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 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. …”

PVloops and isochronous <i>P</i>_<i>lv</i>—<i>V</i>_<i>lv</i> relations. 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. …”

PoRVA infection induces significant changes in cellular metabolites in IPEC-J2 cells. by Haixin Liu (7571234)

Inactivation of NatB destabilized Drk, which mediated activated EGFR-induced MAPK activation. by Zhentao Sheng (107495)

“…(C-F) MARCM clones of <i>psid-D4</i> in wing discs, marked by GFP expression (pointed by arrowheads), showed decreased Drk level (C) which was rescued by expressing WT Psid (D) or nonphosphorylatable Psid^SA (S678A) (F) but not the phosphomimetic mutant Psid^SD (S678D) (E). …”

Expression of 5HT-2AR, 2BR, 3AR, and 3BR mRNA in the mid colon. by Ji Eun Kim (403026)

Expression of c-kit, nNOS, NSE, and PGP9.5. by Ji Eun Kim (403026)

CD8 stimulation induces M1 phenotype. by Jan Boddaert (4775013)

PoRVA G9P[23] strain and PoRVA G5P[7] strain infection differentially affect PEDV-induced cellular metabolic reprogramming. by Haixin Liu (7571234)

Expression of mAChR M1, M2, M3, M4, and M5 mRNA in the mid colon. by Ji Eun Kim (403026)

Characterization of recent and minimally passaged Brazilian dengue viruses inducing robust infection in rhesus macaques by Maria Beatriz Borges (5142965)

Cardamonin inhibited the proliferation of ovarian cancer cells. by Peiguang Niu (17044532)

Upstream regulators for thyroid and plasma using IPA. by Malin Larsson (1616557)

Too much syncopation causes rhythm tracking failure. by Jonathan Cannon (5665774)

Association between the posterior part of the circle of Willis and the vertebral artery hypoplasia by Virginija Gaigalaite (7378229)

“…With the increasing degree of VAH, the proportion of FCW increases, while the proportion of absence/hypoplastic of both PCoA decreases.</p></div>…”

Spleen tissue analysis in SCD mice. by Mayuko Takezaki (12700243)