6 research outputs found

    PCR detection of the <i>NIb8</i> gene in dwarf male-sterile wheat (DMSW) seeding.

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    <p>M, DNA marker; lane1, positive control (N12-1); lanes 2–5, genetically modified (GM) seedling with the <i>NIb8</i> gene; lanes 6–8, nongenetically modified (non-GM) seedling; lane 9, negative control (H<sub>2</sub>O).</p

    The exponential decay models for pollen and gene flow of transgenic wheat and the corresponding determination coefficient (R<sup>2</sup>) in eight compass sectors.

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    <p>The exponential decay models for pollen and gene flow of transgenic wheat and the corresponding determination coefficient (R<sup>2</sup>) in eight compass sectors.</p

    Estimated regression curves showing the decrease of transgene flow frequencies from genetically modified (GM) wheat lines to dwarf male-sterile wheat (DMSW) with the increasing distance from the pollen source in eight compass sectors.

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    <p>Estimated regression curves showing the decrease of transgene flow frequencies from genetically modified (GM) wheat lines to dwarf male-sterile wheat (DMSW) with the increasing distance from the pollen source in eight compass sectors.</p

    Diagrammatic presentation of the experimental design.

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    <p>The circular pollen donor N12-1 plot with radius 5m was planted at the center of experiment field. Pollen recipient dwarf male-sterile wheat (DMSW) was grown at eight compass directions. The radius of concentric circle of the recipient DMSW was 50 m.</p
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