112 research outputs found
Ferroelectric displacements in multiferroic Y(Mn,Ga)O-3
We have studied the effects of substitution of Mn3+ by Ga3+ on the crystal structure of YMnO3. Y(Mn,Ga)O-3 is a magnetoferroelectric in which the ferroelectric displacements from the YO7 polyhedra are associated with buckling and tilting of the MnO5 bipyramids. The differences in ionic radius and orbital occupation between Mn3+ and Ga3+ result in an increase of the c/a lattice parameter ratio. This dilation is not associated with the displacements of MnO5 bipyramids, but with the elongation of the YO6 antiprisms. The magnitude of the local YO6 dipoles decrease with Ga substitution
Magnetodielectric and magnetoelastic coupling in TbFe3(BO3)4
We have studied the magnetodielectric and magnetoelastic coupling in
TbFe3(BO3)4 single crystals by means of capacitance, magnetostriction and Raman
spectroscopy measurements. The data reveal strong magnetic field effects on the
dielectric constant and on the macroscopic sample length which are associated
to long range magnetic ordering and a field-driven metamagnetic transition. We
discuss the coupling of the dielectric, structural, and magnetic order
parameters and attribute the origin of the magnetodielectric coupling to phonon
mode shifts according to the Lyddane-Sachs-Teller (LST) relation.Comment: Accepted for publication in Physical Review
Magnetodielectric coupling of a polar organic-inorganic hybrid Cr(II) phosphonate
Cr[(H(3)N-(CH(2))(2)-PO(3))(Cl)(H(2)O)] represents a rare example of a polar organic-inorganic hybrid material that exhibits a canted antiferromagnetic order below T(N)=5.5 K. The unusual coexistence of a polar crystal structure and magnetic order triggered our investigation of the magnetodielectric coupling. The coupling is evidenced by an anomaly in the temperature dependence of the dielectric constant epsilon below the Neel temperature. The magnetocapacitance is enhanced by one order of magnitude below T(N). The main characteristics of the magnetodielectic response are interpreted by Landau theoretical coupling terms
Scaling behavior of the magnetocapacitance of YbMnO3
We observe a seemingly complex magnetic field dependence of the dielectric constant of hexagonal YbMnO3 near the spin ordering temperature. After rescaling, the data taken at different temperatures and magnetic fields collapse on a single curve describing the sharp anomaly in nonlinear magnetoelectric response at the magnetic transition. We show that this anomaly is a result of the competition between two magnetic phases. The scaling and the shape of the anomaly are explained using the phenomenological Landau description of the competing phases in hexagonal manganites
Ramond-Ramond Fields, Fractional Branes and Orbifold Differential K-Theory
We study D-branes and Ramond-Ramond fields on global orbifolds of Type II
string theory with vanishing H-flux using methods of equivariant K-theory and
K-homology. We illustrate how Bredon equivariant cohomology naturally realizes
stringy orbifold cohomology. We emphasize its role as the correct cohomological
tool which captures known features of the low-energy effective field theory,
and which provides new consistency conditions for fractional D-branes and
Ramond-Ramond fields on orbifolds. We use an equivariant Chern character from
equivariant K-theory to Bredon cohomology to define new Ramond-Ramond couplings
of D-branes which generalize previous examples. We propose a definition for
groups of differential characters associated to equivariant K-theory. We derive
a Dirac quantization rule for Ramond-Ramond fluxes, and study flat
Ramond-Ramond potentials on orbifolds.Comment: 46 pages; v2: typos correcte
Endothelial function in patients with familial Mediterranean fever-related amyloidosis and association with cardiovascular events
Objectives. Secondary amyloidosis is the most important complication of FMF and endothelial function is more severely impaired. Elevated asymmetric dimethyl arginine (ADMA) may mediate the excess cardiovascular disease (CVD) risk of this group. We aimed to compare endothelial function characteristics, including ADMA, in patients with FMF-related amyloidosis and primary glomerulopathies and to define risk factors for a CVD event. Methods. We undertook a cross-sectional study with prospective follow-up including consecutive patients with FMF-related amyloidosis (n = 98) or other non-diabetic glomerulopathies (n = 102). All patients had nephrotic-range proteinuria and normal glomerular filtration rate. Flow-mediated dilatation (FMD) was assessedand ADMA levels, CRP and pentraxin 3 (PTX3) were determined. Patients were followed for cardiovascular events. Results. Amyloidosis patients secondary to FMF showed higher levels of ADMA, CRP and PTX3 and lower FMD as compared with patients with other glomerulopathies. Cardiovascular events (n = 54) were registered during 3 years of follow-up. Increased ADMA levels and lower FMD were observed in patients with cardiovascular risk in both groups, but especially in individuals with amyloidosis.Conclusion. Patients with FMF-related amyloidosis have increased CVD event risk, probably related to the high ADMA levels, elevated inflammatory markers and decreased FMD measures observed in these patients
A combined analysis of outcome following breast cancer: differences in survival based on BRCA1/BRCA2 mutation status and administration of adjuvant treatment
BACKGROUND: The prognostic significance of germline mutations in BRCA1 and BRCA2 in women with breast cancer remains unclear. A combined analysis was performed to address this uncertainty. METHODS: Two retrospective cohorts of Ashkenazi Jewish women undergoing breast-conserving treatment for invasive cancer between 1980 and 1995 (n = 584) were established. Archived tissue blocks were used as the source of DNA for Ashkenazi Jewish BRCA1/BRCA2 founder mutation analysis. Paraffin-embedded tissue and follow-up information was available for 505 women. RESULTS: Genotyping was successful in 496 women, of whom 56 (11.3%) were found to carry a BRCA1/BRCA2 founder mutation. After a median follow-up period of 116 months, breast cancer specific survival was worse in women with BRCA1 mutations than in those without (62% at 10 years versus 86%; P < 0.0001), but not in women with the BRCA2 mutation (84% versus 86% at 10 years; P = 0.76). Germline BRCA1 mutations were an independent predictor of breast cancer mortality in multivariate analysis (hazard ratio 2.4, 95% confidence interval 1.2–4.8; P = 0.01). BRCA1 status predicted breast cancer mortality only among women who did not receive chemotherapy (hazard ratio 4.8, 95% confidence interval 2.0–11.7; P = 0.001). The risk for metachronous ipsilateral cancer was not greater in women with germline BRCA1/BRCA2 founder mutations than in those without mutations (P = 0.68). CONCLUSION: BRCA1 mutations, but not BRCA2 mutations, are associated with reduced survival in Ashkenazi women undergoing breast-conserving treatment for invasive breast cancer, but the poor prognosis associated with germline BRCA1 mutations is mitigated by adjuvant chemotherapy. The risk for metachronous ipsilateral disease does not appear to be increased for either BRCA1 or BRCA2 mutation carriers, at least up to 10 years of follow up
RNA-Seq Mapping and Detection of Gene Fusions with a Suffix Array Algorithm
High-throughput RNA sequencing enables quantification of transcripts (both known and novel), exon/exon junctions and fusions of exons from different genes. Discovery of gene fusions–particularly those expressed with low abundance– is a challenge with short- and medium-length sequencing reads. To address this challenge, we implemented an RNA-Seq mapping pipeline within the LifeScope software. We introduced new features including filter and junction mapping, annotation-aided pairing rescue and accurate mapping quality values. We combined this pipeline with a Suffix Array Spliced Read (SASR) aligner to detect chimeric transcripts. Performing paired-end RNA-Seq of the breast cancer cell line MCF-7 using the SOLiD system, we called 40 gene fusions among over 120,000 splicing junctions. We validated 36 of these 40 fusions with TaqMan assays, of which 25 were expressed in MCF-7 but not the Human Brain Reference. An intra-chromosomal gene fusion involving the estrogen receptor alpha gene ESR1, and another involving the RPS6KB1 (Ribosomal protein S6 kinase beta-1) were recurrently expressed in a number of breast tumor cell lines and a clinical tumor sample
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