Academic literature on the topic 'Genetic regulation'

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Journal articles on the topic "Genetic regulation"

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Humphries, S. E. "Genetic Regulation of Fibrinogen." European Heart Journal 16, suppl A (March 2, 1995): 16–20. http://dx.doi.org/10.1093/eurheartj/16.suppl_a.16.

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Depuydt, Christophe E., Adel Zalata, Christian R. de Potter, John van Emmelo, and Frank H. Comhaire. "Genetic regulation of gametogensis." Molecular Human Reproduction 2, no. 1 (1996): 2–8. http://dx.doi.org/10.1093/molehr/2.1.2.

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Breslow, Jan L. "Genetic regulation of apolipoproteins." American Heart Journal 113, no. 2 (February 1987): 422–27. http://dx.doi.org/10.1016/0002-8703(87)90608-9.

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Osiewacz, Heinz D. "Genetic regulation of aging." Journal of Molecular Medicine 75, no. 10 (October 13, 1997): 715–27. http://dx.doi.org/10.1007/s001090050158.

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Evans, Barbara J. "Economic Regulation of Next-Generation Sequencing." Journal of Law, Medicine & Ethics 42, S1 (2014): 51–66. http://dx.doi.org/10.1111/jlme.12162.

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The genetic testing industry is in a period of potentially major structural change driven by several factors. These include weaker patent protections after Association for Molecular Pathology v. Myriad Genetics (the “Myriad decision”) and Mayo Collaborative Services v. Prometheus Laboratories, Inc.; a continuing shift from single-gene tests to genome-scale sequencing; and a set of February 2014 amendments to the Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations and the Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule. This article explores the nature of these changes and why they strain existing regulatory frameworks for protecting patients, research subjects, and other consumers who receive genetic testing.Oversight of genetic testing has, at least to date, had two major thrusts: (1) privacy and ethical protections and (2) traditional consumer health and safety regulations. Examples of the first are the Genetic Information Nondiscrimination Act and the HIPAA Privacy Rule, which after 2013 amendments expressly protects genetic privacy as well as other medical privacy.
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Jiang, Guanglong, Jill L. Reiter, Chuanpeng Dong, Yue Wang, Fang Fang, Zhaoyang Jiang, and Yunlong Liu. "Genetic Regulation of Human isomiR Biogenesis." Cancers 15, no. 17 (September 4, 2023): 4411. http://dx.doi.org/10.3390/cancers15174411.

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MicroRNAs play a critical role in regulating gene expression post-transcriptionally. Variations in mature microRNA sequences, known as isomiRs, arise from imprecise cleavage and nucleotide substitution or addition. These isomiRs can target different mRNAs or compete with their canonical counterparts, thereby expanding the scope of miRNA post-transcriptional regulation. Our study investigated the relationship between cis-acting single-nucleotide polymorphisms (SNPs) in precursor miRNA regions and isomiR composition, represented by the ratio of a specific 5′-isomiR subtype to all isomiRs identified for a particular mature miRNA. Significant associations between 95 SNP–isomiR pairs were identified. Of note, rs6505162 was significantly associated with both the 5′-extension of hsa-miR-423-3p and the 5′-trimming of hsa-miR-423-5p. Comparison of breast cancer and normal samples revealed that the expression of both isomiRs was significantly higher in tumors than in normal tissues. This study sheds light on the genetic regulation of isomiR maturation and advances our understanding of post-transcriptional regulation by microRNAs.
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Motta-Murguia, Lourdes, and Garbiñe Saruwatari-Zavala. "Mexican Regulation of Biobanks." Journal of Law, Medicine & Ethics 44, no. 1 (2016): 58–67. http://dx.doi.org/10.1177/1073110516644199.

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Biobank-based research in Mexico is mostly governed by research and data protection laws. There is no direct mention of biobanks in either statutory or regulatory law besides a requirement that the Federal Ministry of Health and a Mexican institution devoted to scientific research approve the transfer of biological materials outside of Mexico for population genetics research purposes. Such requirements are the basis of Genomic Sovereignty in Mexico, but such requirements have not prevented international collaboration. In addition, Mexican law singles out genetic research in informed consent provisions, but it does not specify whether all biobank-based research is genetic research. In order to facilitate international collaboration on biobank-based research, Mexico should directly address biobanking in its laws, building on the research framework and data protection framework already in place.
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Meeks, J. J., and E. M. Schaeffer. "Genetic Regulation of Prostate Development." Journal of Andrology 32, no. 3 (October 7, 2010): 210–17. http://dx.doi.org/10.2164/jandrol.110.011577.

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Yue, Shanna, Philip Whalen, and Youn Hee Jee. "Genetic regulation of linear growth." Annals of Pediatric Endocrinology & Metabolism 24, no. 1 (March 31, 2019): 2–14. http://dx.doi.org/10.6065/apem.2019.24.1.2.

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Howard, Sasha R. "Genetic regulation in pubertal delay." Journal of Molecular Endocrinology 63, no. 3 (October 2019): R37—R49. http://dx.doi.org/10.1530/jme-19-0130.

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Delayed puberty represents the clinical presentation of a final common pathway for many different pathological mechanisms. In the majority of patients presenting with significantly delayed puberty, there is a clear family history of delayed or disturbed puberty, and pubertal timing is known to be a trait with strong heritability. Thus, genetic factors clearly play a key role in determining the timing of puberty, and mutations in certain genes are recognised as responsible for delayed or absent puberty in a minority of patients. Through the identification of causal genetic defects such as these we have been able to learn a great deal about the pathogenesis of disrupted puberty and its genetic regulation. Firstly, deficiency in key genes that govern the development of the gonadotropin-releasing hormone system during fetal development may result in a spectrum of conditions ranging from isolated delayed puberty to absent puberty with anosmia. Secondly, a balance of inhibitory and excitatory signals, acting upstream of GnRH secretion, are vital for the correct timing of puberty. These act to repress the hypothalamic–pituitary–gonadal axis during mid-childhood and allow it to reactivate at puberty, and alterations in this equilibrium can cause delayed (or precocious) puberty. Thirdly, disturbances of energy metabolism inputs to the kisspeptin–GnRH system may also lead to late onset of puberty associated with changes in body mass.
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Dissertations / Theses on the topic "Genetic regulation"

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Button, Eric A. "Regulation of T-DNA gene 7." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26177.

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The purpose of this study was two-fold. The first objective was to determine if Saccharomyces cerevisiae is a useful system for investigating the expression of T-DNA (it takes several months to obtain sufficient bacteria-free transformed plant tissue to investigate T-DNA transcription). A short fragment of T-DNA carrying T-DNA gene 7 was cloned into a yeast plasmid in an attempt to investigate the expression of gene 7 in yeast. The second objective was to determine the significance of a heat shock related sequence identified in the 5¹ region of T-DNA gene 7. Primer extension analysis, SI nuclease mapping, and Northern hybridizations indicate that transcription of T-DNA gene 7 in yeast is different from that of transcription of gene 7 in crown gall tumors. Transcription is different because the distance between the TATA box and the transcription initiation sites must be at least 40 nucleotides in yeast. Therefore, Saccharomyces cerevisiae does not appear to be a useful system for investigating the expression of T-DNA. Crown gall tumors were subjected to a number of stress agents, including heat shock, to determine the significance of the heat shock related sequence identified in gene 7. Primer extension analyses indicate that only cadmium and mercury have a significant effect on the expression of T-DNA gene 7. Although gene 7 responds to cadmium and mercury, the increase in transcription does not appear to be heat shock or metallothionein related, indicating that another mechanism is involved in the enhanced transcription of T-DNA gene 7 in crown gall tumors.
Medicine, Faculty of
Medical Genetics, Department of
Graduate
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Robertson, Michael Paul. "Engineered regulation of an RNA ligase ribozyme." Access restricted to users with UT Austin EID Full text (PDF) from UMI/Dissertation Abstracts International, 2001. http://wwwlib.umi.com/cr/utexas/fullcit?p3035968.

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Sigvardsson, Mikael. "Regulation of immunoglobulin transcription during B-cell differentiation." Lund : Lund University, 1995. http://books.google.com/books?id=TJNqAAAAMAAJ.

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Bečanović, Kristina. "Genetic regulation of autoimmune neuroinflammation /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-726-6.

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Fouracre, Jim P. "Genetic regulation of Kranz anatomy." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:7f10306d-d942-49cd-b12f-35b29311ad3c.

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The C₄ photosynthetic cycle acts to concentrate CO₂ around the enzyme Rubisco. By doing so, C₄ photosynthesis leads to increased radiation, water and nitrogen use efficiencies. As such, C₄ photosynthesis is the most productive form of photosynthesis known. Because it enables such high levels of productivity there are large international efforts to introduce C₄ photosynthesis into non-C₄ crop species such as rice. Kranz anatomy is a characteristic leaf cellular arrangement of concentric rings of bundle sheath and mesophyll cells around closely spaced veins and is crucial to C₄ photosynthesis in almost all known examples. Despite the fact that Kranz has evolved on over 60 times independently little is known about the genetic regulation of Kranz development, as attempts to elucidate Kranz regulators using conventional mutagenesis screens have provided few insights. However, the advent of next generation DNA sequencing technologies has enabled the interrogation of genetic networks at a previously unprecedented scale. The work in this thesis describes a genome-wide transcriptomic analysis of leaf development in maize, a C₄ species, that develops both Kranz-type and non-Kranz-type leaves. Detailed bioinformatics analyses identified candidate regulators of both Kranz development and additional aspects of maize leaf development. Three of the identified Kranz candidates were functionally characterised in both C₄ and non-C₄ species. Furthermore, expression and phylogenetic analyses of GOLDEN2-LIKE (GLK) genes, a small transcription factor family previously implicated in C₄ development in maize, were extended to determine the generality of GLK function in C₄ evolution.
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Povinelli, Christine Marie. "Genetic analysis of the dihydrofolate reductase and thymidylate synthase genes of bacteriophage T4." Diss., Georgia Institute of Technology, 1987. http://hdl.handle.net/1853/25347.

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Wasinger, Valerie Christine. "Optimising gene and protein annotations and characterisation of the Mycoplasma genitalium proteome." Thesis, The University of Sydney, 1998. https://hdl.handle.net/2123/27694.

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The PROTEin complement of the genOME (proteome) can provide useful information with respect to that obtained during the analysis of genomic DNA sequence. The proteome has the ability to provide confirmation of the expression of genes / Open Reading Frames (ORF’s), which can only be presumed prior to physical detection. The effects of posttranslational modifications, and multi-gene, co-regulated and compensated pathways, likely to contribute to debilitating disease can also be explored. Two-dimensional electrophoresis (2-DE), the method of choice for delineation of proteomes, has been optimised to broaden the percentage of proteome detected at any one instant. The concept of ‘proteomic contigs’ was applied to Ochrobactrum anthropz', allowing the detection and summation of proteins spanning the gradient pH2.3-11.0. Using the gradients pH2.3-5.0 and pH6.0-11.0, in addition to the commercially available gradient pH4.0-7.0, a total of 1158 gene-products from 6 ‘windows of protein expression’ were detected and compared to the theoretical expression of sequenced genomes. Protein migration at the extreme basic gradient and resolvability below IOkDa were shown to remain a challenge for 2-D electrophoresis.
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Mauro, Vincent Peter. "Structure and regulation of nodulin genes of soybean." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75360.

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The nodulin-23 gene is an abundantly transcribed soybean gene induced in nodules during symbiosis with Rhizobium. Sequencing of the cDNA and genomic clones revealed one intron within an open reading frame. A 24,275 dalton protein was predicted. The transcription of nodulin-23 gene occurs concomitantly with Lbc$ sb3$ and nodulin-24 genes. The 5$ sp prime$-regions of nodulin-23 and Lbc$ sb3$ genes were sequenced and compared with that of nodulin-24. Three potential cis-regulatory sequences were identified. The presence of trans-acting molecule(s), possibly regulating the expression of these genes, was tested for in vitro by preincubating nuclei from embryonic axes with nodule extract and assaying for gene activation. Nodulin-23, nodulin-24, and Lbc$ sb3$ genes were specifically activated and demonstrated similar kinetics. Several genes used as controls were not stimulated. A nodule factor(s) was shown to bind the 5$ sp prime$-region of nodulin-23 gene. The corresponding DNA regions from the other two coordinately expressed nodulin genes specifically competed for this binding, whereas other genes did not bind this factor at all.
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Cleavinger, Peter Jay. "Role of the long terminal repeat in transcriptional regulation of rous sarcoma virus gene expression." free to MU campus, to others for purchase, 1996. http://wwwlib.umi.com/cr/mo/fullcit?p9841207.

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Willadsen, Kai. "Robustness in Boolean models of genetic regulatory systems /." [St. Lucia, Qld.], 2006. http://adt.library.uq.edu.au/public/adt-QU20061115.135112/index.html.

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Books on the topic "Genetic regulation"

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L, McKnight Steven, and Yamamoto Keith R, eds. Transcriptional regulation. Plainview, N.Y: Cold Spring Harbor Laboratory Press, 1992.

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Klaus, Grasser, ed. Regulation of transcription in plants. Oxford: Blackwell Pub., 2006.

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Inc, ebrary, ed. Genetics. 2nd ed. New Delhi: New Age International (P) Ltd., Publishers, 2009.

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Soreq, H. Cholinesterase genes: Multileveled regulation. Basel: Karger, 1990.

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Biochemical Society (Great Britain). Symposium. Gene expression: Regulation at the RNA and protein levels : Biochemical Society Symposium No. 55 held at University of Nottingham, July 1988. London: Biochemical Society, 1989.

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C, Kurzfield Nathan, ed. Developmental gene expression regulation. Hauppauge NY: Nova Science Publishers, 2009.

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A, Haseltine William, Wong-Staal Flossie, and Harvard AIDS Institute, eds. Genetic structure and regulation of HIV. New York: Raven Press, 1991.

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Lawrence, Privalsky Martin, ed. Transcriptional corepressors: Mediators of eukaryotic gene repression. Berlin: Springer, 2001.

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Maxine, Singer, and Berg Paul 1926-, eds. Exploring genetic mechanisms. Sausalito, Calif: University Science Books, 1997.

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C, Conaway Ronald, and Conaway Joan Weliky, eds. Transcription: Mechanisms and regulation. New York: Raven Press, 1994.

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Book chapters on the topic "Genetic regulation"

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Somvanshi, Pramod R., and Kareenhalli V. Venkatesh. "Genetic Regulation Mechanisms." In Encyclopedia of Systems Biology, 827–30. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_705.

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McKeown, Michael. "Regulation of Alternative Splicing." In Genetic Engineering, 139–81. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0641-2_9.

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Danon, Avihai, Christopher B. Yohn, and Stephen P. Mayfield. "Regulation of Translation in Plants." In Genetic Engineering, 41–55. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4899-1666-2_3.

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Weaver, Louis M., Edward Himelblau, and Richard M. Amasino. "Leaf Senescence: Gene Expression and Regulation." In Genetic Engineering, 215–34. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5925-2_12.

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Callis, Judy. "Regulation of Protein Degradation in Plants." In Genetic Engineering, 121–48. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5925-2_7.

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Smith-Keary, Peter. "Genetic regulation in procaryotes." In Molecular Genetics, 165–81. London: Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-11732-1_10.

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Wong-Staal, F. "Genetic Regulation of HIV." In Progress in Immunology, 1016–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83755-5_136.

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Szépfalusi, Zsolt, and Thomas Eiwegger. "Genetic Regulation of IgE." In Encyclopedia of Medical Immunology, 335–39. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9194-1_81.

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Kim, Insoon, Ken Kobayashi, Euna Cho, and Patricia C. Zambryski. "Regulation of Plant Intercellular Communication Via Plasmodesmata." In Genetic Engineering, 1–15. Boston, MA: Springer US, 2007. http://dx.doi.org/10.1007/978-0-387-34504-8_1.

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Hudson, Laurie G., and Gordon N. Gill. "Regulation of Gene Expression by Epidermal Growth Factor." In Genetic Engineering, 137–51. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3760-1_5.

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Conference papers on the topic "Genetic regulation"

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Wang, Junling, and Yan Cai. "Genetic traffic regulation testing system." In 2011 International Conference on Electrical and Control Engineering (ICECE). IEEE, 2011. http://dx.doi.org/10.1109/iceceng.2011.6057898.

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Kazakov, Nikita. "LEGAL REGULATION OF GENETIC INFORMATION." In MODERN PROBLEMS AND PROSPECTS OF DEVELOPMENT PRIVATE LAW AND PUBLIC LAW REGULATION. Baskir State University, 2022. http://dx.doi.org/10.33184/spprchppr-2022-04-22.27.

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"Genetic regulation of wheat inflorescence development." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-191.

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Lalejini, Alexander, Matthew Andres Moreno, and Charles Ofria. "Tag-based module regulation for genetic programming." In GECCO '22: Genetic and Evolutionary Computation Conference. New York, NY, USA: ACM, 2022. http://dx.doi.org/10.1145/3520304.3534060.

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"Genetic aspects of internet-dependence in teenagers." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-160.

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Delecluse, Martin, Stéphane Sanchez, Sylvain Cussat-Blanc, Nicolas Schneider, and Jean-Baptiste Welcomme. "High-level behavior regulation for multi-robot systems." In GECCO '14: Genetic and Evolutionary Computation Conference. New York, NY, USA: ACM, 2014. http://dx.doi.org/10.1145/2598394.2598454.

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Zhongming Han, Dagao Duan, Wenzheng Li, and Hongzhi Liu. "Reconstructing genetic regulation network: Problems and methods." In 2009 2nd IEEE International Conference on Computer Science and Information Technology. IEEE, 2009. http://dx.doi.org/10.1109/iccsit.2009.5234743.

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Wang, Yi, Yichen Liu, Yangyu Fan, and Yilong Niu. "Adaptive hormone regulation operator for genetic algorithm." In TENCON 2013 - 2013 IEEE Region 10 Conference. IEEE, 2013. http://dx.doi.org/10.1109/tencon.2013.6718801.

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Zhang, Yan. "On the Genetic Regulation of Bayesian Networks." In 2019 12th International Symposium on Computational Intelligence and Design (ISCID). IEEE, 2019. http://dx.doi.org/10.1109/iscid.2019.10139.

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Liu, Yichen, Yi Wang, Yangyu Fan, and Yilong Niu. "Adaptive hormone regulation operator for genetic algorithm." In 2013 IEEE Conference Anthology. IEEE, 2013. http://dx.doi.org/10.1109/anthology.2013.6784903.

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Reports on the topic "Genetic regulation"

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Freeling, M. A genetic analysis of Adh1 regulation. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/5821489.

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Freeling, M. A genetic analysis of Adhl regulation. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6854161.

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Shonka, Brittany N., and Diane M. Spurlock. Genetic Regulation of Feed Efficiency in Lactating Holstein Cows. Ames (Iowa): Iowa State University, January 2013. http://dx.doi.org/10.31274/ans_air-180814-656.

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Ntambi, James. Genetic Regulation of Lipid Biogenesis in Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2000. http://dx.doi.org/10.21236/ada383396.

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Wilson, D. B. (Studies of the genetic regulation of the Thermomonospora cellulase complex). Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/7239659.

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Braam, Janet. Genetic analysis of the regulation of TCH gene expression, Final Report. Office of Scientific and Technical Information (OSTI), October 2008. http://dx.doi.org/10.2172/939904.

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Freeling, M. A genetic analysis of Adhl regulation. Progress report, June 1991--May 1993. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10107602.

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Freeling, M. A genetic analysis of Adh1 regulation. Progress report, June 1991--February 1992. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/10124127.

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Perl-Treves, Rafael, Rebecca Grumet, Nurit Katzir, and Jack E. Staub. Ethylene Mediated Regulation of Sex Expression in Cucumis. United States Department of Agriculture, January 2005. http://dx.doi.org/10.32747/2005.7586536.bard.

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Monoecious species such as melon and cucumber develop separate male and female (or bisexual) flowers on the same plant individual. They display complex genetic and hormonal regulation of sex patterns along the plant. Ethylene is known to play an important role in promoting femaleness and inhibiting male development, but many questions regarding critical sites of ethylene production versus perception, the relationship between ethylene and the sex determining loci, and the possible differences between melon and cucumber in this respect are still open. The general goal of the project was to elucidate the role of ethylene in determining flower sex in Cucumis species, melon and cucumber. The specific Objectives were: 1. Clone and characterize expression patterns of cucumber genes involved in ethylene biosynthesis and perception. 2. Genetic mapping of cloned genes and markers with respect to sex loci in melon and cucumber. 3. Produce and analyze transgenic melons altered in ethylene production or perception. In the course of the project, some modifications/adjustments were made: under Objective 2 (genetic mapping) a set of new mapping populations had to be developed, to allow better detection of polymorphism. Under Objective 3, cucumber transformation systems became available to us and we included this second model species in our plan. The main findings of our study support the pivotal role of ethylene in cucumber and melon sex determination and later stages of reproductive development. Modifying ethylene production resulted in profound alteration of sex patterns in melon: femaleness increased, and also flower maturation and fruit set were enhanced, resulting in earlier, more concentrated fruit yield in the field. Such effect was previously unknown and could have agronomic value. Our results also demonstrate the great importance of ethylene sensitivity in sex expression. Ethylene perception genes are expressed in sex-related patterns, e.g., gynoecious lines express higher levels of receptor-transcripts, and copper treatments that activate the receptor can increase femaleness. Transgenic cucumbers with increased expression of an ethylene receptor showed enhanced femaleness. Melons that expressed a defective receptor produced fewer hermaphrodite flowers and were insensitive to exogenous ethylene. When the expression of defective receptor was restricted to specific floral whorls, we saw that pistils were not inhibited by the blocked perception at the fourth whorl. Such unexpected findings suggest an indirect effect of ethylene on the affected whorl; it also points at interesting differences between melon and cucumber regarding the mode of action of ethylene. Such effects will require further study. Finally, our project also generated and tested a set of novel genetic tools for finer identification of sex determining genes in the two species and for efficient breeding for these characters. Populations that will allow easier linkage analysis of candidate genes with each sex locus were developed. Moreover, effects of modifier genes on the major femaleness trait were resolved. QTL analysis of femaleness and related developmental traits was conducted, and a comprehensive set of Near Isogenic Lines that differ in specific QTLs were prepared and made available for the private and public research. Marker assisted selection (MAS) of femaleness and fruit yield components was directly compared with phenotypic selection in field trials, and the relative efficiency of MAS was demonstrated. Such level of genetic resolution and such advanced tools were not used before to study these traits, that act as primary yield components to determine economic yields of cucurbits. In addition, this project resulted in the establishment of workable transformation procedures in our laboratories and these can be further utilized to study the function of sex-related genes in detail.
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Taub, Floyd E., and Richard E. Weller. Proline-Rich Polypeptide 1 and GX-NH2: Molecular and Genetic Mechanisms of Hematopoiesis Regulation. Office of Scientific and Technical Information (OSTI), September 2011. http://dx.doi.org/10.2172/1025686.

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