ライフサイエンスコーパス: motoneuronal

1 ion may be an effective means of controlling motoneuronal activity in a behavior-dependent manner.

2 We conclude that hypoglossal motoneuronal activity is more strongly influenced by che

3 Motoneuronal activity was recorded simultaneously from a

4 e central preparation; recruitment curves of motoneuronal activity were then generated.

5 that allows a temporally specific control of motoneuronal activity within a single phase of motor pro

6 muscle contractions are a graded function of motoneuronal activity, one consequence of the shortening

7 ators (CPGs) may be used to control rhythmic motoneuronal activity.

8 ating inspiratory drive to hypoglossal (XII) motoneuronal activity.

9 e alterations in neuronal properties at both motoneuronal and pre-motoneuronal levels.

10 definitively that TASK channels account for motoneuronal, anesthetic-activated K(+) currents and to

11 he proximal femur and distal tibia, based on motoneuronal birth order.

12 ith labeled and unlabeled dendrites in these motoneuronal cell groups and contain large amounts of sp

13 NRA projects to a somewhat different set of motoneuronal cell groups compared with other species fit

14 nd contains premotor neurons that project to motoneuronal cell groups in the brainstem and spinal cor

15 oneurons involved in vocalization, i.e., the motoneuronal cell groups innervating soft palate, pharyn

16 To identify motoneuronal cell groups receiving input from the NRA, t

17 behavior by means of projections to distinct motoneuronal cell groups.

18 ce in the iliopsoas, axial, and pelvic floor motoneuronal cell groups.

19 hat under certain circumstances even cortico-motoneuronal cells, which make monosynaptic connections

20 uscles of rhesus monkeys to identify cortico-motoneuronal (CM) cells in the primary motor cortex (M1)

21 This enabled us to define cortico-motoneuronal (CM) cells that make monosynaptic connectio

22 rged together with the appearance of cortico-motoneuronal (CM) connections during the evolution of th

23 al system and, in particular, direct cortico-motoneuronal (CM) connections to hand muscles.

24 The significance of direct, cortico-motoneuronal (CM) connections, which were discovered a l

25 and bilateral projections to the respiratory motoneuronal columns.

26 axon initial segment (AIS), but not on other motoneuronal compartments, inhibited the action potentia

27 we show using electrophysiology that cortico-motoneuronal connections from fast conducting CST fibers

28 how that all parts of M1 and 3a have cortico-motoneuronal connections over more slowly conducting CST

29 w M1") and area 3a make monosynaptic cortico-motoneuronal connections with limb motoneurons.

30 nd pharmacological understanding of specific motoneuronal contributions to eye movements might help i

31 a controlling signal of pre- and post-alpha motoneuronal control of the soleus H-reflex.

32 ith retrogradely labeled genioglossus muscle motoneuronal dendrites and perikarya in the hypoglossal

33 cal properties, and consequently altered the motoneuronal dendritic processing of synaptic inputs.

34 ic connections between the interneuronal and motoneuronal elements that generate the two behaviors.

35 vel of the pTRG diminished the contralateral motoneuronal EPSPs as well as a local injection of 6-cya

36 ting a role of phosphorylation in modulating motoneuronal excitability affecting behaviorally relevan

37 These effects of halothane decrease motoneuronal excitability and may contribute to the immo

38 Neurotransmitters increase motoneuronal excitability by inhibiting TWIK-related aci

39 Since protein kinase-dependent modulation of motoneuronal excitability contributes to adaptive change

40 inducing long-term increases in genioglossal motoneuronal excitability to AMPA-mediated drive may hel

41 latile anaesthetics have opposing effects on motoneuronal excitability which appear to reflect contra

42 e--activated 5-HT1A receptors that decreased motoneuronal excitability.

43 ced membrane hyperpolarization and increased motoneuronal excitability.

44 examines the role of polyamine modulation of motoneuronal excitation in situ, with an emphasis on pos

45 otoneurons, thereby diminishing serotonergic motoneuronal excitation.

46 relevant role of the MLF pathway in driving motoneuronal firing and evidenced compensatory mechanism

47 th motoneurons and were active just prior to motoneuronal firing in each segment.

48 (2) The kt value (change in motoneuronal firing necessary to increase motor unit for

49 permanent, 2 months after ATD lesioning all motoneuronal firing parameters were similar to the contr

50 laminae V-VIII, as well as the laterodorsal motoneuronal group of lamina IX (which innervates distal

51 nce of phosphorylated eIF-2a should minimize motoneuronal injury in obstructive sleep apnea.

52 entation of eIF-2a phosphorylation minimizes motoneuronal injury in this model.

53 ckroach Blaberus discoidalis; in particular, motoneuronal inputs and muscle force levels are chosen t

54 s activating protein kinase G (PKG) modulate motoneuronal inspiratory drive currents and long-term pl

55 espiratory-related rhythm, hypoglossal (XII) motoneuronal inspiratory drive currents and respiratory-

56 ruthenium red, we found a major component of motoneuronal isoflurane-sensitive TASK-like current that

57 these transmitters might be detected at the motoneuronal level during muscle tone suppression elicit

58 rd by acting at both the premotoneuronal and motoneuronal levels.

59 onal properties at both motoneuronal and pre-motoneuronal levels.

60 s maintaining muscle strength in the face of motoneuronal loss caused by injury or disease.

61 e association of SOD1-G85R or SOD1-G93A with motoneuronal mitochondria is reduced capacity of the ETC

62 iated by inhibition of rhythmogenic and (pre)motoneuronal networks; and (iii) pre-inspiratory (Pre-I)

63 cytoplasmic ribonucleoprotein complexes from motoneuronal NSC-34 cells.

64 lar circuitry makes it likely that a similar motoneuronal organization is also implemented in other v

65 d show that Zfh1 cell autonomously regulates motoneuronal outgrowth and larval growth of neuromuscula

66 Synchrony strength in cortico-motoneuronal output neurons in primary motor cortex depe

67 edback to the CNS which, in turn, constrains motoneuronal output to the active skeletal muscle.

68 Although motoneuronal output was 21 +/- 12% higher during FENT co

69 Motoneuronal output was estimated through vastus lateral

70 rones and plays an important role in shaping motoneuronal output.

71 ization by activating the prefrontal-PAG-NRA-motoneuronal pathway, and, at the same time, they modula

72 receptors were localized at the membrane of motoneuronal perikarya and dendrites.

73 o enriched at glutamatergic synapses in both motoneuronal perikarya and dendrites.

74 pTRG neurons projecting to the vagal motoneuronal pool were identified in a restricted area o

75 n part, through activation of nonhypoglossal motoneuronal pools innervating the UA muscles.

76 A(A) gamma2 levels towards control values in motoneuronal pools of both muscles.

77 neurons terminate preferentially within the motoneuronal pools of the lumbosacral spinal cord that i

78 study demonstrates the presence of specific motoneuronal populations with pharmacological profiles t

79 Motoneuronal potassium currents were unaffected.

80 r formation prolonged the inhibitory phrenic motoneuronal response to superior laryngeal nerve stimul

81 imulation and abolished or reduced abdominal motoneuronal responses during respiration, vomiting, and

82 Defects in motoneuronal retrograde axonal transport may critically

83 Because both the reticulospinal and the motoneuronal segmental patterns persist in the hindbrain

84 he inability to meet the surge in demand for motoneuronal SMN that was seen in controls.

85 king a functional Scn8a sodium channel gene, motoneuronal sodium current density was comparable at P0

86 Motoneuronal soma size in Nissl stain revealed the same

87 hin Rexed's lamina IX, in close proximity to motoneuronal somata.

88 Because of the spinal motoneuronal somatotopic organization, motor coordinatio

89 In contrast, primary motoneuronal specification depends on the presence of so

90 In addition, a positive correlation between motoneuronal survival and voiding efficiency was observe

91 Modulation of residual corticospinal-motoneuronal synapses may present a novel therapeutic ta

92 ding and peripheral volleys at corticospinal-motoneuronal synapses of an intrinsic finger muscle in h

93 pendent plasticity of residual corticospinal-motoneuronal synapses provides a mechanism to improve mo

94 ion to the nRO spinal autonomic and pudendal motoneuronal targets, projections were observed to regio

95 Some cholinergic motoneuronal terminals on both Renshaw cells and motoneu

96 , and Shh to NSFCs induced the expression of motoneuronal transcription factors, tyrosine hydroxylase