2,525 research outputs found
Spin relaxation in mesoscopic superconducting Al wires
We studied the diffusion and the relaxation of the polarized quasiparticle
spins in superconductors. To that end, quasiparticles of polarized spins were
injected through an interface of a mesoscopic superconducting Al wire in
proximity contact with an overlaid ferromagnetic Co wire in the single-domain
state. The superconductivity was observed to be suppressed near the
spin-injecting interface, as evidenced by the occurrence of a finite voltage
for a bias current below the onset of the superconducting transition. The spin
diffusion length, estimated from finite voltages over a certain length of Al
wire near the interface, was almost temperature independent in the temperature
range sufficiently below the superconducting transition but grew as the
transition temperature was approached. This temperature dependence suggests
that the relaxation of the spin polarization in the superconducting state is
governed by the condensation of quasiparticles to the paired state. The spin
relaxation in the superconducting state turned out to be more effective than in
the normal state.Comment: 9 pages, 8 figure
Kondo-like behaviors in magnetic and thermal properties of single crystal Tm5Si2Ge2
We grew the single crystal of stoichiometric Tm5Si2.0Ge2.0 using a Bridgeman
method and performed XRD, EDS, magnetization, ac and dc magnetic
susceptibilities, specific heat, electrical resistivity and XPS experiments. It
crystallizes in orthorhombic Sm5Ge4-type structure. The mean valence of Tm ions
in Tm5Si2.0Ge2.0 is almost trivalent. The 4f states is split by the crystalline
electric field. The ground state exhibits the long range antiferromagnetic
order with the ferromagnetically coupled magnetic moments in the ac plane below
8.01 K, while the exited states exhibit the reduction of magnetic moment and
magnetic entropy and -log T-behaviors observed in Kondo materials.Comment: 8 pages, 13 figure
Anatomical evaluation of CT-MRI combined femoral model
<p>Abstract</p> <p>Background</p> <p>Both CT and MRI are complementary to each other in that CT can produce a distinct contour of bones, and MRI can show the shape of both ligaments and bones. It will be ideal to build a CT-MRI combined model to take advantage of complementary information of each modality. This study evaluated the accuracy of the combined femoral model in terms of anatomical inspection.</p> <p>Methods</p> <p>Six normal porcine femora (180 ± 10 days, 3 lefts and 3 rights) with ball markers were scanned by CT and MRI. The 3D/3D registration was performed by two methods, i.e. the landmark-based 3 points-to-3 points and the surface matching using the iterative closest point (ICP) algorithm. The matching accuracy of the combined model was evaluated with statistical global deviation and locally measure anatomical contour-based deviation. Statistical analysis to assess any significant difference between accuracies of those two methods was performed using univariate repeated measures ANOVA with the Turkey post hoc test.</p> <p>Results</p> <p>This study revealed that the local 2D contour-based measurement of matching deviation was 0.5 ± 0.3 mm in the femoral condyle, and in the middle femoral shaft. The global 3D contour matching deviation of the landmark-based matching was 1.1 ± 0.3 mm, but local 2D contour deviation through anatomical inspection was much larger as much as 3.0 ± 1.8 mm.</p> <p>Conclusion</p> <p>Even with human-factor derived errors accumulated from segmentation of MRI images, and limited image quality, the matching accuracy of CT-&-MRI combined 3D models was 0.5 ± 0.3 mm in terms of local anatomical inspection.</p
Genetic Effects of FTO and MC4R Polymorphisms on Body Mass in Constitutional Types
Sasang constitutional medicine (SCM), a Korean tailored medicine, categorizes human beings into four types through states of physiological imbalances and responsiveness to herbal medicine. One SCM type susceptible to obesity seems sensitive to energy intake due to an imbalance toward preserving energy. Common variants of fat mass and obesity associated (FTO) and melanocortin 4 receptor (MC4R) genes have been associated with increased body mass index (BMI) by affecting energy intake. Here, we statistically examined the association of FTO and MC4R polymorphisms with BMI in two populations with 1370 Koreans before and after SCM typing, and with the lowering of BMI in 538 individuals who underwent a 1-month lifestyle intervention. The increased BMI replicated the association with FTO haplotypes (effect size ≃ 1.1 kg/m2) and MC4R variants (effect size ≃ 0.64 kg/m2). After the lifestyle intervention, the carriers of the haplotype represented by the minor allele of rs1075440 had a tendency to lose more waist-to-hip ratio (0.76%) than non-carriers. The constitutional discrepancy for the accumulation of body mass by the effects of FTO and/or MC4R variants seemed to reflect the physique differences shown in each group of SCM constitutional types. In conclusion, FTO and MC4R polymorphisms appear to play an important role in weight gain, while only FTO variants play a role in weight loss after lifestyle intervention. Different trends were observed among individuals of SCM types, especially for weight gain. Therefore, classification of individuals based on physiological imbalance would offer a good genetic stratification system in assessing the effects of obesity genes
Forming indium-carbon (In-C) bonds at the edges of graphitic nanoplatelets
Indium (In), one of the soft and malleable post-transition metals, was introduced along the broken edges of graphitic nanoplatelets (GnPs) by mechanochemically ball-milling graphite in the presence of solid state In beads. After completely leaching off unreacted In using royal water (aqua regia), the formation of In-C bonds in the resulting In-doped graphitic nanoplatelets (InGnPs) was confirmed using various analytical techniques, including atomic-resolution transmission electron microscopy (AR-TEM). Scanning TEM (STEM) image shows that In elements instead of In clusters were uniformly distributed in the InGnPs, suggesting the formation of In-C bonds. The content of In in the InGnPs was 0.34 at% (3.01 wt%), as determined by X-ray photoelectron spectroscopy (XPS). The mechanochemically induced chemical reaction was powerful enough to form In-C bonds. Further, the InGnPs demonstrated catalytic activity toward the oxygen reduction reaction (ORR) comparable to commercial Pt/C catalysts, as well as excellent durability and tolerance against impurities (methanol and CO) in alkaline medium
Frequent Occurrence of Mitochondrial DNA Mutations in Barrett’s Metaplasia without the Presence of Dysplasia
BACKGROUND: Barrett's esophagus (BE) is one of the most common premalignant lesions and can progress to esophageal adenocarcinoma (EA). The numerous molecular events may play a role in the neoplastic transformation of Barrett's mucosa such as the change of DNA ploidy, p53 mutation and alteration of adhesion molecules. However, the molecular mechanism of the progression of BE to EA remains unclear and most studies of mitochondrial DNA (mtDNA) mutations in BE have performed on BE with the presence of dysplasia. METHODS/FINDINGS: Thus, the current study is to investigate new molecular events (Barrett's esophageal tissue-specific-mtDNA alterations/instabilities) in mitochondrial genome and causative factors for their alterations using the corresponding adjacent normal mucosal tissue (NT) and tissue (BT) from 34 patients having Barrett's metaplasia without the presence of dysplasia. Eighteen patients (53%) exhibited mtDNA mutations which were not found in adjacent NT. mtDNA copy number was about 3 times higher in BT than in adjacent NT. The activity of the mitochondrial respiratory chain enzyme complexes in tissues from Barrett's metaplasia without the presence of dysplasia was impaired. Reactive oxygen species (ROS) level in BT was significantly higher than those in corresponding samples. CONCLUSION/SIGNIFICANCE: High ROS level in BT may contribute to the development of mtDNA mutations, which may play a crucial role in disease progression and tumorigenesis in BE
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HD CAGnome: A Search Tool for Huntingtin CAG Repeat Length-Correlated Genes
Background: The length of the huntingtin (HTT) CAG repeat is strongly correlated with both age at onset of Huntington’s disease (HD) symptoms and age at death of HD patients. Dichotomous analysis comparing HD to controls is widely used to study the effects of HTT CAG repeat expansion. However, a potentially more powerful approach is a continuous analysis strategy that takes advantage of all of the different CAG lengths, to capture effects that are expected to be critical to HD pathogenesis. Methodology/Principal Findings We used continuous and dichotomous approaches to analyze microarray gene expression data from 107 human control and HD lymphoblastoid cell lines. Of all probes found to be significant in a continuous analysis by CAG length, only 21.4% were so identified by a dichotomous comparison of HD versus controls. Moreover, of probes significant by dichotomous analysis, only 33.2% were also significant in the continuous analysis. Simulations revealed that the dichotomous approach would require substantially more than 107 samples to either detect 80% of the CAG-length correlated changes revealed by continuous analysis or to reduce the rate of significant differences that are not CAG length-correlated to 20% (n = 133 or n = 206, respectively). Given the superior power of the continuous approach, we calculated the correlation structure between HTT CAG repeat lengths and gene expression levels and created a freely available searchable website, “HD CAGnome,” that allows users to examine continuous relationships between HTT CAG and expression levels of ∼20,000 human genes. Conclusions/Significance: Our results reveal limitations of dichotomous approaches compared to the power of continuous analysis to study a disease where human genotype-phenotype relationships strongly support a role for a continuum of CAG length-dependent changes. The compendium of HTT CAG length-gene expression level relationships found at the HD CAGnome now provides convenient routes for discovery of candidates influenced by the HD mutation
Prevalence of the Intestinal Flukes Haplorchis taichui and H. yokogawai in a Mountainous Area of Phongsaly Province, Lao PDR
Phongsaly Province, located in the northernmost area of Lao PDR, was previously suggested to be endemic for the liver fluke Opisthorchis viverrini infection. To confirm, or rule out, this suggestion, the Phonxay village in the Khoua District, Phongsaly Province, was selected for a survey. Ten volunteers (8 men and 2 women aged 31-57 years) who consumed raw freshwater fish and had gastrointestinal troubles were treated with a single dose of praziquantel (40 mg/kg) and pyrantel pamoate (10 mg/kg) and purged with magnesium sulfate to recover any worm parasites. Eight of the 10 volunteers expelled 1 or more species of trematodes, nematodes, or cestodes (worm positive rate; 80%). The worms were morphologically identified as H. taichui (861 worms from 8 people), H. yokogawai (59 from 6 people), Phaneropsolus bonnei (1 from 1 person), Trichostrongylus sp. (2 from 2 people), Ascaris lumbricoides (2 from 1 person), Enterobius vermicularis (11 from 3 people), and Taenia saginata (1 strobila with scolex from 1 person). The results indicate that the mountainous area of Phongsaly Province, Lao PDR, is not endemic for the liver fluke but endemic for intestinal flukes, in particular, Haplorchis taichui and H. yokogawai
Band gap opening by two-dimensional manifestation of Peierls instability in graphene
Using first-principles calculations of graphene having high-symmetry
distortion or defects, we investigate band gap opening by chiral symmetry
breaking, or intervalley mixing, in graphene and show an intuitive picture of
understanding the gap opening in terms of local bonding and antibonding
hybridizations. We identify that the gap opening by chiral symmetry breaking in
honeycomb lattices is an ideal two-dimensional (2D) extension of the Peierls
metal-insulator transition in 1D linear lattices. We show that the spontaneous
Kekule distortion, a 2D version of the Peierls distortion, takes place in
biaxially strained graphene, leading to structural failure. We also show that
the gap opening in graphene antidots and armchair nanoribbons, which has been
attributed usually to quantum confinement effects, can be understood with the
chiral symmetry breaking
Droplet-like Fermi surfaces in the anti-ferromagnetic phase of EuFeAs, an Fe-pnictide superconductor parent compound
Using angle resolved photoemission it is shown that the low lying electronic
states of the iron pnictide parent compound EuFeAs are strongly
modified in the magnetically ordered, low temperature, orthorhombic state
compared to the tetragonal, paramagnetic case above the spin density wave
transition temperature. Back-folded bands, reflected in the orthorhombic/
anti-ferromagnetic Brillouin zone boundary hybridize strongly with the
non-folded states, leading to the opening of energy gaps. As a direct
consequence, the large Fermi surfaces of the tetragonal phase fragment, the low
temperature Fermi surface being comprised of small droplets, built up of
electron and hole-like sections. These high resolution ARPES data are therefore
in keeping with quantum oscillation and optical data from other undoped
pnictide parent compounds.Comment: 4 figures, 6 page
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