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Libros sobre el tema "ADN polymerase I"

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Publicado: 4 de junio de 2021
Última modificación: 3 de febrero de 2022

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1

Newton, C. R. PCR. Oxford: BIOS Scientific in association with the Biochemical Society, 1994.

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2

A, Graham, ed. PCR. 2a ed. Oxford, OX, UK: BIOS Scientific Publishers, 1997.

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3

Tulin, Alexei V., ed. Poly(ADP-ribose) Polymerase. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-270-0.

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4

Tulin, Alexei V., ed. Poly(ADP-Ribose) Polymerase. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6993-7.

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5

Poly (ADP-ribose) polymerase: Methods and protocols. New York: Humana Press, 2011.

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6

1942-, Pethrick R. A. y White J. R. 1943-, eds. Polymer characterization: Physical techniques. 2a ed. Cheltenham, Glos., U.K: S. Thornes, 2000.

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7

1943-, White J. R., ed. Polymer characterization: Physical techniques. London: Chapman and Hall, 1989.

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8

D, Campbell. Polymer characterization: Physical techniques. London: Chapman and Hall, 1989.

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9

Rodriguez, Ferdinand. Principles of polymer systems. 3a ed. New York: Hemisphere Publishing Corporation, 1989.

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10

Schlechter, Mel. Conductive polymers. Norwalk, CT: Business Communications Co., 2003.

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11

Schlechter, Melvin. Biodegradable polymers. Norwalk, CT: Business Communications Co., 2001.

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12

Weizer, William P. Emulsion polymers. Cleveland: Freedonia Group, 2000.

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13

Weizer, William P. Emulsion polymers. Cleveland, OH: Freedonia Group, 1998.

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14

Wieler, Sonya Marlen. Poly(ADP-ribose) polymerase-1 is a positive regulator of the p53-mediated cell cycle response to ionizing radiation. Ottawa: National Library of Canada, 2002.

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15

Structural investigation of polymers. New York: Ellis Horwood, 1991.

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16

Bodor, G. Structural investigation of polymers. Hemel Hempstead: Ellis Horwood, 1990.

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17

Kalia, Susheel. Polymers at Cryogenic Temperatures. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013.

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18

Bhavana, Deore, ed. Self-doped conductiong polymers. Chichester, England: Wiley, 2007.

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19

Ita, Paul A. y Aaron Hackle. Metallocene & single-site polymers. Cleveland, Ohio: Freedonia Group, 2003.

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20

Prane, Joseph W. Introduction to polymers and resins. Philadelphia, PA: Federation of Societies for Coatings Technology, 1986.

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21

1945-, Mittal K. L., ed. Polymers in information storage technology. New York: Plenum Press, 1989.

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22

Vinogradova, S. V. Polikondensat͡s︡ionnye prot͡s︡essy i polimery. Moskva: Nauka, 2000.

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23

Schlechter, Melvin. Conductive and electro-optic polymers. Norwalk, CT: Business Communications Co., 1997.

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24

Scialpi, Angela y Alessio Mengoni, eds. La PCR e le sue varianti. Florence: Firenze University Press, 2008. http://dx.doi.org/10.36253/978-88-6453-159-5.

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The book "La PCR e le sue varianti" is designed as a reference tool for those whose laboratory activities deal with methods based on nucleic acid amplification. The text provides the theoretical bases of the polymerase chain reaction (PCR) and its variants (e.g. RT-PCR, quantitative PCR, isothermic PCR) in a rapid and concise manner and describes the principal applications used for genetic identification and the study of genetic polymorphism, in the form of a protocol that can be easily consulted by the users.
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25

Mathias, Lon J. Solid State NMR of Polymers. Boston, MA: Springer US, 1991.

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26

Minsker, K. S. Degradation and stabilization of vinyl-chloridebased polymers. Oxford: Pergamon Press, 1988.

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27

Minsker, K. S. Degradation and stabilization of vinyl chloride-based polymers. Oxford: Pergamon, 1988.

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28

Batzer, Hans. Introduction to macromolecular chemistry. 2a ed. Ann Arbor: UMI Books on Demand, 1991.

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29

Doi, M. The theory of polymer dynamics. Oxford: Clarendon, 1986.

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30

State University College at Buffalo. Dept. of Art Conservation., ed. Principles of polymer chemistry. Ithaca, NY: Cornell University Press, 1990.

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31

Newton, C. R. Pcr: Essential Data. Wiley & Sons, Incorporated, John, 2009.

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32

Graham, A. y C. R. Newton. Pcr (Introduction to Biotechniques). Coronet Books, 1994.

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33

White, Bruce A. Pcr Cloning Protocols: From Molecular Cloning to Genetic Engineering (Methods in Molecular Biology). Humana Press, 1997.

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34

PCR Cloning Protocols: From Molecular Cloning to Genetic Engineering (Methods in Molecular Biology). Humana Press, 1997.

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35

PCR protocols: A guide to methods and applications. San Diego: Academic Press, 1990.

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36

PCR Protocols: A Guide to Methods and Applications. Academic Press, 1989.

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37

PCR Protocols: A Guide to Methods and Applications. Academic Press, 1989.

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38

(Editor), Michael A. Innis, David H. Gelfand (Editor), John J. Sninsky (Editor) y Thomas J. White (Editor), eds. PCR Protocols: A Guide to Methods and Applications. Academic Press, 1989.

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39

PCR Protocols: A Guide to Methods and Applications. Academic Press, 1989.

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40

(Editor), M. J. McPherson, B. D. Hames (Editor) y G. R. Taylor (Editor), eds. PCR 2: A Practical Approach (Practical Approach Series). Oxford University Press, USA, 1995.

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41

(Editor), M. J. McPherson, B. D. Hames (Editor) y G. R. Taylor (Editor), eds. PCR 2: A Practical Approach (Practical Approach Series). Oxford University Press, USA, 1995.

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42

J, McPherson M. y Hames B. D, eds. PCR 2: A practical approach. Oxford: IRL Press at Oxford University Press, 1995.

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43

(Editor), Sankar Adhya y Susan Garges (Editor), eds. RNA Polymerase and Associated Factors, Part C, Volume 370 (Methods in Enzymology). Academic Press, 2003.

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44

Taberlet, Pierre, Aurélie Bonin, Lucie Zinger y Eric Coissac. DNA amplification and multiplexing. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198767220.003.0006.

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After a brief reminder of the principles underlying the polymerase chain reaction (PCR), Chapter 6 “DNA amplification and multiplexing” discusses the choice of a DNA polymerase for the PCR. In particular, it warns against the use of proofreading polymerases, that can lead to a substantial loss of PCR specificity. Chapter 6 insists on the benefits of including different types of controls in the PCR (e.g., PCR negatives and positives, tagging system controls, etc.). The most common causes of PCR failures and their solutions are addressed, as well as the precautions to take to avoid and monitor contaminations. Chapter 6 also deals with the particular case of blocking oligonucleotides, which aim at reducing the amplification of undesired sequences. It gives some valuable guidelines to design such oligonucleotides and use them efficiently. Finally, Chapter 6 presents different strategies for tagging individual samples during the amplification, to allow subsequent multiplexing during the sequencing step.
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45

D, Szabó Csaba M., ed. Cell death: The role of poly(ADP-ribose) polymerase. Boca Raton: CRC Press, 2000.

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46

H, Persing David, ed. PCR protocols for emerging infectious diseases: A supplement to Diagnostic Molecular Microbiology : principles and applications. Washington, D.C: ASM Press, 1996.

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47

Pcr Protocols for Emerging Infectious Diseases A Supplement to Diagnostic Molecular Microbiology: Principles and Applications. ASM Press, 1996.

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48

E, Cotter Finbarr, ed. Molecular diagnosis of cancer. Totowa, N.J: Humana Press, 1996.

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49

Poly(ADP-Ribosyl)ation. Springer, 2006.

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50

Bensimon, David, Vincent Croquette, Jean-François Allemand, Xavier Michalet y Terence Strick. Single-Molecule Studies of Nucleic Acids and Their Proteins. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198530923.001.0001.

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This book presents a comprehensive overview of the foundations of single-molecule studies, based on manipulation of the molecules and observation of these with fluorescent probes. It first discusses the forces present at the single-molecule scale, the methods to manipulate them, and their pros and cons. It goes on to present an introduction to single-molecule fluorescent studies based on a quantum description of absorption and emission of radiation due to Einstein. Various considerations in the study of single molecules are introduced (including signal to noise, non-radiative decay, triplet states, etc.) and some novel super-resolution methods are sketched. The elastic and dynamic properties of polymers, their relation to experiments on DNA and RNA, and the structural transitions observed in those molecules upon stretching, twisting, and unzipping are presented. The use of these single-molecule approaches for the investigation of DNA–protein interactions is highlighted via the study of DNA and RNA polymerases, helicases, and topoisomerases. Beyond the confirmation of expected mechanisms (e.g., the relaxation of DNA torsion by topoisomerases in quantized steps) and the discovery of unexpected ones (e.g., strand-switching by helicases, DNA scrunching by RNA polymerases, and chiral discrimination by bacterial topoII), these approaches have also fostered novel (third generation) sequencing technologies.
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