46 research outputs found
Rho-Omega Mixing and the Pion Form Factor in the Time-like Region
We determine the magnitude, phase, and -dependence of -
``mixing'' in the pion form factor in the time-like region through fits to
e^+e^- \ra \pi^+ \pi^- data. The associated systematic errors in these
quantities, arising from the functional form used to fit the resonance,
are small. The systematic errors in the mass and width, however, are
larger than previously estimated.Comment: 20 pages, REVTeX, epsfig, 2 ps figures, minor change
Rho-Omega Mixing and Direct CP Violation in Hadronic B-Decays
The extraction of CKM-matrix-element information from hadronic B-decays
generally suffers from discrete ambiguities, hampering the diagnosis of physics
beyond the Standard Model. We show that a measurement of the rate asymmetry,
which is CP-violating, in
, where the
invariant mass of the pair is in the vicinity of the
resonance, can remove the mod() uncertainty in present in standard analyses.Comment: 9 pages, REVTeX, 1 ps figure, major style changes, results unchange
Persistent currents, flux quantization, and magnetomotive forces in normal metals and superconductors (Review Article)
The notion of persistent current comes back to orbital currents in normal metals, semiconductors and even insulators displaying diamagnetic behavior in weak magnetic fields, but came to focus at the discovery of current persistence and magnetic flux quantization at large fields in atomically big but macroscopically small (mesoscopic) objects. The phenomenon bears much similarity with supercurrents in superconductive metals. We will review progress in developing of our understanding of the physical and technological aspects of this phenomenon. The exact solution for currents, magnetic moments and magnetomotive forces (torques) in crossed magnetic fields are presented. Time-dependent phenomena in crossed magnetic and electric fields, and in possibility of spontaneous persistent currents and of work extraction from static and dynamic quantum states are discussed
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
A História da Alimentação: balizas historiográficas
Os M. pretenderam traçar um quadro da História da Alimentação, não como um novo ramo epistemológico da disciplina, mas como um campo em desenvolvimento de práticas e atividades especializadas, incluindo pesquisa, formação, publicações, associações, encontros acadêmicos, etc. Um breve relato das condições em que tal campo se assentou faz-se preceder de um panorama dos estudos de alimentação e temas correia tos, em geral, segundo cinco abardagens Ia biológica, a econômica, a social, a cultural e a filosófica!, assim como da identificação das contribuições mais relevantes da Antropologia, Arqueologia, Sociologia e Geografia. A fim de comentar a multiforme e volumosa bibliografia histórica, foi ela organizada segundo critérios morfológicos. A seguir, alguns tópicos importantes mereceram tratamento à parte: a fome, o alimento e o domínio religioso, as descobertas européias e a difusão mundial de alimentos, gosto e gastronomia. O artigo se encerra com um rápido balanço crítico da historiografia brasileira sobre o tema