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  • 2005-2009  (5)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    International journal of dermatology 44 (2005), S. 0 
    ISSN: 1365-4632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background  Cryotherapy and intralesional corticosteroids have been used separately or in combination as a treatment for hypertrophic and keloidal scars. The addition of silicone gel to the treatment schedule might be of interest.Methods  Twenty patients with hypertrophic and keloidal scars received two 15-s cycles (in total 30 s) of cryotherapy treatments at every session (once monthly for 12 months) with intralesional injections of trimcinolone acetonide 0.1% (10–40 mg/mL, once monthly for 3 months). Topical application of silicone gel was added three times daily (for 12 months). The control group included 10 patients who received treatment with silicone sheeting.Results  After 1 year there was improvement in all the parameters studied, especially in terms of symptoms, cosmetic appearance and associated signs (P 〈 0.0001) compared to baseline and compared to the control group.Conclusion  Our study suggests that polytherapy may be an effective tool in the therapy of hypertrophic and keloidal scars.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2018-03-07
    Description: Structure-based inhibitor design has led to the discovery of a number of potent inhibitors of glycogen phosphorylase b (GPb), N-acyl derivatives of β-d-glucopyranosylamine, that bind at the catalytic site of the enzyme. The first good inhibitor in this class of compounds, N-acetyl-β-d-glucopyranosylamine (NAG) (Ki = 32 μM), has been previously characterized by biochemical, biological and crystallographic experiments at 2.3 Å resolution. Bioisosteric replacement of the acetyl group by trifluoroacetyl group resulted in an inhibitor, N-trifluoroacetyl-β-d-glucopyranosylamine (NFAG), with a Ki = 75 μM. To elucidate the structural basis of its reduced potency, we determined the ligand structure in complex with GPb at 1.8 Å resolution. To compare the binding mode of N-trifluoroacetyl derivative with that of the lead molecule, we also determined the structure of GPb–NAG complex at a higher resolution (1.9 Å). NFAG can be accommodated in the catalytic site of T-state GPb at approximately the same position as that of NAG and stabilize the T-state conformation of the 280s loop by making several favourable contacts to Asn284 of this loop. The difference observed in the Ki values of the two analogues can be interpreted in terms of subtle conformational changes of protein residues and shifts of water molecules in the vicinity of the catalytic site, variations in van der Waals interaction, and desolvation effects.
    Type: Article , PeerReviewed
    Format: text
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  • 3
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    American Society of Limnology and Oceanography
    In:  Limnology and Oceanography: Methods, 6 . pp. 64-74.
    Publication Date: 2018-03-06
    Description: A freshwater magnesium hydroxide coprecipitation method (MAGIC) has been developed to accurately and reproducibly determine low (nanomolar to subnanomolar) soluble reactive phosphorus (SRP) concentrations in freshwater. The method allows investigation of phosphorus distributions and cycling for systems in which SRP is below the detection limits of conventional methods. In natural waters, both inorganic and organic forms of P are coprecipitated; hence the method is essentially a preconcentration rather than a separation technique. Quantification of SRP on dissolved MAGIC precipitates follows a modified version of the standard molybdenum blue colorimetric method, using a spectrophotometer with ~0.1 milliabsorbance (mAbs) noise. Detection limit is 0.15 nM, improving on typical conventional colorimetric methods by a factor of ~50, with precision (RSD of triplicates) of ~10% at the 1 nM SRP level, 10% at ≤0.5 nM, and 4% to 7% at 〉1 nM. Considerable method development was necessary to eliminate or correct for multiple interferences, including a novel finding of potential interference by colored dissolved organic matter, and to optimize recovery, precision, and detection limit. The method was applied to filtered, frozen samples from western Lake Superior, showing that SRP concentrations are characterized by limited seasonal variability, largely uniform vertical distribution, and near-bottom enrichment. Concentrations ranged from 0.4 to 10.9 nM SRP, representing ~10% of the total dissolved phosphorus pool. MAGIC is an easily employed analytical method appropriate for measurement of very low SRP in lakes and rivers.
    Type: Article , PeerReviewed
    Format: text
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  • 4
    Publication Date: 2018-03-07
    Description: The supply of limiting nutrients to the low latitude ocean is controlled by physical processes linked to climate variations, but methods for reconstructing past nutrient concentrations in the surface ocean are few and indirect. Here, we present laser ablation mass spectrometry results that reveal annual cycles of P/Ca in a 4-year record from the scleractinian coral Pavona gigantea (mean P/Ca = 118 μmol mol−1). The P/Ca cycles track variations in past seawater phosphate concentration synchronously with skeletal Sr/Ca-derived temperature variations associated with seasonal upwelling in the Gulf of Panamá. Skeletal P/Ca varies seasonally by 2–3 fold, reflecting the timing and magnitude of dissolved phosphate variations. Solution cleaning experiments on drilled coral powders show that over 60% of skeletal P occurs in intracrystalline organic phases. Coral skeleton P/Ca holds promise as a proxy record of nutrient availability on time scales of decades to millennia.
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2018-03-06
    Description: Lake Superior has exhibited a continuous, century-long increase in nitrate whereas phosphate remains at very low levels. Increasing nitrate and low phosphate has led to a present-day severe stoichiometric imbalance; Lake Superior's deepwater NO3−:PO43− molar ratio is 10,000, more than 600 times the mean requirement ratio for primary producers. We examine the rate of [NO3−] increase relative to budgets for NO3− and fixed N. Nitrate in Lake Superior has continued to rise since 1980, though possibly at a reduced rate. We constructed whole-lake NO3− and N budgets and found that NO3− must be generated in the lake at significant rates. Stable O isotope results indicate that most NO3− in the lake originated by in-lake oxidation. Nitrate in the lake is responding not just to NO3− loading but also to oxidation of reduced forms of nitrogen delivered to the lake. The increasing [NO3−]:[PO43−] stoichiometric imbalance in this large lake is largely determined by these in-situ processes.
    Type: Article , PeerReviewed
    Format: text
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