Academic literature on the topic 'Genetically designed'

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Journal articles on the topic "Genetically designed"

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Tamerler, Candan, and Mehmet Sarikaya. "Genetically Designed Peptide-Based Molecular Materials." ACS Nano 3, no. 7 (July 28, 2009): 1606–15. http://dx.doi.org/10.1021/nn900720g.

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Oliveri, G., M. Donelli, and A. Massa. "Genetically-designed arbitrary length almost difference sets." Electronics Letters 45, no. 23 (2009): 1182. http://dx.doi.org/10.1049/el.2009.1927.

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Anderson, Neil O., and Natalie J. Walker. "Marketing Genetically Modified Organism Carnations by Future Floral Designers: Student-designed Policy Formulation." HortTechnology 23, no. 5 (October 2013): 683–88. http://dx.doi.org/10.21273/horttech.23.5.683.

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Genetically modified organism (GMO) crops provide new trait(s) that may benefit floral designers and consumers. A limited array of GMO cut flower cultivars exist in the floral markets worldwide: nine carnations (Dianthus caryophyllus) and one rose (Rosa ×hybrida). Labeling GMO flowers in the United States is not required. Thus, most distributors, flower auctions, brokers, wholesalers, floral designers and consumers are not aware that they exist. To test the acceptance of GMO cut flowers with potential future floral designers, n = 121 students enrolled in Floral Design (HORT 1013) at the University of Minnesota during 2005–07, 2009, and 2011, designed with standard and miniature GMO Moon™ series carnations. Each student created a Hogarth design with both types of carnations and assembled a price sheet. Students examined the differences between GMO lavender/purple carnations and those created with classic methods of spraying, dipping, or infusion. In 2009 only, students were also assigned to write a marketing paragraph about their GMO floral design. Each year, students were given an identical question on a subsequent midterm examination to determine their position on GMO cut flowers, including development of a floral shop policy to inform customers. Student examination responses ranged from not carrying GMO products [1/121 (0.8% response)], offering GMO/non-GMO carnation options to the consumer [81/121 (66.9% response)], or only selling only GMOs [33/121 (27.3% response)] that differed significantly from a 1:1:1 chi-square (χ2). A significant majority of students would inform their customers of the GMO crops [89/121 (73.6% response)]. In several instances, consumers were not to be informed of the GMO nature unless they queried about the higher price point. Similarly, marketing paragraphs did not uniformly highlight the GMO nature of the flowers. Implications for the next generation of floral designers demonstrate that, with the exception of students in 2005–06, most would sell both GMO and non-GMO flowers with a majority of shops clearly identifying GMOs.
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Yunus, Ian Sofian, and Shen-Long Tsai. "Designed biomolecule–cellulose complexes for palladium recovery and detoxification." RSC Advances 5, no. 26 (2015): 20276–82. http://dx.doi.org/10.1039/c4ra16200e.

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Zhong, Ming, Satish Sharma, and Pawan Lingras. "Genetically Designed Models for Accurate Imputation of Missing Traffic Counts." Transportation Research Record: Journal of the Transportation Research Board 1879, no. 1 (January 2004): 71–79. http://dx.doi.org/10.3141/1879-09.

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Wright, James N., Wan Ling Wong, Joseph A. Harvey, James A. Garnett, Laura S. Itzhaki, and Ewan R. G. Main. "Scalable Geometrically Designed Protein Cages Assembled via Genetically Encoded Split Inteins." Structure 27, no. 5 (May 2019): 776–84. http://dx.doi.org/10.1016/j.str.2019.02.005.

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Aich, Pulakesh, Jaeyeon An, Byeongseon Yang, Young Ho Ko, Junghyun Kim, James Murray, Hyung Joon Cha, Joon Ho Roh, Kyeng Min Park, and Kimoon Kim. "Self-assembled adhesive biomaterials formed by a genetically designed fusion protein." Chemical Communications 54, no. 89 (2018): 12642–45. http://dx.doi.org/10.1039/c8cc07475e.

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Patriarchi, Tommaso, Jounhong Ryan Cho, Katharina Merten, Mark W. Howe, Aaron Marley, Wei-Hong Xiong, Robert W. Folk, et al. "Ultrafast neuronal imaging of dopamine dynamics with designed genetically encoded sensors." Science 360, no. 6396 (May 31, 2018): eaat4422. http://dx.doi.org/10.1126/science.aat4422.

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Neuromodulatory systems exert profound influences on brain function. Understanding how these systems modify the operating mode of target circuits requires spatiotemporally precise measurement of neuromodulator release. We developed dLight1, an intensity-based genetically encoded dopamine indicator, to enable optical recording of dopamine dynamics with high spatiotemporal resolution in behaving mice. We demonstrated the utility of dLight1 by imaging dopamine dynamics simultaneously with pharmacological manipulation, electrophysiological or optogenetic stimulation, and calcium imaging of local neuronal activity. dLight1 enabled chronic tracking of learning-induced changes in millisecond dopamine transients in mouse striatum. Further, we used dLight1 to image spatially distinct, functionally heterogeneous dopamine transients relevant to learning and motor control in mouse cortex. We also validated our sensor design platform for developing norepinephrine, serotonin, melatonin, and opioid neuropeptide indicators.
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Zhong, Ming, Satish Sharma, and Pawan Lingras. "Refining Genetically Designed Models for Improved Traffic Prediction on Rural Roads." Transportation Planning and Technology 28, no. 3 (June 2005): 213–36. http://dx.doi.org/10.1080/03081060500120340.

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FUKUI, Emiko, Tomoko YUZAWA, Hiromichi MATSUMOTO, Akio KAWANOBE, Yumi SAKURAI, Tota OHSHIMA, Susumu HOUJO, et al. "Production of a Japanese Black calf designed genetically using reproductive technologies." Nihon Chikusan Gakkaiho 86, no. 3 (2015): 375–78. http://dx.doi.org/10.2508/chikusan.86.375.

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Dissertations / Theses on the topic "Genetically designed"

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Newcomb, Ellyn Margaret. "Effects of GM Disclosure Statements on Consumer Perceptions of Selected Food Products in Survey and Sensory Panel Settings." BYU ScholarsArchive, 2017. https://scholarsarchive.byu.edu/etd/6699.

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The National Bioengineered Food Disclosure Standard (PL 114-216) will require nearly all foods sold in the U.S. to bear a statement disclosing whether they contain genetically modified (GM) material. Past studies suggest the presence of such a statement could have profound effects on consumers; however, research comparing consumer response towards different GM-disclosure statements is scarce. PL 114-216 states that GM foods shall not be considered more or less safe than their non-bioengineered counterparts, nevertheless it would benefit regulators and food manufacturers to be aware of the possible effects such disclosures might have on consumers. In a nationwide survey, multiple disclosure statements with varying degrees of public familiarity were compared to evaluate consumer perceptions and attitudes associated with each statement. Average consumer knowledge level of GM processes was also measured. The statements were then paired with actual food items to determine whether specific product categories influenced consumer responses. A select few of these statements and foods were included in a taste panel, allowing researchers to analyze if disclosure statements affected a consumer's sensorial experience. Results suggested that consumers were most favorable towards statements indicating the absence of GM-material, however they also responded less negatively towards new disclosure statements that do not have negative connotations. Additionally, consumers may react differently depending on the food accompanying a particular disclosure, although the taste panel data found no evidence that statements affected actual eating experience. Importantly, data from both surveys and taste panel suggested a disclosure statement may affect consumer willingness to buy a product.
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Books on the topic "Genetically designed"

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Designer food: Mutant harvest or breadbasket of the world? Lanham, MD: Rowman & Littlefield, 2002.

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Pence, Gregory E. Designer Food: Mutant Harvest or Breadbasket for the World? Rowman & Littlefield Publishers, Inc., 2002.

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Chassy, Bruce M. Food Safety. Edited by Ronald J. Herring. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780195397772.013.027.

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Most consumers expect the food they eat to be safe. This concern is not lost on governments around the world, which explains why there are numerous laws and regulations intended to ensure food safety. There are many misconceptions about food safety, such as the belief that organic foods are safer than conventional food products. This article examines food safety, first by considering the factors that explain why genetically modified (GM) crops as well as the foods and feeds produced from them, are assumed to be as safe as any other food. It provides an overview of the history of the use of recombinant DNA in food crops and the production of transgenic crops. It then looks at the scientific food-safety risk assessment of crops produced using biotechnology. It also discusses food safety in relation to proteins in food, as well as food allergy and allergens. Finally, it reviews the results of animal studies designed to demonstrate the safety of GM crops and the politics underlying such studies.
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West-Eberhard, Mary Jane. Developmental Plasticity and Evolution. Oxford University Press, 2003. http://dx.doi.org/10.1093/oso/9780195122343.001.0001.

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The first comprehensive synthesis on development and evolution: it applies to all aspects of development, at all levels of organization and in all organisms, taking advantage of modern findings on behavior, genetics, endocrinology, molecular biology, evolutionary theory and phylogenetics to show the connections between developmental mechanisms and evolutionary change. This book solves key problems that have impeded a definitive synthesis in the past. It uses new concepts and specific examples to show how to relate environmentally sensitive development to the genetic theory of adaptive evolution and to explain major patterns of change. In this book development includes not only embryology and the ontogeny of morphology, sometimes portrayed inadequately as governed by "regulatory genes," but also behavioral development and physiological adaptation, where plasticity is mediated by genetically complex mechanisms like hormones and learning. The book shows how the universal qualities of phenotypes--modular organization and plasticity--facilitate both integration and change. Here you will learn why it is wrong to describe organisms as genetically programmed; why environmental induction is likely to be more important in evolution than random mutation; and why it is crucial to consider both selection and developmental mechanism in explanations of adaptive evolution. This book satisfies the need for a truly general book on development, plasticity and evolution that applies to living organisms in all of their life stages and environments. Using an immense compendium of examples on many kinds of organisms, from viruses and bacteria to higher plants and animals, it shows how the phenotype is reorganized during evolution to produce novelties, and how alternative phenotypes occupy a pivotal role as a phase of evolution that fosters diversification and speeds change. The arguments of this book call for a new view of the major themes of evolutionary biology, as shown in chapters on gradualism, homology, environmental induction, speciation, radiation, macroevolution, punctuation, and the maintenance of sex. No other treatment of development and evolution since Darwin's offers such a comprehensive and critical discussion of the relevant issues. Developmental Plasticity and Evolution is designed for biologists interested in the development and evolution of behavior, life-history patterns, ecology, physiology, morphology and speciation. It will also appeal to evolutionary paleontologists, anthropologists, psychologists, and teachers of general biology.
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Desroches, Julie. Peripheral analgesia involves cannabinoid receptors. Edited by Paul Farquhar-Smith, Pierre Beaulieu, and Sian Jagger. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198834359.003.0034.

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This landmark paper by Agarwal and colleagues was published in 2007, when the exact contribution of the activation of the cannabinoid type 1 receptor (CB1) receptors expressed on the peripheral terminals of nociceptors in pain modulation was still uncertain. At that time, while it was clearly demonstrated that the central nervous system (CNS) was involved in the antinociceptive effects induced by the activation of the CB1 receptor, many strains of mice in which the gene encoding the CB1 receptor was deleted by conditional mutagenesis were used to study the specific role of these receptors in pain. Creating an ingenious model of genetically modified mice with a conditional deletion of the CB1 receptor gene exclusively in the peripheral nociceptors, Agarwal and colleagues were the first to unequivocally demonstrate the major role of this receptor in the control of pain at the peripheral level. In fact, these mutant mice lacking CB1 receptors only in sensory neurons (those expressing the sodium channel Nav1.8) have been designed to highlight that CB1 receptors on nociceptors, and not those within the CNS, constitute an important target for mediating local or systemic (but not intrathecal) cannabinoid analgesia. Overall, they have clarified the anatomical locus of cannabinoid-induced analgesia, highlighted the potential significance of peripheral CB1-mediated cannabinoid analgesia, and revealed important insights into how the peripheral endocannabinoid system works in controlling both inflammatory pain and neuropathic pain.
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GMO sapiens: The life-changing science of designer babies. World Scientific, 2016.

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Crowley, Michael J., and Wendy K. Silverman. Coercion Dynamics and Problematic Anxiety in Children. Edited by Thomas J. Dishion and James Snyder. Oxford University Press, 2015. http://dx.doi.org/10.1093/oxfordhb/9780199324552.013.19.

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This chapter discusses contemporary work on parenting and child anxiety. It briefly discusses work on family aggregation and heritability in anxiety research, which highlights the relevance of parenting factors. It then discusses relevant parenting constructs in child anxiety research, followed by work on reciprocal and transactional parent and child effects in the development of anxiety. Next, it reviews recent work on parental control and anxiety considered within a genetically informed design. Research using neuroimaging of the neuroanatomy of negative reinforcement suggests extensions to understanding child–parent dynamics, potentially amplifying childhood anxiety. Finally, the chapter considers implications of this literature for clinical work including parents in youth anxiety treatment.
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Chow, Wong-Ho, Ghislaine Scelo, and Robert E. Tarone. Renal Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0051.

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Renal cancers in adults are classified into two major groups according to the anatomic subsite of origin. The predominant group, originating from the renal parenchyma, is mostly renal cell carcinoma, which, in turn, is further classified into morphologically, clinically, and genetically distinct subtypes. Over 75% of renal cell carcinomas are designated clear cell, which is closely linked to alterations in the VHL gene. Almost all cancers arising from the renal pelvis and ureter are urothelial carcinomas, previously known as transitional cell carcinomas. Renal cell cancer incidence rates have increased globally over the past few decades. In the United States, incidence rates among blacks have surpassed rates for whites. Modifiable risk factors such as cigarette smoking, obesity, and hypertension, are more common among blacks than whites, partly explaining the racial disparity in renal cell cancer incidence. Having a first-degree relative with kidney cancer also has been linked to a two- to five-fold elevated risk.
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McShane, Tony, Peter Clayton, Michael Donaghy, and Robert Surtees. Neurometabolic disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0213.

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Various disorders result from genetically determined abnormalities of enzymes, the metabolic consequences of which affect the development or functioning of the nervous system. The range of metabolic disturbances is wide, as is the resultant range of clinical syndromes. Although most occur in children, some can present in adult life, and increasing numbers of affected children survive into adult life. In some, specific treatments are possible or are being developed. The last 20 years has seen a considerable expansion in our understanding of the genetic and metabolic basis for many neurological conditions. Particular clinical presentations of neurometabolic disorders include ataxias, movement disorders, childhood epilepsies, or peripheral neuropathy. Detailed coverage of the entire range of inherited metabolic diseases of the nervous system is available in other texts (Brett 1997; Scriver et al. 2001; Menkes et al. 2005).Treatment is possible for some metabolic diseases. For instance, the devastating neurological effects of phenylketonuria have been recognized for many years. Neonatal screening for this disorder and dietary modification in the developed world has removed phenylketonuria from the list of important causes of serious neurological disability in children. This success has led to new challenges in the management of the adult with phenylketonuria and unexpected and devastating effect of the disorder on the unborn child of an untreated Phenylketonuria mother. More recently Biotinidase deficiency has been recognized as an important and easily treatable cause of serious neurological disease usually presenting with early onset drug resistant seizures. This and some other neurometabolic diseases can be identified on neonatal blood screening although a full range of screening is not yet routine in the United Kingdom. More disorders are likely to be picked up at an earlier asymptomatic stage as the sophistication of screening tests increases (Wilcken et al. 2003; Bodamer et al. 2007).Although individual metabolic disorders are rare, collectively such disorders are relatively common. In reality most clinicians will see an individual condition only rarely in a career. Furthermore, patients with certain rare conditions are often concentrated in specialist referral centres, further reducing the exposure of general and paediatric neurologists to these disorders. A recent study into progressive intellectual and neurological deterioration, PIND, gives some information about the relative frequency and distribution of some childhood neurodegenerative diseases in the United Kingdom (Verity et al. 2000; Devereux et al. 2004). Although primarily designed to identify any childhood cases of variant Creutzfeldt- Jakob disease, the study also provided much information about the distribution of neurometabolic disease in children in the United Kingdom. The commonest five causes of progressive intellectual and neurological deterioration over 5 years were Sanfilippo syndrome, 41 cases, adrenoleukodystrophy, 32 cases, late infantile neuronal ceroid lipofuschinosis, 32 cases, mitochondrial cytopathy, 30 cases, and Rett syndrome, 29 cases. Notably, geographical foci of these disorders were also found and correlate with high rate of consanguinity in some local populations.
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Book chapters on the topic "Genetically designed"

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Mishra, Raj Gaurav, and Jeevani Jayasinghe. "Broadband Stacked Microstrip Antenna with Genetically Designed Patches." In Advances in Fire and Process Safety, 149–56. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-7281-9_12.

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Hochuli, E. "Genetically Designed Affinity Chromatography Using a Novel Metal Chelate Absorbent." In Biologically Active Molecules, 217–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74582-9_10.

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Zhong, Ming, Satish Sharma, and Pawan Lingras. "Analyzing the Performance of Genetically Designed Short-Term Traffic Prediction Models Based on Road Types and Functional Classes." In Innovations in Applied Artificial Intelligence, 1133–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-540-24677-0_116.

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Kearsey, Michael J., and Harpal S. Pooni. "Designer chromosomes." In The Genetical Analysis of Quantitative Traits, 165–85. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-4441-2_8.

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Jones, Huw D. "Gene silencing or gene editing: the pros and cons." In RNAi for plant improvement and protection, 47–53. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0047.

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Abstract Research into plant genetics often requires the suppression or complete knockout of gene expression to scientifically validate gene function. In addition, the phenotypes obtained from gene suppression can occasionally have commercial value for plant breeders. Until recently, the methodological choices to achieve these goals fell into two broad types: either some form of RNA-based gene silencing; or the screening of large numbers of natural or induced random genomic mutations. The more recent invention of gene editing as a tool for targeted mutation potentially gives researchers and plant breeders another route to block gene function. RNAi is widely used in animal and plant research and functions to silence gene expression by degrading the target gene transcript. Although RNAi offers unique advantages over genomic mutations, it often leads to the formation of a genetically modified organism (GMO), which for commercial activities has major regulatory and acceptance issues in some regions of the world. Traditional methods of generating genomic mutations are more laborious and uncertain to achieve the desired goals but possess a distinct advantage of not being governed by GMO regulations. Gene editing (GE) technologies have some of the advantages of both RNAi and classical mutation breeding in that they can be designed to give simple knockouts or to modulate gene expression more subtly. GE also has a more complex regulatory position, with some countries treating it as another conventional breeding method whilst the EU defines GE as a technique of genetic modification and applies the normal GMO authorization procedures. This chapter explores the pros and cons of RNAi alongside other methods of modulating gene function.
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Jones, Huw D. "Gene silencing or gene editing: the pros and cons." In RNAi for plant improvement and protection, 47–53. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0006.

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Abstract Research into plant genetics often requires the suppression or complete knockout of gene expression to scientifically validate gene function. In addition, the phenotypes obtained from gene suppression can occasionally have commercial value for plant breeders. Until recently, the methodological choices to achieve these goals fell into two broad types: either some form of RNA-based gene silencing; or the screening of large numbers of natural or induced random genomic mutations. The more recent invention of gene editing as a tool for targeted mutation potentially gives researchers and plant breeders another route to block gene function. RNAi is widely used in animal and plant research and functions to silence gene expression by degrading the target gene transcript. Although RNAi offers unique advantages over genomic mutations, it often leads to the formation of a genetically modified organism (GMO), which for commercial activities has major regulatory and acceptance issues in some regions of the world. Traditional methods of generating genomic mutations are more laborious and uncertain to achieve the desired goals but possess a distinct advantage of not being governed by GMO regulations. Gene editing (GE) technologies have some of the advantages of both RNAi and classical mutation breeding in that they can be designed to give simple knockouts or to modulate gene expression more subtly. GE also has a more complex regulatory position, with some countries treating it as another conventional breeding method whilst the EU defines GE as a technique of genetic modification and applies the normal GMO authorization procedures. This chapter explores the pros and cons of RNAi alongside other methods of modulating gene function.
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Kingwell, Ross. "Incentive Design for Introducing Genetically Modified Crops." In Risk Management and the Environment: Agriculture in Perspective, 82–95. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-2915-4_6.

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Kearsey, Michael J., and Harpal S. Pooni. "Experimental design." In The Genetical Analysis of Quantitative Traits, 335–49. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-4441-2_16.

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Jiang, Xi-Ling, and Ai-Ming Yu. "Genetically Modified Mouse Models in ADME Studies." In ADME-Enabling Technologies in Drug Design and Development, 235–454. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118180778.ch28.

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Kearsey, Michael J., and Harpal S. Pooni. "Half-sib mating designs." In The Genetical Analysis of Quantitative Traits, 77–100. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-4441-2_5.

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Conference papers on the topic "Genetically designed"

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Uduwawala, Disala, Jeevani Jayasinghe, and Nimesha Narampanawe. "Genetically Designed High Gain Sierpinski Carpet Fractal Antenna." In 2019 IEEE 14th Conference on Industrial and Information Systems (ICIIS). IEEE, 2019. http://dx.doi.org/10.1109/iciis47346.2019.9063309.

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Muntean, Oana. "Genetically designed heuristics for the bin packing problem." In the 2007 GECCO conference companion. New York, New York, USA: ACM Press, 2007. http://dx.doi.org/10.1145/1274000.1274088.

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Diosan, Laura, Mihai Oltean, Alexandrina Rogozan, and Jean Pierre Pecuchet. "Genetically designed multiple-kernels for improving the SVM performance." In the 9th annual conference. New York, New York, USA: ACM Press, 2007. http://dx.doi.org/10.1145/1276958.1277332.

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Ramos, Fausto de Oliveira, and Ernesto Araujo. "Fuzzy-scored genetically-designed controller for the VLS-1 launcher." In 2008 IEEE 16th International Conference on Fuzzy Systems (FUZZ-IEEE). IEEE, 2008. http://dx.doi.org/10.1109/fuzzy.2008.4630494.

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Bossard, Jeremy A., Yan Tang, Douglas H. Werner, and Theresa S. Mayer. "Genetically designed multiband metallodielectric frequency selective surface filters for the mid-infrared." In 2007 IEEE Antennas and Propagation Society International Symposium. IEEE, 2007. http://dx.doi.org/10.1109/aps.2007.4396268.

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Li, Zikang, Zhengrong Zhang, Jie Huang, and Junbo Yang. "Genetically Designed Ultra-compact Wideband Multiple-use Reflectors with High Reflectivity Appling to Optics Communication." In 2019 IEEE 19th International Conference on Communication Technology (ICCT). IEEE, 2019. http://dx.doi.org/10.1109/icct46805.2019.8947154.

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Wenner, Brett R., Phillip Douglass, Suresh Shrestha, Bethel V. Sharma, Siyi Lai, Marc J. Madou, and Sylvia Daunert. "Genetically designed biosensing systems for high-throughput screening of pharmaceuticals, clinical diagnostics, and environmental monitoring." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Joseph R. Lakowicz and Richard B. Thompson. SPIE, 2001. http://dx.doi.org/10.1117/12.426736.

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Lin, Ying-Ting, Iren Kuznetsova, and Gou-Jen Wang. "Genetically Modified Soybean Detection Using a Biosensor Electrode With Self-Assembled Gold Nanoparticles on a Micro Hemisphere Array." In ASME 2019 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/detc2019-97112.

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Abstract Gene transfer technology changes some of the characteristics of crops. However, genetically modified foods have been reported to have an impact on human health. We proposed a cost effective and highly sensitive biosensor electrode with self-assembled monolayer of gold nanoparticle on a micro hemisphere array to detect genetically modified soybean. An ordered array of micro hemispherical features was formed on a 6-inch reclaimed silicon wafer using photolithography. Then, a thin gold layer was sputtered onto the hemispheres. The wafer was then immersed into a 5 mM ethanol solution of 1,6-hexanedithiol (1,6-HDT) to enable the attachment of one thio-end of 1,6-HDT to the thin gold layer. Next, a colloidal gold (15 nm) solution was dripped onto the wafer and baked on a hot plate in such a way that the monolayer of gold nanoparticles could self-assemble on the 1,6-HDT surface. Finally, we used electrochemical impedance spectroscopy (EIS) analysis to detect genetically modified soybean. Experimental results demonstrate that our biosensor can successfully distinguish the genetically modified soybeans from the normal ones.
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Cohen, Lawrence. "Genetically Encoded Fluorescent Voltage Indicators (GEVIs) in the Mammalian Brain." In Bio-Optics: Design and Application. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/boda.2015.brt2b.6.

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Konur, S., and M. Gheorghe. "Design and Analysis of Genetically Constructed Logic Gates." In University of Sheffield Engineering Symposium. USES, 2015. http://dx.doi.org/10.15445/01012014.44.

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Reports on the topic "Genetically designed"

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Shuler, Michael L. Development of Cell Models as a Basis for Bioreactor Design for Genetically Modified Bacteria. Fort Belvoir, VA: Defense Technical Information Center, October 1986. http://dx.doi.org/10.21236/ada174571.

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