يعرض 1 - 20 نتائج من 71 نتيجة بحث عن '"Microorganismos fitopatógenos"', وقت الاستعلام: 0.73s تنقيح النتائج
  1. 1
    Dissertation/ Thesis

    المؤلفون: Pedro Jové, Roger de

    المساهمون: University/Department: Universitat de Barcelona. Departament de Genètica, Microbiologia i Estadística

    Thesis Advisors: Valls i Matheu, Marc

    المصدر: TDX (Tesis Doctorals en Xarxa)

    وصف الملف: application/pdf

  2. 2
    Dissertation/ Thesis
  3. 3
  4. 4
    Academic Journal
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  6. 6
  7. 7
  8. 8
  9. 9
    Conference

    Relation: XX Congreso Nacional de la Sociedad Española de Fitopatología; Valencia; 24 a 26 de octubre de 2022; Tienda et al., 2021. La producción de gránulos de polihidroxialcanoatos por Pseudomonas chlororaphis PCL1606 tiene un papel durante la interacción con la rizosfera del aguacate. Póster 018, Libro de resúmenes del XX Congreso Nacional de la SEF, pg. 131; https://hdl.handle.net/10630/25365

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  11. 11
  12. 12
    Conference
  13. 13
    Academic Journal
  14. 14
  15. 15
    Book
  16. 16
    Academic Journal
  17. 17
    Academic Journal
  18. 18

    المساهمون: Fabio Ancizar, Aristizabal Gutierrez, Diego Mauricio, Riaño Pachón, Bioprocesos y bioprospección - Linea Caucho Natural, Laboratório de Biologia Computacional, Evolutiva e de Sistemas (LabBCES) Centro de Energia Nuclear na Agricultura (CENA)

    المصدر: Repositorio UN
    Universidad Nacional de Colombia
    instacron:Universidad Nacional de Colombia

    وصف الملف: xx, 164 páginas; application/pdf

  19. 19
    Dissertation/ Thesis

    المؤلفون: Mármol Calle, Mikaela Jazmín

    المساهمون: Chancusig, Francisco Hernán

    وصف الملف: 82 páginas

    Relation: Mármol Calle Mikaela Jazmín (2021); Diagnóstico de enfermedades producidas por hongos de los tres principales parques del espacio público de la ciudad de Latacunga 2021. UTC. Latacunga. 82 p.; PC-002139; http://repositorio.utc.edu.ec/handle/27000/8298

  20. 20
    Dissertation/ Thesis

    المساهمون: Fabio Ancizar, Aristizabal Gutierrez, Diego Mauricio, Riaño Pachón, Bioprocesos y bioprospección - Linea Caucho Natural, Laboratório de Biologia Computacional, Evolutiva e de Sistemas (LabBCES) Centro de Energia Nuclear na Agricultura (CENA)

    وصف الملف: xx, 164 páginas; application/pdf

    Relation: • Akinsanmi, O and Carvalhais L. (2020) Draft Genome of the Macadamia Husk Spot Pathogen, Pseudocercospora macadamiae. Phytopathology. 110:1503-1506 https://doi.org/10.1094/PHYTO-12-19-0460-A • Albera S. (2016). Biotrophic Fungi Infection and Plant Defense Mechanism. Journal of Plant Pathology & Microbiology, 7(9), 1–6. • Alic, A., Ruzafa, D., Dopazo, J., Blanquer, I. (2016). Objective review of de novo stand-alone error correction methods for NGS data. Wiley Interdisciplinary Reviews: Computational Molecular Science, 6(2), 111–146. doi:10.1002/wcms.1239 • Altschul, S.F., Gish, W., Miller, W., Myers, E.W. & Lipman, D.J. (1990) "Basic local alignment search tool." J. Mol. Biol. 215:403-410. • Andrews S. (2010). FastQC: a quality control tool for high throughput sequence data. Available online at: http://www.bioinformatics.babraham.ac.uk/projects/fastqc • Angelo, S., Yamagishi, B., Cruz, C., Silva, G, & Gasparotto, L. (2020). Differential expression and structural polymorphism in rubber tree genes related to South American leaf blight resistance. Physiological and Molecular Plant Pathology, 110, 101477. doi:10.1016/j.pmpp.2020.101477 • Asai, S., & Shirasu, K. (2015). Plant cells under siege: plant immune system versus pathogen effectors. Current Opinion in Plant Biology, 28, 1–8. doi:10.1016/j.pbi.2015.08.008 • Auyong, S. (2015). The Role of Cutinase and its Impact on Pathogenicity of Colletotrichum truncatum. Journal of Plant Pathology & Microbiology, 06(03). https://doi.org/10.4172/2157-7471.1000259 • Bakhshi, Marzanlou, M., Babai-Ahari, A., Groenewald, J., Crous, P. (2014). Multi-gene analyses of Pseudocercospora spp. from Iran. Phytotaxa 184: 245 – 264 • Ballester, A., Marcet-Houben, M., Levin, E., Sela, N., Selma-Lázaro, C., Carmona, L., Wisniewski, M., Droby, S., González, L., Gabaldón, T. (2015). Genome, Transcriptome, and Functional Analyses of Penicillium expansum Provide New Insights Into Secondary Metabolism and Pathogenicity. Molecular Plant-Microbe Interactions, 28(3), 232–248. doi:10.1094/MPMI-09-14-0261-FI • Bankevich, A., Nurk, S., Antipov, D., Gurevich, A., Dvorkin, M., Kulikov, A. S., Lesin, V., Nikolenko, S., Pham S., Prjibelski A., Pyshkin A., Sirotkin A., Vyahhi N., Tesler G., Alekseyev M. A., Pevzner, P. A. (2012). SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing. Journal of Computational Biology • Bao, W., Kojima, K., Kohany, O. (2015). Repbase Update, a database of repetitive elements in eukaryotic genomes. Mob DNA. 2015;6(1):11. Available from: http://www.mobilednajournal.com/content/6/1/11. • Bayry, A., Guijarro, J., Sunde, M., Latgé, J. (2012) Hydrophobins Unique Fungal In Biological Adhesives Vol. 107, pp. 25–55 • Beacham, G. M., Partlow, E. A., Lange, J. J., & Hollopeter, G. (2018). NECAPs are negative regulators of the AP2 clathrin adaptor complex. ELife, 7. https://doi.org/10.7554/eLife.32242 • Beckerman, L., and Ebbole, D. (1996). MPG1, a gene encoding a fungal hydrophobin of Magnaporthe grisea, is involved in surface recognition. Mol. Plant-Microbe Interact. 9:450-456. • Bedre, R., Avila, C., Mandadi, K. (2021). HTSeqQC: A Flexible and One-Step Quality Control Software for High-throughput Sequence Data Analysis. BioRxiv https://doi.org/10.1101/2020.07.23.214536 • Benavidez. T, Jaron. K Schatz. Michael . (2020). GenomeScope 2.0 and Smudgeplot for reference- free profiling of polyploid genomes NATURE COMMUNICATIONS (2020)11:1432:https://doi.org/10.1038/s41467-020-14998-3 • Berlin, K., Koren, S., Chi, X., Drake, J., Landolin, J.,Phillippy, A (2015). Assembling large genomes with single-molecule sequencing and locality-sensitive hashing Nature Biotechnology 33, 623–630 • Bigeard, J., Colcombet, J., Heribert, H. (2015). Signaling Mechanisms in Pattern-Triggered Immunity (PTI). Molecular Plant 8, 521–539 • Blackwell, M. (2011). The Fungi: 1, 2, 3.5.1 million species? American Journal of Botany 98:426-438 • Blango, M., Kniemeyer, O., Brakhage, A., Sheppard, D. (2019). Conidial surface proteins at the interface of fungal infections. PLOS Pathogens, 15(9), e1007939–. doi:10.1371/journal.ppat.1007939 • Blatzer, M., Binder, U., Haas, H. (2011). The metalloreductase FreB is involved in adaptation of Aspergillus fumigatus to iron starvation. , 48(11), 0–1033. doi:10.1016/j.fgb.2011.07.009 • Blin, K., Medema, M., Kazempour, D., Fischbach, M., Breitling, R., Takano, E., et al. (2013). antiSMASH 2.0 a versatile platform for genome mining of secondary metabolite producers. Nucleic Acids Res. 41(1), Pages 204-212. • Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014 Aug 1;30(15):2114-20. doi:10.1093/bioinformatics/btu170. • Boller, T., Yang, S. (2009). Innate immunity in plants: An arms race between pattern recognition receptors in plants and effectors in microbial pathogens. Science. May 8; 324(5928): 742–744. • Bolton, M., van Esse, R., Vossen, J., de Jonge, R et al. (2008). The novel Cladosporium fulvum lysin motif effector Ecp6 is a virulence factor with orthologues in other fungal species. Molecular Microbiology 69(1), 119–136 • Breen, J., Wicker, T., Kong, X., Zhang, J., Ma, W., Paux, E., et al. (2010). A highly conserved gene island of three genes on chromosome 3B of hexaploid wheat: diverse gene function and genomic structure maintained in a tightly linked block. BMC Plant Biol. 2010;10:98. Available from: http://www.ncbi.nlm.nih.gov/ pubmed/20507561. • Breen J, Wicker T, Kong X, Zhang J, Ma W, Paux E, et al. A highly conserved gene island of three genes on chromosome 3B of hexaploid wheat: diverse gene function and genomic structure maintained in a tightly linked block. BMC Plant Biol. 2010;10:98. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20507561 • Brown, A., Antoniw, J., & Hammond-Kosack, K. E. (2012). The Predicted Secretome of the Plant Pathogenic Fungus Fusarium graminearum: A Refined Comparative Analysis. PLoS ONE, 7(4), e33731. doi:10.1371/journal.pone.0033731 • Buermans, J., & Dunnen, T. (2014). Next generation sequencing technology: Advances and applications. BBA - Molecular Basis of Disease, 1842(10), 1932–1941. • Bushnell, B. (2014). BBMap: A Fast, Accurate, Splice-Aware-aligner. LBNL Department of Energy Joint Genome Institute, 2800 Mitchell Drive, Walnut Creek, USA. • Butler, E & Jones, S. (1949) Tomato Leaf Mould, Cladosporium fulvum Cooke. London: Macmillan. • Camargo, A.P., Marin, F.R., Camargo, M.B.P., 2003. Zoneamento Climático da Hevea no Brasil, Documento 24. Embrapa, Campinas, SP, ISSN 0103-78110. • Cantarel, L., Coutinho, M., Rancurel, C., Bernard, T., Lombard,V., Henrissat,B. (2009) The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics. Nucleic Acids Res., 37, D233–D238. • Capella, S., Silla, J., Gabaldón, T. (2009). trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics. 25(15): Pages 1972- 3. • Casadevall, A., Rosas, L., Nosanchuk, D. (2000). Melanin and virulence in Cryptococcus neoformans. Curr Opin Microbiol. 2000 Aug;3(4):354-8. doi:10.1016/s1369-5274(00)00103-x. PMID: 10972493. • Casadevall, A. (2007).Determinants of virulence in the pathogenic fungi. Fungal Biol Rev. 2007 November; 28(5): 511–515 • Tudzynski, P & Sharon, A. (2003). Fungal Pathogenicity Genes. Applied Mycology and Biotechnology (Vol. 3, pp. 187–212). Elsevier. • Urban, M., Cuzick, A., Rutherford, K., Irvine, A., Helder, P., Pant, Ra., Sadanadan, V, Khamari, L., et al. (2017) PHI-base: a new interface and further additions for the multi-species pathogen–host interactions database, Nucleic Acids Research, Volume 45, Issue D1, January 2017, Pages D604–D610, https://doi.org/10.1093/nar/gkw1089 • Van Bel, M., Proost, S., Van Neste, C. et al. TRAPID: an efficient online tool for the functional and comparative analysis of de novoRNA-Seq transcriptomes. Genome Biol 14, R134 (2013). https://doi.org/10.1186/gb-2013-14-12-r134 • Venkatachalam, P., Geetha, N., Sangeetha, P., Thulaseedharan, A. (2013) Natural rubber producing plants: An overview. African J Biotechnol; 12: 1297–1310. https://doi.org/10.5897/AJBX12.016 • Viklund H, Elofsson A. Best alpha-helical transmembrane protein topology predictions are achieved using hidden Markov models and evolutionary information. Protein Sci. 2004;13(7):1908-1917. doi:10.1110/ps.04625404 • Vogel, J. (2008). Unique aspects of the grass cell wall. Current Opinion in Plant Biology; Curr Opin Plant Biol. https://doi.org/10.1016/j.pbi.2008.03.002 • Vurture, W. et al. GenomeScope: fast reference-free genome profiling from short reads. Bioinformatics 33, 2202–2204 (2017). • Walker, J., Abeel, T., Shea, T., Priest, M., Abouelleil, A., Sakthikumar, S., et al. (2014). Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome • Wang, H., Fewer, P., Holm, L., Rouhiainen, L., Sivonen, K. (2014). Atlas of nonribosomal peptide and polyketide biosynthetic pathways reveals common occurrence of non-modular enzymes. Proceedings of the National Academy of Sciences, 111(25), 9259–9264. doi:10.1073/pnas.1401734111 • Wang, Z., Lienemann, M., Qiau, M., Linder, M. (2010). Mechanisms of Protein Adhesion on Surface Films of Hydrophobin. Langmuir, 26(11), 8491–8496. doi:10.1021/la101240e • Warren, L., Yang, C., Vandervalk, P. et al. (2015). LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads. GigaSci 4, 35 . https://doi.org/10.1186/s13742-015-0076-3 • Warris, A., & Ballou, E. R. (2019). Oxidative responses and fungal infection biology. Seminars in Cell & Developmental Biology, 89, 34-46. https://doi.org/10.1016/j.semcdb.2018.03.004 • Waterhouse, A., Procter, J., Martin, D., Clamp, M., Barton, G. (2009). Jalview Version 2-a multiple sequence alignment editor and analysis workbench. Bioinformatics 25: Pages 1189-1191. • Webster, J., & Weber, R., (2007). Introduction to fungí. Cambridge – United Kingdom.http://www.dbbe.fcen.uba.ar/contenido/objetos/webster 30521807395_1400021643840195.pd • Wenger, M., Peluso, P., Rowell, W. J., Chang, P.-C., Hall, R. J., Concepcion, G. T., Hunkapiller, M. W. (2019). Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome. Nature Biotechnology. doi:10.1038/s41587-019-0217-9 • White, T., Bruns, T., Lee, S. & Taylor, J. (1990). Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR protocols a guide to methods and applications Academic Press. • Wicker, T., Oberhaensli, S., Parlange, F., Buchmann, J., Shatalina, M., Roffler, S., Ben-David, R., Doležel, J., Šimková, H., Schulze-Lefert, P., Spanu, P., Bruggmann, R., Amselem, J., Quesneville, H., et al (2013). The wheat powdery mildew genome shows the unique evolution of an obligate biotroph. Nature Genetics, 45(9), 1092–1096. doi:10.1038/ng.2704 • Wicker, T., Sabot, F., Hua-Van, A., Bennetzen, J., Capy, P., Chalhoub, B., Flavell, A., Leroy, P., Morgante, M., Panaud, O. (2007). A unified classification system for eukaryotic transposable elements. , 8(12), 973–982. doi:10.1038/nrg2165 • Wit, P. J. G. M. de, Burgt, A. van der, Ökmen, B., Stergiopoulos, I., Abd-Elsalam, K. A., Aerts, A. L., Bahkali, A. H., Beenen, H. G., Chettri, P., Cox, M. P., Datema, E., Vries, R. P. de, Dhillon, B., Ganley, A. R., Griffiths, S. A., Guo, Y., Hamelin, R. C., Henrissat, B., Kabir, M. S., … Bradshaw, R. E. (2012). The Genomes of the Fungal Plant Pathogens Cladosporium fulvum and Dothistroma septosporum Reveal Adaptation to Different Hosts and Lifestyles But Also Signatures of Common Ancestry. PLOS Genetics, 8(11), e1003088. https://doi.org/10.1371/journal.pgen.1003088 • Xu, Z., Wang, H. (2007). LTR-FINDER: an efficient tool for the prediction of full-length LTR retrotransposons. Nucleic Acids Res. 2007;35 • Yamashita, S., Takahashi, S. (2020). Molecular Mechanisms of Natural Rubber Biosynthesis. Annu Rev Biochem, 2020 89:1, 821-851 • Yandell, M., & Ence, D. (2012). A beginner’s guide to eukaryotic genome annotation. Nature Reviews Genetics, 13(5), 329–342. doi:10.1038/nrg3174 • Yeadon, P. J., and D. E. Catcheside. 1995. Guest: a 98 bp inverted repeat transposable element in Neurospora crassa. Mol. Gen. Genet. 247:105–109. • Yin, Y., Mao, X., Yang, J., Chen, X., Mao, F., Xu, Y. (2012). dbCAN: a web resource for automated carbohydrate- active enzyme annotation. Nucleic Acids Res. 40(Web Server issue): Pages 445–W51. • Zaccaron, A. Z., & Stergiopoulos, I. (2020). First Draft Genome Resource for the Tomato Black Leaf Mold Pathogen Pseudocercospora fuligena. Molecular Plant-Microbe Interactions. https://doi.org/10.1094/MPMI-06-20-0139-A • Zhang, C., Maryam R., Erfan S., Siavash, M. (2018). “ASTRAL-III: Polynomial Time Species Tree Reconstruction from Partially Resolved Gene Trees.” BMC Bioinformatics 19 (S6): Page 153. • Zhang, D., He, J., Haddadi, P., Zhu, j., Yang, Z., Ma, L. (2018). Genome sequence of the potato pathogenic fungus Alternaria solani HWC-168 reveals clues for its conidiation and virulence. BMC Microbiology, 18(1), 176–. doi:10.1186/s12866-018-1324-3 • Zhang, G., Zhang, Q., Zhou, D., Short, L., Wang G., Ma J., Li, F., Kong, T., Wang Z., et al (2017). A Verticillium dahliae Extracellular Cutinase Modulates Plant Immune Responses. Molecular Plant-Microbe Interactions. https://doi.org/10.1094/MPMI-06-17-0136-R • Zhang, H., Jain, C., & Aluru, S. (2020). A comprehensive evaluation of long read error correction methods. BMC Genomics, 21(S6). doi:10.1186/s12864-020-07227-0 • Zhang, H., Yohe, T., Huang, L., Entwistle, S., Wu, P., Yang, Z., Busk, P., Xu, Y., Yin, Y. (2018). dbCAN2: a meta server for automated carbohydrate-active enzyme annotation. Nucleic Acids Research, –. doi:10.1093/nar/gky418 • Zhang, N., Luo, J., Bhattacharya, D. (2017).Advances in Fungal Phylogenomics and Their Impact on Fungal Systematics. Advances in Genetics, Volume 100. ISSN 0065-2660 • Zhang, Q., Arbuckle, J., and Wessler, S.(2000). Recently extensive and preferential insertion of members of the miniature inverted-repeat transposable element family Heartbreaker (Hbr) into genic regions of maize. Proc. Natl. Acad. Sci. USA 97:1160 – 1165. • Zhao, C., Waalwijk, C., de Wit, P. J. G. M., Tang, D., & van der Lee, T. (2013). RNA-Seq analysis reveals new gene models and alternative splicing in the fungal pathogen Fusarium graminearum. BMC Genomics, 14(1), 21. doi:10.1186/1471-2164-14-21 • Zhao, Z., Liu, H., Wang, C., & Xu, J.-R. (2013). Comparative analysis of fungal genomes reveals different plant cell wall degrading capacity in fungi. BMC Genomics, 14(1), 1-15. https://doi.org/10.1186/1471-2164-14-274 • Zhong, Z., Marcel, TC., Hartmann. E., Ma, X., Plissonneau, C., Zala, M., Ducasse, A., Confais, J., Compain, J., Lapalu, N. et al. (2017) A small secreted protein in Zymoseptoria tritici is responsible for avirulence on wheat cultivars carrying the Stb6 resistance gene. • Žifčáková, L., & Baldrian, P. (2012). Fungal polysaccharide monooxygenases: new players in the decomposition of cellulose. Fungal Ecology, 5(5), 481–489. doi:10.1016/j.funeco.2012.05.001 • Zimin, V., Marçais, G., Puiu, D., Roberts, M., Salzberg SL., Yorke, A. (2013). The MaSuRCA genome assembler. Bioinformatics;29:2669–77. • Zipfel, C. (2008). Pattern-recognition receptors in plant innate immunity. Current Opinion in Immunology, 20, 10-16. • Zipfel, C. & Felix, G. (2005). Plants and animals: a different taste for microbes? Current Opinion in Plant Biology, 8, 353-360.; https://repositorio.unal.edu.co/handle/unal/80147; Universidad Nacional de Colombia; Repositorio Institucional Universidad Nacional de Colombia; https://repositorio.unal.edu.co/