D
David E. Evans
Researcher at Oxford Brookes University
Publications - 102
Citations - 3920
David E. Evans is an academic researcher from Oxford Brookes University. The author has contributed to research in topics: LINC complex & Inner membrane. The author has an hindex of 33, co-authored 102 publications receiving 3686 citations. Previous affiliations of David E. Evans include University of Oxford & St Mary's Hospital.
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Journal ArticleDOI
Characterisation of programmed cell death during aerenchyma formation induced by ethylene or hypoxia in roots of maize (Zea mays L.)
Arunika H. L. A. N. Gunawardena,Deborah M.E. Pearce,Michael B. Jackson,Chris Hawes,David E. Evans +4 more
TL;DR: Aerenchyma formation initiated by hypoxia or ethylene appears to be a form of programmed cell death that shows characteristics in part resembling both apoptosis and cytoplasmic cell death in animal cells.
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Aluminium/silicon interactions in higher plants
Martin J. Hodson,David E. Evans +1 more
TL;DR: In this article, it has been suggested that Al toxicity can be ameliorated by Si in a variety of animal systems, including maize, barley, teosinte, and soybean, but not in rice, wheat, cotton, and pea.
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Active Calcium Transport by Plant Cell Membranes
TL;DR: Chez les plantes superieures, le calcium cytosolique est maintenu a une faible concentration grâce a l'action des transporteurs membranaires specifiques ganant un antiport Ca/H +.
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The amelioration of aluminium toxicity by silicon in higher plants : Solution chemistry or an in planta mechanism?
TL;DR: In this paper, the root cell walls are the main internal sites of aluminosilicate (AS) and/or HAS formation and of Al detoxification, and it is shown that Al and Si can ameliorate the toxic effects of Al in hydroponic culture.
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Characterization of SUN-domain proteins at the higher plant nuclear envelope
TL;DR: The study provides evidence suggesting the existence of cytoskeletal-nucleoskeleton bridging complexes at the plant NE, and presents evidence that AtS SUN1 and AtSUN2 are present as homomers and heteromers in vivo, and that the coiled-coil domains are required for this.