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Table S1 . (Continued)

Table S1 . List of primers used for the amplification of DNA fragments that were used as probes for Northern blot analysis. Table S1 . (Continued).

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Table S1 . (Continued)

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  1. Table S1. List of primers used for the amplification of DNA fragments that were used as probes for Northern blot analysis.

  2. Table S1. (Continued)

  3. Fig. S1. Disease severity in wild-type (WT) and transgenic cotton plants expressing AtNPR1 gene, one month following inoculation with Thielaviopsis basicola. The image shown is at the termination of experiment #2 conducted under growth chamber conditions.

  4. ** Fig. S2. Resistance to Thielaviopsis basicola in transgenic cotton lines (#68L-19, #68L-20, and #68L-5) expressing AtNPR1. WT: wild-type. Shoot weight was used as a parameter to score disease-severity in experiment #2, conducted under growth chamber conditions, one month following inoculation with the pathogen. Data represent mean±SE, **P<0.01; n=10.

  5. ** * * Fig. S3. Resistance to Thielaviopsis basicola in transgenic cotton lines (#68L-19, #68L-20, and #68L-5) expressing AtNPR1. WT: wild-type. Root weight was used as a parameter to score disease-severity in experiment #2, conducted under growth chamber conditions, one month following inoculation with the pathogen. Data represent mean±SE, *P<0.05, **P<0.01; n=10.

  6. *** * *** Fig. S4. Resistance to Thielaviopsis basicola in transgenic cotton lines (#68L-19, #68L-20, and #68L-5) expressing AtNPR1. WT: wild-type. Chlamydospore count was obtained from the roots of WT and transgenic cotton plants, one month following inoculation with the pathogen in experiment # 2. Data represent mean±SE; *P<0.05, ***P<0.001; n=3; each replicate is a representative sample obtained from roots pooled from 3-4 infected plants.

  7. WT 68L-20 WT 68L-20 Uninfected Infected Fig. S5. Stunting of growth caused by Thielaviopsis basicola in wild-type (WT) and transgenic cotton plants expressing AtNPR1 gene. The image depicted is of plants three months following inoculation with the pathogen from experiment #4 conducted under greenhouse conditions.

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