2,981 research outputs found
Properties of Heavy B Hadrons
We review recent measurements of heavy B hadron states including masses and
lifetimes of the Bc meson as well as excited B states (B**, Bs**). We discuss
properties of the Bs meson such as lifetime, lifetime difference
delta_Gamma/Gamma and CP violation in Bs -> J/Psi Phi decays. We also summarize
new measurements of the masses and lifetimes of bottom baryons including the
Lambda_b baryon, the Sigma_b baryon states as well as the Xi_b and Omega_b
baryons.Comment: Plenary talk at ICHEP08, Philadelphia, USA, July 2008. 15 pages with
10 figures and 1 table. Fixed typo
The origin and evolution of lactation
The presence of mammary glands is the defining morphological feature of mammals. The recent assembly of the bovine genome and a report in Genome Biology that links the milk and lactation data of bovine and other mammalian genomes will help biologists investigate this economically and medically important feature
Jet shapes in ep collisions at HERA
New measurements of the jet shape in ep collisions at HERA using the
k_T-cluster jet algorithm are presented.Comment: 7 pages, 3 figures; plenary talk given at the 3rd UK Phenomenology
Workshop on HERA Physics, Durham, UK, September 199
Impact of diabetes mellitus on ventricular structure, arterial stiffness, and pulsatile hemodynamics in heart failure with preserved ejection fraction
Background-Heterogeneity in the underlying processes that contribute to heart failure with preserved ejection fraction (HFpEF) is increasingly recognized. Diabetes mellitus is a frequent comorbidity in HFpEF, but its impact on left ventricular and arterial structure and function in HFpEF is unknown. Methods and Results-Weassessed the impact of diabetesmellitus on left ventricular cellular and interstitial hypertrophy (assessedwith cardiacmagnetic resonance imaging, including T1mapping pregadolinium and postgadolinium administration), arterial stiffness (assessed with arterial tonometry), and pulsatile arterial hemodynamics (assessed with in-office pressure-flow analyses and 24-hour ambulatory monitoring) among 53 subjects with HFpEF (32 diabetic and 21 nondiabetic subjects). Despite few differences in clinical characteristics, diabetic subjects with HFpEF exhibited a markedly greater left ventricular mass index (78.1 [95% CI, 70.4-85.9] g versus 63.6 [95% CI, 55.8-71.3] g; P=0.0093) and indexed extracellular volume (23.6 [95% CI, 21.2-26.1] mL/m(2) versus 16.2 [95% CI, 13.1-19.4] mL/m(2); P=0.0008). Pronounced aortic stiffening was also observed in the diabetic group (carotid-femoral pulse wave velocity, 11.86 [95% CI, 10.4-13.1] m/s versus 8.8 [95% CI, 7.5-10.1] m/s; P=0.0027), with an adverse pulsatile hemodynamic profile characterized by increased oscillatory power (315 [95% CI, 258-373] mWversus 190 [95% CI, 144-236] mW; P=0.0007), aortic characteristic impedance (0.154 [95% CI, 0.124-0.183] mmHg/mL per second versus 0.096 [95% CI, 0.072-0.121] mm Hg/mL per second; P=0.0024), and forward (59.5 [95% CI, 52.8-66.1] mm Hg versus 40.1 [95% CI, 31.6-48.6] mm Hg; P=0.0010) and backward (19.6 [95% CI, 16.2-22.9] mm Hg versus 14.1 [95% CI, 10.9-17.3] mm Hg; P=0.0169) wave amplitude. Abnormal pulsatile hemodynamics were also evident in 24-hour ambulatory monitoring, despite the absence of significant differences in 24-hour systolic blood pressure between the groups. Conclusions-Diabetes mellitus is a key determinant of left ventricular remodeling, arterial stiffness, adverse pulsatile hemodynamics, and ventricular-arterial interactions in HFpEF
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