Gene-specific primers for quantitative real-time PCR or Northern blot analysis. (DOC 48 kb
Table S1 Comparison of agronomic traits between WT and ds1. Table S2 Primers used in mapping. Table ...
Table S6. Characteristic fragment ions of the SA standard and its optimized MS/MS condition. (XLSX 1...
The primers (OsWRKY45, NH1, PR1a, Pb1 and Rubq1) were used for quantitative RT-PCR analysis. The oth...
Specific primers for amplification of the full and 5â-deleted promoters of OsWRKY80. (DOC 29 kb
Table S2. Differentially expressed genes in OsWRKY67 overexpressing plants by RNA-seq analysis. (XLS...
Table S3. Gene ontology analysis of up- and down-regulated genes in OsWRKY67-overexpressing plants d...
Table S5. Primers used for quantitative RT-PCR and vector construction. (XLSX 10 kb
Table S4. A statistic pathway enrichment analysis of differentially expressed genes between OsWRKY67...
Table S1. The microarray data of OsWRKY67 after leaf blast and panicle blast infection. (XLSX 9 kb
Figure S10. Relative expression levels of four WRKY genes in wild-type Nipponbare and OsWRKY67 trans...
Figure S8. The results of qRT-PCR showed an excellent concordance with the sequencing data. (JPG 214...
Figure S7. Overexpression of OsWRKY67 influences the expression of defense-related genes. The values...
Figure S1. qRT-PCR validation of 10 genes expressed in IR64 and spl21. (DOCX 340 kb
Table S1. PCR primers used for construction of vectors, detection of positive transgenic plants, mut...
Gene ontology analysis of up- and down-regulated genes in JMJ704 T-DNA mutant detected with RNA-seq ...
Table S1 Comparison of agronomic traits between WT and ds1. Table S2 Primers used in mapping. Table ...
Table S6. Characteristic fragment ions of the SA standard and its optimized MS/MS condition. (XLSX 1...
The primers (OsWRKY45, NH1, PR1a, Pb1 and Rubq1) were used for quantitative RT-PCR analysis. The oth...
Specific primers for amplification of the full and 5â-deleted promoters of OsWRKY80. (DOC 29 kb
Table S2. Differentially expressed genes in OsWRKY67 overexpressing plants by RNA-seq analysis. (XLS...
Table S3. Gene ontology analysis of up- and down-regulated genes in OsWRKY67-overexpressing plants d...
Table S5. Primers used for quantitative RT-PCR and vector construction. (XLSX 10 kb
Table S4. A statistic pathway enrichment analysis of differentially expressed genes between OsWRKY67...
Table S1. The microarray data of OsWRKY67 after leaf blast and panicle blast infection. (XLSX 9 kb
Figure S10. Relative expression levels of four WRKY genes in wild-type Nipponbare and OsWRKY67 trans...
Figure S8. The results of qRT-PCR showed an excellent concordance with the sequencing data. (JPG 214...
Figure S7. Overexpression of OsWRKY67 influences the expression of defense-related genes. The values...
Figure S1. qRT-PCR validation of 10 genes expressed in IR64 and spl21. (DOCX 340 kb
Table S1. PCR primers used for construction of vectors, detection of positive transgenic plants, mut...
Gene ontology analysis of up- and down-regulated genes in JMJ704 T-DNA mutant detected with RNA-seq ...
Table S1 Comparison of agronomic traits between WT and ds1. Table S2 Primers used in mapping. Table ...
Table S6. Characteristic fragment ions of the SA standard and its optimized MS/MS condition. (XLSX 1...
The primers (OsWRKY45, NH1, PR1a, Pb1 and Rubq1) were used for quantitative RT-PCR analysis. The oth...
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