Literatura académica sobre el tema "Mlo genes"
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Artículos de revistas sobre el tema "Mlo genes"
Shi, Jianlei, Hongjian Wan, Wenshan Zai, Zili Xiong y Weiren Wu. "Phylogenetic Relationship of Plant MLO Genes and Transcriptional Response of MLO Genes to Ralstonia solanacearum in Tomato". Genes 11, n.º 5 (29 de abril de 2020): 487. http://dx.doi.org/10.3390/genes11050487.
Texto completoKEMAL, RAHMAT AZHARI, ERIC BERNARDUS L. SANDJAJA, AUDI PUTRA SANTOSA y JEREMIAS IVAN. "Short Communication: Identification of Mildew Locus O (MLO) genes in Durio zibethinus genome corresponding with the Powdery Mildew disease". Biodiversitas Journal of Biological Diversity 19, n.º 6 (9 de octubre de 2018): 2204–12. http://dx.doi.org/10.13057/biodiv/d190628.
Texto completoGe, Cynthia, Paula Moolhuijzen, Lee Hickey, Elzette Wentzel, Weiwei Deng, Eric G. Dinglasan y Simon R. Ellwood. "Physiological Changes in Barley mlo-11 Powdery Mildew Resistance Conditioned by Tandem Repeat Copy Number". International Journal of Molecular Sciences 21, n.º 22 (20 de noviembre de 2020): 8769. http://dx.doi.org/10.3390/ijms21228769.
Texto completoFang, Peihong, Paul Arens, Xintong Liu, Xin Zhang, Deepika Lakwani, Fabrice Foucher, Jérémy Clotault et al. "Analysis of allelic variants of RhMLO genes in rose and functional studies on susceptibility to powdery mildew related to clade V homologs". Theoretical and Applied Genetics 134, n.º 8 (2 de mayo de 2021): 2495–515. http://dx.doi.org/10.1007/s00122-021-03838-7.
Texto completoYaeno, Takashi, Miki Wahara, Mai Nagano, Hikaru Wanezaki, Hirotaka Toda, Hiroshi Inoue, Ayaka Eishima et al. "RACE1, a Japanese Blumeria graminis f. sp. hordei isolate, is capable of overcoming partially mlo-mediated penetration resistance in barley in an allele-specific manner". PLOS ONE 16, n.º 8 (23 de agosto de 2021): e0256574. http://dx.doi.org/10.1371/journal.pone.0256574.
Texto completoJambagi, Shridhar, Shridhar Jambagi, Jim M. Dunwell y Jim M. Dunwell. "Identification and Expression Analysis of Fragaria Vesca MLO Genes Involved in Interaction with Powdery Mildew (Podosphaera Aphanis)". Journal of Advances in Plant Biology 1, n.º 1 (22 de noviembre de 2017): 40–54. http://dx.doi.org/10.14302/issn.2638-4469.japb-17-1838.
Texto completoBaykal, Ulku y Kadriye Özcan. "Analysis of Clade V MLO Gene Expressions in Hazelnut Leaves upon Exposure to Powdery Mildew". Turkish Journal of Agriculture - Food Science and Technology 10, n.º 4 (4 de mayo de 2022): 595–612. http://dx.doi.org/10.24925/turjaf.v10i4.595-612.4686.
Texto completoSaja, Diana, Anna Janeczko, Balázs Barna, Andrzej Skoczowski, Michał Dziurka, Andrzej Kornaś y Gábor Gullner. "Powdery Mildew-Induced Hormonal and Photosynthetic Changes in Barley Near Isogenic Lines Carrying Various Resistant Genes". International Journal of Molecular Sciences 21, n.º 12 (25 de junio de 2020): 4536. http://dx.doi.org/10.3390/ijms21124536.
Texto completoJarosch, Birgit, Karl-Heinz Kogel y Ulrich Schaffrath. "The Ambivalence of the Barley Mlo Locus: Mutations Conferring Resistance Against Powdery Mildew (Blumeria graminis f. sp. hordei) Enhance Susceptibility to the Rice Blast Fungus Magnaporthe grisea". Molecular Plant-Microbe Interactions® 12, n.º 6 (junio de 1999): 508–14. http://dx.doi.org/10.1094/mpmi.1999.12.6.508.
Texto completoPanstruga, R. "Serpentine plant MLO proteins as entry portals for powdery mildew fungi". Biochemical Society Transactions 33, n.º 2 (1 de abril de 2005): 389–92. http://dx.doi.org/10.1042/bst0330389.
Texto completoTesis sobre el tema "Mlo genes"
Geike, Juliane [Verfasser]. "Funktionelle Analyse von MLO Genen im Rosengenom / Juliane Geike". Hannover : Gottfried Wilhelm Leibniz Universität Hannover, 2018. http://d-nb.info/1172414211/34.
Texto completoCóser, Virgínia Maria. "Caracterização dos genes envolvidos nos rearranjos do gene MLL em leucemia aguda de novo de lactentes". reponame:Repositório Institucional da UFPR, 2013. http://hdl.handle.net/1884/32101.
Texto completoDorrance, Adrienne M. "The role of the partial tandem duplication of the MLL (MLL PTD) in leukemogenesis". Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1203712889.
Texto completoLima, Diego Silva. "Avaliação dos genes MLL, RB e TP53 em pacientes com síndrome mielodisplásica". reponame:Repositório Institucional da UFC, 2011. http://www.repositorio.ufc.br/handle/riufc/6887.
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Myelodysplastic syndromes (MDS) represent a heterogeneous group of clonal disorders affecting the hematopoietic pluripotent cell, characterized by low cell counts in peripheral blood, dysplasia in one or more cell lines, inefficient hematopoiesis and increased risk of progression to acute myeloid leukemia. Although the disease can affect patients of other age groups, they are more frequent in those with advanced age with an average 60 to 75 years at diagnosis. Chromosomal abnormalities are observed in approximately 50% of all cases of MDS and are related with clinical and morphological findings. The aim of this study was to determine, through the technique of FISH (fluorescence in situ hybridization), the frequency of changes involving the MLL, RB, and TP53 genes in patients with MDS and associate these changes with cytogenetic findings. The cases included in the study were selected in the ambulatory of SMD from University Hospital Walter Cantídio. Thirty three patients were selected, 17 had aged over 60 years. 52% of patients were classified, according to WHO criteria, as refractory cytopenia with dysplasia in multiple lineages (RCDM) and 61% stratified, according to IPSS, as intermediate risk 1 (INT-1). 78% of patients had abnormalities detected by cytogenetics, among them 31% had complex karyotypes (more than 3 changes per metaphase). 18% of patients had changes at least in one of the three genes valued in this study by FISH. Three patients showed alterations of TP53 gene, being detected in two patients (records 31 and 6) the deletion of a single allele or both alleles of the gene, respectively, and in the third (record 2), we detected amplification of TP53 gene, all this changes were not detected by classical cytogenetics, because it is a less sensitive technique. 6% of patients (records 7 and 22) had rearrangement of MLL gene. In the first case, FISH discarded the gene deletion alleged by cytogenetic, proving that it was present in the genome of the patient, but in a rearranged form, and in the second case cytogenetics failed to demonstrate rearrangement of the gene. For the RB gene, FISH identified only one patient (3%) with deletion of one allele of the gene, and this change was also not detected by classical cytogenetics. During evaluating the TP53 gene, FISH allowed identification of two patients (records 5 and 10) presenting at least six extra copies of chromosome 17, probably representing a small hyperdiploid clone partially detected in the first patient and not detected in the second . In the six patients who showed abnormalities of the genes analyzed, FISH has provided information that added, changed or confirmed the result previously given by classical cytogenetics, which are a major application of this technique due to its high sensitivity compared to the traditional method.
As síndromes mielodisplásicas (SMD) representam um grupo heterogêneo de doenças clonais que acometem a célula precursora hematopoética pluripotente, caracterizando-se por baixa contagem de células no sangue periférico, displasia em uma ou mais linhagens celulares, hematopoese ineficiente, além do risco aumentado de progressão para leucemia mielóide aguda. Embora a doença possa acometer pacientes de outras faixas etárias, é mais frequente naqueles com idade avançada, com média ao diagnóstico de 60 a 75 anos. As anormalidades cromossômicas são observadas em aproximadamente 50% de todos os casos de SMD, estando, em alguns casos, relacionadas com achados clínicos e morfológicos. O objetivo deste trabalho foi determinar, através da técnica de FISH (hibridização in situ por fluorescência), a frequência de alterações envolvendo os genes MLL, RB e TP53 em pacientes com SMD e associar estas alterações com os achados citogenéticos. Os casos inseridos no estudo foram oriundos do ambulatório de SMD do Hospital Universitário Walter Cantídio. Dos 33 pacientes selecionados, 17 pertenciam ao grupo com idade acima de 60 anos. 52% dos pacientes foram classificados, segundo a OMS, como citopenia refratária com displasia em múltiplas linhagens (CRDM) e 61% estratificados, segundo o IPSS, como de risco intermediário 1 (INT-1). Um total de 78% dos pacientes apresentaram alterações citogenéticas, dentre eles 31% possuíam cariótipos complexos (mais de 3 alterações por metáfase). A técnica de FISH permitiu identificar em 18% dos pacientes alterações envolvendo um dos três genes avaliados. Três pacientes apresentaram alteração do gene TP53, sendo detectada em dois deles (registros 31 e 6) a deleção de um único alelo ou de ambos os alelos do gene, respectivamente, e no terceiro (registro 2), detectou-se a amplificação do gene TP53, sendo estas alterações não visualizadas através da citogenética clássica, por se tratar de um técnica menos sensível. Detectou-se em 6% dos pacientes (registros 7 e 22) rearranjo do gene MLL, no primeiro a FISH descartou a suposta deleção do gene alegada pela citogenética, provando que o mesmo estava presente no genoma do paciente, porém de forma rearranjada e no segundo a citogenética não conseguiu demonstrar o rearranjo do gene. Quanto ao gene RB, a FISH permitiu identificar apenas um paciente (3%) com deleção de um dos alelos do gene, sendo esta alteração também não detectada pela citogenética clássica. A FISH possibilitou identificar, durante a avaliação do gene TP53, dois pacientes (registros 5 e 10) apresentando pelo menos 6 cópias extras do cromossomo 17, devendo essa alteração se tratar de um pequeno clone hiperdiplóide detectado parcialmente no primeiro paciente e não detectado no segundo. Nos seis pacientes que apresentaram alteração dos genes avaliados, a FISH proveu informações que adicionaram, confirmaram ou alteraram o resultado previamente emitido pela citogenética clássica, sendo estas uma das principais aplicações desta técnica devido sua alta sensibilidade quando comparada ao método clássico.
Makepeace, Joanne Claire. "The effect of the mlo mildew resistance gene on spotting diseases of barley". Thesis, University of East Anglia, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.437638.
Texto completoBussiere, Marianne. "Characterising the MLL complex : epigenetic regulation of Hoxa genes". Thesis, University of Birmingham, 2010. http://etheses.bham.ac.uk//id/eprint/707/.
Texto completoWong, Piu. "Meis1 and micrornas as collaborating genes in MLL leukemia /". May be available electronically:, 2008. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.
Texto completoCleavinger, Peter Jay. "Role of the long terminal repeat in transcriptional regulation of rous sarcoma virus gene expression". free to MU campus, to others for purchase, 1996. http://wwwlib.umi.com/cr/mo/fullcit?p9841207.
Texto completoNigavekar, Shraddha S. "Regulation of GLC7 encoded PP1 and analysis of synthetic lethal interactions with ade3 and leu2 in saccharomyces cerevisiae". free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3013007.
Texto completoAggelis, Alexandros. "Gene expression in ripening melon (Cucumis melo L.)". Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319646.
Texto completoLibros sobre el tema "Mlo genes"
El poema de mio Cid: El patriarca Rodrigo Díaz de Vivar trasmite sus genes. Kassel [Germany]: Edition Reichenberger, 2001.
Buscar texto completoBiagetti, Biagio. Il mio diario: Pagine scelte e scritti leopardiani : in appendice : La genesi dell'opera pittorica. Recanati [Italy]: CNSL, 1998.
Buscar texto completoUnited States. Congress. House. Committee on Post Office and Civil Service. Gene Taylor Post Office Building: Report (to accompany H.R. 3987). [Washington, D.C.?: U.S. G.P.O., 1988.
Buscar texto completoUnited States. Congress. House. Committee on Veterans' Affairs. Gene Taylor Veterans' Outpatient Clinic: Report (to accompany H.R. 2983). [Washington, D.C.?: U.S. G.P.O., 1989.
Buscar texto completoUnited States. Congress. House. Committee on Veterans' Affairs. Gene Taylor Veterans' Outpatient Clinic: Report (to accompany H.R. 2983). [Washington, D.C.?: U.S. G.P.O., 1989.
Buscar texto completoBaumann, Nicole y Jean-Claude Turpin. Metachromatic Leukodystrophy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0052.
Texto completoThe Bedford Book of Genres: A Guide with 2016 MLA Update. Bedford/St. Martin's, 2017.
Buscar texto completoGayley, Holly. Love Letters from Golok. Columbia University Press, 2017. http://dx.doi.org/10.7312/columbia/9780231180528.001.0001.
Texto completoSongs Only You Know. Soho Press Inc, 2013.
Buscar texto completoDetroit Country Music. The University of Michigan Press, 2013.
Buscar texto completoCapítulos de libros sobre el tema "Mlo genes"
Downing, James R. y A. Thomas Look. "MLL fusion genes in the 11q23 acute leukemias". En Cancer Treatment and Research, 73–92. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1261-1_4.
Texto completoShih, J. C., J. Grimsby y K. Chen. "The expression of human MAO-A and B genes". En Amine Oxidases and Their Impact on Neurobiology, 41–47. Vienna: Springer Vienna, 1990. http://dx.doi.org/10.1007/978-3-7091-9113-2_4.
Texto completoJoseph, Anitta y P. K. Nizar Banu. "Identification of Predominant Genes that Causes Autism Using MLP". En Smart Intelligent Computing and Applications, Volume 1, 269–79. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-9669-5_25.
Texto completoMacrina, Francis L. y C. Jeffrey Smith. "Gene Transmission, MLS, and Tetracycline Resistance in Bacteroides". En Brock/Springer Series in Contemporary Bioscience, 474–89. New York, NY: Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4615-7087-5_35.
Texto completoMeyer, Claus y Rolf Marschalek. "LDI-PCR: Identification of Known and Unknown Gene Fusions of the Human MLL Gene". En Leukemia, 71–83. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-418-6_5.
Texto completoShih, J. C., Q. S. Zhu, J. Grimsby y K. Chen. "Identification of human monoamine oxidase (MAO) A and B gene promoters". En Amine Oxidases: Function and Dysfunction, 27–33. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9324-2_3.
Texto completoMatthieu, J. M., F. X. Omlin, J. M. Roch y B. J. Cooper. "Myelin Basic Protein Gene Expression, Oligodendrocyte Metabolism and Myelin Stability in the MLD Mutant Mouse". En A Multidisciplinary Approach to Myelin Diseases, 13–28. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4757-0354-2_2.
Texto completoSantin, Yohan, Angelo Parini y Jeanne Mialet-Perez. "Expression and Function of MAO A in Cardiac Cells by Means of Adenovirus-Mediated Gene Transfer". En Methods in Molecular Biology, 163–70. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2643-6_12.
Texto completoRossi, André L. D., Carlos Soares y André C. P. L. F. Carvalho. "Bioinspired Parameter Tuning of MLP Networks for Gene Expression Analysis: Quality of Fitness Estimates vs. Number of Solutions Analysed". En Advances in Neuro-Information Processing, 252–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03040-6_31.
Texto completoKlaus, M., S. Schnittger, T. Haferlach, M. Dreyling, W. Hiddemann y C. Schoch. "Different Mechanisms Lead to Rearrangements of the MLL Gene in Cases with Acute Myeloid Leukemia (AML) and Translocation t(10;l1)". En Haematology and Blood Transfusion Hämatologie und Bluttransfusion, 67–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-59358-1_14.
Texto completoActas de conferencias sobre el tema "Mlo genes"
Volinia, S., P. Patracchini, F. Vannini, L. Felloni, F. Panicucci y F. Beranardi. "HAGEMAN TRAIT INVESTIGATED BY FACTOR XII cDNA PROBES". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643299.
Texto completoChakraborty, Goutam, Jagdish Patra, Seiryo Noda y Basabi Chakraborty. "A MLP-SOM Combination to Select Relevant Genes from High-dimensional DNA Microarray Data". En 2007 IEEE International Symposium on Signal Processing and Information Technology. IEEE, 2007. http://dx.doi.org/10.1109/isspit.2007.4458020.
Texto completoPoppen, Steven y Manuel Diaz. "Abstract 4034: The role of CYP33 in MLL target gene repression". En Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-4034.
Texto completoVaughan, Andrew T., Rebecca Wright y Katrina Slemmons. "Abstract B35: Estradiol drives MLL gene fusions in infant acute leukemia". En Abstracts: AACR Special Conference: Pediatric Cancer at the Crossroads: Translating Discovery into Improved Outcomes; November 3-6, 2013; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.pedcan-b35.
Texto completoRossi, André L. D., André C. P. L. F. Carvalho y Carlos Soares. "Bio-Inspired Parameter Tunning of MLP Networks for Gene Expression Analysis". En 2008 8th International Conference on Hybrid Intelligent Systems (HIS). IEEE, 2008. http://dx.doi.org/10.1109/his.2008.152.
Texto completoAlkotami, Linah, Brice Jarvis, Chaofu Lu, Doug Allen, Jianhui Zhang, John Sedbrook, Kathleen Schuler, Somnath Koley y Timothy Durrett. "Targeted genome editing of industrial oilseed crops to enhance synthesis of functional lipids". En 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/orfd6797.
Texto completoBernardi, F., G. Marchetti, F. Vannini, L. Felloni, F. Panicucci y F. Conconi. "SPORADISM INVESTIGATION AND CARRIER DETECTION IN HAEMOPHILIA A BY RFLP ANALYSIS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644011.
Texto completoZhang, Junying, Hongyi Zhang, Shenling Liu y Yue Wang. "A Novel Multiclass Gene Selection Method based on SVM/MLP Cross Validation". En 2006 International Conference on Mechatronics and Automation. IEEE, 2006. http://dx.doi.org/10.1109/icma.2006.257654.
Texto completoBenhattar, Jean y Isabelle Guilleret. "Abstract 3023: Rapid methylation profiling of multiple genes at the same time using the methylation ligation-dependent macroarray (MLM)". En Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-3023.
Texto completoEssing, Mirko, Alberto Zambon, Vera Gallo, Cristina Baldoli, Federica Cugnata, Paola M. V. Rancoita, Fabiola De Mattia et al. "Lentiviral Hematopoietic Stem and Progenitor Cell Gene Therapy for Metachromatic Leukodystrophy (MLD): Clinical Outcomes from 38 Patients". En Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1739647.
Texto completoInformes sobre el tema "Mlo genes"
Katzir, Nurit, James Giovannoni, Marla Binzel, Efraim Lewinsohn, Joseph Burger y Arthur Schaffer. Genomic Approach to the Improvement of Fruit Quality in Melon (Cucumis melo) and Related Cucurbit Crops II: Functional Genomics. United States Department of Agriculture, enero de 2010. http://dx.doi.org/10.32747/2010.7592123.bard.
Texto completoLi, Li, Joseph Burger, Nurit Katzir, Yaakov Tadmor, Ari Schaffer y Zhangjun Fei. Characterization of the Or regulatory network in melon for carotenoid biofortification in food crops. United States Department of Agriculture, abril de 2015. http://dx.doi.org/10.32747/2015.7594408.bard.
Texto completoGrumet, Rebecca, Rafael Perl-Treves y Jack Staub. Ethylene Mediated Regulation of Cucumis Reproduction - from Sex Expression to Fruit Set. United States Department of Agriculture, febrero de 2010. http://dx.doi.org/10.32747/2010.7696533.bard.
Texto completoAharoni, Asaph, Zhangjun Fei, Efraim Lewinsohn, Arthur Schaffer y Yaakov Tadmor. System Approach to Understanding the Metabolic Diversity in Melon. United States Department of Agriculture, julio de 2013. http://dx.doi.org/10.32747/2013.7593400.bard.
Texto completoZhao, Bingyu, Saul Burdman, Ronald Walcott y Gregory E. Welbaum. Control of Bacterial Fruit Blotch of Cucurbits Using the Maize Non-Host Disease Resistance Gene Rxo1. United States Department of Agriculture, septiembre de 2013. http://dx.doi.org/10.32747/2013.7699843.bard.
Texto completoBadami, Kaswan, Budi Setiadi Daryono, Achmad Amzeri y Syaiful Khoiri. COMBINING ABILITY AND HETEROTIC STUDIES ON HYBRID MELON (Cucumis melo L.) POPULATIONS FOR FRUIT YIELD AND QUALITY TRAITS. SABRAO Journal of Breeding and Genetics, octubre de 2020. http://dx.doi.org/10.21107/amzeri.2020.3.
Texto completoBarefoot, Susan F., Bonita A. Glatz, Nathan Gollop y Thomas A. Hughes. Bacteriocin Markers for Propionibacteria Gene Transfer Systems. United States Department of Agriculture, junio de 2000. http://dx.doi.org/10.32747/2000.7573993.bard.
Texto completoKatzir, Nurit, James Giovannoni y Joseph Burger. Genomic approach to the improvement of fruit quality in melon (Cucumis melo) and related cucurbit crops. United States Department of Agriculture, junio de 2006. http://dx.doi.org/10.32747/2006.7587224.bard.
Texto completoArnett, Clint, Justin Lange, Ashley Boyd, Martin Page y Donald Cropek. Expression and secretion of active Moringa oleifera coagulant protein in Bacillus subtilis. Engineer Research and Development Center (U.S.), agosto de 2021. http://dx.doi.org/10.21079/11681/41546.
Texto completoFriedmann, Michael, Charles J. Arntzen y Hugh S. Mason. Expression of ETEC Enterotoxin in Tomato Fruit and Development of a Prototype Transgenic Tomato for Dissemination as an Oral Vaccine in Developing Countries. United States Department of Agriculture, marzo de 2003. http://dx.doi.org/10.32747/2003.7585203.bard.
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