PLUG markers results of M11003-3-1-15-8.

<p>The arrow indicates an <i>L</i>. <i>mollis</i> specific band. All PCR products are digested by <i>Taq</i>I or <i>Hae</i>III. M DL2000, 1 7182, 2 <i>L</i>.<i>mollis</i>, 3 M11003-3-1-15-8. a TNAC1811-<i>Hae</i>III, b TNAC1812-<i>Hae</i>III, c TNAC1926-<i>Hae</i>III, d TNAC1956-<i>Hae</i>III, e TNAC1812-<i>Taq</i>I, f TNAC1926-<i>Taq</i>I, g TNAC1826-<i>Taq</i>I, h TNAC1903-<i>Taq</i>I, i TNAC1957-<i>Taq</i>I.</p

Hazard ratios for cause-specific mortality according joint categories of body mass index.

<p>Hazard ratios (95% CI) indicates the risk of body mass index (BMI) <18 kg/m² compared with the risk in all the other BMI groups. The adjusted model includes sex and age. The fully adjusted model includes smoking, drinking, physical activity, systolic blood pressure, history of cardiovascular disorders, serum lipid disturbance, diabetes mellitus and antihypertensive drug treatment additionally.</p>*<p>p<0.05,</p>§<p>p<0.01,</p>¶<p>p<0.001.</p

Planar FAPbBr₃ Solar Cells with Power Conversion Efficiency above 10%

Bromide-based hybrid perovskites are of particular interest not only due to the fact that they offer a way to go beyond the Shockley–Queisser limit via the tandem cell scheme but single-junction devices of them can also achieve reasonably high efficiency with high stability for solar energy conversion. However, the highest power conversion efficiency achieved up to now for FAPbBr₃ single-junction solar cells is only 8.2%, which is far below the efficiency of ∼17% predicted from detailed balance analysis. Here, a two-step method (the intermolecule exchange pathway) was systematically optimized for the fabrication of high-quality FAPbBr₃ films. A molecule of urea, structurally similar to formamidinium, is introduced as an additive to tune the intermolecular ion exchange procedure. SnO₂ is introduced as an electron-selective contact to the planar structured FAPbBr₃ solar cells. As a result, a power conversion efficiency of 10.61% and a <i>V</i>_oc of 1.56 V are achieved with planar structured solar cells, both of which represent the highest value ever reported for FAPbBr₃ solar cells

EST-STS markers results of M11003-3-1-15-8.

<p>The arrow indicates an <i>L</i>. <i>mollis</i> specific band. M DL2000, 1 7182, 2 <i>L</i>.<i>mollis</i>, 3 M11003-3-1-15-8. <i>BE482781-</i>7<b>A</b>L 7<b>B</b>L 7<b>D</b>L, <i>BE404955-</i>7<b>A</b> 7<b>B</b>S 7<b>D</b>.</p

Fluorescence <i>in situ</i> hybridization (FISH) analysis using Oligo-pTa535 (red), Oligo-pSc119.2 as probes on root tip metaphase chromosomes of M11003-3-1-15-8 (a), Genomic <i>in situ</i> hybridization (GISH) analysis using <i>L</i>. <i>mollis</i> genomic DNA (green) as probe on root tip metaphase chromosomes of M11003-3-1-15-8.

<p>Chromosomes were counterstained with DAPI (blue). The yellow arrows indicate the introduced <i>L</i>. <i>mollis</i> chromosomes in M11003-3-1-15-8.</p

Nullisomic-tetrasomic analysis of M11003-3-1-15-8.

<p>The arrow indicates an <i>L</i>. <i>mollis</i> specific band. M DL2000, 1 7182, 2 <i>L</i>.<i>mollis</i>, 3 M11003-3-1-15-8, 4 M47, 5 CS, 6 CSN7AT7D, 7 CSN7BT7A, 8 CSN7DT7B; a TNAC1826-<i>Taq</i>I, b TNAC1957-<i>Taq</i>I, c TNAC1926-<i>Hae</i>III, d TNAC1926-<i>Taq</i>I.</p

Fluorescence <i>in situ</i> hybridization (FISH) analysis using Oligo-pTa535 (red), Oligo-pSc119.2 (green) as probes on root tip metaphase chromosomes of 7182.

<p>Chromosomes were counterstained with DAPI (blue). The pair of wheat chromosomes 7<b>D</b> was indicated in a small white rectangular box.</p

Baseline characteristics of the community hypertensive patients by category of body-mass index.

<p>Data are No. (%) or mean±SD. SBP and DBP indicate systolic and diastolic blood pressures. P values are for the difference among the eight groups. P values less than 0.05 are shown in bold and italics.</p

Multivariable-adjusted hazard ratios (95% CI) for all causes mortality, cardiovascular mortality and non-cardiovascular mortality across eight groups of body mass index (BMI).

<p>The hazard ratio express the risk in the BMI group compared with the average risk in the whole study population, which were adjusted for sex, age, smoking, drinking, physical activity, systolic blood pressure, history of cardiovascular disorders, serum lipid disturbance, diabetes mellitus and antihypertensive drug treatment.</p

Genomic <i>in situ</i> hybridization (GISH) analysis using <i>L</i>. <i>mollis</i> genomic DNA (green) as probe on root tip metaphase chromosomes of M11003-3-1-15-8.

<p>Chromosomes were counterstained with PI (red).</p