175 research outputs found

    Factors determining social participation in the first year after kidney transplantation: a prospective study

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    BACKGROUND: This study describes changes in social participation in the first year after kidney transplantation and examines the influence of clinical factors, health status, transplantation-related symptoms, and psychological characteristics on change in social participation. METHODS: A prospective study was performed on a cohort of primary kidney transplant recipients, transplanted between March 2002 and March 2003. Data on participation in obligatory activities (i.e., employment, education, household tasks) and leisure activities (i.e., volunteer work, assisting others, sports, clubs/associations, recreation, socializing, going out) were collected by in-home interviews (n=61) at 3 months (T1) and 1 year posttransplantation (T2). Analysis of covariance was performed. RESULTS: Data showed an increase in participation in obligatory activities and diversity of leisure participation between T1 and T2, although pre-end-stage renal disease level was not regained and differed from the general population. On T1, the majority of employed recipients were on sick leave, but returned to work on T2. Employment rate remained stable. An increase in obligatory participation was predicted by clinical factors (i.e., peritoneal dialysis, initial hospitalization), whereas change in leisure participation was related to serum albumin and cognitive capacity. No effects were found for type of donation, comorbidity, and renal function. CONCLUSIONS: We found that mainly clinical factors were associated with an increase in participation in society. Although health-status related factors and the psychological attribute self-efficacy may be related to recovery of social participation, their effect was outweighed by the strength of clinical predictors in multivariate analysis

    Validation of a major QTL for salinity tolerance on chromosome 1 of rice in three different breeding populations

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    The effect of a major quantitative trait locus (QTL) for salinity tolerance in rice, designated as SalTol in a previous study, was tested using three F2 breeding populations. The populations were derived from the following F1 hybrids: 'BRRI dhan40' (susceptible)/ 'IR61920-3B-22-2-1' (highly tolerant); 'BRRI dhan28' (highly susceptible)/ 'IR50184-3B-18-2B-1' (moderately tolerant); and 'Kajalsail' (tolerant)/ 'IR52713-2B-8-2B-1-2' (tolerant). Targeted mapping of the chromosome region containing SolTol (49.6 to 87.1 cM) on chromosome 1 was conducted using 20 SSR and two EST markers. Comparisons of linkage maps of the three populations were very similar to the previous QTL map that identified SolTol. A QTL was only detected for 'BRRI dhan40'/ 'IR61920-3B-22-2-1' population. The SSR marker RM8094 was the most tightly-linked marker (P<0.001); four other markers, RM1287, RM3412, RM493 and CP03970, were also significantly associated with salinity tolerance (P<0.05). An F-3 population of the cross 'BRRI dhan40'/ 'IR61920' was used to reconfirm this result. This was interesting because the tolerant parent in this population was not related to the tolerant parent used for the original mapping population. QTLs were not detected at the SalTol locus for either of the other two populations. This was consistent with the phenotypes of the parents used to construct these populations, and indicates that the SolTol QTL may only be effective in specific populations

    Characterizing the Saltol quantitative trait locus for salinity tolerance in rice

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    This study characterized Pokkali-derived quantitative trait loci (QTLs) for seedling stage salinity tolerance in preparation for use in marker-assisted breeding. An analysis of 100 SSR markers on 140 IR29/Pokkali recombinant inbred lines (RILs) confirmed the location of the Saltol QTL on chromosome 1 and identified additional QTLs associated with tolerance. Analysis of a series of backcross lines and near-isogenic lines (NILs) developed to better characterize the effect of the Saltol locus revealed that Saltol mainly acted to control shoot Na +/K + homeostasis. Multiple QTLs were required to acquire a high level of tolerance. Unexpectedly, multiple Pokkali alleles at Saltol were detected within the RIL population and between backcross lines, and representative lines were compared with seven Pokkali accessions to better characterize this allelic variation. Thus, while the Saltol locus presents a complex scenario, it provides an opportunity for markerassisted backcrossing to improve salt tolerance of popular varieties followed by targeting multiple loci through QTL pyramiding for areas with higher salt stress

    The "Persuadable Middle" on Same-Sex Marriage: Formative Research to Build Support among Heterosexual College Students

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    Same-sex marriage is a controversial policy issue that affects the welfare of gay and lesbian couples throughout the USA. Considerable research examines opinions about same-sex marriage; however, studies have not investigated the covariates of the “persuadable middle”— those individuals who are neutral or unsure about their views. This group of people is often the target of same-sex marriage campaigns, yet they have received no empirical attention.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/89607/1/Woodford et al 2011 Persuadable Middle.pd

    Erratum to: Combined analysis of Belle and Belle II data to determine the CKM angle ϕ3 using B+ → D(K0Sh+h−)h+ decays

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    Combined analysis of Belle and Belle II data to determine the CKM angle ϕ3 using B+ → D(K0S h+h−)h+ decays

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    Search for an invisible ZZ^\prime in a final state with two muons and missing energy at Belle II

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    The LμLτL_{\mu}-L_{\tau} extension of the standard model predicts the existence of a lepton-flavor-universality-violating ZZ^{\prime} boson that couples only to the heavier lepton families. We search for such a ZZ^\prime through its invisible decay in the process e+eμ+μZe^+ e^- \to \mu^+ \mu^- Z^{\prime}. We use a sample of electron-positron collisions at a center-of-mass energy of 10.58GeV collected by the Belle II experiment in 2019-2020, corresponding to an integrated luminosity of 79.7fb1^{-1}. We find no excess over the expected standard-model background. We set 90%\%-confidence-level upper limits on the cross section for this process as well as on the coupling of the model, which ranges from 3×1033 \times 10^{-3} at low ZZ^{\prime} masses to 1 at ZZ^{\prime} masses of 8GeV/c2GeV/c^{2}

    Measurement of the Λc+\Lambda_c^+ lifetime

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    An absolute measurement of the Λc+\Lambda^{+}_c lifetime is reported using Λc+pKπ+\Lambda_c^+\rightarrow pK^-\pi^+ decays in events reconstructed from data collected by the Belle II experiment at the SuperKEKB asymmetric-energy electron-positron collider. The total integrated luminosity of the data sample, which was collected at center-of-mass energies at or near the Υ(4S)\Upsilon(4S) resonance, is 207.2~\mbox{fb}^{-1}. The result, τ(Λc+)=203.20±0.89(stat)±0.77(syst)\tau(\Lambda^{+}_c) = 203.20 \pm 0.89 \,\mathrm{(stat)} \pm 0.77 \,\mathrm{(syst)} fs, is the most precise measurement to date and is consistent with previous determinations.Comment: Accepted for publication in PR

    Measurement of CPCP asymmetries in B0ϕKS0B^0\to \phi K^0_S decays with Belle II

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    We present a measurement of time-dependent rate asymmetries in B0ϕKS0B^0\to \phi K^0_S decays to search for non-standard-model physics in bqqsb\to q \overline{q}s transitions. The data sample is collected with the Belle II detector at the SuperKEKB asymmetric-energy e+ee^{+}e^{-} collider in 2019-2022 and contains (387±6)×106(387\pm 6)\times 10^6 bottom-antibottom mesons from Υ(4S)\Upsilon(4S) resonance decays. We reconstruct 162±17162\pm17 signal events and extract the charge-parity (CPCP) violating parameters from a fit to the distribution of the proper-decay-time difference of the two BB mesons. The measured direct and mixing-induced CPCP asymmetries are A=0.31±0.20±0.05A=0.31\pm0.20\pm0.05 and S=0.54±0.260.08+0.06S=0.54\pm0.26^{+0.06}_{-0.08}, respectively, where the first uncertainties are statistical and the second are systematic. The results are compatible with the CPCP asymmetries observed in bccsb\to c\overline{c} s transitions
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