ライフサイエンスコーパス: triceps surae

1 s and gastrocnemius and contraction force of triceps surae.

2 uromuscular electrical stimulation (NMES) of triceps surae.

3 nships, and neural drive distribution to the triceps surae.

4 uctor pollicis brevis, anterior tibialis and triceps surae.

5 was determined by stereological analysis of triceps surae (a limb muscle) and extraocular muscles of

6 le, fibre length and muscle thickness in the triceps surae complex in man in response to changes in a

7 reatments, the contractile properties of the triceps surae complex were assessed in situ.

8 Increasing triceps surae contraction velocity during cyclic contrac

9 Voluntary isometric contraction of triceps surae elicited a significant HR change in the fi

10 Sustained passive stretch of triceps surae for 1 min, by dorsiflexion of the foot, ca

11 surae motoneurons from animals in which the triceps surae H-reflex in one leg had been increased (HR

12 Operant conditioning of the primate triceps surae H-reflex, the electrical analog of the spi

13 e analyzed the synaptic terminal coverage of triceps surae motoneurons from animals in which the tric

14 Evidence on how triceps surae motor unit firing properties are influence

15 e uneven distribution of neural drive to the triceps surae muscle at low force levels, characterised

16 We investigated the isolated effect of triceps surae muscle contraction velocity on whole-body

17 with comparable metabolic rates but distinct triceps surae muscle force and velocity demands (walking

18 y lean mass, tibialis anterior (TA) mass and triceps surae muscle mass in response to castration.

19 Static contractions of the triceps surae muscle of one hindlimb were evoked by elec

20 The volume of triceps surae muscle was also increased in 2G compared w

21 es elicited during static contraction of the triceps surae muscle.

22 tely dissociated rat DRG neurons innervating triceps surae muscle.

23 ally on primary afferent neurons innervating triceps surae muscle.

24 al root ganglion (DRG) cells innervating the triceps surae muscles (n = 12).

25 five weeks of rhythmic manual stimulation of triceps surae muscles (non-specific training) and withou

26 lly contracting and passively stretching the triceps surae muscles before and after injection of GsMT

27 lex was evoked by statically contracting the triceps surae muscles before and after injection of the

28 puts drive the motor neurons innervating the triceps surae muscles during isometric ankle plantarflex

29 hetized rats having one of the nerves to the triceps surae muscles either untreated or cut and immedi

30 ex evoked by intermittent contraction of the triceps surae muscles in decerebrated, unanaesthetized r

31 We suggest that the triceps surae muscles maintain balance by predictively c

32 Our measurements suggest that the triceps surae muscles maintain balance via a spring-like

33 are components of NADPH oxidase, compared to triceps surae muscles of 'freely perfused' rats.

34 Western blots showed that the triceps surae muscles of 'ligated' rats expressed more N

35 n of ribosomes) in response to detraining in triceps surae muscles of C57BL/6 mice.

36 alpain and cathepsin L, were measured in the triceps surae muscles of wild-type (WT) and MuRF1-knocko

37 Resistive force and electromyograms from triceps surae muscles were measured during dorsiflexion

38 erebrated rats by statically contracting the triceps surae muscles with or without muscle ischaemia.

39 Of the DRG cells innervating the triceps surae muscles, 85% stained positive for the TRPC

40 receiving group III afferent input from the triceps surae muscles.

41 e the force generating capacity of the TA or triceps surae muscles.

42 was evoked by isometrically contracting the triceps surae muscles.

43 ly identified group Ia muscle afferents from triceps surae or plantaris muscles were labeled intraaxo

44 earch suggests that the moment arm of the m. triceps surae tendon (i.e., Achilles tendon), is positiv

45 The response of the triceps surae (TS) and tibialis anterior (TA) muscles to

46 gely governed by the forces generated by the triceps surae (TS) muscles (gastrocnemius-GAS, soleus-SO

47 ed that segmental reflex excitability of the triceps surae was also modulated in a manner associated

48 ressor response to isometric exercise of the triceps surae was examined in the trained dominant limb

49 the present study, static contraction of the triceps surae was induced by electrical stimulation of L

50 ally evoked isometric exercise (Stim) of the triceps surae was performed for 2 min at 30 % maximum vo

51 CMT Neuropathy Score); in fact, the dominant triceps surae was slightly stronger than the non-dominan

52 PS of the triceps surae was tested in 14 healthy human volunteers.

53 non-painful stimulation was measured in the triceps surae; we found that the soleus reflexes were sm