18 research outputs found

    file3. measurements on selected trichomes

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    This table contains measurements on the selected trichomes with consistent diameter (67–70 μm). From these data, we can get the positive linear correlation of complete cross-walls spacing and the intercalated incomplete cross-walls length

    file2. Parallel to bedding

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    The table contains series of measurements for Megathrix longus in thin sections parallel to the bedding

    Analysis of association of SNP rs9943582 with echocardiographic parameters.

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    <p>CAD: coronary artery disease, LV: left ventricle, LVSD: left ventricle systolic dysfunction, LVEF: left ventricle eject fraction.</p><p>Analysis of association of SNP rs9943582 with echocardiographic parameters.</p

    Characteristics of the study population for CAD.

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    <p>Data are shown as mean +/- standard deviation (SD) for quantitative variables and % for qualitative variables.</p><p>CAD: coronary artery disease; HDL-c: high density lipoprotein cholesterol levels; LDL-c, low density lipoprotein cholesterol levels; n.a: no data</p><p>*Age at the first diagnosis of the disease in CAD cases and age at enrollment for CAD controls.</p><p><sup>†</sup><i>P</i> value for comparison of means for quantitative data with a student t-test, and for comparison of distribution of qualitative variables between cases and controls with a Chi-square test.</p><p>Characteristics of the study population for CAD.</p

    Characteristics of the CAD group with LVSD and the CAD group with normal LVEF.

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    <p>Data are shown as mean +/- standard deviation (SD) for quantitative variables and % for qualitative variables.</p><p>CAD: coronary artery disease, HDL-c: high density lipoprotein cholesterol levels; LDL-c, low density lipoprotein cholesterol levels, LVSD: left ventricle systolic dysfunction, LVEF: left ventricle eject fraction.</p><p>*Age at the first diagnosis of the disease for CAD cases and age at enrollment for CAD controls.</p><p><sup>†</sup><i>P</i> values for comparison of means for quantitative data with a student t-test, and for comparison of distribution of qualitative variables between CAD patients with LVSD and CAD patients with normal LVEF with a Chi-square test.</p><p>Characteristics of the CAD group with LVSD and the CAD group with normal LVEF.</p

    Analysis of Allelic Association of SNP rs9943582 with LVSD among the CAD population.

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    <p>Freq _A: Frequency of A allele. LVSD: left ventricle systolic dysfunction, LVEF: left ventricle eject fraction.</p><p>*Uncorrected <i>P</i> value and odds ratio (OR) using Chi-square tests with Pearson’s 2×2.</p><p><sup>†</sup>Adjusted <i>P</i> value by multivariate logistic regression analysis for potential confounders including age, gender, smoking, hypertension, diabetes mellitus and lipid concentrations (Tch, TG, HDL-c and LDL-c).</p><p><sup>‡</sup> Empirical P values were calculated using 100,000 Monte Carlo simulations</p><p><sup>‖</sup>Multiple testing was adjusted by Bonferroni correction</p><p>Analysis of Allelic Association of SNP rs9943582 with LVSD among the CAD population.</p

    <i>PITX2c</i> and <i>ZFHX3</i> regulate expression of <i>NKX2</i>.<i>5</i>, <i>TBX5</i>, <i>KCNQ1</i> and <i>SCN1B</i>.

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    <p>HCT116 cells were transfected with siRNA specific for <i>PITX2c</i> or <i>ZFHX3</i> and used for isolation of total RNA samples and real-time RT-PCR analysis. Transfection of siRNA for <i>PITX2c</i> increased expression of <i>NKX2</i>.<i>5</i>, <i>TBX5</i>, <i>KCNQ1</i> and <i>SCN1B</i>. Transfection of siRNA for <i>ZFHX3</i> increased expression of <i>NKX2</i>.<i>5</i> and <i>TBX5</i>,but decreased expression of <i>SCN1B</i>. <i>ZFHX3</i> did not affect on the expression of <i>KCNQ1</i>. Transfection of siRNAs for both <i>PITX2c</i> and <i>ZFHX3</i> increased expression of <i>NKX2</i>.<i>5</i> and <i>TBX5</i>.</p

    The <i>ZFHX3</i> gene positively regulates expression of the <i>PITX2c</i> gene.

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    <p>HCT116 cells were transfected with siRNA specific for <i>ZFHX3</i> or an expression plasmid for <i>ZFHX3</i> and used for isolation of total RNA samples, real time RT-PCR analysis and Luciferase assays. A. Real-time RT-PCR analysis for <i>ZFHX3</i>. Transfection of siRNA for <i>ZFHX3</i> successfully reduced expression of <i>ZFHX3</i>. B. Real-time RT-PCR analysis for <i>ZFHX3</i>. Transfection of an expression plasmid for <i>ZFHX3</i> successfully increased expression of <i>ZFHX3</i>. C. Real-time RT-PCR analysis for <i>PITX2c</i>. Transfection of siRNA for <i>ZFHX3</i> reduced expression of <i>PITX2c</i>. D. Real-time RT-PCR analysis for <i>PITX2c</i>. Transfection of an expression plasmid for <i>ZFHX3</i> successfully increased expression of <i>PITX2c</i>. E. Luciferase assays for the <i>PITX2c</i> promoter activity in cells transfected with a siRNA specific for <i>ZFHX3</i> or a control scramble siRNA. *<i>P</i><0.05; **<i>P</i><0.01.</p

    Both <i>PITX2c</i> and <i>ZFHX3</i> positively regulate expression of the <i>NPPA</i> transcription.

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    <p>HCT116 cells were co-transfected with an expression plasmid for either <i>PITX2c</i>, <i>ZFHX3</i> or both, or siRNA for either <i>PITX2c</i>, <i>ZFHX3</i> or both and used for measurements of RT-PCR. A. Knockdown of <i>PITX2c</i>, <i>ZFHX3</i> or both by siRNAs down-regulated <i>NPPA</i> expression. B. Overexpression of either <i>PITX2c</i> or <i>ZFHX3</i> up-regulated <i>NPPA</i> expression. Co-expression of both <i>PITX2c</i> and <i>ZFHX3</i> dramatically increased <i>NPPA</i> expression. *<i>P</i><0.05; **<i>P</i><0.01.</p
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