Transcriptome of Arabidopsis leaf senescence
By Yongfeng Guo, Z. Cai, S. Gan. 2004
576 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/1334a99bdbe2704338e5b48c7fe1f14d346b908c
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- R. Oelmüller
- Madhunita Bakshi
- A. Fischer
- I. Somssich
- Sara K. El-Esawe
- P. Roberts
- Wim Van den Ende
- J. D. Ehlers
In Plant Science
- J. Specht
- K. Cassman
- A. Dobermann
- R. Oelmüller
- Madhunita Bakshi
- A. Fischer
- I. Somssich
- Sara K. El-Esawe
Citations in the corpus
- Sucrose signaling pathways leading to fructan and anthocyanin accumulation: A dual function in abiotic and biotic stress responses? (2014, background): “More in particular, plant-specific NACs (NAM, 5 ATAF1, ATAF2 and CUC2) constitute a major TF family with well-known roles in plant 6 developmental programs (Singh et al., 2002; Guo et al., 2004; Huang et al., 2012) and 7 stress responses (Nakashima et al.”
- ORS1, an H2O2-Responsive NAC Transcription Factor, Controls Senescence in Arabidopsis thaliana (2011, unknown): “Transcription factors (TFs) of the NAC (for NAM, ATAF1, 2, and CUC2) domain family represent an appreciable portion of the senescence-regulated genes in many plant species including crops and trees, suggesting an important role in the control of senescence (e.g. Andersson et al., 2004; Guo et al., 2”
- Leaf area index simulation in soybean grown under near-optimal conditions (2008, background): “The use of cumulative xs in Equation (14) allowed the effect of temperature on phenology to drive senescence, emphasizing the concept that senescence is a highly regulated process (Gepstein, 2004; Guo et al., 2004).”
- The Complex Regulation of Senescence (2012, background): “…of differentially regulated genes were also found in other studies exploring the Arabidopsis senescence transcriptome (Gepstein et al., 2003; Guo et al., 2004; Lin and Wu, 2004), and in senescing leaves of wheat (Gregersen and Holm, 2007), barley (Parrott et al., 2007; Jukanti et al.,…”
- Cloning and expression profiles of 15 genes encoding WRKY transcription factor in wheat (Triticum aestivem L.) (2008, background): “WRKY genes constituted the second largest group of Arabidopsis transcription factors in the transcriptome of senescing leaves [47], and the transcript levels of several Arabidopsis genes (AtWRKY4, AtWRKY6, AtWRKY7, AtWRKY11 and AtWRKY53) were enhanced in senescent leaves [37–39].”
- WRKY transcription factors: from DNA binding towards biological function. (2004, background): “In fact, WRKY transcripts constitute the second largest group of Arabidopsis transcription factors in the transcriptome of senescing leaves [26 ].”
- WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis1[C][W][OA] (2007, background): “The involvement of WRKY75 during senescence has also been suggested based on a microarray analysis (Guo et al., 2004) as well as unpublished data (Y. Guo and S. Gan).”
- WRKY transcription factors (2014, background): “Expression profiling in Arabidopsis revealed that WRKY TFs are the second largest family of TFs in reprogramming the Arabidopsis genome toward senescence.(139) Mutual regulation exists between WRKY22, WRKY6, WRKY53, and WRKY70.”
- Seedling Stage Drought-Induced Phenotypes and Drought-Responsive Genes in Diverse Cowpea Genotypes (2008, background): “Phospholipase D (El-Maarouf et al., 1999), galactolipid acyl hydrolase (Matos et al., 2001), lipoxygenase homolog CPRD46 (Iuchi et al., 1996a), and 12-oxophytodienoic acid reductase homolog CPRD8 (Iuchi et al., 1996b) are all known membrane lipid metabolism and leaf senescence responsive genes (He e”