Shape coexistence and evolution in neutron-deficient krypton isotopes

Total Routhian Surface (TRS) calculations have been performed to investigate shape coexistence and evolution in neutron-deficient krypton isotopes 72,74,76Kr. The ground-state shape is found to change from oblate in 72Kr to prolate in 74,76Kr, in agreement with experimental data. Quadrupole deformations of the ground states and coexisting 0+2 states as well as excitation energies of the latter are also well reproduced. While the general agreement between calculated moments of inertia and those deduced from observed spectra confirms the prolate nature of the low-lying yrast states of all three isotopes (except the ground state of 72Kr), the deviation at low spins suggests significant shape mixing. The role of triaxiality in describing shape coexistence and evolution in these nuclei is finally discussed

The Mineral Nutrients Content and the Organic Manure Quality Appraisal for the \u3cem\u3eStylosanthes\u3c/em\u3e Green Manure

Stylo (Stylosanthes spp.) is a leguminous crop planted widely in the world tropics. In the past the stylo was commonly used as pasture with high quality, and was less used as a green manure. However, stylo is recently used more as a green manure in tropical plantations. As there is little relevant research on the organic manure quality for stylo, the purpose of this research was to evaluate the quality of stylo green manure. Selection of stylo green manure with the highest quality was based on the analysis of nutrients and organic matter content in stylo

Prevalence, incidence and mortality of hypertrophic cardiomyopathy based on a population cohort of 21.9 million in China

There are limited studies on the prevalence and incidence of clinically diagnosed hypertrophic myocardiopathy (HCM) and its mortality in the Chinese population, and the projected population burden of HCM over the next decades. We collected data on HCM and its mortality from the Beijing Municipal Health Commission Information Center (BMHCIC) database and estimated the prevalence and incidence based on the whole Beijing population. Calculation of population trends was performed using annual percentage change (APC) and average annual percentage change (AAPC). Finally, future HCM incidence was built by modelling projection of HCM to the next decades using Poisson regression analysis and Gray Model 1,1(GM [1,1]). The prevalence of HCM was 0.0069% (95%CI, 0.0065–0.0072%; N = 1343) in 2010, rising to 0.076% (95% CI, 0.074–0.077%; N = 16,616) in 2019, and the incidence of HCM was 6.85 per 100 000 person-year in 2010, rising to 11.76 per 100 000 person-year in 2019. Males had higher prevalence and incidence of HCM than females. The APPC for the rising incidence of HCM was 5.8% and the expected numbers will double increase in 2029 by assuming the same increase trend as the last decades. HCM had increased annual incidence of HF (APPC: 8.4, 4.4–12.6, p  0.05) during the studied period. Males had lower mortality (2.70% vs. 4.20%, p < 0.001) than females. The calculated HCM prevalence was much lower compared to prior screening studies from 2004, although the predicted HCM incidence would double over the next decades. HCM was associated with a stable risk of mortality during the studied period

Identification and functional characterization of an N-terminal oligomerization domain for polycystin-2*

Autosomal dominant polycystic kidney disease (ADPKD), the most common inherited cause of kidney failure, is caused by mutations in either PKD1 (85%) or PKD2 (15%). The PKD2 protein, polycystin-2 (PC2 or TRPP2), is a member of the transient receptor potential (TRP) superfamily and functions as a non-selective calcium channel. PC2 has been found to form oligomers in native tissues suggesting that it may form functional homo- or heterotetramers with other subunits, similar to other TRP channels. Our experiments unexpectedly revealed that PC2 mutant proteins lacking the known C-terminal dimerization domain were still able to form oligomers and co-immunoprecipitate full-length PC2, implying the possible existence of a proximal dimerization domain. Using yeast two-hybrid and biochemical assays, we have mapped an alternative dimerization domain to the N terminus of PC2 (NT2-1-223, L224X). Functional characterization of this domain demonstrated that it was sufficient to induce cyst formation in zebrafish embryos and inhibit PC2 surface currents in mIMCD3 cells probably by a dominant-negative mechanism. In summary, we propose a model for PC2 assembly as a functional tetramer which depends on both C- and N-terminal dimerization domains. These results have significant implications for our understanding of PC2 function and disease pathogenesis in ADPKD and provide a new strategy for studying PC2 function