Semaphorins and their receptors in immune cell interactions

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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

Plexin-Neuropilin-1 Complexes Form Functional Semaphorin-3A Receptors

Takahashi, T., Fournier, A. E., Nakamura, F., Wang, L.-H., Murakami, Y., Kalb, R. G., Fujisawa, H., & Strittmatter, S. M. (1999) · Cell · doi:10.1016/s0092-8674(00)80062-8 · Cited by 817

Neuropilin-1 conveys semaphorin and VEGF signaling during neural and cardiovascular development.

Gu, C.-H., Rodríguez, E., Reimert, D. V., Shu, T., Fritzsch, B., Richards, L. J., Kolodkin, A., & Ginty, D. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00169-2 · Cited by 756

TREMs in the immune system and beyond

Colonna, M. (2003) · Nature Reviews Immunology · doi:10.1038/nri1106 · Cited by 701

Regulation of B-cell fate by antigen-receptor signals

Niiro, H., & Clark, E. A. (2002) · Nature reviews. Immunology · doi:10.1038/nri955 · Cited by 653

Semaphorin III is needed for normal patterning and growth of nerves, bones and heart

Behar, O., Golden, J. A., Mashimo, H. L., Schöen, F. J., & Fishman, M. C. (1996) · Nature · doi:10.1038/383525a0 · Cited by 583

Class 3 semaphorins control vascular morphogenesis by inhibiting integrin function

Serini, G., Valdembri, D., Zanivan, S. R., Morterra, G., Burkhardt, C., Caccavari, F., Zammataro, L. A., Primo, L., Tamagnone, L., Logan, M. P. O., et al. (2003) · Nature · doi:10.1038/nature01784 · Cited by 575

CD40 expression by human monocytes: regulation by cytokines and activation of monocytes by the ligand for CD40.

Alderson, M. R., Armitage, R. J., Tough, T. W., Strockbine, L. D., Fanslow, W. C., & Spriggs, M. K. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.178.2.669 · Cited by 570

Semaphorin 3E and Plexin-D1 Control Vascular Pattern Independently of Neuropilins

Gu, C., Yoshida, Y., Livet, J., Reimert, D. V., Mann, F., Merte, J., Henderson, C. E., Jessell, T. M., Kolodkin, A. L., & Ginty, D. D. (2004) · Science · doi:10.1126/science.1105416 · Cited by 543

A Role in B Cell Activation for CD22 and the Protein Tyrosine Phosphatase SHP

Doody, G. M., Justement, L. B., Delibrias, C., Matthews, R. J., Lin, J., Thomas, M. L., & Fearon, D. T. (1995) · Science · doi:10.1126/science.7618087 · Cited by 538

Hyperresponsive B Cells in CD22-Deficient Mice

O’Keefe, T. L., Williams, G. T., Davies, S. L., & Neuberger, M. S. (1996) · Science · doi:10.1126/science.274.5288.798 · Cited by 532

From Form to Function: Signaling by Protein Tyrosine Phosphatases

Tonks, N. K., & Neel, B. G. (1996) · Cell · doi:10.1016/s0092-8674(00)81357-4 · Cited by 530

Semaphorin 7A promotes axon outgrowth through integrins and MAPKs

Pasterkamp, R. J., Peschon, J. J., Spriggs, M. K., & Kolodkin, A. L. (2003) · Nature · doi:10.1038/nature01790 · Cited by 517

Semaphorins command cells to move

Kruger, R. P., Aurandt, J., & Guan, K. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1740 · Cited by 508

CD22 is both a positive and negative regulator of B lymphocyte antigen receptor signal transduction: altered signaling in CD22-deficient mice.

Sato, S., Miller, A. S., Inaoki, M., Bock, C., Jansen, P. J., Tang, M., & Tedder, T. F. (1996) · Immunity · doi:10.1016/s1074-7613(00)80270-8 · Cited by 470

Unified nomenclature for the semaphorins/collapsins [1]

Bamberg, J., Baumgartner, S., Betz, H., Bolz, J., Chédotal, A., Christensen, C., Comoglio, P., Culotti, J., Doherty, P., Drabkin, H., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80766-7 · Cited by 427

Regulation of T-cell activation by the cytoskeleton

Billadeau, D. D., Nolz, J. C., & Gomez, T. S. (2007) · Nature reviews. Immunology · doi:10.1038/nri2021 · Cited by 389

The Semaphorin 4D Receptor Plexin-B1 Is a GTPase Activating Protein for R-Ras

Oinuma, I., Ishikawa, Y., Katoh, H., & Negishi, M. (2004) · Science · doi:10.1126/science.1097545 · Cited by 383

Role of the cytoskeleton during leukocyte responses

Vicente‐Manzanares, M., & Sánchez‐Madrid, F. (2004) · Nature reviews. Immunology · doi:10.1038/nri1268 · Cited by 375

PlexinD1 and Semaphorin Signaling Are Required in Endothelial Cells for Cardiovascular Development

Gitler, A. D., Lu, M. M., & Epstein, J. A. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.06.002 · Cited by 372

Plexin-B1 Directly Interacts with PDZ-RhoGEF/LARG to Regulate RhoA and Growth Cone Morphology

Swiercz, J. M., Kuner, R., Behrens, J., & Offermanns, S. (2002) · Neuron · doi:10.1016/s0896-6273(02)00750-x · Cited by 363

Identification of CD72 as a Lymphocyte Receptor for the Class IV Semaphorin CD100

Kumanogoh, A., Watanabe, C., Lee, I.-S., Wang, X., Shi, W., Araki, H., Hirata, H., Iwahori, K., Uchida, J., Yasui, T., et al. (2000) · Immunity · doi:10.1016/s1074-7613(00)00062-5 · Cited by 354

Class IV semaphorin Sema4A enhances T-cell activation and interacts with Tim-2

Kumanogoh, A., Marukawa, S., Suzuki, K., Takegahara, N., Watanabe, C., Ch’ng, E. S., Ishida, I., Fujimura, H., Sakoda, S., Yoshida, K., et al. (2002) · Nature · doi:10.1038/nature01037 · Cited by 336

Semaphorin junction: making tracks toward neural connectivity

Pasterkamp, R. J., & Kolodkin, A. L. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00003-5 · Cited by 320

The Collagen Binding α1β1 Integrin VLA-1 Regulates CD8 T Cell-Mediated Immune Protection against Heterologous Influenza Infection

Ray, S. J., Franki, S. N., Pierce, R. H., Dimitrova, S., Koteliansky, V., Sprague, A., Doherty, P. C., de Fougerolles, A. R., & Topham, D. J. (2004) · Immunity · doi:10.1016/s1074-7613(04)00021-4 · Cited by 317

Semaphorin 7A initiates T-cell-mediated inflammatory responses through α1β1 integrin

Suzuki, K., Okuno, T., Yamamoto, M., Pasterkamp, R. J., Takegahara, N., Takamatsu, H., Kitao, T., Takagi, J., Rennert, P. D., Kolodkin, A. L., et al. (2007) · Nature · doi:10.1038/nature05652 · Cited by 309

Dual roles of Sema6D in cardiac morphogenesis through region-specific association of its receptor, Plexin-A1, with off-track and vascular endothelial growth factor receptor type 2Preprint

Toyofuku, T., Zhang, H., Kumanogoh, A., Takegahara, N., Suto, F., Kamei, J., Aoki, K., Yabuki, M., Hori, M., Fujisawa, H., et al. (2004) · Genes & Development · doi:10.1101/gad.1167304 · Cited by 282

Dynamic imaging of the immune system: progress, pitfalls and promise

Germain, R. N., Miller, M. J., Dustin, M. L., & Nussenzweig, M. C. (2006) · Nature reviews. Immunology · doi:10.1038/nri1884 · Cited by 275

Plexin-A1 and its interaction with DAP12 in immune responses and bone homeostasis

Takegahara, N., Takamatsu, H., Toyofuku, T., Tsujimura, T., Okuno, T., Yukawa, K., Mizui, M., Yamamoto, M., Prasad, D. V., Suzuki, K., et al. (2006) · Nature Cell Biology · doi:10.1038/ncb1416 · Cited by 270

Human CD100, a novel leukocyte semaphorin that promotes B-cell aggregation and differentiation.

Hall, K. T., Boumsell, L., Schultze, J. L., Boussiotis, V. A., Dorfman, D. M., Cardoso, A. A., Bensussan, A., Nadler, L. M., & Freeman, G. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11780 · Cited by 266

The Class IV Semaphorin CD100 Plays Nonredundant Roles in the Immune System

Shi, W., Kumanogoh, A., Watanabe, C., Uchida, J., Wang, X., Yasui, T., Yukawa, K., Ikawa, M., Okabe, M., Parnes, J. R., et al. (2000) · Immunity · doi:10.1016/s1074-7613(00)00063-7 · Cited by 257

Requirement of Rac1 and Rac2 Expression by Mature Dendritic Cells for T Cell Priming

Benvenuti, F., Hugues, S., Walmsley, M. J., Ruf, S., Fetler, L., Popoff, M. R., Tybulewicz, V. L. J., & Amigorena, S. (2004) · Science · doi:10.1126/science.1099159 · Cited by 239

A Poxvirus-Encoded Semaphorin Induces Cytokine Production from Monocytes and Binds to a Novel Cellular Semaphorin Receptor, VESPR

Comeau, M. R., Johnson, R., DuBose, R. F., Petersen, M., Gearing, P., VandenBos, T., Park, L., Farrah, T., Buller, R. M. L., Cohen, J. I., et al. (1998) · Immunity · doi:10.1016/s1074-7613(00)80552-x · Cited by 237

Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patterns.

Sekido, Y., Bader, S., Latif, F., Chen, J. Y., Duh, F.-M. C., Wei, M. H., Albanesi, J. P., Lee, C. C., Lerman, M. I., & Minna, J. D. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.9.4120 · Cited by 232

Inhibition of lung cancer cell growth and induction of apoptosis after reexpression of 3p21.3 candidate tumor suppressor gene SEMA3B

Tomizawa, Y., Sekido, Y., Kondo, M., Gao, B., Yokota, J., Roche, J., Drabkin, H. A., Lerman, M. I., Gazdar, A. F., & Minna, J. D. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231490898 · Cited by 208

CD72-Deficient Mice Reveal Nonredundant Roles of CD72 in B Cell Development and Activation

Pan, C., Baumgarth, N., & Parnes, J. R. (1999) · Immunity · doi:10.1016/s1074-7613(00)80124-7 · Cited by 207

The ITAM-bearing transmembrane adaptor DAP12 in lymphoid and myeloid cell function

Lanier, L. L., & Bakker, A. B. H. (2000) · Immunology Today · doi:10.1016/s0167-5699(00)01745-x · Cited by 203

Guidance of myocardial patterning in cardiac development by Sema6D reverse signalling

Toyofuku, T., Zhang, H., Kumanogoh, A., Takegahara, N., Yabuki, M., Harada, K., Hori, M., & Kikutani, H. (2004) · Nature Cell Biology · doi:10.1038/ncb1193 · Cited by 196

In vivo imaging of leukocyte trafficking in blood vessels and tissues

Mempel, T. R., Scimone, M. L., Mora, J. R., & von Andrian, U. H. (2004) · Current Opinion in Immunology · doi:10.1016/j.coi.2004.05.018 · Cited by 184

Immunosuppressive role of semaphorin‐3A on T cell proliferation is mediated by inhibition of actin cytoskeleton reorganization

Lepelletier, Y., Moura, I. C., Hadj-Slimane, R., Renand, A., Susana Fiorentino, G., Baude, C., Shirvan, A., Barzilai, A., & Hermine, O. (2006) · European Journal of Immunology · doi:10.1002/eji.200535601 · Cited by 178

Semaphorin 7A plays a critical role in TGF-β1–induced pulmonary fibrosis

Kang, H., Lee, C. G., Homer, R., & Elias, J. A. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061273 · Cited by 177

Semaphorin‐4A, an activator for T‐cell‐mediated immunity, suppresses angiogenesis via Plexin‐D1

Toyofuku, T., Yabuki, M., Kamei, J., Kamei, M., Makino, N., Kumanogoh, A., & Hori, M. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601589 · Cited by 175

Nonredundant Roles of Sema4A in the Immune System: Defective T Cell Priming and Th1/Th2 Regulation in Sema4A-Deficient Mice

Kumanogoh, A., Shikina, T., Suzuki, K., Uematsu, S., Yukawa, K., Kashiwamura, S., Tsutsui, H., Yamamoto, M., Takamatsu, H., Ko-Mitamura, E. P., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.01.014 · Cited by 174

Semaphorin-3A is expressed by tumor cells and alters T-cell signal transduction and function.

Catalano, A., Caprari, P., Moretti, S., Faronato, M., Tamagnone, L., & Procopio, A. (2006) · Blood · doi:10.1182/blood-2005-06-2445 · Cited by 167

CD100/Plexin-B1 interactions sustain proliferation and survival of normal and leukemic CD5+ B lymphocytes

Granziero, L., Circosta, P., Scielzo, C., Frisaldi, E., Stella, S., Geuna, M., Giordano, S., Ghia, P., & Caligaris‐Cappio, F. (2003) · Blood · doi:10.1182/blood-2002-05-1339 · Cited by 163

Biological Activity of Soluble CD100. II. Soluble CD100, Similarly to H-SemaIII, Inhibits Immune Cell Migration

Delaire, S., Billard, C., Tordjman, R., Chédotal, A., Elhabazi, A., Bensussan, A., & Boumsell, L. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.7.4348 · Cited by 161

The B cell surface protein CD72 recruits the tyrosine phosphatase SHP-1 upon tyrosine phosphorylation.

Adachi, T., Flaswinkel, H., Yakura, H., Reth, M. G., & Tsubata, T. (1998) · PubMed · Cited by 156

Requirement for the Lymphocyte Semaphorin, CD100, in the Induction of Antigen-Specific T Cells and the Maturation of Dendritic Cells

Kumanogoh, A., Suzuki, K., Ch’ng, E. S., Watanabe, C., Marukawa, S., Takegahara, N., Ishida, I., Sato, T., Habu, S., Yoshida, K., et al. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.3.1175 · Cited by 152

Sema7A is a Potent Monocyte Stimulator

HOLMES, S., DOWNS, A. ‐., Fosberry, A. P., Hayes, P. D., Michalovich, D., MURDOCH, P., Moores, K., Fox, J. M., Deen, K. C., Pettman, G. R., et al. (2002) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.2002.01129.x · Cited by 148

Cutting Edge: The B Cell Surface Protein CD72 Recruits the Tyrosine Phosphatase SHP-1 upon Tyrosine Phosphorylation

Adachi, T., Flaswinkel, H., Yakura, H., Reth, M. G., & Tsubata, T. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.10.4662 · Cited by 146

Increased surface expression of a newly identified 150-kDa dimer early after human T lymphocyte activation

Bougeret, C., Mansur, I. G., Dastot, H., Schmid, M., Mahouy, G., Bensussan, A., & Boumsell, L. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.2.318 · Cited by 145

The B-cell transmembrane protein CD72 binds to and is an in vivo substrate of the protein tyrosine phosphatase SHP-1.

Wu, Y.-J., Nadler, M. J. S., Brennan, L., Gish, G., Timms, J., Fusaki, N., Jongstra-Bilen, J., Tada, N., Pawson, T., Wither, J., et al. (1998) · Current Biology · doi:10.1016/s0960-9822(07)00421-6 · Cited by 143

Human Semaphorin 3B (SEMA3B) located at chromosome 3p21.3 suppresses tumor formation in an adenocarcinoma cell line.

Tse, C., Xiang, R. H., Bracht, T., & Naylor, S. L. (2002) · PubMed · Cited by 142

CIITA-regulated plexin-A1 affects T-cell–dendritic cell interactions

Wong, A. W., Brickey, W. J., Taxman, D. J., van Deventer, H. W., REED, W. A., Gao, J. X., Zheng, P., Liu, Y., Li, P., Blum, J. S., et al. (2003) · Nature Immunology · doi:10.1038/ni960 · Cited by 136

Semaphorin 3F gene from human 3p21.3 suppresses tumor formation in nude mice.

Xiang, R., Davalos, A. R., Hensel, C. H., Zhou, X., Tse, C., & Naylor, S. L. (2002) · PubMed · Cited by 132

Tim-2 regulates T helper type 2 responses and autoimmunity

Chakravarti, S., Sabatos, C. A., Xiao, S., Illés, Z., Cha, E. K., Sobel, R. A., Zheng, X. X., Strom, T. B., & Kuchroo, V. K. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050308 · Cited by 130

Semaphorin 7A Is a Negative Regulator of T Cell Responses

Czopik, A. K., Bynoe, M. S., Palm, N. W., Raine, C. S., & Medzhitov, R. M. (2006) · Immunity · doi:10.1016/j.immuni.2006.03.013 · Cited by 112

TIM Family of Genes in Immunity and Tolerance

Kuchroo, V. K., Meyers, J. H., Umetsu, D. T., & DeKruyff, R. H. (2006) · Advances in immunology · doi:10.1016/s0065-2776(06)91006-2 · Cited by 111

Human Semaphorin K1 Is Glycosylphosphatidylinositol-linked and Defines a New Subfamily of Viral-related Semaphorins

Xu, X., Ng, S., Wu, Z., Nguyen, D., Homburger, S. A., Seidel‐Dugan, C., Ebens, A. J., & Luo, Y. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.35.22428 · Cited by 108

Regulation of B cell fates by BCR signaling components

Kurosaki, T. (2002) · Current Opinion in Immunology · doi:10.1016/s0952-7915(02)00344-8 · Cited by 106

CD100 is a leukocyte semaphorin

Delaire, S., Elhabazi, A., Bensussan, A., & Boumsell, L. (1998) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050252 · Cited by 106

Involvement of CD100, a lymphocyte semaphorin, in the activation of the human immune system via CD72: implications for the regulation of immune and inflammatory responses

Ishida, I. (2003) · International Immunology · doi:10.1093/intimm/dxg098 · Cited by 96

Soluble CD100 functions on human monocytes and immature dendritic cells require plexin C1 and plexin B1, respectively

Ponnat, I. C.-D. (2005) · International Immunology · doi:10.1093/intimm/dxh224 · Cited by 92

Plexin C1 Engagement on Mouse Dendritic Cells by Viral Semaphorin A39R Induces Actin Cytoskeleton Rearrangement and Inhibits Integrin-Mediated Adhesion and Chemokine-Induced Migration

Walzer, T., Galibert, L., Comeau, M. R., & Smedt, T. D. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.1.51 · Cited by 85

SHP-1 Requires Inhibitory Co-receptors to Down-modulate B Cell Antigen Receptor-mediated Phosphorylation of Cellular Substrates

Adachi, T., Wienands, J., Wakabayashi, C., Yakura, H., Reth, M. G., & Tsubata, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100997200 · Cited by 81

Molecular Cloning of a Glycosylphosphatidylinositol-Anchored Molecule CDw108

Yamada, A., Kubo, K., Takeshita, T., Harashima, N., Kawano, K., Mine, T., Sagawa, K., Sugamura, K., & Itoh, K. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.7.4094 · Cited by 80

The role of very late antigen-1 in immune-mediated inflammation

Ben‐Horin, S., & Bank, I. (2004) · Clinical Immunology · doi:10.1016/j.clim.2004.06.007 · Cited by 73

T Cell, Ig Domain, Mucin Domain-2 Gene-Deficient Mice Reveal a Novel Mechanism for the Regulation of Th2 Immune Responses and Airway Inflammation

Rennert, P. D., Ichimura, T., Sizing, I. D., Bailly, V., Li, Z., Rennard, R., McCoon, P., Pablo, L., Miklasz, S., Tarilonte, L., et al. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.7.4311 · Cited by 67

Shared resources between the neural and immune systems: semaphorins join the ranks

Spriggs, M. K. (1999) · Current Opinion in Immunology · doi:10.1016/s0952-7915(99)80065-x · Cited by 61

Requirement for CD100-CD72 interactions in fine-tuning of B-cell antigen receptor signaling and homeostatic maintenance of the B-cell compartment.

Kumanogoh, A., Shikina, T., Watanabe, C., Takegahara, N., Suzuki, K., Yamamoto, M., Takamatsu, H., Prasad, D. V., Mizui, M., Toyofuku, T., et al. (2005) · International Immunology · doi:10.1093/intimm/dxh307 · Cited by 58

Enhanced Immune Responses in Transgenic Mice Expressing a Truncated Form of the Lymphocyte Semaphorin CD100

Watanabe, C., Kumanogoh, A., Shi, W., Suzuki, K., Yamada, S., Okabe, M., Yoshida, K., & Kikutani, H. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.8.4321 · Cited by 56

The SH2 Domain Containing Tyrosine Phosphatase-1 Down-regulates Activation of Lyn and Lyn-induced Tyrosine Phosphorylation of the CD19 Receptor in B Cells

Somani, A.-K. B., Yuen, K., Xu, F., Zhang, J., Branch, D. R., & Siminovitch, K. A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006820200 · Cited by 49

CDw108 expression during T‐cell development

Mine, T., Harada, K., Matsumoto, T., Yamana, H., Shirouzu, K., Itoh, K., & Yamada, A. (2000) · Tissue Antigens · doi:10.1034/j.1399-0039.2000.550505.x · Cited by 45

Expression and Functional Importance of Collagen-Binding Integrins, α1β1 and α2β1, on Virus-Activated T Cells

Andreasen, S. Ø., Thomsen, A. R., Koteliansky, V., Novobrantseva, T. I., Sprague, A., de Fougerolles, A. R., & Christensen, J. P. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.6.2804 · Cited by 45

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

Inflammation, metaflammation and immunometabolic disorders

Hotamisligil, G. S. (2017) · Nature · doi:10.1038/nature21363 · Cited by 2,570

Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells

Florencio-Silva, R., Sasso, G. R. D. S., Sasso-Cerri, E., Simões, M. J., & Cerri, P. S. (2015) · BioMed Research International · doi:10.1155/2015/421746 · Cited by 2,044

Free Fatty Acid Receptors in Health and Disease

Kimura, I., Ichimura, A., Ohue‐Kitano, R., & Igarashi, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00041.2018 · Cited by 1,058

Osteoclast–osteoblast communication

Matsuo, K., & Irie, N. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.03.027 · Cited by 780

Immune proteins in brain development and synaptic plasticity

Boulanger, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.001 · Cited by 555

Regulation of immune cell responses by semaphorins and their receptors

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