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Zhang, C. J.,Lim, S. H.,Kim, J. W.,Song, J. S.,Yook, M. J.,Nah, G.,Valverde, B. E.,Kim, D. S. Canadian Science Publishing 2015 Canadian journal of plant science. Revue canadienn Vol.95 No.6
<P> Zhang, C. J., Lim, S. H., Kim, J. W., Song, J. S., Yook, M. J., Nah, G., Valverde, N. E. and Kim, D. S. 2015. Quantifying herbicide dose-response and resistance in Echinochloa spp. by measuring root length in growth pouches. Can. J. Plant Sci. 95: 1181-1192. The aim of the presented study was to develop a bioassay for rapid diagnosis of herbicide dose-response and resistance in Echinochloa. Pre-germinated seeds of Echinochloa spp. were incubated in growth pouches (18 cm×16.5 cm) containing herbicide solutions in a range of concentrations. Shoot and root lengths were measured after 6 d of incubation. Dose-responses estimated by measuring root lengths in the growth pouches were well-described by the log-logistic dose-response model and similar to those estimated by a whole-plant assay. Accurate dose-response curves were successfully generated for several herbicides with different modes of action, suggesting that the growth pouch method can be used for herbicide bioassays. The suitability of the growth pouch method for rapid diagnosis of acetyl coenzyme-A carboxylase (ACCase) and acetolactate synthase (ALS) inhibitor resistance in Echinochloa spp. was also tested. For cyhalofop-butyl, resistant and susceptible biotypes were discriminated at 180-300 mg a.i. L<SUP>−1</SUP> and 80-120 mg a.i. L<SUP>−1</SUP> for barnyardgrass (E. crus-galli) and late watergrass (E. oryzicola), respectively. For penoxsulam, the discriminatory dosage was 350-500 mg a.i. L<SUP>−1</SUP> for barnyardgrass and 650-1000 mg a.i. L<SUP>−1</SUP> for late watergrass. The method was further used to identify late watergrass biotypes resistant and susceptible to two other ALS inhibitors, azimsulfuron and bispyribac-sodium. Our results show that the growth pouch method can be reliably used in herbicide dose-response studies and to diagnose herbicide resistance in Echinochloa spp., with significant time and cost savings compared with conventional whole-plant assays. </P>
Radio-frequency characteristics of graphene monolayer via nitric acid doping
Lee, H.J.,Kim, E.,Park, J.,Song, W.,An, K.S.,Kim, Y.S.,Yook, J.G.,Jung, J. Pergamon Press ; Elsevier Science Ltd 2014 Carbon Vol.78 No.-
The radio-frequency, i.e. 0.5-40GHz, characteristics of chemical vapor deposition-grown graphene monolayer via HNO<SUB>3</SUB> doping is experimentally investigated. According to the obtained results, the sheet resistance of HNO<SUB>3</SUB>-treated graphene decreases about half compared to bare graphene. In the case of radio-frequency characteristics, the transmission coefficient and effective conductivity of the HNO<SUB>3</SUB>-treated graphene are more enhanced than those of the bare graphene. Moreover, the intrinsic resistance and inductance of the HNO<SUB>3</SUB>-treated graphene itself show diminishing tendency with frequency increase. As a result, it is verified that the direct current as well as high frequency characteristics of graphene are improved by using the chemical doping method.
Lee, S.J.,Yook, S.,Yhee, J.Y.,Yoon, H.Y.,Kim, M.G.,Ku, S.H.,Kim, S.H.,Park, J.H.,Jeong, J.H.,Kwon, I.C.,Lee, S.,Lee, H.,Kim, K. Elsevier Science Publishers 2015 Journal of controlled release Vol.220 No.2
Cancer is a multifactorial disease which involves complex genetic mutation and dysregulation. Combinatorial RNAi technology and concurrent multiple gene silencing are expected to provide advanced strategies for effective cancer therapy, but a safe and effective carrier system is a prerequisite to successful siRNA delivery in vivo. We previously developed an effective tumor-targeting siRNA delivery system for in vivo application. In response to the success of this development, herein we present a dual-gene targeted siRNA and its delivery system, to achieve synergistic effects in cancer therapy. Two different sequences of siRNA were chemically modified to be randomly copolymerized in a single backbone of siRNA polymer (Dual-poly-siRNA), and the resulting Dual-poly-siRNA was incorporated into tumor-homing glycol chitosan nanoparticles. Based on the stability in serum and delivery in a tumor-targeted manner, intravenously administered Dual-poly-siRNA carrying glycol chitosan nanoparticles (Dual-NP) demonstrated successful dual-gene silencing in tumors. Notably, co-delivery of VEGF and Bcl-2 targeting siRNA led to more effective cancer therapy for convenient application.