13 research outputs found
Persistent edge currents for paired quantum hall states
We study the behavior of the persistent edge current for paired quantum Hall
states on the cylinder. We show that the currents are periodic with the unit
flux . At low temperatures, they exhibit anomalous oscillations in
their flux dependence.The shape of the functions converges to the sawtooth
function periodic with .Comment: RevTex 8 pages. one figure. to appear in Phys.Rev.
Antioxidant effect of phycocyanin on oxidative stress induced with monosodium glutamate in rats
The objective of this work was to study the antioxidant effect of phycocyanin on the oxidative stress induced by monosodium glutamate in the rats. The tests were performed with 32 rats of Wistar breed, divided into four groups, which were administered saline solution of phycocyanin, monosodium glutamate and monosodium glutamate plus phycocyanin. Sulfhydryl groups and the secondary substances derived from lipid oxidation were determined through the level of TBA. The evaluation of these values and the level of sulfhydryl showed that the administration of phycocyanin presented significant antioxidant effect (p < 0.05) reducing the oxidative stress induced by the monosodium glutamate in vivo
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy.
Clinical presentation of congenital heart disease is heterogeneous,
making identification of the disease-causing genes and their genetic
pathways and mechanisms of action challenging. By using in vivo
electrocardiography, transthoracic echocardiography and microcomputed
tomography imaging to screen 3,894 single-gene-null mouse lines for
structural and functional cardiac abnormalities, here we identify 705
lines with cardiac arrhythmia, myocardial hypertrophy and/or ventricular
dilation. Among these 705 genes, 486 have not been previously
associated with cardiac dysfunction in humans, and some of them
represent variants of unknown relevance (VUR). Mice with mutations in Casz1, Dnajc18, Pde4dip, Rnf38 or Tmem161b
genes show developmental cardiac structural abnormalities, with their
human orthologs being categorized as VUR. Using UK Biobank data, we
validate the importance of the DNAJC18 gene for cardiac
homeostasis by showing that its loss of function is associated with
altered left ventricular systolic function. Our results identify
hundreds of previously unappreciated genes with potential function in
congenital heart disease and suggest causal function of five VUR in
congenital heart disease