retrotransposon sequence
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Mobile DNA ◽  
2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Zhuqing Wang ◽  
Hayden McSwiggin ◽  
Simon J. Newkirk ◽  
Yue Wang ◽  
Daniel Oliver ◽  
...  

2017 ◽  
Vol 53 (9) ◽  
pp. 988-997 ◽  
Author(s):  
L. S. Melnikova ◽  
M. V. Kostyuchenko ◽  
I. V. Krivega ◽  
I. S. Shapovalov ◽  
P. G. Georgiev ◽  
...  

2013 ◽  
Vol 92 (1) ◽  
pp. 103-108 ◽  
Author(s):  
JIE ZHANG ◽  
HAI LONG ◽  
ZHIFEN PAN ◽  
JUNJUN LIANG ◽  
SHUIYANG YU ◽  
...  

2007 ◽  
Vol 97 (8) ◽  
pp. 987-996 ◽  
Author(s):  
Matias Pasquali ◽  
Flavia Dematheis ◽  
Maria Lodovica Gullino ◽  
Angelo Garibaldi

Fusarium wilt of lettuce, caused worldwide by Fusarium oxysporum f. sp. lactucae, is an emerging seed-transmitted disease on Lactuca sativa. In order to develop a molecular diagnostic tool for identifying race 1 (VCG0300) of the pathogen on vegetable samples, an effective technique is presented. Inter-retrotransposon amplified polymorphism polymerase chain reaction (PCR), a technique based on the amplification of genomic regions between long terminal repeats, was applied. It was shown to be useful for grouping F. oxysporum f. sp. lactucae race 1 isolates. Inter-retrotransposon sequence-characterized amplified regions (IR-SCAR) was used to develop a specific set of PCR primers to be utilized for differentiating F. oxysporum f. sp. lactucae isolates from other F. oxysporum isolates. The specific primers were able to uniquely amplify fungal genomic DNA from race 1 isolates obtained in Italy, Portugal, the United States, Japan, and Taiwan. The primers also were specific to pathogen DNA obtained from artificially infected lettuce seed and naturally and artificially infected plants.


2006 ◽  
Vol 62 (4) ◽  
pp. 375-387 ◽  
Author(s):  
T. Roderick Docking ◽  
Fabienne E. Saadé ◽  
Miranda C. Elliott ◽  
Daniel J. Schoen

2001 ◽  
Vol 13 (1/2) ◽  
pp. 1-6
Author(s):  
Masaru MIYANO ◽  
Takahiro OKABE ◽  
Takahiro KUSAKABE

1992 ◽  
Vol 233 (1-2) ◽  
pp. 322-326 ◽  
Author(s):  
Andrew J. Flavell ◽  
Donald B. Smith

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