يعرض 1 - 20 نتائج من 113 نتيجة بحث عن '"Caracteres cuantitativos"', وقت الاستعلام: 0.56s تنقيح النتائج
  1. 1
    Dissertation/ Thesis

    المؤلفون: Garrido Martín, Diego

    المساهمون: University/Department: Universitat Pompeu Fabra. Departament de Ciències Experimentals i de la Salut

    Thesis Advisors: Guigó Serra, Roderic, Calvo, Miquel (Calvo Llorca)

    المصدر: TDX (Tesis Doctorals en Xarxa)

    وصف الملف: application/pdf

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    Academic Journal
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    Academic Journal
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    Dissertation/ Thesis

    المؤلفون: Pérez Vega, Elena

    Thesis Advisors: Escuela Superior y Tecnica de Ingenieria Agraria, Otros, Ferreira Fernández, Juan José, Giráldez Ceballos-Escalera, Ramón

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    Academic Journal
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    Academic Journal
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    Conference

    المساهمون: Universidad Politécnica de Cartagena

    وصف الملف: application/pdf

    Relation: Zarid, Mohamed.; Esteras, C.; Sifres, A.G.; Cañizares, X.; Belén Picó, M.; Monforte Gilabert, Antonio José; Fernández Trujillo, Juan Pablo. Mayor expresión de dos genes en una línea de melón casi isogénica versus su parental durante la maduración. En: Proceedings of the 7th Workshop on agri-food research: WiA.18. Cartagena: Universidad Politécnica de Cartagena, CRAI Biblioteca, 2019. Pp. 14-17. ISBN: 978-84-16325-89-4; http://hdl.handle.net/10317/11100

  11. 11
    Conference

    المساهمون: Universidad Politécnica de Cartagena

    وصف الملف: application/pdf

    Relation: Zarid, Mohamed; Esteras, C.; Gemma Sifres, A.; Cañizares, X.; Esteva Pascual, JuanBelén Picó, M.; Monforte Gilabert, Antonio José; Fernández Trujillo, Juan Pablo. Expresión génica y producción de volátiles durante la maduración del melón. En: Proceedings of the 6th Workshop on agri-food research: WiA.17. Cartagena: Universidad Politécnica de Cartagena, CRAI Biblioteca, 2018. Pp. 27-30. ISBN: 978-84-16325-64-1; http://hdl.handle.net/10317/11044

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    Academic Journal
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    Academic Journal

    المصدر: Acta Biológica Colombiana; Vol. 23 Núm. 1 (2018); 5-16 ; Acta Biológica Colombiana; Vol. 23 No. 1 (2018); 5-16 ; 1900-1649 ; 0120-548X

    وصف الملف: application/pdf; application/xml

    Relation: https://revistas.unal.edu.co/index.php/actabiol/article/view/66487/pdf_23%281%29_art1; https://revistas.unal.edu.co/index.php/actabiol/article/view/66487/65740; Afzal AJ, Wood AJ, Lightfoot DA. Plant receptor-like serine threonine kinases: roles in signaling and plant defense. Mol Plant Microbe Interact. 2008;21:507-517. Doi:10.1094/MPMI-21-5-0507.; Ansorge WJ. Next-generation DNA sequencing techniques. New biotechnology. 2009;25:195-203. Doi:10.1016/j.nbt.2008.12.009.; Araus JL, Cairns JE. Field high-throughput phenotyping: the new crop breeding frontier. Trends Plant Sci. 2014;19:52-61. Doi:10.1016/j.tplants.2013.09.008; Arruda MP, Brown P, Brown-Guedira G, Krill A, Thurber C, Merrill K, Foresman B, Kolb F. Genome-wide association mapping of fusarium head blight resistance in wheat using genotyping-by-sequencing. The Plant Genome. 2016;9(1). Doi:10.3835/plantgenome2015.04.0028; Baker NR. Chlorophyll fluorescence: a probe of photosynthesis in vivo. Annu Rev Plant Biol. 2008;59:89-113. Doi:10.1146/annurev.arplant.59.032607.092759; Basu PS, Srivastava M, Singh P, Porwal P, Kant R, Singh J. High-precision phenotyping under controlled versus natural environments. In. Phenomics in Crop Plants: Trends, Options and Limitations. Springer: India; 2015. p. 27-40.; Bauriegel E, Herppich WB. Hyperspectral and chlorophyll fluorescence imaging for early detection of plant diseases, with special reference to Fusarium spec. infections on wheat. Agriculture 2014;4:32-57. Doi:10.3390/agriculture4010032; Benson JM, Poland JA, Benson BM, Stromberg EL, Nelson RJ. Resistance to gray leaf spot of maize: genetic architecture and mechanisms elucidated through nested association mapping and near-isogenic line analysis. PLoS Genet. 2015;11(13):e1005045. Doi:10.1371/journal.pgen.1005045; Bonierbale MW, Plaisted RL, Tanksley SD. RFLP maps based on a common set of clones reveal modes of chromosomal evolution in potato and tomato. Genetics. 1988;120:1095-103.; Bozsó Z, Maunoury N, Szatmari A, Mergaert P, Ott P, Zsíros L, Szabó E, Kondorosi E, Klement Z. Transcriptome analysis of a bacterially induced basal and hypersensitive response of Medicago truncatula. Plant Mol Biol. 2009;70(6):627-46. Doi:10.1007/s11103-009-9496-8; Bozso Z, Ott PG, Kaman-Toth E, Bognar GF, Pogany M, Szatmari A. Overlapping yet response-specific transcriptome alterations characterize the nature of tobacco-Pseudomonas syringae interactions. Front. Plant Sci. 2016;7(251). Doi:10.3389/fpls.2016.00251; Brachi B, Morris GP, Borevitz JO. Genome-wide association studies in plants: the missing heritability is in the field. Genome Biol. 2011;12(10):232. Doi:10.1186/gb-2011-12-10-232; Brun H, Chèvre AM, Fitt BD, Powers S, Besnard A, Ermel L, Huteau V, et al. Quantitative resistance increases the durability of qualitative resistance to Leptosphaeria maculans in Brassica napus. New Phytol. 2010;185(1):285-99. 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Euphytica. 2005;142:169-196. Doi:10.1007/s10681-005-1681-5; Cook DE, Mesarich CH, Thomma BP. Understanding plant immunity as a surveillance system to detect invasion. Annu Rev Phytopathol. 2015;53,541-563. Doi:10.1146/annurev-phyto-080614-120114; Corwin JA, Copeland D, Feusier J, Subedy A, Eshbaugh R, Palmer C, Maloof J, Kliebenstein D. The quantitative basis of the Arabidopsis innate immune system to endemic pathogens depends on pathogen genetics. PLoS Genet. 2016;12(2):e1005789. Doi:10.1371/journal.pgen.1005789; Cui H, Tsuda K, Parker JE. Effector-triggered immunity: from pathogen perception to robust defense. Annu Rev Plant Biol. 2015;66:487-511. Doi:10.1146/annurev-arplant-050213-040012; Chisholm ST, Coaker G, Day B, Staskawicz BJ. Host-microbe interactions: shaping the evolution of the plant immune response. Cell. 2006;124(4):803-814. Doi:10.1016/j.cell.2006.02.008; De Smet I, Voss U, Jurgens G, Beeckman T. Receptor-like kinases shape the plant. Nat Cell Biol. 2009;11(10):1166-1173. Doi:10.1038/ncb1009-1166; Dinesh-Kumar SP, Baker BJ. Alternatively spliced N resistance gene transcripts: their possible role in tobacco mosaic virus resistance. Proc Natl Acad Sci USA. 2000;97(4):1908-1913. Doi:10.1073/pnas.020367497; Druka A, Potokina E, Luo Z, et al. Exploiting regulatory variation to identify genes underlying quantitative resistance to the wheat stem rust pathogen Puccinia graminis f. sp. tritici in barley. Theor Appl Genet. 2008;117(2):261-272. Doi:10.1007/s00122-008-0771-x; El-Soda M, Malosetti M, Zwaan BJ, Koornneef M, Aarts MG. Genotype x environment interaction QTL mapping in plants: lessons from Arabidopsis. Trends Plant Sci. 2014;19(6):390-398. Doi:10.1016/j.tplants.2014.01.001; Falconer DS, Mackay TFC. Introduction to Quantitative Genetics London, UK: Prentice Hall; 1996. p. 56-70.; Flor HH. Host-parasite interaction in flax rust—Its genetics and other implications. Phytopathology. 1955;45:680–685. Doi:10.1016/S0065-2660(08)60498-8; Fu D, Uauy C, Distelfeld A, Blechl A, Epstein L, Chen Z, Sela H, et al. A kinase-START gene confers temperature-dependent resistance to wheat stripe rust. Science. 2009;23(5919):1357-1360. Doi:10.1126/science.1166289; Fukuoka S, Saka N, Koga H, Ono K, Shimizu T, Ebana K, Hayashi N, Takahashi A, Hirochika H, Okuno K, Yano M. Loss of function of a proline-containing protein confers durable disease resistance in rice. Science. 2009;325(5943):998-1001. Doi:10.1126/science.1175550; Gautami B, Foncéka D, Pandey MK, Moretzsohn M, Sujay V, Qin H, Hong Y. An international reference consensus genetic map with 897 marker loci based on 11 mapping populations for tetraploid groundnut (Arachis hypogaea L.). PLoS ONE. 2012;7(7):e41213. Doi:10.1371/journal.pone.0041213; Giannakopoulou A, Steele JF, Segretin ME, Bozkurt T, Zhou J, Robatzek S, Banfield M, Pais M, Kamoun S. Tomato I2 immune receptor can be engineered to confer partial resistance to the oomycete Phytophthora infestans in addition to the fungus Fusarium oxysporum. Mol Plant Microbe Interact. 2015;28(12):1316-1329. Doi:10.1094/MPMI-07-15-0147-R; Glazier AM, Nadeau JH, Aitman TJ. Finding genes that underlie complex traits. Science. 2002;298(5602):2345-2349. Doi:10.1126/science.1076641; Griffiths AJ. An introduction to genetic analysis. Macmillan. 2005. p. 61-67.; Gutiérrez L, Germán S, Pereyra S, Hayes PM, Pérez CA, Capettini F, Locatelli A, et al. Multi-environment multi-QTL association mapping identifies disease resistance QTL in barley germplasm from Latin America. Theor Appl Genet. 2015;128(3);501-516. Doi:10.1007%2Fs00122-014-2448-y; Heffner EL, Sorrells ME, Jannink J-L. Genomic selection for crop improvement. Crop Science. 2009;49(1):1-12. Doi:10.2135/cropsci2008.08.0512; Helentjaris T, Weber D, Wright S. Identification of the genomic locations of duplicate nucleotide sequences in maize by analysis of restriction fragment length polymorphisms. Genetics. 1988;118(2):353-363.; Hematy K, Hofte H. Novel receptor kinases involved in growth regulation. Curr Opin Plant Biol. 2008;11(3):321-328. Doi:10.1016/j.pbi.2008.02.008; Houterman PM, Ma L, Van Ooijen G, de Vroomen M, Cornelissen B, Takken F, Rep M. The effector protein Avr2 of the xylem-colonizing fungus Fusarium oxysporum activates the tomato resistance protein I-2 intracellularly. Plant J. 2009;58(6):970-978. Doi:10.1111/j.1365-313X.2009.03838.x; Huard-Chauveau C, Perchepied L, Debieu M, Rivas S, Kroj T, Kars I, Bergelson J, Roux F, Roby D. An atypical kinase under balancing selection bonfers broad-spectrum disease resistance in Arabidopsis. PLoS Genet. 2013;9(9):e1003766. Doi:10.1371/journal.pgen.1003766; Iquira E, Humira S, François B. Association mapping of QTLs for sclerotinia stem rot resistance in a collection of soybean plant introductions using a genotyping by sequencing (GBS) approach. BMC Plant Biol. 2015;15(1):5. Doi:10.1186/s12870-014-0408-y; Johnson R. Genetic Background of Durable Resistance. In: Lamberti F, Waller JM, Graaff NA, editors. Durable Resistance in Crops. Boston, MA: Springer New York; 1983. p. 5-26.; Jones JD, Dangl JL. The plant immune system. Nature. 2006;444(7117):323. Doi:10.1038/nature05286; Kou Y, Wang S. Broad-spectrum and durability: understanding of quantitative disease resistance. Curr Opin Plant Biol. 2010;13(2):181-185. Doi:10.1016/j.pbi.2009.12.010; Krattinger SG, Lagudah ES, Spielmeyer W, Singh RP, Huerta-Espino J, McFadden H, Bossolini E, Selter LL, Keller B. A putative ABC transporter confers durable resistance to multiple fungal pathogens in wheat. Science. 2009;323(5919):1360-1363. Doi:10.1126/science.1166453; Kushalappa AC, Yogendra KN, Karre S. Plant innate immune response: qualitative and quantitative resistance. Crit Rev Plant Sci. 2016;35(1):38-55. Doi:10.1080/07352689.2016.1148980; Lopez C. Descifrando las bases moleculares de la resistencia cuantitativa. Acta biol Col. 2011;16(2):3-14.; Mackay TFC, Stone EA, Ayroles JF. The genetics of quantitative traits: challenges and prospects. Nat Rev Genet. 2009;10(8):565. Doi:10.1038/nrg2612; Mahlein A-K, Steiner U, Hillnhütter C, Dehne H-W, Oerke E-C. Hyperspectral imaging for small-scale analysis of symptoms caused by different sugar beet diseases. Plant Methods. 2012;8(1):3. Doi:10.1186/1746-4811-8-3; Miklas PN, Kelly JD, Beebe SE, Blair MW. Common bean breeding for resistance against biotic and abiotic stresses: from classical to MAS breeding. Euphytica. 2006;147(1-2):105-131. Doi:10.1007/s10681-006-4600-5; Mittler R, Blumwald E. Genetic engineering for modern agriculture: challenges and perspectives. Annu Rev Plant Biol. 2010;61:443-462. Doi:10.1146/annurev-arplant-042809-112116; Mutka AM, Bart RS. Image-based phenotyping of plant disease symptoms. Front Plant Sci. 2015;5:734. Doi:10.3389/fpls.2014.00734; Mutka AM, Fentress SJ, Sher JW, Berry J, Pretz C, Nusinow D, Bart R. Quantitative, image-based phenotyping methods provide insight into spatial and temporal dimensions of plant disease. Plant Physiol. 2016;172(2):650-660. Doi:10.1104/pp.16.00984; Narusaka M, Shirasu K, Noutoshi Y, Kubo Y, Shiraishi T, Iwabuchi M, Narusaka Y. RRS1 and RPS4 provide a dual Resistance-gene system against fungal and bacterial pathogens. Plant J. 2009;60(2):218-226. Doi:10.1111/j.1365-313X.2009.03949.x; Navabi A, Singh RP, Huerta-Espino J, Tewari JP. Phenotypic association of adult-plant resistance to leaf and stripe rusts in wheat. Can J Plant Pathol. 2005;27(3):396-403. Doi:10.1080/07060660509507238; Navarro L, Zipfel C, Rowland O, Keller I, Robatzek S, Boller T, Jones JD. The transcriptional innate immune response to flg22. Interplay and overlap with Avr gene-dependent defense responses and bacterial pathogenesis. Plant Physiol. 2004;135(2):1113-1128. Doi:10.1104/pp.103.036749; Niks RE, Qi X, Marcel TC. Quantitative resistance to biotrophic filamentous plant pathogens: concepts, misconceptions, and mechanisms. Annu Rev Phytopathol. 2015;53:445-470. Doi:10.1146/annurev-phyto-080614-115928; Ntare B, Williams J. Heritability and genotype x environment interaction for yield and components of a yield model in segregating population of groundnut under semi-arid conditions. Afr Crop Sci. 1998;6:119-127.; Olukolu BA, Tracy WF, Wisser R, De Vries B, Balint-Kurti PJ. A genome-wide association study for partial resistance to maize common rust. Phytopathology. 2016;106(7):745-751. Doi:10.1094/PHYTO-11-15-0305-R; Parniske M. Arbuscular mycorrhiza: the mother of plant root endosymbioses. Nat Rev Micro. 2008;6(10):763-775. Doi:10.1038/nrmicro1987; Phillips RL, Vasil IK. DNA-based markers in plants. Springer Science & Business Media. 2013. p. 55-56; Poland JA, Balint-Kurti PJ, Wisser RJ, Pratt RC, Nelson RJ. Shades of gray: the world of quantitative disease resistance. Trends Plant Sci. 2009;14(1):21-29. Doi:10.1016/j.tplants.2008.10.006; Rafalski A. Applications of single nucleotide polymorphisms in crop genetics. Curr Opin Plant Biol. 2002;5(2):94-100. Doi:10.1016/S1369-5266(02)00240-6; Roux F, Noël L, Rivas S, Roby D. ZRK atypical kinases: emerging signaling components of plant immunity. New Phytologist. 2014a;203(3):713-716. Doi:10.1111/nph.12841; Roux F, Voisin D, Badet T, Balagué C, Barlet X, Huard-Chauveau C, Roby D, Raffaele S. Resistance to phytopathogens e tutti quanti: placing plant quantitative disease resistance on the map. Mol Plant Pathol. 2014b;15(5):427-432. Doi:10.1111/mpp.12138; Sadhu MJ, Bloom JS, Day L, Kruglyak L. CRISPR-directed mitotic recombination enables genetic mapping without crosses. Science. 2016;352(6289):1113-1116. Doi:10.1126/science.aaf5124; Salvi S, Tuberosa R. The crop QTLome comes of age. Curr Opin Biotechnol. 2015;32:179-185. Doi:10.1016/j.copbio.2015.01.001; Santner A, Estelle M. Recent advances and emerging trends in plant hormone signalling. Nature. 2009;459(7250):1071. Doi:10.1038/nature08122; Sax K. The association of size differences with seed-coat pattern and pigmentation in Phaseolus vulgaris. Genetics. 1923;8:552-60.; Schwessinger B, Zipfel C. News from the frontline: recent insights into PAMP-triggered immunity in plants. Curr Opin Plant Biol. 2008;11(4):389-395. Doi:10.1016/j.pbi.2008.06.001; Segretin ME, Pais M, Franceschetti M, Chaparro-Garcia A, Bos JI, Banfield MJ, Kamoun S. et al. Single amino acid mutations in the potato immune receptor R3a expand response to Phytophthora effectors. Mol Plant Microbe Interact. 2014;27(7):624-637. Doi:10.1094/MPMI-02-14-0040-R; Sehgal D. Advances in Molecular Breeding of Pearl Millet. In: Molecular Breeding for Sustainable Crop Improvement. Springer; 2016. p. 397-419.; Soriano JM, Royo C. Dissecting the genetic architecture of leaf rust resistance in wheat by QTL meta-analysis. Phytopathology. 2015;105(12):1585-1593. Doi:10.1094/PHYTO-05-15-0130-R; Soto JC, Ortiz JF, Perlaza-Jiménez L, Vásquez AX, Lopez-Lavalle LA, Mathew B, Léon J, Bernal AJ, Ballvora A, López CE. A genetic map of cassava (Manihot esculenta Crantz) with integrated physical mapping of immunity-related genes. BMC Genomics. 2015;16(1):190. Doi:10.1186/s12864-015-1397-4; St. Clair DA. Quantitative disease resistance and quantitative resistance loci in breeding. Annu Rev Phytopathol. 2010;48:247-268. Doi:10.1146/annurev-phyto-080508-081904; Stephens A, Lombardi M, Cogan NO, Forster J, Hobson K, Materne M, Kaur S. Genetic marker discovery, intraspecific linkage map construction and quantitative trait locus analysis of Ascochyta blight resistance in chickpea (Cicer arietinum L.). Molecular Breeding. 2014;33(2):297-313. Doi:10.1007/s11032-013-9950-9; Summers R, Brown J. Constraints on breeding for disease resistance in commercially competitive wheat cultivars. Plant Pathology. 2013;62(S1):115-121. Doi:10.1111/ppa.12165; Tanksley SD, Medina-Filho H, Rick CM. Use of naturally-occurring enzyme variation to detect and map genes controlling quantitative traits in an interspecific backcross of tomato. Heredity. 1982;49:11-25.; Tao Y, Xie Z, Chen W, Glazebrook J, Chang HS, Han B, Zhu T, Zou G, Katagiri F. Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen Pseudomonas syringae. Plant Cell. 2003;15(2):317-330. Doi:10.1105/tpc.007591; Thoday JM. Location of Polygenes. Nature. 1961;191:368-370.; Turuspekov Y, Ormanbekova D, Rsaliev A, Abugalieva S. Genome-wide association study on stem rust resistance in Kazakh spring barley lines. BMC Plant Biol. 2016;16(1):6. Doi:10.1186/s12870-015-0686-z; Venuti S, Copetti D, Foria S, Falginella L, Hoffmann S, Bellin D, Cindrić P, et al. Historical introgression of the downy mildew resistance gene Rpv12 from the Asian species Vitis amurensis into grapevine varieties. Plos One. 2013;8(4):e61228. Doi:10.1371/journal.pone.0061228; Wang Y, Xu J, Deng D, Ding H, Bian Y, Yin Z, et al. A comprehensive meta-analysis of plant morphology, yield, stay-green, and virus disease resistance QTL in maize (Zea mays L.). Planta. 2016;243(2):459-471. Doi:10.1007/s00425-015-2419-9; Xiao S, Ellwood S, Calis O, Patrick E, Li T, Coleman M, Turner JG. Broad-spectrum mildew resistance in Arabidopsis thaliana mediated by RPW8. Science. 2001;291(5501):118-120. Doi:10.1126/science.291.5501.118; Xu Y, Crouch JH. Marker-assisted selection in plant breeding: from publications to practice. Crop Science. 2008;48(2):391-407. Doi:10.2135/cropsci2007.04.0191; Yang J, Jiang H, Yeh CT, Jeddeloh JA, Nettleton D, Schnable PS. Extreme‐phenotype genome‐wide association study (XP‐GWAS): a method for identifying trait‐associated variants by sequencing pools of individuals selected from a diversity panel. Plant J. 2015; 84(3):587-596. Doi:10.1111/tpj.13029; Zhang J, Yu J, Pei W, Li X, Said J, Song M, Sanogo S. Genetic analysis of Verticillium wilt resistance in a backcross inbred line population and a meta-analysis of quantitative trait loci for disease resistance in cotton. BMC Genomics. 2015;16(1):577. Doi:10.1186/s12864-015-1682-2; Zhao BY, Ardales E, Brasset E, Claflin LE, Leach JE, Hulbert SH. The Rxo1/ Rba1 locus of maize controls resistance reactions to pathogenic and non-host bacteria. Theor Appl Genet. 2004;109(1):71-79.; Zhu C, Gore M, Buckler ES, Yu J. Status and prospects of association mapping in plants. Plant Genome. 2008;1(1):5-20. Doi:10.3835/plantgenome2008.02.0089; Zipfel C. Plant pattern-recognition receptors. Trends Immunol. 2014;35(7):345-351. Doi:10.1016/j.it.2014.05.004; Zuo W, Chao Q, Zhang N, Ye J, Tan Q, Li B, Xing Y, et al. A maize wall-associated kinase confers quantitative resistance to head smut. Nat Genet. 2015;47(2):151-157. Doi:10.1038/ng.3170; https://revistas.unal.edu.co/index.php/actabiol/article/view/66487

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    Academic Journal

    وصف الملف: application/pdf

    Relation: https://revistas.unal.edu.co/index.php/actabiol/article/view/66487; Universidad Nacional de Colombia Revistas electrónicas UN Acta Biológica Colombiana; Acta Biológica Colombiana; Vásquez, Andrea Ximena and Soto Sedano, Johana Carolina and López Carrascal, Camilo Ernesto (2018) Unraveling the molecules hidden in the gray shadows of quantitative disease resistance to pathogens. Acta Biológica Colombiana, 23 (1). pp. 5-16. ISSN 1900-1649; https://repositorio.unal.edu.co/handle/unal/68167; http://bdigital.unal.edu.co/69200/

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    Dissertation/ Thesis
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