about
Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species.Matching roots to their environmentNew insights to lateral rooting: Differential responses to heterogeneous nitrogen availability among maize root typesEvolutionary origins of abnormally large shoot sodium accumulation in nonsaline environments within the Caryophyllales.Selenium accumulation by plants.High-throughput phenotyping (HTP) identifies seedling root traits linked to variation in seed yield and nutrient capture in field-grown oilseed rape (Brassica napus L.).Root morphology and seed and leaf ionomic traits in a Brassica napus L. diversity panel show wide phenotypic variation and are characteristic of crop habitA conceptual model of root hair ideotypes for future agricultural environments: what combination of traits should be targeted to cope with limited P availability?Root traits for infertile soilsDistribution of calcium (Ca) and magnesium (Mg) in the leaves of Brassica rapa under varying exogenous Ca and Mg supplyPhysiological limits to zinc biofortification of edible crops.Plant nutrition for sustainable development and global health.Tandem quadruplication of HMA4 in the zinc (Zn) and cadmium (Cd) hyperaccumulator Noccaea caerulescensDietary requirements for magnesium, but not calcium, are likely to be met in Malawi based on national food supply data.Analysis of root growth from a phenotyping data set using a density-based model.Optimising the analysis of transcript data using high density oligonucleotide arrays and genomic DNA-based probe selection.Genetic responses to phosphorus deficiency.Breeding histories and selection criteria for oilseed rape in Europe and China identified by genome wide pedigree dissection.A Brassica exon array for whole-transcript gene expression profiling.Interactions between light intensity and phosphorus nutrition affect the phosphate-mining capacity of white lupin (Lupinus albus L.).Gene expression changes in phosphorus deficient potato (Solanum tuberosum L.) leaves and the potential for diagnostic gene expression markersCalcium in plants.Dietary mineral supplies in Africa.The three-dimensional distribution of minerals in potato tubers.Continuous, high-resolution biospeckle imaging reveals a discrete zone of activity at the root apex that responds to contact with obstacles.Maize varieties released in different eras have similar root length density distributions in the soil, which are negatively correlated with local concentrations of soil mineral nitrogen.A large and deep root system underlies high nitrogen-use efficiency in maize productionInter-cultivar variation in soil-to-plant transfer of radiocaesium and radiostrontium in Brassica oleracea.A cellular hypothesis for the induction of blossom-end rot in tomato fruit.Biological costs and benefits to plant-microbe interactions in the rhizosphere.Mutation increasing β-carotene concentrations does not adversely affect concentrations of essential mineral elements in pepper fruit.Biofortifying crops with essential mineral elements.Biofortification of UK food crops with selenium.How do plants respond to nutrient shortage by biomass allocation?Zinc in plants.High-throughput root phenotyping screens identify genetic loci associated with root architectural traits in Brassica napus under contrasting phosphate availabilitiesSucrose transport in the phloem: integrating root responses to phosphorus starvation.QTL meta-analysis of root traits in Brassica napus under contrasting phosphorus supply in two growth systems.Biofortification of crops with seven mineral elements often lacking in human diets--iron, zinc, copper, calcium, magnesium, selenium and iodine.Moving cationic minerals to edible tissues: potassium, magnesium, calcium.
P50
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P50
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Philip J White
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Philip J White
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P1053
C-5860-2008
P106
P1960
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P2038
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P21
P31
P3829
P496
0000-0003-0827-288X