Proteomics for Investigation of Secreted Factors: Focus on Muscle Secretome

Henningsen, J., Blagoev, B., & Kratchmarov, I. (2012) · InTech eBooks · doi:10.5772/30820 · Cited by 1

Mechanisms Regulating Epidermal Innervation in Pruritus of Atopic Dermatitis

Tominaga, M., & Takamori, K. (2011) · InTech eBooks · doi:10.5772/22442 · Cited by 1

Frequency of appearance of anemias at rheumatoid arthritis - a disease of autoimmune genesis (on the data of retrospective study)

Aripov, A. N., Karimov, M. S., & Eshmurzaeva, A. A. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3608 · Cited by 1

Effect of B cell depletion using peptide tetramers in collagen-induced arthritis

Michishita, K., Kawahata, K., Kanzaki, T., Akahira, L., Eri, T., & Yamamoto, K. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3634 · Cited by 1

SPACIA1/SAAL1: a newly identified gene associated with aberrant proliferation of synovial fibroblasts

Sato, T., Fujii, R., Konomi, K., Yagishita, N., Aratani, S., Araya, N., Aono, H., Yudoh, K., Suzuki, N., Beppu, M., et al. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3662 · Cited by 1

Inhibition of Syndecan-4 by therapeutic antibodies reduces TNFα dependent joint destruction in mice

Stratis, A., Neugebauer, K., Fröhling, M., Paruzel, P., Dankbar, B., Wemeyer, C., Cromme, C., Godmann, L., Bertrand, J., Korb, A., et al. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3665 · Cited by 1

Abnormal osteogenesis in osteoarthritis: gone with the Wnt?

Lajeunesse, D., Chan, T. F., Delalandre, A., Pelletier, J., Martel‐Pelletier, J., & Abed, É. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3574 · Cited by 1

Directed induction of chondrogenic cells from mouse dermal fibroblast culture

Tsumaki, N. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3582 · Cited by 1

Uncoupling protein 3 attenuates generation of reactive oxygen species by interacting with thioredoxin 2 in the mitochondrial intermembrane space

Hirasaka, K., Mills, E., Kohno, S., Abe, T., Ikeda, C., Maeda, T., Kondo, S., Maita, A., Okumura, Y., & Nikawa, T. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3625 · Cited by 1

Semaphorin-3A in autoimmune rheumatic diseases: immunological and pathological aspects

Lotfi, R., Rahmani, H., & Nasirifar, A. (2025) · Inflammopharmacology · doi:10.1007/s10787-025-01881-0 · Cited by 1

Risk factors for latent tuberculosis infection in RA patients treated with anti-tumor necrosis factor

Huang, S., Su, W., Ruan, S., Yu, C., Hsieh, S., Liu, Y., Wu, Y. J., & Lin, H.-Y. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3641 · Cited by 1

Peripheral tolerance induced by apoptotic cells and PD-1+ CD8 T cells

Kazama, H., Iyoda, T., Yokoyama, S., Inaba, K., Ferguson, T. A., & Yonehara, S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3635 · Cited by 1

Active repression by Blimp1 play an important role in osteoclast differentiation

Nishikawa, K., Nakashima, T., Hayashi, M., Fukunaga, T., Kato, S., Kodama, T., Takahashi, S., Calame, K. L., & Takayanagi, H. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3655 · Cited by 1

A novel role for monosodium urate monohydrate crystals and gouty synovial fluids in monocyte migration in gout

Amin, M. A., Shu, Q., Vargo, J. W., Ruth, J. H., Isozaki, T., Lee, S., & Koch, A. E. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3606 · Cited by 1

Assessment of histological alterations in cartilage and extracellular matrix driven by collagen-induced arthritis in Macaca fascicularis

Amizuka, N., Hongo, H., Sasaki, M., Hasegawa, T., de Freitas, P. H. L., Mori, H., & Li, M. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3569 · Cited by 1

Osteoprotegerin induction in response to microbial infection

Takada, Y., & Matsuo, K. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3668 · Cited by 1

Methods for Quantitation of Leukocyte Chemotaxis and Fugetaxis

Vianello, F., Righi, E., & Poznansky, M. C. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-461-6_8 · Cited by 1

The role of mRNA degradation in immunity and inflammation

Akira, S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3562 · Cited by 1

Microglial metabolic reprogramming drives cognitive decline in heart failure with preserved ejection fractionPreprint

Patil, S., Lantz, C. W., Marinovic, A., Sarkar, R., Lee, B. R., & DeBerge, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.10.675257 · Cited by 1

Semaphorins and Adhesion Molecules

Robert, J. (2014) · Springer eBooks · doi:10.1007/978-3-319-14340-8_11

Microparticles as antigenic targets in human and murine SLE

Ullal, A. J., & Pisetsky, D. S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3589

Análise da atividade de CD100 na modulação da ativação de macrófagos e sua infectividade por Leishmania (Leishmania) amazonensis.

Galuppo, M. K. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2012.tde-21092012-085336

Crosstalk Between the Immune and Central Nervous Systems with Special Reference to Drug Development

Kubo, T., Tokita, S., & Yamashit, T. (2011) · InTech eBooks · doi:10.5772/29057

JMH Blood Group System

Daniels, G. L. (2013) · Wiley eBooks · doi:10.1002/9781118493595.ch24

Metastasis Genes: Epigenetics

Lujambio, A., & Esteller, M. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511976117.010

Pathfinding Molecules Branch Out: Semaphorin Family Members Regulate Synapse Development

Paradis, S. (2009) · Springer eBooks · doi:10.1007/978-0-387-92708-4_15

IL-17, synoviolin and rheumatoid arthritis chronicity

Miossec, P. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3579

TGF-β signaling induces SnoN to suppress BMP-induced hypertrophic maturation of chondrocytes

Maeda, S., Kawamura, I., Ishidou, Y., Imamura, K., Yokouchi, M., & Komiya, S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3642

Clinical-experimental assessment of simvastatin efficiency in the treatment of rheumatoid arthritis

Tadjikhodjaeva, R. N., & Khabibullaeva, N. G. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3666

SNP algorithms for prediction of efficacy and adverse events of abatacept (ABT)

Middleton, J. E., Matsubara, T., Funahashi, K., Koyano, S., Hagiwara, T., Miura, T., Kosuke, O., Nakamura, T., Iwahashi, M., Tsuru, T., et al. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3649

Combined effects of the hedgehog pathway inhibitor LDE225 and nilotinib in a random mutagenesis screen

Tauchi, T. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3598

Anti-TNF antibody therapy induces IL-17 suppressing regulatory T cells in patients with rheumatoid arthritis

McGovern, J. L., Notley, C. A., Nguyen, D. X., Mauri, C., Isenberg, D. A., & Ehrenstein, M. R. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3597

New mechanisms of action and signaling by TNF-α

Ivashkiv, L. B. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3590

Combined depletion of interleukin-1 and interleukin-6 does not exceed single depletion of interleukin -1 in TNF-mediated arthritis

Hayer, S., Niederreiter, B., Smolen, J. S., & Redlich, K. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3645

Skeletal involvement in the pathogenesis and outcomes of rheumatoid arthritis and osteoarthritis

Pelletier, J. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3571

Cancer immunotherapy; integration of T cell biology with nanogel- and vector-technology in translational research

Shiku, H. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3564

Peptide therapy in sepsis and inflammation: a novel strategy to suppress inflammation

Okada, H., & Okada, A. K. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3595

Postnatal Syk deletion in mice clarifies the function of Syk in an anti-collagen antibody-induced arthritis model

Ozaki, N., Suzuki, S., Hara, H., & Yoshida, H. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3577

Autoimmune arthritis caused by altered thymic T-cell selection due to a mutation of the ZAP-70 gene

Ito, Y., & Sakaguchi, S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3565

Smoking induces expression of ligands of the immune receptor NKG2D

Ospelt, C., Camici, G. G., Brentano, F., Künzler, P., Kolling, C., Gay, R. E., Michel, B. A., & Gay, S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3659

The bacterial effector protein YopM reduces rheumatoid arthritis (RA) outcome by inhibiting inflammation and bone destruction

Bertrand, J., Rüter, C., Cromme, C., Scharnert, J., Schmidt, A., & Pap, T. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3609

Reconstruction of injured spinal cord by epigenetic regulation of transplanted neural stem cells

Abematsu, M., Tsujimura, K., Yamano, M., Saito, M., Kohno, K., Setoguchi, T., Yone, K., Nakashima, K., & Komiya, S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3602

Novel regulatory T cells controlling antibody production and systemic autoimmunity

Yamamoto, K., Okamura, T., & Fujio, K. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3586

Adult stem cell-based therapy for degenerative joint diseases

Alexander, P. G., & Tuan, R. S. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3594

Role of HLA-antigens class 1 in the development of rheumatoid arthritis in Uzbek women

Mirakhmedova, N. N., & Mirzakhanova, M. I. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3648

Roles of S ema4 A in multiple sclerosis and interferon‐β therapy efficacy

Nakatsuji, Y., Okuno, T., Koda, T., Takata, K., Honorat, J. A., Mochizuki, H., & Kumanogoh, A. (2013) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12070

Abnormal expressions of immune response-related genes in RA bone marrow cells

Lee, H.-M., Aoki, C., Shimaoka, Y., Ochi, K., Ochi, T., & Nishimoto, N. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3640

Tks5-dependent formation of circumferential podosomes mediates cell-cell fusion

Oikawa, T., Oyama, M., Kozuka‐Hata, H., Uehara, S., Udagawa, N., Saya, H., & Matsuo, K. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3690

SEMA4D in osteoporosis

Martz, L. (2011) · Science-Business eXchange · doi:10.1038/scibx.2011.1255

Cartilage-specific deletion of prar-gamma in mice results in early endochondral ossification defects and accelerated aging-dependent development of osteoarthritis

Monemdjou, R., Vasheghani, F., Fahmi, H., Pérez, G., Blati, M., Taniguchi, N., Lotz, M., St‐Arnaud, R., Pelletier, J., Martel‐Pelletier, J., et al. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3632

Etiology and molecular pathogenesis of RA; how can we best use European initiatives to advance our knowledge?

Klareskog, L. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3558

Interleukin-6 as a therapeutic target in locomotor disorders

Nishimoto, N., Murakami, M., Matsutani, T., Hashi­moto, J., & Takagi, N. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3592

Evidence for synovial fibroblasts spreading rheumatoid arthritis

Müller‐Ladner, U., Lefèvre, S., Zimmermann, B., Tarner, I. H., Dinser, R., Pap, T., Gay, S., & Neumann, E. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3570

The function of a novel guidance molecule, Plexin-A1, on immune dendritic cells

Eun, S.-Y. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/3hnp-bf62

Nogo-A knockout mice: a systems biology approach to understand regeneration

Montani, L. (2008) · Zurich Open Repository and Archive (University of Zurich) · doi:10.3929/ethz-a-005746408

Sema4A and Chronic Inflammation

Ito, D., & Kumanogoh, A. (2016) · Springer eBooks · doi:10.1007/978-4-431-56068-5_3

Characterizing Semaphorin-Mediated Immune Responses Using an Antigen-Presentation Assay

Nojima, S., & Kumanogoh, A. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6448-2_27

Immunoaffinity Purification of the Glycosylated Extracellular Fragment of Mouse Plexin A2 Produced in a Mammalian Expression System

Nogi, T., Mihara, E., Yasui, N., & Takagi, J. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6448-2_4

The Role of Semaphorin 5A in Pancreatic Cancer Progression and Metastasis

Saxena, S. (2017) · DigitalCommons@UNMC

Elucidating the pathomechanism behind the neurocristopathy CHARGE syndrome

Freese, L. (2018) · doi:10.53846/goediss-6403

PlexinD1 deficiency in macrophage exacerbates house dust mite-induced allergic asthma

Aktar, A. (2019) · Mspace (University of Manitoba)

Research Progress on the Effect of Semaphorin 3A on Immune Cells

史, 卓. (2021) · Advances in Clinical Medicine · doi:10.12677/acm.2021.119633

La voie des sémaphorines

Robert, J. (2010) · Springer eBooks · doi:10.1007/978-2-8178-0028-8_11

Transcriptional Analysis of TH2 Primed Dendritic Cells and T cells

Morgan, C. (2021) · doi:10.26686/wgtn.16850506.v1

Faculty Opinions recommendation of Structural basis of semaphorin-plexin recognition and viral mimicry from Sema7A and A39R complexes with PlexinC1.

Gabbiani, G., & Serini, G. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.4886960.4832057

Functional Analysis of Semaphorin 3A in Retinal Ganglion Cells under Hypoxia In Vitro

Komatsu, K., Ko, J.-A., Shimizu, A., Okumichi, H., & Kiuchi, Y. (2023) · Biology Bulletin · doi:10.1134/s1062359022700017

Relationship of Semaphorin Proteins with Blood Markers in Patients with COVID-19

Okuyan, H. M., Doğan, S., Bal, T., & Çabalak, M. (2023) · Journal of Turkish Clinical Biochemistry · doi:10.56615/tkbd.2023.10

Determination of SIRT7, SEMA3A, SEMA3F Gene Expressions in Patients with Multiple Sclerosis

Cetin, F., Güldiken, Y. C., Kargün, K., & Demir, C. F. (2024) · Journal of Multiple Sclerosis Research · doi:10.4274/jmsr.galenos.2023.2023-9-1

Additional file 2 of A pan-cancer study of class-3 semaphorins as therapeutic targets in cancer

Zhang, X., Klamer, B. G., Li, J., Fernández, S., & Li, L. (2020) · Figshare · doi:10.6084/m9.figshare.12072375

Additional file 1 of A pan-cancer study of class-3 semaphorins as therapeutic targets in cancer

Zhang, X., Klamer, B. G., Li, J., Fernández, S., & Li, L. (2020) · Figshare · doi:10.6084/m9.figshare.12072366

A single-nucleus census of immune and non-immune cell types for the major immune organ systems of chickenPreprint

Sculley, E. R., Ricemeyer, E. S., Carroll, R. A., Driver, J. P., Smith, J., Kaufman, J., Hearn, C. J., Balic, A., Chen, P. R., Lamont, S. J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.05.606414

Evaluation of the Relationship Between Semaphorin 4D Levels and the Coronary Slow Flow Phenomenon

Çakmak, H. A., Karakurt, Ö., Kanat, S., & Uyanık, K. Ç. P. (2025) · Interventional Cardiology Perspectives · doi:10.4274/intercardiopers.2025.2025-2-8

The role of angiogenic and neuronal factors in the mechanisms of thymic involution in tumor growth

Kiseleva, E. P. (2010) · Medical academic journal · doi:10.17816/maj104201-209

Additional file 3 of A pan-cancer study of class-3 semaphorins as therapeutic targets in cancer

Zhang, X., Klamer, B., Li, J., Fernández, S., & Li, L. (2020) · Figshare · doi:10.6084/m9.figshare.12072381

Additional file 4 of Semaphorin 7A interacts with nuclear factor NF-kappa-B p105 via integrin β1 and mediates inflammation

Li, X., Xie, W., Pan, Q., Zhang, X., Zhang, L., Zhao, N., Xie, Q., Ding, J., & Chai, J. (2023) · Figshare · doi:10.6084/m9.figshare.22603565

Additional file 1 of SEMA6A/RhoA/YAP axis mediates tumor-stroma interactions and prevents response to dual BRAF/MEK inhibition in BRAF-mutant melanoma

Loria, R., Laquintana, V., Scalera, S., Fraioli, R., Caprara, V., Falcone, I., Bazzichetto, C., Martile, M. D., Rosanò, L., Bufalo, D. D., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19619337

Additional file 3 of Semaphorin 7A interacts with nuclear factor NF-kappa-B p105 via integrin β1 and mediates inflammation

Li, X., Xie, W., Pan, Q., Zhang, X., Zhang, L., Zhao, N., Xie, Q., Ding, J., & Chai, J. (2023) · Figshare · doi:10.6084/m9.figshare.22603562

Additional file 4 of A pan-cancer study of class-3 semaphorins as therapeutic targets in cancer

Zhang, X., Klamer, B., Li, J., Fernandez, S., & Li, L. (2020) · Figshare · doi:10.6084/m9.figshare.12072387

Additional file 2 of Semaphorin 7A interacts with nuclear factor NF-kappa-B p105 via integrin β1 and mediates inflammation

Li, X., Xie, W., Pan, Q., Zhang, X., Zhang, L., Zhao, N., Xie, Q., Ding, J., & Chai, J. (2023) · Figshare · doi:10.6084/m9.figshare.22603559

Additional file 5 of Semaphorin 7A interacts with nuclear factor NF-kappa-B p105 via integrin β1 and mediates inflammation

Li, X., Xie, W., Pan, Q., Zhang, X., Zhang, L., Zhao, N., Xie, Q., Ding, J., & Chai, J. (2023) · Figshare · doi:10.6084/m9.figshare.22603568

Potentiating dendritic cell immunotherapy by interrupting the Semaphorin 4D-induced immune-suppressive barrier

Garg†, S. K., Snyder, C., Ramamoorthi, G., Kodumudi, K. N., Evans, E. E., Lok, V. M., Bußler, H., Nguyen, J. V., Yao, J., Basu, A., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117050

Neuropilin-2 is an entry receptor for Chikungunya virusPreprint

Chen, Y., Zhang, K., Tang, H., He, Z., Shu-dan, L. U. O., Qi, Z., Zhao, P., & Ding, C. (2026) · Research Square · doi:10.21203/rs.3.rs-9056403/v1

Biology of bone and cartilage

Boyce, B. F., Zuscik, M. J., & Xing, L. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-13683-2.00003-7

Guidage axonal commissural : mécanismes de sensibilisation au signal de la ligne médiane Sémaphorine 3B

Nawabi, H. (2009) · theses.fr (ABES) · doi:10.70675/deb0a9b9zc7a5z4312za23azbee7d3622018

Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux

Leclerc, M. (2018) · theses.fr (ABES) · doi:10.70675/13aee211zad7bz4b07z9a5fz29b15750d99c

Cell-autonomous co-stimulatory function of membrane-bound CD100 promotes activation and differentiation of HBcAg-specific CD8+ T cells

Zhao, M., Chen, L., Chen, Y., Wang, L. L., Yang, X., Sutter, K., Lu, M., Chen, J., Zheng, X., Yang, D., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1826036

Differences in immune-related semaphorin levels in the CSF and serum of newly diagnosed, treatment-naive patients with relapsing–remitting multiple sclerosis: a case–control study

Sarıdaş, F., Aydın, B., Özpar, R., Koç, E. R., Hakyemez, B., ALKAN, T., & Turan, Ö. F. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1851383

Semaphorin3E is a novel regulator of germinal center responses in a mouse model of allergic asthma

Sedaghat, F., Matloubi, M., Shan, L., Onyilagha, C., & GOUNNI, A. S. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkag220

A teleost - Specific Sema4E - like protein promotes grass carp reovirus infection by upregulating HSP70 expression

Shao, Y., Lei, J., Xie, J., Jia, Z., Gui, B., Chen, L., Li, Y., Wang, Y., & Huang, R. (2026) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2026.111750

Genome‐Wide Analysis of Resistance to Gastrointestinal Parasites in Portuguese Merino and Merino‐Related Sheep

Gaspar, D., Ginja, C., Carolino, N., Leão, C., Monteiro, H., Tábuas, L., Branco, S., Caetano, P., Romão, R., Matos, C., et al. (2026) · Animal Genetics · doi:10.1002/age.70218

Anti-Fas IgM monoclonal antibody (anti-Fas mAb) effect on haemophilic arthropathy (HA) synoviocytes

Guiducci, S., Romano, E., Ceccarelli, C., Melchiorre, D., Manetti, M., Milia, A. F., Manneshi, L. I., Nishioka, K., & Matucci‐Cerinic, M. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3566

Regulation of immune cell responses by semaphorins and their receptors

Takamatsu, H., Okuno, T., & Kumanogoh, A. (2010) · Cellular and Molecular Immunology · doi:10.1038/cmi.2009.111 · Cited by 108

Immune Semaphorins: Increasing Members and Their Diverse Roles

Kikutani, H., Suzuki, K., & Kumanogoh, A. (2007) · Advances in immunology · doi:10.1016/s0065-2776(06)93003-x · Cited by 37

Semaphorins: a new class of immunoregulatory molecules

Takegahara, N., Kumanogoh, A., & Kikutani, H. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1696 · Cited by 45

The role of Semaphorin family in immune systems

Ito, D., Nojima, S., & Kumanogoh, A. (2014) · Japanese Journal of Clinical Immunology · doi:10.2177/jsci.37.1 · Cited by 5

Diverse roles for semaphorin−plexin signaling in the immune system

Takamatsu, H., & Kumanogoh, A. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.01.008 · Cited by 167