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Hypoglycemia Abrogates the Vascular Endothelial Protective Effect of Exenatide in Type 2 Diabetes Mellitus
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Molecular Transformations of Unsaturated Thiacrown Ethers
Unsaturated thiacrown ethers with 15, 18, and 21 members were oxidized to sulfoxides by the reaction
with m-CPBA. The reaction with t-BuOCl at −20 °C also afforded sulfoxides, whereas the reaction at
room temperature yielded cis−trans isomerized compounds. The cis−trans isomerized compound was
also obtained by the photochemical reaction or by the reaction with NCS and NCP. Meanwhile, the
reaction with NBS and NBP provided an acetal via 1,2-bridged bromonium intermediate
Molecular Transformations of Unsaturated Thiacrown Ethers
Unsaturated thiacrown ethers with 15, 18, and 21 members were oxidized to sulfoxides by the reaction
with m-CPBA. The reaction with t-BuOCl at −20 °C also afforded sulfoxides, whereas the reaction at
room temperature yielded cis−trans isomerized compounds. The cis−trans isomerized compound was
also obtained by the photochemical reaction or by the reaction with NCS and NCP. Meanwhile, the
reaction with NBS and NBP provided an acetal via 1,2-bridged bromonium intermediate
Molecular Transformations of Unsaturated Thiacrown Ethers
Unsaturated thiacrown ethers with 15, 18, and 21 members were oxidized to sulfoxides by the reaction
with m-CPBA. The reaction with t-BuOCl at −20 °C also afforded sulfoxides, whereas the reaction at
room temperature yielded cis−trans isomerized compounds. The cis−trans isomerized compound was
also obtained by the photochemical reaction or by the reaction with NCS and NCP. Meanwhile, the
reaction with NBS and NBP provided an acetal via 1,2-bridged bromonium intermediate
Molecular Transformations of Unsaturated Thiacrown Ethers
Unsaturated thiacrown ethers with 15, 18, and 21 members were oxidized to sulfoxides by the reaction
with m-CPBA. The reaction with t-BuOCl at −20 °C also afforded sulfoxides, whereas the reaction at
room temperature yielded cis−trans isomerized compounds. The cis−trans isomerized compound was
also obtained by the photochemical reaction or by the reaction with NCS and NCP. Meanwhile, the
reaction with NBS and NBP provided an acetal via 1,2-bridged bromonium intermediate
Molecular Transformations of Unsaturated Thiacrown Ethers
Unsaturated thiacrown ethers with 15, 18, and 21 members were oxidized to sulfoxides by the reaction
with m-CPBA. The reaction with t-BuOCl at −20 °C also afforded sulfoxides, whereas the reaction at
room temperature yielded cis−trans isomerized compounds. The cis−trans isomerized compound was
also obtained by the photochemical reaction or by the reaction with NCS and NCP. Meanwhile, the
reaction with NBS and NBP provided an acetal via 1,2-bridged bromonium intermediate
Supplementary data for "Pathological role of Th17 cells in Graves' disease."
Supplementary data for "Pathological role of Th17 cells in Graves' disease.
IL-17 suppressed the expression of chondrogenic marker genes.
<p>Human MSCs were cultured as aggregates in TGF-β3-containing medium with the indicated concentrations of IL-17. After 14 days, type II collagen (<i>COL2A1</i>), aggrecan (<i>ACAN</i>), type X collagen (<i>COL10A1</i>), and alkaline phosphatase (<i>ALP</i>) mRNA levels were determined by real-time PCR and expressed relative to β-actin expression level. Values are mean±SD of 3 aggregates from 1 of 3 independent experiments with similar findings.</p
IL-17 treatment reduces PKA activity during chondrogenesis.
<p>A, Human MSCs were cultured as aggregates with TGF-β3 in the presence of IL-17 (100 ng/mL) or H89 (10 µM). After 7 days, 3 aggregates were pooled and lysed in each group, and PKA activity within the soluble protein fraction was determined using PepTag non-radioactive PKA assay (top). Recombinant PKA catalytic subunit (2 µg/mL) was used as a positive control and water was used as a negative control. Densitometric analyses of the band intensities were performed and results were expressed as the test band intensity relative to that of the “no TGF-β3” sample (bottom). B, The DNA content of three aggregates in each group was measured after 7-day culture. Values shown in A and B are mean±SD of three independent experiments. **<i>P<</i>0.01 compared to no cytokine (+TGF-β3), by Dunnett’s multiple comparison test.</p
PKA activation is required for chondrogenic differentiation of human MSCs.
<p>A, Paraffin sections from aggregates cultured in the presence of 10 µM H89 for 21 days were stained with Safranin O and anti-type II collagen antibody. Original magnification×10. Scale bars represent 500 µm. B, <i>COL2A1, ACAN, COL10A1</i>, and <i>ALP</i> mRNA levels in aggregates treated with the indicated concentrations of H89 for 21 days were determined by real-time PCR. Values are mean±SD of three aggregates from 1 of 2 independent experiments with similar findings. See <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0079463#pone-0079463-g001" target="_blank">Figures 1</a> and <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0079463#pone-0079463-g002" target="_blank">2</a> for the definition of other symbols.</p
