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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
  
     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
  
    11  tension development in detergent-extracted (skinned) fiber bundles isolated from mouse left ventricu
  
  
  
  
    16  with nonischemic control hearts, bundles of skinned fibers from hearts subjected to ischemia alone d
  
    18 amidotetramethylrhodamine and exchanged into skinned fibers from rabbit psoas muscle without signific
  
  
  
    22  influence in intact hearts, trabeculae, and skinned fibers from wild-type (+/+) and homozygous trunc
  
  
    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
  
  
    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
  
  
    36 both the Ca(2+) binding measurements and the skinned fiber tension measurements, the presence of cTnI
  
  
    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 
  
    43 ot other contractile proteins in "chemically skinned" fibers, we substantially reduced the contractil
  
  
  
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