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1 t major architectural chromatin proteins are hyperdynamic and bind loosely to chromatin in ES cells.
2 uction did not prevent the occurrence of the hyperdynamic and hypercardiovascular response during the
3 ous, unrestrained rats prevented LPS-induced hyperdynamic and hypodynamic circulatory shock, hyperlac
6 ures enriched for active chromatin marks and hyperdynamic binding of structural chromatin proteins.
8 ction may exist to coordinately maintain the hyperdynamic cardiac contractile performance of the PLN-
9 ngendorff perfusion indicated that the basal hyperdynamic cardiac function of the knockout mouse was
16 Lipoic acid prevented the development of the hyperdynamic circulation (cardiac index [CI]: 15.7 +/- 2
18 al hypertension develops differently, with a hyperdynamic circulation and angiogenic biomarker profil
19 l hypertensive (PHT) gastric mucosa leads to hyperdynamic circulation and increased susceptibility to
20 aused haemodynamic changes consistent with a hyperdynamic circulation and induced increases in muscle
21 ent hypermetabolic response characterized by hyperdynamic circulation and severe muscle catabolism an
23 dilatation (splanchnic and systemic) and the hyperdynamic circulation are hemodynamic abnormalities t
25 Vasodilatation (splanchnic and systemic) and hyperdynamic circulation are hemodynamic abnormalities t
26 dilatation (splanchnic and systemic) and the hyperdynamic circulation are hemodynamic abnormalities t
27 olely from portal hypertension, although the hyperdynamic circulation contributes to variceal growth
28 olely from portal hypertension, although the hyperdynamic circulation contributes to variceal growth
31 We have previously demonstrated that the hyperdynamic circulation in the partial portal vein-liga
32 lipoic acid prevents the development of the hyperdynamic circulation in the rat model of biliary cir
35 NO production, blunts the development of the hyperdynamic circulation, and decreases portal pressure
36 ment of liver cirrhosis, is characterized by hyperdynamic circulation, angiogenesis, and portosystemi
45 day 4, portal vein-ligated rats developed a hyperdynamic circulatory state with a normal central blo
46 receiving the bacterial infusion developed a hyperdynamic circulatory state with hypotension, decreas
47 fter 24 hrs of sepsis, all sheep developed a hyperdynamic circulatory state with increased cardiac in
48 is and ascites showed a typical pattern of a hyperdynamic circulatory state, when compared with their
49 Pseudomonas infusion, all sheep developed a hyperdynamic circulatory state, with increased cardiac i
54 econd, experimental models used to study the hyperdynamic circulatory syndrome; and third, the vasodi
55 vity was correlated with a prevention of the hyperdynamic contractile response and enhanced myocardia
56 bserved in most infants (29/40; 72%); 17 had hyperdynamic contractility, and 24 had altered LV geomet
59 the hearts of older mutant mice also showed hyperdynamic contraction, with increased end-systolic ch
60 ncreased wall thickness, small chamber size, hyperdynamic ejection fraction, and left ventricular con
63 ncy in mice did not alter cardiac structure, hyperdynamic function, or antifibrotic effects induced b
65 months after thermal injury, ameliorates the hyperdynamic, hypermetabolic, hypercatabolic, and osteop
66 and prolonged QT interval) and functionally (hyperdynamic left ventricular [LV] contractility along w
68 data are consistent with the hypothesis that hyperdynamic microtubules impair axonal transport and ac
71 icrobial sepsis is characterized by an early hyperdynamic phase (2-10 hrs after cecal ligation and pu
73 crobial sepsis is characterized by an early, hyperdynamic phase followed by a late, hypodynamic phase
74 crobial sepsis is characterized by an early, hyperdynamic phase followed by a late, hypodynamic phase
75 gulated CYP4A3 is associated with the early, hyperdynamic phase of sepsis and the down-regulated CYP2
76 ays or even prevents the transition from the hyperdynamic phase to the hypodynamic phase of sepsis, a
77 ays or even prevents the transition from the hyperdynamic phase to the hypodynamic phase of sepsis, a
78 o be responsible for the transition from the hyperdynamic phase to the hypodynamic phase of sepsis.
79 sequently observed that produced a transient hyperdynamic phase; however, progressive RV distension d
89 rotects against I/R injury by preventing the hyperdynamic response of isolated perfused hearts during
93 lop a standardized and reproducible model of hyperdynamic sepsis after smoke inhalation in sheep.
94 ensin II and norepinephrine and induction of hyperdynamic sepsis by administration of live Escherichi
97 nthase inhibitors in a large animal model of hyperdynamic sepsis in which acute kidney injury occurs
98 ures and maintains mean arterial pressure in hyperdynamic sepsis without reversal of sepsis-induced v
106 tion of TNF-alpha attenuated the severity of hyperdynamic shock induced by a subsequent infusion of e
107 5 hrs or 10 hrs after CLP (i.e., the early, hyperdynamic stage of sepsis), the thoracic aorta was is
112 All three doses of hemoglobin reversed this hyperdynamic state by increasing mean arterial pressure
114 ponse syndrome of fever, leukocytosis, and a hyperdynamic state is common in trauma patients, especia
116 The E. coli infusions were associated with a hyperdynamic state, pulmonary hypertension, systemic hyp
117 ndotoxemia induced an immediate hypotensive, hyperdynamic, tachycardic state with progressive lactic
118 1 (AMBP-1) prevented the transition from the hyperdynamic to the hypodynamic stage in the progression
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