Methionine synthase reductase polymorphisms are associated with serum osteocalcin levels in postmenopausal women

Homocysteine (Hcy) is thought to play an important role in the development of osteoporosis and fracture. Methionine synthase reductase (MTRR) is an enzyme involved in the conversion of Hcy to methionine. We hypothesized that certain genetic polymorphisms of MTRR leading to reduced enzyme activity may cause hyperhomocysteinemia and affect bone metabolism. We therefore examined the associations of the A66G and C524T polymorphisms of the MTRR gene with bone mineral density (BMD) and serum osteocalcin levels in postmenopausal women. Although we did not detect any significant associations between MTRR polymorphisms and BMD or serum osteocalcin levels, we found that the 66G/524C haplotype, which has reduced enzyme activity, was significantly associated with serum osteocalcin levels in a gene-dose dependent manner (P = 0.002). That is, the highest osteocalcin levels (34.5 +/- 16.8 ng/ml) were observed in subjects bearing two copies, intermediate osteocalcin levels (32.6 +/- 14.4 ng/ml) were observed in subjects bearing one copy, and the lowest levels of osteocalcin (28.8 +/- 10.9 ng/ml) were observed in subjects bearing no copies. These results suggest that the 66G/524C haplotype of the MTRR gene affect bone turn over rate.     

Eta1 and eta2 complexes of lambda3-1,2,4,6-thiatriazinyls with CpCr(CO)x

The title heterocyclic radicals coordinate to either 17e CpCr(CO)3 or 15e CpCr(CO)2 moieties as one-electron or as three-electron donors, respectively; in the former the bonding is via the perpendicular p orbital of the sulfur atom, while in the latter bonding is via p(pi) orbitals on both sulfur and nitrogen.     

Euler calculations with embedded Cartesian grids and small-perturbation boundary conditions

This study examines the use of stationary Cartesian mesh for steady and unsteady flow computations. The surface boundary conditions are imposed by reflected points. A cloud of nodes in the vicinity of the surface is used to get a weighted average of the flow properties via a gridless least-squares technique. If the displacement of the moving surface from the original position is typically small, a small-perturbation boundary condition method can be used. To ensure computational efficiency, multigrid solution is made via a framework of embedded grids for local grid refinement. Computations of airfoil wing and wing-body test cases show the practical usefulness of the embedded Cartesian grids with the small-perturbation boundary conditions approach.     

Triode field emitters with planar carbon-nanoparticle cathodes

We designed and fabricated three different types of triode field emitters with planar carbon-nanoparticle (CNP) cathodes such as a normal-gate structure, a double-gate structure, and a well-structure. A normal-gate structure CNP triode emitter showed good field emission properties. The field emission started at the gate-voltage of 45 V, and the anode current reached the level of 120 nA at the gate-voltage of 60 V. However, in general, normal-gate structure suffered from large gate current. Using the double-gate structure, we successfully reduced the gate current to the level less than 4% of anode currents up to the anode current of 250 nA. To simplify fabrication process while maintaining the gate current reduction effect of the double-gate structure, a triode emitter with a well-structure cathode was fabricated via reactive-ion etching of a heavily doped n-type silicon wafer. The triode emitter with a well-structure cathode and a recessed gate structure showed negligible gate current.     

An Upper Bound for the Total Restrained Domination Number of Graphs

Let G be a graph with vertex set V. A set ${D \subseteq V}$ is a total restrained dominating set of G if every vertex in V has a neighbor in D and every vertex in ${V \setminus D}$ has a neighbor in ${V \setminus D}$ . The minimum cardinality of a total restrained dominating set of G is called the total restrained domination number of G, and is denoted by γ _tr (G). In this paper, we prove that if G is a connected graph of order n ≥ 4 and minimum degree at least two, then ${\gamma_{tr}(G) \leq n-\sqrt[3]{n \over 4}}$ .     

Mesogenic Schiff base esters with benzothiazole core: synthesis and phase transition studies

A series of new rod-shaped mesomorphic compounds, 6-ethoxy-2-(4-alkanoyloxybenzylidenamino)benzothiazoles, consisting of a 2,6-disubstituted benzothiazole core and a Schiff base central linkage, were synthesized and their structures were ascertained via elemental analysis and spectroscopic techniques. Their mesomorphic properties were studied using differential scanning calorimetry (DSC), polarized optical microscopy (POM) and X-ray diffraction (XRD) analysis. All compounds showed enantiotropic mesomorphism. Whilst the lower members of the series, hexanoyloxy and octanoyloxy derivatives exhibited nematic phase, the higher members (decanoyloxy, dodecanoyloxy, tetradecanoyloxy, hexadecanoyloxy and octadecanoyloxy derivatives) exhibited nematic and smectic C phases.     

The Effect of a Finite Interaction Cross-Section on the Hanle Signal

Hanle technique is used for the lifetime measurement of the atomic excited states. Field dependent Hanle signal is Lorentzian under ideal conditions. Any departure from ideal situation is reflected in the shape of the Hanle signal resulting in erroreous measurements. The effect of one such factor, a finite interaction cross section, is discussed here.     

Idempotents in a compact ring

In this paper we investigate stable range conditions by virtue of elements in 2-dimensional general linear groups. Also we give the substitutions of modules over rings with stable range conditions. As an application, we prove that 2-fold stable condition is left-right symmetric.     

Strain‐Induced Isomerization in One‐Dimensional Metal–Organic Chains

The ability to use mechanical strain to steer chemical reactions creates completely new opportunities for solution‐ and solid‐phase synthesis of functional molecules and materials. However, this strategy is not readily applied in the bottom‐up on‐surface synthesis of well‐defined nanostructures. We report an internal strain‐induced skeletal rearrangement of one‐dimensional (1D) metal–organic chains (MOCs) via a concurrent atom shift and bond cleavage on Cu(111) at room temperature. The process involves Cu‐catalyzed debromination of organic monomers to generate 1,5‐dimethylnaphthalene diradicals that coordinate to Cu adatoms, forming MOCs with both homochiral and heterochiral naphthalene backbone arrangements. Bond‐resolved non‐contact atomic force microscopy imaging combined with density functional theory calculations showed that the relief of substrate‐induced internal strain drives the skeletal rearrangement of MOCs via 1,3‐H shifts and shift of Cu adatoms that enable migration of the monomer backbone toward an energetically favorable registry with the Cu(111) substrate. Our findings on this strain‐induced structural rearrangement in 1D systems will enrich the toolbox for on‐surface synthesis of novel functional materials and quantum nanostructures.