[1] Zhao L N,SQin Z,SWei P, et al. Elongation factor 1β gene from Spodoptera exigua: characterization and function identification through RNA interference[J]. Int J Mol Sci. 2012, 13(7):8126-41. [2] 晏琛,邵江华. 真核翻译延伸因子1A1在肿瘤发生和发展中作用的研究进展[J]. 肿瘤,2014,34(4):378-382. [3] Qi X L,SSu X F,SLu G Q,Set al. The effect of silencingSarginine kinaseSby RNAi on the larval development of Helicoverpa armigera[J]. Bull Entomol Res, S2015, 105(5):555-65. [4] Sahu S,SSamanta S,SHarish D R,S et al. Molecular cloning and characterization ofSarginine kinaseSgene of Toxocara canis[J]. J Parasit Dis, S2015, 39(2):211-5. [5] Hornáková D, Matousková P, Kindl J, et al. Selection of Reference genes for real-time polymerase chain reaction analysis in tissues from Bombus terrestris and Bombus lucorum of different ages[J]. Anal Biochem. 2010, 397(1):118-20. [6] Lu Y H, Yuan M, Gao X W, et al. Identification and validation of Reference genes for gene expression analysis using quantitative PCR in Spodoptera litura (Lepidoptera: Noctuidae) [J]. PLoS One, 2013, 8(7):e68059. [7] 岳秀利,高新菊,王进军,等. 二斑叶螨内参基因的筛选及解毒酶基因的表达水平[J]. 中国农业科学,2013, 46(21) : 4542-4549. [8] Yang Q P, Li Z, Cao J J, et al. Selection and Assessment of Reference Genes for Quantitative PCR Normalization in Migratory Locust Locusta migratoria (Orthoptera: Acrididae) [J]. Plos one, 2014, 9(6): e98164. [9] Yuan M, Lu Y H, Zhu X, et al. Selection and evaluation of potential Reference genes for gene expression analysis in the brown planthopper, Nilaparvata lugens (Hemiptera: Delphacidae) using reverse-transcription quantitative PCR[J]. PLoS One, 2014, 9(1):e86503. [10] Wang S,SWang Y,SSun X,Set al. Protective immunity against acute toxoplasmosis in BALB/c mice induced by a DNA vaccine encoding Toxoplasma gondiiSelongation factor 1-alpha[J]. BMC Infect Dis, 2015, 15:448. [11] Chen X,SYao P,SChu X,Set al. Isolation ofSarginine kinaseSfrom Apis cerana cerana and its possible involvement in response to adverse stress[J]. Cell Stress Chaperones,S2015, 20(1):169-83. [12] Fu W, Xie W, Zhang Z, et al. Exploring valid Reference genes for quantitative real-time PCR analysis in Plutella xylostella (Lepidoptera: Plutellidae) [J]. Int J Biol Sci, 2013, 9(8):792-802. [13] Chandra G S, Asokan R, Manamohan M, et al. Evaluation of Reference genes for quantitative real-time PCR normalization in cotton bollworm, Helicoverna armigera[J]. Mol Biol (Mosk), 2014, 48(6):927-38. [14] Zhu X, Yuan M, Shakeel M, et al. Selection and evaluation of Reference genes for expression analysis using qRT-PCR in the beet armyworm Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae) [J]. PLoS One, 2014, 9(1):e84730. [15] Bustin S, Benes V, Nolan T, et al. Quantitative real-time RT-PCR a perspective[J]. Journal of Molecular Endocrinology, 2005, 34: 597-601. [16] 王梨嬛,潘永娟,杨莉,等.‘琯溪蜜柚’荧光定量PCR 内参基因的筛选[J].果树学报,2013,30(1):48-54. [17] Pan H P, Yang X W, Siegfried B D, et al. A Comprehensive Selection of Reference Genes for RT-qPCR Analysis in a Predatory Lady Beetle, Hippodamia convergens (Coleoptera: Coccinellidae) [J]. Plos one, 2015, 10(4): e0125868. [18] Derveaux S, Vandesompele J, Hellemans J. How to do successful gene expression analysis using real-time PCR[J]. Methods, 2010, 50: 227-230. [19] Diego R, Jorge HU, Rosa MC, et al. Analysis of qPCR Reference gene stability determination methods and a practical approach for efficiency calculation on a turbot (Scophthalmus maximus) gonad dataset[J]. BMC Genomics, 2014, 15: 648. [20] 张云慧,张智,姜玉英,等. 2012年三代粘虫大发生原因初步分析[J].植物保护,2012, 38(5):1-8. [21] 江幸福,张蕾,程云霞,等.我国粘虫研究现状及发展趋势[J].应用昆虫学报,2014,51(4): 881-889. [22] 李柯,阴环,奚耕思,等.粘虫β-actin基因cDNA的克隆、序列分析及表达量检测[J].昆虫知识,2010,47(6): 1089-1094.
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