Biology Reference
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Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.M. Seldman, J.G. and Smith, J.A. Eds., (1991).
Current Protocols in Molecular Biology , Greene Publishing, New York.
Ayliffe, M.A., Lawrence, G.J., Ellis, J.G., and Pryor, A.J., (1994). Heteroduplex molecules formed
between allelic sequences cause nonparental RAPD bands. Nucleic Acids Res. 22 : 1632-1636.
Ayyadevara, S., Thaden, J.J., and Shmookler Reis, R.J., (2000). Discrimination of primer
3 -nucleotide mismatch by Taq DNA polymerase during polymerase chain reaction. Analyt.
Biochem. 284 : 11-18.
Azad, A.F., Webb, L., Carl, M., and Dasch, G.A., (1990). Detection of rickettsiae in arthropod vectors
by DNA amplification using the polymerase chain reaction, pp. 557-563. In: Rickettsiology:
Current Issues and Perspectives , Volume 590 . Annals of the New York Academy of Sciences,
The New York Academy of Sciences, New York.
Baker, M., (2011). qPCR: quicker and easier but don't be sloppy. Nat. Methods 8 : 207-212.
Baldrich, E., Xamena, N., and Cabre, O., (1999). Overcoming false negatives due to the genomic
context in polymerase chain reaction amplification. J. Biochem. Biophys. Methods 40 : 45-48.
Barker Jr., R.H., (1994). Use of PCR in the field. Parasitol. Today 10 : 117-119.
Barnes, W.M., (1994). PCR amplification of up to 35-kb DNA with high fidelity and high yield from
λ bacteriophage templates. Proc. Natl. Acad. Sci. USA 91 : 2216-2220.
Beckenbach, A.T., (1995). Age of bacteria from amber. Science 270 : 2015-2016.
Bennett, B.L., and Molenaar, A.J., (1994). Cloning of PCR products can be inhibited by Taq
polymerase carryover. BioTechniques 16 : 32-33.
Brass, N., Heckel, D., and Meese, E., (1998). Comparative PCR: An improved method to detect gene
amplification. BioTechniques 24 : 22-26.
Brooke, B.D., Hunt, R.H., Koekemoer, L.L., Dossou-Yovo, J., and Coetzee, M., (1999). Evaluation of a
polymerase chain reaction assay for detection of pyrethroid insecticide resistance in the malaria
vector species of the Anopheles gambiae complex. J. Am. Mosq. Control Assoc. 15 : 565-568.
Brownie, J., Shawcross, S., Theaker, J., Whitcombe, D., Ferrie, R., and Newton, C., et al. (1997). The
elimination of primer-dimer accumulation in PCR. Nucleic Acids Res. 25 : 3235-3241.
Burt, A., Carter, D.A., White, T.J., and Taylor, J.W., (1994). DNA sequencing with arbitrary primer
pairs. Mol. Ecol. 3 : 523-535.
Bustin, S.A., (2004). A-Z of Quantitative PCR (IUL Biotechnology, No. 5) . International University
Line, La Jolla, CA.
Bustin, S.A., Benes, V., Garson, J.A., Hellemans, J., Huggett, J., and Kubista, M., et al. (2009).
The MIQE Guidelines: M inimum I nformation for publication of Q uantitative real-time PCR
E xperiments. Clin. Chem. 55 : 611-622.
Cano, R.J., and Borucki, M.K., (1995). Revival and identification of bacterial spores in 25- to
40-million-year-old Dominican amber. Science 268 : 1060-1063.
Cano, R.J., Poinar, H.N., Pieniazek, N.J., Acra, A., and Poinar, G.O., (1993a). Amplification and
sequencing of DNA from a 120-135-million-year-old weevil. Nature 363 : 536-538.
Cano, R.J., Poinar, H.N., Roubik, D.W., and Poinar, G.O., (1993b). Enzymatic amplification and
nucleotide sequencing of portions of the 18s rRNA gene of the bee Proplebeia dominicana
(Apidae: Hymenoptera) isolated from 25-40 million year old Dominican amber. Med. Sci. Res.
20 : 619-622.
Carbonari, M., Sbarigia, D., Cibati, M., and Fiorilli, M., (1993). Optimization of PCR performance.
Trends Genet. 9 : 42-43.
Chan, C.K., Petersen, D.J., and Vrain, T.C., (1999). DNA fingerprinting of single aphid embryos by
random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR). Can. Entomol.
131 : 229-230.
Chehab, F.F., and Kan, Y.W., (1989). Detection of specific DNA sequences by fluorescence
amplification: a color complementation assay. Proc. Natl. Acad. Sci. USA 86 : 9178-9182.
Cheng, S., (1995). Longer PCR amplifications. In: Innis, M.A., Gelfand, D.H., and Sninsky, J.J., Eds.,
PCR Strategies , Academic Press, San Diego, CA, pp. 313-324.
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