Relevant bibliographies by topics / Superbugs

Academic literature on the topic 'Superbugs'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Superbugs"

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Khan, M. Karim. "Superbugs." Community Based Medical Journal 6, no. 2 (September 10, 2017): 1–2. http://dx.doi.org/10.3329/cbmj.v6i2.54721.

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Rogers, Rob. "Superbugs." Chest 143, no. 3 (March 2013): 596. http://dx.doi.org/10.1378/chest.143.3.596.

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Yin, Xiaoyan, Toshimitsu Hamasaki, Dean Follmann, and Scott R. Evans. "OutSMARTing Superbugs." CHANCE 33, no. 3 (July 2, 2020): 22–30. http://dx.doi.org/10.1080/09332480.2020.1820248.

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Yuhas, Daisy. "Stopping Superbugs." Scientific American 308, no. 2 (January 14, 2013): 17. http://dx.doi.org/10.1038/scientificamerican0213-17b.

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Harmon, Katherine. "Stopping Superbugs." Scientific American 308, no. 2 (January 18, 2013): 18. http://dx.doi.org/10.1038/scientificamerican0213-18a.

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Hicks, B. "Farm-grown superbugs?" Canadian Medical Association Journal 184, no. 15 (October 16, 2012): 1716. http://dx.doi.org/10.1503/cmaj.112-2074.

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Davies, S. "Superfuels from superbugs." Engineering & Technology 5, no. 5 (March 27, 2010): 42–45. http://dx.doi.org/10.1049/et.2010.0509.

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Lorenzi, Rossella. "EU researches superbugs." Genome Biology 4 (2003): spotlight—20031202–01. http://dx.doi.org/10.1186/gb-spotlight-20031202-01.

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Fleming, Nic. "The other superbugs." New Scientist 249, no. 3315 (January 2021): 39–43. http://dx.doi.org/10.1016/s0262-4079(20)32268-5.

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Honigsbaum, Mark. "Superbugs and us." Lancet 391, no. 10119 (February 2018): 420. http://dx.doi.org/10.1016/s0140-6736(18)30110-7.

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Dissertations / Theses on the topic "Superbugs"

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Pérez-Peinado, Clara 1991. "Hitchhiking with Nature : exploring snake venom peptides to fight cancer and superbugs." Doctoral thesis, Universitat Pompeu Fabra, 2020. http://hdl.handle.net/10803/668411.

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This work describes the discovery and optimization of efficient, selective, cost-effective and proteolytic-resistant antimicrobial and antitumoral peptides. To this end, we first identified novel cathelicidin-related peptides from the venom gland of South American pit vipers, collectively named vipericidins. In particular, crotalicidin (Ctn), a 34-mer helical peptide from the Crotalus durissus terrificus venom, highlighted due to its promising antimicrobial and antitumoral properties. Its fragment Ctn[15-34] also stood out due to its overall preserved activity, improved selectivity, serum stability and significant size reduction. Their mechanisms of action were stepwise characterized against Escherichia coli and a leukemic cell line. The unusually high lifespan of Ctn[15-34] in serum was also investigated to ascertain its structural determinants and molecular interaction with serum proteins. Altogether, this thesis proposes two novel bioactive peptides as potential drug candidates to fight bacterial infections and cancer, particularly leukemia. Beyond specific results, this thesis provides a set of valuable methodologies to discover, optimize and evaluate bioactive molecules from natural sources.
Esta tesis aborda el descubrimiento y optimización de péptidos antimicrobianos y antitumorales eficientes, selectivos, rentables y resistentes a la proteólisis. Con este fin, inicialmente identificamos nuevas catelicidinas en la glándula venenosa de diferentes víboras de América del Sur, denominadas vipericidinas. En particular la crotalicidina (Ctn), un péptido helicoidal de 34 residuos aislado del veneno de la serpiente Crotalus durissus terrificus destacó por sus propiedades antimicrobianas y antitumorales, así como su fragmento Ctn[15-34], que mostró una selectividad y estabilidad en suero mejoradas y una reducción de tamaño considerable. Los mecanismos de acción de ambos péptidos contra Escherichia coli y una línea celular de leucemia fueron investigados. También se investigó en profundidad la inusual estabilidad en suero de Ctn[15-34], con el fin de conocer sus determinantes estructurales y las posibles interacciones con proteínas del suero. En conjunto, esta tesis propone dos nuevos péptidos bioactivos como posibles candidatos para combatir infecciones bacterianas y la leucemia, además de proporcionar un conjunto de metodologías útiles en el descubrimiento, optimización y caracterización de moléculas bioactivas a partir de fuentes naturales.
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Wong, Choon Kit Adison. "Programming microbes to treat superbug infection." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/31369.

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Superbug infection is one of the greatest public health threat with grave implications across all levels of society. Towards a new solution to combat infection by multi-drug resistant bacteria, this thesis presents an engineering framework and genetic tools applied to repurpose commensal bacteria into 'micro-robots' for the treatment of superbug infection. Specifically, a prototype of designer probiotic was developed using the human commensal bacteria Escherichia coli. The engineered commensal was reprogrammed with user-specified functions to sense superbug, produced pathogen-specific killing molecules and released the killing molecules via a lytic mechanism. The engineered commensal was effective in suppressing ~99% of planktonic Pseudomonas and preventing ~ 90% of biofilm formation. To enhance the sensing capabilities of engineered commensal, genetic interfaces comprising orthogonal AND & OR logic devices were developed to mediate the integration and interpretation of binary input signals. Finally, AND, OR and NOT logic gates were networked to generate a myriad of cellular logic operations including half adder and half subtractor. The creation of half adder logic represents a significant advancement of engineering human commensal to be biological equivalent of microprocessor chips in programmable computer with the ability to process input signals into diversified actions. Importantly, this thesis provides exemplary case studies to the attenuation of cellular and genetic context dependent effects through principles elucidated herein, thereby advancing our capability to engineer commensal bacteria.
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Wilke, Mark Steven. "Structural characterization of superbug proteins involved in regulating beta-lactam resistance." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/725.

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The widespread use of β-lactams has undermined their effectiveness as chemotherapeutic agents by fueling the evolution and dissemination of multiple resistance mechanisms, including: (1) production of hydrolytic β-lactamase enzymes that inactivate β-­lactams, (2) expression of PBPs with low-affinity for β-­lactams and (3) overexpression of multidrug efflux pumps which actively expunge β-­lactams and other toxic substances. The overall goal of this thesis is the structural characterization of bacterial proteins involved in regulating β-lactam resistance. The notorious resistance of Staphylococcus aureus primarily stems from the production of β-lactamases and PBP2a, a low-affinity PBP which confers broad-spectrum β-­lactam resistance in methicillin-resistant S. aureus (MRSA) strains. Expression of these resistance determinants is controlled by a β-­lactam-inducible transmembrane receptor (BlaR1/MecR1) and repressor (BlaI/MecI). This dissertation presents the crystal structure of the BlaR1 sensor domain (BlaRs) from S. aureus, determined in its apo form and acylated with penicillin G. These structures reveal that acylation by β-lactams is not accompanied by a BlaRs conformational change. It is also shown that mutation of the BlaR1 L2 loop prevents induction of β-­lactamase expression in vivo, supporting that the L2 loop plays an important role in signal transduction. The intrinsic resistance of Pseudomonas aeruginosa to a variety of antibiotics (including β-lactams) is exacerbated in mutant strains that overexpress multidrug efflux pumps such as MexAB-OprM. Production of MexAB-OprM is controlled by the MarR family repressor, MexR, and several hyper-resistant strains of P. aeruginosa appear to involve mutations in either MexR or additional regulatory factors upstream of MexR. The allosteric effectors of MarR proteins are typically small lipophenolic compounds. This dissertation confirms that MexR is uniquely modulated by the 53 residue protein, ArmR. Electromobility gel shift assays and isothermal titration calorimetry demonstrate that a direct MexR-ArmR interaction is responsible for neutralizing the affinity of MexR for its DNA operator. The allosteric conformational change induced by ArmR-binding was assessed by determining the crystal structure of MexR double mutant Q106L/A110L (MexRLL) in complex with ArmR residues 29-53 (ArmRC). This structure shows that ArmR induces a dramatic conformational change which repositions the MexR DNA-binding lobes into an orientation that is incompatible with binding DNA.
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Davies, Abigail. "Structure and biochemical analysis of toxins from the superbug Clostridium difficile." Thesis, University of Bath, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.619282.

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Clostridium difficile is a gram positive, anaerobic bacterium that is the leading cause of antibiotic-associated pseudomembranous colitis worldwide. C. difficile is an extremely infectious bacterium that produces spores that are highly resistant to standard disinfectant agents and can survive on surfaces for long periods of time. Both the resistance of the spores combined with multiple patients with low-immune systems has lead to an increase in hospital-acquired C. difficile infection, which has had a severe economic impact on the healthcare system. Due to the emerging antibiotic resistance problems and the common occurrence of patient relapse using the current drugs of choice, alternative therapeutic avenues are being explored. C.difficile produces two potent exotoxins; Toxin A and Toxin B that are the causative agents of infection. These toxins have multi-modular domain organisations, with each domain playing a role in cytotoxicity. Some of these domains have been characterised structurally using X-ray crystallography. In this thesis, the low resolution SAXS structure of Toxin A will be presented along with the advances made towards determining the X-ray crystallographic structure of the full-length Toxin A. In addition to Toxins A and B, some strains of C. difficile produce a binary toxin, CDT, which is made up of two individually produced components, CDTa and CDTb. The CDTa component is the enzymatically active component, whereas CDTb is the transport component, directly involved in translocating CDTa into target cells. The precise role of CDT in pathogenesis is unclear, however there is evidence that CDT ADP-ribosylates monomeric actin in target cells, but the detailed mechanism by which this reaction takes place is unknown. Here site directed mutagenesis of key residues of the active site of CDTa was performed and the effect of these mutations on the enzyme’s cytotoxicity tested. By separately mutating three active site residues, the cytotoxic effect of CDTa can be completely eradicated, details of which will be discussed in this thesis. Additionally, the progress made towards determining the X-ray crystallographic structure of the transport component, CDTb, will be discussed.
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Damann, Margaret S. "Juvenility and flowering responses in Chrysanthemum x superbum and Coreopsis grandiflora and lanceolata." Thesis, This resource online, 1991. http://scholar.lib.vt.edu/theses/available/etd-08042009-040254/.

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Barrett, Cindy L. "Range-wide Prevalence and Impacts of Pseudocercosporella inconspicua on Lilium grayi and an Assessment of L. superbum and L. michauxii as Reservoirs." Digital Commons @ East Tennessee State University, 2017. https://dc.etsu.edu/etd/3249.

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Lilium grayi (Gray’s Lily), a southern Appalachian endemic species, is threatened by a Lilium-specific fungal pathogen, Pseudocercosporella inconspicua. The disease is characterized by tan lesions that can cause early senescence, while also lowering seed production and viability. This project tested for P. inconspicua conidia and accessed health at nine locations. The disease was present and ubiquitous across the range of L. grayi. Through identification of P. inconspicua conidia in the field, L. superbum (Turk’s Cap Lily) was identified as an additional host, while L. michauxii (Michaux’s Lily) was disease-free. However, infection was inducible in both species. With the disease widespread in L. superbum and this species represented by many large populations, L. superbum may act as disease reservoir, further complicating the outlook for L. grayi. The disease should be considered an epidemic because of its impact on individual plants, its commonness within populations, and its ubiquity across the geographical range.
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Dobrovolný, Ondřej. "Koncept závodního vozu pro autokros." Master's thesis, Vysoké učení technické v Brně. Fakulta strojního inženýrství, 2016. http://www.nusl.cz/ntk/nusl-241914.

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Diploma thesis deals with the design and simulation of torsional stiffness of the frame for autocross racing car. The design put emphasis on observe the regulations of international automobile federation and the result of torsional rigidity and weight. The first part focuses on the design of vehicles for autocross and its regulations. The main part is the structural design of the frame, following with simulation analysis using finite element method and computing torsional stiffness. In conclusion, results are evaluate and referred for further development.
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Hsieh, Pei-Wen, and 謝珮文. "Studies on The Chemical Constituents of Drymaria diandra, Dianthus superbus, and Dianthus superbus var. logicalycinus, and the Synthetic` Dianthramide Alkaloid Analogues, and Their Biological Activities." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/70194536196718378537.

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博士
高雄醫學大學
藥學研究所博士班
93
The aim of this dissertation is building up the data including the isolation, structural elucidation, and bioactivities, eg. antiplatelet aggregation, anti-inflammatory, and cytotoxicities of cyclic peptides from three Formosan Caryophyllaceous plants, Drymaria diandra, Dianthus superbus, and Dianthus superbus var. longicalycinus. Fourty compounds were isolated including two alkaloids, drymaritin (DR-15) and 2’-methoxydianthramide B (DS-A12); five flavonoids, torosaflavone A (DR-26), diandraflavone (DR-31), isovitexin (DR-30), isofurcatain (DR-32), and 7-methoxyisofurcatain (DR-33); nine cyclic peptides, diandrine A~ D (DR-22、23、28、29), dianthin C-F (DS-P3~6), and longicalycinin A (DS-P7); two steroids, spinasterol (DR-21) and spinasterol-β-D-glycoside (DR-27); five triterpenoid saponins, dianthoside A, B, G, H (DS-T1, 2, 7, 8), and vaccaroside A (DS-T22); two norsesquiterpenes, 3-oxo-α-ionol (DR-11) and megastigma-4,7-diene-3,9-dione (DR-12), and the other fifteen misllenous compounds, anemonin (DR-9), hexadecanoic acid (DR-10), methyl 5-hydroxy-4-oxopentanoate (DR-13), glycerol-α-lignocerate (DR-14), p-hydroxybenzoic acid (DR-16), p-hydroxybenaldehyde (DR-17), vallinic acid (DR-18), isovanillin (DR-19), 4-methoxy-benzoic aicd methyl ester (DR-20), cis-p-coumarate (DR-24), 3,4-dihydroxybenzoic acid (DR-25), aurantiamide benzoate (DS-O10), 4-(2-hydroxy-ethyl)-2-methoxy-phenol (DS-O11), vanillin (DS-O12), and 3-(4-hydroxy-3-methoxy-phenyl)-propionic acid methyl ester (DS-O13). The structures of them were elucidated and established on the basis of spectoscopic data and chemical derivates. Among them, twelve compounds are new, and twenty-three ones were firstly derived from these plants. Additionally, compound DR-23 exhibited highly slective inhibitory effect on the platelet aggregation induced by collagen; compound DR-31 showed inhibitory activity to neutrophil superoxide generation stimulated by fMLP. Furthermore, drymaritin exhibited anti-HIV effect with an EC50 value of 2.80 µM and a TI value of 20.6 The dianthramide alkaloids and their analogues, which were isolated from the genus Dianthus, were selected as the targets for the further medicinal chemistry study. Seventy-one compounds were synthesized and screened for their cytotoxicity, antiplatelet activity, antiinflammatory, inhibition of neutrophil elastase release, ICAM-1 expression inhibition, and anti-HCoVs activities. On the basis of these screenings, the SARs of these compounds were established or proposed. The mechanisms of the most potent compounds, DS-R14, DS-R15, DS-R16, DS-R21, DS-R31, and DS-R41 are underinvestiged for the pharmacological mechanism to anti-platelet aggregation, inhibition of neutrophil elastase release, and ICAM-1 expression inhibition, respectively.
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Janovčíková, Jana. "Superbia, superbus. Sémantická studie a kulturně-historická sonda do hodnotového systému." Master's thesis, 2010. http://www.nusl.cz/ntk/nusl-280480.

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The purpose of this thesis is to explore and explain the meaning of the Latin word superbus plus it's derivatives (superbia, superbe, superbiter, superbire) and the way in which it is usually or not-so-usually used. In particular, during this exploration we will look into the works of Lucius Annaeus Seneca and Cornelius Tacitus, two authors of the 1st century AD. Analysis of kinds of behavior, situations and characters which bore the negative evaluative name of superbia in the mind (and texts) of a historian and a philosopher shall open an insight into the Roman system of values in political and social context. That is the reason, why the first field with which we will compare the data obtained by our analysis will be the general trend in the usage of this word which we will find in the textual corpus of Rome's republican era and the Principate era authors. Our second comparatory field will be formed by meanings and evaluations carried by Czech words, which are usually used as translations of Latin superbus, especially the words pyšný and povýšený. Those meanings and evaluations we will seek in the CzechNational Corpus.
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Wu, Chun-Ming, and 吳浚銘. "Thermal strain analysis of SuperBGA by moire interferometry." Thesis, 2000. http://ndltd.ncl.edu.tw/handle/45976222926498030750.

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碩士
國立成功大學
工程科學系
88
When the temperature of electronic package components circulate repeatedly, they cause the horizontal and vertical displacement between components and I/O along with the difference of coefficient of thermal expansion(CTE), solder joints, encapsulate resin, heat sink and substrate material. Due to this reason, the materials are under the circumstance of fatigue and warpage. Therefore, the components place on the surface of touching point, they lost the operation function because of the destructive fatigue. This research based on moiré interfermety as an experiment to measure the new Super BGA in package style and compare with PBGA on understanding the difference of CTE among electronic packages. They produce fatigue failure. Beside, the result of this experiment will provide the further data to IC designer engineer on the reliability analysis for the best solution in convenience and reduce the product cost.
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Books on the topic "Superbugs"

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Superbugs. London: Raintree, 2012.

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Superbugs. Chicago, Ill: Heinemann Library, 2012.

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Häusler, Thomas. Viruses vs. Superbugs. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9.

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Drug-resistant diseases and superbugs. Tarrytown, NY: Marshall Cavendish Benchmark, 2010.

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Koki, Horikoshi, and Grant W. D, eds. Superbugs: Microorganisms in extreme environments. Berlin: Springer-Verlag, 1991.

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Watson, Stephanie. Superbugs: The rise of drug-resistant germs. New York: Rosen Pub., 2010.

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Superbugs: The rise of drug-resistant germs. New York, NY: Rosen Pub., 2010.

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Watson, Stephanie. Superbugs: The rise of drug-resistant germs. New York: Rosen Pub., 2010.

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author, Wilker Ian, and Ambrose Marylou author, eds. Tuberculosis and superbugs: Examining TB and bacterial infections. Berkeley Heights, NJ: Jasmine Health, 2014.

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Viruses vs. superbugs: A solution to the antibiotics crisis? London: Macmillan, 2006.

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Book chapters on the topic "Superbugs"

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Marcus, Bernard. "Superbugs." In SpringerBriefs in Evolutionary Biology, 41–47. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6126-6_6.

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Horikoshi, Koki. "Superbugs Project." In Extremophiles, 83–92. Tokyo: Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-55408-0_6.

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Zaccheo, Aleardo, Eleonora Palmaccio, Morgan Venable, Isabella Locarnini-Sciaroni, and Salvatore Parisi. "Biocides and “Superbugs”." In Food Hygiene and Applied Food Microbiology in an Anthropological Cross Cultural Perspective, 63–72. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-44975-3_11.

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Häusler, Thomas. "at the limits of medicine." In Viruses vs. Superbugs, 1–14. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_1.

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Häusler, Thomas. "invincible microbes." In Viruses vs. Superbugs, 15–47. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_2.

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Häusler, Thomas. "the wild pioneer era." In Viruses vs. Superbugs, 48–104. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_3.

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Häusler, Thomas. "the renaissance of phages during the war." In Viruses vs. Superbugs, 105–25. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_4.

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Häusler, Thomas. "a parallel universe." In Viruses vs. Superbugs, 126–74. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_5.

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Häusler, Thomas. "keepers of the grail in peril." In Viruses vs. Superbugs, 175–202. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_6.

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Häusler, Thomas. "resurrection." In Viruses vs. Superbugs, 203–47. London: Palgrave Macmillan UK, 2006. http://dx.doi.org/10.1007/978-0-230-55228-9_7.

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Conference papers on the topic "Superbugs"

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Hogan, A., and N. Hauter. "2. Microbes, Emerging Resistance, and Superbugs: Health Care Worker Safety, the New Frontier." In AIHce 2006. AIHA, 2006. http://dx.doi.org/10.3320/1.2753418.

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Skender, Kristina, Anna Machowska, Vivek Singh, Varun Goel, Yogyata Marothi, Cecilia Stålsby Lundborg, and Megha Sharma. "Antibiotic Use, Incidence and Risk Factors for Orthopedic Surgical Site Infections in a Teaching Hospital in Madhya Pradesh, India." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12706.

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Melro, Liliana, Tânia D. Tavares, Jorge Padrão, Fernando Dourado, Miguel Gama, Carla Silva, Joana C. Antunes, Helena P. Felgueiras, and Andrea Zille. "Antimicrobial Activity of a Bacterial Nanocellulose Film Functionalized with Nisin Z for Prospective Burn Wounds Treatment." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12708.

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Shen, Justin, and Davesh Valagolam. "A Systematic Implementation of Machine Learning Algorithms for Multifaceted Antimicrobial Screening of Lead Compounds." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12751.

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Chaurasia, Surabhi, and Anima Pandey. "A Systematic In Silico Investigation of Phytochemicals from Artocarpus Species against Plasmodium falciparum Inhibitors." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12712.

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Gracia, Raquel, Mercedes Arenere, Beatriz Bonaga, Maria Angeles Allende, Alberto Jose Frutos, Transito Salvador, Raquel Fresquet, Oihana Pascual, and Jose Manuel Vinuesa. "Experience of Real-Life Use of Dalbavancin as an Off-Label Treatment of Complicated Infectious Diseases in a Tertiary Care Hospital Experience." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12736.

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Bartolomeu, Maria, Cátia Vieira, Marta Gomes, Ana T. P. C. Gomes, Maria Amparo F. Faustino, Maria Graça P. M. S. Neves, and Adelaide Almeida. "Photodynamic Inactivation of Phage Phi6 as SARS-CoV-2 Model in Wastewater Disinfection: Effectivity and Safety." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12707.

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Brożyna, Malwina, Justyna Paleczny, and Adam Junka. "The Antibiofilm Potential of Vapor Fractions of Selected Essential Oils against Pseudomonas aeruginosa." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12702.

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Uaraksakul, Pataraporn, and Pragatsawat Chanprapai. "In Vitro Antifungal Activity of Boesenbergia rotundo Linn. and Syzygium aromaticum L. Merr. and Perry Extracts against Aspergillus flavus." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12687.

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Jaroszewicz, Weronika, Patrycja Bielańska, Daria Lubomska, Katarzyna Kosznik-Kwaśnicka, Piotr Golec, Łukasz Grabowski, Ewa Wieczerzak, et al. "Antimicrobial Activities of Compounds Produced by Newly Isolated Streptomyces Strains from Mountain Caves." In The 2nd International Electronic Conference on Antibiotics—Drugs for Superbugs: Antibiotic Discovery, Modes of Action And Mechanisms of Resistance. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/eca2022-12749.

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Reports on the topic "Superbugs"

1

Segelke, B. 19-LW-045 Full Length Final Report. Molecular Mechanisms of Bacterial Pathogenesis: Waging the Arms Race with Superbugs. Office of Scientific and Technical Information (OSTI), January 2021. http://dx.doi.org/10.2172/1756727.

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Marti-Arbona, Ricardo. Superbug Recon and Destroy-Discovery of Minimal Invasive Signatures and Validation of Novel Antimicrobial Targets. Office of Scientific and Technical Information (OSTI), June 2018. http://dx.doi.org/10.2172/1441278.

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Fisker, J. Computational Models of X-Ray Burst Quenching Times and 12C Nucleosynthesis Following a Superburst. Office of Scientific and Technical Information (OSTI), March 2009. http://dx.doi.org/10.2172/989344.

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National infection control campaigns led to a rapid decline in superbug infections in UK intensive care units. National Institute for Health Research, November 2020. http://dx.doi.org/10.3310/alert_42408.

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