Identification of In Vivo–Expressed Antigens of Staphylococcus aureus and Their Use in Vaccinations for Protection against Nasal Carriage

Principles and Practice of Infectious Diseases.

(1991) · Annals of Internal Medicine · doi:10.7326/0003-4819-114-9-818_5 · Cited by 12,045 · see citing works

Bacterial iron homeostasis

Andrews, S. C., Robinson, A. K., & Rodríguez-Quiñones, F. (2003) · FEMS Microbiology Reviews · doi:10.1016/s0168-6445(03)00055-x · Cited by 2,702 · see citing works

Nasal Carriage as a Source of<i>Staphylococcus aureus</i>Bacteremia

von Eiff, C., Becker, K., Machka, K., Stammer, H., & Peters, G. (2001) · New England Journal of Medicine · doi:10.1056/nejm200101043440102 · Cited by 1,984 · see citing works

Whole genome sequencing of meticillin-resistant Staphylococcus aureus

Kuroda, M., Ohta, T., Uchiyama, I., Baba, T., Yuzawa, H., Kobayashi, I., Cui, L., Oguchi, A., Aoki, K.-I., Nagai, Y., et al. (2001) · The Lancet · doi:10.1016/s0140-6736(00)04403-2 · Cited by 1,950 · see citing works

Identification of Vaccine Candidates Against Serogroup B Meningococcus by Whole-Genome Sequencing

Pizza, M., Scarlato, V., Masignani, V., Giuliani, M. M., Aricò, B., Comanducci, M., Jennings, G. T., Baldi, L., Bartolini, E., Capecchi, B., et al. (2000) · Science · doi:10.1126/science.287.5459.1816 · Cited by 1,403 · see citing works

An overview of nosocomial infections, including the role of the microbiology laboratory

Emori, T. G., & Gaynes, R. P. (1993) · Clinical Microbiology Reviews · doi:10.1128/cmr.6.4.428 · Cited by 1,262 · see citing works

Risk and outcome of nosocomial Staphylococcus aureus bacteraemia in nasal carriers versus non-carriers

Wertheim, H. F. L., Vos, M. D., Ott, A., van Belkum, A., Voß, A., Kluytmans, J. A. J. W., van Keulen, P. H. J., Vandenbroucke‐Grauls, C. M. J. E., Meester, M. H. M., & Verbrugh, H. A. (2004) · The Lancet · doi:10.1016/s0140-6736(04)16897-9 · Cited by 891 · see citing works

Properties of a cryptic high-frequency transducing phage in Staphylococcus aureus

Novick, R. P. (1967) · Virology · doi:10.1016/0042-6822(67)90105-5 · Cited by 745 · see citing works

σ B Modulates Virulence Determinant Expression and Stress Resistance: Characterization of a Functional rsbU Strain Derived from Staphylococcus aureus 8325-4

Horsburgh, M. J., Aish, J., White, I. J., Shaw, L., Lithgow, J. K., & Foster, S. J. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.19.5457-5467.2002 · Cited by 699 · see citing works

Staphylococcal Coagulase: Mode of Action and Antigenicity

Duthie, E. S., & Lorenz, L. (1952) · Microbiology · doi:10.1099/00221287-6-1-2-95 · Cited by 623 · see citing works

Role of teichoic acids in Staphylococcus aureus nasal colonization, a major risk factor in nosocomial infections

Weidenmaier, C., Kokai‐Kun, J. F., Kristian, S. A., Chanturiya, T., Kalbacher, H., Gross, M., NICHOLSON, G. J., Neumeister, B., Mond, J. J., & Peschel, A. (2004) · Nature Medicine · doi:10.1038/nm991 · Cited by 553 · see citing works

Staphylococcus aureusNasal Carriage and Infection in Patients on Hemodialysis

Yu, V. L., Goetz, A., Wagener, M. M., Smith, P. B., Rihs, J. D., Hanchett, J. E., & Zuravleff, J. J. (1986) · New England Journal of Medicine · doi:10.1056/nejm198607103150204 · Cited by 472 · see citing works

Clumping factor B (ClfB), a new surface‐located fibrinogen‐binding adhesin of Staphylococcus aureus

Eidhin, D. N., Perkins, S., François, P., Vaudaux, P. E., Höök, M., & Foster, T. J. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.01050.x · Cited by 418 · see citing works

Reduction of Oropharyngeal Carriage of Haemophilus influenzae Type b (Rib) in Children Immunized with an Rib Conjugate Vaccine

Takala, A. K., Eskola, J., Leinonen, M., Käyhty, H. M., Nissinen, A. E. T., Pekkanen, E., & Mäkelä, P. H. (1991) · The Journal of Infectious Diseases · doi:10.1093/infdis/164.5.982 · Cited by 375 · see citing works

Staphylococcus aureus Nasal Carriage and Infection in Patients on Continuous Ambulatory Peritoneal Dialysis

Luzar, M. A., Coles, G. A., Faller, B., Slingeneyer, A., Dah, G. D., Briat, C., Wone, C., Knefati, Y., Kessler, M., & Peluso, F. (1990) · New England Journal of Medicine · doi:10.1056/nejm199002223220804 · Cited by 353 · see citing works

Use of a Whole Genome Approach To Identify Vaccine Molecules Affording Protection against Streptococcus pneumoniae Infection

Wizemann, T. M., Heinrichs, J. H., Adamou, J. E., Erwin, A. L., KUNSCH, C. A., Choi, G. H., Barash, S. C., Rosen, C. A., Masure, H. R., TUOMANEN, E. I., et al. (2001) · Infection and Immunity · doi:10.1128/iai.69.3.1593-1598.2001 · Cited by 351 · see citing works

Nosocomial and Community-Acquired Staphylococcus aureus Bacteremias from 1980 to 1993: Impact of Intravascular Devices and Methicillin Resistance

Steinberg, J. P., Clark, C. C., & Hackman, B. (1996) · Clinical Infectious Diseases · doi:10.1093/clinids/23.2.255 · Cited by 313 · see citing works

Immunoglobulin transport across polarized epithelial cells

Rojas, R. E., & Apodaca, G. L. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm972 · Cited by 309 · see citing works

The pathogenesis of respiratory syncytial virus infection in cotton rats.

Prince, G. A., Jenson, A. B., Horswood, R. L., Camargo, E., & Chanock, R. M. (1978) · PubMed Central · Cited by 296 · see citing works

The Immune Response to Pneumococcal Proteins during Experimental Human Carriage

McCool, T. L., Cate, T. R., Moy, G., & Weiser, J. N. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20011576 · Cited by 270 · see citing works

Staphylococcus aureus clumping factor B (ClfB) promotes adherence to human type I cytokeratin 10: implications for nasal colonization

O'Brien, L. M., Walsh, E. J., Massey, R. C., Peacock, S. J., & Foster, T. J. (2002) · Cellular Microbiology · doi:10.1046/j.1462-5822.2002.00231.x · Cited by 229 · see citing works

Determinants of Staphylococcus aureus Nasal Carriage

Cole, A. M., Tahk, S., Oren, A., Yoshioka, D., Kim, Y., Park, A., & Ganz, T. (2001) · Clinical and Diagnostic Laboratory Immunology · doi:10.1128/cdli.8.6.1064-1069.2001 · Cited by 225 · see citing works

Lack of Wall Teichoic Acids in Staphylococcus aureus Leads to Reduced Interactions with Endothelial Cells and to Attenuated Virulence in a Rabbit Model of Endocarditis

Weidenmaier, C., Peschel, A., Xiong, Y.-Q., Kristian, S. A., Dietz, K., Yeaman, M. R., & Bayer, A. S. (2005) · The Journal of Infectious Diseases · doi:10.1086/429692 · Cited by 225 · see citing works

The Relation between the Nasal-Staphylococcal-Carrier State and the Incidence of Postoperative Complications

Weinstein, H. J. (1959) · New England Journal of Medicine · doi:10.1056/nejm195906252602601 · Cited by 220 · see citing works

Identification of <i>in vivo</i> expressed vaccine candidate antigens from <i>Staphylococcus aureus</i>

Etz, H., Minh, D. B., Henics, T., Dryla, A., Winkler, B., Triska, C., Boyd, A. P., Söllner, J., Schmidt, W., von Ahsen, U., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092569199 · Cited by 218 · see citing works

The Staphylococcus aureus surface protein SasG and its homologues promote bacterial adherence to human desquamated nasal epithelial cells

Roche, F. M., Meehan, M., & Foster, T. J. (2003) · Microbiology · doi:10.1099/mic.0.26412-0 · Cited by 218 · see citing works

Characterization of novel LPXTG-containing proteins of Staphylococcus aureus identified from genome sequences

Roche, F. M., Massey, R. C., Peacock, S. J., Day, N., Visai, L., Speziale, P., Lam, A., Pallen, M. J., & Foster, T. J. (2003) · Microbiology · doi:10.1099/mic.0.25996-0 · Cited by 212 · see citing works

Comparison of Antibody Repertoires against Staphylococcus aureus in Healthy Individuals and in Acutely Infected Patients

Dryla, A., Prustomersky, S., Gelbmann, D., Hanner, M., Bettinger, E., Kocsis, B., Kustos, T., Henics, T., Meinke, A. L., & Nagy, E. (2005) · Clinical and Vaccine Immunology · doi:10.1128/cdli.12.3.387-398.2005 · Cited by 183 · see citing works

Lysostaphin Cream Eradicates Staphylococcus aureus Nasal Colonization in a Cotton Rat Model

Kokai‐Kun, J. F., Walsh, S. M., Chanturiya, T., & Mond, J. J. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.5.1589-1597.2003 · Cited by 161 · see citing works

Bactericidal Function of Neutrophils from Patients with Acute Bacterial Infections and from Diabetics

Repine, J. E., Clawson, C. C., & Goetz, F. C. (1980) · The Journal of Infectious Diseases · doi:10.1093/infdis/142.6.869 · Cited by 160 · see citing works

Identification of a novel iron regulated staphylococcal surface protein with haptoglobin‐haemoglobin binding activity

Dryla, A., Gelbmann, D., Von Gabain, A., & Nagy, E. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03542.x · Cited by 153 · see citing works

IsdA of <i>Staphylococcus aureus</i> is a broad spectrum, iron‐regulated adhesin

Clarke, S. R., Wiltshire, M. D., & Foster, S. J. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2003.03938.x · Cited by 150 · see citing works

An overview of nosocomial infections, including the role of the microbiology laboratory.

Emori, T. G., & Gaynes, R. P. (1993) · Clinical Microbiology Reviews · doi:10.1128/cmr.6.4.428-442.1993 · Cited by 135 · see citing works

Analysis of Ebh, a 1.1-Megadalton Cell Wall-Associated Fibronectin-Binding Protein of Staphylococcus aureus

Clarke, S. R., Harris, L. G., Richards, R. G., & Foster, S. J. (2002) · Infection and Immunity · doi:10.1128/iai.70.12.6680-6687.2002 · Cited by 133 · see citing works

Clumping Factor B, a Fibrinogen-binding MSCRAMM (Microbial Surface Components Recognizing Adhesive Matrix Molecules) Adhesin of Staphylococcus aureus, Also Binds to the Tail Region of Type I Cytokeratin 10

Walsh, E. J., O'Brien, L. M., Liang, X., Höök, M., & Foster, T. J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m408713200 · Cited by 116 · see citing works

Diversifying animal models: the use of hispid cotton rats ( Sigmodon hispidus ) in infectious diseases

Niewiesk, S., & Prince, G. A. (2002) · Laboratory Animals · doi:10.1258/002367702320389026 · Cited by 115 · see citing works

Bacterial adherence to nasal mucosal cells

Aly, R., Shinefield, H., Strauss, W. G., & Maïbach, H. I. (1977) · Infection and Immunity · doi:10.1128/iai.17.3.546-549.1977 · Cited by 113 · see citing works

Nasal Carriage as a Source of Staphylococcus aureus Bacteremia

Pugliese, G., & Favero, M. S. (2001) · Infection Control and Hospital Epidemiology · doi:10.1017/s0195941700069356 · Cited by 90 · see citing works

Importance of the Keratinized Epithelial Cell in Bacterial Adherence

Bibel, D. J., Aly, R., Shinefield, H. R., Maïbach, H. I., & Strauss, W. G. (1982) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12500072 · Cited by 89 · see citing works

Anti-capsular polysaccharide antibody concentrations in saliva after immunization with Haemophilus influenzas type b conjugate vaccines

KAUPPI, M., Eskola, J., & Käyhty, H. M. (1995) · The Pediatric Infectious Disease Journal · doi:10.1097/00006454-199504000-00008 · Cited by 88 · see citing works

Extracellular-matrix-binding proteins as targets for the prevention of Staphylococcus aureus infections

Flock, J. (1999) · Molecular Medicine Today · doi:10.1016/s1357-4310(99)01597-x · Cited by 87 · see citing works

Determinants of Staphylococcus aureus nasal carriage

Nouwen, J. L. (2001) · The Netherlands Journal of Medicine · doi:10.1016/s0300-2977(01)00150-4 · Cited by 76 · see citing works

Pulmonary Innate Immune Proteins and Receptors that Interact with Gram-positive Bacterial Ligands

Palaniyar, N. (2002) · Immunobiology · doi:10.1078/0171-2985-00156 · Cited by 63 · see citing works

Anti-Capsular Polysaccharide Antibodies Reduce Nasopharyngeal Colonization byHaemophilus influenzaeType b in Infant Rats

Kauppi, M., Saarinen, L., & Käyhty, H. M. (1993) · The Journal of Infectious Diseases · doi:10.1093/infdis/167.2.365 · Cited by 62 · see citing works

Conservation, Surface Exposure, and In Vivo Expression of the Frp Family of Iron-Regulated Cell Wall Proteins in Staphylococcus aureus

Morrissey, J. A., Cockayne, A., Hammacott, J. E., Bishop, K., Denman-Johnson, A., Hill, P. J., & Williams, P. M. (2002) · Infection and Immunity · doi:10.1128/iai.70.5.2399-2407.2002 · Cited by 49 · see citing works

Mechanism of Antibody-Mediated Reduction of Nasopharyngeal Colonization by Haemophilus influenzae Type b Studied in an Infant Rat Model

Kauppi-Korkeila, M., van Alphen, L., Madore, D. V., Saarinen, L., & Käyhty, H. M. (1996) · The Journal of Infectious Diseases · doi:10.1093/infdis/174.6.1337 · Cited by 40 · see citing works

Whole genome sequencing of methicillin resistant Staphylococcus aureus

Cookson, B. D. (2001) · Weekly releases (1997–2007) · doi:10.2807/esw.05.17.01764-en · Cited by 35 · see citing works

Evoluzione della Chemioresistenza nei Batteri Patogeni Gram-Positivi

Marchese, A. E., Schito, G. C., & Debbia, E. A. (2000) · Journal of Chemotherapy · doi:10.1080/1120009x.2000.11782295 · Cited by 12 · see citing works

Identification of the secreted macromolecular immunogens of Staphylococcus aureus by analysis of serum

Royan, S., Sharp, L., Nair, S. P., Crean, S., Henderson, B. E., Poole, S., Scott, G., & Evans, A. W. (2000) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2000.tb01539.x · Cited by 11 · see citing works

Molecular analysis of Staphylococcus aureus adhesins.

Lg, H. (2002) · Europe PMC (PubMed Central) · Cited by 1 · see citing works

Adhesion, invasion and evasion: the many functions of the surface proteins of Staphylococcus aureus

Foster, T. J., Geoghegan, J. A., Ganesh, V. K., & Höök, M. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro3161 · Cited by 1,534 · see citing works

Atopic dermatitis: a disease of altered skin barrier and immune dysregulation

Boguniewicz, M., & Leung, D. Y. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01027.x · Cited by 1,081 · see citing works

Staphylococcus aureus Nasal Colonization: An Update on Mechanisms, Epidemiology, Risk Factors, and Subsequent Infections

Sakr, A., Brégeon, F., Mège, J., Rolain, J., & Blin, O. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02419 · Cited by 566 · see citing works

Staphylococcus aureus and Atopic Dermatitis: A Complex and Evolving Relationship

Geoghegan, J. A., Irvine, A. D., & Foster, T. J. (2017) · Trends in Microbiology · doi:10.1016/j.tim.2017.11.008 · Cited by 517 · see citing works

Scenery of Staphylococcus Implant Infections in Orthopedics

Montanaro, L., Speziale, P., Campoccia, D., Ravaioli, S., Cangini, I., Pietrocola, G., Giannini, S., & Arciola, C. R. (2011) · Future Microbiology · doi:10.2217/fmb.11.117 · Cited by 368 · see citing works

Catalase (KatA) and Alkyl Hydroperoxide Reductase (AhpC) Have Compensatory Roles in Peroxide Stress Resistance and Are Required for Survival, Persistence, and Nasal Colonization in <i>Staphylococcus aureus</i>

Cosgrove, K., Coutts, G., Jonsson, I.-M., Tarkowski, A., Kokai-Kun, J. F., Mond, J. J., & Foster, S. J. (2007) · Journal of Bacteriology · doi:10.1128/jb.01524-06 · Cited by 334 · see citing works

The role of Staphylococcus aureus surface protein SasG in adherence and biofilm formation

Corrigan, R. M., Rigby, D., Handley, P. S., & Foster, T. J. (2007) · Microbiology · doi:10.1099/mic.0.2007/006676-0 · Cited by 335 · see citing works

Recent insights into atopic dermatitis and implications for management of infectious complications

Boguniewicz, M., & Leung, D. Y. M. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2009.11.027 · Cited by 328 · see citing works

<i>Staphylococcus aureus</i> IsdB Is a Hemoglobin Receptor Required for Heme Iron Utilization

Torres, V. J., Pishchany, G., Humayun, M., Schneewind, O., & Skaar, E. P. (2006) · Journal of Bacteriology · doi:10.1128/jb.01335-06 · Cited by 302 · see citing works

Recent developments in understanding the iron acquisition strategies of gram positive pathogens

Sheldon, J. R., & Heinrichs, D. E. (2015) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuv009 · Cited by 272 · see citing works

Staphylococcus aureus Colonization: Modulation of Host Immune Response and Impact on Human Vaccine Design

Brown, A. F., Leech, J. M., Rogers, T. R., & McLoughlin, R. M. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00507 · Cited by 247 · see citing works

Cell wall peptidoglycan architecture in Bacillus subtilis

Hayhurst, E. J., Kailas, L., Hobbs, J. K., & Foster, S. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804138105 · Cited by 244 · see citing works

Effect of filaggrin breakdown products on growth of and protein expression by Staphylococcus aureus

Miajlović, H., Fallon, P. G., Irvine, A. D., & Foster, T. J. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.09.015 · Cited by 242 · see citing works

Iron acquisition strategies of bacterial pathogens

Sheldon, J. R., Laakso, H. A., & Heinrichs, D. E. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0010-2015 · Cited by 219 · see citing works

The Staphylococcus aureus surface protein IsdA mediates resistance to innate defenses of human skin

Clarke, S. R., Mohamed, R., Bian, L., Routh, A. F., Kokai-Kun, J. F., Mond, J. J., Tarkowski, A., & Foster, S. J. (2007) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2007.04.005 · Cited by 225 · see citing works

Surface proteins that promote adherence of Staphylococcus aureusto human desquamated nasal epithelial cells

Corrigan, R. M., Miajlovic, H., & Foster, T. J. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-22 · Cited by 226 · see citing works

Antimicrobial Agents in Orthopaedic Surgery

Trampuž, A., & Zimmerli, W. (2006) · Drugs · doi:10.2165/00003495-200666080-00005 · Cited by 225 · see citing works

Identification of Staphylococcus aureus Proteins Recognized by the Antibody-Mediated Immune Response to a Biofilm Infection

Brady, R. A., Leid, J. G., Camper, A. K., Costerton, J. W., & Shirtliff, M. E. (2006) · Infection and Immunity · doi:10.1128/iai.00392-06 · Cited by 219 · see citing works

Differential Expression and Roles of Staphylococcus aureus Virulence Determinants during Colonization and Disease

Jenkins, A. L., Diep, B. A., Mai, T. T., Vo, N. H., Warrener, P., Suzich, J., Stover, C. K., & Sellman, B. R. (2015) · mBio · doi:10.1128/mbio.02272-14 · Cited by 202 · see citing works

Staphylococcus aureus colonisation and strategies for decolonisation

Piewngam, P., & Otto, M. J. (2024) · The Lancet Microbe · doi:10.1016/s2666-5247(24)00040-5 · Cited by 189 · see citing works

Anti-Staphylococcal Humoral Immune Response in Persistent Nasal Carriers and Noncarriers ofStaphylococcus aureus

Verkaik, N. J., de Vogel, C. P., Boelens, H. A. M., Grumann, D., Hoogenboezem, T., Vink, C., Hooijkaas, H., Foster, T. J., Verbrugh, H. A., van Belkum, A., et al. (2009) · The Journal of Infectious Diseases · doi:10.1086/596743 · Cited by 178 · see citing works

Global analysis of community-associated methicillin-resistant Staphylococcus aureus exoproteins reveals molecules produced in vitro and during infection

Burlak, C., Hammer, C. H., Robinson, M.-A., Whitney, A. R., Mcgavin, M. J., Kreiswirth, B. N., & DeLeo, F. R. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00858.x · Cited by 177 · see citing works

Haem recognition by a <i>Staphylococcus aureus</i> NEAT domain

Grigg, J. C., Vermeiren, C. L., Heinrichs, D. E., & Murphy, M. E. P. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05502.x · Cited by 166 · see citing works

Inferring Reasons for the Failure of Staphylococcus aureus Vaccines in Clinical Trials

Bagnoli, F., Bertholet, S., & Grandi, G. (2012) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00016 · Cited by 172 · see citing works

Nasal Colonisation by Staphylococcus aureus Depends upon Clumping Factor B Binding to the Squamous Epithelial Cell Envelope Protein Loricrin

Mulcahy, M. E., Geoghegan, J. A., Monk, I. R., O’Keeffe, K. M., Walsh, E. J., Foster, T. J., & McLoughlin, R. M. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1003092 · Cited by 170 · see citing works

Structural biology of heme binding in the Staphylococcus aureus Isd system

Grigg, J. C., Ukpabi, G., Gaudin, C. F. M., & Murphy, M. E. P. (2010) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2009.09.012 · Cited by 169 · see citing works

Staphylococcus aureus Toxins and Diabetic Foot Ulcers: Role in Pathogenesis and Interest in Diagnosis

Dunyach‐Remy, C., Essebe, C. N., Sotto, A., & Lavigne, J. (2016) · Toxins · doi:10.3390/toxins8070209 · Cited by 173 · see citing works

A review on nanosystems as an effective approach against infections of Staphylococcus aureus

Zhou, K., Li, C., Chen, D., Pan, Y., Tao, Y., Qu, W., Liu, Z., Wang, X., & Xie, S. (2018) · International Journal of Nanomedicine · doi:10.2147/ijn.s169935 · Cited by 164 · see citing works

Characterization of IsaA and SceD, Two Putative Lytic Transglycosylases of Staphylococcus aureus

Stapleton, M. R., Horsburgh, M. J., Hayhurst, E. J., Wright, L., Jonsson, I., Tarkowski, A., Kokai‐Kun, J. F., Mond, J. J., & Foster, S. J. (2007) · Journal of Bacteriology · doi:10.1128/jb.00734-07 · Cited by 164 · see citing works

Proteomics uncovers extreme heterogeneity in the Staphylococcus aureus exoproteome due to genomic plasticity and variant gene regulation

Ziebandt, A., Kusch, H., Degner, M., Jaglitz, S., Sibbald, M. J. J. B., Arends, J. P., Chlebowicz, M. A., Albrecht, D., Pantůček, R., Doškař, J., et al. (2010) · PROTEOMICS · doi:10.1002/pmic.200900313 · Cited by 158 · see citing works

Metal ion acquisition in Staphylococcus aureus: overcoming nutritional immunity

Cassat, J. E., & Skaar, E. P. (2012) · Seminars in Immunopathology · doi:10.1007/s00281-011-0294-4 · Cited by 155 · see citing works

Staphylococcus aureus determinants for nasal colonization

Weidenmaier, C., Goerke, C., & Wolz, C. (2012) · Trends in Microbiology · doi:10.1016/j.tim.2012.03.004 · Cited by 153 · see citing works

Surface Proteins ofStaphylococcus aureus

Foster, T. J. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.gpp3-0046-2018 · Cited by 160 · see citing works

Host–pathogen interactions between the skin and Staphylococcus aureus

Krishna, S. M., & Miller, L. S. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.11.003 · Cited by 148 · see citing works

The Role of Staphylococcus aureus Virulence Factors in Skin Infection and Their Potential as Vaccine Antigens

Lacey, K. A., Geoghegan, J. A., & McLoughlin, R. M. (2016) · Pathogens · doi:10.3390/pathogens5010022 · Cited by 149 · see citing works

Colonization and infection of the human host by staphylococci: adhesion, survival and immune evasion

Foster, T. J. (2009) · Veterinary Dermatology · doi:10.1111/j.1365-3164.2009.00825.x · Cited by 144 · see citing works

Molecular Characterization of a Novel Staphylococcus Aureus Surface Protein (SasC) Involved in Cell Aggregation and Biofilm Accumulation

Schroeder, K., Jularic, M., Horsburgh, S. M., Nina, H., Neumann, C., Bertling, A., Schulte, A., Foster, S. J., Kehrel, B. E., Peters, G., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007567 · Cited by 143 · see citing works

Temporal Expression of Adhesion Factors and Activity of Global Regulators during Establishment ofStaphylococcus aureusNasal Colonization

Burian, M., Rautenberg, M., Kohler, T. P., Fritz, M., Krismer, B., Unger, C., Hoffmann, W. H., Peschel, A., Wolz, C., & Goerke, C. (2010) · The Journal of Infectious Diseases · doi:10.1086/651619 · Cited by 140 · see citing works

Colonization and Infection of the Skin by S. aureus: Immune System Evasion and the Response to Cationic Antimicrobial Peptides

Ryu, S., Song, P. I., Seo, C., Cheong, H., & Park, Y. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15058753 · Cited by 138 · see citing works

Efficacy of Staphylococcus aureus vaccines for bovine mastitis: A systematic review

Pereira, U. D. P., de Oliveira, D. G. S., Mesquita, L. D. R., da Costa, G. M., & Pereira, L. J. (2010) · Veterinary Microbiology · doi:10.1016/j.vetmic.2010.10.003 · Cited by 130 · see citing works

Active Immunization with Extracellular Vesicles Derived from Staphylococcus aureus Effectively Protects against Staphylococcal Lung Infections, Mainly via Th1 Cell-Mediated Immunity

Choi, S. J., Kim, M.-H., Jeon, J., Kim, O. Y., Choi, Y., Seo, J., Hong, S., Lee, W. H., Jeon, S. G., Gho, Y. S., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136021 · Cited by 129 · see citing works

Vaccination and passive immunisation against Staphylococcus aureus

Schaffer, A. C., & Lee, J. C. (2008) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2008.06.009 · Cited by 127 · see citing works

Structural and functional role of Staphylococcus aureus surface components recognizing adhesive matrix molecules of the host

Speziale, P., Pietrocola, G., Rindi, S., Provenzano, M., Provenza, G., Poto, A. D., Visai, L., & Arciola, C. R. (2009) · Future Microbiology · doi:10.2217/fmb.09.102 · Cited by 127 · see citing works

Crystal Structure of the Heme-IsdC Complex, the Central Conduit of the Isd Iron/Heme Uptake System in Staphylococcus aureus

Sharp, K. H., Schneider, S., Cockayne, A., & Paoli, M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700234200 · Cited by 120 · see citing works

A Nasal Epithelial Receptor for Staphylococcus aureus WTA Governs Adhesion to Epithelial Cells and Modulates Nasal Colonization

Baur, S., Rautenberg, M., Faulstich, M., Grau, T., Severin, Y., Unger, C., Hoffmann, W. H., Rudel, T., Autenrieth, I. B., & Weidenmaier, C. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004089 · Cited by 117 · see citing works

Towards the immune proteome of Staphylococcus aureus – The anti-S. aureus antibody response

Holtfreter, S., Kolata, J., & Bröker, B. M. (2009) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2009.10.002 · Cited by 115 · see citing works

Host–Bacterial Crosstalk Determines Staphylococcus aureus Nasal Colonization

Mulcahy, M. E., & McLoughlin, R. M. (2016) · Trends in Microbiology · doi:10.1016/j.tim.2016.06.012 · Cited by 113 · see citing works

Is there a future for a Staphylococcus aureus vaccine?

Proctor, R. A. (2011) · Vaccine · doi:10.1016/j.vaccine.2011.11.006 · Cited by 109 · see citing works

Differential roles of sortase-anchored surface proteins and wall teichoic acid in Staphylococcus aureus nasal colonization

Weidenmaier, C., Kokai‐Kun, J. F., Kulauzovic, E., Kohler, T. P., Thumm, G., Stoll, H., Götz, F., & Peschel, A. (2008) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2007.11.006 · Cited by 108 · see citing works

Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization

Winstel, V., Kühner, P., Salomon, F., Larsen, J., Skov, R. L., Hoffmann, W. H., Peschel, A., & Weidenmaier, C. (2015) · mBio · doi:10.1128/mbio.00632-15 · Cited by 105 · see citing works

Iron-Regulated Surface Determinant Protein A Mediates Adhesion of<i>Staphylococcus aureus</i>to Human Corneocyte Envelope Proteins

Clarke, S. R., Andre, G., Walsh, E. J., Dufrêne, Y. F., Foster, T. J., & Foster, S. J. (2009) · Infection and Immunity · doi:10.1128/iai.01304-08 · Cited by 105 · see citing works

Molecular imaging of glycan chains couples cell-wall polysaccharide architecture to bacterial cell morphology

Turner, R. D., Mesnage, S., Hobbs, J. K., & Foster, S. J. (2018) · Nature Communications · doi:10.1038/s41467-018-03551-y · Cited by 101 · see citing works

Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis

Anderson, A. S., Scully, I. L., Timofeyeva, Y., Murphy, E., McNeil, L. K., Mininni, T., Nuñez, L., Carrière, M. B., Singer, C. L., Dilts, D. A., et al. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis272 · Cited by 100 · see citing works

Host- and microbe determinants that may influence the success of S. aureus colonization

Johannessen, M., Sollid, J. E., & Hanssen, A.-M. (2012) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00056 · Cited by 100 · see citing works

Potentials of nanotechnology in treatment of methicillin-resistant Staphylococcus aureus

Gao, Y., Chen, Y., Cao, Y., Mo, A., & Peng, Q. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.113056 · Cited by 99 · see citing works

Staphylococcal Vaccines and Immunotherapies

Schaffer, A. C., & Lee, J. C. (2009) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2008.10.005 · Cited by 97 · see citing works

The interaction between Staphylococcus aureus SdrD and desmoglein 1 is important for adhesion to host cells

Askarian, F., Ajayi, C., Hanssen, A.-M., van Sorge, N. M., Pettersen, I., Diep, D. B., Ericson, J. U., & Johannessen, M. (2016) · Scientific Reports · doi:10.1038/srep22134 · Cited by 97 · see citing works

Bacterial Cell Enlargement Requires Control of Cell Wall Stiffness Mediated by Peptidoglycan Hydrolases

Wheeler, R., Turner, R. D., Bailey, R. G., Salamaga, B., Mesnage, S., Mohamad, S. A. S., Hayhurst, E. J., Horsburgh, M. J., Hobbs, J. K., & Foster, S. J. (2015) · mBio · doi:10.1128/mbio.00660-15 · Cited by 96 · see citing works

Structural and Biochemical Characterization of Staphylococcus aureus Clumping Factor B/Ligand Interactions

Ganesh, V. K., Barbu, E. M., Deivanayagam, C. C. S., Le, B. V., Anderson, A. S., Matsuka, Y. V., Lin, S. L., Foster, T. J., Narayana, S. V. L., & Höök, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.217414 · Cited by 91 · see citing works

Staphylococcus aureusantigens and challenges in vaccine development

Middleton, J. R. (2008) · Expert Review of Vaccines · doi:10.1586/14760584.7.6.805 · Cited by 90 · see citing works

Biofilm Matrix Exoproteins Induce a Protective Immune Response against Staphylococcus aureus Biofilm Infection

Gil, C., Solano, C., Burgui, S., Latasa, C., García, B., Toledo‐Arana, A., Lasa, Í., & Valle, J. (2013) · Infection and Immunity · doi:10.1128/iai.01419-13 · Cited by 88 · see citing works

Hemoglobin Promotes Staphylococcus aureus Nasal Colonization

Pynnonen, M. A., Stephenson, R. E., Schwartz, K., Hernandez, M., & Boles, B. R. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002104 · Cited by 84 · see citing works

Heterogeneity of the humoral immune response following Staphylococcus aureus bacteremia

Verkaik, N. J., Boelens, H. A. M., de Vogel, C. P., Tavakol, M., Bode, L. G. M., Verbrugh, H. A., van Belkum, A., & van Wamel, W. J. B. (2010) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-010-0888-0 · Cited by 83 · see citing works

Staphylococcus aureus-Associated Skin and Soft Tissue Infections: Anatomical Localization, Epidemiology, Therapy and Potential Prophylaxis

Olaniyi, R., Pozzi, C., Grimaldi, L., & Bagnoli, F. (2016) · Current topics in microbiology and immunology · doi:10.1007/82_2016_32 · Cited by 82 · see citing works

Novel targeted immunotherapy approaches for staphylococcal infection

Otto, M. J. (2010) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2010.495115 · Cited by 84 · see citing works

Proteomics-Based Identification of Anchorless Cell Wall Proteins as Vaccine Candidates againstStaphylococcus aureus

Glowalla, E., Tosetti, B., Krönke, M., & Krut, O. (2009) · Infection and Immunity · doi:10.1128/iai.00617-08 · Cited by 81 · see citing works

Staphylococcus aureus keratinocyte invasion is dependent upon multiple high-affinity fibronectin-binding repeats within FnBPA

Edwards, A. M., Potter, U., Meenan, N. A. G., Potts, J. R., & Massey, R. C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018899 · Cited by 80 · see citing works

Induction of antibodies by Staphylococcus aureus nasal colonization in young children

Verkaik, N. J., Lebon, A., de Vogel, C. P., Hooijkaas, H., Verbrugh, H. A., Jaddoe, V. W. V., Albert Hofman, D., Moll, H. A., van Belkum, A., & van Wamel, W. J. B. (2009) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2009.03073.x · Cited by 76 · see citing works

IsdA Protects<i>Staphylococcus aureus</i>against the Bactericidal Protease Activity of Apolactoferrin

Clarke, S. R., & Foster, S. J. (2008) · Infection and Immunity · doi:10.1128/iai.01530-07 · Cited by 75 · see citing works

Sortases, Surface Proteins, and Their Roles in Staphylococcus aureus Disease and Vaccine Development

Schneewind, O., & Missiakas, D. M. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.psib-0004-2018 · Cited by 75 · see citing works

Characterization of the Heme Binding Properties of Staphylococcus aureus IsdA

Vermeiren, C. L., Pluym, M., Mack, J. P., Heinrichs, D. E., & Stillman, M. J. (2006) · Biochemistry · doi:10.1021/bi0607711 · Cited by 74 · see citing works

Distinctive patterns in the human antibody response to Staphylococcus aureus bacteremia in carriers and non‐carriers

Kolata, J., Bode, L. G. M., Holtfreter, S., Steil, L., Kusch, H., Holtfreter, B., Albrecht, D., Hecker, M., Engelmann, S., van Belkum, A., et al. (2011) · PROTEOMICS · doi:10.1002/pmic.201000760 · Cited by 73 · see citing works

Immune evasion by Staphylococcus aureus conferred by iron-regulated surface determinant protein IsdH

Visai, L., Yanagisawa, N., Josefsson, E., Tarkowski, A., Pezzali, I., Rooijakkers, S. H. M., Foster, T. J., & Speziale, P. (2009) · Microbiology · doi:10.1099/mic.0.025684-0 · Cited by 73 · see citing works

Immune control of Staphylococcus aureus – Regulation and counter-regulation of the adaptive immune response

Bröker, B. M., Holtfreter, S., & Bekeredjian‐Ding, I. (2013) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2013.11.008 · Cited by 72 · see citing works

Haemophore functions revisited

Wandersman, C., & Delepelaire, P. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08136.x · Cited by 70 · see citing works

Levels of Antibody against 11 Staphylococcus aureus Antigens in a Healthy Population

Colque‐Navarro, P., Jacobsson, G., Andersson, R., Flock, J., & Möllby, R. (2010) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00506-09 · Cited by 70 · see citing works

Cell Wall-Anchored Surface Proteins of Staphylococcus aureus: Many Proteins, Multiple Functions

Geoghegan, J. A., & Foster, T. J. (2015) · Current topics in microbiology and immunology · doi:10.1007/82_2015_5002 · Cited by 69 · see citing works

Generation of a Novel Staphylococcus aureus Ghost Vaccine and Examination of Its Immunogenicity against Virulent Challenge in Rats

Vinod, N., Oh, S. J., Park, H. J., Koo, J. M., Choi, C. W., & Kim, S. C. (2015) · Infection and Immunity · doi:10.1128/iai.00009-15 · Cited by 66 · see citing works

Human Defensins: A Novel Approach in the Fight against Skin Colonizing Staphylococcus aureus

Scudiero, O., Brancaccio, M., Mennitti, C., Laneri, S., Lombardo, B., Biasi, M.-G. D., Gregorio, E. D., Pagliuca, C., Colicchio, R., Salvatore, P., et al. (2020) · Antibiotics · doi:10.3390/antibiotics9040198 · Cited by 66 · see citing works

Immunotherapeutic strategies to combat staphylococcal infections

Ohlsen, K., & Lorenz, U. (2010) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2010.04.015 · Cited by 61 · see citing works

A Diagnostic Serum Antibody Test for Patients With Staphylococcus aureus Osteomyelitis

Nishitani, K., Beck, C. A., Rosenberg, A. F., Kates, S. L., Schwarz, E. M., & Daiss, J. L. (2015) · Clinical Orthopaedics and Related Research · doi:10.1007/s11999-015-4354-2 · Cited by 60 · see citing works

Identification of Key Determinants of Staphylococcus aureus Vaginal Colonization

Deng, L., Schilcher, K., Burcham, L. R., Kwiecinski, J. M., Johsnon, P. M., Head, S. R., Heinrichs, D. E., Horswill, A. R., & Doran, K. S. (2019) · mBio · doi:10.1128/mbio.02321-19 · Cited by 60 · see citing works

Iron-Regulated Surface Determinant (Isd) Proteins of Staphylococcus lugdunensis

Zapotoczna, M., Heilbronner, S., Speziale, P., & Foster, T. J. (2012) · Journal of Bacteriology · doi:10.1128/jb.01195-12 · Cited by 56 · see citing works

A randomized phase I study of the safety and immunogenicity of three ascending dose levels of a 3-antigen Staphylococcus aureus vaccine (SA3Ag) in healthy adults

Nissen, M. D., Marshall, H. S., Richmond, P., Shakib, S., Jiang, Q. L., Cooper, D., Rill, D., Baber, J., Eiden, J. J., Gruber, W. C., et al. (2015) · Vaccine · doi:10.1016/j.vaccine.2015.02.024 · Cited by 59 · see citing works

A human monoclonal antibody targeting the conserved staphylococcal antigen IsaA protects mice against Staphylococcus aureus bacteremia

van den Berg, S., Bonarius, H. P. J., van Kessel, K. P. M., Elsinga, G. S., Kooi, N. M., Westra, H., Bosma, T., van der Kooi‐Pol, M. M., Koedijk, D. G. A. M., Groen, H., et al. (2014) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2014.11.002 · Cited by 59 · see citing works

Localization of Staphylococcus aureus in tissue from the nasal vestibule in healthy carriers

Hanssen, A.-M., Kindlund, B., Stenklev, N. C., Furberg, A., Fismen, S., Olsen, R. S., Johannessen, M., & Ericson, J. U. (2017) · BMC Microbiology · doi:10.1186/s12866-017-0997-3 · Cited by 59 · see citing works

Structural Basis for Hemoglobin Capture by Staphylococcus aureus Cell-surface Protein, IsdH

Kumar, K. K., Jacques, D. A., Pishchany, G., Caradoc-Davies, T. T., Spirig, T., Malmirchegini, G. R., Langley, D. B., Dickson, C. F., Mackay, J. P., Clubb, R., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.287300 · Cited by 58 · see citing works

Iron-Coordinating Tyrosine Is a Key Determinant of NEAT Domain Heme Transfer

Grigg, J. C., Mao, C. X., & Murphy, M. E. P. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.08.047 · Cited by 58 · see citing works

Functional Antibodies Targeting IsaA of Staphylococcus aureus Augment Host Immune Response and Open New Perspectives for Antibacterial Therapy

Lorenz, U., Lorenz, B., Schmitter, T., Streker, K., Erck, C., Wehland, J., Nickel, J., Zimmermann, B., & Ohlsen, K. (2010) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01144-10 · Cited by 57 · see citing works

Targeted Immunotherapy for Staphylococcal Infections

Otto, M. J. (2008) · BioDrugs · doi:10.2165/00063030-200822010-00003 · Cited by 54 · see citing works

Staphylococcal Protein A Contributes to Persistent Colonization of Mice with Staphylococcus aureus

Sun, Y., Emolo, C., Holtfreter, S., Wiles, S., Kreiswirth, B. N., Missiakas, D. M., & Schneewind, O. (2018) · Journal of Bacteriology · doi:10.1128/jb.00735-17 · Cited by 55 · see citing works

Does Staphylococcus Aureus Nasal Colonization Involve Biofilm Formation?

Krismer, B., & Peschel, A. (2011) · Future Microbiology · doi:10.2217/fmb.11.37 · Cited by 54 · see citing works

Strategies for and advances in the development ofStaphylococcus aureusprophylactic vaccines

Broughan, J. H., Anderson, R., & Anderson, A. S. (2011) · Expert Review of Vaccines · doi:10.1586/erv.11.54 · Cited by 52 · see citing works

Comparison of carboxylated and Penta-His microspheres for semi-quantitative measurement of antibody responses to His-tagged proteins

Verkaik, N. J., Brouwer, E., Hooijkaas, H., van Belkum, A., & van Wamel, W. J. B. (2008) · Journal of Immunological Methods · doi:10.1016/j.jim.2008.02.022 · Cited by 52 · see citing works

Protection from the acquisition of Staphylococcus aureus nasal carriage by cross-reactive antibody to a pneumococcal dehydrogenase

Lijek, R. S., Luque, S. L., Liu, Q., Parker, D., Bae, T., & Weiser, J. N. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208075109 · Cited by 50 · see citing works

Innate Immune Memory Contributes to Host Defense against Recurrent Skin and Skin Structure Infections Caused by Methicillin-Resistant Staphylococcus aureus

Chan, L. C., Chaili, S., Filler, S. G., Miller, L. S., Solis, N. V., Wang, H., Johnson, C. W., Lee, H. K., Diaz, L. F., & Yeaman, M. R. (2016) · Infection and Immunity · doi:10.1128/iai.00876-16 · Cited by 50 · see citing works

Immunotherapeutic Approaches against Staphylococcus Aureus

Verkaik, N. J., van Wamel, W. J. B., & van Belkum, A. (2011) · Immunotherapy · doi:10.2217/imt.11.84 · Cited by 49 · see citing works

Staphylococcus aureus seroproteomes discriminate ruminant isolates causing mild or severe mastitis

Maréchal, C. L., Jardin, J., Jan, G., Even, S., Pulido, C., Guibert, J.-M., Hernández, D., François, P., Schrenzel, J., Demon, D., et al. (2011) · Veterinary Research · doi:10.1186/1297-9716-42-35 · Cited by 47 · see citing works

Selection and Characterization of Murine Monoclonal Antibodies toStaphylococcus aureusIron-Regulated Surface Determinant B with Functional Activity In Vitro and In Vivo

Brown, M. J., Kowalski, R., Zorman, J. K., Wang, X.-M., Towne, V., Zhao, Q., Secore, S., Finnefrock, A. C., Ebert, T., Pancari, G., et al. (2009) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00085-09 · Cited by 45 · see citing works

The iron-regulated staphylococcal lipoproteins

Sheldon, J. R., & Heinrichs, D. E. (2012) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00041 · Cited by 43 · see citing works

Identification of In Vivo–Expressed Antigens of Staphylococcus aureus and Their Use

Kokai‐Kun, J. F., & Foster, S. J. (2016)

Human Immune Proteome in Experimental Colonization with Staphylococcus aureus

Holtfreter, S., Nguyen, T. T. H., Wertheim, H. F. L., Steil, L., Kusch, H., Truong, Q. P., Engelmann, S., Hecker, M., Völker, U., van Belkum, A., et al. (2009) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00263-09 · Cited by 71 · see citing works

Vaccination as infection control: A pilot study to determine the impact of Staphylococcus aureus vaccination on nasal carriage

Creech, C. B., Johnson, B. G., Alsentzer, A., Hohenboken, M. J., Edwards, K. M., & Talbot, T. R. (2009) · Vaccine · doi:10.1016/j.vaccine.2009.09.088 · Cited by 43 · see citing works

Induction of antibodies by Staphylococcus aureus nasal colonization in young children

Verkaik, N. J., Lebon, A., de Vogel, C. P., Hooijkaas, H., Verbrugh, H. A., Jaddoe, V. W. V., Albert Hofman, D., Moll, H. A., van Belkum, A., & van Wamel, W. J. B. (2009) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2009.03073.x · Cited by 76 · see citing works

Evaluation of Approaches to Monitor Staphylococcus aureus Virulence Factor Expression during Human Disease

Rozemeijer, W., Fink, P. S., Rojas, E. A. P., Jones, C. H., Pavliakova, D., Giardina, P. C., Murphy, E., Liberator, P., Jiang, Q. L., Girgenti, D., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116945 · Cited by 44 · see citing works