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Artículos de revistas sobre el tema "DNA systems"

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Publicado: 6 de septiembre de 2023

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1

Chakarov, Stoyan, Rumena Petkova y George Russev. "DNA repair systems". BioDiscovery, n.º 13 (22 de septiembre de 2014): 2. http://dx.doi.org/10.7750/biodiscovery.2014.13.2.

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2

Teo, Yin Nah y Eric T. Kool. "DNA-Multichromophore Systems". Chemical Reviews 112, n.º 7 (16 de marzo de 2012): 4221–45. http://dx.doi.org/10.1021/cr100351g.

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3

Kaina, Bernd. "DNA repair systems". Toxicology Letters 164 (septiembre de 2006): S320. http://dx.doi.org/10.1016/j.toxlet.2006.07.328.

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4

Rao, D. N. y Yedu Prasad. "DNA repair systems". Resonance 21, n.º 10 (octubre de 2016): 925–36. http://dx.doi.org/10.1007/s12045-016-0401-x.

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5

Walker, G. C. "Inducible DNA Repair Systems". Annual Review of Biochemistry 54, n.º 1 (junio de 1985): 425–57. http://dx.doi.org/10.1146/annurev.bi.54.070185.002233.

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6

Aerts, Diederik y Marek Czachor. "Abstract DNA-type systems". Nonlinearity 19, n.º 3 (31 de enero de 2006): 575–89. http://dx.doi.org/10.1088/0951-7715/19/3/003.

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7

Luo, Dan y W. Mark Saltzman. "Synthetic DNA delivery systems". Nature Biotechnology 18, n.º 1 (enero de 2000): 33–37. http://dx.doi.org/10.1038/71889.

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8

Ma, Ke, Alexander W. Harris y Jennifer N. Cha. "DNA assembled photoactive systems". Current Opinion in Colloid & Interface Science 38 (noviembre de 2018): 18–29. http://dx.doi.org/10.1016/j.cocis.2018.08.003.

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9

Handelsman, Jo. "Call for Papers: Unique Model Systems". DNA and Cell Biology 27, n.º 6 (junio de 2008): 287. http://dx.doi.org/10.1089/dna.2008.1504.

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10

Jolly, Pawan, Pedro Estrela y Michael Ladomery. "Oligonucleotide-based systems: DNA, microRNAs, DNA/RNA aptamers". Essays in Biochemistry 60, n.º 1 (30 de junio de 2016): 27–35. http://dx.doi.org/10.1042/ebc20150004.

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There are an increasing number of applications that have been developed for oligonucleotide-based biosensing systems in genetics and biomedicine. Oligonucleotide-based biosensors are those where the probe to capture the analyte is a strand of deoxyribonucleic acid (DNA), ribonucleic acid (RNA) or a synthetic analogue of naturally occurring nucleic acids. This review will shed light on various types of nucleic acids such as DNA and RNA (particularly microRNAs), their role and their application in biosensing. It will also cover DNA/RNA aptamers, which can be used as bioreceptors for a wide range of targets such as proteins, small molecules, bacteria and even cells. It will also highlight how the invention of synthetic oligonucleotides such as peptide nucleic acid (PNA) or locked nucleic acid (LNA) has pushed the limits of molecular biology and biosensor development to new perspectives. These technologies are very promising albeit still in need of development in order to bridge the gap between the laboratory-based status and the reality of biomedical applications.
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11

Bonincontro, A., R. Caneva y F. Pedone. "Hydration of aminoacid-DNA and protein-DNA systems". Biochemical Pharmacology 37, n.º 9 (mayo de 1988): 1839–40. http://dx.doi.org/10.1016/0006-2952(88)90472-8.

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12

Winogradoff, David, Pin‐Yi Li, Himanshu Joshi, Lauren Quednau, Christopher Maffeo y Aleksei Aksimentiev. "Chiral Systems Made from DNA". Advanced Science 8, n.º 5 (21 de enero de 2021): 2003113. http://dx.doi.org/10.1002/advs.202003113.

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13

Sáez, Guillermo. "DNA Injury and Repair Systems". International Journal of Molecular Sciences 19, n.º 7 (28 de junio de 2018): 1902. http://dx.doi.org/10.3390/ijms19071902.

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14

Kozulin, R. A., V. E. Kurochkin y V. M. Zolotarev. "Fluorescence-based DNA-monitoring systems". Journal of Optical Technology 72, n.º 1 (1 de enero de 2005): 20. http://dx.doi.org/10.1364/jot.72.000020.

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15

Martin, F. L. "DNA Repair Protocols: Eukaryotic Systems". Mutagenesis 14, n.º 6 (1 de noviembre de 1999): 657. http://dx.doi.org/10.1093/mutage/14.6.657.

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16

DOERFLER, WALTER, RAINER SCHUBBERT, HILDE HELLER, JENNIFER HERTZ, RALPH REMUS, JÖRG SCHRÖER, CHRISTINA KÄMMER et al. "Foreign DNA in mammalian systems". APMIS 106, S84 (noviembre de 1998): 62–68. http://dx.doi.org/10.1111/j.1600-0463.1998.tb05650.x.

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17

Brzeski, Henry. "DNA cloning 2. Expression systems". Biochemical Systematics and Ecology 24, n.º 1 (enero de 1996): 92. http://dx.doi.org/10.1016/s0305-1978(96)90010-1.

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18

Glazer, Peter M. "DNA Repair Protocols: Eukaryotic Systems". Radiation Research 153, n.º 2 (febrero de 2000): 241–42. http://dx.doi.org/10.1667/0033-7587(2000)153[0241:drpes]2.0.co;2.

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19

Mardian, Rizki y Kosuke Sekiyama. "Ant Systems-Based DNA Circuits". BioNanoScience 5, n.º 4 (11 de noviembre de 2015): 206–16. http://dx.doi.org/10.1007/s12668-015-0182-9.

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20

Mayran, Alexandre y Christopher Chase Bolt. "Transgenic Model Systems Have Revolutionized the Study of Disease". DNA and Cell Biology 41, n.º 1 (1 de enero de 2022): 49–52. http://dx.doi.org/10.1089/dna.2021.0514.

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21

TAVERNIER, JAN, RENE DEVOS, JOSE VAN DER HEYDEN, GUIDO HAUQUIER, RITA BAUDEN, INA FACHE, ERIC KAWASHIMA, JOEL VANDEKERCKHOVE, ROLAND CONTRERAS y WALTER FIERS. "Expression of Human and Murine Interleukin-5 in Eukaryotic Systems". DNA 8, n.º 7 (septiembre de 1989): 491–501. http://dx.doi.org/10.1089/dna.1.1989.8.491.

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22

Huckenbeck, W., H. G. Scheil, H. D. Schmidt, L. Efremovska y N. Xirotiris. "Population genetic studies in the Balkans. II. DNA-STR-systems". Anthropologischer Anzeiger 59, n.º 3 (12 de septiembre de 2001): 213–25. http://dx.doi.org/10.1127/anthranz/59/2001/213.

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23

Bhandari, Deepika. "Touch DNA: Revolutionizing Evidentiary DNA Forensics". International Journal of Forensic Sciences 8, n.º 3 (2023): 1–8. http://dx.doi.org/10.23880/ijfsc-16000314.

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Touch DNA is an advanced technique widely employed in modern criminal justice systems in many developed countries. It aims to extract genetic information from biological substances, specifically the cells shed from the outermost layer of skin, that are left behind on touched objects. This method involves recovering trace amounts of DNA from the biological cells released during contact, even though the quantity is usually very low. The recovered DNA is further analyzed to generate a person's DNA profile. Since dead cells are not really visible to the naked eye, successfully locating and recovering them can be challenging. Performing DNA profiling from the samples that are just touched is quite difficult, hence, requires a highly sensitive approach to its proper recovery, extraction, and amplification of the segment. The methods which are used for the collection, sampling procedure, preservation, removal of contaminants, quantification of DNA, the amplifying of the genetic material, and the subsequent analysis and interpretation of the findings all play a role in how well touch DNA analysis works. Various techniques have been created over time to gather touch DNA. Reliable DNA profiles are produced thanks to the use of sophisticated kits, tools, and well-equipped forensic laboratories, which benefit the criminal justice system.
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24

Patil, Siddhesh D., David G. Rhodes y Diane J. Burgess. "DNA-based therapeutics and DNA delivery systems: A comprehensive review". AAPS Journal 7, n.º 1 (marzo de 2005): E61—E77. http://dx.doi.org/10.1208/aapsj070109.

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25

Chiaramoni, N. S., L. C. Baccarini, M. C. Taira y S. del V. Alonso. "Liposome/DNA Systems: Correlation Between Hydrophobicity and DNA Conformational Changes". Journal of Biological Physics 34, n.º 1-2 (abril de 2008): 179–88. http://dx.doi.org/10.1007/s10867-008-9103-2.

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26

SEKIGUCHI, Mutsuo. "Genetic systems for stability of DNA." Seibutsu Butsuri 37, n.º 3 (1997): 100–105. http://dx.doi.org/10.2142/biophys.37.100.

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27

Guan, Chaoyang, Xiaoli Zhu y Chang Feng. "DNA Nanodevice-Based Drug Delivery Systems". Biomolecules 11, n.º 12 (10 de diciembre de 2021): 1855. http://dx.doi.org/10.3390/biom11121855.

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DNA, a natural biological material, has become an ideal choice for biomedical applications, mainly owing to its good biocompatibility, ease of synthesis, modifiability, and especially programmability. In recent years, with the deepening of the understanding of the physical and chemical properties of DNA and the continuous advancement of DNA synthesis and modification technology, the biomedical applications based on DNA materials have been upgraded to version 2.0: through elaborate design and fabrication of smart-responsive DNA nanodevices, they can respond to external or internal physical or chemical stimuli so as to smartly perform certain specific functions. For tumor treatment, this advancement provides a new way to solve the problems of precise targeting, controllable release, and controllable elimination of drugs to a certain extent. Here, we review the progress of related fields over the past decade, and provide prospects for possible future development directions.
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28

Lu, Shasha, Jianlei Shen, Chunhai Fan, Qian Li y Xiurong Yang. "DNA Assembly‐Based Stimuli‐Responsive Systems". Advanced Science 8, n.º 13 (14 de mayo de 2021): 2100328. http://dx.doi.org/10.1002/advs.202100328.

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29

Linko, Veikko, Sami Nummelin, Laura Aarnos, Kosti Tapio, J. Toppari y Mauri Kostiainen. "DNA-Based Enzyme Reactors and Systems". Nanomaterials 6, n.º 8 (27 de julio de 2016): 139. http://dx.doi.org/10.3390/nano6080139.

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30

Xue, Han, Xihui Gao y Chuan Zhang. "DNA nanostructure-based siRNA delivery systems". Chinese Science Bulletin 64, n.º 10 (25 de enero de 2019): 1053–66. http://dx.doi.org/10.1360/n972018-00893.

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31

RADMAN, M., F. TADDEI y I. MATIC. "DNA Repair Systems and Bacterial Evolution". Cold Spring Harbor Symposia on Quantitative Biology 65 (1 de enero de 2000): 11–20. http://dx.doi.org/10.1101/sqb.2000.65.11.

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32

Pannier, Angela K. y Lonnie D. Shea. "Controlled release systems for DNA delivery". Molecular Therapy 10, n.º 1 (julio de 2004): 19–26. http://dx.doi.org/10.1016/j.ymthe.2004.03.020.

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33

Mai, Danielle J., Christopher Brockman y Charles M. Schroeder. "Microfluidic systems for single DNA dynamics". Soft Matter 8, n.º 41 (2012): 10560. http://dx.doi.org/10.1039/c2sm26036k.

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34

Radman, Miroslav. "DNA repair systems and genetic toxicology". Toxicology Letters 164 (septiembre de 2006): S3. http://dx.doi.org/10.1016/j.toxlet.2006.06.009.

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35

Ibraheem, D., A. Elaissari y H. Fessi. "Gene therapy and DNA delivery systems". International Journal of Pharmaceutics 459, n.º 1-2 (enero de 2014): 70–83. http://dx.doi.org/10.1016/j.ijpharm.2013.11.041.

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36

Morling, Niels y Hanna E. Hansen. "Paternity testing with VNTR DNA systems". International Journal of Legal Medicine 105, n.º 4 (julio de 1993): 189–96. http://dx.doi.org/10.1007/bf01642792.

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37

Hansen, Hanna E. y Niels Morling. "Paternity testing with VNTR DNA systems". International Journal of Legal Medicine 105, n.º 4 (julio de 1993): 197–202. http://dx.doi.org/10.1007/bf01642793.

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38

Kari, Lila, Gheorghe Păun, Grzegorz Rozenberg, Arto Salomaa y Sheng Yu. "DNA computing, sticker systems, and universality". Acta Informatica 35, n.º 5 (1 de mayo de 1998): 401–20. http://dx.doi.org/10.1007/s002360050125.

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39

Lee, Lan-Ying y Stanton B. Gelvin. "T-DNA Binary Vectors and Systems". Plant Physiology 146, n.º 2 (febrero de 2008): 325–32. http://dx.doi.org/10.1104/pp.107.113001.

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40

Toumpanakis, Dimitrios y Stamatios E. Theocharis. "DNA repair systems in malignant mesothelioma". Cancer Letters 312, n.º 2 (diciembre de 2011): 143–49. http://dx.doi.org/10.1016/j.canlet.2011.08.021.

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41

Furniss, Caroline S. M., A. Bryan Hanley, Alan R. Mackie y James Mingins. "DNA manipulation in low water systems". Enzyme and Microbial Technology 13, n.º 6 (junio de 1991): 525. http://dx.doi.org/10.1016/0141-0229(91)90043-a.

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42

Malinina, L. V., V. V. Makhaldiani, V. A. Tereshko, V. F. Zarytova y E. M. Ivanova. "Phase Diagrams for DNA Crystallization Systems". Journal of Biomolecular Structure and Dynamics 5, n.º 2 (octubre de 1987): 405–33. http://dx.doi.org/10.1080/07391102.1987.10506402.

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43

Nakakuki, Takashi, Jun-ichi Imura, Ibuki Kawamata y Satoshi Murata. "Robustness of DNA Strand Displacement Systems⋆". IFAC-PapersOnLine 51, n.º 33 (2018): 32–37. http://dx.doi.org/10.1016/j.ifacol.2018.12.081.

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44

Feldkamp, Udo y Christof M Niemeyer. "Rational Engineering of Dynamic DNA Systems". Angewandte Chemie International Edition 47, n.º 21 (13 de mayo de 2008): 3871–73. http://dx.doi.org/10.1002/anie.200800675.

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45

Yu, Zhe, Jian Chen, Barry N. Ford, Moyra E. Brackley y Barry W. Glickman. "Human DNA repair systems: An overview". Environmental and Molecular Mutagenesis 33, n.º 1 (1999): 3–20. http://dx.doi.org/10.1002/(sici)1098-2280(1999)33:1<3::aid-em2>3.0.co;2-l.

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46

Lo, Chen-Yu y Yang Gao. "DNA Helicase–Polymerase Coupling in Bacteriophage DNA Replication". Viruses 13, n.º 9 (31 de agosto de 2021): 1739. http://dx.doi.org/10.3390/v13091739.

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Bacteriophages have long been model systems to study the molecular mechanisms of DNA replication. During DNA replication, a DNA helicase and a DNA polymerase cooperatively unwind the parental DNA. By surveying recent data from three bacteriophage replication systems, we summarized the mechanistic basis of DNA replication by helicases and polymerases. Kinetic data have suggested that a polymerase or a helicase alone is a passive motor that is sensitive to the base-pairing energy of the DNA. When coupled together, the helicase–polymerase complex is able to unwind DNA actively. In bacteriophage T7, helicase and polymerase reside right at the replication fork where the parental DNA is separated into two daughter strands. The two motors pull the two daughter strands to opposite directions, while the polymerase provides a separation pin to split the fork. Although independently evolved and containing different replisome components, bacteriophage T4 replisome shares mechanistic features of Hel–Pol coupling that are similar to T7. Interestingly, in bacteriophages with a limited size of genome like Φ29, DNA polymerase itself can form a tunnel-like structure, which encircles the DNA template strand and facilitates strand displacement synthesis in the absence of a helicase. Studies on bacteriophage replication provide implications for the more complicated replication systems in bacteria, archaeal, and eukaryotic systems, as well as the RNA genome replication in RNA viruses.
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47

Fiebig, Torsten y Hans-Achim Wagenknecht. "DNA Photonics – Photoinduced Electron Transfer in Synthetic DNA-Donor–Acceptor Systems". CHIMIA International Journal for Chemistry 61, n.º 4 (25 de abril de 2007): 133–39. http://dx.doi.org/10.2533/chimia.2007.133.

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48

George, Aby K. y Harpreet Singh. "DNA Implementation of Fuzzy Inference Engine: Towards DNA Decision-Making Systems". IEEE Transactions on NanoBioscience 16, n.º 8 (diciembre de 2017): 773–82. http://dx.doi.org/10.1109/tnb.2017.2760821.

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49

Lu, Chun-Hua, Bilha Willner y Itamar Willner. "DNA Nanotechnology: From Sensing and DNA Machines to Drug-Delivery Systems". ACS Nano 7, n.º 10 (26 de septiembre de 2013): 8320–32. http://dx.doi.org/10.1021/nn404613v.

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50

Thompson, Marlo K., Robert W. Sobol y Aishwarya Prakash. "Exploiting DNA Endonucleases to Advance Mechanisms of DNA Repair". Biology 10, n.º 6 (14 de junio de 2021): 530. http://dx.doi.org/10.3390/biology10060530.

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The earliest methods of genome editing, such as zinc-finger nucleases (ZFN) and transcription activator-like effector nucleases (TALENs), utilize customizable DNA-binding motifs to target the genome at specific loci. While these approaches provided sequence-specific gene-editing capacity, the laborious process of designing and synthesizing recombinant nucleases to recognize a specific target sequence, combined with limited target choices and poor editing efficiency, ultimately minimized the broad utility of these systems. The discovery of clustered regularly interspaced short palindromic repeat sequences (CRISPR) in Escherichia coli dates to 1987, yet it was another 20 years before CRISPR and the CRISPR-associated (Cas) proteins were identified as part of the microbial adaptive immune system, by targeting phage DNA, to fight bacteriophage reinfection. By 2013, CRISPR/Cas9 systems had been engineered to allow gene editing in mammalian cells. The ease of design, low cytotoxicity, and increased efficiency have made CRISPR/Cas9 and its related systems the designer nucleases of choice for many. In this review, we discuss the various CRISPR systems and their broad utility in genome manipulation. We will explore how CRISPR-controlled modifications have advanced our understanding of the mechanisms of genome stability, using the modulation of DNA repair genes as examples.
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