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Relevant bibliographies by topics / Control by RNA

Academic literature on the topic 'Control by RNA'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Control by RNA"

1

Zong, Xinying, Vidisha Tripathi, and Kannanganattu V. Prasanth. "RNA splicing control." RNA Biology 8, no. 6 (November 2011): 968–77. http://dx.doi.org/10.4161/rna.8.6.17606.

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Sheppard, Terry L. "RNA takes control." Nature Chemical Biology 9, no. 12 (November 14, 2013): 754. http://dx.doi.org/10.1038/nchembio.1397.

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Blencowe, Benjamin J., and May Khanna. "RNA in control." Nature 447, no. 7143 (May 2007): 391–93. http://dx.doi.org/10.1038/447391a.

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HASEGAWA, TAKEMA, JUNKO TAKAHASHI, and HITOSHI IWAHASHI. "RNA Quality Control Using External Standard RNA." Polish Journal of Microbiology 67, no. 3 (2018): 347–53. http://dx.doi.org/10.21307/pjm-2018-042.

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Bellacosa, Alfonso, and Eric G. Moss. "RNA Repair: Damage Control." Current Biology 13, no. 12 (June 2003): R482—R484. http://dx.doi.org/10.1016/s0960-9822(03)00408-1.

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Chetnani, Bhaskar, and Alfonso Mondragón. "RNA exerts self-control." Nature 500, no. 7462 (July 28, 2013): 279–80. http://dx.doi.org/10.1038/nature12460.

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Li, Z. "RNA quality control: degradation of defective transfer RNA." EMBO Journal 21, no. 5 (March 1, 2002): 1132–38. http://dx.doi.org/10.1093/emboj/21.5.1132.

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Crombach, Anton, and Paulien Hogeweg. "Is RNA-dependent RNA polymerase essential for transposon control?" BMC Systems Biology 5, no. 1 (2011): 104. http://dx.doi.org/10.1186/1752-0509-5-104.

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Zhan, Y., J. S. Dhaliwal, P. Adjibade, J. Uniacke, R. Mazroui, and W. Zerges. "Localized control of oxidized RNA." Journal of Cell Science 128, no. 22 (October 8, 2015): 4210–19. http://dx.doi.org/10.1242/jcs.175232.

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Velema, Willem A., Anna M. Kietrys, and Eric T. Kool. "RNA Control by Photoreversible Acylation." Journal of the American Chemical Society 140, no. 10 (February 23, 2018): 3491–95. http://dx.doi.org/10.1021/jacs.7b12408.

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Dissertations / Theses on the topic "Control by RNA"

1

Xu, Ning. "Adenoviral Control of RNAi/miRNA Pathways in Human Cells." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Universitetsbiblioteket [distribution], 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-9387.

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Fritz, Sarah E. "Molecular basis of the DExH-box RNA helicase RNA helicase A (RHA/DHX9) in eukaryotic protein synthesis." The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1437413252.

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Giacometti, Simone. "CBC bound proteins and RNA fate." Thesis, Montpellier, 2016. http://www.theses.fr/2016MONTS028.

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Le complexe de liaison de la coiffe des ARN (CBC) joue un rôle essentiel dans leur maturation et déclenche une variété de réactions biochimiques, via son interaction avec différents partenaires. Deux complexes, CBC-ARS2-PHAX (CBCAP), et CBC-ARS2-ZC3H18-NEXT (CBCN), ont récemment été montré comme important pour cibler les ARN vers l'export (CBCAP) ou la dégradation (CBCN). Cependant, les mécanismes par lesquels la sélection se fait pour l'une voie ou l'autre reste mystérieuse. Ainsi, une question majeure qui reste à résoudre est de savoir quand et comment ces complexes sont recrutés sur les ARN. Dans ce travail, j'ai utilisé la procédure du iCLIP (Cross-Linking and Immuno-Precipitation), afin d'identifier les cibles de ces complexes sur l'ensemble du transcriptome humain. J'ai réalisé un iCLIP sur cinq composants de CBCAP et CBCN, et j'ai comparé les résultats à ceux obtenus avec RBM7, un composant de NEXT précédemment étudié par iCLIP. Mes résultats indiquent que: (i) CBP20, ARS2, PHAX et ZC3H18 se lient près de la coiffe des ARN, tandis que RBM7 et MTR4 se lient partout; (ii) CBP20, ARS2, PHAX et ZC3H18 s'associent à un large ensemble d'ARN transcrits par l'ARN polymérase II et montrent une faible sélectivité; (iii) la liaison de ces protéines varie avec l'état de maturation des ARN, avec le CBC enrichi sur les ARN matures, tout comme ARS2/PHAX/ZC3H18 et MTR4 (bien que dans une moindre mesure), tandis que RBM7 est préférentiellement lié sur les pre-mRNAs non épissés; (iv) une liaison différentielle de RBM7 et MTR4 sur les ARN, avec RBM7 enrichi sur les introns et les PROMPTs, et MTR4 plus présent sur les ARN mature. Bien que des expériences additionnelles soient requises, nous proposons que le CBCAP et le CBCN se lient à un même ensemble d'ARN, ce qui indique à la fois une compétition entre ZC3H18 et PHAX pour la liaison à ces ARN, et l'absence de voies de routage bien déterminées qui ciblerait les ARN vers l'une ou l'autre de ces protéines. Le devenir des ARN pourrait ainsi être déterminé par d'autres caractéristiques des ARN, ou encore par des protéines additionnelles. Ces facteurs pourraient s'allier aux protéines liées à la coiffe afin de favoriser la formation du CBCAP ou du CBCN. Dans le but d’identifier des facteurs additionnels, j'ai réalisé un screen d'interaction par spectrométrie de masse après purification de ARS2 ou CBP80. Ceci a été fait dans des conditions natives ou après un cross-link des complexes à la formaldéhyde, afin de stabiliser les interactions transitoires. Ceci a permis d'identifier de nouveaux partenaires de ARS2 et de CBP80, dont la majorité sont impliqués dans l'épissage des ARN. Des expériences additionnelles seront nécessaires pour valider ces interactions
The cap-binding complex (CBC) plays a pivotal role in post-transcriptional processing events and orchestrates a variety of metabolic pathways, through association with different interaction partners. Two CBC sub-complexes, the CBC-ARS2-PHAX (CBCAP) and the CBC-nuclear exosome targeting (NEXT) complex (CBCN), were recently shown to target capped RNA either toward export or degradation, but the mechanisms by which they can discriminate between different RNA families and route them toward different metabolic pathways still remain unclear. A major question to be answered is how and when the different CBC subcomplexes are recruited to the RNP. Here, we used an individual nucleotide-resolution UV cross-linking and immunoprecipitation (iCLIP) approach to identify the transcriptome-wide targets for 5 different components of the CBCAP and CBCN complexes, and compared results to the previously analysed NEXT-component RBM7. We report that: (i) CBP20, ARS2, PHAX and ZC3H18 bind close to the cap, while RBM7 and MTR4 bind throughout the mRNA body; (ii) CBP20, ARS2, PHAX and ZC3H18 associate with a broad set of RNA polymerase II (PolII)-derived RNAs and have only mild species preferences; (iii) binding varies with the RNA maturation stage, with the CBC being highly enriched on mature mRNA, ARS2/PHAX/ZC3H18/MTR4 less so, and RMB7 preferentially bound to pre-mRNAs; (iv) MTR4 and RBM7 show different specificities, with RBM7 being highly enriched on introns and promoter upstream transcripts (PROMPTs), while MTR4 is additionally present on mature RNAs. Although more experimental work is needed to fully support our model, we propose that CBCAP and CBCN bind overlapping sets of RNAs, indicating a competition between the proteins ZC3H18 and PHAX, and the lack of a strict RNA sorting mechanism. RNA fate may therefore be determined by additional RNA features and/or by other RNA-binding proteins, which may synergize with the cap and drive the formation of one specific CBC subcomplex instead of another. In an attempt to identify yet unknown factors that may interact with cap-bound CBCAP and CBCN, we performed a protein interaction screen leveraging affinity capture-mass spectrometry (ACMS), using ARS2 and CBP80 as bait proteins. As a complementary approach, we also employed a formaldehyde-based chemical cross-linking strategy, aimed at stabilizing weak/transient interactions. Although we failed to detect any transient interactions involving the CBC, we identified several potential CBC80 and ARS2 interactors, the majority of which are involved in pre-mRNA splicing. Additional quantitative experiments are required to validate our ACMS results and confirm the existence of such protein interactions in vivo

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Hitchcock, Robert Arthur. "Epigenetic control of the kinetoplastid spliced leader RNA." Diss., Restricted to subscribing institutions, 2009. http://proquest.umi.com/pqdweb?did=1998392041&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Wilson, Sean. "Control of messenger RNA stability in Saccharomyces cerevisiae." Thesis, University of Aberdeen, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368535.

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The effect of glucose on ribosomal protein mRNA stability was examined. The addition of glucose, to a final concentration as low as 0.01%, resulted in a dramatic, transient increase in ribosomal protein mRNA stability. It has been demonstrated that protein kinase A (PKA) activity plays an important role in the up-regulation of ribosomal protein gene transcription in response to glucose addition. PKA pathway is required for the transient stabilisation of ribosomal protein mRNA following glucose addition, mRNA half-lives were determined in a PKA mutant strain. The data indicated that this glucose effect is not dependent upon a functional Ras-cAMP-PKA signalling pathway. Previously it was shown that the glucose-induced upshift in ribosomal protein gene transcription could be triggered by the addition of exogenous cAMP. However, that dibutyryl cAMP did not act efficiently as a second messenger in the signalling pathway mediating the glucose effect, or that cAMP signalling is not required for the transient stabilisation of ribosomal protein mRNAs. The involvement of specific glucose signalling factors was also examined. The glucose sensors, Snf3p and Rgt2p, were not required for the stabilisation of the ribosomal protein mRNAs. It was noted however, that phosphorylation of glucose by any one of the three yeast hexose kinases (Hxk1p, Hxk2p or Glk1p) was required to mediate this effect.

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Brown, Justin Travis. "MRNA degradation in the control of gene expression in yeast." Access restricted to users with UT Austin EID Full text (PDF) from UMI/Dissertation Abstracts International, 2001. http://wwwlib.umi.com/cr/utexas/fullcit?p3024999.

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Carlberg, Konstantin. "In Situ RNA Quality Control : A spatial heat map of RNA integrity with single cell resolution." Thesis, KTH, Skolan för bioteknologi (BIO), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-176873.

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The quality of RNA is of great importance in gene expression studies. It is mostly measured using the RNA integrity number (RIN). Lately it has been shown that samples with low RIN and different fragmentation patterns could affect quality of sequencing data. For such low RIN samples a new approach has been developed by Illumina called the DV200 metric, which is the percentage of fragments >200 nucleotides. For samples with low RIN, DV200 has proved to be a better method to predict if good quality data from RNA sequencing can be generated. However, neither RIN nor DV200 provide spatial infromation on the RNA integrity. Thus, tissues with areas of heterogeneous RNA integrity, where regions of good quality RNA sequencing data could be generated from are missed. We have designed a method to spatially evaluate the RNA integrity in tissue, which we named in situ RNA QC. The method uses three probes with three different fluorophores, each bound to three specific cDNA regions synthesized from the high abundant and well conserved 18S rRNA. With the help of in-house technology from the Spatial Transcriptomics (ST) group at SciLifeLab, we enable creation of heat maps over the RNA integrity to show spatial fragmentation patterns of RNA in tissue. This could reveal the regional quality of transcripts in situ, which is crucial knowledge when selecting samples for further RNA sequencing. The assay has been tried using different tissue fixation methods in order to show a proof of concept that formalin gives shorter cDNA fragments than acetone. The generated heat-map provides a visual overview of RNA integrity in situ; hence this method could be used to select samples for sequencing by evaluation the spatial quality of RNA. For instance from fresh frozen and formalin fixated paraffin embedded (FFPE) tissue (biobanks contain large number of longterm storage FFPE samples). With this assay we will be able to determine which samples are suitable for sequencing.

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Zhang, Ze. "The control of ribosomal RNA synthesis in mammalian cells." Thesis, University of Southampton, 2013. https://eprints.soton.ac.uk/350477/.

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The biogenesis of ribosomes is a fundamental process that occurs in all living cells. In mammalian cells, it is a highly complex process consisting of the coordinated synthesis and assembly of four ribosomal RNAs (rRNAs) with about 80 ribosomal proteins (RPs). More than 150 non-ribosomal proteins are involved in the processing of rRNAs. The main focus of this project is to use adult rat ventricular cardiomyocytes (ARVCs) as a model to address how mTOR complex 1 (mTORC1) and other signalling pathways regulate the synthesis of rRNAs. A new technique has been developed to monitor the synthesis of new rRNAs using 4-thiouridine (4-SU) and I have applied it in both HeLa cells and heart muscle cells to study the control of ribosome synthesis. HeLa cells were treated with different mTOR inhibitors to identify effects on the transcription and/or decay of rRNA. We analysed both the synthesis rate and the decay rate of new RNAs made by Pol I and Pol III using real-time RT-PCR. Interestingly, rapamycin not only blocked the synthesis of 18S, 28S and 5S rRNA, but also induced the decay of newly synthesized rRNAs. This demonstrates that mTORC1 regulates Pol I and Pol III transcription, as well as the decay of rRNA. In cardiomyocytes, hypertrophic agents such as phenylephrine (PE) strongly activate protein synthesis and lead to heart cell growth. The boost of protein synthesis drives the increase of cell size and leads to hypertrophy. Cardiac hypertrophy (CH) is a major risk factor for heart failure. Therefore, it is important to understand the mechanisms that how hypertrophic agents which cause the overgrowth of heart muscle increase ribosome production. Although it is known that inhibiting mTORC1 largely blocks the rapid activation of protein synthesis by PE, here it did not affect the synthesis of new 18S rRNAs. However, inhibitors of the MEK/Erk pathway and p90RSK each block the new rRNA synthesis. These data reveal that, in contrast to many other types of cell, ribosome biogenesis is controlled by MEK/ERK/p90RSK signalling, not mTORC1, in cardiomyocytes. Taken together, the data presented here may provide cues for potential valuable therapy of cardiac left ventricular hypertrophy.

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Tzelos, Thomas. "RNA interference in parasitic nematodes : from genome to control." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/15906.

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Teladorsagia circumcincta is a parasitic nematode which is a major cause of ovine parasitic gastroenteritis in temperate climatic regions. The parasite has developed resistance to the major anthelmintic drug classes and this challenges its future control. Vaccination is a potential alternative control method since sheep are able to develop protective immunity against this parasite. Although potential vaccine candidates have been revealed, the increasing gene datasets suggest that vaccinetarget selection may be aided by screening methods such as RNAi. This is a reverse genetic mechanism that causes highly specific gene silencing which was initially described and applied to defining gene function in Caenorhabditis elegans. Nevertheless, its application was more difficult than anticipated in parasitic nematodes because of the inconsistency of the silencing effect. In the unsuccessful cases, did the dsRNA penetrate the parasite and activate the RNAi pathway? Thus far, there are no internal controls that indicate the activation of the pathway. Are the RNAi pathway genes constantly transcribed or are they ‘switched on’ in response to the dsRNA exposure? The initial aim of the study was to determine potential marker genes in the RNAi pathway that could indicate the activation of the pathway in C. elegans. After the exposure to dsRNA from two target genes, the transcript levels of three candidate marker genes (Ce-dcr-1, Ce-ego-1 and Ce-rsd-3) were examined and showed that exposure to dsRNA has no effect on the transcript levels of these genes making them inappropriate markers for the activation of the RNAi pathway. The two target-genes were Ce-cpr-4 and Ce-sod-4 which had been proven to be consistently susceptible and refractory to RNAi, respectively. Another aim of the project was to develop an RNAi platform in T. circumcincta for use as a screening method for potential vaccine candidates. The targets selected for the in vitro RNAi included: five members of the Activation-associated Secreted Proteins (ASPs); a Macrophage migration Inhibitory Factor-like (Tci-mif-1) and a Surface Associated Antigen gene (Tci-saa-1), all of which have been associated with vaccine-induced protective immunity. The selection of the ASPs was based on a bioinformatic and transcriptomic analysis of the ASPs in T. circumcincta. The results showed successful knock-down only for three out of five ASP targets after 1 hour of soaking in gene-specific double stranded RNA (dsRNA) which illustrates the inconsistency and the target specificity of RNAi in T. circumcincta which has been observed in the past with other parasitic nematodes. Inconsistencies were also observed within the successful ASP targets with the results not being reproducible after several successful experiments. Potential reasons for the inconsistencies were examined with the duration of larval storage being a critical factor. Larvae stored for a short or long period of time were susceptible and refractory to RNAi, respectively. Experiments were also conducted to investigate how the ASPs relate to extracellular microvesicles (EMVs). These vesicles are considered to play an important role in the intercellular communication between parasites and their hosts, and thus represent potentially useful vaccine and/or drug targets. Transmission electron microscopy (TEM) confirmed that EMVs are excreted / secreted by the parasite and the proteomic analysis revealed several types of proteins within the vesicles such as: ASPs, Actins, Metallopeptidases, and RAB proteins. A comparative analysis of EMVs, EMV-free ES (Excretory / Secretory) and total ES products showed that approximately 35% of the proteins found in the vesicles could also be identified in EMV-free ES and in total ES products, whilst the remaining 65% were present only in EMVs.

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Peele, Price Jason. "Control of RNA Structure by CspA Proteins in Rhizobia." Thesis, Washington State University, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10605605.

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Rhizobia are soil bacteria that can associate with some legumes and participate in symbiotic nitrogen fixation. Bacterial CspA family members are small, single stranded nucleic acid binding proteins conserved throughout all domains of life. Here, the role of CspA family proteins in the symbiotic development of Sinorhizobium meliloti with Medicago sativa (alfalfa) is investigated. Expression and genetic deletion strain analysis revealed that CspA family proteins are differentially expressed in symbiosis and contribute to symbiotic effectiveness. RNAseq analysis of native co-immunoprecipitated RNAs identified a novel interaction between several CspA family proteins and the αR14 family of small non-coding RNA (sRNAs). Whole transcriptome analysis defined transcriptional defects associated with loss of CspA function. The development of a new in vitro RNA binding assay using broccoli, a Green Fluorescent Protein (GFP) RNA mimic, is described as well as its use in defining binding specificity of CspA family proteins with synthetic and native ?R14 family sRNA structures. This work concludes that CspA family proteins interact with and influence the stability of specific RNA structures and these interactions control RNA regulated processes important for symbiotic development.

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Books on the topic "Control by RNA"

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Post-transcriptional regulation by STAR proteins : control of RNA metabolism in development and disease. New York: Springer Science+Business Media, LLC, 2010.

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Artsimovitch, Irina, and Thomas J. Santangelo. Bacterial transcriptional control: Methods and protocols. New York: Humana Press, 2015.

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NATO/CEC, Advanced Research Workshop on "Post-Transcriptional Control of Gene Expression" (1990 Goslar Germany). Post-transcriptional control of gene expression. Berlin: Springer-Verlag, 1990.

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Myers, Fiona Alice. Factors effecting the control [sic.] of maternal messenger RNA stability in early Drosophila development. Portsmouth: University of Portsmouth, School of Biological Sciences, 1995.

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Mallory, Ellen B. John Rea farm: Case study. [Pullman, WA]: Washington State University Cooperative Extension, 1999.

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Ivanishchev, Viktor (Victor). Molecular biology. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/01857-6.

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The textbook presents the main range of issues in molecular biology — the most rapidly developing area of biological science. The logic of the presentation of the material includes sequential coverage of the structural organization and functions of DNA, RNA, proteins. Important attention is paid to the mechanisms of signal transmission in living systems, the problems of creating and using genetically engineered organisms. Each chapter ends with control questions and assignments for independent work. The textbook includes a set of laboratory and practical works that do not require specialized equipment and materials. The new edition has been supplemented and clarified, reflecting the current state of science. The content of the textbook corresponds to a number of competencies, the development of which is provided for by the Federal State Educational Standard of Higher Education in the preparation of bachelors in the fields of "Pedagogical Education" (profiles "Biology" and "Chemistry"), "Biology". Certain topics can be used in the preparation of masters in the fields of "Biology", "Chemistry", "Natural Science Education". The book is intended for students studying in natural sciences, and will also be useful for teachers of biology and chemistry of high school.

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Shui wu ran kong zhi gong cheng. Beijing Shi: Hua xue gong ye chu ban she, 2008.

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Fa ding chuan ran bing yu fang yu kong zhi. Beijing Shi: Zhongguo da di chu ban she, 2009.

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Ran qi lun ji zi dong kong zhi xi tong she ji. Beijing: Ji xie gong ye chu ban she, 1986.

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Fan, Chengxin, and Lu Zhang. Tai hu: Chen ji wu wu ran yu xiu fu yuan li. Bei jing: Ke xue chu ban she, 2009.

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Book chapters on the topic "Control by RNA"

1

Hilliker, Angela K. "RNA Quality Control." In Molecular Life Sciences, 1080–82. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4614-1531-2_763.

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Hilliker, Angela. "RNA Quality Control." In Molecular Life Sciences, 1–3. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-6436-5_763-1.

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Nordström, Kurt, Stanley N. Cohen, and Robert W. Simons. "Antisense RNA." In Post-transcriptional Control of Gene Expression, 231–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-60929-9_20.

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Zeiler, Brian N., and Robert W. Simons. "Control by Antisense RNA." In Regulation of Gene Expression in Escherichia coli, 67–83. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4684-8601-8_5.

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Fladung, Matthias, Hely Häggman, and Suvi Sutela. "Application of RNAi technology in forest trees." In RNAi for plant improvement and protection, 54–71. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0054.

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Abstract A diverse set of small RNAs is involved in the regulation of genome organization and gene expression in plants. These regulatory sRNAs play a central role for RNA in evolution and ontogeny in complex organisms, including forest tree species, providers of indispensable ecosystem services. RNA interference is a process that inhibits gene expression by double-stranded RNA and thus causes the degradation of target messenger RNA molecules. Targeted gene silencing by RNAi has been utilized in various crop plants in order to enhance their characteristics. For forest tree species, most of the successful RNAi modification has been conducted in poplar. Over the past 20 years, successful RNAi-mediated suppression of gene expression has been achieved with a variety of economically important traits. Moreover, the stability of RNAi-mediated transgene suppression has been confirmed in field-grown poplars. In this chapter, we describe examples of successful RNAi applications mainly in poplar but also provide some information about application of RNAi in pest control in forest tree species. Advantages and disadvantages of this technology with respect to the particular features of forest tree species will be discussed.

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Fladung, Matthias, Hely Häggman, and Suvi Sutela. "Application of RNAi technology in forest trees." In RNAi for plant improvement and protection, 54–71. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789248890.0007.

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Abstract A diverse set of small RNAs is involved in the regulation of genome organization and gene expression in plants. These regulatory sRNAs play a central role for RNA in evolution and ontogeny in complex organisms, including forest tree species, providers of indispensable ecosystem services. RNA interference is a process that inhibits gene expression by double-stranded RNA and thus causes the degradation of target messenger RNA molecules. Targeted gene silencing by RNAi has been utilized in various crop plants in order to enhance their characteristics. For forest tree species, most of the successful RNAi modification has been conducted in poplar. Over the past 20 years, successful RNAi-mediated suppression of gene expression has been achieved with a variety of economically important traits. Moreover, the stability of RNAi-mediated transgene suppression has been confirmed in field-grown poplars. In this chapter, we describe examples of successful RNAi applications mainly in poplar but also provide some information about application of RNAi in pest control in forest tree species. Advantages and disadvantages of this technology with respect to the particular features of forest tree species will be discussed.

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Tanaka, Takahiro, Yoshiya Ikawa, and Shigeyoshi Matsumura. "Rational Engineering of a Modular Group I Ribozyme to Control Its Activity by Self-Dimerization." In RNA Nanostructures, 325–40. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7138-1_21.

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Endo, Kei, and Hirohide Saito. "mRNA Engineering for the Control of Mammalian Cells in Medical Applications." In Applied RNA Bioscience, 95–114. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-8372-3_7.

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Smiley, James R. "Organization and Control of the mRNA of the HSV TK Gene." In Viral Messenger RNA, 101–25. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2585-7_6.

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Haque, Farzin, Congcong Xu, Daniel L. Jasinski, Hui Li, and Peixuan Guo. "Using Planar Phi29 pRNA Three-Way Junction to Control Size and Shape of RNA Nanoparticles for Biodistribution Profiling in Mice." In RNA Nanostructures, 359–80. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7138-1_23.

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Conference papers on the topic "Control by RNA"

1

Shatters, Jr., Robert. "Application of RNA interference (RNAi) as an invasive pest control strategy in Florida." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.94273.

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Aviran, Sharon, Julius B. Lucks, and Lior Pachter. "RNA structure characterization from chemical mapping experiments." In 2011 49th Annual Allerton Conference on Communication, Control, and Computing (Allerton). IEEE, 2011. http://dx.doi.org/10.1109/allerton.2011.6120379.

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Desai, Suresh. "Control of pests of canola using RNA interference technologies." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.93852.

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Wang, Tong, Jianxin Xue, and Yi Du. "A Method For The RNA-Protein Complexes Recognition." In ICCIR 2021: 2021 International Conference on Control and Intelligent Robotics. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3473714.3473756.

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Liu, Xiu, Ning Wang, and Jili Tao. "Grey wolf RNA-GA modeling method for FCCU main fractionator." In 2018 Chinese Control And Decision Conference (CCDC). IEEE, 2018. http://dx.doi.org/10.1109/ccdc.2018.8407406.

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Blanchini, Franco, Christian Cuba Samaniego, Elisa Franco, and Giulia Giordano. "Design of a molecular clock with RNA-mediated regulation." In 2014 IEEE 53rd Annual Conference on Decision and Control (CDC). IEEE, 2014. http://dx.doi.org/10.1109/cdc.2014.7040109.

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Wang, Zengmiao, Jun Wang, and Minghua Deng. "Estimation of isoform expression using hierarchical Bayesian model by RNA-seq." In 2015 34th Chinese Control Conference (CCC). IEEE, 2015. http://dx.doi.org/10.1109/chicc.2015.7260993.

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Liu, Xiu, and Ning Wang. "RNA-GA with Whale Search based LSSVMs for Modeling Multivariable Systems." In 2018 37th Chinese Control Conference (CCC). IEEE, 2018. http://dx.doi.org/10.23919/chicc.2018.8482951.

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Vu, Ly, Camila Prieto, Eliana M. Amin, Gerard Minuesa, Sagar Chhangawala, Maria C. Vidal, Andrei Krivtsov, et al. "Abstract IA13: RNA regulators and the control of self-renewal." In Abstracts: Second AACR Conference on Hematologic Malignancies: Translating Discoveries to Novel Therapies; May 6-9, 2017; Boston, MA. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1557-3265.hemmal17-ia13.

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Zhang, Bengong, and Ya-Zhou Shi. "3D structure stability of RNA hairpin controlled by loop size." In 2017 29th Chinese Control And Decision Conference (CCDC). IEEE, 2017. http://dx.doi.org/10.1109/ccdc.2017.7978407.

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Reports on the topic "Control by RNA"

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Lomboy, Gilson, Douglas Cleary, Seth Wagner, Yusef Mehta, Danielle Kennedy, Benjamin Watts, Peter Bly, and Jared Oren. Long-term performance of sustainable pavements using ternary blended concrete with recycled aggregates. Engineer Research and Development Center (U.S.), May 2021. http://dx.doi.org/10.21079/11681/40780.

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Abstract:

Dwindling supplies of natural concrete aggregates, the cost of landfilling construction waste, and interest in sustainable design have increased the demand for recycled concrete aggregates (RCA) in new portland cement concrete mixtures. RCA repurposes waste material to provide useful ingredients for new construction applications. However, RCA can reduce the performance of the concrete. This study investigated the effectiveness of ternary blended binders, mixtures containing portland cement and two different supplementary cementitious materials, at mitigating performance losses of concrete mixtures with RCA materials. Concrete mixtures with different ternary binder combinations were batched with four recycled concrete aggregate materials. For the materials used, the study found that a blend of portland cement, Class C fly ash, and blast furnace slag produced the highest strength of ternary binder. At 50% replacement of virgin aggregates and ternary blended binder, some specimens showed comparable mechanical performance to a control mix of only portland cement as a binder and no RCA substitution. This study demonstrates that even at 50% RCA replacement, using the appropriate ternary binder can create a concrete mixture that performs similarly to a plain portland cement concrete without RCA, with the added benefit of being environmentally beneficial.

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In-depth survey report: field evaluation of Champion engineering controls designed to reduce occupational exposures during asphalt paving operations; Manufacturer: Champion Road Machinery, Inc.; Paving contractor: Rea Construction; Paving location: Ridgeland, South Carolina. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, March 2000. http://dx.doi.org/10.26616/nioshectb20820a.

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