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Articles de revues sur le sujet « DNA Synthesis »

Auteur : Grafiati
Publié le 4 juin 2021
Mis à jour le 28 juillet 2024

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1

Burke, Cassandra R., et Andrej Lupták. « DNA synthesis from diphosphate substrates by DNA polymerases ». Proceedings of the National Academy of Sciences 115, no 5 (16 janvier 2018) : 980–85. http://dx.doi.org/10.1073/pnas.1712193115.

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The activity of DNA polymerase underlies numerous biotechnologies, cell division, and therapeutics, yet the enzyme remains incompletely understood. We demonstrate that both thermostable and mesophilic DNA polymerases readily utilize deoxyribonucleoside diphosphates (dNDPs) for DNA synthesis and inorganic phosphate for the reverse reaction, that is, phosphorolysis of DNA. For Taq DNA polymerase, the KMs of the dNDP and phosphate substrates are ∼20 and 200 times higher than for dNTP and pyrophosphate, respectively. DNA synthesis from dNDPs is about 17 times slower than from dNTPs, and DNA phosphorolysis about 200 times less efficient than pyrophosphorolysis. Such parameters allow DNA replication without requiring coupled metabolism to sequester the phosphate products, which consequently do not pose a threat to genome stability. This mechanism contrasts with DNA synthesis from dNTPs, which yield high-energy pyrophosphates that have to be hydrolyzed to phosphates to prevent the reverse reaction. Because the last common ancestor was likely a thermophile, dNDPs are plausible substrates for genome replication on early Earth and may represent metabolic intermediates later replaced by the higher-energy triphosphates.
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2

Shilkin, E. S., E. O. Boldinova, A. D. Stolyarenko, R. I. Goncharova, R. N. Chuprov-Netochin, M. P. Smal et A. V. Makarova. « Translesion DNA Synthesis and Reinitiation of DNA Synthesis in Chemotherapy Resistance ». Biochemistry (Moscow) 85, no 8 (août 2020) : 869–82. http://dx.doi.org/10.1134/s0006297920080039.

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3

Shaista Sabir and Naghmmana Rashid, Shaista Sabir and Naghmmana Rashid. « Organocatalyzed Synthesis, DNA Binding and Microbial Studies of Warfarin Analogues ». Journal of the chemical society of pakistan 46, no 1 (2024) : 107. http://dx.doi.org/10.52568/001426/jcsp/46.01.2024.

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A noval chiral sec-amine/amidine-base hybrid catalyst, N [S-carbonylprolyl] cyclohexyl Amine is described, which is able to catalyze conjugate addition of 6-Methyl-4-hydroxypyran and 2-Hydroxy-naphthaquinone with various benzylideneacetones through Michael reactions that directly gives anticoagulant Warfarin analogues. These analogues were prepared in good yields (54–82%) and in good enantiomeric excess (50–75%). Identification of synthesized compounds was done by physio-chemical properties and spectral analysis (1H-NMR andamp; 13C-NMR).These compounds were further investigated for their antimicrobial (antibacterial andamp; antifungal) activities and DNA-binding studies. Antimicrobial studies were carried out by Disc Diffusion while DNA-binding studies were carried out by Cyclic Voltammetry and UV-Visible spectroscopy. These studies showed that the compounds showed significant interaction with DNA. Some analogues also imparted prominent antimicrobial activities.
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4

Caruthers, Marvin H. « Chemical synthesis of DNA and DNA analogs ». Accounts of Chemical Research 24, no 9 (septembre 1991) : 278–84. http://dx.doi.org/10.1021/ar00009a005.

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5

Church, Geoffrey A., Anindya Dasgupta et Duncan W. Wilson. « Herpes Simplex Virus DNA Packaging without Measurable DNA Synthesis ». Journal of Virology 72, no 4 (1 avril 1998) : 2745–51. http://dx.doi.org/10.1128/jvi.72.4.2745-2751.1998.

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ABSTRACT Herpes simplex virus (HSV) type 1 DNA synthesis and packaging occur within the nuclei of infected cells; however, the extent to which the two processes are coupled remains unclear. Correct packaging is thought to be dependent upon DNA debranching or other repair processes, and such events commonly involve new DNA synthesis. Furthermore, the HSV UL15 gene product, essential for packaging, nevertheless localizes to sites of active DNA replication and may link the two events. It has previously been difficult to determine whether packaging requires concomitant DNA synthesis due to the complexity of these processes and of the viral life cycle; however, we have recently described a model system which simplifies the study of HSV assembly. Cells infected with HSV strain tsProt.A accumulate unpackaged capsids at the nonpermissive temperature of 39°C. Following release of the temperature block, these capsids proceed to package viral DNA in a single, synchronous wave. Here we report that, when DNA replication was inhibited prior to release of the temperature block, DNA packaging and later events in viral assembly nevertheless occurred at near-normal levels. We conclude that, under our conditions, HSV DNA packaging does not require detectable levels of DNA synthesis.
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6

Turgay Tun, Turgay Tun, Nadir Demirel Nadir Demirel, Mahmut Emir Mahmut Emir, Asl han G. nel Asl han G nel, R. fk Kad o. lu R fk Kad o lu et Nurcan Karacan Nurcan Karacan. « Three New Copper (II) Complexes with CHIRAL SCHIFF BASES : Synthesis, Characterization, DNA Binding and DNA-Cleavage Studies ». Journal of the chemical society of pakistan 41, no 2 (2019) : 334. http://dx.doi.org/10.52568/000730/jcsp/41.02.2019.

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New mononuclear copper (II) complexes (1, 2 and 3) were synthesized from Schiff bases (H2L) of chiral amino alcohols. The structures of the copper complexes were proposed by a combination of elemental analyses, FTIR, LCMS, magnetic susceptibility and molar conductance measurement methods. Spectroscopic and analytical data of the complexes suggest four-coordinated structures. Geometry optimization carried out with DFT/6-31G (d,p) were proposed to be distorted square planar geometry for the complexes. The similarity between experimental and theoretical IR spectra confirms the proposed structures. The interaction of copper (II) complexes with calf thymus (CT-DNA) was investigated using absorption titration method. The results suggest that the complex 1 and 2 can bind to DNA by intercalation. Binding constants Kb were found to be 2.46and#215;105 for 1, 5.41and#215;105 for 2 and 7.00and#215;104 for 3. Moreover, agarose gel electrophoresis assay demonstrates that all complexes were found to cleavage of plasmid pentry/d-topo plasmid DNA. Complex 2 shows the best cleavage activity (5 and#181;M).
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7

Leslie, Mitch. « Double-checking DNA synthesis ». Journal of Cell Biology 204, no 2 (13 janvier 2014) : 148. http://dx.doi.org/10.1083/jcb.2042iti1.

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8

Doerr, Allison. « DNA synthesis lights up ». Nature Methods 5, no 4 (avril 2008) : 286. http://dx.doi.org/10.1038/nmeth0408-286.

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9

Uppenbrink, J. « ORGANIC SYNTHESIS : Sugarcoated DNA ». Science 290, no 5492 (27 octobre 2000) : 675b—675. http://dx.doi.org/10.1126/science.290.5492.675b.

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10

LeBrasseur, Nicole. « Geminin halts DNA synthesis ». Journal of Cell Biology 165, no 4 (24 mai 2004) : 455. http://dx.doi.org/10.1083/jcb1654iti3.

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11

MILLS, W. RONALD, MICHELE REEVES, DIANA L. FOWLER et STEPHEN F. CAPO. « DNA Synthesis in Chloroplasts ». Journal of Experimental Botany 40, no 4 (1989) : 425–29. http://dx.doi.org/10.1093/jxb/40.4.425.

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12

Caruthers, Marvin H. « Chemical synthesis of DNA ». Journal of Chemical Education 66, no 7 (juillet 1989) : 577. http://dx.doi.org/10.1021/ed066p577.

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13

HENRY, CELIA M. « DNA-PROGRAMMED ORGANIC SYNTHESIS ». Chemical & ; Engineering News Archive 83, no 5 (31 janvier 2005) : 35–36. http://dx.doi.org/10.1021/cen-v083n005.p035.

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14

Leake, Devin. « DNA Synthesis Steps Up ». Genetic Engineering & ; Biotechnology News 36, no 8 (15 avril 2016) : 14–15. http://dx.doi.org/10.1089/gen.36.08.09.

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15

Wright, N. A. « DNA Synthesis and Genotoxicity ». Digestion 47, no 1 (1990) : 24–30. http://dx.doi.org/10.1159/000200511.

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16

Hansen, Bjarke N., Kim S. Larsen, Daniel Merkle et Alexei Mihalchuk. « DNA-templated synthesis optimization ». Natural Computing 17, no 4 (31 juillet 2018) : 693–707. http://dx.doi.org/10.1007/s11047-018-9697-7.

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17

LUCK, DENNIS N., JOHNNY K. NGSEE, FRITZ M. ROTTMAN et MICHAEL SMITH. « Synthesis of Bovine Prolactin inEscherichia coli ». DNA 5, no 1 (février 1986) : 21–28. http://dx.doi.org/10.1089/dna.1986.5.21.

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18

Hogg, Matthew, A. Elisabeth Sauer-Eriksson et Erik Johansson. « Promiscuous DNA synthesis by human DNA polymerase θ ». Nucleic Acids Research 40, no 6 (30 novembre 2011) : 2611–22. http://dx.doi.org/10.1093/nar/gkr1102.

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19

Bridges, Bryn A. « Error-prone DNA repair and translesion DNA synthesis ». DNA Repair 4, no 6 (juin 2005) : 725–39. http://dx.doi.org/10.1016/j.dnarep.2004.12.009.

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20

Ebara, Y., T. Sugiyama, K. Kaihatsu et S. i. Ueji. « Synthesis of non-natural DNA using DNA polymerase ». Nucleic Acids Symposium Series 44, no 1 (1 octobre 2000) : 143–44. http://dx.doi.org/10.1093/nass/44.1.143.

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21

Chary, Parvathi, William A. Beard, Samuel H. Wilson et R. Stephen Lloyd. « DNA Polymerase β Gap-Filling Translesion DNA Synthesis ». Chemical Research in Toxicology 25, no 12 (15 novembre 2012) : 2744–54. http://dx.doi.org/10.1021/tx300368f.

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22

Sariban, E., R. S. Wu, L. C. Erickson et W. M. Bonner. « Interrelationships of protein and DNA syntheses during replication of mammalian cells ». Molecular and Cellular Biology 5, no 6 (juin 1985) : 1279–86. http://dx.doi.org/10.1128/mcb.5.6.1279-1286.1985.

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During the replication of chromatin, the syntheses of the histone protein and DNA components are closely coordinated but not totally linked. The interrelationships of total protein synthesis, histone protein synthesis, DNA synthesis, and mRNA levels have been investigated in Chinese hamster ovary cells subjected to several different types of inhibitors in several different temporal combinations. The results from these studies and results reported elsewhere can be brought together into a consistent framework which combines the idea of autoregulation of histone biosynthesis as originally proposed by W. B. Butler and G. C. Mueller (Biochim. Biophys. Acta 294:481-496, 1973] with the presence of basal histone synthesis and the effects of protein synthesis on DNA synthesis. The proposed framework obviates the difficulties of Butler and Mueller's model and may have wider application in understanding the control of cell growth.
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23

Sariban, E., R. S. Wu, L. C. Erickson et W. M. Bonner. « Interrelationships of protein and DNA syntheses during replication of mammalian cells. » Molecular and Cellular Biology 5, no 6 (juin 1985) : 1279–86. http://dx.doi.org/10.1128/mcb.5.6.1279.

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During the replication of chromatin, the syntheses of the histone protein and DNA components are closely coordinated but not totally linked. The interrelationships of total protein synthesis, histone protein synthesis, DNA synthesis, and mRNA levels have been investigated in Chinese hamster ovary cells subjected to several different types of inhibitors in several different temporal combinations. The results from these studies and results reported elsewhere can be brought together into a consistent framework which combines the idea of autoregulation of histone biosynthesis as originally proposed by W. B. Butler and G. C. Mueller (Biochim. Biophys. Acta 294:481-496, 1973] with the presence of basal histone synthesis and the effects of protein synthesis on DNA synthesis. The proposed framework obviates the difficulties of Butler and Mueller's model and may have wider application in understanding the control of cell growth.
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24

Zhang, Yanbin, Xiaohua Wu, Fenghua Yuan, Zhongwen Xie et Zhigang Wang. « Highly Frequent Frameshift DNA Synthesis by Human DNA Polymerase μ ». Molecular and Cellular Biology 21, no 23 (1 décembre 2001) : 7995–8006. http://dx.doi.org/10.1128/mcb.21.23.7995-8006.2001.

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ABSTRACT DNA polymerase μ (Polμ) is a newly identified member of the polymerase X family. The biological function of Polμ is not known, although it has been speculated that human Polμ may be a somatic hypermutation polymerase. To help understand the in vivo function of human Polμ, we have performed in vitro biochemical analyses of the purified polymerase. Unlike any other DNA polymerases studied thus far, human Polμ catalyzed frameshift DNA synthesis with an unprecedentedly high frequency. In the sequence contexts examined, −1 deletion occurred as the predominant DNA synthesis mechanism opposite the single-nucleotide repeat sequences AA, GG, TT, and CC in the template. Thus, the fidelity of DNA synthesis by human Polμ was largely dictated by the sequence context. Human Polμ was able to efficiently extend mismatched bases mainly by a frameshift synthesis mechanism. With the primer ends, containing up to four mismatches, examined, human Polμ effectively realigned the primer to achieve annealing with a microhomology region in the template several nucleotides downstream. As a result, human Polμ promoted microhomology search and microhomology pairing between the primer and the template strands of DNA. These results show that human Polμ is much more prone to cause frameshift mutations than base substitutions. The biochemical properties of human Polμ suggest a function in nonhomologous end joining and V(D)J recombination through its microhomology searching and pairing activities but do not support a function in somatic hypermutation.
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25

HAYDEN, MARK A., et WLODEK MANDECKI. « Gene Synthesis by Serial Cloning of Oligonucleotides ». DNA 7, no 8 (octobre 1988) : 571–77. http://dx.doi.org/10.1089/dna.1.1988.7.571.

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26

EBE, KAZUYU, MONICA SCHÖLD, JOHN J. ROSSI et R. BRUCE WALLACE. « Enzymatic Synthesis of Oligoribonucleotides of Defined Sequence ». DNA 6, no 5 (octobre 1987) : 497–504. http://dx.doi.org/10.1089/dna.1987.6.497.

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27

Xiong, X., J. L. Smith et M. S. Chen. « Effect of incorporation of cidofovir into DNA by human cytomegalovirus DNA polymerase on DNA elongation. » Antimicrobial Agents and Chemotherapy 41, no 3 (mars 1997) : 594–99. http://dx.doi.org/10.1128/aac.41.3.594.

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Cidofovir (CDV) (HPMPC) has potent in vitro and in vivo activity against human cytomegalovirus (HCMV), CDV diphosphate (CDVpp), the putative antiviral metabolite of CDV, is an inhibitor and an alternate substrate of HCMV DNA polymerase. CDV is incorporated with the correct complementation to dGMP in the template, and the incorporated CDV at the primer end is not excised by the 3'-to-5' exonuclease activity of HCMV DNA polymerase. The incorporation of a CDV molecule causes a decrease in the rate of DNA elongation for the addition of the second natural nucleotide from the singly incorporated CDV molecule. The reduction in the rate of DNA (36-mer) synthesis from an 18-mer by one incorporated CDV is 31% that of the control. However, the fidelity of HCMV DNA polymerase is maintained for the addition of the nucleotides following a single incorporated CDV molecule. The rate of DNA synthesis by HCMV DNA polymerase is drastically decreased after the incorporation of two consecutive CDV molecules; the incorporation of a third consecutive CDV molecule is not detectable. Incorporation of two CDV molecules separated by either one or two deoxynucleoside monophosphates (dAMP, dGMP, or dTMP) also drastically decreases the rate of DNA chain elongation by HCMV DNA polymerase. The rate of DNA synthesis decreases by 90% when a template which contains one internally incorporated CDV molecule is used. The inhibition by CDVpp of DNA synthesis by HCMV DNA polymerase and the inability of HCMV DNA polymerase to excise incorporated CDV from DNA may account for the potent and long-lasting anti-CMV activity of CDV.
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28

SHIMKUS, MARY L., PERRY GUAGLIANONE et TIMOTHY M. HERMAN. « Synthesis and Characterization of Biotin-Labeled Nucleotide Analogs ». DNA 5, no 3 (juin 1986) : 247–55. http://dx.doi.org/10.1089/dna.1986.5.247.

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29

BODESCOT, MYRIAM, et OLIVIER BRISON. « Efficient Second-Strand cDNA Synthesis Using T7 DNA Polymerase ». DNA and Cell Biology 13, no 9 (septembre 1994) : 977–85. http://dx.doi.org/10.1089/dna.1994.13.977.

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30

MacCulloch, Tara, Alexandra Novacek et Nicholas Stephanopoulos. « Proximity-enhanced synthesis of DNA–peptide–DNA triblock molecules ». Chemical Communications 58, no 25 (2022) : 4044–47. http://dx.doi.org/10.1039/d1cc04970d.

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31

Chaput, John C., Justin K. Ichida et Jack W. Szostak. « DNA Polymerase-Mediated DNA Synthesis on a TNA Template ». Journal of the American Chemical Society 125, no 4 (janvier 2003) : 856–57. http://dx.doi.org/10.1021/ja028589k.

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32

Arana, M. E., M. Seki, R. D. Wood, I. B. Rogozin et T. A. Kunkel. « Low-fidelity DNA synthesis by human DNA polymerase theta ». Nucleic Acids Research 36, no 11 (28 mai 2008) : 3847–56. http://dx.doi.org/10.1093/nar/gkn310.

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33

Gomez Godinez, Veronica, Sami Kabbara, Adria Sherman, Tao Wu, Shirli Cohen, Xiangduo Kong, Jose Luis Maravillas-Montero et al. « DNA damage induced during mitosis undergoes DNA repair synthesis ». PLOS ONE 15, no 4 (28 avril 2020) : e0227849. http://dx.doi.org/10.1371/journal.pone.0227849.

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34

Paz-Elizur, Tamar, Masaru Takeshita, Myron Goodman, Michael O'Donnell et Zvi Livneh. « Mechanism of Translesion DNA Synthesis by DNA Polymerase II ». Journal of Biological Chemistry 271, no 40 (4 octobre 1996) : 24662–69. http://dx.doi.org/10.1074/jbc.271.40.24662.

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35

Lee, S. H., Z. Q. Pan, A. D. Kwong, P. M. Burgers et J. Hurwitz. « Synthesis of DNA by DNA polymerase epsilon in vitro. » Journal of Biological Chemistry 266, no 33 (novembre 1991) : 22707–17. http://dx.doi.org/10.1016/s0021-9258(18)54626-3.

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36

Tomiyasu, Shinjiro, Kazuhiko Kuwahara, Nobuo Sakaguchi et Michio Ogawa. « GANP DNA primase associated with MCM3 and DNA synthesis ». International Congress Series 1255 (août 2003) : 283–88. http://dx.doi.org/10.1016/s0531-5131(03)00917-8.

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37

Liang, X., T. Kato et H. Asanuma. « Mechanism of DNA elongation during de novo DNA synthesis ». Nucleic Acids Symposium Series 52, no 1 (1 septembre 2008) : 411–12. http://dx.doi.org/10.1093/nass/nrn209.

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38

Barone, G., L. De Napoli, G. Di Fabio, E. Erra, C. Giancola, A. Messere, D. Montesarchio, L. Petraccone et G. Piccialli. « Synthesis and DNA Binding Properties of DNA-PNA Chimeras ». Nucleosides, Nucleotides and Nucleic Acids 22, no 5-8 (octobre 2003) : 1089–91. http://dx.doi.org/10.1081/ncn-120022743.

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39

Matsuda, Toshiro, Katarzyna Bebenek, Chikahide Masutani, Fumio Hanaoka et Thomas A. Kunkel. « Low fidelity DNA synthesis by human DNA polymerase-η ». Nature 404, no 6781 (avril 2000) : 1011–13. http://dx.doi.org/10.1038/35010014.

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40

CARUTHERS, M. H. « ChemInform Abstract : Chemical Synthesis of DNA and DNA Analogues ». ChemInform 23, no 4 (22 août 2010) : no. http://dx.doi.org/10.1002/chin.199204308.

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41

Zhang, Hui Yong. « Solid-Phase Synthesis of DNA Chemical Sensor ». Advanced Materials Research 815 (octobre 2013) : 305–11. http://dx.doi.org/10.4028/www.scientific.net/amr.815.305.

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Oligonucleotides are essential components of many applications in molecular biology. The synthesis chemistry is robust and commercial oligonucleotide synthesizers have taken advantage of the chemistry to provide oligonucleotides of high quality and purity. This paper established nucleic acid synthesis platform to carry out the synthesis of the labeled nucleic acid probes based on the DNA synthesizer and solid-phase synthesis technology. We chose to study the automated synthesis starting from DMT protected FAM labeled amidite attached to controlled pore glass (CPG) support and the standard trityl-off oligonucleotide synthesis cycle was performed, yielding the solid-supported oligonucleotide. The reported automated solid-phase oligonucleotide synthesis procedure successfully employs the common iterative synthesis, deblocking, activation, coupling, capping, oxidation, and isolation steps in standard oligonucleotide synthesis. The automated synthetic approach can also be applied to oligonucleotides of different length, composition of nucleotide, demonstrating the universality of the method. Moreover, the synthesis involved the use of commercially available, safe, stable, and inexpensive reagents, particularly advantageous and attractive for their use in automated solid-phase synthesis. The synthesis allows custom tailoring of their structure to the requirements of biological assays within hours, as opposed to traditional approaches that require weeks or months of work in the laboratory. Therefore it will become much easier to investigate biological interactions and optimize for objectives such as the receptor mediated targeting of oligonucleotides.
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Bügl, Hans, John P. Danner, Robert J. Molinari, John T. Mulligan, Han-Oh Park, Bas Reichert, David A. Roth et al. « DNA synthesis and biological security ». Nature Biotechnology 25, no 6 (juin 2007) : 627–29. http://dx.doi.org/10.1038/nbt0607-627.

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43

Shivalingam, Arun, et Tom Brown. « Synthesis of chemically modified DNA ». Biochemical Society Transactions 44, no 3 (9 juin 2016) : 709–15. http://dx.doi.org/10.1042/bst20160051.

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Naturally occurring DNA is encoded by the four nucleobases adenine, cytosine, guanine and thymine. Yet minor chemical modifications to these bases, such as methylation, can significantly alter DNA function, and more drastic changes, such as replacement with unnatural base pairs, could expand its function. In order to realize the full potential of DNA in therapeutic and synthetic biology applications, our ability to ‘write’ long modified DNA in a controlled manner must be improved. This review highlights methods currently used for the synthesis of moderately long chemically modified nucleic acids (up to 1000 bp), their limitations and areas for future expansion.
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44

Yamashita, Takayuki, Tsukasa Oda et Takayuki Sekimoto. « Translesion DNA Synthesis and Hsp90 ». Genes and Environment 34, no 2 (2012) : 89–93. http://dx.doi.org/10.3123/jemsge.34.89.

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45

Pincus, SH, KS Ramesh et DJ Wyler. « Eosinophils stimulate fibroblast DNA synthesis ». Blood 70, no 2 (1 août 1987) : 572–74. http://dx.doi.org/10.1182/blood.v70.2.572.572.

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Abstract Fibrosis complicates a number of chronic inflammatory diseases and occurs in some conditions following chronic hypereosinophilic syndromes. We assessed whether eosinophils might be a source of fibrogenic factors. Extracts of human and guinea pig cell populations enriched for eosinophils contained substances that stimulated tritiated thymidine incorporation by human fibroblasts. Supernatants derived from resting eosinophils and extracts prepared from eosinophil granules also contained fibrogenic factors. Our findings demonstrate a new potential role for eosinophils and suggest a causal relationship between tissue eosinophilia and scar formation in certain parasitic condition.
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46

Pincus, SH, KS Ramesh et DJ Wyler. « Eosinophils stimulate fibroblast DNA synthesis ». Blood 70, no 2 (1 août 1987) : 572–74. http://dx.doi.org/10.1182/blood.v70.2.572.bloodjournal702572.

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Fibrosis complicates a number of chronic inflammatory diseases and occurs in some conditions following chronic hypereosinophilic syndromes. We assessed whether eosinophils might be a source of fibrogenic factors. Extracts of human and guinea pig cell populations enriched for eosinophils contained substances that stimulated tritiated thymidine incorporation by human fibroblasts. Supernatants derived from resting eosinophils and extracts prepared from eosinophil granules also contained fibrogenic factors. Our findings demonstrate a new potential role for eosinophils and suggest a causal relationship between tissue eosinophilia and scar formation in certain parasitic condition.
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HANNIGAN, B. H., K. L. O'NEILL, R. H. PEARCE, P. G. McKENNA et W. P. ABRAM. « Lymphocyte DNA synthesis in malignancy ». Biochemical Society Transactions 14, no 1 (1 février 1986) : 81–82. http://dx.doi.org/10.1042/bst0140081.

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Bong, Dennis, et Jie Mao. « Synthesis of DNA-Binding Peptoids ». Synlett 26, no 11 (11 mai 2015) : 1581–85. http://dx.doi.org/10.1055/s-0034-1380698.

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Chow, B. Y., C. J. Emig et J. M. Jacobson. « Photoelectrochemical synthesis of DNA microarrays ». Proceedings of the National Academy of Sciences 106, no 36 (21 août 2009) : 15219–24. http://dx.doi.org/10.1073/pnas.0813011106.

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Nicolaou, K. C., Brian Smith, Joaquin Pastor, Yoshihiko Watanabe et David Weinstein. « Synthesis of DNA-Binding Oligosaccharides ». Synlett 1997, Sup. I (juin 1997) : 401–10. http://dx.doi.org/10.1055/s-1997-6114.

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