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Sökning: WFRF:(Sillanpää E)

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1.
  • 2019
  • Tidskriftsartikel (refereegranskat)
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2.
  • Li, Chen, et al. (författare)
  • Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
  • 2020
  • Ingår i: American Journal of Human Genetics. - : CELL PRESS. - 0002-9297 .- 1537-6605. ; 106:3, s. 389-404
  • Tidskriftsartikel (refereegranskat)abstract
    • Leukocyte telomere length (LTL) is a heritable biomarker of genomic aging. In this study, we perform a genome-wide meta-analysis of LTL by pooling densely genotyped and imputed association results across large-scale European-descent studies including up to 78,592 individuals. We identify 49 genomic regions at a false dicovery rate (FDR) < 0.05 threshold and prioritize genes at 31, with five highlighting nucleotide metabolism as an important regulator of LTL. We report six genome-wide significant loci in or near SENP7, MOB1B, CARMIL1 , PRRC2A, TERF2, and RFWD3, and our results support recently identified PARP1, POT1, ATM, and MPHOSPH6 loci. Phenome-wide analyses in >350,000 UK Biobank participants suggest that genetically shorter telomere length increases the risk of hypothyroidism and decreases the risk of thyroid cancer, lymphoma, and a range of proliferative conditions. Our results replicate previously reported associations with increased risk of coronary artery disease and lower risk for multiple cancer types. Our findings substantially expand current knowledge on genes that regulate LTL and their impact on human health and disease.
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4.
  • Ambashta, Ritu D., et al. (författare)
  • Supported iron-based catalysts under influence of static magnetic field for the removal of TBP and EDTA
  • 2015
  • Ingår i: Desalination and Water Treatment. - : Informa UK Limited. - 1944-3994 .- 1944-3986. ; 54:10, s. 2700-2709
  • Tidskriftsartikel (refereegranskat)abstract
    • Zerovalent metals offer decontamination of organic toxins in aqueous medium. In the present study, alumina-based iron and iron-nickel in the presence and the absence of magnetic field for the decontamination of tributyl phosphate (TBP) and ethylene diamine tetraacetic acid (EDTA) has been compared. TBP decontamination was improved in the presence of zerovalent metals. EDTA decontamination was not enhanced in the presence of zerovalent metals. The decontamination of TBP using iron-based alumina was higher than iron-nickel. The surface interaction on alumina surface, as characterized by attentuated total reflectance-Fourier transform infrared spectroscopy, and the surface interaction on metallic elements, as characterized by evaluating the magnetic moment values helped to understand the reason for the difference in role of alumina-based iron and iron-nickel on decontamination of TBP and EDTA.
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5.
  • Bhatnagar, Amit, et al. (författare)
  • Heavy metals adsorption by novel EDTA-modified chitosan-silica hybrid materials
  • 2011
  • Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 358:1, s. 261-267
  • Tidskriftsartikel (refereegranskat)abstract
    • Novel adsorbents were synthesized by functionalizing chitosan-silica hybrid materials with (ethylenediaminetetraacetic acid) EDTA ligands. The synthesized adsorbents were found to combine the advantages of both silica gel (high surface area, porosity, rigid structure) and chitosan (surface functionality). The Adsorption potential of hybrid materials was investigated using Co(II), Ni(II), Cd(II), and Pb(II) as target metals by varying experimental conditions such as pH, contact time, and initial metal concentration. The kinetic results revealed that the pore diffusion process played a key role in adsorption kinetics, which might be attributed to the porous structure of synthesized adsorbents. The obtained maximum adsorption capacities of the hybrid materials for the metal ions ranged from 0.25 to 0.63 mmol/g under the studied experimental conditions. The adsorbent with the highest chitosan content showed the best adsorption efficiency. Bi-Langmuir and Sips isotherm model fitting to experimental data suggested the surface heterogeneity of the prepared adsorbents. In multimetal solutions, the hybrid adsorbents showed the highest affinity toward Pb(II).
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6.
  • Bhatnagar, Amit, et al. (författare)
  • Removal of phenolic pollutants from water utilizing Mangifera indica (Mango) seed waste and cement fixation
  • 2009
  • Ingår i: Separation science and technology (Print). - : Informa UK Limited. - 0149-6395 .- 1520-5754. ; 44:13, s. 3150-3169
  • Tidskriftsartikel (refereegranskat)abstract
    • A process for the removal of two chlorophenols (2-chlorophenol and 2,4-dichlorophenol) from water using surface modified mango seed waste by adsorption process followed by cement fixation of the phenols-laden adsorbent is investigated. The two main objectives of this study were to develop efficient adsorbent utilizing mango seed waste by physiochemical activation and to an environmentally-friendly disposal of phenols-laden adsorbent into cement by a fixation process. The results of the present study reveal that the modified mango seed adsorbent showed an efficient adsorption potential for chlorophenols removal from water. The maximum adsorption potential of modified mango seed adsorbent for 2-chlorophenol and 2,4-dichlorophenol was 40.6 and 72.3 mg g−1, respectively at 25°C. Adsorption kinetic data of chlorophenols adsorption on mango seed adsorbent could be described more favorably by a pseudo-second-order kinetic model. After the adsorption studies, the phenol-laden adsorbent was immobilized in cement for its ultimate disposal. Leachates from the fixed phenols-laden adsorbent exhibit phenols concentrations lower than the drinking water standards. Results from this study suggest the potential utility of agricultural wastes as one of the most promising activated carbon precursors for phenols removal from water and wastewater and the safe disposal of phenol-laden adsorbent into cement by fixation process.
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7.
  • Clark, M. S., et al. (författare)
  • Deciphering mollusc shell production: the roles of genetic mechanisms through to ecology, aquaculture and biomimetics
  • 2020
  • Ingår i: Biological Reviews. - : Wiley. - 1464-7931 .- 1469-185X. ; 95:6, s. 1812-37
  • Tidskriftsartikel (refereegranskat)abstract
    • Most molluscs possess shells, constructed from a vast array of microstructures and architectures. The fully formed shell is composed of calcite or aragonite. These CaCO(3)crystals form complex biocomposites with proteins, which although typically less than 5% of total shell mass, play significant roles in determining shell microstructure. Despite much research effort, large knowledge gaps remain in how molluscs construct and maintain their shells, and how they produce such a great diversity of forms. Here we synthesize results on how shell shape, microstructure, composition and organic content vary among, and within, species in response to numerous biotic and abiotic factors. At the local level, temperature, food supply and predation cues significantly affect shell morphology, whilst salinity has a much stronger influence across latitudes. Moreover, we emphasize how advances in genomic technologies [e.g. restriction site-associated DNA sequencing (RAD-Seq) and epigenetics] allow detailed examinations of whether morphological changes result from phenotypic plasticity or genetic adaptation, or a combination of these. RAD-Seq has already identified single nucleotide polymorphisms associated with temperature and aquaculture practices, whilst epigenetic processes have been shown significantly to modify shell construction to local conditions in, for example, Antarctica and New Zealand. We also synthesize results on the costs of shell construction and explore how these affect energetic trade-offs in animal metabolism. The cellular costs are still debated, with CaCO(3)precipitation estimates ranging from 1-2 J/mg to 17-55 J/mg depending on experimental and environmental conditions. However, organic components are more expensive (similar to 29 J/mg) and recent data indicate transmembrane calcium ion transporters can involve considerable costs. This review emphasizes the role that molecular analyses have played in demonstrating multiple evolutionary origins of biomineralization genes. Although these are characterized by lineage-specific proteins and unique combinations of co-opted genes, a small set of protein domains have been identified as a conserved biomineralization tool box. We further highlight the use of sequence data sets in providing candidate genes forin situlocalization and protein function studies. The former has elucidated gene expression modularity in mantle tissue, improving understanding of the diversity of shell morphology synthesis. RNA interference (RNAi) and clustered regularly interspersed short palindromic repeats - CRISPR-associated protein 9 (CRISPR-Cas9) experiments have provided proof of concept for use in the functional investigation of mollusc gene sequences, showing for example that Pif (aragonite-binding) protein plays a significant role in structured nacre crystal growth and that theLsdia1gene sets shell chirality inLymnaea stagnalis. Much research has focused on the impacts of ocean acidification on molluscs. Initial studies were predominantly pessimistic for future molluscan biodiversity. However, more sophisticated experiments incorporating selective breeding and multiple generations are identifying subtle effects and that variability within mollusc genomes has potential for adaption to future conditions. Furthermore, we highlight recent historical studies based on museum collections that demonstrate a greater resilience of molluscs to climate change compared with experimental data. The future of mollusc research lies not solely with ecological investigations into biodiversity, and this review synthesizes knowledge across disciplines to understand biomineralization. It spans research ranging from evolution and development, through predictions of biodiversity prospects and future-proofing of aquaculture to identifying new biomimetic opportunities and societal benefits from recycling shell products.
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8.
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9.
  • Hokkanen, S., et al. (författare)
  • Adsorption of Ni2+, Cd2+, PO4 3- and NO3 - from aqueous solutions by nanostructured microfibrillated cellulose modified with carbonated hydroxyapatite
  • 2014
  • Ingår i: Chemical Engineering Journal. - : Elsevier BV. - 1385-8947. ; 252, s. 64-74
  • Tidskriftsartikel (refereegranskat)abstract
    • The adsorption of Ni2+, Cd2+, PO4 3- and NO3 - by carbonated hydroxyapatite (CHA) modified microfibrillated cellulose (MFC) was studied in the aqueous solution. The modified adsorbent was characterized using elemental analysis, FTIR, SEM and EDAX analysis. The adsorption studies were conducted in batch mode. The effects of pH, contact time, the concentration of metals and the regeneration efficiency were studied. The removal of Ni2+, Cd2+, PO4 3- and NO3 - was not pH dependent. The maximum removal capacities of the CHA/MFC adsorbent for Ni2+, Cd2+, PO4 3- and NO3 - were 2.021, 1.224, 0.843 and 0.209mmol/g, respectively. The Langmuir and Sips models were representative to simulate adsorption isotherms. The results of adsorption kinetic indicate that adsorption was very fast for all studied compounds.
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10.
  • Hossain, Kamal, et al. (författare)
  • Syntheses and catalytic oxotransfer actiVIties of oxo molybdenum(VI) complexes of a new aminoalcohol phenolate ligand
  • 2017
  • Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; 46:21, s. 7051-7060
  • Tidskriftsartikel (refereegranskat)abstract
    • The new aminoalcohol phenol 2,4-di-tert-butyl-6-(((2-hydroxy-2-phenylethyl)amino)methyl)phenol (H2L) was prepared by a facile solvent-free synthesis and used as a tridentate ligand for new cis-dioxomolybdenum(vi)(L) complexes. In the presence of a coordinating solvent (DMSO, MeOH, pyridine), the complexes crystallise as monomeric solvent adducts while in the absence of such molecules, a trimer with asymmetric MoO→Mo bridges crystallises. The complexes can catalyse epoxidation of cis-cyclooctene and sulfoxidation of methyl-p-tolylsulfide, using tert-butyl hydroperoxide as oxidant.
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