Trade-Off for Better Balanced Nonlinear Optical Performance with Disordered Si in ZnGeP₂ by Shunda Yang (8086265)

“…Theoretical calculations with special quasirandom structures show that the NLO coefficient decreases gradually with increasing Si content, but the decrease is tiny in the 0–50% range and acute in the 50–100% range of Si. …”

Trade-Off for Better Balanced Nonlinear Optical Performance with Disordered Si in ZnGeP₂ by Shunda Yang (8086265)

“…Theoretical calculations with special quasirandom structures show that the NLO coefficient decreases gradually with increasing Si content, but the decrease is tiny in the 0–50% range and acute in the 50–100% range of Si. …”

Fig 4 - by Corantin Maurin (9155070)

Identification and characterization of transposon insertion locations that alter fitness in single amino acid media. by Alison K. Hottes (22470601)

Effect of MA-5 on mitochondrial dynamics in sIBM skin fibroblasts. by Yoshitsugu Oikawa (9721356)

Representative immunostaining of ACE-2, TMPRSS2, Cathepsin B, and Cathepsin L in cryosections of 0.5% PFA-fixed fresh human corneas. by Corantin Maurin (9155070)

Time course of ribosome clearance following lincomycin treatment in light <i>versus</i> dark. by Prakitchai Chotewutmontri (3153774)

“…LIN was applied to seedlings at midday in the light or after 30 minutes of dark adaptation; this period of dark adaptation is sufficient for ribosome occupancy on <i>psbA</i> mRNA to decrease to its dark steady-state level (see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1007555#pgen.1007555.g005" target="_blank">Fig 5</a>). …”

Titan cells generation is dependent on various genes and requires signaling through the Gpr/PKA/Rim101 pathway <i>in vitro</i>. by Benjamin Hommel (523072)

FTY720 treatment reduces the establishment of latency and total and integrated HIV-1 DNA in T_CM. by Rachel S. Resop (9238645)

Depletion of RipA results in a reversible arrest in growth of <i>M. smegmatis.</i> by Erik C. Hett (244859)

“…Bacteria were visualized with a 100× objective. (D) Depletion strains of <i>M. smegmatis</i> grown on plates containing a gradient of inducer created by placing 10 µl of 10 ng/ml Tet on a paper disc in the center of the plate, resulting in a concentration of inducer highest at the middle of the plate and lowest at the edges. …”

Effect of MA-5 on sIBM myoblasts. by Yoshitsugu Oikawa (9721356)

Variables of the simplified circulation model. by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Parameters in Eq (23). by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Circulation model. by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Contains C program code of the model. by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Parameters of the circulation model. by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Parameters of the LV geometry model. by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Parameters used in Eqs (16) and (17). by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Time course of half-sarcomere length (<i>L</i>). by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”

Time course of the crossbridge length (<i>h</i>_<i>p</i>). by Shiro Kato (2444047)

“…On the other hand, end-systolic elastance (<i>E</i>_<i>max</i>) is known to be a good index of LV contractility, which is measured by the slope of several end-systolic <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> points obtained by using different loads. …”