ライフサイエンスコーパス: muscle force

1 to how myosin both generates and responds to muscle force.

2 terminant of physiological levels of passive muscle force.

3 n myosin structure, myosin biochemistry, and muscle force.

4 age-related decreases in DHPR number and in muscle force.

5 sistance to muscle fatigue, despite reducing muscle force.

6 s impairs regeneration, leading to decreased muscle force.

7 biochemistry, and significant enhancement of muscle force.

8 he dystrophin-associated protein complex and muscle force.

9 advances to explain how they could influence muscle force.

10 tor nerve activity served as a surrogate for muscle force.

11 enge, as well as greater decrement in biceps muscle force.

12 ce and those that assess evoked (stimulated) muscle force.

13 accounts for Ca(2+) sensitization of smooth muscle force.

14 eeded to reduce muscle pathology and improve muscle force.

15 by a dynamic balance of surface, tissue, and muscle forces.

16 ment of new IOLs designed to harness ciliary muscle forces.

17 uscles determines the magnitude of joint and muscle forces.

18 ATP hydrolysis (ATPase) reaction coupled to muscle force?.

19 macrophage density and a faster recovery in muscle force (20%), combined with an increase in muscle

20 otor deficit characterized by a reduction in muscle force, abnormal muscle contractile characteristic

21 ide a continuous mechanical link to transmit muscle forces across the hypodermis to the cuticle.

22 apted through evolution to complement active muscle forces acting at the same joint.

23 y shift facilitated a large increase in peak muscle force and an increase in MG power output.

24 muscle generated significantly less absolute muscle force and became more susceptible to contraction-

25 terized by decreased development of skeletal muscle force and cardiac conduction disorders.

26 Arimoclomol significantly improved hindlimb muscle force and contractile characteristics, rescued mo

27 w diet, and it determines the maintenance of muscle force and exercise performance upon a HFD regimen

28 ematically and correlates significantly with muscle force and fatigue.

29 Muscle force and functional capacity generally decrease

30 keletal-troponin complex to calcium improves muscle force and grip strength immediately after adminis

31 survived at least 18 months, and had normal muscle force and intracellular organization of muscle fi

32 tic stage of disease, resulting in increased muscle force and motor unit survival and a significant i

33 st cancer, caused remarkable improvements of muscle force and of diaphragm and cardiac structure in t

34 els are expressed on ASM and regulate smooth muscle force and offer a novel target for therapeutic re

35 n (SA), a mechanical property that increases muscle force and oscillatory power generation, is not kn

36 low-level dystrophin expression, we compared muscle force and pathology in mdx3cv and mdx4cv mice.

37 ponin activator that may be used to increase muscle force and power in conditions of muscle weakness.

38 osed with CK-2066260 show increased hindlimb muscle force and power in response to submaximal rates o

39 atment ameliorated histopathology, increased muscle force and protected against eccentric contraction

40 cal conditions in one ALS patient, improving muscle force and respiratory efficacy.

41 ween the rate of actomyosin dissociation and muscle force and shortening velocity.

42 the mean number of attached bridges, depress muscle force and stiffness, and increase force-length hy

43 thetized, tracheotomized rat in which tongue muscle force and the neural drive to the protrudor and r

44 el with the user's calf muscles, off-loading muscle force and thereby reducing the metabolic energy c

45 bute substantially to the initial changes in muscle force and work.

46 Ross et al. is not only due to variations in muscle forces and cranial morphology, but also due to va

47 ed to simulate MU firing rates and isometric muscle forces and, to that model, we added fatigue-relat

48 and organ masses, muscle histology, in vitro muscle force, and creatine kinase levels were measured.

49 amping properties that may aid or oppose the muscle force; and the environment produces reaction forc

50 and grip is a common task during which high muscle forces are sustained, especially at the proximal

51 man skeletal muscles because the majority of muscle forces are transmitted through this region.

52 bed by a muscle equation of state containing muscle force as a state variable.

53 After assessment of muscle force at days 1, 4, 14, and 42 after injury, samp

54 gested to cause a progressive decline in the muscle force at which motor units are recruited during r

55 This tissue modulates the transfer of muscle forces between two materials, i.e. tendon and bon

56 del of the skull that can be used to predict muscle forces, bite forces, and joint reaction forces wo

57 d utrophin levels, may help maintain minimal muscle force but not arrest muscle degeneration or necro

58 cycle and contributed almost elastically to muscle force, but the rapidly cycling cross-bridge distr

59 st muscle fatigue and increased mdx hindlimb muscle force by 40%, a value comparable to current dystr

60 n an isometric task, where joint torques and muscle forces can be straightforwardly computed from lim

61 tion determines the trajectory of changes in muscle force capacity during prolonged activity.

62 A very large number of possible muscle force combinations will satisfy a particular func

63 s significantly decreased the maintenance of muscle force compared to control.

64 t then level off at modest rates even though muscle force continues to increase.

65 t then level off at modest rates even though muscle force continues to increase.

66 with confidence when model input parameters (muscle forces, detailed material properties) and/or outp

67 Muscle forces determine joint loads, but the objectives

68 Changes in muscle force development as a result of ricin-mAb 35 inj

69 and rate of demembranated (skinned) cardiac muscle force development by exchanging native cardiac tr

70 S; an adapter protein associated with smooth muscle force development) from cytoskeletal vimentin.

71 ion of actin polymerization depresses smooth muscle force development.

72 o diminished actin polymerization and smooth muscle force development.

73 ired for extracellular matrix attachment and muscle force development.

74 cessfully prevented chronic exercise-induced muscle force drop.

75 Whole-muscle force drops from peak force production to zero wi

76 Muscle forces during isometric biting appear to be consi

77 However, after nerve crush, reflex muscle forces during stretch do recover after muscle rei

78 mdx-knockout mice exhibited lower muscle force/endurance as well as increased muscle damag

79 study tested the hypothesis that masticatory muscle forces exerted during static biting are consisten

80 timal length), the steady-state value of the muscle force, F, approximates the isometric force, the m

81 quencies of these oscillations are above the muscle force frequency range.

82 coupling deficits, we compared the papillary muscle force generated by electrically stimulated versus

83 es a myopathy characterized by reductions in muscle force-generating capacity, atrophy (loss of muscl

84 -I, there were significant increases both in muscle force generation and cross-sectional area at all

85 ificantly increased cross-sectional area and muscle force generation lasting over 3 months.

86 ance were independent of central command and muscle force generation, were not activated in anticipat

87 that an endothermic molecular step underlies muscle force generation.

88 apidly improved in movement acceleration and muscle force generation.

89 ine kinase levels, but had limited effect on muscle force generation.

90 uscular transmission and faithfully reported muscle force generation.

91 cross-sectional area and decreased skeletal muscle force generation.

92 les, taking into consideration surrogates of muscle force [ie, muscle cross-sectional area (MCSA) and

93 or, improved muscle relaxation and increased muscle force in HSALR mice without affecting splicing.

94 The specific single twitch and tetanic muscle force in old transgenic soleus and extensor digit

95 that CK-2017357 increases the production of muscle force in situ at sub-maximal nerve stimulation ra

96 sease symptomology that causes resistance in muscle force initiation.

97 ads, but the objectives governing the mix of muscle forces involved are unknown.

98 n equilibrium between agonist and antagonist muscle force is achieved.

99 Our results show that muscle force is associated with a transition of the cros

100 Muscle force is dictated by micrometer-scale contractile

101 Muscle force is generated by myosin crossbridges interac

102 erefore, quantitative assessment of skeletal muscle force is important for diagnosis of intensive car

103 Thus, the temperature sensitivity of muscle force is markedly increased with velocity during

104 The question of whether complicated muscle forcing is required to create the observed deform

105 alis; in particular, motoneuronal inputs and muscle force levels are chosen to approximately achieve

106 meters provide a mechanistic explanation for muscle force loss after EC.

107 In addition, muscle force measured after exercise decreases upon HFD

108 tor activity, histopathology, and individual muscle force measurements of mdx and mdx((5)cv) mice.

109 ither provide resistance against extraocular muscle forces or limit globe axial elongation.

110 x (M1): relatively low-level parameters like muscle force, or more abstract parameters like handpath?

111 tates of a key behavior produce asymmetry in muscle forces, passive joint forces can be coadapted to

112 mpt)) leading to a hypermuscular yet reduced muscle-force phenotype was compared to that in wild-type

113 orylation plays a prominent role in skeletal muscle force potentiation of fast-twitch type IIb but no

114 tal issue in locomotion is to understand how muscle forcing produces apparently complex deformation k

115 of events that contribute to reduced smooth muscle force production during altered metabolism.

116 whether and to what extent 4AP could enhance muscle force production in HCSMA.

117 In addition, muscle force production in isometric contraction was inc

118 icle-shortening velocity at the time of peak muscle force production increased with walking speed, im

119 future investigations and models of skeletal muscle force production must incorporate Tmods.

120 zed expression of NMJ-related genes, in situ muscle force production, and clearance of glycogen in co

121 e model regarding the possibility of maximal muscle force production, and suggest that only 97% of th

122 With no effect on muscle force production, inhibiting alphaARs (phentolami

123 With no effect on muscle force production, inhibiting alphaARs improved RO

124 cted tissue and modify AChR mRNA expression, muscle force production, motor endplate area, and innerv

125 muscle weakness by decreasing Ca(2+)-induced muscle force production.

126 mically modulate stiffness along the axis of muscle force production.

127 taking into account the state dependence of muscle-force production and multijoint mechanics, I show

128 stress we predict working to balancing side muscle force ratios, peak bite forces, and joint reactio

129 assive muscle fire in direct relationship to muscle force-related variables, rather than length-relat

130 Muscle force studies showed more severe strength deficit

131 stimating or measuring the joint torques and muscle forces that underlie movements made by biological

132 factors regulate and/or maintain extraocular muscle force through a rapid mechanism that appears to i

133 sibly through more efficient transmission of muscle force through stiffer intestinal tissue.

134 rom contraction-induced injury and corrected muscle force to the same level as that observed in contr

135 This enhanced the diaphragm muscle force, to a greater extent with lower lung volume

136 dynamic parameters of jaw function including muscle force, torque, effective mechanical advantage, ja

137 For molecular motors and for muscle, force-velocity curves have provided key biophysi

138 Net tongue muscle force was always consistent with tongue retractio

139 wisdom, is based in part on studies in which muscle force was shown to decline more rapidly when stim

140 week after injection, muscle morphology and muscle force were compared between the IGF-treated and c

141 n, systolic blood pressure, and LV papillary muscle force while LV end-diastolic and systolic volume

142 ing, and calculations of how quickly passive muscle force would slow limb movement as limb size varie