基因工程学术论文范文参考文献

［3］ 赵艳,于彦春,钱前,等.无载体主干序列的bar和cecropin B基因表达框共转化水稻［J］. 遗传学报,2003,30（2）:135-141. ［4］ 安韩冰,朱祯,李慧芬,等.基因枪法转化水稻（Oryza sativa L.）获得可育的转抗虫基因水稻再生植株［J］. 高技术通讯,2001,2:12-17. ［5］ CHU Qi-ren, CAO Hua-xin, FAN Hui-qin, et al.. Preliminary report on transienexpression of gus gene in transgene rice protoplast-derived calli via PEG-mediated DNA transformation［J］. shanghai nongye xue bao,1995,11(3):63-68. ［6］ 赵凌,王才林,宗寿余,等. 花粉管介导的转bar基因水稻植株的获得及其遗传［J］. 中国生物工程杂志,2003,23（8）:92-95. ［7］ LI L C, QU R D, KOCHKO A,et al.. An improved transformation of embryogenic grape cell suspensions［J］. Plant Cell Report,1993,12:250-255. ［8］ 范钦,许新萍,黄小乐,等. 早籼稻培矮64S愈伤组织形成及植株再生［J］. 西北植物学报,2002,22（6）:1 469-1 473. ［9］ 易自力,曹守云,王力,等. 提高农杆菌转化水稻频率的研究［J］. 遗传学报,2001,28（4）:352-358. ［10］ 郑宏红,何锶洁,戴顺洪,等. 提高水稻基因枪转化效率的研究［J］. 生物工程学报,1996,（增）:111-115. ［11］ 田文忠,IAN RANCE,ELUNIALAI,等. 提高籼稻愈伤组织再生频率的研究［J］. 遗传学报,1994,21（3）:215-221. ［12］ 叶松青,储成才,曹守云,等. 提高水稻转化率几个因素的研究［J］. 遗传学报,2001,28（10）:933-938. ［13］ 刁现民,陈振玲,段胜军,等. 影响谷子愈伤组织基因枪转化的因素［J］. 华北农学报,1999,14（3）:31-36. ［14］ 易自力,王力,曹守云,等. 提高籼稻基因枪转化频率的研究［J］. 高技术通讯,2000,10(11):12-15. ［15］ 薛锐,曹守云,杨炜,等. 基因枪法转化籼稻有关因素的评价［J］. 中国水稻科学,1998,12（1）:21-26. ［16］ LI L C, TIAN W Z, YANG M, et al.. Establishment of an efficient transformation system for rice(Oryza Sativa L.) ［A］.农业的未来-转基因技术研究［C］. 长沙,湖南科学技术出版社,2002. ［17］ 马炳田,朱祯,李平,等. 水稻遗传转化选择系统优化初探［J］. 西南农业学报,2003,16（1）:28-31. ［18］ 唐祚舜,王象坤,李良才,等. 基因枪法转基因水稻中HPT基因稳定遗传［J］. 遗传学报,2000,27（1）:26-33. ［19］ 陶利珍,凌定厚,张世平,等. 基因枪介导的籼稻遗传转化及外源基因在受体中的遗传研究［J］. 武汉植物学研究,1999,17（4）:289-296. ［20］ CHENG Zai-quan,HUANG Xing-qi,RAY Wu,et al..Comparison of biolistic and agrobacterium-mediated transformation methods on transgene copy number and rearrangement frequency in rice［J］. Acta Botanica Sinica, 2001,43(8):826-833.

生物基因工程论文参考文献汇总 生物基因工程论文参考文献怎么写?有哪些格式要求，下面我就为大家推荐一些优秀的范例，希望大家喜欢![1] Brackett B G, Baranska W, Sawicki W，et al. Uptake of heterologous genome by mammalianspermatozoa and its transfer to ova through fertilization. Proc Natl Acad Sci USA,1971,68(2):353-357. [2] Jaenisch R, Mintz B. Simian virus 40 DNA sequences in DNA of healthy adult mice derived frompreimp antation blastocysts injected with viral DNA. Proc Natl Acad Sci USA, 1974,71 (4): 1250-1254. [3] Palmiter R D, Brinster R L, Hammer R E, et al. Dramatic growth of mice that develop from eggsmicroinjected with metallothionein-growth hormone fusion genes. Nature, 1982,300(5893):611-615. [4] 李宁.动物克隆与基因组编辑.中国农业大学出版社，2012. [5] Hammer R E, Pursel V G, Rexroad C J, et al. Production of transgenic rabbits, sheep and pigs bymicroinjection. Nature, 1985,315(6021):680-683 [6] 杜伟，崔海信，王 琰 ，等.精子载体法制备转基因动物的'研究进展.生物技术通报，2012(12):13-18. [7] Maione B，Lavitrano M, Spadafora C, et al. Sperm-mediated gene transfer in mice. Mol ReprodDev, 1998,50(4):406-409. [8] Lavitrano M, Bacci M L, Forni M, et al. Efficient production by sperm-mediated gene transfer ofhuman decay accelerating factor (hDAF) transgenic pigs for xenotransplantation. Proc Matl Acad SciUSA, 2002,99(22):14230-14235. [9] Sperandio S, Lulli V，Bacci M L, et al. Sperm - mediated DNA transfer in bovine and swinespecies. Animal biotechnology, 1996,7(1):59-77. [10] 武坚，刘明军，李文蓉，等.精子载体介导法生产转基因绵羊的研究.草食家畜，2001(S2):186-190. [11] Pfeifer A, Kessler T, Yang M, et al. Transduction of liver cells by lentiviral vectors: analysis inliving animals by fluorescence imaging. Mol Ther，2001,3(3):319-322. [12] Lois C, Hong E J, Pease S, et al. Germline transmission and tissue-specific expression oftransgenes delivered by lentiviral vectors. Science, 2002,295(5556):868-872. [13] Hofmann A, Kessler B, Ewerling S，et al. Efficient transgenesis in farm animals by lentiviralvectors. EMBO Rep, 2003,4( 11): 1054-1060. [14] Hofmann A, Zakhartchenko V, Weppert M, et al. Generation of transgenic cattle by lentiviral genetransfer into oocytes’ Biol Reprod, 2004,71 (2):405-409 [15] Lillico S G, Sherman A, McGrew M J，et al. Oviduct-specific expression of two therapeuticproteins in transgenic hens. Proc Natl Acad Sci USA，2007,104(6): 1771-1776. [16] Lyall J，Irvine R M, Sherman A, et al. Suppression of avian influenza transmission in geneticallymodified chickens. Science，2011,331(6014):223-226. [17] Golding M C, Long C R，Carmell M A, et al. Suppression of prion protein in livestock by RNAinterference. Proc Natl Acad Sci USA, 2006,103(14):5285-5290. [18] 杨春荣，窦忠英.利用干细胞生产转基因动物研究进展.西北农林科技大学学报(自然科学版)，2006(07):37-40. [19] Hai T, Teng F，Guo R, et al. One-step generation of knockout pigs by zygote injection ofCRISPR/Cas system. Cell Res, 2014,24(3):372-375. [20] Hongbing H, Yonghe M A, Tao W, et al. One-step generation of myostatin gene knockout sheepvia the CRISPR/Cas9 system. Frontiers of Agricultural Science and Engineering, 2014,1(1):2-5. [21] Swanson M E，Martin M J, O'Donnell J K, et al. Production of functional human hemoglobin intransgenic swine. Biotechnology (N Y)，1992,10(5):557-559. [22] Zbikowska H M，Soukhareva N, Behnam R, et al. Uromodulin promoter directs high-levelexpression of biologically active human alpha 1-antitrypsin into mouse urine. Biochem J, 2002,365(Pt1):7-11. [23] Golovan S P，Hayes M A, Phillips J P，et al. Transgenic mice expressing bacterial phytase as amodel for phosphorus pollution control. Nat Biotechnol, 2001,19(5):429-433. [24] Rapp J C, Harvey A J, Speksnijder G L, et al. Biologically active human interferon alpha-2bproduced in the egg white of transgenic hens. Transgenic Res, 2003,12(5):569-575. [25] Wright G, Carver A, Cottom D, et al. High level expression of active human alpha-1 -antitrypsin inthe milk of transgenic sheep. Biotechnology (N Y), 1991,9(9):830-834. [26] Li S, Ip D T, Lin H Q, et al. High-level expression of functional recombinant humanbutyrylcholinesterase in silkworm larvae by Bac-to-Bac system. Chem Biol Interact,2010,187(1-3):101-105. [27] 刘英，张瑞君，伍志伟，等.转基因疾病动物模型的研究进展.动物医学进展，2006(12):44-49. [28] Kragh P M, Nielsen A L, Li J, et al. Hemizygous minipigs produced by random gene insertion andhandmade cloning express the Alzheimer's disease-causing dominant mutation APPsw. Transgenic Res,2009,18(4):545-558. [29] Lee M K, Stirling W, Xu Y, et al. Human alpha-synuclein-harboring familial Parkinson'sdisease-linked Ala-53 Thr mutation causes neurodegenerative disease with alpha-synucleinaggregation in transgenic mice. Proc Natl Acad Sci USA, 2002,99(13):8968-8973. ;