ライフサイエンスコーパス: fusimotor

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1 ed as evidence for a higher level of dynamic fusimotor activity maintained during active movements th

2 There was clear evidence of fusimotor activity occurring during active jaw closing s

3 muscle length changes and static and dynamic fusimotor activity to determine primary afferent firing

4 The underlying patterns of fusimotor activity were deduced by comparing afferent di

5 not therefore be able to respond to dynamic fusimotor activity.

6 was taken to represent the profile of static fusimotor activity.

7 vements repeated passively in the absence of fusimotor activity.

8 However, they were not innervated by fusimotor axons and they did not express glial derived n

9 increased numbers of large sensory and small fusimotor axons.

10 rent gains and/or the integrity of automatic fusimotor control.

11 tate of their parent muscle and by efferent (fusimotor) control, and their discharges represent futur

12 erefore attributed to a modulation of static fusimotor discharge approximately in parallel with alpha

13 This need to control gamma-static fusimotor drive explicitly as a function of muscle lengt

14 ntly required the modulation of gamma-static fusimotor drive to produce increases in physiological tr

15 igate the nature (i.e. static or dynamic) of fusimotor drive to the flexor hallucis longus (FHL) and

16 servations are compatible with the view that fusimotor drive varies in different muscles during locom

17 hy humans likely increase their gamma-static fusimotor drive when muscles shorten.

18 ve and active movements, indicating that the fusimotor effects associated with active contractions ha

19 he intrafusal fibres activated by individual fusimotor efferents) were separated by a minimum conduct

20 y selectively operated by static and dynamic fusimotor efferents.

21 This indicated increased dynamic fusimotor firing during active locomotion.

22 iasing activity, presynaptic inhibition, and fusimotor gain).

23 intrafusal muscle fiber differentiation and fusimotor innervation homeostasis.

24 This human-based fusimotor model and its incorporation into the reflex ar

25 rophic factor (GDNF), which is essential for fusimotor neuron survival.

26 Dynamic fusimotor neurone firing appears to be set at a raised l

27 or a variety of active jaw movements, static fusimotor neurone firing is modulated roughly in paralle

28 s, operated separately by static and dynamic fusimotor neurones, and the topological structure of the

29 ion to the concept that the modulated static fusimotor pattern may represent a 'temporal template' of

30 signal matched the predictions of the static fusimotor signal derived from secondary afferents.

31 and separate and combined static and dynamic fusimotor stimulation were recorded in physiological exp

32 This suggests that the way in which the fusimotor system works may differ between the two muscle

33 l not only the skeletal muscles but also the fusimotor system.

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