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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 re recently, in axoplasm isolated from squid giant axons.
9 he Na+ activation gate were studied in squid giant axons.
10 rt along microtubules in axoplasm from squid giant axons.
11 vity inhibits the sealing of crayfish medial giant axons.
12 his pathway in axoplasms isolated from squid giant axons.
13 The temperature difference between the squid giant axon (6.3 degrees C) and RGCs (37 degrees C) is br
14 eratively during the action potential (squid giant axon); a wasteful 85% enter during the falling pha
15 stablished that sodium currents in the squid giant axons activate after a delay, which is explained b
16 onal transport using axoplasm from the squid giant axon and suggest that axonal transport defects may
17 he cortex may reach layer I by virtue of the giant axons, and that several laminar patterns of audito
19 s, which form after transection of earthworm giant axons, are very dynamic in the short term (35 minu
21 H) description of Na and K channels in squid giant axons as the basis of the calculations and find th
22 ut ends of invertebrate myelinated earthworm giant axons beginning with the formation of a dye barrie
25 we internally dialyzed isolated intact squid giant axons (GAs) and showed that elevation of intracell
26 ionic currents in the membrane of the squid giant axon has become the standard model for the electro
28 s because FD Ca channels are absent from the giant axon in situ but, rather, suggest a potential role
30 ciatic or spinal axons and myelinated medial giant axons is measured by the restored conduction of ac
31 II is synthesized in the cell bodies of the giant axon, is present in the axon, and is associated wi
32 of the 70-kDa family in the crayfish medial giant axon (MGA), we analyzed axoplasmic proteins separa
34 examined transected GAs and crayfish medial giant axons (MGAs) with time-lapse confocal fluorescence
35 Organelles in the axoplasm from the squid giant axon move along exogenous actin filaments toward t
36 xoplasmic organelles obtained from the squid giant axon move on actin filaments at an average velocit
38 Abnormal GFAP aggregation also occurs in giant axon neuropathy (GAN), which is caused by recessiv
39 the initial observation that vesicles in the giant axon of the squid move on both microtubules and ac
40 fficient for this recruitment; and (iii) the giant axon of the squid provides a unique system to diss
41 ular and the extracellular potentials of the giant axon of the squid resembles that observed during t
42 the roles of myosins in the axon we used the giant axon of the squid, a powerful model for studies of
43 tor axoplasmic transport of HSV, we used the giant axon of the squid, Loligo pealei, a well known sys
46 ears ago C.A.G. Wiersma established that the giant axons of the crayfish nerve cord drive tail-flip e
47 ssays performed with axoplasm from the squid giant axon showed a requirement for a Rab GTPase in Myo5
48 compose the "delayed rectifier" in the squid giant axon system, but discrepancies regarding inactivat
49 expected nuclear convergence of two types of giant axon terminals, each of which must have independen
51 ling phase of action potentials in the squid giant axon, the diversity of voltage-gated potassium (Kv
52 ley model and for eliciting a spike in squid giant axons, the preparation for which the model was dev
53 nvelopes by detergent were injected into the giant axon, thereby bypassing the infective process.
55 By applying rapid voltage steps to squid giant axons, we previously identified three components i
56 the bath saline induces the sealing of squid giant axons, whereas the addition of inhibitors of calpa
57 anently maintain earthworm myelinated medial giant axons whose functional and morphological integrity
58 acellular perfusion of voltage-clamped squid giant axons with a solution containing K+ and TEA+ irrev
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