1-21 of 21
Keywords: Arabidopsis thaliana
Close
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Articles
Articles
Biochem Soc Trans (2024) 52 (1): 291–299.
Published: 04 January 2024
...). Published by Portland Press Limited on behalf of the Biochemical Society 2024 Arabidopsis thaliana DUB endocytosis ubiquitin Plants are sessile organisms that need to adapt to local and global environmental changes in their habitat. For the perception of these changes and the timely...
Articles
Biochem Soc Trans (2023) 51 (1): 31–39.
Published: 25 January 2023
... quality control and imply its involvement in regulating gene expression in a wide range of physiological processes. Studies in moss Physcomitrella patens and Arabidopsis thaliana have shown that NMD is also important in plants where it contributes to the regulation of pathogen defence, hormonal signalling...
Articles
Biochem Soc Trans (2021) 49 (3): 1133–1146.
Published: 20 May 2021
...-hohenheim.de ) 28 2 2021 16 4 2021 23 4 2021 © 2021 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2021 Arabidopsis thaliana crops nutrient uptake root hair transporter Mineral nutrients can be essential, beneficial or toxic...
Articles
Biochem Soc Trans (2020) 48 (6): 2779–2789.
Published: 10 November 2020
...Jie Shu; Chen Chen; Chenlong Li; Yuhai Cui Polycomb repressive complex 2 (PRC2) is an evolutionally conserved multisubunit complex essential for the development of eukaryotes. In Arabidopsis thaliana ( Arabidopsis ), CURLY LEAF (CLF) and SWINGER (SWN) are PRC2 catalytic subunits that repress gene...
Articles
Biochem Soc Trans (2018) 46 (4): 957–966.
Published: 31 July 2018
.... In addition to the core subunits, an exponentially increasing number of PRC1-associated factors have been identified in Arabidopsis thaliana . Recent studies have also unraveled cross-component interactions and intertwined roles of PRC1 and PRC2 in chromatin modulation. In addition, complexities...
Articles
Biochem Soc Trans (2016) 44 (1): 150–158.
Published: 09 February 2016
... (e.g. xyloglucans and Rhamnogalacturonan I, RGI [ 24 ]). A biologically relevant substrate for BGALs during fruit ripening of tomato is galactan, a polymer of β-(1-4) D-galactose attached to RGI [ 25 – 27 ]. In this mini review, we discuss the BGALs from Arabidopsis thaliana and Solanum lycopersicum...
Articles
Biochem Soc Trans (2014) 42 (2): 383–387.
Published: 20 March 2014
... phosphorylation. Protein phosphorylation belongs among the most rapid post-translational modifications. To date, only Arabidopsis thaliana and tobacco ( Nicotiana tabacum ) mature pollen have been subjected to phosphoproteomic studies in order to identify the phosphoproteins present. In the present mini-review...
Articles
Biochem Soc Trans (2014) 42 (2): 408–412.
Published: 20 March 2014
... ] ( Figure 2 ). Furthermore, it restricts the developmental progression of meristemoids to guard mother cells, possibly by regulating the activity of the bHLH transcription factor MUTE, although MUTE does not appear to be a direct MAPK target on the basis of in vitro data [ 25 ]. Arabidopsis thaliana...
Articles
Biochem Soc Trans (2010) 38 (5): 1197–1201.
Published: 24 September 2010
... the sources of error in a nascent model rapidly, and the generation of tenable hypotheses concerning solutions that would improve a model. We will illustrate these issues with approaches we have developed in the course of building metabolic models of Streptococcus agalactiae and Arabidopsis thaliana...
Articles
Biochem Soc Trans (2010) 38 (2): 593–597.
Published: 22 March 2010
... or Mark_Johnson_1@brown.edu ) 2 9 2009 © The Authors Journal compilation © 2010 Biochemical Society 2010 Arabidopsis thaliana functional genomics pistil pollen tube Co-ordinated development in multicellular organisms involves cells responding to signals from neighbouring cells...
Includes: Multimedia, Supplementary data
Articles
Biochem Soc Trans (2010) 38 (2): 635–640.
Published: 22 March 2010
... of the female gametes and technical limitations. Over the last couple of years, however, the use of advanced methodologies, new imaging tools and new mutants has provided deeper insights into double fertilization, at both the cellular and the molecular level, especially for the model plant Arabidopsis thaliana...
Articles
Biochem Soc Trans (2010) 38 (2): 672–676.
Published: 22 March 2010
... ). 4 9 2009 © The Authors Journal compilation © 2010 Biochemical Society 2010 Arabidopsis thaliana assembly factor Cajal body RNA modification small nucleolar RNA (snoRNA) The snoRNAs represent an abundant class of ~50–300 nucleotide trans -acting RNAs in all eukaryotes...
Articles
Biochem Soc Trans (2007) 35 (6): 1643–1647.
Published: 23 November 2007
...@cyllene.uwa.edu.au ). 2 7 2007 © The Authors Journal compilation © 2007 Biochemical Society 2007 Arabidopsis thaliana chloroplast mitochondrion pentatricopeptide repeat (PPR) RNA binding tetratricopeptide repeat (TPR) As most PPR proteins lack any known catalytic sites, the RNA...
Articles
Biochem Soc Trans (2006) 34 (4): 531–534.
Published: 21 July 2006
.... In Arabidopsis thaliana , we have identified several DNA fragments (less than 5 kb in size) with genetic recombination rates at least 5 times higher than the whole-chromosome average [4.6 cM (centimorgan)/Mb], which are therefore probable hotspots for meiotic recombination. Most crossover breakpoints lie...
Articles
Biochem Soc Trans (2005) 33 (5): 943–944.
Published: 26 October 2005
... in leaves but not in roots. Preliminary experiments suggest that the same is true for at least one gene in Arabidopsis thaliana . It will be important to define the extent and function of this phenomenon and the underlying mechanism. Arabidopsis thaliana carbon allocation circadian control gene...
Articles
Biochem Soc Trans (2005) 33 (1): 283–286.
Published: 01 February 2005
..., agamous, deficiens and SRF) box gene ( ANR1 ) in Arabidopsis thaliana that is involved in modulating the rate of lateral root growth in response to changes in the external NO 3 − supply. Transgenic plants have been generated in which a constitutively expressed ANR1 protein can be post-translationally...
Articles
Biochem Soc Trans (2004) 32 (4): 575–577.
Published: 01 August 2004
... strategy designed to isolate mutants of Arabidopsis thaliana that fail to recognize these sequences is described. In this strategy, a selectable gene and a screenable marker gene are put under the control of the sequence element being analysed and mutants are selected with altered abundance...
Articles
Biochem Soc Trans (2004) 32 (4): 581–584.
Published: 01 August 2004
.... The TOR protein is specifically inhibited by a rapamycin–FKBP12 complex (where FKBP stands for FK506-binding protein) in yeast and animal cells. Whereas plants appear insensitive to rapamycin, Arabidopsis thaliana harbours a single TOR gene, which is essential for embryonic development. It was found...
Articles
Articles
Biochem Soc Trans (2000) 28 (6): 940–942.
Published: 01 December 2000
... fatty acids to normal levels and results in a 2-fold increase in total epoxy fatty acids. Arabidopsis thaliana Crepis palaestina Δ12-desaturase Δ12-epoxygenase epoxygenated fatty acid 18:1E, 12,13-epoxy- cis -9-octadecenoic acid 18:2E, 12,13-epoxy- cis -9,15-octadec-2-enoic acid ODP...