Publications

Found 12 results
Filters: Author is J. Luo  [Clear All Filters]
2016
X. H. Zhang, Liu, H. Q., Guo, Q. W., Zheng, C. F., Li, C. S., Xiang, X. M., Zhao, D. F., Liu, J., Luo, J., Zhao, D. K., Zheng, J. Q., Wan, H. J., Zhang, X. H., Liu, H. Q., Guo, Q. W., Zheng, C. F., Li, C. S., Xiang, X. M., Zhao, D. F., Liu, J., Luo, J., Zhao, D. K., Zheng, J. Q., and Wan, H. J., Genome-wide identification, phylogenetic relationships, and expression analysis of the carotenoid cleavage oxygenase gene family in pepper, vol. 15, p. -, 2016.
X. H. Zhang, Liu, H. Q., Guo, Q. W., Zheng, C. F., Li, C. S., Xiang, X. M., Zhao, D. F., Liu, J., Luo, J., Zhao, D. K., Zheng, J. Q., Wan, H. J., Zhang, X. H., Liu, H. Q., Guo, Q. W., Zheng, C. F., Li, C. S., Xiang, X. M., Zhao, D. F., Liu, J., Luo, J., Zhao, D. K., Zheng, J. Q., and Wan, H. J., Genome-wide identification, phylogenetic relationships, and expression analysis of the carotenoid cleavage oxygenase gene family in pepper, vol. 15, p. -, 2016.
Y. Cheng, Yao, Z. P., Ruan, M. Y., Ye, Q. J., Wang, R. Q., Zhou, G. Z., Luo, J., Li, Z. M., Yang, Y. J., Wan, H. J., Cheng, Y., Yao, Z. P., Ruan, M. Y., Ye, Q. J., Wang, R. Q., Zhou, G. Z., Luo, J., Li, Z. M., Yang, Y. J., and Wan, H. J., In silico identification and characterization of the WRKY gene superfamily in pepper (Capsicum annuum L.), vol. 15, p. -, 2016.
Y. Cheng, Yao, Z. P., Ruan, M. Y., Ye, Q. J., Wang, R. Q., Zhou, G. Z., Luo, J., Li, Z. M., Yang, Y. J., Wan, H. J., Cheng, Y., Yao, Z. P., Ruan, M. Y., Ye, Q. J., Wang, R. Q., Zhou, G. Z., Luo, J., Li, Z. M., Yang, Y. J., and Wan, H. J., In silico identification and characterization of the WRKY gene superfamily in pepper (Capsicum annuum L.), vol. 15, p. -, 2016.
2013
X. Z. Qi, Yin, S. W., Luo, J., and Huo, R., Complete mitochondrial genome sequence of the humphead wrasse, Cheilinus undulatus, vol. 12, pp. 1095-1105, 2013.
Boore JL (1999). Animal mitochondrial genomes. Nucleic Acids Res. 27: 1767-1780. http://dx.doi.org/10.1093/nar/27.8.1767 PMid:10101183 PMCid:148383   Bourlat SJ, Rota-Stabelli O, Lanfear R and Telford MJ (2009). The mitochondrial genome structure of Xenoturbella bocki (phylum Xenoturbellida) is ancestral within the deuterostomes. BMC Evol. Biol. 9: 107. http://dx.doi.org/10.1186/1471-2148-9-107 PMid:19450249 PMCid:2697986   Cao J, Liu WD, Ge LL, Gao XG, et al. (2007). Structure of mtDNA control region in variegate flounder verasper variegate. Fish. Sci. 26: 678-681.   Craig MT, Pondella DJ, Franck JP and Hafner JC (2001). On the status of the Serranid fish genus Epinephelus: evidence for paraphyly based upon 16S rDNA sequence. Mol. Phylogenet. Evol. 19: 121-130. http://dx.doi.org/10.1006/mpev.2000.0913 PMid:11286497   Ding S, Zhuang X, Guo F, Wang J, et al. (2006). Molecular phylogenetic relationships of China Seas groupers based on cytochrome b gene fragment sequences. Sci. China C Life Sci. 49: 235-242. http://dx.doi.org/10.1007/s11427-006-0235-y PMid:16856492   Hou WR, Chen Y, Wu X, Hu JC, et al. (2007). A complete mitochondrial genome sequence of Asian black bear Sichuan subspecies (Ursus thibetanus mupinensis). Int. J. Biol. Sci. 3: 85-90. http://dx.doi.org/10.7150/ijbs.3.85 PMCid:1752227   Maggio T, Andaloro F, Hemida F and Arculeo M (2005). A molecular analysis of some Eastern Atlantic grouper from the Epinephelus and Mycteroperca genus. J. Exp. Mar. Biol. Ecol. 321: 83-92. http://dx.doi.org/10.1016/j.jembe.2005.01.004   Miya MM and Nishida (2000). Use of mitogenomic information in teleostean molecular phylogenetics: a tree-based exploration under the maximumparsimony optimality criterion. Mol. Phylogenet. Evol. 17: 437-455. http://dx.doi.org/10.1006/mpev.2000.0839 PMid:11133198   Ojala D, Montoya J and Attardi G (1981). tRNA punctuation model of RNA processing in human mitochondria. Nature 290: 470-474. http://dx.doi.org/10.1038/290470a0 PMid:7219536   Pereira SL (2000). Mitochondrial genome organization and vertebrate phylogenetics. Genet. Mol. Biol. 23: 745-752. http://dx.doi.org/10.1590/S1415-47572000000400008   Sadovy YJ (2002). The Humphead Wrasse - A Threatened Reef Fish. SPC Live Reef Fish Information Bulletin #10.   Sadovy YJ and Vincent ACJ (2002). Ecological Issues and the Trades in Live Reef Fishes. In: Coral Reef Fishes Dynamics and Diversity in a Complex Ecosystem (Sale PP, ed.). Academic Press, San Diego, 391-420. http://dx.doi.org/10.1016/B978-012615185-5/50023-2   Sadovy YJ, Kulbicki M, Labrose P, Letourneur Y, et al. (2003). Humphead wrasse, Cheilinus undulatus: synopsis of a threatened and poorly known giant coral reef fish. Rev. Fish Biol. Fish. 13: 327-364. http://dx.doi.org/10.1023/B:RFBF.0000033122.90679.97   Sbisa E, Tanzariello F, Reyes A, Pesole G, et al. (1997). Mammalian mitochondrial D-loop region structural analysis: identification of new conserved sequences and their functional and evolutionary implications. Gene 205: 125-140. http://dx.doi.org/10.1016/S0378-1119(97)00404-6   Shadel GS and Clayton DA (1997). Mitochondrial DNA maintenance in vertebrates. Annu. Rev. Biochem. 66: 409-435. http://dx.doi.org/10.1146/annurev.biochem.66.1.409 PMid:9242913   Sheffield NC, Song H, Cameron SL and Whiting MF (2008). A comparative analysis of mitochondrial genomes in Coleoptera (Arthropoda: Insecta) and genome descriptions of six new beetles. Mol. Biol. Evol. 25: 2499-2509. http://dx.doi.org/10.1093/molbev/msn198 PMid:18779259 PMCid:2568038   Tamura K, Dudley J, Nei M and Kumar S (2007). MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol. Biol. Evol. 24: 1596-1599. http://dx.doi.org/10.1093/molbev/msm092 PMid:17488738   Tan W, Guo YS, Wang ZD and Liu CW (2010). Structure of the mitochondrial DNA control region of snapper species and their phylogenetic relationship. Acta Oceanol. Sin. 32: 139-145.   Tang QY, Liu HZ, Yang XP and Xiong BX (2009). Studies on the structure of the mitochondrial DNA control region and phylogenetic relationships of the subfamily Botiinae. Acta Hydrobiol. Sin. 29: 645-653.   Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, et al. (1997). The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 25: 4876-4882. http://dx.doi.org/10.1093/nar/25.24.4876 PMid:9396791 PMCid:147148
H. L. Zheng, Liu, X. M., Yu, Q., Xing, R. F., Yang, Z. Y., and Luo, J., Construction of recombinant adenoviruses carrying the optimal shRNA template against goat PTHrP and successful suppression of PTHrP expression in mammary epithelial cells, vol. 12, pp. 3363-3374, 2013.
J. Hu, Zhu, X. P., Luo, J., Yin, S. W., Peng, Y. H., Hu, Y. L., and Zhu, F., Development and characterization of microsatellite loci in a threatened marine fish, Cheilinus undulatus (humphead wrasse), vol. 12, pp. 2633-2636, 2013.
J. Luo, Zhu, X. P., Peng, Y. H., and Yin, S. W., Isolation and characterization of 16 microsatellite loci in marble goby (Oxyeleotris marmoratus), vol. 12, pp. 2020-2023, 2013.
2012
L. Shi, Fan, J. Q., Hu, C. G., Luo, J., and Yao, J. L., Improved production of transgenic Dioscorea zingiberensis (Dioscoreaceae) by Agrobacterium tumefaciens-mediated transformation, vol. 11, pp. 244-253, 2012.
Catlin DW (1990). The effect of antibiotics on the inhibition of callus induction and regeneration from cotyledons of sugarbeet. Plant Cell Rep. 9: 285-288. http://dx.doi.org/10.1007/BF00232303 Chen Y, Fan J, Yi F, Luo Z, et al. (2003). Rapid clonal propagation of Dioscorea zingiberensis. Plant Cell Tissue Org. Cult. 73: 75-80. Cheng M, Fry JE, Pang S, Zhou H, et al. (1997). Genetic transformation of wheat mediated by Agrobacterium tumefaciens. Plant Physiol. 115: 971-980. PMid:12223854    PMCid:158560 Cheng M, Lowe B, Spencer T, Ye X, et al. (2004). Factors influencing Agrobacterium-mediated transformation of monocotyledonous species. In Vitro Cell Dev. Biol. Plant. 40: 31-45. http://dx.doi.org/10.1079/IVP2003501 Dutt M and Grosser JW (2009). Evaluation of parameters affecting Agrobacterium-mediated transformation of citrus. Plant Cell Tissue Org. Cult. 98: 331-340. Hiei Y, Ohta S, Komari T and Kumashiro T (1994). Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 6: 271-282. http://dx.doi.org/10.1046/j.1365-313X.1994.6020271.x PMid:7920717 Jia K, Yuan X and Su Y (2004). Problems ought to be focused on in the breeding of Dioscorea zingiberensis. J. Hubei Agric. Sci. 50: 83-84. Kim KH, Lee YH, Kim D, Park YH, et al. (2004). Agrobacterium-mediated genetic transformation of Perilla frutescens. Plant Cell Rep. 23: 386-390. http://dx.doi.org/10.1007/s00299-004-0825-8 PMid:15368075 Lee YH, Lee SB, Suh SC and Byun MO (2000). Herbicide-resistant cabbage (Brassica oleracea ssp capitata) plants by Agrobacterium-mediated transformation. J. Plant Biol. 2: 35-41. Liu J and Liu XM (2005). Genetic transformation mediated by Ri T-DNA and the accumulation of diosgenin of Dioscrea zigiberensis C.H.Wright. Nat. Prod. Res. 17: 59-64. Mo Y, Lan LQ, Qin RW and Deng Y (2004). Study on the germination terms of seeds of Dioscorea zingiberensis and its explant callus culture. J. Sichuan Univ. 41: 837-841. Murashige T and Skoog F (1962). A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol. Plant 15: 473-497. http://dx.doi.org/10.1111/j.1399-3054.1962.tb08052.x Qin TC, Zhang YD and Zhang JZ (1996). The present situation and exploitation of Dioscorea zingiberensis in Hubei province. Natl. Res. 3: 58-61. Stachel SE, Messens E, Montagu MV and Zambryski P (1985). Identification of the signal molecules produced by wounded plant cells which activate the T-DNA transfer in Agrobacterium tumefaciens. Nature 318: 624-629. http://dx.doi.org/10.1038/318624a0 Yan LX, Hu CG and Yao JL (2007). Haploid callus and plantlets regenerated from anther culture of Dioscorea zingiberensis (Dioscoreaceae). Acta Bot. Yunnanica 29: 33-37. Yan YC, Lin HH, Dai QL and Huang QQ (2002). Studies on tissue culture and rapid propagation of Dioscorea zingiberensis. J. Sichuan Univ. 39: 136-140. Yu C, Huang S, Chen C, Deng Z, et al. (2002). Factors affecting Agrobacterium-mediated transformation and regeneration of sweet orange and citrange. Plant Cell Tissue Org. Cult. 71: 147-155. Yuan S, Yan YC and Lin HH (2005). Plant regeneration through somatic embryogenesis from callus cultures of Dioscorea zingiberensis. Plant Cell Tissue Org. Cult. 80: 157-161. Zhu Q, Wu F, Ding F, Ye D, et al. (2009). Agrobacterium-mediated transformation of Dioscorea zingiberensis Wright, an important pharmaceutical crop. Plant Cell Tissue Org. Cult. 96: 317-324.