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1 red abilities to inhibit ATPase and to relax skinned fibers.
2 osin complex in myofibrils and in chemically skinned fibers.
3 nC (cardiac and slow skeletal troponin C) in skinned fibers.
4 3% decrease in maximum developed force), and skinned fibers (14% decrease in maximally activated forc
5 mbinant HCTnTs was incorporated into porcine skinned fibers along with human cardiac troponin I (HCTn
6 related with increased Ca(2+) sensitivity in skinned fibers and vice versa.
7 and structural role of the RLC in chemically skinned fibers at various thick and thin filament lattic
8 depression in tension and ATPase activity in skinned fiber bundles from a TG model in which cTnI is r
9  of tension and ATPase activity of detergent-skinned fiber bundles from left ventricular papillary mu
10                          Exchange of cTnI in skinned fiber bundles with cTnI(146G) induced enhanced C
11  tension development in detergent-extracted (skinned) fiber bundles isolated from mouse left ventricu
12 cross-bridge cycling kinetics as measured in skinned fibers derived from the diseased muscle.
13                            Porcine papillary skinned fibers displaced with HSSTnT1, -2, or -3 and rec
14                        In troponin-exchanged skinned fibers, each mutant caused a significant increas
15  with severe mitochondrial damage, and their skinned fibers failed to activate with calcium.
16  with nonischemic control hearts, bundles of skinned fibers from hearts subjected to ischemia alone d
17                                      Single, skinned fibers from rabbit psoas muscle were used to tes
18 amidotetramethylrhodamine and exchanged into skinned fibers from rabbit psoas muscle without signific
19 ric tension over a wide range of [Ca(2+)] in skinned fibers from rabbit psoas muscle.
20 C-5'ATR), in sTnC-5'ATR reconstituted single skinned fibers from rabbit psoas muscle.
21  exchanged for the endogenous RLC in single, skinned fibers from rabbit psoas muscle.
22  influence in intact hearts, trabeculae, and skinned fibers from wild-type (+/+) and homozygous trunc
23                                           In skinned fibers, I79N increased myofilamental calcium sen
24         Ca(2+) sensitivity of contraction in skinned fibers increased with mutant gene dose: KI-TnC-A
25 ction in elastic modulus in Dmlc2(Delta2-46) skinned fibers is consistent with the N-terminal extensi
26 ps) of 3-7 degrees C were examined in single skinned fibers isolated from rabbit psoas (fast) and sol
27            Surprisingly when the kinetics of skinned fibers isolated from the ELC1vDelta5-14 or ELC1a
28                     Investigation of cardiac skinned fibers isolated from WT and heterozygous mice re
29 ated hearts, isolated papillary muscles, and skinned fiber preparations), biochemical and molecular b
30 oncentration (Vmax) have been assessed using skinned fibers prepared from two oxidative muscles (vent
31 lopment of cardiac disease include increased skinned fiber sensitivity to calcium and, at the whole o
32 roteins reconstituted into porcine papillary skinned fibers showed decreased Ca(2+) sensitivity of fo
33 ), were expressed, purified, and utilized in skinned fiber studies and in reconstituted actomyosin AT
34 ions in cTnI, actomyosin ATPase activity and skinned fiber studies were carried out.
35                                           In skinned fiber studies, TnT1-wild-type (WT)-treated fiber
36 both the Ca(2+) binding measurements and the skinned fiber tension measurements, the presence of cTnI
37                       In maximally activated skinned fibers, the rate of tension redevelopment (ktr)
38                                  Exposure of skinned fiber to caspase-3 decreased maximal Ca(2+)-acti
39 e/decrease the Ca(2+) sensitivity of cardiac skinned fibers to create the characteristic effects of D
40 spacing of dissected, osmotically compressed skinned fibers to native muscle fibers in living flies.
41 ociated with increased Ca(2+) sensitivity in skinned fibers was identified; and 3) the F27W reporter
42           The maximal force in reconstituted skinned fibers was significantly greater for the cTnT1 (
43 ot other contractile proteins in "chemically skinned" fibers, we substantially reduced the contractil
44                                              Skinned fibers were maximally Ca(2+)-activated at 20 deg
45                        TnC-extracted cardiac skinned fibers were reconstituted with the cTnC-A31S mut
46               Small step-stretches of single skinned fibers were used to study the effect of phosphor

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