Titlebook: Citrus Tristeza Virus; Methods and Protocol Antonino F. Catara,Moshe Bar-Joseph,Grazia Licciar Book 2019 Springer Science+Business Media, L

充裕

書目名稱Citrus Tristeza Virus影響因子(影響力)




書目名稱Citrus Tristeza Virus影響因子(影響力)學(xué)科排名




書目名稱Citrus Tristeza Virus網(wǎng)絡(luò)公開度




書目名稱Citrus Tristeza Virus網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Citrus Tristeza Virus被引頻次




書目名稱Citrus Tristeza Virus被引頻次學(xué)科排名




書目名稱Citrus Tristeza Virus年度引用




書目名稱Citrus Tristeza Virus年度引用學(xué)科排名




書目名稱Citrus Tristeza Virus讀者反饋




書目名稱Citrus Tristeza Virus讀者反饋學(xué)科排名

消息靈通

A Brief Historical Account of the Family , taxon comprising plant viruses that possess very long helically constructed filamentous particles and a positive-sense single-stranded, monopartite or bipartite RNA genome and are transmitted either by aphids (genus .), pseudococcid mealybugs/soft scale insects (genus .), or whiteflies (genus .) or

彈藥

Phenotyping Biological Properties of CTV Isolates,ogical properties of a single isolate of . complex (CTV). It enables the phenotypic profile of the isolates to be defined and to infer the associated tristeza diseases (decline, seedling yellows, or stem pitting), to assess their aggressiveness or potential cross protectiveness (if any), and to moni

fructose

逢迎春日

Tissue-Print and Squash Capture Real-Time RT-PCR Method for Direct Detection of , (CTV) in Plant orto polymerase chain reaction (RT-PCR) neither with extract preparation nor nucleic acid purification. Immobilized CTV targets are amplified from fresh sections of plant tissues or squashes of fresh or already caught vectors onto paper, nitrocellulose, or positively charged nylon membranes. The print

含鐵

Detection of , and Coinfecting Viroids, programs require pathogen detection systems which must be economical and sensitive to maintain a healthy citrus industry. Rapid diagnostic tests for simultaneous detection of major graft-transmissible disease agents enable reduction of cost and time. The genetic and biological features of viruses a

含鐵

Assessment of Genetic Variability of , by SSCP and CE-SSCP,tes. It is a simple, low-cost, and highly specific method for mutation detection of specific genes, mostly of the CTV major coat protein gene (.). The technique is based on a comparison on polyacrylamide gel of electrophoretic profiles of single-stranded (ss) DNA sequences in terms of their spatial

HEPA-filter

Inordinate

颶風(fēng)

Rapid and Sensitive Detection of , Using Reverse Transcription Loop-Mediated Isothermal Amplificatil for early detection of nucleic acid targets. The LAMP technique works on the principle of strand displacement activity of . polymerase. It contains a set of four specially designed primers, which recognizes six different regions on the target nucleotide sequence. In the LAMP reaction, amplificatio