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1.
Ottavia Colombo Simona Villani Giovanna Pinelli Claudia Trentani Maurizia Baldi Orazio Tomarchio Anna Tagliabue 《Nutrition journal》2008,7(1):5
Background
Excess body fat is a major risk factor for disease primarily due to its endocrine activity. In recent years several criteria have been introduced to evaluate this factor. Nevertheless, treatment need is currently assessed only on the basis of an individual's Body Mass Index (BMI), calculated as body weight (in kg) divided by height in m2. The aim of our study was to determine whether application of the BMI, compared to adiposity-based criteria, results in underestimation of the number of subjects needing lifestyle intervention. 相似文献2.
Summary The polymerization of 1-hexyne, 3,3-dimethyl-1-butyne, 2-hexyne and 1-chloro-1-hexyne by using metal halide based initiators was studied. By analogy with ionic ring opening polymerization systems, living acetylene polymerizations resulted when backbiting and interchain reactions were suppressed, i.e., ktr, kt=0. Large acetylenic substituents suppress the formation of cis-cisoidal propagating chains and subsequently eliminate backbiting reactions and also propagating carbene interchain reactions. Possible explanations for differences in polymer dispersities which result under different reaction conditions were also provided. 相似文献
3.
This paper describes the synthesis and cation-radical polymerization of 1,5-bis(1-naphthoxy)-3-oxapentane. This monomer contains a flexible diethylene oxide unit between two 1-naphthalene rings. The FT-IR analysis of the resulted polymer indicates that it contains 1,4-disubstituted naphthalene structural units, i.e. 4,4-disubstituted-1,1-binaphthalene units. The polymer is crystalline with a melting point of 236 °C.Part IX: V. Percec and J. H. Wang: J. Mater. Chem., in press 相似文献
4.
Summary Living cationic copolymerization of 11-[(4-cyano-4-biphenyl)oxy]undecanyl vinyl ether (6-11) with 2-vinyloxyethyloxy methacrylate (16-2) leads to reactive copolymers poly[(6-11)-co-(16-2)]X/Y (where X/Y is the mol ratio between the two monomers in copolymer) containing methacryloyl side groups. Upon thermal crosslinking via the polymerization of their methacryloyl side groups, the copolymers with X/Y=5/5 to 9/1 lead to liquid crystalline networks displaying a SA mesophase. These results have demonstrated that a shorter spacer in the reactive bifunctional monomer 16-2 than in the mesogenic 6-11 monomer leads to networks with broader range of mesomorphism than those derived from a reactive monomer containing a spacer length equal to that of the mesogenic monomer.This paper is part 27 in the series: Molecular engineering of liquid-crystalline polymers by living polymerization. Part 26: V. Percec, Q. Zheng: Polym. Bull., previous paper in the issue 相似文献
5.
Luiza Ghila Thomas Aga Legy Andreas Frslev Mathisen Shadab Abadpour Joao A. Paulo Hanne Scholz Helge Rder Simona Chera 《International journal of molecular sciences》2021,22(7)
The past decade revealed that cell identity changes, such as dedifferentiation or transdifferentiation, accompany the insulin-producing β-cell decay in most diabetes conditions. Mapping and controlling the mechanisms governing these processes is, thus, extremely valuable for managing the disease progression. Extracellular glucose is known to influence cell identity by impacting the redox balance. Here, we use global proteomics and pathway analysis to map the response of differentiating human pancreatic progenitors to chronically increased in vitro glucose levels. We show that exogenous high glucose levels impact different protein subsets in a concentration-dependent manner. In contrast, regardless of concentration, glucose elicits an antipodal effect on the proteome landscape, inducing both beneficial and detrimental changes in regard to achieving the desired islet cell fingerprint. Furthermore, we identified that only a subgroup of these effects and pathways are regulated by changes in redox balance. Our study highlights a complex effect of exogenous glucose on differentiating pancreas progenitors characterized by a distinct proteome signature. 相似文献
6.
7.
Summary Free radical copolymerization of acrylonitrile (AN, M1) with poly(2,6-dimethyl-1,4-phenylene oxide)--vinylbenzyl ether (PPO-VBE, M2,
n + 4200g/mol,
w/
n + 1.04) was performed at 60°C in either a mixture of N,N-dimethylformamide/toluene or tetrahydrofuran, using 2,2-azoisobutyronitrile (AIBN) as initiator. The characterization of the resulting polyacrylonitrile grafted with poly(2,6-dimethyl-1,4-phenylene oxide) (PAN-g-PPO) was performed by 200 MHz 1H-NMR spectroscopy and solubility. 相似文献
8.
Summary Three new phenothiazine-containing electrono-donor monomers: methacryloyl-2-hydroxyethyl-2-(N-phenothiazinyl)propionate (i) acryloyl-2-hydroxyethyl-2-(N-phenothiazinyl) propionate (ii) and 2-(N-phenothiazinyl) propionic acid vinyl ester (iii) were synthesized and radically polymerized. The ionization potentials of poly(i), poly(iii) and of the model for the structural unit of the acrylic polymers: acetyl-2-hydroxyethyl-2-(N-phenothiazinyl) propionate determined with two small acceptors were discussed in terms of sterical hindrances. 相似文献
9.
Simona Caudo Gabriele Centi Chiara Genovese Siglinda Perathoner 《Topics in Catalysis》2006,40(1-4):207-219
Homogeneous (Cu2+ ions) and heterogeneous (Cu2+-pillared clay) Fenton-like catalysts have been compared in the conversion of p-coumaric acid. The performances of the two classes of catalysts are similar for an analogous amount of copper, but there are
some relevant differences in terms of (i) the presence of an induction time, (ii) the turnover frequency, (iii) the efficiency
in the use of H2O2, (iv) the initial attack of p-coumaric acid (hydroxylation on the aromatic ring or oxidative attack on the double bond of the lateral chain), and (v) the
effect of dissolved oxygen on the removal of total organic carbon (TOC). These differences were interpreted in terms of reaction
network of generation of radical oxygen species and of organics conversion. The possible formation of a surface peroxo adduct
coordinated to a copper binulcear site was also evidenced for the solid heterogeneous catalyst. 相似文献
10.
A systematic reactivity study of N2O, NO, and NO2 on highly dispersed CuO phases over modified silica supports (SiO2–Al2O3, SiO2–TiO2, and SiO2–ZrO2) has been performed. Different reaction paths for the nitrogen oxide species abatement were studied: from direct decomposition (N2O) to selective reductions by hydrocarbons (N2O, NO, and NO2) and oxidation (NO to NO2). The oxygen concentration, temperature, and contact time, were varied within suitable ranges in order to investigate the activity and in particular the selectivity in the different reactions studied. The support deeply influenced the catalytic properties of the active copper phase. The most acidic supports, SiO2–Al2O3 and SiO2–ZrO2, led to a better activity and selectivity of CuO for the reactions of N2O, NO, and NO2 reductions and N2O decomposition than SiO2–TiO2. The catalytic results are discussed in terms of actual turnover frequencies starting from the knowledge of the copper dispersion values. 相似文献