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  1. MAGIC, an in vivo genetic method for the rapid construction of recombinant DNA molecules: Nature Genetics, Vol. 37, No. 3. (30 January 2005), pp. 311-319.

    Source: Nature Genetics, Vol. 37, No. 3. (30 January 2005), pp. 311-319.

  2. PCR-suppressio n effect: Kinetic analysis and application to representative or long-molecule biased PCR-based amplification of complex samples: Journal of Biotechnology, Vol. In Press, Corrected ProofIn the present study, we analyzed the kinetics of the PCR-suppressio n effect (PS-effect) and firstly demonstrate that lower annealing temperature enhances PS-effect. Furthermore, we controlled the average size of complex PCR products over a wide range, and simultaneously amplified targets from 0.25 to 10 kb by regulating the degree of suppression in a single-primer PCR. In addition, we describe an improved template-switc hing full-length cDNA synthesis method that greatly reduces truncated cDNA. This study provides a general guide for the design of PS-effect related PCR and is useful for representative or long-transcrip t enriched cDNA library construction, especially when only a small amount of total RNA is available.

    Source: Journal of Biotechnology, Vol. In Press, Corrected Proof

  3. Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC: Nature Methods, Vol. 4, No. 3. (11 February 2007), pp. 251-256.

    Source: Nature Methods, Vol. 4, No. 3. (11 February 2007), pp. 251-256.

  4. Generation and Characterizati on of SCARs by Cloning and Sequencing of RAPD Products: A Strategy for Species-specif ic Marker Development in Bamboo: Annals of Botany, Vol. 95, No. 5. (16 April 2005), pp. 835-841.

    Source: Annals of Botany, Vol. 95, No. 5. (16 April 2005), pp. 835-841.

  5. Structure of a cannabinoid receptor and functional expression of the cloned cDNA.: Nature, Vol. 346, No. 6284. (9 August 1990), pp. 561-564.Mariju ana and many of its constituent cannabinoids influence the central nervous system (CNS) in a complex and dose-dependent manner. Although CNS depression and analgesia are well documented effects of the cannabinoids, the mechanisms responsible for these and other cannabinoid-in duced effects are not so far known. The hydrophobic nature of these substances has suggested that cannabinoids resemble anaesthetic agents in their action, that is, they nonspecificall y disrupt cellular membranes. Recent evidence, however, has supported a mechanism involving a G protein-couple d receptor found in brain and neural cell lines, and which inhibits adenylate cyclase activity in a dose-dependent , stereoselectiv e and pertussis toxin-sensitiv e manner. Also, the receptor is more responsive to psychoactive cannabinoids than to non-psychoacti ve cannabinoids. Here we report the cloning and expression of a complementary DNA that encodes a G protein-couple d receptor with all of these properties. Its messenger RNA is found in cell lines and regions of the brain that have cannabinoid receptors. These findings suggest that this protein is involved in cannabinoid-in duced CNS effects (including alterations in mood and cognition) experienced by users of marijuana.

    Source: Nature, Vol. 346, No. 6284. (9 August 1990), pp. 561-564.

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