地域における高齢者の社会的孤立を予防する支援に関する文献検討 : 高齢者の程よい社会関係を基盤とした支援のあり方

application/pdf大阪府立大学看護学雑誌. 2021, 27 (1), P.57-65departmental bulletin pape

Observation of D_s1(2536)^+ → D^+π^-K^+ and angular decomposition of D_s1(2536)^+ →D^*+K_S^0

Using 462 fb^{-1} of e^+e^- annihilation data recorded by the Belle detector, we report the first observation of the decay D_s1(2536)^+　→　D+π^-K^+. The ratio of branching fractions \frac{B(D_s1(2536)^+ → D^+π^- K^+}{B(D_s1(2536)^+ → D+K^0}is measured to be (3.27±0.18±0.37)%. We also study the angular distributions in the D_s1(2536)^+　→D*+K_S^0 decay and measure the ratio of D- and S-wave amplitudes. The S-wave dominates, with a partial width of Γ_S/Γtotal=0.72±0.05±0.01.journal articl

Evidence for Direct CP Violation in B0→K+π-Decays

journal articl

Different Frequencies between Power and Efficiency in Wireless Power Transfer

Wireless Power Transfer (WPT) has been recognized as a common power transfer method because it transfers electric power without any cable from source to the load. One of the physical principle of WPT is the law of electromagnetic induction, and the WPT system is driven by alternative current power source under specific frequency. The frequency that provides maximum gain between voltages or currents is called resonance frequency. On the other hand, some studies about WPT said that resonance frequency is able to produce high power and high efficiency on the WPT system. There are cases that make WPT system has two different frequencies. One leads maximum power and another leads maximum efficiency. If WPT system works under the resonance frequency, WPT produces maximum power with lower efficiency on it. As the solution of that, the intersection frequency able to balance both power and efficiency.departmental bulletin pape

The transgene programs full level, tissue-specific and copy number dependent expression

<p><b>Copyright information:</b></p><p>Taken from "The human vitamin D-binding protein gene contains locus control determinants sufficient for autonomous activation in hepatic chromatin"</p><p>Nucleic Acids Research 2006;34(8):2154-2165.</p><p>Published online 28 Apr 2006</p><p>PMCID:PMC1450336.</p><p>© The Author 2006. Published by Oxford University Press. All rights reserved</p> () Tissue specificity of transgene expression. The autoradiograph shows a Northern blot surveying a set of tissues from a representative transgenic line (mouse line 6). RNAs from the indicated tissues and control RNA from wild-type mouse liver (WT) were analyzed. The Northern blot was hybridized with an hDBP cDNA fragment and then with a mouse ribosomal protein L32 (mrpL32) cDNA fragment to normalize for RNA loading. The hDBP cDNA probe was specific for the human DBP mRNA and did not cross-hybridize to the mouse DBP mRNA. The blot was stripped then re-hybridized with rat DBP cDNA to detect the cross-hybridizing, endogenous mouse DBP mRNA. The transgene was expressed predominantly in the livers and at lower level in the kidney of each line. The table summarizes the tissue distribution of transgene expression in an adult male mouse of each transgenic line (-; no signal detected). Expression in the liver is defined as 100 and all values in other tissues are calculated as using this as a reference. Very low-level expression was detected in intestines of three lines and occasionally in spleen or testis. () Copy number dependency of transgene expression. Northern blots containing liver RNA from the five transgenic lines were hybridized with cDNA and then cDNA. Three animals from each line were analyzed and a representative Northern blot is shown. mRNA was quantified for each line and normalized to the signal to correct for RNA loading. The corrected expression value was divided by transgene copy number and the mean ratio for line 1 was arbitrarily set to 1.0. The ratios from the remaining lines were normalized to line 1 and were plotted on the bar graph (±SD). All quantifications were done by phosphoimager analysis and all were in the linear range of detection (Materials and Methods). There were no statistically significant differences among the lines when hDBP expression was normalized to transgene copy number. A radial immunodiffusion assay was used to quantify levels of serum hDBP in each transgenic line. The serum hDBP levels per transgene copy number were plotted in the bottom panel using a logarithmic scale. The results demonstrated that the liver hDBP mRNA and serum hDBP levels were remarkably consistent from line to line in a copy number dependent fashion

Comparisons between human and rodent genomic sequences in the vicinity of the DBP locus

<p><b>Copyright information:</b></p><p>Taken from "The human vitamin D-binding protein gene contains locus control determinants sufficient for autonomous activation in hepatic chromatin"</p><p>Nucleic Acids Research 2006;34(8):2154-2165.</p><p>Published online 28 Apr 2006</p><p>PMCID:PMC1450336.</p><p>© The Author 2006. Published by Oxford University Press. All rights reserved</p> A map of the gene is displayed in the center of the figure showing the exon-intron arrangement and location of the HS in liver (downward arrows) and brain (upward arrows). An expanded view of the sequence comparisons (human compared to rodent) in the 5′-flanking region (upper panel) and intron 1 (lower panel) are shown. The numbering on the -axis refers to the position in the human sequence. The level of similarity in sequence is displayed on the -axis as a percentage (mVISTA program; window size 50 bp, homology threshold 70%). The 75% level of sequence similarity is marked by a horizontal line and regions of the sequence representing repeated elements are indicated by the shaded rectangles, LINE elements (stippled) and SINE (solid). The positions of liver-specific HSI, HSIII, HSIV and HSV sequence comparisons are each indicated by the downward arrows. Note the peaks of sequence identity at each of the indicated DNase I HS

M. Tullii Ciceronis Operum tomus octauus : continens De Philosophia volumen primum [et] in ipsum Aldi Mannuccij commentarium.

Mode of access: Internet.Contiene el texto de Cicerón y el comentario de Aldo Manuzio.Marca tip. en port.Según CCPB, existe al menos una emisión con el mismo pie de imprenta pero diferente composición tipográfica de la portada y título diferente; una lleva marca tip. y otra en su lugar retrato de Manuzio.Sign. : [asterisco]4, A-2R4, 2S6