[1]林俊城,吴秋云,高灿红,等. 青花菜硫、硒代谢竞争及其对保健功能的影响研究进展[J]. 中国细胞生物学学报,2011,33(4):422-432.
[2]解鸿蕾,车文静,苏越, 等. 十字花科蔬菜的抗癌作用[J]. 食品安全导刊,2022(34):172-175.
[3]李占省,戚如诗,刘玉梅,等. 我国青花菜生产布局、价格变化及趋势[J]. 长江蔬菜,2021(4):1-5.
[4]吴名. 利用分子标记辅助选育甘蓝型油菜自交不亲和系[D]. 武汉:华中农业大学,2015.
[5]寇小培. 分子标记辅助选育甘蓝型油菜自交不亲和系[D]. 武汉:华中农业大学,2012.
[6]郑敏,朱陈曾,刘梦慈,等. 基于SRK基因序列分析的甘蓝自交不亲和系单倍型鉴定及验证[J]. 中国蔬菜,2018(3):32-39.
[7]许明超,黄倩,张康妮,等. 甘蓝型油菜隐性细胞核雄性不育系LY31AB的选育及利用[J]. 浙江大学学报(农业与生命科学版),2023,49(4):507-515.
[8]Takasaki T,Hatakeyama K,Suzuki G,et al. The S receptor kinase determines self-incompatibility in Brassica stigma[J]. Nature,2000,403(6772):913-916.
[9]Murase K,Shiba H,Iwano M,et al. A membrane-anchored protein kinase involved in Brassica self-incompatibility signaling[J]. Science,2004,303(5663):1516-1519.
[10]Horisaki A,Niikura S. Developmental and environmental factors affecting level of self-incompatibility response in Brassica rapa L.[J]. Sexual Plant Reproduction,2008,21(2):123-132.
[11]蓝兴国,杨佳,赵昕,等. 羽衣甘蓝ARC1的基因分离、表达及与SRK相互作用的分析[J]. 园艺学报,2011,38(12):2342-2348.
[12]Kusaba M,Matsushita M,Okazaki K,et al. Sequence and structural diversity of the S locus genes from different lines with the same self-recognition specificities in Brassica oleracea[J]. Genetics,2000,154(1):413-420.
[13]Schopfer C R,Nasrallah M E,Nasrallah J B,et al. The male determinant of self-incompatibility in Brassica[J]. Science,1999,286(5445):1697-1700.
[14]魏小春,姚秋菊,原玉香,等. 大白菜高代自交系S单元型的分布[J]. 河南农业科学,2015,44(11):109-113,119.
[15]Die J V,Román B,Nadal S,et al. Evaluation of candidate reference genes for expression studies in Pisum sativum under different experimental conditions[J]. Planta,2010,232(1):145-53.
[16]Fu J X,Wang Y,Huang H,et al. Reference gene selection for RT-qPCR analysis of Chrysanthemum lavandulifolium during its flowering stages[J]. Molecular Breeding,2013,31(1):205-215.
[17]王成. 不结球白菜自交不亲和相关基因及转录组分析[D]. 南京:南京农业大学,2017.
[18]江汉民,刘莉莉,徐嘉艺,等. 青花菜高代自交系S单元型的鉴定及SRK基因表达分析[J]. 南开大学学报(自然科学版),2018,51(3):60-65.
[19]Gachon C,Mingam A,Charrier B. Real-time PCR:what relevance to plant studies?[J]. Journal of Experimental Botany,2004,55(402):1445-1454.
[20]袁伟,万红建,杨悦俭. 植物实时荧光定量PCR内参基因的特点及选择[J]. 植物学报,2012,47(4):427-436.
[21]Albuquerque G M R,Fonseca F C A,Boiteux L S,et al. Stability analysis of reference genes for RT-qPCR assays involving compatible and incompatible Ralstonia solanacearum-tomato ‘Hawaii 7996’ interactions[J]. Scientific Reports,2021,11(1):18719.
[22]孙静. 铁皮石斛qPCR内参基因的筛选及开花相关基因的表达分析[D]. 南京:南京师范大学,2017.
[23]Song J H,Yang J,Pan F,et al. Differential expression of micro RNAs may regulate pollen development in Brassica oleracea[J]. Genetics and Molecular Research,2015,14(4):15024-15034.
[24]de Spiegelaere W,Dern-Wieloch J,Weigel R,et al. Reference gene validation for RT-qPCR,a note on different available software packages[J]. PLoS One,2017,10(3):e0122515.
[25]Leelatanawit R,Saetung T,Phuengwas S,et al. Selection of reference genes for quantitative real-time PCR in postharvest tomatoes(Lycopersicon esculentum)treated by continuous low-voltage direct current electricity to increase secondary metabolites[J]. International Journal of Food Science & Technology,2017,52(9):1942-1950.
[26]张颖,陈婉婷,陈冉红,等. 杉木实时荧光定量PCR分析中内参基因的选择[J]. 林业科学研究,2019,32(2):65-72.
[27]Xiao X L,Ma J B,Wang J R,et al. Validation of suitable reference genes for gene expression analysis in the halophyte Salicornia europaea by real-time quantitative PCR[J]. Frontiers in Plant Science,2015,5(1):788.
[28]Delporte M,Legrand G,Hilbert J L,et al. Selection and validation of reference genes for quantitative real-time PCR analysis of gene expression in Cichorium intybus[J]. Frontiers in Plant Science,2015,6(1):651.
[29]左同鸿.甘蓝SI相关基因BoPUB3L和BoGSTL21的克隆与分析[D]. 重庆:西南大学,2020.
[30]张彤. 甘蓝型油菜自交不亲和反应候选基因的功能研究及挖掘[D]. 湖北:华中农业大学,2018.
[31]郭怡婷,孙世英,赵文菊,等. 球茎甘蓝qRT-PCR内参基因的筛选及稳定性验证[J]. 甘肃农业大学学报,2024,59(1):144-152.
[32]李晗,李治龙,李晓屿,等. 羽衣甘蓝不同组织及柱头发育实时荧光定量PCR内参基因的筛选[J]. 植物研究,2016,36(4):565-572.
[33]张冠,杨迎霞,陆国清,等. 花椰菜花球中花青素合成相关基因qRT-PCR内参基因的筛选[J]. 分子植物育种,2024,22(9):2938-2946.
[34]Yan X,Zhang Q L,Zou J,et al. Selection of optimized reference genes for qRT-PCR normalization in Xanthomonas campestris pv. campestris cultured in different media[J]. Current Microbiology,2019,76(5):613-619.
[35]Vandesompele J,de Preter K,Pattyn F,et al. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes[J]. Genome Biology,2002,3(7):RESEARCH0034.
[36]Andersen C L,Jensen J L,rntoft T F. Normalization of real-time quantitative reverse transcription-PCR data:a model-based variance estimation approach to identify genes suited for normalization,applied to bladder and colon cancer data sets[J]. Cancer Research,2004,64(15):5245-5250.
[37]Pfaffl M W,Tichopad A,Prgomet C,et al. Determination of stable housekeeping genes,differentially regulated target genes and sample integrity:BestKeeper-Excel-based tool using pair-wise correlations[J]. Biotechnology Letters,2004,26(6):509-515.
[38]吴建阳,何冰,杜玉洁,等. 利用geNorm、NormFinder和BestKeeper软件进行内参基因稳定性分析的方法[J]. 现代农业科技,2017(5):278-281.
[39]杨琳. 受体激酶SRK与FERONIA调控大白菜远缘杂交生殖隔离的分子机制[D]. 山东:山东农业大学,2023.
[40]张以忠,曾文艺,邓琳琼,等. 甘蓝S-位点基因SRK、SLG和SP11/SCR密码子偏好性分析[J]. 作物学报,2022,48(5):1152-1168.
[41]Chen W D,Zhang B,Ren W J,et al. An identification system targeting the SRK gene for selecting S-haplotypes and self-compatible lines in cabbage[J]. Plants,2022,11(10):1372-1372.
[42]裴徐梨,冯鹏宇,唐征,等. 青花菜花蕾发育LncRNAs内参基因筛选[J]. 河南农业科学,2023,52(1):125-133.
[43]裴徐梨,焦鹏,荆赞革,等. 非生物胁迫下青花菜LncRNA内参基因的筛选[J]. 西北农业学报,2023,32(4):593-599.
[44]Zeng A S,Xu Y Y,Song L X,et al. Validation of suitable reference genes for qRT-PCR in cabbage(Brassica oleracea L.)under different abiotic stress experimental conditions[J]. Journal of Plant Biochemistry and Biotechnology,2021,30(1):184-195.
[45]李浩霞,黄稳娥,柳西宁,等. 枸杞实时荧光定量RT-qPCR内参基因筛选与验证[J]. 江苏农业科学,2023,51(9):41-51.
[46]穆德添,万凌云,章瑶,等. 钩藤管家基因筛选及生物碱合成相关基因的表达分析[J]. 生物技术通报,2023,39(2):126-138.
[47]Lee J M,Roche J R,Donaghy D J,et al. Validation of reference genes for quantitative RT-qPCR studies of gene expression in perennial ryegrass(Lolium perenne L.)[J]. BMC Molecular Biology,2010,11(1):8.
[48]Li H,Qin Y,Xiao X,et al. Screening of valid reference genes for real-time RT-qPCR data normalization in Hevea brasiliensis and expression validation of a sucrose transporter gene HbSUT3[J]. Plant Science,2011,181(2):132-139.
[1]邓艳美,王红妹,万从庆.青花菜中硫代葡萄糖苷的提取工艺[J].江苏农业科学,2013,41(06):254.
Deng Yanmei,et al.Extraction technology of glucosinolates from broccoli[J].Jiangsu Agricultural Sciences,2013,41(2):254.
[2]秦文斌,戴忠良,张振超,等.应用轮回选择改良青花菜侧花茎长度[J].江苏农业科学,2013,41(07):132.
Qin Wenbin,et al.Lengthening of broccoli (Brassica oleracea var. italica) lateral scape length by recurrent selection[J].Jiangsu Agricultural Sciences,2013,41(2):132.
[3]赵志刚.人工合成的甘蓝型油菜自交亲和性分析[J].江苏农业科学,2013,41(08):95.
Zhao Zhigang.Self-compatibility analysis of artificially synthetic Brassica napus L.[J].Jiangsu Agricultural Sciences,2013,41(2):95.
[4]戴忠良,张振超,潘永飞,等.青花菜新品种瑞绿5号的选育[J].江苏农业科学,2013,41(10):94.
Dai Zhongliang,et al.Breeding of new Brassica oleracea var. italica cultivar “Ruilü No.5”[J].Jiangsu Agricultural Sciences,2013,41(2):94.
[5]荆赞革,裴徐梨,唐征,等.青花菜早中熟种质资源遗传多样性SRAP标记分析[J].江苏农业科学,2014,42(01):41.
Jing Zange,et al.Genetic diversity analysis of early-mid mature broccoli germplasm by SRAP marker[J].Jiangsu Agricultural Sciences,2014,42(2):41.
[6]马越,丁云花,刘光敏,等.青花菜花球及叶片中硫代葡萄糖苷组分及含量分析[J].江苏农业科学,2016,44(07):300.
Ma Yue,et al.Analysis of glucosinolate composition and contents in flowers and leaves of broccoli (Brassica oleracea L. var. botrytis L.)[J].Jiangsu Agricultural Sciences,2016,44(2):300.
[7]滕昀,陈奎,刘雯倩,等.不同装箱方式对适宜温度下青花菜商品苗贮运质量的影响[J].江苏农业科学,2018,46(02):100.
Teng Yun,et al.Effects of different packing methods on storage and transportation quality of broccoli seedlings under suitable temperature[J].Jiangsu Agricultural Sciences,2018,46(2):100.
[8]宋立晓,侯忠乐,任一鸣,等.利用PEI-SWNT介导的瞬时转化检测青花菜基因编辑效率[J].江苏农业科学,2021,49(13):56.
Song Lixiao,et al.Detection of gene editing efficiency in broccoli by PEI-SWNT mediated transient transformation[J].Jiangsu Agricultural Sciences,2021,49(2):56.
[9]宋立晓,曾爱松,高兵,等.青花菜新品种苏青3号的选育[J].江苏农业科学,2014,42(12):216.
Song Lixiao,et al.Breeding of new broccoli cultivar “Suqing No.3”[J].Jiangsu Agricultural Sciences,2014,42(2):216.