Innate Immunity and Its Regulation by Mast Cells

The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors

Kawai, T., & Akira, S. (2010) · Nature Immunology · doi:10.1038/ni.1863 · Cited by 9,304 · see citing works

Toll-like receptors and their crosstalk with other innate receptors in infection and immunity

Kawai, T., & Akira, S. (2011) · Immunity · doi:10.1016/j.immuni.2011.05.006 · Cited by 3,658 · see citing works

Cryopyrin activates the inflammasome in response to toxins and ATP

Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080 · see citing works

Inflammasomes in health and disease

Strowig, T., Henao-Mejia, J., Elinav, E., & Flavell, R. (2012) · Nature · doi:10.1038/nature10759 · Cited by 2,230 · see citing works

TRANSFORMING GROWTH FACTOR-β REGULATION OF IMMUNE RESPONSES

Li, M. O., Wan, Y. Y., Sanjabi, S., Robertson, A.-K. L., & Flavell, R. A. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.24.021605.090737 · Cited by 2,199 · see citing works

Intracellular pattern recognition receptors in the host response

Meylan, E., Tschopp, J., & Karin, M. (2006) · Nature · doi:10.1038/nature04946 · Cited by 1,196 · see citing works

Mast cell modulation of neutrophil influx and bacterial clearance at sites of infection through TNF-α

Malaviya, R., Ikeda, T., Ross, E., & Abraham, S. N. (1996) · Nature · doi:10.1038/381077a0 · Cited by 1,123 · see citing works

Mast cell-orchestrated immunity to pathogens

Abraham, S. N., & John, A. L. S. (2010) · Nature reviews. Immunology · doi:10.1038/nri2782 · Cited by 959 · see citing works

Induction of Direct Antimicrobial Activity Through Mammalian Toll-Like Receptors

Thoma-Uszynski, S., Stenger, S., Takeuchi, O., Ochoa, M. T., Engele, M., Sieling, P. A., Barnes, P. F., Röllinghoff, M., Bölcskei, P., Wagner, M., et al. (2001) · Science · doi:10.1126/science.291.5508.1544 · Cited by 729 · see citing works

Mycobacterium tuberculosis: success through dormancy

Gengenbacher, M., & Kaufmann, S. H. E. (2012) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2012.00331.x · Cited by 698 · see citing works

Intestinal mucosal mast cells in normal and nematode-infected rat intestines are in intimate contact with peptidergic nerves.

Stead, R. H., Tomioka, M., Quinonez, G. E., Simon, G. T., Felten, S. Y., & Bienenstock, J. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.9.2975 · Cited by 554 · see citing works

The Membrane Attack Complex of Complement

Müller‐Eberhard, H. J. (1986) · Annual Review of Immunology · doi:10.1146/annurev.iy.04.040186.002443 · Cited by 507 · see citing works

Differential responses of mast cell Toll-like receptors 2 and 4 in allergy and innate immunity

Supajatura, V., Ushio, H., Nakao, A., Akira, S., Okumura, K., Ra, C., & Ogawa, H. (2002) · Journal of Clinical Investigation · doi:10.1172/jci14704 · Cited by 491 · see citing works

Mast cell–derived interleukin 10 limits skin pathology in contact dermatitis and chronic irradiation with ultraviolet B

Grimbaldeston, M. A., Nakae, S., Kalesnikoff, J., Tsai, M. M., & Galli, S. J. (2007) · Nature Immunology · doi:10.1038/ni1503 · Cited by 486 · see citing works

Activation of Airway Epithelial Cells by Toll-Like Receptor Agonists

Sha, Q., Truong-Tran, A. Q., Plitt, J. R., Beck, L. A., & Schleimer, R. P. (2004) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2003-0388oc · Cited by 485 · see citing works

Heterogeneity of Mast Cells and Phenotypic Change Between Subpopulations

Kitamura, Y. (1989) · Annual Review of Immunology · doi:10.1146/annurev.iy.07.040189.000423 · Cited by 475 · see citing works

Differential release of mast cell mediators and the pathogenesis of inflammation

Theoharides, T. C., Kempuraj, D., Tagen, M., Conti, P., & Kalogeromitros, D. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00519.x · Cited by 425 · see citing works

Cutting Edge: Mast Cell Antimicrobial Activity Is Mediated by Expression of Cathelicidin Antimicrobial Peptide

Nardo, A. D., Vitiello, A., & Gallo, R. L. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.5.2274 · Cited by 405 · see citing works

Differential responses of mast cell Toll-like receptors 2 and 4 in allergy and innate immunity

Supajatura, V., Ushio, H., Nakao, A., Akira, S., Okumura, K., Ra, C., & Ogawa, H. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0214704 · Cited by 404 · see citing works

Mast Cells Can Enhance Resistance to Snake and Honeybee Venoms

Metz, M., Piliponsky, A. M., Chen, C., Lammel, V., Åbrink, M., Pejler, G., Tsai, M. M., & Galli, S. J. (2006) · Science · doi:10.1126/science.1128877 · Cited by 381 · see citing works

Activation of mast cells by double-stranded RNA: evidence for activation through Toll-like receptor 3

Kulka, M., Alexopoulou, L., Flavell, R. A., & Metcalfe, D. D. (2004) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2004.03.049 · Cited by 354 · see citing works

Cutting Edge: Distinct Toll-Like Receptor 2 Activators Selectively Induce Different Classes of Mediator Production from Human Mast Cells

McCurdy, J. D., Olynych, T., Maher, L. H., & Marshall, J. S. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.4.1625 · Cited by 349 · see citing works

Roles of mast cells and basophils in innate and acquired immunity

Wedemeyer, J., Tsai, M. M., & Galli, S. J. (2000) · Current Opinion in Immunology · doi:10.1016/s0952-7915(00)00154-0 · Cited by 345 · see citing works

Lipopolysaccharide-Dependent Prostaglandin E2 Production Is Regulated by the Glutathione-Dependent Prostaglandin E2 Synthase Gene Induced by the Toll-Like Receptor 4/MyD88/NF-IL6 Pathway

Uematsu, S., Matsumoto, M., Takeda, K., & Akira, S. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.11.5811 · Cited by 308 · see citing works

Imiquimod clears tumors in mice independent of adaptive immunity by converting pDCs into tumor-killing effector cells

Drobits, B., Holcmann, M., Amberg, N., Swiecki, M. K., Grundtner, R., Hammer, M., Colonna, M., & Sibilia, M. C. (2012) · Journal of Clinical Investigation · doi:10.1172/jci61034 · Cited by 295 · see citing works

IL-10 Overexpression Decreases Inflammatory Mediators and Promotes Regenerative Healing in an Adult Model of Scar Formation

Peranteau, W. H., Zhang, L., Muvarak, N. E., Badillo, A. T., Radu, A. P., Zoltick, P. W., & Liechty, K. W. (2008) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5701232 · Cited by 286 · see citing works

Extracellular ATP mediates mast cell-dependent intestinal inflammation through P2X7 purinoceptors

Kurashima, Y., Amiya, T., Nochi, T., Fujisawa, K., Haraguchi, T., Iba, H., Tsutsui, H., Sato, S., Nakajima, S., Iijima, H., et al. (2012) · Nature Communications · doi:10.1038/ncomms2023 · Cited by 286 · see citing works

Mast cells and eicosanoid mediators: a system of reciprocal paracrine and autocrine regulation

Boyce, J. A. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00512.x · Cited by 255 · see citing works

Mucosal mast cells are functionally active during spontaneous expulsion of intestinal nematode infections in rat

Woodbury, R. G., Miller, H. R. P., Huntley, J. F., Newlands, G. F. J., Palliser, A. C., & Wakelin, D. (1984) · Nature · doi:10.1038/312450a0 · Cited by 255 · see citing works

The mast cell tumor necrosis factor α response to FimH-expressing Escherichia coli is mediated by the glycosylphosphatidylinositol-anchored molecule CD48

Malaviya, R., Gao, Z., Thankavel, K., van der Merwe, P. A., & Abraham, S. N. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.14.8110 · Cited by 255 · see citing works

The Role of Leukocytes, Keratinocytes, and Allergen-Specific IgE in the Development of Atopic Dermatitis

Werfel, T. (2009) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.71 · Cited by 249 · see citing works

IL-10, an inflammatory/inhibitory cytokine, but not always

Conti, P., Kempuraj, D., Kandere‐Grzybowska, K., Gioacchino, M. D., Barbacane, R. C., Castellani, M. L., Felaco, M., Boucher, W. S., Létourneau, R., & Theoharides, T. C. (2003) · Immunology Letters · doi:10.1016/s0165-2478(03)00002-6 · Cited by 236 · see citing works

Immune surveillance by mast cells during dengue infection promotes natural killer (NK) and NKT-cell recruitment and viral clearance

John, A. L. S., Rathore, A. P. S., Yap, H., Ng, M. L., Metcalfe, D. D., Vasudevan, S. G., & Abraham, S. N. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105079108 · Cited by 225 · see citing works

Mast cell modulation of the vascular and lymphatic endothelium

Kunder, C. A., John, A. L. S., & Abraham, S. N. (2011) · Blood · doi:10.1182/blood-2011-07-358432 · Cited by 219 · see citing works

Modulation of Inflammasome Pathways by Bacterial and Viral Pathogens

Lamkanfi, M., & Dixit, V. M. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100229 · Cited by 217 · see citing works

Transcriptional Regulation of β-Defensin Gene Expression in Tracheal Epithelial Cells

Diamond, G., Kaiser, V. L., Rhodes, J., Russell, J. P., & Bevins, C. L. (2000) · Infection and Immunity · doi:10.1128/iai.68.1.113-119.2000 · Cited by 215 · see citing works

Susceptibility and immunity to helminth parasites

Maizels, R. M., Hewitson, J. P., & Smith, K. A. (2012) · Current Opinion in Immunology · doi:10.1016/j.coi.2012.06.003 · Cited by 215 · see citing works

Mast cell activators: a new class of highly effective vaccine adjuvants

McLachlan, J. B., Shelburne, C. P., Hart, J. P., Pizzo, S. V., Goyal, R., Brooking-Dixon, R., Staats, H. F., & Abraham, S. N. (2008) · Nature Medicine · doi:10.1038/nm1757 · Cited by 206 · see citing works

Activation of paracrine TGF‐β1 signaling upon stimulation and degranulation of rat serosal mast cells: a novel function for chymase

Lindstedt, K. A., Wang, Y., Shiota, N., Saarinen, J., Hyytiäinen, M. M., Kokkonen, J. O., Keski‐Oja, J., & Kovanen, P. T. (2001) · The FASEB Journal · doi:10.1096/fj.00-0273com · Cited by 197 · see citing works

New models for analyzing mast cell functions in vivo

Reber, L. L., Marichal, T., & Galli, S. J. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.09.008 · Cited by 188 · see citing works

Characterization of Toll-like receptors in primary lung epithelial cells: strong impact of the TLR3 ligand poly(I:C) on the regulation of Toll-like receptors, adaptor proteins and inflammatory response

Ritter, M., Mennerich, D., Weith, A., & Seither, P. (2005) · Journal of Inflammation · doi:10.1186/1476-9255-2-16 · Cited by 184 · see citing works

Mast cells mediate neutrophil recruitment and vascular leakage through the NLRP3 inflammasome in histamine-independent urticaria

Nakamura, Y., Kambe, N., Saito, M. K., Nishikomori, R., Kim, Y., Murakami, M., Núñez, G., & Matsue, H. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20082179 · Cited by 181 · see citing works

Immune cells in the healing skin wound: Influential players at each stage of repair

Wilgus, T. A. (2008) · Pharmacological Research · doi:10.1016/j.phrs.2008.07.009 · Cited by 181 · see citing works

TLR3-induced activation of mast cells modulates CD8+ T-cell recruitment

Orinska, Z., Bulanova, E., Budagian, V., Metz, M., Maurer, M., & Bulfone‐Paus, S. (2005) · Blood · doi:10.1182/blood-2004-07-2656 · Cited by 181 · see citing works

Mast cell–derived particles deliver peripheral signals to remote lymph nodes

Kunder, C. A., John, A. L. S., Li, G., Leong, K. W., Berwin, B. L., Staats, H. F., & Abraham, S. N. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20090805 · Cited by 176 · see citing works

Accelerated Wound Closure in Mice Deficient for Interleukin-10

Eming, S. A., Werner, S., Bugnon, P., Wickenhauser, C., Siewe, L., Utermöhlen, O., Davidson, J. M., Krieg, T. M., & Roers, A. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.060370 · Cited by 172 · see citing works

Mast Cell Interleukin-10 Drives Localized Tolerance in Chronic Bladder Infection

Chan, C. Y., John, A. L. S., & Abraham, S. N. (2013) · Immunity · doi:10.1016/j.immuni.2012.10.019 · Cited by 156 · see citing works

Mouse Mast Cell Tryptase mMCP-6 Is a Critical Link between Adaptive and Innate Immunity in the Chronic Phase of Trichinella spiralis Infection

Shin, K., Watts, G. F., Oettgen, H. C., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.7.4885 · Cited by 152 · see citing works

Mast Cells Augment Adaptive Immunity by Orchestrating Dendritic Cell Trafficking through Infected Tissues

Shelburne, C. P., Nakano, H., John, A. L. S., et al. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.09.004 · Cited by 140 · see citing works

Myocardial Ischemia Activates an Injurious Innate Immune Signaling via Cardiac Heat Shock Protein 60 and Toll-like Receptor 4

Li, Y., Si, R., Feng, Y., Chen, H. H., Zou, L., Wang, E., Zhang, M., Warren, H. S., Sosnovik, D. E., & Chao, W. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.246124 · Cited by 139 · see citing works

Direct evidence of mast cell involvement in Clostridium difficile toxin a—induced enteritis in mice☆☆☆

Wershil, B. K., Castagliuolo, I., & Pothoulakis, C. (1998) · Gastroenterology · doi:10.1016/s0016-5085(98)70315-4 · Cited by 135 · see citing works

Tryptophan hydroxylase-1 regulates immune tolerance and inflammation

Nowak, E. C., de Vries, V. C., Wasiuk, A., Ahonen, C. L., Bennett, K. A., Mercier, I. L., Ha, D.-G., & Noelle, R. J. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20120408 · Cited by 125 · see citing works

Toll-like Receptor 4 (TLR4) Is Essential for Hsp70-like Protein 1 (HSP70L1) to Activate Dendritic Cells and Induce Th1 Response

Fang, H., Wu, Y., Huang, X., Wang, W., Ang, B., Cao, X., & Wan, T. Y. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.266528 · Cited by 122 · see citing works

Mast cells are crucial for early inflammation, migration of Langerhans cells, and CTL responses following topical application of TLR7 ligand in mice

Heib, V., Becker, M., Warger, T., et al. (2007) · Blood · doi:10.1182/blood-2006-07-036889 · Cited by 115 · see citing works

Critical Role for Mast Cells in Interleukin-1β-Driven Skin Inflammation Associated with an Activating Mutation in the Nlrp3 Protein

Nakamura, Y., Franchi, L., Kambe, N., Meng, G., Strober, W., & Núñez, G. (2012) · Immunity · doi:10.1016/j.immuni.2012.04.013 · Cited by 104 · see citing works

Skin Mast Cells Protect Mice against Vaccinia Virus by Triggering Mast Cell Receptor S1PR2 and Releasing Antimicrobial Peptides

Wang, Z., Lai, Y., Bernard, J. J., MacLeod, D. T., Cogen, A. L., Moss, B., & Nardo, A. D. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1101703 · Cited by 100 · see citing works

Signaling through Toll-Like Receptors Triggers HIV-1 Replication in Latently Infected Mast Cells

Sundstrom, J. B., Little, D. M., Villinger, F. J., Ellis, J. E., & Ansari, A. A. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.7.4391 · Cited by 99 · see citing works

Synthetic mast-cell granules as adjuvants to promote and polarize immunity in lymph nodes

John, A. L. S., Chan, C. Y., Staats, H. F., Leong, K. W., & Abraham, S. N. (2012) · Nature Materials · doi:10.1038/nmat3222 · Cited by 96 · see citing works

Cutting Edge: Mast Cells Critically Augment Myeloid-Derived Suppressor Cell Activity

Saleem, S. J., Martin, R., Morales, J. K., Sturgill, J., Gibb, D. R., Graham, L., Bear, H. D., Manjili, M. H., Ryan, J. J., & Conrad, D. H. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200647 · Cited by 93 · see citing works

Neuroimmune communication in the submucous plexus of guinea pig colon after infection with Trichinella spiralis

Frieling, T., Palmer, J. M., Cooke, H. J., & Wood, J. D. (1994) · Gastroenterology · doi:10.1016/0016-5085(94)90798-6 · Cited by 92 · see citing works

“Host Tissue Damage” Signal ATP Promotes Non-directional Migration and Negatively Regulates Toll-like Receptor Signaling in Human Monocytes

Kaufmann, A. M., Musset, B., Limberg, S. H., Renigunta, V., Sus, R., Dalpke, A. H., Heeg, K. M., Robaye, B., & Hanley, P. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m505301200 · Cited by 88 · see citing works

Pseudomonas aeruginosa Activates Human Mast Cells to Induce Neutrophil Transendothelial Migration Via Mast Cell-Derived IL-1α and β

Lin, T., Garduño, R. A., Boudreau, R. T. M., & Issekutz, A. C. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.8.4522 · Cited by 86 · see citing works

Cooperative Activation of TLR2 and Bradykinin B2 Receptor Is Required for Induction of Type 1 Immunity in a Mouse Model of Subcutaneous Infection by Trypanosoma cruzi

Monteiro, A. C., Schmitz, V., Svensjö, E., et al. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.9.6325 · Cited by 86 · see citing works

Mast cells elicit proinflammatory but not type I interferon responses upon activation of TLRs by bacteria

Dietrich, N. L., Rohde, M., Geffers, R., Kröger, A., Häuser, H., Weiß, S., & Gekara, N. O. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912551107 · Cited by 78 · see citing works

Cholera toxin increases IL-6 synthesis and decreases TNF-α production by rat peritoneal mast cells

Leal‐Berumen, I., Snider, D. P., Barajas‐López, C., et al. (1996) · The Journal of Immunology · doi:10.4049/jimmunol.156.1.316 · Cited by 77 · see citing works

Fate of Shed Mast Cell Granules.

Higginbotham, R. D., Dougherty, T. F., & Jee, W. S. S. (1956) · Experimental Biology and Medicine · doi:10.3181/00379727-92-22445 · Cited by 69 · see citing works

Colocalization of heparin and histamine in the intracellular granules of test cells from the invertebrate Styela plicata (Chordata-Tunicata)

Cavalcante, M. C. M. (2002) · Journal of Structural Biology · doi:10.1016/s1047-8477(02)00007-2 · Cited by 67 · see citing works

Co‐option of endocytic functions of cellular caveolae by pathogens

Shin, J., & Abraham, S. N. (2001) · Immunology · doi:10.1046/j.1365-2567.2001.01173.x · Cited by 67 · see citing works

Mast Cells Play a Crucial Role in Staphylococcus aureus Peptidoglycan-Induced Diarrhea

Feng, B., He, S., Zheng, P., Wu, L. H., & Yang, P. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.061274 · Cited by 63 · see citing works

Substance P primes lipoteichoic acid‐ and Pam3CysSerLys4‐mediated activation of human mast cells by up‐regulating Toll‐like receptor 2

Tancowny, B. P., Karpov, V. G., Schleimer, R. P., & Kulka, M. (2010) · Immunology · doi:10.1111/j.1365-2567.2010.03296.x · Cited by 62 · see citing works

Mast Cell Stabilizer Ketotifen [4-(1-Methyl-4-piperidylidene)-4 H-benzo[4,5]cyclohepta[1,2-b]thiophen-10(9 H)-one Fumarate] Prevents Mucosal Mast Cell Hyperplasia and Intestinal Dysmotility in Experimental Trichinella spiralis Inflammation in the Rat

de la Serna, H., Porras, M., & Vergara, P. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.106.104620 · Cited by 60 · see citing works

FcεR1-Mediated Mast Cell Reactivity Is Amplified through Prolonged Toll-Like Receptor-Ligand Treatment

Saluja, R., Delin, I., Nilsson, G. P., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043547 · Cited by 55 · see citing works

Repeated intranasal TLR7 stimulation reduces allergen responsiveness in allergic rhinitis

Greiff, L., Cervin, A., Ahlström‐Emanuelsson, C., Almqvist, G., Andersson, M., Dolata, J., Eriksson, L. T., Högestätt, E. D., Källén, A., Norlén, P., et al. (2012) · Respiratory Research · doi:10.1186/1465-9921-13-53 · Cited by 51 · see citing works

Lipopolysaccharide-Mediated Mast Cell Activation Induces IFN-γ Secretion by NK Cells

Voßkuhl, K., Greten, T. F., Manns, M. P., Korangy, F., & Wedemeyer, J. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0902406 · Cited by 44 · see citing works

Interaction of Bordetella pertussis with mast cells, modulation of cytokine secretion by pertussis toxin

Mielcarek, N., Hörnquist, E. H., Johansson, B. R., et al. (2001) · Cellular Microbiology · doi:10.1046/j.1462-5822.2001.00106.x · Cited by 41 · see citing works

Histamine H 2 receptor-mediated airway goblet cell secretion and its modulation by histamine-degrading enzymes

Tamaoki, J., Nakata, J., Takeyama, K., et al. (1997) · Journal of Allergy and Clinical Immunology · doi:10.1016/s0091-6749(97)70102-7 · Cited by 35 · see citing works

Leukotriene D4(LTD4) Induces Mucus Secretion from Goblet Cells in the Guinea Pig Respiratory Epithelium

Hoffstein, S. T., Malo, P. E., Bugelski, P. J., et al. (1990) · Experimental Lung Research · doi:10.3109/01902149009087890 · Cited by 34 · see citing works

Mast cell regulation of airway smooth muscle function in asthma

Bradding, P. (2007) · European Respiratory Journal · doi:10.1183/09031936.00017707 · Cited by 34 · see citing works

Systemic mast cell degranulation increases mortality during polymicrobial septic peritonitis in mice

Seeley, E. J., Sutherland, R. E., Kim, S. S., & Wolters, P. J. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.0910531 · Cited by 32 · see citing works

In Vitro Desensitization of Human Skin Mast Cells

Zhao, W., Gomez, G., Macey, M., et al. (2011) · Journal of Clinical Immunology · doi:10.1007/s10875-011-9605-8 · Cited by 25 · see citing works

Immunity to intestinal parasites: role of mast cells and goblet cells.

Levy, D. A., & Frondoza, C. G. (1983) · PubMed · Cited by 23 · see citing works

Impaired Mast Cell-Driven Immune Responses in Mice Lacking the Transcription Factor NFATc2

Becker, M., Heib, V., Klein, M., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802878 · Cited by 16 · see citing works

Long-term management of asthma

Kabra, S. K., & Lodha, R. (2003) · The Indian Journal of Pediatrics · doi:10.1007/bf02722747 · Cited by 11 · see citing works

Mast Cell-Mediated Inhibition of Abdominal Neutrophil Inflammation by a PEGylated TLR7 Ligand

Hayashi, T., Yao, S., Crain, B., Chan, M., Cottam, H. B., Lao, F. S., Carson, D. A., & Corr, M. (2012) · Mediators of Inflammation · doi:10.1155/2012/262394 · Cited by 9 · see citing works

Gender differences in autoimmune disease

Ngo, S. T., Steyn, F. J., & McCombe, P. A. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.04.004 · Cited by 1,074 · see citing works

Human mast cell tryptase in biology and medicine

Vitte, J. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2014.04.001 · Cited by 152 · see citing works

Gender-Related Effects of Sex Steroids on Histamine Release and Fc<i>ε</i>RI Expression in Rat Peritoneal Mast Cells

Muñoz-Cruz, S., Mendoza-Rodríguez, Y., Nava-Castro, K. E., Yepez-Mulia, L., & Morales-Montor, J. (2015) · Journal of Immunology Research · doi:10.1155/2015/351829 · Cited by 54 · see citing works

IVIG activates FcγRIIB-SHIP1-PIP3 Pathway to stabilize mast cells and suppress inflammation after ICH in mice

Akyol, G. Y., Manaenko, A., Akyol, O., Solaroglu, I., Ho, W. M., Ding, Y., Flores, J., Zhang, J. H., & Tang, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-15455-w · Cited by 25 · see citing works

Serum concentrations of mast cell tryptase are reduced in heavy drinkers

Beceiro, C., Campos, J., Valcarcel, M.-A., Fenger, R. V., Lojo, S., Linneberg, A., Vidal, C., & Gonzalez-Quintela, A. (2015) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12682 · Cited by 9 · see citing works

The OWEZ Meteorological Mast. Analysis of mast-top displacements

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