Magnetic and electrical properties of NdNiSn

Magnetization and resistivity measurements have been carried out on the equiatomic ternary compound NdNiSn in the temperature range 2–200 K. The compound crystallizes in the orthorhombic CeNiSn-type structure with space group Pna21. Magnetic susceptibility shows a distinct feature at TN=3 K (Néel temperature), typical of a phase transition from an antiferromagnetic to paramagnetic state. In the paramagnetic regime, the magnetic susceptibility obeys Curie–Weiss behavior yielding an effective magnetic moment μeff=3.32μB at lower temperatures, and 3.88 μB at higher temperatures. The reduction in the magnetic moment at lower temperatures is attributed to a crystalline electric field (CEF) effect, while the slight excess of magnetic moment at high temperatures compared to that of the free Nd3+ ion (3.62 μB) indicates that only a very small magnetic moment, at most 0.3 μB, is induced at the Ni sites. The electrical resistivity exhibits metallic behavior and no anomaly is observed at the respective Néel temperature. Analysis of the resistivity data in terms of crystalline electric fields including s–d electron scattering reveals that the ground magnetic state for the Nd3+ ions is a doublet of J=±5/2 states, with a first exited doublet of J=±7/2 states having an energy splitting of 56 K, with the next exited multiplet 139 K above the ground levels. These results are in fairly good agreement with those reported in the literature based on magnetic susceptibility and heat capacity measurements

Effect of exchange bias on the electrical resistivity of Pd doped NiMn thin films: Two-Channel Kondo system

Electrical resistivity measurements have been carried out for both flash-evaporated reentrant spin glasses (RSGs) (Ni76−xPdx)Mn24 and Ni74.5Mn23.5Pd2, as well as Ni75Mn23Pd2, a pure SG. These measurements were carried out at temperatures down to 4K. We observed a very deep resistivity minimum at about 75K for Ni74Mn24Pd2. It was found previously [Öner et al., J. Appl. Phys.89, 7044 (2001)] that this sample shows the largest coercivity and exchange unidirectional anisotropy among these films. In addition, magnetization measurements show that this takes place just on the border of the RSG such that it could be handled as a superparamagnetic sample. Previously it was assumed that the exchange bias created in the sample between the domains plays the dominant role in the resistivity minimum. On the other hand, in order to account for the temperature dependence of the resistivity below the minimum we have analyzed these data using the Kondo, two-channel Kondo, weak localization, and Cochrane models for structural disorder based on the Anderson mechanism. We have deduced that the two-channel Kondomodel gives the best agreement with the data; a logarithmic temperature dependence Δρ(T)=βlog10(T∕TK), was observed at the temperatures below Tf accompanied by a resistivity behavior Δρ(T)=ρ0m(0)(1−αT1∕2), at lower temperatures. All parameters deduced from the fitting correlate consistently with the strength of the exchange anisotropy and coercivity in the RSG films, and thus provide a separate measure of the presence of antiferromagnetically coupled domains in these materials

Dietary elimination of children with food protein induced gastrointestinal allergy – micronutrient adequacy with and without a hypoallergenic formula?

Background: The cornerstone for management of Food protein-induced gastrointestinal allergy (FPGIA) is dietary exclusion; however the micronutrient intake of this population has been poorly studied. We set out to determine the dietary intake of children on an elimination diet for this food allergy and hypothesised that the type of elimination diet and the presence of a hypoallergenic formula (HF) significantly impacts on micronutrient intake. Method: A prospective observational study was conducted on children diagnosed with FPIGA on an exclusion diet who completed a 3 day semi-quantitative food diary 4 weeks after commencing the diet. Nutritional intake where HF was used was compared to those without HF, with or without a vitamin and mineral supplement (VMS). Results: One-hundred-and-five food diaries were included in the data analysis: 70 boys (66.7%) with median age of 21.8 months [IQR: 10 - 67.7]. Fifty-three children (50.5%) consumed a HF and the volume of consumption was correlated to micronutrient intake. Significantly (p <0.05) more children reached their micronutrient requirements if a HF was consumed. In those without a HF, some continued not to achieve requirements in particular for vitamin D and zinc, in spite of VMS. Conclusion: This study points towards the important micronutrient contribution of a HF in children with FPIGA. Children, who are not on a HF and without a VMS, are at increased risk of low intakes in particular vitamin D and zinc. Further studies need to be performed, to assess whether dietary intake translates into actual biological deficiencies

Functional Analysis of Conserved Motifs in Influenza Virus PB1 Protein

The influenza virus RNA polymerase complex is a heterotrimer composed of the PB1, PB2, and PA subunits. PB1, the catalytic core and structural backbone of the polymerase, possesses four highly conserved amino acid motifs that are present among all viral RNA-dependent RNA polymerases. A previous study demonstrated the importance of several of these conserved amino acids in PB1 for influenza polymerase activity through mutational analysis. However, a small number of viruses isolated in nature possesses non-consensus amino acids in one of the four motifs, most of which have not been tested for their replicative ability. Here, we assessed the transcription/replication activities of 25 selected PB1 mutations found in natural isolates by using minireplicon assays in human and avian cells. Most of the mutations tested significantly reduced polymerase activity. One exception was mutation K480R, observed in several pandemic (H1N1) 2009 viruses, which slightly increased polymerase activity relative to wild-type. However, in the background of the pandemic A/California/04/2009 (H1N1) virus, this mutation did not affect virus titers in cell culture. Our results further demonstrate the functional importance of the four conserved PB1 motifs in influenza virus transcription/replication. The finding of natural isolates with non-consensus PB1 motifs that are nonfunctional in minireplicon assays suggests compensatory mutations and/or mixed infections which may have ‘rescued’ the inactive PB1 protein

The Mitochondrial Ca(2+) Uniporter: Structure, Function, and Pharmacology.

Mitochondrial Ca(2+) uptake is crucial for an array of cellular functions while an imbalance can elicit cell death. In this chapter, we briefly reviewed the various modes of mitochondrial Ca(2+) uptake and our current understanding of mitochondrial Ca(2+) homeostasis in regards to cell physiology and pathophysiology. Further, this chapter focuses on the molecular identities, intracellular regulators as well as the pharmacology of mitochondrial Ca(2+) uniporter complex

MICU2, a Paralog of MICU1, Resides within the Mitochondrial Uniporter Complex to Regulate Calcium Handling

Mitochondrial calcium uptake is present in nearly all vertebrate tissues and is believed to be critical in shaping calcium signaling, regulating ATP synthesis and controlling cell death. Calcium uptake occurs through a channel called the uniporter that resides in the inner mitochondrial membrane. Recently, we used comparative genomics to identify MICU1 and MCU as the key regulatory and putative pore-forming subunits of this channel, respectively. Using bioinformatics, we now report that the human genome encodes two additional paralogs of MICU1, which we call MICU2 and MICU3, each of which likely arose by gene duplication and exhibits distinct patterns of organ expression. We demonstrate that MICU1 and MICU2 are expressed in HeLa and HEK293T cells, and provide multiple lines of biochemical evidence that MCU, MICU1 and MICU2 reside within a complex and cross-stabilize each other's protein expression in a cell-type dependent manner. Using in vivo RNAi technology to silence MICU1, MICU2 or both proteins in mouse liver, we observe an additive impairment in calcium handling without adversely impacting mitochondrial respiration or membrane potential. The results identify MICU2 as a new component of the uniporter complex that may contribute to the tissue-specific regulation of this channel.National Institutes of Health (U.S.) (GM0077465)National Institutes of Health (U.S.) (DK080261

TMPRSS2/ERG Promotes Epithelial to Mesenchymal Transition through the ZEB1/ZEB2 Axis in a Prostate Cancer Model

Prostate cancer is the most common non-dermatologic malignancy in men in the Western world. Recently, a frequent chromosomal aberration fusing androgen regulated TMPRSS2 promoter and the ERG gene (TMPRSS2/ERG) was discovered in prostate cancer. Several studies demonstrated cooperation between TMPRSS2/ERG and other defective pathways in cancer progression. However, the unveiling of more specific pathways in which TMPRSS2/ERG takes part, requires further investigation. Using immortalized prostate epithelial cells we were able to show that TMPRSS2/ERG over-expressing cells undergo an Epithelial to Mesenchymal Transition (EMT), manifested by acquisition of mesenchymal morphology and markers as well as migration and invasion capabilities. These findings were corroborated in vivo, where the control cells gave rise to discrete nodules while the TMPRSS2/ERG-expressing cells formed malignant tumors, which expressed EMT markers. To further investigate the general transcription scheme induced by TMPRSS2/ERG, cells were subjected to a microarray analysis that revealed a distinct EMT expression program, including up-regulation of the EMT facilitators, ZEB1 and ZEB2, and down-regulation of the epithelial marker CDH1(E-Cadherin). A chromatin immunoprecipitation assay revealed direct binding of TMPRSS2/ERG to the promoter of ZEB1 but not ZEB2. However, TMPRSS2/ERG was able to bind the promoters of the ZEB2 modulators, IL1R2 and SPINT1. This set of experiments further illuminates the mechanism by which the TMPRSS2/ERG fusion affects prostate cancer progression and might assist in targeting TMPRSS2/ERG and its downstream targets in future drug design efforts

A Search for a Narrow Radial Excitation of the D∗±D^{*\pm} Meson

A sample of 3.73 million hadronic Z decays, recorded with the OPAL detector at LEP in the years 1991-95, has been used to search for a narrow resonance corresponding to the decay of the D*'+/-(2629) meson into D*+/- pi+ pi-. The D*+ mesons are reconstructed in the decay channel D*+ -> D0 pi+ with D0 -> K- pi+. No evidence for a narrow D*'+/-(2629) resonance is found. A limit on the production of D*'+/-(2629) in hadronic Z decays is derived: f(Z -> D*'+/-(2629)) x Br(D*'+ -> D*+ pi+ pi-) D0 pi+ with D0 -> K- pi+. No evidence for a narrow D*'+/-(2629) resonance is found. A limit on the production of D*'+/-(2629) in hadronic Z decays is derived: f(Z -> D*'+/-(2629)) x Br(D*'+ -> D*+ pi+ pi-) < 3.1 x 10^{-3} (95% C.L.