A Survey of the Difference in Language Sensitivity Between Japanese and Americans : A Preliminary Study

論文(Article)The goal of this survey is to discover the difference in sensitivity that Americans and Japanese have towards their languages. Thank you for taking time to cooperate with us by answering the following questions. ...departmental bulletin pape

Correlations of pathologic scores (Ph score) and concentrations of energy substances at 24 h post-TBI.

<p>All of uncorrected energy substances were negatively correlated with pathologic scores (Spearman test) at 24 h post-TBI. All of DNA content-corrected energy substances were negatively correlated with pathologic scores (Spearman test) at 24 h post-TBI except DNA content-corrected AMP.</p

The levels of ATP, ADP, AMP and TAN for different dose irradiated groups and control group at 24

<p> <b>h post-TBI.</b> The bars represent the means of energy substances. X axis indicates the content of energy substances and Y axis indicates the different group. *: p<0.05, **: p<0.01(versus control); ^#: p<0.05, ^##: p<0.01 (post hoc LSD or Games-Howell test).</p

Ultrastructure of mitochondria.

<p>Compared with control group, electron micrographs show enlarged mitochondria and reduced electron density for 2 and 5 Gy. The increased electron lucent and vacuolization were shown for 8, 11 and 14 Gy. (×15 000–20 000).</p

Histological analysis and pathological scores in small intestine.

<p><b>A.</b> the pathologic alterations in the various doses of irradiated groups and the control group at 24 h post-TBI were observed in H.E. stained sections of small intestine.(arrows indicate apoptosis and hemorrhage) e (×400). <b>B.</b> pathologic alterations in the sections of small intestine were scored and graphed. Y-axis indicates pathologic severity.</p

MOESM1 of Abnormalities of hair structure and skin histology derived from CRISPR/Cas9-based knockout of phospholipase C-delta 1 in mice

Additional file 1: Table S1. Target loci of mouse PLCD1 gene. Table S2. Generation of PLCD1-modified mice (F0). Table S3. Primers for qRT-PCR analysis of PLCD1and the related gene expression. Table S4. List of putative off-target sites (OTSs). Table S5. Primer pairs for PCR amplification of OTSs

MOESM2 of TZAP plays an inhibitory role in the self-renewal of porcine mesenchymal stromal cells and is implicated the regulation of premature senescence via the p53 pathway

Additional file 2: Table S1. Primers for qRT-PCR analysis of porcine TZAP and related gene expression

MOESM1 of TZAP plays an inhibitory role in the self-renewal of porcine mesenchymal stromal cells and is implicated the regulation of premature senescence via the p53 pathway

Additional file 1: Fig. S1. TZAP was knocked out in pMSCs by CRISPR/Cas9 gene editing. (A) A diagram of the porcine TZAP locus targeted by CRISPR editing and sequencing results for the edited porcine TZAP gene in the KO-sg2 clone. The sgRNA target region and PAM sequences are highlighted in cyan and red, respectively. (B and C) Pools of pMSCs treated with the control and pMSCs treated with Cas9 and TZAP-targeting sgRNA LV-sg2 were analyzed by TIDE [40]; (B) the spectra and frequency of Indels were determined by TIDE. (C) Visualization of the aberrant signal sequence in LV-sg2 (green) and the control sample (black), the region used for decomposition (gray bar) and the expected cutting site (blue dotted line)