15 research outputs found
Logistic regression models of associated factors, including radial quantitative ultrasound (QUS), for falls in men and women.
<p>Model I: SOS by radial QUS as continuous variable. Model II: categorical T-score by radial QUS.</p>a<p>p<0.05,</p>b<p>p<0.01, SOS = speed of sound.</p
Logistic regression models of associated factors, including the lowest T-score derived by either calcaneal or radial quantitative ultrasound, for falls in men and women.
a<p>p<0.05,</p>b<p>p<0.01.</p
Basic characteristics between faller and non-faller men and women.
<p>Comparisons between faller and non-faller.</p>a<p>p<0.05,</p>b<p>p<0.01, QUS = quantitative ultrasound, BUA = broadband of ultrasound attenuation, SOS = speed of sound.</p
BMJopen-Role of Broadband Ultrasound Attenuation Measured by Calcaneal Quantitative Ultrasound in the Fall Incidence in Middle-Aged and Old People
This data file was the raw data of the article which is submitted to BMJ open journal with the article title named as:Role of Broadband Ultrasound Attenuation Measured by Calcaneal Quantitative Ultrasound in the Fall Incidence in Middle-Aged and Old People. Thanks
Logistic regression models of associated factors, including calcaneal quantitative ultrasound (QUS), for falls in men and women.
<p>Model I: BUA by calcaneal QUS as continuous variable. Model II: categorical T-score by calcaneal QUS.</p>a<p>p<0.05,</p>b<p>p<0.01, BUA = broadband of ultrasound attenuation.</p
Smooth muscle specific antibodies used for analysis
<p>Smooth muscle specific antibodies used for analysis</p
Fluorescence-conjugated monoclonal antibodies used for FACS analysis
<p>Fluorescence-conjugated monoclonal antibodies used for FACS analysis</p
Primers for reverse transcription-polymerase chain reaction
1<p>Ref. 21.</p>2<p>We used a single pair of PCR primers that cover the sequence specific to SM2, because these two isoforms are produced from a single gene by alternative splicing.</p>3<p>Ref. 22.</p>4<p>Ref. 23.</p
Characterization of transplanted human VPC-derived vascular cells.
<p>a) Flow cytometric analysis of cell surface markers on expanded human VPC-derived VEGF-R2<sup>+</sup>VE-cadherin<sup>+</sup> cells ( = EC). b) Immunofluorescence image of CD31 (green) and αSMA (red) with nuclear staining (blue) in expanded EC. Scale bar: 100 µm. c) Immunostaining of mural cell markers (brown) with hematoxyline counter-staining of expanded VPC-derived VEGF-R2<sup>+</sup>VE<sup>−</sup>cadherin- cells ( = MC). Scale bar: 100 µm. d, e) RT-PCR analysis of mural cell (d) and skeletal/cardiac specific (e) markers in human VPC-derived vascular cells.</p
Characterization of peripheral blood and umbilical cord-derived EPC (pEPC and uEPC, respectively) by flow cytometer.
<p>a) Representative forward and side scatter profile of cultured pEPC. b-d) Flow cytometric analysis of ulex-lectin binding/acLDL uptake (b, c) and various cell surface markers (d) in pEPC. e) Flow cytometric analysis of cell surface markers in uEPC.</p