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Imaging studies that track the expression of regulators of the plant's proliferative centers, meristems, in conjunction with mutant analysis have shed new light on the earliest organizational cues during regenerative organ formation.
Moreover, inhibition studies and mutant analysis have shown that CA is important to the function of photosynthesis in Chlamydomonas [ 83].
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Knock-out mutant analysis has identified light response-defective phenotypes in T-DNA insertional mutant lines for nine gene family members that are predominantly expressed under high illumination (Jung et al. 2008).
Mutant analysis has been an excellent tool to dissect the major regulators controlling plant morphology.
Mutant analysis has shown that ACL5 is involved in xylem specification.
Mutant analysis had previously determined that mus-101 (tm1761 ∆) was sterile and/or lethal.
Furthermore, mutant analysis has demonstrated that loss of Pcdh10 can influence different aspects of development and post-natal life [ 48].
Mutant analysis has revealed that sugar signaling interacts with ethylene [ 70], ABA [ 71, 72], cytokinins [ 73], and light [ 74, 75].
Mutant analysis has suggested the involvement of a MATE transporter for proanthocyanins in Arabidopsis [ 13], anthocyanins in tomato (Solanum lycopersicum, [ 14]) and maize (Zea mays, [ 15]).
Although mutant analysis has not been reported for all components of TAC, plants with mutations in PEP and pTAC encoding genes have diverse pleiotropic phenotypes, but all share, to some degree, loss of pigmentation and abnormal plastid development.
Double mutant analysis has also revealed several redundancies between ABF3 and ABI5, including sensitivity to ABA during germination, stress sensitivity of root growth, resistance to glucose, and regulation of the ABA-induced vegetative expression of RAB18 and RD29B [ 88].
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