Bibliografías temáticas / Gene Array

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Literatura académica sobre el tema "Gene Array"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 20 de febrero de 2023

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Artículos de revistas sobre el tema "Gene Array"

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Zhang, Xiaoling, Marc E. Lenburg, and Avrum Spira. "Comparison of Nasal Epithelial Smoking-Induced Gene Expression on Affymetrix Exon 1.0 and Gene 1.0 ST Arrays." Scientific World Journal 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/951416.

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We have previously defined the impact of tobacco smoking on nasal epithelium gene expression using Affymetrix Exon 1.0 ST arrays. In this paper, we compared the performance of the Affymetrix GeneChip Human Gene 1.0 ST array with the Human Exon 1.0 ST array for detecting nasal smoking-related gene expression changes. RNA collected from the nasal epithelium of five current smokers and five never smokers was hybridized to both arrays. While the intersample correlation within each array platform was relatively higher in the Gene array than that in the Exon array, the majority of the genes most cha
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Aschheim, Kathy. "Gene detection by array." Nature Biotechnology 18, no. 11 (November 2000): 1129. http://dx.doi.org/10.1038/81066.

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Thomas, E. V., K. H. Phillippy, B. Brahamsha, D. M. Haaland, J. A. Timlin, L. D. H. Elbourne, B. Palenik, and I. T. Paulsen. "Statistical Analysis of Microarray Data with Replicated Spots: A Case Study withSynechococcusWH8102." Comparative and Functional Genomics 2009 (2009): 1–11. http://dx.doi.org/10.1155/2009/950171.

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Until recently microarray experiments often involved relatively few arrays with only a single representation of each gene on each array. A complete genome microarray with multiple spots per gene (spread out spatially across the array) was developed in order to compare the gene expression of a marine cyanobacterium and a knockout mutant strain in a defined artificial seawater medium. Statistical methods were developed for analysis in the special situation of this case study where there is gene replication within an array and where relatively few arrays are used, which can be the case with curre
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Gellert, Pascal, Mizue Teranishi, Katharina Jenniches, Piera De Gaspari, David John, Karsten grosse Kreymborg, Thomas Braun, and Shizuka Uchida. "Gene Array Analyzer: alternative usage of gene arrays to study alternative splicing events." Nucleic Acids Research 40, no. 6 (November 28, 2011): 2414–25. http://dx.doi.org/10.1093/nar/gkr1110.

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Walsh, James Bruce. "Persistence of Tandem Arrays: Implications for Satellite and Simple-Sequence DNAs." Genetics 115, no. 3 (March 1, 1987): 553–67. http://dx.doi.org/10.1093/genetics/115.3.553.

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ABSTRACT Recombination processes acting on tandem arrays are suggested here to have probable intrinsic biases, producing an expected net decrease in array size following each event, in contrast to previous models which assume no net change in array size. We examine the implications of this by modeling copy number dynamics in a tandem array under the joint interactions of sister-strand unequal crossing over (rate γ per generation per copy) and intrastrand recombination resulting in deletion (rate ∊ per generation per copy). Assuming no gene amplification or selection, the expected mean persiste
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Alkahtani, Mohammed, Yihua Hu, Zuyu Wu, Colin Sokol Kuka, Muflih S. Alhammad, and Chen Zhang. "Gene Evaluation Algorithm for Reconfiguration of Medium and Large Size Photovoltaic Arrays Exhibiting Non-Uniform Aging." Energies 13, no. 8 (April 14, 2020): 1921. http://dx.doi.org/10.3390/en13081921.

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Aging is known to exert various non-uniform effects on photovoltaic (PV) modules within a PV array that consequently can result in non-uniform operational parameters affecting the individual PV modules, leading to a variable power output of the overall PV array. This study presents an algorithm for optimising the configuration of a PV array within which different PV modules are subject to non-uniform aging processes. The PV array reconfiguration approach suggests maximising power generation across non-uniformly aged PV arrays by merely repositioning, rather than replacing, the PV modules, ther
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Mocellin, Simone, Maurizio Provenzano, Carlo Riccardo Rossi, Pierluigi Pilati, Donato Nitti, and Mario Lise. "DNA Array-Based Gene Profiling." Annals of Surgery 241, no. 1 (January 2005): 16–26. http://dx.doi.org/10.1097/01.sla.0000150157.83537.53.

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O'Neill, Paul. "Gene array breakthrough for glioblastoma." Trends in Molecular Medicine 7, no. 9 (September 2001): 387. http://dx.doi.org/10.1016/s1471-4914(01)02145-1.

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AOKI, Hiroshi, Akiko KITAJIMA, and Hiroaki TAO. "Electrochemical Gene Sensor Arrays Prepared Using Non-contact Nanoliter Array Spotting of Gene Probes." Analytical Sciences 26, no. 3 (2010): 367–70. http://dx.doi.org/10.2116/analsci.26.367.

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Johnston, Mark. "Gene chips: Array of hope for understanding gene regulation." Current Biology 8, no. 5 (February 1998): R171—R174. http://dx.doi.org/10.1016/s0960-9822(98)70103-4.

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Tesis sobre el tema "Gene Array"

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Li, Yan 1978 July 15. "Gene expression array simulator." Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/87263.

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Thesis (M.Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, June 2002.<br>"May 10, 2002.<br>Includes bibliographical references (leaf 141).<br>by Yan Li.<br>M.Eng.
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Mapiye, Darlington S. "Normalization and statistical methods for crossplatform expression array analysis." University of the Western Cape, 2012. http://hdl.handle.net/11394/4586.

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>Magister Scientiae - MSc<br>A large volume of gene expression data exists in public repositories like the NCBI’s Gene Expression Omnibus (GEO) and the EBI’s ArrayExpress and a significant opportunity to re-use data in various combinations for novel in-silico analyses that would otherwise be too costly to perform or for which the equivalent sample numbers would be difficult to collects exists. For example, combining and re-analysing large numbers of data sets from the same cancer type would increase statistical power, while the effects of individual study-specific variability is weakened, whic
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Lundén, Karl. "Heterobasidion - conifer pathosystem : heterologous array analysis and transcriptional shift from saprotrophic to necrotrophic growth /." Uppsala : Department of Forest Mycology and Pathology, Swedish University of Agricultural Sciences, 2010. http://epsilon.slu.se/201019.pdf.

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Norouzi, Masoud. "Development of an RNA array to Protein array (RAPA) platform and its application to gene expression analysis of synthetic riboregulators." Thesis, University of Portsmouth, 2018. https://researchportal.port.ac.uk/portal/en/theses/development-of-an-rna-array-to-protein-array-rapa-platform-and-its-application-to-gene-expression-analysis-of-synthetic-riboregulators(5867a39c-55a4-410a-8e5a-53c347b8a81a).html.

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Bjork, Kathe Elizabeth. "Robust identification of differential gene expression and discrimination /." Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2006.

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Thesis (Ph.D. in Biostatistics) -- University of Colorado at Denver and Health Sciences Center, 2006.<br>Typescript. Includes bibliographical references (leaves 237-239). Free to UCDHSC affiliates. Online version available via ProQuest Digital Dissertations;
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Araujo, Tânia Kawasaki de 1985. "Utilização da técnica de Open Array para investigação de genes associados a fendas labiopalatais em amostra da população brasileira." [s.n.], 2015. http://repositorio.unicamp.br/jspui/handle/REPOSIP/313118.

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Orientador: Vera Lúcia Gil da Silva Lopes<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-08-27T00:02:24Z (GMT). No. of bitstreams: 1 Araujo_TaniaKawasakide_D.pdf: 3447671 bytes, checksum: 97911848c6334882843e4b270b9c6771 (MD5) Previous issue date: 2015<br>Resumo: A fenda de labiopalatal (FLP) isolada é o defeito craniofacial mais comum em humanos. O objetivo deste estudo foi avaliar associações entre 39 genes e a etiologia de FLP isolada em uma amostra da população brasileira. Este estudo de associação do tipo caso-c
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Arlinde, Christina. "Gene expression profiling in animal models of alcoholism /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7140-133-4/.

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Sandgren, Johanna. "Array-based Genomic and Epigenomic Studies in Healthy Individuals and Endocrine Tumours." Doctoral thesis, Uppsala universitet, Institutionen för kirurgiska vetenskaper, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-129533.

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The human genome is a dynamic structure, recently recognized to present with significant large-scale structural variation. DNA-copy number changes represent one common type of such variation and is found both between individuals and within the somatic cells of the same individual, especially in disease states like cancer.  Apart from DNA-rearrangements, epigenomic changes are increasingly acknowledged as important events in the maintenance of genomic integrity. In this thesis, different array-based methods have been applied for global genomic and epigenomic profiling of both normal and cancer
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Dumas, Laura Jane. "Gene copy number variation in human and primate evolution /." Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2008. http://proquest.umi.com/pqdweb?did=1545571861&sid=1&Fmt=6&clientId=18952&RQT=309&VName=PQD.

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Thesis (Ph.D. in Human Medical Genetics) -- University of Colorado Denver, 2008.<br>Typescript. Includes bibliographical references (leaves 98-112). Free to UCD Anschutz Medical Campus. Online version available via ProQuest Digital Dissertations;
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Tong, Lily. "Probing the function of RNase E family using biochemical techniques and gene array technology." Thesis, University of Leeds, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.414514.

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Libros sobre el tema "Gene Array"

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Muller, Hans-Joachim. Microarrays. Burlington, MA: Elsevier Academic Press, 2005.

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Gene network inference: Verification of methods for systems genetics data. Heidelberg: Springer, 2013.

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1966-, Scherer Andreas, ed. Batch effects and noise in microarray experiments, sources, and solutions. Chichester, West Sussex: J. Wiley, 2009.

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Thomas, Roeder, ed. Microarrays. Burlington, MA: Elsevier Academic Press, 2006.

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T, Kho Alvin, and Butte Atul J, eds. Microarrays for an integrative genomics. Cambridge, Mass: MIT Press, 2003.

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1965-, Blalock Eric M., ed. A beginner's guide to microarrays. Boston: Kluwer Academic Publishers, 2003.

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Formalin-fixed paraffin-embedded tissues: Methods and protocols. New York: Humana Press, 2011.

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1961-, Ye S., and Day Ian N. M, eds. Microarrays & microplates: Applications in biomedical sciences. Oxford: BIOS, 2003.

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Microarray analysis. Hoboken, NJ: Wiley-Liss, 2003.

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Beadchip molecular immunohematology: Toward routine donor and patient antigen profiling by DNA analysis. New York: Springer, 2011.

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Capítulos de libros sobre el tema "Gene Array"

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Lam, Ching-Wan, and Kin-Chong Lau. "Candidate Screening through High-Density SNP Array." In Gene Discovery for Disease Models, 195–214. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9780470933947.ch10.

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Dorris, David, Chang-gong Liu, Ramesh Ramakrishnan, Richard Shippy, Sangeet Singh-Gasson, Anna Lublinsky, Edward Touma, et al. "Oligonucleotide Array Technologies for Gene Expression Profiling." In Biochips, 1–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05092-7_1.

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Jovanovic, Borko D., Raymond C. Bergan, and Warren A. Kibbe. "Some Aspects of Analysis of Gene Array Data." In Biostatistical Applications in Cancer Research, 71–89. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4757-3571-0_5.

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Dickson, Glenda J., Terence R. Lappin, and Alexander Thompson. "Complete Array of HOX Gene Expression by RQ-PCR." In Leukemia, 369–93. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-418-6_19.

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Lidén, Per, Lars Asker, and Henrik Bostróm. "Rule Induction for Classification of Gene Expression Array Data." In Principles of Data Mining and Knowledge Discovery, 338–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45681-3_28.

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González Calabozo, José María, Carmen Peláez-Moreno, and Francisco José Valverde-Albacete. "Gene Expression Array Exploration Using $\mathcal{K}$ -Formal Concept Analysis." In Formal Concept Analysis, 119–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-20514-9_11.

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Archer, T. K., M. G. Cordingley, V. Marsaud, H. Richard-Foy, and G. L. Hager. "Steroid Transactivation at a Promoter Organized in a Specifically-Positioned Array of Nucleosomes." In The Steroid/Thyroid Hormone Receptor Family and Gene Regulation, 221–38. Basel: Birkhäuser Basel, 1989. http://dx.doi.org/10.1007/978-3-0348-5466-5_16.

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Aigner, Thomas, Pia M. Gebhard, and Alexander Zien. "Gene expression profiling by the cDNA array technology: Molecular portraying of chondrocytes." In The Many Faces of Osteoarthritis, 293–96. Basel: Birkhäuser Basel, 2002. http://dx.doi.org/10.1007/978-3-0348-8133-3_29.

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Wong, Kwong-Kwok. "Use of Single-Nucleotide Polymorphism Array for Tumor Aberrations in Gene Copy Numbers." In Genomics and Pharmacogenomics in Anticancer Drug Development and Clinical Response, 75–88. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-088-5_6.

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Jovanovic, Borko D., Shuguang Huang, Yuequin Liu, Karen N. Naguib, and Raymond C. Bergan. "An Analysis of Gene Array Data Related to Cell Adhesion and Prostate Cancer." In Biostatistical Applications in Cancer Research, 91–111. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4757-3571-0_6.

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Actas de conferencias sobre el tema "Gene Array"

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Neitz, Maureen. "Molecular genetics of red-green color vision." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fm2.

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Genes encoding cone pigments sensitive to middle-to-long wavelengths lie in a head-to-tail tandem array on the X-chromosome. Although two X-encoded genes, one for long-wavelength-sensitive pigments and one for middle-wavelength-sensitive pigments, are sufficient to serve trichromatic color vision, most people have more than two such genes. The arrangement, location, and degree of homology of the pigment genes promote recombination within the tandem arrays. Such recombination events produce pigment-gene complements that differ in the number and sequences of individual genes and in the interrela
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Caffarena, G., S. Bojanic, J. A. Lopez, C. Pedreira, and O. Nieto-Taladriz. "High-speed systolic array for gene matching." In Proceeding of the 2004 ACM/SIGDA 12th international symposium. New York, New York, USA: ACM Press, 2004. http://dx.doi.org/10.1145/968280.968325.

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Paik, S. J., S. Park, V. Zarnitsyn, M. R. Prausnitz, M. G. Allen, S. Choi, and X. D. Guo. "A HIGHLY DENSE NANONEEDLE ARRAY FOR INTRACELLULAR GENE DELIVERY." In 2012 Solid-State, Actuators, and Microsystems Workshop. San Diego: Transducer Research Foundation, 2012. http://dx.doi.org/10.31438/trf.hh2012.40.

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Venkatesh, E. T., P. Tangaraj, and S. Chitra. "Classification of cancer gene expressions from micro-array analysis." In 2010 International Conference on Innovative Computing Technologies (ICICT). IEEE, 2010. http://dx.doi.org/10.1109/icinnovct.2010.5440095.

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Hu, Jing, Jianbo Gao, Yinhe Cao, and Weijia Zhang. "Detection of gene copy number change in array CGH data." In 2006 IEEE/NLM Life Science Systems and Applications Workshop. IEEE, 2006. http://dx.doi.org/10.1109/lssa.2006.250402.

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Rehna, V. J., and G. Raju. "Signal extraction from microarray images for gene array data analysis." In 2nd International Conference on Computer and Automation Engineering (ICCAE 2010). IEEE, 2010. http://dx.doi.org/10.1109/iccae.2010.5451859.

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Dror, Ron O., Jonathan G. Murnick, Nicola A. Rinaldi, Voichita D. Marinescu, Ryan M. Rifkin, and Richard A. Young. "A bayesian approach to transcript estimation from gene array data." In the sixth annual international conference. New York, New York, USA: ACM Press, 2002. http://dx.doi.org/10.1145/565196.565213.

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Tian, David, and Keith Burley. "Classification of micro-array gene expression data using neural networks." In 2010 International Joint Conference on Neural Networks (IJCNN). IEEE, 2010. http://dx.doi.org/10.1109/ijcnn.2010.5596568.

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Ramalingam, Naveen, Long-Qing Chen, Xin-Hao Yang, Liqun Deng, Qing-Hui Wang, Eric Yap Peng Huat, Chiew Hoon Neo, and Hai-Qing Gong. "A Surface-Directed Microfluidic Scheme for Parallel Nanoliter PCR Array Suitable for Point-of-Care Testing." In ASME 2009 7th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2009. http://dx.doi.org/10.1115/icnmm2009-82052.

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In resource-limited settings, it is impractical to get access to a diagnostic laboratory having sophisticated instruments, and it is desirable to use disposable point-of-care diagnostic chips that do not require liquid handling or pumping instruments for sample distribution among an array of reactors. In addition to the pump-less sample loading method, the challenge to seal an array of reactors without the use of microvalves or mechanical parts still persists. Implementation of microvalve array adds complexity to the chip fabrication and operation processes, and also reduces the space on the m
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Chretien, Stephane, Christophe Guyeux, Michael Boyer-Guittaut, Regis Delage-Mouroux, and Francoise Descotes. "Investigating gene expression array with outliers and missing data in bladder cancer." In 2015 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2015. http://dx.doi.org/10.1109/bibm.2015.7359819.

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Informes sobre el tema "Gene Array"

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Fluhr, Robert, and Volker Brendel. Harnessing the genetic diversity engendered by alternative gene splicing. United States Department of Agriculture, December 2005. http://dx.doi.org/10.32747/2005.7696517.bard.

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Our original objectives were to assess the unexplored dimension of alternative splicing as a source of genetic variation. In particular, we sought to initially establish an alternative splicing database for Arabidopsis, the only plant for which a near-complete genome has been assembled. Our goal was to then use the database, in part, to advance plant gene prediction programs that are currently a limiting factor in annotating genomic sequence data and thus will facilitate the exploitation of the ever increasing quantity of raw genomic data accumulating for plants. Additionally, the database was
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Tu, Q., Ye Deng, Lu Lin, Chris L. Hemme, Zhili He, and Jizhong Zhou. HuMiChip: Development of a Functional Gene Array for the Study of Human Microbiomes. Office of Scientific and Technical Information (OSTI), May 2010. http://dx.doi.org/10.2172/1008326.

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Xu, Jin-Rong, and Amir Sharon. Comparative studies of fungal pathogeneses in two hemibiotrophs: Magnaporthe grisea and Colletotrichum gloeosporioides. United States Department of Agriculture, May 2008. http://dx.doi.org/10.32747/2008.7695585.bard.

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Plant pathogenic fungi have various life styles and different plant infection strategies. Hemibiotrophs like Magnaporthe grisea and Colletotrichum species develop specialized structures during plant infection. The goal of this study was to identify, characterize, and compare genes required for plant infection in M. grisea and C. gloeosporioides. Specific objectives are to: 1) further characterize genes identified in the preliminary studies of C. gloeosporioides and M. grisea;2) identify and characterize additional fungal genes tagged by GFP; and 3) identify in planta growth and appressorium-sp
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Steffens, John, Eithan Harel, and Alfred Mayer. Coding, Expression, Targeting, Import and Processing of Distinct Polyphenoloxidases in Tissues of Higher Plants. United States Department of Agriculture, November 1994. http://dx.doi.org/10.32747/1994.7613008.bard.

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Polyphenol oxidase (PPO) catalyzes the oxidation of phenols to quinones at the expense of O2. PPOs are ubiquitous in higer plants, and their role in oxidative browning of plant tissues causes large annual losses to food production. Despite the importance of PPOs to agriculture, the function(s) of PPOs in higher plants are not understood. Among other roles, PPOs have been proposed to participate in aspects of chloroplast metabolism, based on their occurrence in plastids and high Km for O2. Due to the ability of PPO to catalyze formation of highly reactive quinones, PPOs have also been proposed
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Levin, Ilan, Avtar K. Handa, Avraham Lalazar, and Autar K. Mattoo. Modulating phytonutrient content in tomatoes combining engineered polyamine metabolism with photomorphogenic mutants. United States Department of Agriculture, December 2006. http://dx.doi.org/10.32747/2006.7587724.bard.

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Fruit constitutes a major component of our diet, providing fiber, vitamins, minerals, and many other phytonutrients that promote good health. Fleshy fruits, such as tomatoes, already contain high levels of several of these ingredients. Nevertheless, efforts have been invested in increasing and diversifying the content of phytonutrients, such as carotenoids and flavonoids, in tomato fruits. Increasing levels of phytonutrients, such as lycopene, is highly justified from the perspective of the lycopene extraction industry due to cost effectiveness reasons. Diversifying phytonutrients, in particul
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Seroussi, Eyal, and George Liu. Genome-Wide Association Study of Copy Number Variation and QTL for Economic Traits in Holstein Cattle. United States Department of Agriculture, September 2010. http://dx.doi.org/10.32747/2010.7593397.bard.

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Copy number variation (CNV) has been recently identified in human and other mammalian genomes and increasing awareness that CNV might be a major source for heritable variation in complex traits has emerged. Despite this, little has been published on CNVs in Holsteins. In order to fill this knowledge-gap, we proposed a genome-wide association study between quantitative trait loci (QTL) for economic traits and CNV in the Holstein cattle. The approved feasibility study was aimed at the genome-wide characterization of CNVs in Holstein cattle and at the demonstrating of their possible association w
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Abbo, Shahal, Hongbin Zhang, Clarice Coyne, Amir Sherman, Dan Shtienberg, and George J. Vandemark. Winter chickpea; towards a new winter pulse for the semiarid Pacific Northwest and wider adaptation in the Mediterranean basin. United States Department of Agriculture, January 2011. http://dx.doi.org/10.32747/2011.7597909.bard.

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Original objectives: [a] Screen an array of chickpea and wild annual Cicer germplasm for winter survival. [b] Genetic analysis of winter hardiness in domesticated x wild chickpea crosses. [c] Genetic analysis of vernalization response in domesticated x wild chickpea crosses. [d] Digital expression analysis of a core selection of breeding and germplasm lines of chickpea that differ in winter hardiness and vernalization. [e] Identification of the genes involved in the chickpea winter hardiness and vernalization and construction of gene network controlling these traits. [f] Assessing the phenotyp
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Bercovier, Herve, and Ronald P. Hedrick. Diagnostic, eco-epidemiology and control of KHV, a new viral pathogen of koi and common carp. United States Department of Agriculture, December 2007. http://dx.doi.org/10.32747/2007.7695593.bard.

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Original objectives and revisions-The proposed research included these original objectives: field validation of diagnostic tests (PCR), the development and evaluation of new sensitive tools (LC-PCR/TaqManPCR, antibody detection by ELISA) including their use to study the ecology and the epidemiology of KHV (virus distribution in the environment and native cyprinids) and the carrier status of fish exposed experimentally or naturally to KHV (sites of virus replication and potential persistence or latency). In the course of the study we completed the genome sequence of KHV and developed a DNA arra
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Porat, Ron, Gregory T. McCollum, Amnon Lers, and Charles L. Guy. Identification and characterization of genes involved in the acquisition of chilling tolerance in citrus fruit. United States Department of Agriculture, December 2007. http://dx.doi.org/10.32747/2007.7587727.bard.

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Citrus, like many other tropical and subtropical fruit are sensitive to chilling temperatures. However, application of a pre-storage temperature conditioning (CD) treatment at 16°C for 7 d or of a hot water brushing (HWB) treatment at 60°C for 20 sec remarkably enhances chilling tolerance and reduces the development of chilling injuries (CI) upon storage at 5°C. In the current research, we proposed to identify and characterize grapefruit genes that are induced by CD, and may contribute to the acquisition of fruit chilling tolerance, by two different molecular approaches: cDNA array analysis an
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Horwitz, Benjamin, and Barbara Gillian Turgeon. Secondary Metabolites, Stress, and Signaling: Roles and Regulation of Peptides Produced by Non-ribosomal Peptide Synthetases. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7696522.bard.

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Fungal pathogens of plants produce a diverse array of small molecules. Often referred to as secondary metabolites because they were thought to be dispensable for basic functions, they may indeed have central roles as signals for the fungal cell, and in interactions with the host. We have identified more than a dozen genes encoding nonribosomal peptide synthetases (NPS) in Cochliobolusheterostrophus, the agent of southern corn leaf blight. The aim of this project was to identify roles of these genes in stress responses and signaling. The first objective was to test a complete collection of C. h
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