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Gotowe bibliografie tematyczne / Polymerase chain reaction / Artykuły w czasopismach

Artykuły w czasopismach na temat „Polymerase chain reaction”

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Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 28 lipca 2024

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1

Namuth, Deana M. "Polymerase Chain Reaction". Journal of Natural Resources and Life Sciences Education 33, nr 1 (2004): 179–80. http://dx.doi.org/10.2134/jnrlse.2004.0179b.

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2

Sheppard, Haynes W. (Chip). "Polymerase Chain Reaction". Infection Control and Hospital Epidemiology 12, nr 8 (sierpień 1991): 476–77. http://dx.doi.org/10.2307/30146878.

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3

Seemayer, Thomas A. "Polymerase Chain Reaction". Pediatric Pathology 10, nr 3 (styczeń 1990): 311–17. http://dx.doi.org/10.3109/15513819009067120.

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4

Teba, Luis. "Polymerase chain reaction". Critical Care Medicine 27, nr 5 (maj 1999): 860–61. http://dx.doi.org/10.1097/00003246-199905000-00005.

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5

Schochetman, G., C. Y. Ou i W. K. Jones. "Polymerase Chain Reaction". Journal of Infectious Diseases 158, nr 6 (1.12.1988): 1154–57. http://dx.doi.org/10.1093/infdis/158.6.1154.

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6

Sheppard, Haynes W. (Chip). "Polymerase Chain Reaction". Infection Control and Hospital Epidemiology 12, nr 8 (sierpień 1991): 476–77. http://dx.doi.org/10.1086/646386.

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7

Morrison, Karen E. "Polymerase Chain Reaction". Practical Neurology 2, nr 5 (październik 2002): 288–93. http://dx.doi.org/10.1046/j.1474-7766.2002.00088.x.

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8

Chesters, John K. "Polymerase chain reaction". Proceedings of the Nutrition Society 55, nr 1B (marzec 1996): 599–604. http://dx.doi.org/10.1079/pns19960053.

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9

Green, Michael R., i Joseph Sambrook. "Polymerase Chain Reaction". Cold Spring Harbor Protocols 2019, nr 6 (czerwiec 2019): pdb.top095109. http://dx.doi.org/10.1101/pdb.top095109.

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10

Ling, Mark R. "Polymerase chain reaction". Journal of the American Academy of Dermatology 28, nr 2 (luty 1993): 279. http://dx.doi.org/10.1016/s0190-9622(08)81159-0.

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11

Williamson, R. "Polymerase chain reaction". Pathology 23 (1991): 17. http://dx.doi.org/10.1016/s0031-3025(16)36213-4.

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12

ARNHEIM, NORMAN, i COREY H. LEVENSON. "POLYMERASE CHAIN REACTION". Chemical & Engineering News 68, nr 40 (październik 1990): 36–47. http://dx.doi.org/10.1021/cen-v068n040.p036.

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13

York, David. "Polymerase Chain Reaction". Biochemical Education 18, nr 1 (styczeń 1990): 55. http://dx.doi.org/10.1016/0307-4412(90)90037-o.

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14

Bréchot, Christian. "Polymerase chain reaction". Journal of Hepatology 11, nr 1 (lipiec 1990): 124–29. http://dx.doi.org/10.1016/0168-8278(90)90282-v.

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15

Erlich, Henry A. "Polymerase chain reaction". Journal of Clinical Immunology 9, nr 6 (listopad 1989): 437–47. http://dx.doi.org/10.1007/bf00918012.

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16

Tyrrell, D. A. J. "Polymerase chain reaction". BMJ 314, nr 7073 (4.01.1997): 5. http://dx.doi.org/10.1136/bmj.314.7073.5.

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17

Garibyan, Lilit, i Nidhi Avashia. "Polymerase Chain Reaction". Journal of Investigative Dermatology 133, nr 3 (marzec 2013): 1–4. http://dx.doi.org/10.1038/jid.2013.1.

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18

Patil, PrakashV. "Polymerase chain reaction". Journal of Cytology 12, nr 1 (1995): 1. http://dx.doi.org/10.4103/0970-9371.237221.

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19

INABA, Hiroshi. "Polymerase chain reaction (PCR)." Blood & Vessel 20, nr 4 (1989): 365–67. http://dx.doi.org/10.2491/jjsth1970.20.365.

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20

Ochman, Howard, James W. Ajioka, Dan Garza i Daniel L. Hartl. "Inverse Polymerase Chain Reaction". Nature Biotechnology 8, nr 8 (sierpień 1990): 759–60. http://dx.doi.org/10.1038/nbt0890-759.

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21

Arnheim, Norman, i Henry Erlich. "Polymerase Chain Reaction Strategy". Annual Review of Biochemistry 61, nr 1 (czerwiec 1992): 131–56. http://dx.doi.org/10.1146/annurev.bi.61.070192.001023.

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22

Maltezos, George, Alvaro Gomez, Jiang Zhong, Frank A. Gomez i Axel Scherer. "Microfluidic polymerase chain reaction". Applied Physics Letters 93, nr 24 (15.12.2008): 243901. http://dx.doi.org/10.1063/1.3046789.

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23

Timmer, William C., i Juanita M. Villalobos. "The polymerase chain reaction". Journal of Chemical Education 70, nr 4 (kwiecień 1993): 273. http://dx.doi.org/10.1021/ed070p273.

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24

Archibald, Alan L. "The polymerase chain reaction". Livestock Production Science 48, nr 1 (kwiecień 1997): 79–80. http://dx.doi.org/10.1016/s0301-6226(97)89732-1.

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25

Huang, Sheng-He. "Inverse polymerase chain reaction". Molecular Biotechnology 2, nr 1 (sierpień 1994): 15–22. http://dx.doi.org/10.1007/bf02789286.

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26

Jester, Joy D. "The polymerase chain reaction". Clinics in Dermatology 9, nr 2 (kwiecień 1991): 137–41. http://dx.doi.org/10.1016/0738-081x(91)90004-5.

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27

O'Brien, John. "The polymerase chain reaction". Trends in Food Science & Technology 2 (styczeń 1991): 27. http://dx.doi.org/10.1016/0924-2244(91)90609-m.

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28

White, Thomas J., Norman Arnheim i Henry A. Erlich. "The polymerase chain reaction". Trends in Genetics 5 (1989): 185–89. http://dx.doi.org/10.1016/0168-9525(89)90073-5.

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29

Rollo, F., R. Salvi, A. Amici i A. Anconetani. "Polymerase chain reaction fingerprints". Nucleic Acids Research 15, nr 21 (1987): 9094. http://dx.doi.org/10.1093/nar/15.21.9094.

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30

Peake, I. "The polymerase chain reaction." Journal of Clinical Pathology 42, nr 7 (1.07.1989): 673–76. http://dx.doi.org/10.1136/jcp.42.7.673.

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31

Desforges, Jane F., i Barry I. Eisenstein. "The Polymerase Chain Reaction". New England Journal of Medicine 322, nr 3 (18.01.1990): 178–83. http://dx.doi.org/10.1056/nejm199001183220307.

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32

Bell, John. "The polymerase chain reaction". Immunology Today 10, nr 10 (październik 1989): 351–55. http://dx.doi.org/10.1016/0167-5699(89)90193-x.

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33

SNOW, JOHN L., KAREN SNOW i MARK R. PITTELKOW. "The Polymerase Chain Reaction". Journal of Dermatologic Surgery and Oncology 19, nr 9 (wrzesień 1993): 831–45. http://dx.doi.org/10.1111/j.1524-4725.1993.tb01016.x.

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34

Powledge, Tabitha M. "The polymerase chain reaction". Advances in Physiology Education 28, nr 2 (czerwiec 2004): 44–50. http://dx.doi.org/10.1152/advan.00002.2004.

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This essay on the polymerase chain reaction is one of a series developed as part of FASEB’S efforts to educate the general public, and the legislators whom it elects, about the benefits of fundamental biomedical research—particularly how investment in such research leads to scientific progress, improved health, and economic well-being. 1

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35

McNicol, P. "Polymerase Chain Reaction Text". Canadian Journal of Infectious Diseases 5, nr 6 (1994): 281. http://dx.doi.org/10.1155/1994/450873.

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36

Miller, James RC, i Ralph Andre. "Quantitative polymerase chain reaction". British Journal of Hospital Medicine 75, Sup12 (grudzień 2014): C188—C192. http://dx.doi.org/10.12968/hmed.2014.75.sup12.c188.

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37

Haas, David W. "The polymerase chain reaction". Infectious Diseases Newsletter 8, nr 5 (maj 1989): 36–39. http://dx.doi.org/10.1016/0278-2316(89)90031-5.

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38

Gibbs, Richard A. "Polymerase chain reaction techniques". Current Opinion in Biotechnology 2, nr 1 (luty 1991): 69–75. http://dx.doi.org/10.1016/0958-1669(91)90063-b.

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39

Hsu, James T., Simantini Das i Satish Mohapatra. "Polymerase chain reaction engineering". Biotechnology and Bioengineering 55, nr 2 (20.07.1997): 359–66. http://dx.doi.org/10.1002/(sici)1097-0290(19970720)55:2<359::aid-bit13>3.0.co;2-c.

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40

Coen, Donald M. "The Polymerase Chain Reaction". Current Protocols in Molecular Biology 73, nr 1 (styczeń 2006): 15.0.1–15.0.3. http://dx.doi.org/10.1002/0471142727.mb1500s73.

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41

DeMarchi, Jean M. "The polymerase chain reaction". Clinical Microbiology Newsletter 12, nr 11 (czerwiec 1990): 81–84. http://dx.doi.org/10.1016/0196-4399(90)90018-7.

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42

Sudarwanto, Mirnawati, Surachmi Setiyaningsih i Harsi Dewantari Kusumaningrum. "Isolation of Campylobacter from Poultry Carcasses using Conventional and Polymerase Chain Reaction Methods". Jurnal Teknologi dan Industri Pangan 24, nr 1 (czerwiec 2013): 27–32. http://dx.doi.org/10.6066/jtip.2013.24.1.27.

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43

Amalia, Ulfah, Ratih Dewanti-Hariyadi i Achmad Poernomo. "RAPID DETECTION OF Salmonella IN SHRIMP BY POLYMERASE CHAIN REACTION". Jurnal Teknologi dan Industri Pangan 25, nr 1 (czerwiec 2014): 78–82. http://dx.doi.org/10.6066/jtip.2014.25.1.78.

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44

Kalina, J., J. Mucksová, H. Yan i P. Trefil. " Rapid sexing of selected Galliformes by polymerase chain reaction". Czech Journal of Animal Science 57, No. 4 (27.04.2012): 187–92. http://dx.doi.org/10.17221/5894-cjas.

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Vent sexing of one-day-old chicks in commercial hatcheries has long been common practice and can be highly accurate. However, there are circumstances when this technique is not applicable such as smaller breeds, non-domestic birds, or where is the necessity of precise sexing. In this study we present a simple and reliable method for fast gender determination in selected Galliformes for which phenotypic determination of sex is difficult until maturity. Four species were tested: two commercial species – chicken (Gallus gallus) and turkey (Meleagris gallopavo), and two game birds – common pheasant (Phasianus colchicus) and wood grouse (Tetraro urogallus). DNA was tested with universal single-pair primers polymerase chain reaction (PCR) detecting W chromosome specific sequence yielding a single band of length specific for each species. The method was developed with regards to time consumption and cost-effectiveness giving results in less than two hours. The method may also be used for early sexing in commercial chicken and turkey flocks as well as sexing of smaller game birds flocks or for research laboratories when rapid sexing of selected Galliformes cells is required.  

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45

Kumari, S., K. Kundu J i J. Polák. "Identification of Xiphinema vuittenezi by polymerase chain reaction". Plant Protection Science 40, No. 1 (7.03.2010): 1–4. http://dx.doi.org/10.17221/3120-pps.

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So far, the identification of the nematode species <I>Xiphinema vuittenezi</I> relied mainly on time-consuming morphological and morphometrical studies. Therefore, a polymerase chain reaction (PCR) protocol was optimised that both reliably and rapidly identifies <I>X. vuittenezi</I>. The internal transcribed spacer (ITS) species-specific primer of ribosomal DNA gene of <I>X. vuittenezi </I>was used. Nine populations of this species from Central Bohemia were investigated by means of PCR.

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46

Mohsen, A. "Molecular detection of Brucella in milk using polymerase chain reaction". Czech Journal of Food Sciences 18, No. 3 (1.01.2000): 95–97. http://dx.doi.org/10.17221/8318-cjfs.

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Brucellosis is a highly contagious disease affecting a wide variety of farm animals. It is also an important zoonosis, and man is often infected following contact with infected animals or the consumption of contaminated milk and milk products. At present, mainly bacteriological and serological detection methods are used. A bacteriological method takes days to weeks to grow the organism besides its health hazard. Serological tests are faster but antigen–antibody interactions can be faulted by non-specific interactions. A method for direct detection of Brucella melitensis in 1 ml of milk was developed on the basis of enzymatic treatment of milk components and subsequent PCR and line probe assay (LPA). After PCR, 3 × 104 CFU/ml sensitivity was obtained by agarose gel electrophoresis and LPA. The safety and sensitivity of LPA combined with its speed suggests the potential of this technique for diagnosis of brucellosis in milk rather than the time consuming classical methods.

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47

Rud, Yu P. "POLYMERASE CHAIN REACTION FOR IDENTIFICATION OF CYPRINID HERPESVIRUSES IN UKRAINE". Biotechnologia Acta 11, nr 1 (luty 2018): 58–63. http://dx.doi.org/10.15407/biotech11.01.058.

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48

YAMADA, Akira, Jiro IMANISHI i Etsuro NAKAJIMA. "Detection of Influenza Virus with PCR (Polymerase Chain Reaction)". Journal of the Japanese Association for Infectious Diseases 65, nr 6 (1991): 759–60. http://dx.doi.org/10.11150/kansenshogakuzasshi1970.65.759.

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49

McInerney, Peter, Paul Adams i Masood Z. Hadi. "Error Rate Comparison during Polymerase Chain Reaction by DNA Polymerase". Molecular Biology International 2014 (17.08.2014): 1–8. http://dx.doi.org/10.1155/2014/287430.

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As larger-scale cloning projects become more prevalent, there is an increasing need for comparisons among high fidelity DNA polymerases used for PCR amplification. All polymerases marketed for PCR applications are tested for fidelity properties (i.e., error rate determination) by vendors, and numerous literature reports have addressed PCR enzyme fidelity. Nonetheless, it is often difficult to make direct comparisons among different enzymes due to numerous methodological and analytical differences from study to study. We have measured the error rates for 6 DNA polymerases commonly used in PCR applications, including 3 polymerases typically used for cloning applications requiring high fidelity. Error rate measurement values reported here were obtained by direct sequencing of cloned PCR products. The strategy employed here allows interrogation of error rate across a very large DNA sequence space, since 94 unique DNA targets were used as templates for PCR cloning. The six enzymes included in the study, Taq polymerase, AccuPrime-Taq High Fidelity, KOD Hot Start, cloned Pfu polymerase, Phusion Hot Start, and Pwo polymerase, we find the lowest error rates with Pfu, Phusion, and Pwo polymerases. Error rates are comparable for these 3 enzymes and are >10x lower than the error rate observed with Taq polymerase. Mutation spectra are reported, with the 3 high fidelity enzymes displaying broadly similar types of mutations. For these enzymes, transition mutations predominate, with little bias observed for type of transition.

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50

Gál, József, Róbert Schnell i Miklós Kálmán. "Polymerase Dependence of Autosticky Polymerase Chain Reaction". Analytical Biochemistry 282, nr 1 (czerwiec 2000): 156–58. http://dx.doi.org/10.1006/abio.2000.4593.

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