ライフサイエンスコーパス: giant axon

1 example in the well-known case of the squid giant axon.

2 ort of peptide-conjugated beads in the squid giant axon.

3 ntains the cell bodies that give rise to the giant axon.

4 ctifier K+ channel (SqK(v)1.1A) in the squid giant axon.

5 ating action potential repolarization in the giant axon.

6 neurofilaments (NFs) isolated from the squid giant axon.

7 mitter release at the motor terminals of the giant axon.

8 his pathway in axoplasms isolated from squid giant axons.

9 ures are the following: (a) Comb nerves with giant axons.

10 he Na+ activation gate were studied in squid giant axons.

11 rt along microtubules in axoplasm from squid giant axons.

12 vity inhibits the sealing of crayfish medial giant axons.

13 re recently, in axoplasm isolated from squid giant axons.

14 The temperature difference between the squid giant axon (6.3 degrees C) and RGCs (37 degrees C) is br

15 eratively during the action potential (squid giant axon); a wasteful 85% enter during the falling pha

16 stablished that sodium currents in the squid giant axons activate after a delay, which is explained b

17 onal transport using axoplasm from the squid giant axon and suggest that axonal transport defects may

18 The squid giant axon and synapse, for example, laid the foundation

19 y studied jellyfish because of its system of giant axons and unique fast swimming/escape behaviors.

20 he cortex may reach layer I by virtue of the giant axons, and that several laminar patterns of audito

21 Squid giant axons are formed by giant fiber lobe (GFL) neurons

22 s, which form after transection of earthworm giant axons, are very dynamic in the short term (35 minu

23 rane excitability and results from the squid giant axon as an experimental data base.

24 H) description of Na and K channels in squid giant axons as the basis of the calculations and find th

25 ings from acutely dissociated single lamprey giant axon AZs, and by lattice light sheet microscopy of

26 ut ends of invertebrate myelinated earthworm giant axons beginning with the formation of a dye barrie

27 In addition, working with the squid giant axon, Cole and Moore noted that strong hyperpolari

28 ape activation by enhancing the amplitude of giant axon depolarization.

29 In contrast, squid giant axons do not seal, even though injury-induced vesi

30 central nervous system with three subsets of giant axons, dozen subtypes of neurons, muscles, and a v

31 we internally dialyzed isolated intact squid giant axons (GAs) and showed that elevation of intracell

32 Giant axons (>=160 mum(2)) enlarged by disorganized IFs,

33 ionic currents in the membrane of the squid giant axon has become the standard model for the electro

34 osin motors that transport S-ER in the squid giant axon has been determined.

35 s because FD Ca channels are absent from the giant axon in situ but, rather, suggest a potential role

36 Following severance of crayfish medial giant axons in physiological saline, vesicles accumulate

37 tions within the Aglantha lineage (including giant axons innervating striated muscles) strongly suppo

38 ciatic or spinal axons and myelinated medial giant axons is measured by the restored conduction of ac

39 II is synthesized in the cell bodies of the giant axon, is present in the axon, and is associated wi

40 of the 70-kDa family in the crayfish medial giant axon (MGA), we analyzed axoplasmic proteins separa

41 Crayfish medial giant axons (MGAs) transected in physiological saline fo

42 examined transected GAs and crayfish medial giant axons (MGAs) with time-lapse confocal fluorescence

43 Organelles in the axoplasm from the squid giant axon move along exogenous actin filaments toward t

44 xoplasmic organelles obtained from the squid giant axon move on actin filaments at an average velocit

45 ication of native cysteines present in squid giant axon Na channels with methanethiosulfonates.

46 Abnormal GFAP aggregation also occurs in giant axon neuropathy (GAN), which is caused by recessiv

47 the initial observation that vesicles in the giant axon of the squid move on both microtubules and ac

48 fficient for this recruitment; and (iii) the giant axon of the squid provides a unique system to diss

49 ular and the extracellular potentials of the giant axon of the squid resembles that observed during t

50 the roles of myosins in the axon we used the giant axon of the squid, a powerful model for studies of

51 tor axoplasmic transport of HSV, we used the giant axon of the squid, Loligo pealei, a well known sys

52 ER) is transported on actin filaments in the giant axon of the squid.

53 on and its experimental confirmation for the giant axon of the squid.

54 ears ago C.A.G. Wiersma established that the giant axons of the crayfish nerve cord drive tail-flip e

55 ssays performed with axoplasm from the squid giant axon showed a requirement for a Rab GTPase in Myo5

56 compose the "delayed rectifier" in the squid giant axon system, but discrepancies regarding inactivat

57 expected nuclear convergence of two types of giant axon terminals, each of which must have independen

58 nal, relationship between the populations of giant axon terminals.

59 es) are edited more extensively in the squid giant axon than in its cell bodies.

60 ling phase of action potentials in the squid giant axon, the diversity of voltage-gated potassium (Kv

61 ley model and for eliciting a spike in squid giant axons, the preparation for which the model was dev

62 nvelopes by detergent were injected into the giant axon, thereby bypassing the infective process.

63 After injection into the squid giant axon, tubulin was transported in an anterograde di

64 By applying rapid voltage steps to squid giant axons, we previously identified three components i

65 the bath saline induces the sealing of squid giant axons, whereas the addition of inhibitors of calpa

66 anently maintain earthworm myelinated medial giant axons whose functional and morphological integrity

67 acellular perfusion of voltage-clamped squid giant axons with a solution containing K+ and TEA+ irrev