A SIMPLE METHOD OF ESTIMATING FIFTY PER CENT ENDPOINTS12

A SARS-CoV-2 protein interaction map reveals targets for drug repurposing

Gordon, D. E., Jang, G. M., Bouhaddou, M., Xu, J., Obernier, K., White, K. M., O’Meara, M. J., Rezelj, V. V., Guo, J. Z., Swaney, D. L., et al. (2020) · Nature · doi:10.1038/s41586-020-2286-9 · Cited by 4,405

An oral SARS-CoV-2 M pro inhibitor clinical candidate for the treatment of COVID-19

Owen, D. R., Allerton, C. M. N., Anderson, A. S., Aschenbrenner, L., Avery, M., Berritt, S., Boras, B., Cardin, R. D., Carlo, A., Coffman, K. J., et al. (2021) · Science · doi:10.1126/science.abl4784 · Cited by 2,033

Zika Virus

Musso, D., & Gubler, D. J. (2016) · Clinical Microbiology Reviews · doi:10.1128/cmr.00072-15 · Cited by 1,469

SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion

Mlcochova, P., Kemp, S. A., Dhar, M. S., Papa, G., Meng, B., Ferreira, I. A. T. M., Datir, R., Collier, D. A., Albecka, A., Singh, S., et al. (2021) · Nature · doi:10.1038/s41586-021-03944-y · Cited by 1,337

Replication of human noroviruses in stem cell–derived human enteroids

Ettayebi, K., Crawford, S. E., Murakami, K., Broughman, J. R., Karandikar, U., Tenge, V. R., Neill, F. H., Blutt, S. E., Zeng, X.-L., Qu, L., et al. (2016) · Science · doi:10.1126/science.aaf5211 · Cited by 1,305

N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2

McCallum, M., De Marco, A., Lempp, F. A., Tortorici, M. A., Pinto, D., Walls, A. C., Beltramello, M., Chen, A., Liu, Z., Zatta, F., et al. (2021) · Cell · doi:10.1016/j.cell.2021.03.028 · Cited by 901

Dissolving polymer microneedle patches for influenza vaccination

Sullivan, S. P., Koutsonanos, D. G., del Pilar Martin, M., Lee, J. W., Zarnitsyn, V., Choi, S.-O., Murthy, N., Compans, R. W., Skountzou, I., & Prausnitz, M. R. (2010) · Nature Medicine · doi:10.1038/nm.2182 · Cited by 948

Aberrant innate immune response in lethal infection of macaques with the 1918 influenza virus.

Kobasa, D., Jones, S. M., Shinya, K., Kash, J. C., Copps, J., Ebihara, H., Hatta, Y., Hyun Kim, J., Halfmann, P., Hatta, M., et al. (2007) · Nature · doi:10.1038/nature05495 · Cited by 934

Paclitaxel is incorporated by mesenchymal stromal cells and released in exosomes that inhibit in vitro tumor growth: A new approach for drug delivery

Pascucci, L., Coccè, V., Bonomi, A., Ami, D., Ceccarelli, P., Ciusani, E., Viganò, L., Locatelli, A., Sisto, F., Doglia, S. M., et al. (2014) · Journal of Controlled Release · doi:10.1016/j.jconrel.2014.07.042 · Cited by 846

Seasonal coronavirus protective immunity is short-lasting

Edridge, A. W. D., Kaczorowska, J., Hoste, A. C. R., Bakker, M., Klein, M., Loens, K., Jebbink, M. F., Matser, A., Kinsella, C. M., Rueda, P., et al. (2020) · Nature Medicine · doi:10.1038/s41591-020-1083-1 · Cited by 767

Ultrapotent human antibodies protect against SARS-CoV-2 challenge via multiple mechanisms

Tortorici, M. A., Beltramello, M., Lempp, F. A., Pinto, D., Dang, H. V., Rosen, L. E., McCallum, M., Bowen, J., Minola, A., Jaconi, S., et al. (2020) · Science · doi:10.1126/science.abe3354 · Cited by 510

Quantitation of human immunodeficiency virus type 1 infection kinetics

Dimitrov, D. S., Willey, R. L., Sato, H., Chang, L. J., Blumenthal, R., & Martin, M. A. (1993) · Journal of Virology · doi:10.1128/jvi.67.4.2182-2190.1993 · Cited by 515

Protective efficacy of in vitro synthesized, specific mRNA vaccines against influenza A virus infection

Petsch, B., Schnee, M., Vogel, A. B., Lange, E., Hoffmann, B., Voss, D., Schlake, T., Thess, A., Kallen, K.-J., Stitz, L., et al. (2012) · Nature Biotechnology · doi:10.1038/nbt.2436 · Cited by 464

Characterisation of the transcriptome and proteome of SARS-CoV-2 reveals a cell passage induced in-frame deletion of the furin-like cleavage site from the spike glycoprotein

Davidson, A. D., Williamson, M. K., Lewis, S., Shoemark, D., Carroll, M. W., Heesom, K. J., Zambon, M., Ellis, J., Lewis, P. A., Hiscox, J. A., et al. (2020) · Genome Medicine · doi:10.1186/s13073-020-00763-0 · Cited by 457

Antimicrobial Actions of the Nadph Phagocyte Oxidase and Inducible Nitric Oxide Synthase in Experimental Salmonellosis. II. Effects on Microbial Proliferation and Host Survival in Vivo

Mastroeni, P., Vazquez-Torres, A., Fang, F. C., Xu, Y., Khan, S., Hormaeche, C. E., & Dougan, G. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.2.237 · Cited by 399

Inactivation of SARS coronavirus by means of povidone-iodine, physical conditions and chemical reagents.

Kariwa, H., Fujii, N., & Takashima, I. (2006) · Dermatology · doi:10.1159/000089211 · Cited by 458

Autophagy is a critical regulator of memory CD8+ T cell formation

Puleston, D. J., Zhang, H., Powell, T. J., Lipina, E., Sims, S., Panse, I., Watson, A. S., Cerundolo, V., Townsend, A. R., Klenerman, P., et al. (2014) · eLife · doi:10.7554/elife.03706 · Cited by 360

Role of iron in the pathogenesis of Vibrio vulnificus infections

Wright, A. C., Simpson, L. M., & Oliver, J. D. (1981) · Infection and Immunity · doi:10.1128/iai.34.2.503-507.1981 · Cited by 343

Microbiota-Driven Tonic Interferon Signals in Lung Stromal Cells Protect from Influenza Virus Infection

Bradley, K. C., Finsterbusch, K., Schnepf, D., Crotta, S., Llorian, M., Davidson, S., Fuchs, S. Y., Staeheli, P., & Wack, A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.105 · Cited by 313

Antimicrobial and antiviral activities of polyphenolics from Cocos nucifera Linn. (Palmae) husk fiber extract

Esquenazi, D., Wigg, M. D., Miranda, M. M. F. S., Rodrigues, H. M., Tostes, J. B. F., Rozental, S., da Silva, A. J. R., & Alviano, C. S. (2002) · Research in Microbiology · doi:10.1016/s0923-2508(02)01377-3 · Cited by 291

Recurrent herpes simplex virus-1 infection induces hallmarks of neurodegeneration and cognitive deficits in mice

De Chiara, G., Piacentini, R., Fabiani, M., Mastrodonato, A., Marcocci, M. E., Limongi, D., Napoletani, G., Protto, V., Coluccio, P., Celestino, I., et al. (2019) · PLOS Pathogens · doi:10.1371/journal.ppat.1007617 · Cited by 266

Depletion of Human DNA in Spiked Clinical Specimens for Improvement of Sensitivity of Pathogen Detection by Next-Generation Sequencing

Hasan, M. R., Rawat, A., Tang, P., Jithesh, P. V., Thomas, E., Tan, R., & Tilley, P. (2016) · Journal of Clinical Microbiology · doi:10.1128/jcm.03050-15 · Cited by 243

The Yfe system of Yersinia pestis transports iron and manganese and is required for full virulence of plague

Bearden, S. W., & Perry, R. D. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01360.x · Cited by 254

Maternal infection leads to abnormal gene regulation and brain atrophy in mouse offspring: implications for genesis of neurodevelopmental disorders

Fatemi, S. H., Reutiman, T. J., Folsom, T. D., Huang, H., Oishi, K., Mori, S., Smee, D. F., Pearce, D. A., Winter, C., Sohr, R., et al. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2007.11.018 · Cited by 250

Bacillus anthracis requires siderophore biosynthesis for growth in macrophages and mouse virulence

Cendrowski, S., MacArthur, W., & Hanna, P. (2004) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03861.x · Cited by 229

Experimental aerosol survival of SARS-CoV-2 in artificial saliva and tissue culture media at medium and high humidity

Smither, S. J., Eastaugh, L. S., Findlay, J. S., & Lever, M. S. (2020) · Emerging Microbes & Infections · doi:10.1080/22221751.2020.1777906 · Cited by 208

Influenza virus neuraminidase contributes to secondary bacterial pneumonia.

Peltola, V. T., Murti, K. G., & McCullers, J. A. (2005) · The Journal of Infectious Diseases · doi:10.1086/430954 · Cited by 219

An mRNA Vaccine Encoding Rabies Virus Glycoprotein Induces Protection against Lethal Infection in Mice and Correlates of Protection in Adult and Newborn Pigs

Schnee, M., Vogel, A. B., Voss, D., Petsch, B., Baumhof, P., Kramps, T., & Stitz, L. (2016) · PLOS Neglected Tropical Diseases · doi:10.1371/journal.pntd.0004746 · Cited by 212

Effect of Wastewater-Borne Bacteria on Algal Growth and Nutrients Removal in Wastewater-Based Algae Cultivation System

Ma, X., Zhou, W., Fu, Z., Cheng, Y., Min, M., Liu, Y., Zhang, Y., Chen, P., & Ruan, R. (2014) · Bioresource Technology · doi:10.1016/j.biortech.2014.05.087 · Cited by 197

Monoclonal antibodies to the spike protein of feline infectious peritonitis virus mediate antibody-dependent enhancement of infection of feline macrophages

Olsen, C. W., Corapi, W. V., Ngichabe, C. K., Baines, J. D., & Scott, F. W. (1992) · Journal of Virology · doi:10.1128/jvi.66.2.956-965.1992 · Cited by 179

Contribution of TonB- and Feo-mediated iron uptake to growth of Salmonella typhimurium in the mouse

Tsolis, R. M., Bäumler, A. J., Heffron, F., & Stojiljkovic, I. (1996) · Infection and Immunity · doi:10.1128/iai.64.11.4549-4556.1996 · Cited by 174

miR-146a facilitates replication of dengue virus by dampening interferon induction by targeting TRAF6

Wu, S., He, L., Li, Y., Wang, T., Feng, L., Jiang, L., Zhang, P., & Huang, X. (2013) · Journal of Infection · doi:10.1016/j.jinf.2013.05.003 · Cited by 173

In vivo testing of an Enterococcus faecalis efaA mutant and use of efaA homologs for species identification

Singh, K. V., Coque, T. M., Weinstock, G. M., & Murray, B. E. (1998) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.1998.tb01180.x · Cited by 179

Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long‐wavelength ultraviolet light

Lin, L., Hanson, C. V., Alter, H. J., Jauvin, V., Bernard, K. A., Murthy, K. K., Metzel, P., & Corash, L. (2005) · Transfusion · doi:10.1111/j.0041-1132.2005.04316.x · Cited by 172

Molecular Characterization of the Hemin Uptake Locus ( hmu ) from Yersinia pestis and Analysis of hmu Mutants for Hemin and Hemoprotein Utilization

Thompson, J. M., Jones, H. A., & Perry, R. D. (1999) · Infection and Immunity · doi:10.1128/iai.67.8.3879-3892.1999 · Cited by 154

The Y ersinia pestis siderophore, yersiniabactin, and the ZnuABC system both contribute to zinc acquisition and the development of lethal septicaemic plague in mice

Bobrov, A. G., Kirillina, O., Fetherston, J. D., Miller, M. C., Burlison, J. A., & Perry, R. D. (2014) · Molecular Microbiology · doi:10.1111/mmi.12693 · Cited by 149

Lethal Synergism of 2009 Pandemic H1N1 Influenza Virus and Streptococcus pneumoniae Coinfection Is Associated with Loss of Murine Lung Repair Responses

Kash, J. C., Walters, K.-A., Davis, A. S., Sandouk, A., Schwartzman, L. M., Jagger, B. W., Chertow, D. S., Qi, L., Kuestner, R. E., Ozinsky, A., et al. (2011) · mBio · doi:10.1128/mbio.00172-11 · Cited by 143

Intranasal Vaccination with 1918 Influenza Virus-Like Particles Protects Mice and Ferrets from Lethal 1918 and H5N1 Influenza Virus Challenge

Perrone, L. A., Ahmad, A., Veguilla, V., Lu, X., Smith, G., Katz, J. M., Pushko, P., & Tumpey, T. M. (2009) · Journal of Virology · doi:10.1128/jvi.00207-09 · Cited by 143

Determinants of attenuation and temperature sensitivity in the type 1 poliovirus Sabin vaccine

Bouchard, M. J., Lam, D. H., & Racaniello, V. R. (1995) · Journal of Virology · doi:10.1128/jvi.69.8.4972-4978.1995 · Cited by 140

Lethal Dissemination of H5N1 Influenza Virus Is Associated with Dysregulation of Inflammation and Lipoxin Signaling in a Mouse Model of Infection

Cilloniz, C., Pantin-Jackwood, M. J., Ni, C., Goodman, A. G., Peng, X., Proll, S. C., Carter, V. S., Rosenzweig, E. R., Szretter, K. J., Katz, J. M., et al. (2010) · Journal of Virology · doi:10.1128/jvi.00553-10 · Cited by 136

ICAM-5/Telencephalin Is a Functional Entry Receptor for Enterovirus D68

Wei, W., Guo, H., Chang, J., Yu, Y., Liu, G., Zhang, N., Willard, S. H., Zheng, S., & Yu, X.-F. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.09.013 · Cited by 131

Artemisia annua L. extracts inhibit the in vitro replication of SARS-CoV-2 and two of its variants

Nair, M. S., Huang, Y., Fidock, D. A., Polyak, S. J., Wagoner, J., Towler, M. J., & Weathers, P. J. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114016 · Cited by 122

A Procedure for High-Yield Spore Production by Bacillus s ubtilis

Monteiro, S. M., Clemente, J. J., Henriques, A. O., Gomes, R. J., Carrondo, M. J., & Cunha, A. E. (2008) · Biotechnology Progress · doi:10.1021/bp050062z · Cited by 119

Recombination between Polioviruses and Co-Circulating Coxsackie A Viruses: Role in the Emergence of Pathogenic Vaccine-Derived Polioviruses

Jegouic, S., Joffret, M.-L., Blanchard, C., Riquet, F. B., Perret, C., Pelletier, I., Colbere-Garapin, F., Rakoto-Andrianarivelo, M., & Delpeyroux, F. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000412 · Cited by 116

Low thymic activity and dendritic cell numbers are associated with the immune response to primary viral infection in elderly humans

Schulz, A. R., Mälzer, J. N., Domingo, C., Jürchott, K., Grützkau, A., Babel, N., Nienen, M., Jelinek, T., Niedrig, M., & Thiel, A. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500598 · Cited by 112

Deliberate reduction of hemagglutinin and neuraminidase expression of influenza virus leads to an ultraprotective live vaccine in mice

Yang, C., Skiena, S., Futcher, B., Mueller, S., & Wimmer, E. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307473110 · Cited by 103

Pathogenesis of Infection by Clinical and Environmental Strains of Vibrio vulnificus in Iron-Dextran-Treated Mice

Starks, A. M., Schoeb, T. R., Tamplin, M. L., Parveen, S., Doyle, T. J., Bomeisl, P. E., Escudero, G. M., & Gulig, P. A. (2000) · Infection and Immunity · doi:10.1128/iai.68.10.5785-5793.2000 · Cited by 101

Pneumococcal IgA1 protease subverts specific protection by human IgA1

Janoff, E. N., Rubins, J. B., Fasching, C., Charboneau, D., Rahkola, J. T., Plaut, A. G., & Weiser, J. N. (2014) · Mucosal Immunology · doi:10.1038/mi.2013.41 · Cited by 98

Susceptibility of inbred mice to chronic central nervous system infection by Theiler's murine encephalomyelitis virus

Lipton, H. L., & Dal Canto, M. C. (1979) · Infection and Immunity · doi:10.1128/iai.26.1.369-374.1979 · Cited by 98

A nickel ABC-transporter of Staphylococcus aureus is involved in urinary tract infection: Nickel uptake and virulence in Staphylococcus aureus

Hiron, A., Posteraro, B., Carrière, M., Remy, L., Delporte, C., La Sorda, M., Sanguinetti, M., Juillard, V., & Borezée-Durant, E. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2010.07287.x · Cited by 97

Co-Circulation and Evolution of Polioviruses and Species C Enteroviruses in a District of Madagascar

Rakoto-Andrianarivelo, M., Guillot, S., Iber, J., Balanant, J., Blondel, B., Riquet, F., Martin, J., Kew, O., Randriamanalina, B., Razafinimpiasa, L., et al. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030191 · Cited by 96

Influenza virus coinfection with Bordetella bronchiseptica enhances bacterial colonization and host responses exacerbating pulmonary lesions

Loving, C. L., Brockmeier, S. L., Vincent, A. L., Palmer, M. V., Sacco, R. E., & Nicholson, T. L. (2010) · Microbial Pathogenesis · doi:10.1016/j.micpath.2010.06.004 · Cited by 95

Development of a chimeric Zika vaccine using a licensed live-attenuated flavivirus vaccine as backbone

Li, X.-F., Dong, H.-L., Wang, H.-J., Huang, X.-Y., Qiu, Y.-F., Ji, X., Ye, Q., Li, C., Liu, Y., Deng, Y.-Q., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-02975-w · Cited by 94

Dopamine and serotonin levels following prenatal viral infection in mouse—implications for psychiatric disorders such as schizophrenia and autism

Winter, C., Reutiman, T. J., Folsom, T. D., Sohr, R., Wolf, R. J., Juckel, G., & Fatemi, S. H. (2008) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2008.06.001 · Cited by 92

Identification and Characterization of the Hemophore-Dependent Heme Acquisition System of Yersinia pestis

Rossi, M.-S., Fetherston, J. D., Létoffé, S., Carniel, E., Perry, R. D., & Ghigo, J.-M. (2001) · Infection and Immunity · doi:10.1128/iai.69.11.6707-6717.2001 · Cited by 91

Mutations in the cueA gene encoding a copper homeostasis P-type ATPase reduce the pathogenicity of Pseudomonas aeruginosa in mice

Schwan, W. R., Warrener, P., Keunz, E., Kendall Stover, C., & Folger, K. R. (2005) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2005.05.005 · Cited by 86

Clinical activity of pleconaril in an experimentally induced coxsackievirus A21 respiratory infection

Schiff, G. M., & Sherwood, J. R. (2000) · The Journal of Infectious Diseases · doi:10.1086/315176 · Cited by 87

Development and evaluation of nucleic acid sequence based amplification (NASBA) for diagnosis of enterovirus infections using the NucliSens® Basic Kit

Fox, J. D., Han, S., Samuelson, A., Zhang, Y., Neale, M. L., & Westmoreland, D. (2002) · Journal of Clinical Virology · doi:10.1016/s1386-6532(01)00241-4 · Cited by 84

Bacillus anthracis Sortase A (SrtA) Anchors LPXTG Motif-Containing Surface Proteins to the Cell Wall Envelope

Gaspar, A. H., Marraffini, L. A., Glass, E. M., DeBord, K. L., Ton-That, H., & Schneewind, O. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.13.4646-4655.2005 · Cited by 82

Development of a nucleoside-modified mRNA vaccine against clade 2.3.4.4b H5 highly pathogenic avian influenza virus

Furey, C., Scher, G., Ye, N., Kercher, L., DeBeauchamp, J., Crumpton, J. C., Jeevan, T., Patton, C., Franks, J., Rubrum, A., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48555-z · Cited by 79

Evaluation of the attenuation, immunogenicity, and efficacy of a live virus vaccine generated by codon-pair bias de-optimization of the 2009 pandemic H1N1 influenza virus, in ferrets

Broadbent, A. J., Santos, C. P., Anafu, A., Wimmer, E., Mueller, S., & Subbarao, K. (2016) · Vaccine · doi:10.1016/j.vaccine.2015.11.054 · Cited by 79

Antibody pressure by a human monoclonal antibody targeting the 2009 pandemic H1N1 virus hemagglutinin drives the emergence of a virus with increased virulence in mice

O’Donnell, C. D., Vogel, L., Wright, A., Das, S. R., Wrammert, J., Li, G.-M., McCausland, M., Zheng, N.-Y., Yewdell, J. W., Ahmed, R., et al. (2012) · mBio · doi:10.1128/mbio.00120-12 · Cited by 77

Pharmacologic Inhibition of COX-1 and COX-2 in Influenza A Viral Infection in Mice

Carey, M. A., Bradbury, J. A., Rebolloso, Y. D., Graves, J. P., Zeldin, D. C., & Germolec, D. R. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011610 · Cited by 77

Coxsackievirus B3 infection leads to the generation of cardiac myosin heavy chain-α-reactive CD4 T cells in A/J mice

Gangaplara, A., Massilamany, C., Brown, D. M., Delhon, G., Pattnaik, A. K., Chapman, N., Rose, N., Steffen, D., & Reddy, J. (2012) · Clinical Immunology · doi:10.1016/j.clim.2012.07.003 · Cited by 69

Differences in replication kinetics and cell tropism between neurovirulent and non-neurovirulent EHV1 strains during the acute phase of infection in horses.

Gryspeerdt, A. C., Vandekerckhove, A. P., Garré, B., Barbé, F., Van de Walle, G. R., & Nauwynck, H. J. (2010) · Veterinary Microbiology · doi:10.1016/j.vetmic.2009.10.015 · Cited by 69

In Vivo Effects of Cefazolin, Daptomycin, and Nafcillin in Experimental Endocarditis with a Methicillin-Susceptible Staphylococcus aureus Strain Showing an Inoculum Effect against Cefazolin

Nannini, E. C., Singh, K. V., Arias, C. A., & Murray, B. E. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00856-13 · Cited by 64

Calcium Flux between the Endoplasmic Reticulum and Mitochondrion Contributes to Poliovirus-Induced Apoptosis

Brisac, C., Téoulé, F., Autret, A., Pelletier, I., Colbère-Garapin, F., Brenner, C., Lemaire, C., & Blondel, B. (2010) · Journal of Virology · doi:10.1128/jvi.00994-10 · Cited by 65

Comparison of the Effects of Deferiprone versus Deferoxamine on Growth and Virulence of Yersinia enterocolitica

Lesic, B., Foulon, J., & Carniel, E. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.6.1741-1745.2002 · Cited by 65

Effect of essential oils on the immune response to some viral vaccines in broiler chickens, with special reference to Newcastle disease virus

El-Shall, N. A., Shewita, R. S., Abd El-Hack, M. E., AlKahtane, A., Alarifi, S., Alkahtani, S., Abdel-Daim, M. M., & Sedeik, M. E. (2020) · Poultry Science · doi:10.1016/j.psj.2020.03.008 · Cited by 64

Imprinted antibody responses against SARS-CoV-2 Omicron sublineages

Park, Y.-J., Pinto, D., Walls, A. C., Liu, Z., De Marco, A., Benigni, F., Zatta, F., Silacci-Fregni, C., Bassi, J., Sprouse, K. R., et al. (2022) · doi:10.1101/2022.05.08.491108 · Cited by 251

Influenza A virus infection predisposes hosts to secondary infection with different Streptococcus pneumoniae serotypes with similar outcome but serotype-specific manifestation.

Sharma-Chawla, N., Sender, V., Kershaw, O., Gruber, A. D., Volckmar, J., Henriques-Normark, B., Stegemann-Koniszewski, S., & Bruder, D. (2016) · Infection and Immunity · doi:10.1128/iai.00422-16 · Cited by 63

Active hexose correlated compound enhances resistance to Klebsiella pneumoniae infection in mice in the hindlimb-unloading model of spaceflight conditions

Aviles, H., Belay, T., Fountain, K., Vance, M., Sun, B., & Sonnenfeld, G. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00259.2003 · Cited by 59

Molecular characterization of an Indian isolate of Japanese encephalitis virus that shows an extended lag phase during growth.

Vrati, S., Agarwal, V, Malik, P., Wani, S. A., & Saini, M. (1999) · Journal of General Virology · doi:10.1099/0022-1317-80-7-1665 · Cited by 57

Gemcitabine-releasing mesenchymal stromal cells inhibit in vitro proliferation of human pancreatic carcinoma cells

Bonomi, A., Sordi, V., Dugnani, E., Ceserani, V., Dossena, M., Coccè, V., Cavicchini, L., Ciusani, E., Bondiolotti, G., Piovani, G., et al. (2015) · Cytotherapy · doi:10.1016/j.jcyt.2015.09.005 · Cited by 56

Increasing the Recruitment of Neutrophils to the Site of Infection Dramatically Attenuates Borrelia burgdorferi Infectivity

Xu, Q., Seemanapalli, S. V., Reif, K. E., Brown, C. R., & Liang, F. T. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.8.5109 · Cited by 55

Effects of the hindlimb-unloading model of spaceflight conditions on resistance of mice to infection with Klebsiella pneumoniae

Belay, T., Aviles, H., Vance, M., Fountain, K., & Sonnenfeld, G. (2002) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2002.126459 · Cited by 54

Formatted single-domain antibodies can protect mice against infection with influenza virus (H5N2)

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Distinct functions of polysaccharide deacetylases in cell shape, neutral polysaccharide synthesis and virulence of Bacillus anthracis

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