Bibliographies thématiques / Biology - biotechnology

Littérature scientifique sur le sujet « Biology - biotechnology »

Auteur : Grafiati
Publié le 26 juillet 2024

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Articles de revues sur le sujet "Biology - biotechnology"

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Penders, Bart. « Biotechnology : DIY biology ». Nature 472, no 7342 (avril 2011) : 167. http://dx.doi.org/10.1038/472167a.

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Kadam, Komal, et Ram Kulkarni. « Connecting Biology With Biotechnology ». Resonance 27, no 10 (19 octobre 2022) : 1741–59. http://dx.doi.org/10.1007/s12045-022-1469-0.

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Roig, Manuel G. « Molecular Biology and Biotechnology ». Biochemical Education 15, no 1 (janvier 1987) : 54. http://dx.doi.org/10.1016/0307-4412(87)90178-6.

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Parslow, G. « Molecular Biology and Biotechnology ». Biochemical Education 20, no 2 (avril 1992) : 124. http://dx.doi.org/10.1016/0307-4412(92)90138-c.

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Svendsen, A. Baerheim. « Molecular biology and biotechnology ». TrAC Trends in Analytical Chemistry 6, no 4 (avril 1987) : XXIII—XXIV. http://dx.doi.org/10.1016/0165-9936(87)87045-0.

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Plant, Nick. « Molecular Biology and Biotechnology ». Drug Discovery Today 6, no 23 (décembre 2001) : 1206. http://dx.doi.org/10.1016/s1359-6446(01)02053-0.

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Fonseca, Maria João, Patrício Costa, Leonor Lencastre et Fernando Tavares. « Disclosing biology teachers’ beliefs about biotechnology and biotechnology education ». Teaching and Teacher Education 28, no 3 (avril 2012) : 368–81. http://dx.doi.org/10.1016/j.tate.2011.11.007.

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Wray, Francis P., Mary C. Fox, Carl A. Huether et Eric R. Schurdak. « Biotechnology for Non-Biology Majors ». American Biology Teacher 63, no 5 (mai 2001) : 363–67. http://dx.doi.org/10.1662/0002-7685(2001)063[0363:bfnbm]2.0.co;2.

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Hinata, Kokichi. « Molecular Biology : Biotechnology in Plants ». TRENDS IN THE SCIENCES 3, no 2 (1998) : 80–81. http://dx.doi.org/10.5363/tits.3.2_80.

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Singh, Zora, Rajesh K. Singh, Vidhu A. Sane et Pravendra Nath. « Mango - Postharvest Biology and Biotechnology ». Critical Reviews in Plant Sciences 32, no 4 (4 juillet 2013) : 217–36. http://dx.doi.org/10.1080/07352689.2012.743399.

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Thèses sur le sujet "Biology - biotechnology"

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Cupples, Gemma. « Fibre-laden flows in biology and biotechnology ». Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8308/.

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Fibre-laden fluids are ubiquitous in biological and physical systems; the fibres alter the rheology of the fluid and hence the emergent behaviour of the system. This thesis investigates two physical situations associated with fibrous media. Firstly we optimise the shear-induced alignment of suspensions of elongated particles, motivated by collaboration with Linear Diagnostics Ltd who are developing handheld devices to detect disruptions in fibre alignment due to pathogen presence in biological samples. Incorporating the effects of fibre dispersion and the mechanical anisotropy induced by the particles, we model suspensions of elongated particles undergoing steady or oscillating ow using a Fokker-Planck framework, producing recommendations for designs which optimise the signal to noise ratio. Next, we investigate microscopic propulsion in perfectly aligned media; for example the evolving fibrous structure of cervical mucus and more generally the problem of propulsion and pumping of an active fluid with alignment. We model the swimming of spermatozoa by adapting Taylor's classical swimming sheet model using Ericksen's transversely isotropic constitutive law (a limit of the Fokker-Planck model), to account for an aligned fibrous network. We find that propulsion in fibre-laden fluids is drastically different from Newtonian fluids, supporting the requirement to investigate fibrous rheology.
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Willrodt, Christian. « Synthetic biology for synthetic chemistry - Microbial production and selective functionalization of limonene ». Doctoral thesis, Universitätsbibliothek Leipzig, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-201140.

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The progress in biotechnological disciplines such as metabolic engineering or synthetic biology increased the interest of chemical and pharmaceutical industries to implement microbial processes for chemical synthesis. However, most microorganisms, e.g., Escherichia coli or Saccharomyces cerevisiae, used in biotechnological applications are not evolved by nature for the production of industrially relevant compounds, which are often hydrophobic, non-charged, volatile, or toxic to the microbial organisms. Bioprocess design relies on an integrated approach addressing pathway, cellular, reaction, and process engineering to combine the results of natural evolution with the demands of industrial applicability. In this thesis, the microbial de novo production and selective oxyfunctionalization of the highly volatile isoprenoid limonene has been investigated as a model system featuring reactants with challenging physicochemical characteristics. Key constraints that limit limonene biosynthesis and its oxyfunctionalization in recombinant E. coli, related to genetics, physiology, and reaction engineering, were identified and relieved.
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Hudson, Cheryl A. « Impact of biotechnology labs on high school biology students ». Montana State University, 2011. http://etd.lib.montana.edu/etd/2011/hudson/HudsonC0811.pdf.

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There is a growing interest and emphasis on teaching biotechnology methods and concepts to high school level students in order to help prepare them to be able to participate in highly technological careers. Numerous biotechnology professional development programs exist for science teachers to gain knowledge and skills that are necessary to teach biotechnology. While it is an easy transition to teach biotechnology methods in advanced and AP level courses, there is uncertainty about the limitations and accommodations that will be necessary to incorporate biotechnology labs into a regular high school biology classroom with 28 students or more of various levels and exceptionalities. The additional expense and time necessary to incorporate biotechnology are justified if students gain increased conceptual understanding and demonstrate improved attitude toward science as a result of the labs. The primary question I sought to answer with this project was what are the effects of incorporating biotechnology labs on high school students' understanding of molecular biology concepts? Secondary questions related to the project are: What were the effects of incorporating biotechnology labs on students' interest in science, students' confidence in their abilities to do science, and on my teaching practices? The sequence of biotechnology labs that occurred within the curriculum of compulsory high school biology were quantitative protein analysis of food, DNA fingerprinting, pGLO bacterial transformation, and GMO investigation of food. The labs utilized Vernier Probeware and Bio-Rad Explorer kits. Conceptual understanding of molecular biology concepts was assessed using student developed concept maps and free-response questions. Anonymous student surveys and one-on-one student interviews were used to assess attitude toward science, which is defined in this project as interest, confidence, and relevance. Results for improved attitude were inconclusive; however gains in conceptual understanding were substantial with the biotechnology labs.
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Madani, Fatemeh. « Biophysical studies of peptides with functions in biotechnology and biology ». Doctoral thesis, Stockholms universitet, Institutionen för biokemi och biofysik, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-66948.

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My thesis concerns spectroscopic studies (NMR, CD and fluorescence) of peptides with functions in biotechnology and biology, and their interactions with a model membrane (large unilamellar phospholipid vesicles). The resorufin-based arsenical hairpin binder (ReAsH) bound to a short peptide is a useful fluorescent tag for genetic labeling of proteins in living cells. A hairpin structure with some resemblance to type II β-turn was determined by NMR structure calculations (Paper I). Cell-penetrating peptides (CPPs) are short (30-35 residues), often rich in basic amino acids such as Arg. They can pass through the cell membrane and deliver bioactive cargoes, making them useful for biotechnical and pharmacological applications. The mechanisms of cellular uptake and membrane translocation are under debate. Understanding the mechanistic aspects of CPPs is the major focus of Papers II, III, and IV. The effect of the pyrenebutyrate (PB) on the cellular uptake, membrane translocation and perturbation of several CPPs from different subgroups was investigated (Paper II). We concluded that both charge and hydrophobicity of the CPP affect the cellular uptake and membrane translocation efficiency. Endosomal escape is a crucial challenge for the CPP applications. We modeled the endosome and endosomal escape for different CPPs to investigate the corresponding molecular mechanisms (Papers III and IV). Hydrophobic CPPs were able to translocate across the model membrane in the presence of a pH gradient, produced by bacteriorhodopsin proton pumping, whereas a smaller effect was observed for hydrophilic CPPs. Dynorphin A (Dyn A) peptide mutations are associated with neurodegenerative disorders, without involvement of the opioid receptors. The non-opioid activities of Dyn A may involve membrane perturbations. Model membrane-perturbations by three Dyn A mutants were investigated (Paper V). The results showed effects to different degrees largely in accordance with their neurotoxic effects.

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 4: Manuscript.

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Funder, Joshua V. « Biology, information and property : the legal appropriation of plant biotechnology ». Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365449.

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Soenksen, Martinez Luis Rubén. « Cell-free freeze-dried synthetic biology for wearable biotechnology applications ». Thesis, Massachusetts Institute of Technology, 2019. https://hdl.handle.net/1721.1/127730.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2020
Cataloged from PDF of thesis. "February 2020."
Includes bibliographical references (pages 163-173).
Synthetic biology aims to develop modular genetic networks for computation, sensing, and control of biological systems, holding great promise for next-generation biosensing platforms. Similarly, advances in material sciences have allowed for the design of substrates and textiles engineered to exhibit novel mechanical, electrical, and optical properties for sensing and actuation. Wearable biosensors using synthetic biology principles and smart materials could expand on this potential, especially as solutions for continuous, fine-grained monitoring of physiological status, disease states, and pathogen/toxin exposure difficult to assess with other methods. Despite this, only few examples of synthetic biology sensors compatible with wearable use-cases have been described, all of which rely on the use of live engineered bacteria with sustainment limitations.
Thus, we report on the development of novel shelf-stable, genetically-programmable, and highly sensitive wearable sensing platforms based on cell-free synthetic biology components freeze-dried into flexible substrates and textiles; as well as on a new class of smart programmable synthetic biology materials capable of reacting to environmental queues. These systems were designed to exhibit colorimetric, fluorescent, luminescence, electrical, or mechanical outputs that can be passively or actively interrogated within isolated modules or in larger-scale garments with wireless networking capabilities. We functionally validated such platforms using a variety of synthetic biology circuits for detecting several relevant environmental exposure targets such as metabolites, chemicals, and pathogen-associated nucleic acids.
These findings suggest that cell-free synthetic biology tools have the potential to enable highly programmable wearable systems for rapid on-body detection or adaptation to external threats in first responders, warfighters or clinical personnel, as well as the assessment of athletic performance and monitoring to complex disease states.
by Luis Rubén Soenksen Martinez.
Ph. D.
Ph.D. Massachusetts Institute of Technology, Department of Mechanical Engineering
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Camsund, Daniel. « Engineering Transcriptional Systems for Cyanobacterial Biotechnology ». Doctoral thesis, Uppsala universitet, Molekylär biomimetik, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-223599.

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Cyanobacteria are solar-powered cell factories that can be engineered to supply us with renewable fuels and chemicals. To do so robust and well-working biological parts and tools are necessary. Parts for controlling gene expression are of special importance in living systems, and specifically promoters are needed for enabling and simplifying rational design. Synthetic biology is an engineering science that incorporates principles such as decoupling, standardization and modularity to enable the design and construction of more advanced systems from simpler parts and the re-use of parts in new contexts. For these principles to work, cross-talk must be avoided and therefore orthogonal parts and systems are important as they are decoupled by definition. This work concerns the design and development of biological parts and tools that can enable synthetic biology in cyanobacteria. This encompasses parts necessary for the development of other systems, such as vectors and translational elements, but with a focus on transcriptional regulation. First, to enable the development and characterization of promoters in different cyanobacterial chassis, a broad-host-range BioBrick plasmid, pPMQAK1, was constructed and confirmed to function in several cyanobacterial strains. Then, ribosome binding sites, protease degradation tags and constitutive, orthogonal promoters were characterized in the model strain Synechocystis PCC 6803. These tools were then used to design LacI-regulated promoter libraries for studying DNA-looping and the behaviour of LacI-mediated loops in Synechocystis. Ultimately, this lead to the design of completely repressed LacI-regulated promoters that could be used for e.g. cyanobacterial genetic switches, and was used to design a destabilized version of the repressed promoter that could be induced to higher levels. Further, this promoter was used to implement an orthogonal transcriptional system based on T7 RNAP that was shown to drive different levels of T7 promoter transcription depending on regulation. Also, Gal4-repressed promoters for bacteria were engineered and examined in Escherichia coli as an initial step towards transferring them to cyanobacteria. Attempts were also made to implement a light-regulated one-component transcription factor based on Gal4. This work provides a background for engineering transcription and provides suggestions for how to develop the parts further.
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Bigler, Amber L. « Student Content Knowledge Increases After Participation in a Hands-on Biotechnology Intervention ». BYU ScholarsArchive, 2010. https://scholarsarchive.byu.edu/etd/2522.

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Hands-on learning is at the heart of science learning. This study examined increased changes of student content knowledge in biology, particularly biotechnology, after a hands-on biotechnology intervention was implemented into a secondary school. A traditional learning school was selected for a control. Both teachers had participated in a biotechnology professional development program called Project Crawfish. Students from both schools took the same assessment before and after their respective units (biotechnology intervention and genetics unit), and the classroom was the unit of analysis (n=5, n=6, respectively). The assessment was compared as a whole and then divided into five components, eight questions each: DNA extraction/gel electrophoresis, polymerase chain reaction (PCR), DNA sequencing, bioinformatics, and phylogenetics. The pre-tests were compared to establish a baseline between the two schools. The biotechnology intervention school began with a higher pre-test raw score than the traditional learning school. After adjusting for the pre-test scores, each school was analyzed for increases in student content knowledge and then compared to each other for any significant increases between the two schools. When the entire assessment was analyzed, each school had statistically significant increases in student content knowledge (<0.0001 for the biotechnology intervention school and 0.0481 for the traditional learning school). When the schools were compared to each other, a p-value of 0.0543 provided a suggestive relationship that the biotechnology intervention school had a larger increase in student content knowledge. When the assessment was divided into the five components, the traditional learning school had statistically significant increases in student content knowledge in the PCR and DNA sequencing components (0.0459, 0.0043, respectively). The biotechnology intervention school had statistically significant increases in student content knowledge in all five components. However, there were no significant differences in learning between the two schools. Implementing biotechnology through hands-on teaching methods should be considered by secondary science teachers. Further research would scale up this study to include more classrooms.
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Dias, Camila Arnaldo Olhê [UNESP]. « Análise estrutural e funcional de eIF5A selvagem e mutadas ». Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/100727.

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Made available in DSpace on 2014-06-11T19:31:00Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-01-22Bitstream added on 2014-06-13T18:41:22Z : No. of bitstreams: 1 dias_cao_dr_araiq.pdf: 1123564 bytes, checksum: ea894f973e080c3d5cae0ce5cf5f2c2e (MD5)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
O fator de início de tradução 5A (eIF5A) é altamente conservado de arqueas a mamíferos e é essencial para a viabilidade celular. Este fator tem sido associado com o início da tradução, proliferação celular, transporte nucleocitoplasmático e decaimento de mRNA. Estudos recentes associam eIF5A com a elongação, ao invés do inicio da tradução. eIF5A é a única proteína conhecida que contém o aminoácido essencial hipusina, gerado pelas enzimas desoxihipusina sintase e desoxihipusina hidroxilase. O objetivo deste estudo foi a caracterização estrutural e funcional de eIF5A de S. cerevisiae. Primeiramente, a estrutura terciária de eIF5A foi determinada por cristalografia e foi demonstrada a sua dimerização em solução, independentemente do resíduo hipusina. Foram obtidos e caracterizados 40 mutantes novos de eIF5A, dos quais 19 não complementaram o nocaute do gene selvagem, 13 apresentaram fenótipo de termossensibilidade e 8 não apresentaram nenhuma alteração nos fenótipos investigados. A maioria dos mutantes novos tem seus fenótipos resultantes da degradação da proteína eIF5A. Curiosamente, este é o primeiro estudo que sugere que a α-hélice presente no C-terminal de eIF5A é essencial para a manutenção da sua estrutura. Descrevemos também, que a extensão N-terminal de eIF5A, presente apenas em eucariotos, não é essencial para estrutura e função dessa proteína. Além disso, os mutantes contendo substituições na alça onde está localizado o aminoácido hipusina são inviáveis ou termossensíveis. Embora estes mutantes produzam eIF5A, inclusive na temperatura não permissiva, a proteína produzida não é hipusinada. Finalmente, dois mutantes termossensíveis (tif51AK56A e tif51AQ22H/L93F) produzem a proteína eIF5A estável na temperatura não permissiva, no entanto, apresentam...
The translation initiation factor 5A (eIF5A) is highly conserved from archae to mammals and is essential for cell viability. This factor has been associated with translation initiation, cell proliferation, nucleocytoplasmatic transport and mRNA decay. Recent studies show eIF5A involved in elongation, rather than translation initiation. eIF5A is the only protein known to contain the essential amino acid residue hypusine, generated by the enzymes deoxyhypusine synthase and deoxyhypusine hydroxylase. The main goal of this study was the structural and functional characterization of S. cerevisiae eIF5A. First of all, the tertiary structure of eIF5A was determined by crystallography and this protein was defined as a dimer in solution, independently of the hipusine residue. We obtained and characterized 40 new mutants, which 19 cannot complement tif51A knockout cells, 13 are temperature-sensitive and 8 show no detectable phenotype. The phenotypes of most mutantes are caused by protein folding defects. Interestingly, this is the first study suggesting that the C-terminal -helix present in yeast eIF5A may be an essential structural element. Moreover, we describe that the eIF5A N-terminal extension present only in eukaryotic homologues is not essential in yeast. Furthermore, the mutants containing substitutions surrounding the hypusine modification site showed unviable or temperature-sensitive phenotypes. Although these mutant proteins were stable, they were defective in hypusine modification. Finally, two of the temperature-sensitive mutant strains (tif51AK56A and tif51AQ22H/L93F) produced stable eIF5A protein but showed defects in growth and protein synthesis and these mutants revealed polysome profile defect similar to that described for mutations in factors involved in translation... (Complete abstract click electronic access below)
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Kim, Daniel. « Characterization of the MATα pre-/pro- peptide by mutagenesis as a means to optimize secretion in pichia pistoris ». Scholarly Commons, 2009. https://scholarlycommons.pacific.edu/uop_etds/738.

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The unicellular yeast, Pichia pastoris has currently emerged as one of the most popular host systems for heterologous proteins due to its relatively cheap cost, easy genetic manipulability, ability to perform post-translational modifications on proteins, and respiratory growth capabilities which allow it to be cultured in very high concentrations. Over 700 foreign proteins have been recombinantly expressed using P. pastoris. Although P. pastoris appears to be an ideal host system, its main drawback is its inability to efficiently export some heterologous proteins into the extracellular medium. The incorporation of S. cerevisiae's MATα pre-pro signal leader (MATα) has led to increased protein secretion in most cases. MATα is thus used in the production of 90% of all proteins secreted in P. pastoris. However secretion efficiency still remains a problem. It has been suspected that low secretion may be attributed to improper extracellular targeting (a function of MATα). In order to address these issues there has been a precedent for performing limited mutagenesis of a signal leader peptide (like MATα) to increase protein secretion. In one study the insertion of a 10 amino-acid residue into MATα resulted in a 5-fold increase in secretion of bacterial phytase, an important industrial enzyme. Despite this success there have been no systematic mutagenesis processes which would help elucidate the reason behind this case of increased secretion. In our study, we performed a series of mutagenesis events, both random and site directed, with the intent of illuminating the mechanisms of MATα that contribute to secretion. As a result were able to create a novel secretion signal (pLL3) with enhanced secretion levels of our reporter protein HRP.
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Livres sur le sujet "Biology - biotechnology"

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Kreuzer, Helen, et Adrianne Massey. Biology and Biotechnology. Washington, DC, USA : ASM Press, 2005. http://dx.doi.org/10.1128/9781555816094.

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Kreuzer, Helen, et Adrianne Massey. Molecular Biology and Biotechnology. Washington, DC, USA : ASM Press, 2007. http://dx.doi.org/10.1128/9781555817480.

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Walker, John M., et Ralph Rapley, dir. Molecular Biology and Biotechnology. Cambridge : Royal Society of Chemistry, 2000. http://dx.doi.org/10.1039/9781847551498.

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Kreuzer, Helen, et Adrianne Massey. Molecular Biology and Biotechnology. Washington, DC, USA : ASM Press, 2007. http://dx.doi.org/10.1128/9781555816100.

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Bahadur, Bir, Manchikatla Venkat Rajam, Leela Sahijram et K. V. Krishnamurthy, dir. Plant Biology and Biotechnology. New Delhi : Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2283-5.

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Bahadur, Bir, Manchikatla Venkat Rajam, Leela Sahijram et K. V. Krishnamurthy, dir. Plant Biology and Biotechnology. New Delhi : Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2286-6.

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Hansen, Alexander P., Devendra K. Choudhary, Pawan Kumar Agrawal et Ajit Varma, dir. Rhizobium Biology and Biotechnology. Cham : Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-64982-5.

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Smith, C. A., et E. J. Wood. Molecular Biology and Biotechnology. Boston, MA : Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3866-0.

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Rapley, Ralph, dir. Molecular Biology and Biotechnology. Cambridge : Royal Society of Chemistry, 2009. http://dx.doi.org/10.1039/9781849730211.

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Oka, Melvin S., et Randall G. Rupp, dir. Cell Biology and Biotechnology. New York, NY : Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4684-9418-1.

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Chapitres de livres sur le sujet "Biology - biotechnology"

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Sutton, Julian. « Biotechnology ». Dans Biology, 489–503. London : Macmillan Education UK, 1998. http://dx.doi.org/10.1007/978-1-349-15201-8_31.

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Smith, George P. « Biotechnology ». Dans The New Biology, 1–13. Boston, MA : Springer US, 1989. http://dx.doi.org/10.1007/978-1-4899-0803-2_1.

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Priyadarshan, P. M. « Biotechnology ». Dans Biology of Hevea Rubber, 185–89. Cham : Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-54506-6_12.

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Hammann, Marcus. « Biotechnology ». Dans Teaching Biology in Schools, 192–203. New York : Routledge, 2018. | Series : Teaching and learning in science series : Routledge, 2018. http://dx.doi.org/10.4324/9781315110158-16.

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Otero, José Manuel, et Jens Nielsen. « Industrial Systems Biology ». Dans Industrial Biotechnology, 79–147. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527630233.ch2.

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Zdobnov, Evgeni M., Rodrigo Lopez, Rolf Apweiler et Thure Etzold. « Using the Molecular Biology Data ». Dans Biotechnology, 281–300. Weinheim, Germany : Wiley-VCH Verlag GmbH, 2008. http://dx.doi.org/10.1002/9783527620876.ch12.

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Fioroni, Marco, Tamara Dworeck et Francisco Rodríguez-Ropero. « Biotechnology ». Dans Advances in Experimental Medicine and Biology, 95–140. Dordrecht : Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7429-2_5.

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Koul, Bhupendra, et Joginder Singh. « Lychee Biology and Biotechnology ». Dans The Lychee Biotechnology, 137–92. Singapore : Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3644-6_5.

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Hahn, S. K., K. V. Bai, R. Asiedu, A. G. O. Dixon, S. Tavoletti, A. Mariani, F. Veronesi et al. « Biotechnology in Reproductive Biology ». Dans Angiosperm Pollen and Ovules, 340–46. New York, NY : Springer New York, 1992. http://dx.doi.org/10.1007/978-1-4612-2958-2_55.

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Besharati, Hossein, Nasser Aliasgharzad, Kazem Khavazi et Hadi Asadi Rahmani. « Soil Biology and Biotechnology ». Dans World Soils Book Series, 189–211. Cham : Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-69048-3_11.

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Actes de conférences sur le sujet "Biology - biotechnology"

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Sypsas, Athanasios, et Dimitris Kalles. « Virtual laboratories in biology, biotechnology and chemistry education ». Dans PCI '18 : 22nd Pan-Hellenic Conference on Informatics. New York, NY, USA : ACM, 2018. http://dx.doi.org/10.1145/3291533.3291560.

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Polizzi, K. M., et P. S. Freemont. « Synthetic biology biosensors for healthcare and industrial biotechnology applications ». Dans IET/SynbiCITE Engineering Biology Conference. Institution of Engineering and Technology, 2016. http://dx.doi.org/10.1049/cp.2016.1235.

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Duda, Hilarius Jago, F. Rahayu Esti Wahyuni et Antonius Edy Setyawan. « Plant biotechnology : Studying the misconception of biology education students ». Dans INTERNATIONAL CONFERENCE ON SCIENCE AND APPLIED SCIENCE (ICSAS2020). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0030449.

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Martin, Stephen. « Annual International Conference on BioInformatics and Computational Biology / Advances in Biotechnology ». Dans Annual International Conference on BioInformatics and Computational Biology / Advances in Biotechnology. Global Science & Technology Forum (GSTF), 2011. http://dx.doi.org/10.5176/978-981-08-8227-3_bicb-biotech-2011.

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Mak, Benjamin, Liam Birkett, Maurice Klee, Eoin Cunneen et Alain Colombet. « Intellectual property in medical devices and biotechnology ». Dans 2007 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2007. http://dx.doi.org/10.1109/iembs.2007.4353308.

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« Preface : Proceeding of International Biology Conference 2016 Biodiversity and Biotechnology for Human Welfare ». Dans PROCEEDING OF INTERNATIONAL BIOLOGY CONFERENCE 2016 : Biodiversity and Biotechnology for Human Welfare. Author(s), 2017. http://dx.doi.org/10.1063/1.4985390.

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Gu, Lemin. « Generalized Least Absolute Deviation Method and Its Application in Biology ». Dans 2012 International Conference on Biomedical Engineering and Biotechnology (iCBEB). IEEE, 2012. http://dx.doi.org/10.1109/icbeb.2012.233.

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« Systems biology study on the WOX5 role in the distal part of the root meristem in Arabidopsis thaliana ». Dans Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-157.

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Fontova, A., A. Soley, J. Galvez, E. Sarro, M. Lecina, J. Rosell, P. Riu, J. Cairo, F. Godia et R. Bragos. « Multiple automated minibioreactor system for multifunctional screening in biotechnology ». Dans Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.260628.

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Fontova, A., A. Soley, J. Galvez, E. Sarro, M. Lecina, J. Rosell, P. Riu, J. Cairo, F. Godia et R. Bragos. « Multiple automated minibioreactor system for multifunctional screening in biotechnology ». Dans Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.4397480.

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Rapports d'organisations sur le sujet "Biology - biotechnology"

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Prange, C. 2003 Biology and Biotechnology Research Program Overview and Highlights. Office of Scientific and Technical Information (OSTI), mars 2003. http://dx.doi.org/10.2172/15005878.

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Carter, Sarah R., Michael Rodemeyer, Michele S. Garfinkel et Robert M. Friedman. Synthetic Biology and the U.S. Biotechnology Regulatory System : Challenges and Options. Office of Scientific and Technical Information (OSTI), mai 2014. http://dx.doi.org/10.2172/1169537.

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ARMY WAR COLL CARLISLE BARRACKS PA. VI International Congress on Pseudomonas : Molecular Biology and Biotechnology, Scientific Program and Abstracts. Fort Belvoir, VA : Defense Technical Information Center, septembre 1997. http://dx.doi.org/10.21236/ada390535.

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Revill, James, Alisha Anand et Giacomo Persi Paoli. Exploring Science and Technology Review Mechanisms Under the Biological Weapons Convention. The United Nations Institute for Disarmament Research, juin 2021. http://dx.doi.org/10.37559/sectec/2021/sandtreviews/01.

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Since the Biological Weapons Convention (BWC) opened for signature in 1972, biology and other converging disciplines have advanced considerably. These changes could have profound implications for a science-based disarmament agreement like the BWC. To address changes in biology and biotechnology, BWC States Parties have established processes to review developments in science and technology (S&T), including annual expert meetings on this topic. However, shortcomings are evident in the current approaches and many BWC States Parties have expressed support for a more systematic review of science and technology under the Convention. This study seeks to inform discussions on establishing a dedicated and systematic S&T review process under the BWC through an examination of existing S&T review-type mechanisms employed in different regimes beyond the BWC, a survey of States Parties views on a possible review mechanism and a study of past and present discourse on this issue in the BWC. Based on the analysis conducted, this study also presents options for BWC States Parties to consider ahead of the Ninth BWC Review Conference.
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Sherman, A., D. N. Kuhn, Y. Cohen, R. Ophir et R. Goenaga. Exploring the polyembryonic seed trait in mango as a basis for a biotechnology platform for fruit tree crops. Israel : United States-Israel Binational Agricultural Research and Development Fund, 2021. http://dx.doi.org/10.32747/2021.8134176.bard.

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Mango is one of the most important fruit crops. However, the biology of this fruit tree is under studied. The lack of genetic and genomic resources has limited progress in mango research and breeding. Several research groups have recently started developing genomic tools for mango by creating transcriptome and genomic data. Sexual reproduction in plants is the main pathway for the creation of new genetic combinations. In modern agriculture, breeders exploit the genetic diversity generated through sexual reproduction to develop elite cultivars; however, these cultivars require genetic stabilization before they are suitable for mass propagation for uniform crop production. In heterozygous plants such as fruit trees, vegetative propagation (cloning) is the primary path for the propagation of genetically uniform plants. Another natural plant mechanism that can create genetically uniform plants (clones) is apomixes. Apomixis is defined as asexual reproduction through seeds that lead to the production of clonal progeny whose genotype is identical to that of the mother plant. In fruit crops like citrus and mango, sporophytic apomixes result in polyembryony, where seeds contain multiple embryos, one of which is sexually originated, and the others are clones of the mother tree. As part of this research, the reference genome of mango was established as a basic platform for mango breeding and research. It was used to map two important mango traits fruit size and polyembryony. The draft genome 'Tommy Atkins' sequence was generated using NRGene de-novo Magic on high molecular weight DNA of 'Tommy Atkins,' supplemented by 10X Genomics long read sequencing to improve the initial assembly. The final 'Tommy Atkins' genome assembly was a consensus sequence that included 20 pseudomolecules representing the 20 chromosomes of mango. The availability of a genome enables the genetic dissection of important traits. We demonstrated the utility of the genome assembly and the 'Tommy Atkins' x 'Kensington Pride' map by analyzing fruit weight phenotypic data and identifying two QTLs for this trait.
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Harris, J. M. International Conference on Partitioning in Aqueous Two-Phase Systems : Advances in Separation in Biochenistry, Cell Biology and Biotechnology (7th) Held in New Orleans, Louisiana on 2-7 June 1991. Fort Belvoir, VA : Defense Technical Information Center, juin 1991. http://dx.doi.org/10.21236/ada250766.

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