Literatura académica sobre el tema "Transcriptional autoregulation"
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Artículos de revistas sobre el tema "Transcriptional autoregulation"
De Siervi, Adriana, Paola De Luca, Jung S. Byun, Li Jun Di, Temesgen Fufa, Cynthia M. Haggerty, Elba Vazquez, Cristian Moiola, Dan L. Longo y Kevin Gardner. "Transcriptional Autoregulation by BRCA1". Cancer Research 70, n.º 2 (12 de enero de 2010): 532–42. http://dx.doi.org/10.1158/0008-5472.can-09-1477.
Texto completoCrews, Stephen T. y Joseph C. Pearson. "Transcriptional autoregulation in development". Current Biology 19, n.º 6 (marzo de 2009): R241—R246. http://dx.doi.org/10.1016/j.cub.2009.01.015.
Texto completoHobert, Oliver. "Maintaining a memory by transcriptional autoregulation". Current Biology 21, n.º 4 (febrero de 2011): R146—R147. http://dx.doi.org/10.1016/j.cub.2011.01.005.
Texto completoHearing, P. y T. Shenk. "Sequence-independent autoregulation of the adenovirus type 5 E1A transcription unit". Molecular and Cellular Biology 5, n.º 11 (noviembre de 1985): 3214–21. http://dx.doi.org/10.1128/mcb.5.11.3214-3221.1985.
Texto completoHearing, P. y T. Shenk. "Sequence-independent autoregulation of the adenovirus type 5 E1A transcription unit." Molecular and Cellular Biology 5, n.º 11 (noviembre de 1985): 3214–21. http://dx.doi.org/10.1128/mcb.5.11.3214.
Texto completoSassone-Corsi, Paolo, John C. Sisson y Inder M. Verma. "Transcriptional autoregulation of the proto-oncogene fos". Nature 334, n.º 6180 (julio de 1988): 314–19. http://dx.doi.org/10.1038/334314a0.
Texto completoMAGENHEIM, Judith, Rachel HERTZ, Ina BERMAN, Janna NOUSBECK y Jacob BAR-TANA. "Negative autoregulation of HNF-4α gene expression by HNF-4α1". Biochemical Journal 388, n.º 1 (10 de mayo de 2005): 325–32. http://dx.doi.org/10.1042/bj20041802.
Texto completoDelahodde, A., T. Delaveau y C. Jacq. "Positive autoregulation of the yeast transcription factor Pdr3p, which is involved in control of drug resistance." Molecular and Cellular Biology 15, n.º 8 (agosto de 1995): 4043–51. http://dx.doi.org/10.1128/mcb.15.8.4043.
Texto completoBell, Stephen D. y Stephen P. Jackson. "Mechanism of Autoregulation by an Archaeal Transcriptional Repressor". Journal of Biological Chemistry 275, n.º 41 (18 de julio de 2000): 31624–29. http://dx.doi.org/10.1074/jbc.m005422200.
Texto completoSoncini, F. C., E. G. Véscovi y E. A. Groisman. "Transcriptional autoregulation of the Salmonella typhimurium phoPQ operon." Journal of bacteriology 177, n.º 15 (1995): 4364–71. http://dx.doi.org/10.1128/jb.177.15.4364-4371.1995.
Texto completoTesis sobre el tema "Transcriptional autoregulation"
Zhu, Cong. "GENE REGULATORY NETWORKS OF AGL15 A PLANT MADS TRANSCRIPTION FACTOR". UKnowledge, 2005. http://uknowledge.uky.edu/gradschool_diss/446.
Texto completoUnoarumhi, Yvette Ochuwa. "Evolution of a Bacterial Global Regulator- Lrp". University of Toledo Health Science Campus / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=mco1461859521.
Texto completoVernié, Tatiana. "Analyse fonctionnelle d'EFD, un régulateur transcriptionnel de la nodulation au cours de l'interaction symbiotique entre Medicago truncatula et Sinorhizobium meliloti". Toulouse 3, 2008. http://thesesups.ups-tlse.fr/222/.
Texto completoLeguminous plants can establish symbiotic interaction with bacteria from the rhizosphere, called Rhizobia. During this interaction, plants control tightly two mechanisms: bacterial infection and formation of a new organ, the nodule in which nitrogen is fixed. But how plants control these mechanisms is still largely unknown. Starting from transcriptomic studies, we selected a potential regulator, EFD (Ethylene response Factor required for nodule Differentiation), coding for a transcription factor belonging to the ERF family. The expression profile of EFD has been characterized by quantitative RT-PCR, in situ hybridization and promoter:GUS fusion. These studies revealed a specific expression of EFD in nodule and root primordia, and in the infection zone of mature nodules, where bacteria and plant tissues differentiate. Using overexpression and RNAi approaches on transformed roots, and study of a deletion mutant, we then showed that EFD plays a role to control the number of nodules and their differentiation. Finally, we identified a major target of EFD by a transcriptomic approach. This target, Mt RR4, encodes a cytokinin response regulator. Cytokinins have recently been shown to be positive regulators of nodule initiation. Consequently, we propose that by regulating RR4 expression, EFD modulates the cytokinin pathway during nodulation to coordinate nodule initiation and development. .
Wu, Tian-Yu y 吳天宇. "Autoregulation of gbsR, identification of GbsR-binding sites, and transcriptional regulation of opuB and opuC operons in Bacillus subtilis". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/47042651578494871587.
Texto completo國立陽明大學
生化暨分子生物研究所
101
The soil bacterium Bacillus subtilis can use glycine betaine, which is one of the most important osmoprotectants in nature, to cope with the environmental osmotic stress. Choline oxidation by GbsB (choline dehydrogenase) and GbsA (glycine betaine aldehyde dehydrogenase) is the only known pathway for the synthesis of glycine betaine in B. subtilis. Choline cannot be synthesized by B. subtilis cells, but can be imported from the environment by osmoinducible ABC transporters OpuB and OpuC. GbsR is a choline-sensing regulator that negatively controls transcription of gbsAB and opuB operons. A previous study from our laboratory demonstrated that the opcR gene, which is located upstream of opuC, encodes a negative regulator for transcription of opuB and opuC operons. In this study, results from deletion and mutation analyses suggest the presence of putative GbsR operators in gbsA and opuB promoter regions, whose sequences and locations are somewhat different from the previously predicted ones. Electrophoretic mobility shift assays confirmed that these putative operators are required for the binding of GbsR. We also identified a previously unknown cis-acting element that negatively regulates opuB expression. In addition, we have found that gbsR expression is subject to negative autoregulation through the binding of GbsR to an operator in the gbsR promoter region. Moreover, we show that, in the absence of OpcR, choline exerts a suppressive effect on opuC expression during normal growth and under osmotic stress. In the absence of the choline-sensing repressor GbsR, opuB expression is also suppressed by choline.
Dar, Roy David. "Adaptation and Stochasticity of Natural Complex Systems". 2011. http://trace.tennessee.edu/utk_graddiss/959.
Texto completoChandra, Soumyanetra. "Probing Protein Sequence-Function Relationships using Deep Mutational Scanning". Thesis, 2021. https://etd.iisc.ac.in/handle/2005/5662.
Texto completoLibros sobre el tema "Transcriptional autoregulation"
Gill, Robert James Montgomery. Characterization of the human RB1 promoter and of elements involved in transcriptional autoregulation. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.
Buscar texto completoCapítulos de libros sobre el tema "Transcriptional autoregulation"
Draper, David E. "Mechanisms of Ribosomal Protein Translational Autoregulation". En Post-Transcriptional Control of Gene Expression, 299–308. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75139-4_28.
Texto completoOei, Shiao Li, Herbert Herzog, Monica Hirsch-Kauffmann, Rainer Schneider, Bernhard Auer y Manfred Schweiger. "Transcriptional regulation and autoregulation of the human gene for ADP-ribosyltransferase". En ADP-Ribosylation: Metabolic Effects and Regulatory Functions, 99–104. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2614-8_13.
Texto completoBateman, Erik. "Autoregulation of Eukaryotic Transcription Factors". En Progress in Nucleic Acid Research and Molecular Biology, 133–68. Elsevier, 1998. http://dx.doi.org/10.1016/s0079-6603(08)60892-2.
Texto completoActas de conferencias sobre el tema "Transcriptional autoregulation"
Herlinger, Alice Laschuk, Min Gao, Ren-Chin Wu, Tian-Li Wang, Leticia B. A. Rangel y Ie-Ming Shih. "Abstract A80: NAC1 attenuates BCL6 negative autoregulation and functions as a BCL6 coactivator of FOXQ1 transcription in ovarian cancer (OVCA)." En Abstracts: AACR Special Conference: Advances in Ovarian Cancer Research: Exploiting Vulnerabilities; October 17-20, 2015; Orlando, FL. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1557-3265.ovca15-a80.
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