Institution
University of Natal
About: University of Natal is a based out in . It is known for research contribution in the topics: Population & Cytokinin. The organization has 5898 authors who have published 8588 publications receiving 230533 citations.
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TL;DR: In Complexity and Postmodernism as mentioned in this paper, Cilliers explores the idea of complexity in the light of contemporary perspectives from philosophy and science, and offers us a unique approach to understand complexity and computational theory by integrating postmodern theory (like that of Derrida and Lyotard) into his discussion.
Abstract: In Complexity and Postmodernism, Paul Cilliers explores the idea of complexity in the light of contemporary perspectives from philosophy and science. Cilliers offers us a unique approach to understanding complexity and computational theory by integrating postmodern theory (like that of Derrida and Lyotard) into his discussion. Complexity and Postmodernism is an exciting and an original book that should be read by anyone interested in gaining a fresh understanding of complexity, postmodernism and connectionism.
1,641 citations
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TL;DR: A mechanism is proposed whereby the interconversions of proline and P5C in different cell types and the associated transfer of redox potential between tissues may constitute a form of metabolic signalling within higher plants.
Abstract: In many plants, free proline accumulates in response to the imposition of a wide range of biotic and abiotic stresses. Controversy has surrounded the extent to which this shift in nitrogen metabolism benefits plants under adverse environmental conditions. Most attempts to account for the phenomenon have focused on the ability of proline to mediate osmotic adjustment, stabilise subcellular structures and scavenge free radicals. However, often the cytoplasmic pool of free proline even after the imposition of stress is insufficient size to account for pronounced biophysical effects. Alternatively, selective preservation of this stress-induced response may relate to endpoints other than simply augmenting the cellular pool of free proline. Proline accumulation may reduce stress-induced cellular acidification or prime oxidative respiration to provide energy needed for recovery. High levels of proline synthesis during stress may maintain NAD(P)+/NAD(P)H ratios at values compatible with metabolism under normal conditions. Consideration of the cofactor preference of plant Δ1-pyrroline-5-carboxylate (P5C) reductase as well as the in vivo concentrations of the two pyridine nucleotide cofactors and their respective redox ratios suggests that even a small increase in proline biosynthesis might have a large impact on the level of reduction of the cellular NADP pool. The increased NADP+/NADPH ratio mediated by proline biosynthesis is likely to enhance activity of the oxidative pentose phosphate pathway. This would provide precursors to support the demand for increased secondary metabolite production during stress as well as nucleotide synthesis accompanying the accelerated rate of cell division upon relief from stress, when oxidation of proline is likely to provide an important energy source for ADP phosphorylation. Thus, the extreme sensitivity of the metabolic processes of proline synthesis and degradation themselves may be of benefit by regulating metabolic processes adversely affected by stress. This viewpoint is supported by consideration of other physiological phenomena not directly related to stress responses, but in which proline metabolism may also play a regulatory role. A mechanism is proposed whereby the interconversions of proline and P5C in different cell types and the associated transfer of redox potential between tissues may constitute a form of metabolic signalling within higher plants. Stress-related alterations in proline metabolism may impinge on systems of redox control of plant gene expression.
1,320 citations
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TL;DR: The rhBMP-2 implant was safe and, when 1.50 mg/mL was used, significantly superior to the standard of care in reducing the frequency of secondary interventions and the overall invasiveness of the procedures, accelerating fracture and wound-healing, and reducing the infection rate in patients with an open fracture of the tibia.
Abstract: Background:The treatment of open fractures of the tibial shaft is often complicated by delayed union and nonunion. The objective of this study was to evaluate the safety and efficacy of the use of recombinant human bone morphogenetic protein-2 (rhBMP-2; dibotermin alfa) to accelerate healing of open
1,220 citations
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TL;DR: In re-assessing the functional significance of compatible solute accumulation, it is suggested that proline and glycine betaine synthesis may buffer cellular redox potential and contribute to stress-tolerant phenotypes observed.
Abstract: Many plants accumulate organic osmolytes in response to the imposition of environmental stresses that cause cellular dehydration. Although an adaptive role for these compounds in mediating osmotic adjustment and protecting subcellular structure has become a central dogma in stress physiology, the evidence in favour of this hypothesis is largely correlative. Transgenic plants engineered to accumulate proline, mannitol, fructans, trehalose, glycine betaine or ononitol exhibit marginal improvements in salt and/or drought tolerance. While these studies do not dismiss causative relationships between osmolyte levels and stress tolerance, the absolute osmolyte concentrations in these plants are unlikely to mediate osmotic adjustment. Metabolic benefits of osmolyte accumulation may augment the classically accepted roles of these compounds. In re-assessing the functional significance of compatible solute accumulation, it is suggested that proline and glycine betaine synthesis may buffer cellular redox potential. Disturbances in hexose sensing in transgenic plants engineered to produce trehalose, fructans or mannitol may be an important contributory factor to the stress-tolerant phenotypes observed. Associated effects on photoassimilate allocation between root and shoot tissues may also be involved. Whether or not osmolyte transport between subcellular compartments or different organs represents a bottleneck that limits stress tolerance at the whole-plant level is presently unclear. None the less, if osmolyte metabolism impinges on hexose or redox signalling, then it may be important in long-range signal transmission throughout the plant.
1,194 citations
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TL;DR: The results of asking subjects to choose the most attractive faces from continua that enhanced or diminished differences between the average shape of female and male faces indicate a selection pressure that limits sexual dimorphism and encourages neoteny in humans.
Abstract: Testosterone-dependent secondary sexual characteristics in males may signal immunological competence1 and are sexually selected for in several species2,3. In humans, oestrogen-dependent characteristics of the female body correlate with health and reproductive fitness and are found attractive4,5,6. Enhancing the sexual dimorphism of human faces should raise attractiveness by enhancing sex-hormone-related cues to youth and fertility in females5,7,8,9,10,11, and to dominance and immunocompetence in males5,12,13. Here we report the results of asking subjects to choose the most attractive faces from continua that enhanced or diminished differences between the average shape of female and male faces. As predicted, subjects preferred feminized to average shapes of a female face. This preference applied across UK and Japanese populations but was stronger for within-population judgements, which indicates that attractiveness cues are learned. Subjects preferred feminized to average or masculinized shapes of a male face. Enhancing masculine facial characteristics increased both perceived dominance and negative attributions (for example, coldness or dishonesty) relevant to relationships and paternal investment. These results indicate a selection pressure that limits sexual dimorphism and encourages neoteny in humans.
1,141 citations
Authors
Showing all 5898 results
Name | H-index | Papers | Citations |
---|---|---|---|
David W. Johnson | 160 | 2714 | 140778 |
Bruce D. Walker | 155 | 779 | 86020 |
Robert J. Norman | 103 | 755 | 45147 |
Basil S. Lewis | 96 | 651 | 60124 |
Roy Maartens | 86 | 432 | 23747 |
Philip J. R. Goulder | 84 | 295 | 32080 |
Andrew Forbes | 83 | 931 | 26849 |
Bongani M. Mayosi | 78 | 403 | 68737 |
J. Van Staden | 76 | 898 | 28266 |
Keertan Dheda | 75 | 357 | 24757 |
Miroslav Strnad | 75 | 478 | 20220 |
Roy M. Robins-Browne | 74 | 309 | 19093 |
Salim S. Abdool Karim | 74 | 429 | 23650 |
Peter C. Appelbaum | 71 | 411 | 19292 |
Paul A. Webley | 70 | 374 | 18633 |