Literatura científica selecionada sobre o tema "Antifungal activiy"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Índice
Consulte a lista de atuais artigos, livros, teses, anais de congressos e outras fontes científicas relevantes para o tema "Antifungal activiy".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Artigos de revistas sobre o assunto "Antifungal activiy"
Pranata, Kadek Dwipayana, I. Gede Putu Wirawan, I. Putu Agus Hendra Wibawa, I. Ketut Suada, I. Nyoman Wijaya e Trisna Agung Phabiola. "ANTIFUNGAL ACTIVITY OF SIAM CITRUS (Citrus nobilis L.) ESSENTIAL OIL AGAINTS Lasiodiplodia theobromae THE PATHOGEN OF BLENDOK DISEASE". International Journal of Biosciences and Biotechnology 11, n.º 2 (30 de abril de 2024): 61. http://dx.doi.org/10.24843/ijbb.2024.v11.i02.p08.
Texto completo da fonteAndrade, B. S., R. Matias, B. O. Corrêa, A. K. M. Oliveira, D. G. F. Guidolin e A. R. Roel. "Phytochemistry, antioxidant potential and antifungal of Byrsonima crassifolia on soil phytopathogen control". Brazilian Journal of Biology 78, n.º 1 (10 de julho de 2017): 140–46. http://dx.doi.org/10.1590/1519-6984.166532.
Texto completo da fonteVahedi-Shahandashti, Roya, e Cornelia Lass-Flörl. "Novel Antifungal Agents and Their Activity against Aspergillus Species". Journal of Fungi 6, n.º 4 (9 de outubro de 2020): 213. http://dx.doi.org/10.3390/jof6040213.
Texto completo da fonteBouz, Ghada, e Martin Doležal. "Advances in Antifungal Drug Development: An Up-To-Date Mini Review". Pharmaceuticals 14, n.º 12 (16 de dezembro de 2021): 1312. http://dx.doi.org/10.3390/ph14121312.
Texto completo da fonteBurger-Kentischer, Anke, Doris Finkelmeier, Petra Keller, Jörg Bauer, Holger Eickhoff, Gerald Kleymann, Walid Abu Rayyan et al. "A Screening Assay Based on Host-Pathogen Interaction Models Identifies a Set of Novel Antifungal Benzimidazole Derivatives". Antimicrobial Agents and Chemotherapy 55, n.º 10 (11 de julho de 2011): 4789–801. http://dx.doi.org/10.1128/aac.01657-10.
Texto completo da fonteKlochenko, Peter D., Irina A. Elanskaya, Tatyana F. Shevchenko e Elena V. Sokolova. "Antifungal activity of freshwater cyanobacteria". Algological Studies/Archiv für Hydrobiologie, Supplement Volumes 103 (3 de dezembro de 2001): 143–49. http://dx.doi.org/10.1127/algol_stud/103/2001/143.
Texto completo da fonteWiederhold, Nathan P. "Pharmacodynamics, Mechanisms of Action and Resistance, and Spectrum of Activity of New Antifungal Agents". Journal of Fungi 8, n.º 8 (16 de agosto de 2022): 857. http://dx.doi.org/10.3390/jof8080857.
Texto completo da fonteLemriss, S., F. Laurent, A. Couble, E. Casoli, J. M. Lancelin, D. Saintpierre-Bonaccio, S. Rifai, A. Fassouane e P. Boiron. "Screening of nonpolyenic antifungal metabolites produced by clinical isolates of actinomycetes". Canadian Journal of Microbiology 49, n.º 11 (1 de novembro de 2003): 669–74. http://dx.doi.org/10.1139/w03-088.
Texto completo da fonteBrilhante, Raimunda SN, Vandbergue S. Pereira, Jonathas S. Oliveira, Anderson M. Rodrigues, Zoilo P. de Camargo, Waldemiro A. Pereira-Neto, Nilberto RF Nascimento et al. "Terpinen-4-ol inhibits the growth of Sporothrix schenckii complex and exhibits synergism with antifungal agents". Future Microbiology 14, n.º 14 (setembro de 2019): 1221–33. http://dx.doi.org/10.2217/fmb-2019-0146.
Texto completo da fonteGrayton, Quincy E., Ivie L. Conlon, Christopher A. Broberg e Mark H. Schoenfisch. "Impact of Nitric Oxide-Release Kinetics on Antifungal Activity". Journal of Fungi 10, n.º 5 (24 de abril de 2024): 308. http://dx.doi.org/10.3390/jof10050308.
Texto completo da fonteTeses / dissertações sobre o assunto "Antifungal activiy"
Pham, Giang Nam. "Développement de nouveaux antibiotiques dirigés contre des bactéries multirésistantes à partir de microorganismes marins inexploités". Electronic Thesis or Diss., Université Côte d'Azur, 2024. http://www.theses.fr/2024COAZ5028.
Texto completo da fonteThe enormous biological and chemical diversity in the marine environment is making it a valuable resource for the discovery of new antibiotics, in response to the emergence of antibiotic crisis worldwide. However, the rate of discovery of new marine-derived drugs seems insufficient compared to its potential. In an effort to contribute to the search for hit compounds for the development of new antibiotics, we investigated the secondảy metabolites and biological activity of four fungi strains: Fusarium equiseti, Anthracocystis flocculosa, Scedosporium dehoogii, and Amesia nigricolor.Regarding chemical components, 45 compounds were isolated, mainly belonging to chromones, alkaloids, cyclic polyketides, glycolipids, sesquiterpenes, and naphthalenes classes. 18 compounds (accounting for 40%) were identified as new compounds. The structures of these compounds were elucidated using a combination of HRMS, NMR, X-ray diffraction, modified Mosher's method, and quantum chemical calculations (ECD, ML-J-DP4, and DP4+ probability analysis). Among them, dehoogiiketones A-B (C3.1-2) isolated from the fungus S. dehoogii possessed rearranged bergamotene skeletons, described for the first time in nature.Regarding biological activity, six fusarochromanone derivatives (C2.1-6) isolated from F. equiseti (two of which are new: C2.2, C2.6) showed cytotoxicity ranging from strong to moderate on three tested cell lines (RPE1, HCT-116, U2OS). Only two of these compounds exhibited inhibition activity against three (ABL1, JAK3, EphB1) out of sixteen tested protein kinases. Only three flocculosins A-C (C3.1-3) out of eight derivatives isolated from A. flocculosa showed antibacterial activity against S. aureus S25. These findings revealed the structure-activity relationship of fusarochromanone and flocculosin derivatives.Equisetin (C2.8) isolated from F. equiseti exhibited strong antibacterial activity against S. aureus S25 but showed no cytotoxicity on three tested cell lines (RPE1, HCT-116, U2OS). Chaetochromins A and B (C5.7-8) exhibited strong antibacterial activity but showed cell toxicity ranging from weak to moderate on tested cell line (THP-1) and primary cells (RBC, PBMC) isolated from the blood of healthy donors, indicating a possible therapeutic window. These three compounds are worthy of further research stages in antibiotic development
Magnusson, Jesper. "Antifungal activity of lactic acid bacteria /". Uppsala : Dept. of Microbiology, Swedish Univ. of Agricultural Sciences, 2003. http://epsilon.slu.se/a397.pdf.
Texto completo da fonteMusso, L. "Analogues of natural products with antifungal activity". Doctoral thesis, Università degli Studi di Milano, 2007. http://hdl.handle.net/2434/49159.
Texto completo da fonteHansen, Bruce Richard. "Antifungal activity of some New Zealand fungal isolates". Thesis, University of Canterbury. Plant and Microbial Sciences, 1998. http://hdl.handle.net/10092/6849.
Texto completo da fonteFewell, Alison. "Interactive antifungal activity between co-occurring Solanum glycoalkaloids". Thesis, University of Exeter, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359158.
Texto completo da fontede, Beer Irving. "Screening of plant-mediated nanoparticles for antifungal activity". University of the Western Cape, 2020. http://hdl.handle.net/11394/7955.
Texto completo da fonteNanotechnology is spreading rapidly across the world as an extremely powerful technology. Nanoscience and nanotechnology are innovative scientific advancements that have been introduced only in this century. Nanotechnology has developed as the scientific advancement to grow and transform the entire agri-food area, with the potential to elevate global food production, in addition to the nutritional value, quality, and safety of food and food products. It has gained recognition due to its variability in shape, size, and dimension and how it correlates to its possibilities. One of those functions is nanoparticles’ (NPs) ability to have antimicrobial activity, more specifically its antifungal activity. One particular pathway of synthesising NPs is through phytonanotechnology which is the use of biomaterial to synthesis the NPs.
2024
Palamar, A. O. "Antimicrobial and antifungal activity of certain imidazole compounds". Thesis, БДМУ, 2021. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/18908.
Texto completo da fonteLe, Lay Céline. "Recherche de microorganismes antifongiques pour la réduction des risques de contaminations fongiques dans les produits de BVP et étude des molécules actives". Thesis, Brest, 2015. http://www.theses.fr/2015BRES0092/document.
Texto completo da fonteMolds are responsible for the spoilage of bakery products and thus, cause substantial economic losses. In this context, bioprotective cultures represent a growing interest as an alternative to chemical preservatives. The aims of the first part of this study was to evaluate the in vitro and in situ antifungal activity of lactic acid bacteria (LAB) and propionibacteria against five moulds species isolated from bakery products. The most inhibitorybacteria found during the in vitro test were evaluated in situ after surface spraying. In WFH medium, the most active LAB isolates belonged to the Lactobacillus plantarum, reuteri and buchneri groups. The most active strains were added directly during “pains au lait” preparation and differents strains present delayed effect in particular a strain of Leuconostoc citreum which seems to delay the growth of Penicillium corylophilum after 10 days. In the second part, supernatants were analyzed to identified and quantified antifungal compounds by different treatments and different methods like HPLC, mass spectrometry. The results suggested that organic acids played the most important role in the antifungal activity and show that the main antifungal compounds corresponded to lactic, acetic and propionic acids, ethanol and hydrogen peroxide, as well as other compounds present at low levels. Based on these results, various combinations of the identified compounds were used to evaluate their effect on spore germination and fungal growth of P. corylophilum and E. repens. Some combinations presented the same activity than the bacterial culture supernatant thus confirming the involvement of the molecules in the antifungal activity. The results suggested that acetic acid was responsible of the entire antifungal activity against Penicillium corylophilum and played an important role in Eurotium repens inhibition. The selected bacteria provide a future prospect for use as bioprotective cultures on bakery products
Marija, Mojićević. "Antifungalni potencijal streptomiceta izolovanih iz rizosfera medicinski značajnih biljaka: karakterizacija i optimizacija biosinteze staurosporina, produkta metabolizma Streptomyces sp. BV410". Phd thesis, Univerzitet u Novom Sadu, Tehnološki fakultet Novi Sad, 2019. https://www.cris.uns.ac.rs/record.jsf?recordId=111226&source=NDLTD&language=en.
Texto completo da fonteDifferent soils are still a source of remarkable microbial diversitywhich also reflects in the unexplored chemical diversity. Recentadvances in assessment of microbial diversity from soil haverevealed the extraordinarily rich biosynthetic potential for theproduction of new natural products among different microbialstrains, especially within the group of Actinobacteria. Amongbacterial soil isolates, representatives of Streptomyces genus arethe most prolific producers of bioactive compounds. One of theobjectives of the present study was to isolate Streptomyces spp.from the rhizosphere soils of three ethno-medicinal plantscollected in Serbia (Papaver rhoeas, Matricaria chamomilla, andUrtica dioica) and to screen their antifungal activity againstCandida spp. Morphologically different sporulating isolates (103in total) were collected from rhizosphere soil samples anddetermined as Streptomyces spp. Two different media and twoextraction procedures were used to induce the production andfacilitate identification of antifungals. Overall, 412 crude cellextracts were tested against Candida albicans using diskdiffusion assays, with 42% (43/103) of the strains showing theability to produce antifungal agents. Also, extracts inhibitedgrowth of other important human pathogens: Candida krusei,Candida parapsilosis, and Candida glabrata. Based on theestablished degree and range of antifungal activity, nine isolateswere selected for further testing. Their ability to inhibit Candidagrowth in liquid culture, to inhibit biofilm formation, and todisperse pre-formed biofilms was assessed with activeconcentrations from 8 to 250 pg/ml. High-performance liquidchromatographic profiles of extracts derived from selectedstrains were recorded, revealing moderate metabolic diversity.The most potent extracts were subjected to comprehensiveidentification and structural characterization of antifungalcompounds. Applying a bioactivity-guided isolation approach,active compounds of three extracts were separated, and basedon NMR structure elucidation it was shown that activecompounds were genistein, daidzein and staurosporine.Genistein and daidzein, soy phytoestrogens, are known to inhibitkey enzymes in the steroid metabolism pathway and werecoming from the fermentation medium containing soy flower.Since isolated Streptomyces spp. showed good ability to extractthese molecules from complex medium, they can be furtherconsidered for biotechnological production of thesephytoestrogens. One of the isolates, Streptomyces sp. BV410,was characterized as an efficient staurosporine producer.Staurosporine is a potent inhibitor of protein kinases and isconsidered in anticancer therapy. The biotechnologicalproduction of staurosporine by strain BV410 was optimized toyield 36.94 mg/l after 14 days of incubation in soy flowerglucose-starch-mannitol based fermentation medium (JS).Further optimization of medium for biosynthesis ofstaurosporine indicated the following optimal values of theexamined factors: the content of glucose of 20 g/l, starch 0.36g/l, mannitol 21.46 g/l, soy flower 17.32 g/l. By applying thedefined optimal values and using the appropriate mathematicalmodels, the following responses were predicted: concentrationof staurosporine 46.88 mg/l and biomass yield 12.05 mg/ml. Thevalidity of the results was confirmed by performing thebiosynthesis of the staurosporine in the medium with optimalcomposition (JSSta). Kinetics of staurosporine and biomassproduction and carbon source consumption were examined andprocess models were developed. Additionally, optimization ofstaurosporine production was performed with differentsupplements which, according to literature data, had stimulativeeffect on secondary metabolism (Zn, Fe and P salts, methyloleate, grape seed oil). In order to improve the production ofstaurosporine, effects of pH (6.5, 7.5 and 8.5) and incubation time(7, 10 and 14 days) were also examined. It was found thataddition of FeS04 significantly improved the staurosporine yieldin comparison to the starting conditions (increase of 25%). Ourresults proved that rhizosphere soils of ethno-medicinal plantsare a prolific source of streptomycetes, producers of compoundswith good antifungal activity. Isolation of the new staurosporineproducing strain, allowed for its detailed bioactivity assessment.Staurosporine scaffold might serve as a lead structure for thedevelopment of new antifungal and antiangiogenic agents. Also,results obtained within this research represent the basis for thefurther scale-up and potential industrialization of the proposedproduction process.
Ta, Chieu Anh Kim. "Bacterial Biofilm Inhibition and Antifungal Activity of Neotropical Plants". Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32419.
Texto completo da fonteLivros sobre o assunto "Antifungal activiy"
Gifford, Jennifer Ann. Antifungal activity of trihalogenmethylthio compounds in controlled release paints. Birmingham: University of Birmingham, 1994.
Encontre o texto completo da fontePaola, Bonsi, ed. Up to date review of toxicological data of some plant volatiles with antifungal activity. Roma: Istituto superiore di sanità, 1999.
Encontre o texto completo da fonteJohnson, Elizabeth M. Antifungal susceptibility testing and resistance. Editado por Christopher C. Kibbler, Richard Barton, Neil A. R. Gow, Susan Howell, Donna M. MacCallum e Rohini J. Manuel. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198755388.003.0047.
Texto completo da fonteEstes, Lynn L., e John W. Wilson. Antimicrobials. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0412.
Texto completo da fonteMathew, Jiby John, Nissy Mary Joseph, Sajeshkumar N. K, P. E. Sreejith e M. Sabu. Green Synthesis of Copper and Zinc Nanoparticles from Plant Extracts and Evaluation of Their Antifungal Activity Against Fusarium Oxysporum Cubense: An Overview. Independently Published, 2019.
Encontre o texto completo da fonteWalton, Katherine E., e Sally Ager. Antimicrobial agents. Editado por Rob Pickard. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0002.
Texto completo da fonteCapítulos de livros sobre o assunto "Antifungal activiy"
Ryley, John F., e Keith Barrett-Bee. "Screening for Antifungal Activity". In Emerging Targets in Antibacterial and Antifungal Chemotherapy, 546–67. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3274-3_21.
Texto completo da fonteSingaraj, Ranjani, Thenmozhli Geetha Saravanan, Kishore Kumar Annamalai, Abirami Baskaran, Radhakrishnan Manikkam, Gopikrishnan Venugopal e Balagurunathan Ramasamy. "Antifungal Activity of Postbiotics". In Methods and Protocols in Food Science, 195–200. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3421-9_27.
Texto completo da fonteGómez-Serranillos, María Pilar, Olga María Palomino, María Teresa Ortega e María Emilia Carretero. "Recent Advances on Medicinal Plants with Antifungal Activity". In Antifungal Metabolites from Plants, 167–220. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38076-1_6.
Texto completo da fonteAbbink, J., M. Plempel e D. Berg. "Expression of Keratinolytic Activity by Trichophyton mentagrophytes". In Advances in Topical Antifungal Therapy, 21–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71717-8_3.
Texto completo da fonteRoddick, James G. "Antifungal Activity of Plant Steroids". In ACS Symposium Series, 286–303. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0325.ch018.
Texto completo da fonteYap, M. C. H., B. A. Dreikorn, L. N. Davis, R. G. Suhr, S. V. Kaster, N. V. Kirby, G. Paterson, P. R. Graupner e W. R. Erickson. "4-Arylalkoxyquinazolines with Antifungal Activity". In ACS Symposium Series, 258–72. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch026.
Texto completo da fonteWang, Jianpeng. "Biological Active Antifungal Peptides". In Springer Theses, 15–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-53399-4_2.
Texto completo da fonteBullerman, Lloyd B., Marketa Giesova, Yousef Hassan, Dwayne Deibert e Dojin Ryu. "Antifungal activity of sourdough bread cultures". In Advances in Experimental Medicine and Biology, 307–16. Boston, MA: Springer US, 2006. http://dx.doi.org/10.1007/0-387-28391-9_20.
Texto completo da fonteGhahramani, Yasmin, Pardis Abolghasemi, Seyyed Mojtaba Mousavi, Seyyed Alireza Hashemi, Wei-Hung Chiang e Chin Wei Lai. "Antifungal Activity of Graphene-Based Nanomaterials". In Encyclopedia of Green Materials, 1–13. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-4921-9_71-1.
Texto completo da fonteKirubakari, Balasupramaniam, Shanmugapriya, Thiagarajan Sangeetha, Soundararajan Vijayarathna, Yeng Chen, Jagat R. Kanwar, Chiuan Herng Leow et al. "Antibacterial and Antifungal Agents of Higher Plants". In Natural Bio-active Compounds, 493–508. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7154-7_16.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Antifungal activiy"
Guo, Zhanyong, Ronge Xing, Huahua Yu, Song Liu e Pengcheng Li. "Antifungal Activity of Quaternized Carboxymethyl Chitosan". In 2008 2nd International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2008. http://dx.doi.org/10.1109/icbbe.2008.305.
Texto completo da fonteMangalagiu, Violeta, Dumitrela Diaconu e Ionel Mangalagiu. "Quinoline - sulfonamide - complexes with antimicrobial activity". In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab26.
Texto completo da fonteLiu, Junang, Gouying Zhou, Aixian Jin e Yuanhao He. "Antifungal Activity of Chitosan Against Colletotrichum Gloeosporioides". In 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2009). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5162373.
Texto completo da fonteMichnová, Hana, Šárka Pospíšilová, Ewelina Spaczynska, Wioleta Cieslik, Alois Čížek, Robert Musiol e Josef Jampílek. "Antibacterial and Antifungal Activity of Styrylquinoline Derivatives". In 4th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05588.
Texto completo da fonteRoldi, Larissa Lopes, Sandro José Greco, Valdemar Lacerda Júnior, Reginaldo Bezerra dos Santos e Eustáquio V. R. de Castro. "Synthesis of new naphthoquinones with antifungal activity." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0296-2.
Texto completo da fonteDolezal, Martin, Josef Jampilek, Jiri Kunes e Vladimir Buchta. "Quinaldine Derivatives Preparation and Their Antifungal Activity". In The 8th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01976.
Texto completo da fonte"Antifungal Activity of Seaweed Agains Aspergillus flavus". In International Seminar of Research Month Science and Technology for People Empowerment. Galaxy Science, 2019. http://dx.doi.org/10.11594/nstp.2019.0202.
Texto completo da fonteCardoso, Joana, Joana Freitas-Silva, Fernando Durães, Madalena Pinto, Emília Sousa e Eugénia Pinto. "Synthesis and Antifungal Activity of Thioxanthone Derivatives". In ECMC 2022. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecmc2022-13478.
Texto completo da fonteRogozin, E. "Biotechnology for production of recombinant hybrid proteins from plants and microbes with antifungal activity". In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.206.
Texto completo da fonteMangalagiu, Violeta, Dumitrela Diaconu, Costel Moldoveanu, Gheorghita Zbancioc, Ramona Danac, Dorina Amariucai-Mantu, Vasilichia Antoci e Ionel Mangalagiu. "Hybrid and chimeric nitrogen heterocycles with biological activity". In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab01.
Texto completo da fonteRelatórios de organizações sobre o assunto "Antifungal activiy"
Sikes, A., T. Yang, M. Richardson e R. Ehioba. Antifungal Activity of Volatile Oil of Mustard (VOM). Fort Belvoir, VA: Defense Technical Information Center, março de 2005. http://dx.doi.org/10.21236/ada430743.
Texto completo da fonteNemska, Veronica, Nelly Georgieva, Jeny Miteva-Staleva, Ekaterina Krumova e Svetla Danova. Antifungal Activity of Lactobacillus spp. from Traditional Bulgarian Dairy Products. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, dezembro de 2019. http://dx.doi.org/10.7546/crabs.2019.12.10.
Texto completo da fontePrusky, Dov, Noel Keen e John Browse. Modulation of the synthesis of the main preformed antifungal compound as abasis for the prevention of postharvest disease of C. gloeosporioides in avocado fruits. United States Department of Agriculture, dezembro de 2001. http://dx.doi.org/10.32747/2001.7575273.bard.
Texto completo da fontePrusky, Dov, Noel Keen e Rolf Christoffersen. Involvement of Epicatechin in the Regulation of Natural Resistance of Avocado Fruit against Postharvest Pathogens. United States Department of Agriculture, janeiro de 1997. http://dx.doi.org/10.32747/1997.7613028.bard.
Texto completo da fonteCytryn, E., Sean F. Brady e O. Frenkel. Cutting edge culture independent pipeline for detection of novel anti-fungal plant protection compounds in suppressive soils. Israel: United States-Israel Binational Agricultural Research and Development Fund, 2022. http://dx.doi.org/10.32747/2022.8134142.bard.
Texto completo da fontePrusky, Dov, Noel T. Keen e Stanley Freeman. Elicitation of Preformed Antifungal Compounds by Non-Pathogenic Fungus Mutants and their Use for the Prevention of Postharvest Decay in Avocado Fruits. United States Department of Agriculture, janeiro de 1996. http://dx.doi.org/10.32747/1996.7570573.bard.
Texto completo da fonteMevarech, Moshe, Jeremy Bruenn e Yigal Koltin. Virus Encoded Toxin of the Corn Smut Ustilago Maydis - Isolation of Receptors and Mapping Functional Domains. United States Department of Agriculture, setembro de 1995. http://dx.doi.org/10.32747/1995.7613022.bard.
Texto completo da fonteThomashow, Linda, Leonid Chernin, Ilan Chet, David M. Weller e Dmitri Mavrodi. Genetically Engineered Microbial Agents for Biocontrol of Plant Fungal Diseases. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7696521.bard.
Texto completo da fonteAnnunziato, Dominick. HPLC Sample Prep and Extraction SOP v1.3 for Fungi. MagicMyco, agosto de 2023. http://dx.doi.org/10.61073/sopv1.3.08.11.2023.
Texto completo da fonteWatad, Abed A., Paul Michael Hasegawa, Ray A. Bressan, Alexander Vainstein e Yigal Elad. Osmotin and Osmotin-Like Proteins as a Novel Source for Phytopathogenic Fungal Resistance in Transgenic Carnation and Tomato Plants. United States Department of Agriculture, janeiro de 2000. http://dx.doi.org/10.32747/2000.7573992.bard.
Texto completo da fonte