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Mutant analyses have revealed that root-type-specific genetic regulators intrinsically determine the maize root system architecture.
Mutant analyses have identified genes regulating shoot-borne root initiation (RTCS) and root hair elongation (RTH1 and RTH3).
CPK10-overexpression and T-DNA insertion mutant analyses have shown that CPK10 is involved in drought stress tolerance.
This is in contrast to IXB, where mutant analyses have identified specific cellulose synthase (CesA) complexes (CesA3 and CesA6) from the plasma membrane as toxin targets [ 8, 9].
Besides, mutant analyses have also revealed that the conserved histone chaperone ASF1 is required for cell proliferation during development in Arabidopsis [ 19].
Furthermore, mutant analyses have demonstrated that Nodal signalling is required for nkx2.5 signalling and, in a similar manner to the scenario in swirl/bmp2b mutants, nkx2.5 expression in Nodal mutants can be restored by ectopic expression of gata5.
Similar(51)
Lack of correlation between transcriptional profiling and deletion mutant analyses has been reported in the literature by investigators using both selected individual mutants as well as whole-genome mutant populations [ 53- 57].
Several analyses have been performed on Drosophila lamin Dm0 mutants [24].
Ultrastructural analyses have revealed that the grana of Chl1 and Chl9 mutants are poorly stacked, resulting in the underdevelopment of chloroplasts (Zhang et al. 2006).
In tomato, most ecophysiological analyses have focused on genetically based variation within domesticated tomato (including between mutant types) (Hsiao 1973).
In addition, whole-genome expression analyses have dissected the inducible heat shock transcriptional response in wild-type and mutant flies.
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