The molecular analysis of leaf senescence--a genomics approach.
By V. Buchanan-Wollaston, S. Earl, E. Harrison, E. Mathas, S. Navabpour, T. Page, D. Pink. Plant Biotechnology Journal, 2002
751 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/5defc9524d8bf0e8fcec638648790d1ffcb0158e
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In Molecular Biology
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Citations in the corpus
- Oxidative Stress and Antioxidant Responses in Young Leaves of Mulberry Plants Grown Under Nitrogen, Phosphorus or Potassium Deficiency (2007, background): “Degradation of chloroplastic pigments and proteins, and increased lipid peroxidation are also indices of senescence that are due to increased ROS generation (Buchanan-Wollaston et al. 2003).”
- Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications (2009, positive): “The timing of senescence is also altered in the ascorbate-deficient Arabidopsis mutant vtc1 (28), but this may be due to the enhanced susceptibility of individual ascorbate-deficient cells to PCD (318).”
- Control of Jasmonate Biosynthesis and Senescence by miR319 Targets (2008, background): “Thus, JA likely plays a role in the control of senescence, but is not essential for it, as pointed out before [47].”
- Ethylene Role in Plant Growth, Development and Senescence: Interaction with Other Phytohormones (2017, background): “, 1996), membrane disruption, lipid degradation, peroxidation (Buchanan-Wollaston, 1997; Thompson et al., 1998; Buchanan-Wollaston et al., 2003), and leaf pigment breakdown (Matile et al.”
- Aging in Perennials (2007, background): “…physiological aspects related to the leaf senescence occurring in plants, with most of the reviews based on experiments performed on the annual, model plant Arabidopsis thaliana (Hadfield and Bennett, 1997; Noodén et al., 1997; Chandlee, 2001; Buchanan-Wollaston et al., 2003; Lim and Nam, 2005).”
- Significance of inducible defense-related proteins in infected plants. (2006, background): “Secreted PRs accumulate in senescing leaves of some species when yellowing is becoming apparent and in ripening fruits (14, 30, 110), as well as in the medium of cell suspension cultures in the absence of visible necrosis (12, 139), indicating that at least some inducible defense-related proteins ar”
- Targets of the WRKY53 transcription factor and its role during leaf senescence in Arabidopsis (2004, background): “Expression profiles of Arabidopsis revealed that approximately 16% of the Arabidopsis genes change their expression during senescence (Buchanan-Wollaston et al., 2003; Zentgraf et al., 2004) and that the mRNA level of at least 43 transcription factors is increased (Chen et al.”
- Defense enzyme activities and biochemical variations of Pelargonium zonale in response to nanosilver application and dark storage (2014, background): “This process has some similarities with natural senescence, which suggests that dark-induced cell death is a result of an active program that include the participation of signaling molecules, transcription factors, and catabolic enzymes (Buchanan-Wollaston et al., 2003).”
- Effect of 5-sulfosalicylic acid on antioxidant activity in relation to vase life of Gladiolus cut flowers (2007, background): “Senescence is determined genetically and governed by environmental factors during development (Buchanan-Wollaston et al. 2003).”
- WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis1[C][W][OA] (2007, background): “For example, many of the genes involved in Pi starvation responses, such as RNases, ATPases, and purple acid phosphatases, are induced during senescence and vice versa (Buchanan-Wollaston et al., 2003).”