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  • Articles  (39)
  • American Association for the Advancement of Science (AAAS)  (17)
  • Springer  (17)
  • Blackwell Publishing Ltd  (5)
  • American Association of Petroleum Geologists (AAPG)
  • American Meteorological Society
  • Copernicus
  • 2015-2019  (15)
  • 2000-2004  (13)
  • 1975-1979  (11)
  • Medicine  (33)
  • Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition  (6)
Collection
  • Articles  (39)
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Year
Journal
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant breeding 123 (2004), S. 0 
    ISSN: 1439-0523
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Broccoli is well recognized as a source of glucosinolates and their isothiocyanate breakdown products. Glucoraphanin is one of the most abundant glucosinolates present in broccoli and its cognate isothiocyanate is sulphoraphane, a potent inducer of mammalian detoxication (phase 2) enzyme activity and anti-cancer agent. This study was designed to measure: glucosinolate levels in broccoli florets from an array of genotypes grown in several environments; the elevation of a key phase 2 enzyme, quinone reductase, in mammalian cells exposed to floret extracts; and total broccoli head content. There were significant environmental and genotype-by-environment effects on levels of glucoraphanin and quinone reductase induction potential of broccoli heads; however, the effect of genotype was greater than that of environmental factors. The relative rankings among genotypes for glucoraphanin and quinone reductase induction potential changed, when expressed on a per head basis, rather than on a concentration basis. Correlations of trait means in one environment vs. means from a second were stronger for glucoraphanin and quinone reductase induction potential on a per head basis than on a fresh weight concentration basis. Results of this study indicate that development of a broccoli phenotype with a dense head and a high concentration of glucoraphanin to deliver maximum chemoprotective potential (high enzyme induction potential/glucoraphanin content) is a feasible goal.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant pathology 24 (1975), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: When the aggregates of fairly dry, medium-coarse soil were broken down and firmed over the seed by moderate or heavy pressure, slug damage was reduced. Coarse soil aggregates did not break down so well, particularly under heavy pressure; many seeds remained exposed and were damaged. The seed was also protected by deep planting, with the penalty of late emergence of the seedlings.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant pathology 24 (1975), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The choice of resting places in bare soil of both immature and mature slugs Was influenced by the size of the soil aggregates. A moderate to coarse soil was preferred and it is suggested that response to contact stimuli may be partly responsible for this behaviour. Soil composed of fine aggregates was preferred for egg-laying sites.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Weed research 17 (1977), S. 0 
    ISSN: 1365-3180
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: A semi-open circuit system for measuring changes in net CO2 exchange (NCE) in single leaves of intact grasses following herbicide treatment is described and evaluated. There were significant differences in levels of inhibition and subsequent recovery of NCE in maize and eight weedy panicoid grasses following limited root uptake of atrazine (2-chloro-4-ethyl-amino-6-isopropylamino-1,3,5-triazine). cyanazine [2-chloro-4-(1-cyano-1-methylethylamino)-6-ethylamino-1,3,5-triazine] and cyprazine (2-chloro-4-cyclopropylamino-6-isopropyl-amino-1,3.5-triazine). Rate of NCE recovery was positively correlated (P = 0.05) with growth of seedlings in nutrient solution containing the herbicides. Rates of NCE recovery 〉0.9 mg CO2 per dm2 per h/h reflected rapid rates of herbicide detoxification in the leaves and a significant tolerance to preplant incorporated and postemergence applications of atra-zine, cyanazine and cyprazine. In contrast, some species, e.g. large crabgrass [Digitaria sanguinalis (L.) Scop.] and proso millet (Panicum miliaceum L.) treated with cyanazine demonstrated considerable tolerance to these treatments in spite of low NCE recovery rates indicating that factors other than foliar detoxification may play an important role in the tolerance of some grasses to 2-chloro- 1,3,5-triazine herbicides.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1365-3180
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Atrazine [2-chloro-4-(ethylaminol-6-(isopropyl-amino)-s-triazine] resistant biotypes of lamb's quarters (Chenopodium athum L) were reported in the maize growing areas of Ontario, where the herbicide had been used fur a number of years. Field samples from four locations proved tolerant to higber than recommended rates of atrazine in controlled environment screening trials. A resistant biotype was not killed with up to 40 kg/ha atrazine. Diuron at 5 x10-5 M inhibited the Hill reaction with isolated chloroplasts of resisiant and susceptible biotypes of lamb's-quarters. However, with 10-4 M atrazine, the photochemical activity was inhibited in chloroplasts isolated from the susceptible biotype but not in chloroplasts from the resisiant biotype. With maize chloroplasts, inhibition with 10-4 M atrazine was the same as with the susceptible biotype of lamb's-quarters. These studies suggested that a new mechanism of intraspecific resistance in lamb's quarters to atrazine was involved, other than differences in uptake, translocation and metabolism reported with interspecific comparisons involving the s-triazines and other herbicides, It was also concluded that atrazine and diuron did not have precisely the same mechanism of action as photosynthetic inhibitors with lamb's-quarters, and that external and or internal structure or function of chloroplasts in relation to atrazine inhibition can vary significantly even in biotypes of the same species.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 14 (1975), S. 304-308 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 31 (1975), S. 1473-1474 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Coverslips coated with rat-tail collagen dried at 37°C were placed in a hot-air sterilizing oven at 160°C for 2 h. The resulting transparent sterile film was found to be a useful multipurpose substrate for cell culture and for subsequent histological sectioning.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 58 (1976), S. 41-50 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The DNA coding for 28 S and 18 S ribosomal RNA, including the spacer regions, has been isolated from calf (Bos taurus) thymus gland. The method used included shearing of the total DNA to a highly homogeneous size population, selective heat denaturation and S 1 nuclease treatment to remove single stranded DNA. Repeated centrifugation on density gradients yields a 140-fold purified rDNA fraction with a GC content of 61.2%. Eco RI nuclease cleaves this DNA into two fragments of 16.4 and 4.9×106 daltons. Hybridization of these fragments with 28 S and 18 S rRNA shows that the 28 S coding sequence is located mostly on the 4.9×106 dalton fragment, while both the 16.4 and 4.9×106 dalton fragments contain the 18 S sequence. The data indicate that the ribosomal RNA gene has a repeat unit of 21.3×106 daltons which includes a nontranscribed spacer of about 12.5×106 daltons.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of muscle research and cell motility 21 (2000), S. 481-489 
    ISSN: 1573-2657
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Mechanisms of fatigue were studied in single muscle fibres of the cane toad (Bufo marinus) in which force, intracellular calcium ([Ca2+]i), [Mg2+]i, glycogen and the rapidly releasable Ca2+ from the sarcoplasmic reticulum (SR) were measured. Fatigue was produced by repeated tetani continued until force had fallen to 50%. Two patterns of fatigue in the absence of glucose were studied. In the first fatigue run force fell to 50% in 8–10 min. Fatigue runs were then repeated until force fell to 50% in 〈3 min in the final fatigue run. Addition of extracellular glucose after the final fatigue run prolonged a subsequent fatigue run. In the first fatigue run peak tetanic [Ca2+]i initially increased and then declined and at the time when force had fallen to 50% tetanic [Ca2+]i was 54 ± 5% of initial value. In the final fatigue run force and peak tetanic [Ca2+]i declined more rapidly but to the same level as in first fatigue runs. At the end of the first fatigue run, the rapidly releasable SR Ca2+ store fell to 46 ± 6% of the pre-fatigue value. At the end of the final fatigue run the rapidly releasable SR Ca2+ store was 109 ± 16% of the pre-fatigue value. In unstimulated fibres the nonwashable glycogen content was 176 ± 30 mmol glycosyl units/l fibre. After one fatigue run the glycogen content was 117 ± 17 mmol glycosyl units/l fibre; at the end of the final fatigue run the glycogen content was reduced to 85 ± 9 mmol glycosyl units/l fibre. [Mg2+]i did not change significantly at the end of fatigue in either the first or the final fatigue run suggesting that globally-averaged ATP does not decline substantially in either pattern of fatigue. These results suggest that different mechanisms are involved in the decline of tetanic [Ca2+]i in first compared to final fatigue runs. The SR Ca2+ store is reduced in first fatigue runs; this is not the case for the final fatigue run which is associated with a decline in glycogen and possibly related to either a non-metabolic effect of glycogen or a spatially-localised metabolic decline.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of muscle research and cell motility 21 (2000), S. 655-662 
    ISSN: 1573-2657
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract There is increasing evidence that endogenous glycogen depletion may affect excitation–contraction (E–C) coupling events in vertebrate skeletal muscle. One approach employed in physiological investigations of E–C coupling involves the use of mechanically skinned, single fibre preparations obtained from tissues stored under paraffin oil, at room temperature (RT: 20–24°C) and 4°C for several hours. In the present study, we examined the effect of these storage conditions on the glycogen content in three muscles frequently used in research on E–C coupling: rat extensor digitorum longus (EDL) and soleus (SOL) and toad iliofibularis (IF). Glycogen content was determined fluorometrically in homogenates prepared from whole muscles, stored under paraffin oil for up to 6 h at RT or 4°C. Control muscles and muscles stored for 0.5 and 6 h were also analysed for total phosphorylase (Phostotal) and phosphorylase a (Phos a) activities. No significant change was observed in the glycogen content of EDL and SOL muscles stored at RT for 0.5 h. In rat muscles stored at RT for longer than 0.5 h, the glycogen content decreased to 67.6% (EDL) and 78.7% (SOL) of controls after 3 h and 25.3% (EDL) and 37.4% (SOL) after 6 h. Rat muscles stored at 4°C retained 79.0% (EDL) and 92.5% (SOL) of glycogen after 3 h and 75.2% (EDL) and 61.1% (SOL) after 6 h. The glycogen content of IF muscles stored at RT or 4°C for 6 h was not significantly different from controls. Phostotal was unchanged in all muscles over the 6 h period, at both temperatures. Phos a was also unchanged in the toad IF muscles, but in rat muscles it decreased rapidly, particularly in EDL (4.1-fold after 0.5 h at RT). Taken together these results indicate that storage under paraffin oil for up to 6 h at RT or 4°C is accompanied by minimal glycogen loss in toad IF muscles and by a time- and temperature-dependent glycogen loss in EDL and SOL muscles of the rat.
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