ライフサイエンスコーパス: backpropagate

1 somadendritic patch-clamp recording to track backpropagated action potentials (APs) in rat AOB primar

2 Backpropagated action potentials recorded at the soma we

3 The backpropagating action potential (BAP) is hypothesised t

4 The [Ca(2+)](i) increase from a backpropagating action potential (bAP) or subthreshold d

5 es via local active conductances, making the backpropagating action potential a candidate for dendrit

6 amplitudes of 10-70% of that generated by a backpropagating action potential at the same location.

7 K(v)7 channels are strongly activated by the backpropagating action potential to attenuate the afterd

8 al neurons is regulated by the spread of the backpropagating action potential to the synapse.

9 nputs and global activation of a neuron by a backpropagating action potential within a dendritic spin

10 pike, the interaction of this spike with the backpropagating action potential, the mechanism responsi

11 ct on the time course of localized events or backpropagating action potential-evoked Ca(2+) signals i

12 re present in spines and can be activated by backpropagating action potentials (APs).

13 Backpropagating action potentials (bAPs) (three at 50 Hz

14 Backpropagating action potentials (bAPs) are an importan

15 Backpropagating action potentials (bAPs) are an importan

16 Backpropagating action potentials (bAPs) are indispensab

17 Dendritic, backpropagating action potentials (bAPs) facilitate the

18 In layer 5 neocortical pyramidal neurons, backpropagating action potentials (bAPs) firing at rates

19 These studies revealed that single backpropagating action potentials (bAPs) produced more r

20 bles that incorporate fast transients due to backpropagating action potentials (bAPs), or other forms

21 However, backpropagating action potentials (BPAPs) have been stud

22 rons, in which dendritic sodium channels and backpropagating action potentials allow somatic spikes t

23 tinguishes LTS from other signals, including backpropagating action potentials and dendritic Ca(2+)/N

24 rites are electrically excitable, exhibiting backpropagating action potentials and fast dendritic cal

25 Second, backpropagating action potentials are able to serve as a

26 Pairing synaptic stimulation with backpropagating action potentials enhanced the likelihoo

27 oral state-dependent manner and suggest that backpropagating action potentials faithfully inform prox

28 KC) leads to an increase in the amplitude of backpropagating action potentials in distal dendrites th

29 endritic tree can exert a powerful impact on backpropagating action potentials in hippocampal pyramid

30 s of [Ca(2+)](i) changes that were evoked by backpropagating action potentials in pyramidal neurons i

31 ential from spines demonstrate directly that backpropagating action potentials invade the spines.

32 n lead to dendritic depolarization, and that backpropagating action potentials may be neither necessa

33 We propose that backpropagating action potentials open glutamate-bound N

34 r dendritic spikes in the same branch, while backpropagating action potentials trigger a widespread r

35 he postsynaptic action potential, carried by backpropagating action potentials, can be strongly degra

36 ic glutamate receptors (mGluRs), paired with backpropagating action potentials, causes large, wave-li

37 indings demonstrate the presence of actively backpropagating action potentials, shifting our understa

38 In contrast, actively backpropagating action potentials, typical of wakefulnes

39 through voltage-gated channels, activated by backpropagating action potentials, was detected at all d

40 Despite the lack of active backpropagating action potentials, we find that trains o

41 d on a Na(+) channel-dependent broadening of backpropagating action potentials.

42 nhibition during dendritic depolarization by backpropagating action potentials.

43 tion, which many current models attribute to backpropagating action potentials.

44 m local NMDA application in conjunction with backpropagating action potentials.

45 voked a larger dendritic calcium influx than backpropagating action potentials.

46 aired soma- dendritic whole-cell recordings, backpropagated APs were unattenuated up to approximately

47 cium influx into dendrites and spines during backpropagating APs (average increase, ~40%).

48 As a result SK channel activation by backpropagating APs gated STDP induction during low-freq

49 midal neurons regulate calcium influx during backpropagating APs in a distance-dependent manner, and

50 that activation of SK channels in spines by backpropagating APs plays a key role in regulating both

51 Voltage waveforms of backpropagating APs were minimally altered in the same d

52 ttle amplitude and time course modulation on backpropagating APs; (2) are strongly invaded by the som

53 Next, the somatic sink backpropagated at a speed of millimeters per minute into

54 the execution of the sequence and ultimately backpropagated away from stereotyped sequence actions, b

55 dritic spiking by adjusting the amplitude of backpropagating axonal action potentials.

56 mputing through intelligent, neural networks backpropagated by Levenberg-Marquardt scheme (NNs-BLMS)

57 nge in the baseline-to-peak amplitude of the backpropagating dendritic action potential (bAP) was not

58 s or by weak synaptic inputs coinciding with backpropagating dendritic action potentials.

59 : a unique, localized, superdissipative, and backpropagating flow structure coexisting with the lamin

60 We measured backpropagated gradients for phase-shifter voltages by i

61 Here, we show that by backpropagating gradients through the transform-restrain

62 ma, triggering axonal action potentials that backpropagate into the dendrites.

63 + rise from single action potentials as they backpropagate into the oblique dendrites from the main t

64 iring caused by axosomatic Kv7 channel block backpropagated into distal dendrites affecting their act

65 Somatically generated APs actively backpropagated into the dendritic tree and evoked instan

66 id reduce the amplitude of action potentials backpropagating into the apical dendrite.

67 are always recorded first at the soma before backpropagating into the dendrites while undergoing subs

68 tile framework that performs optimization by backpropagating LLM-generated feedback to improve AI sys

69 n that the N20 component presumably reflects backpropagating membrane potentials toward the apical de

70 s reduced through the block of Ca(2+) entry, backpropagating Na(+) spikes and synaptically evoked EPS

71 Imaging studies revealed that backpropagating Na(+) spikes and synaptically evoked EPS

72 hippocampus, Na+-dependent action potentials backpropagate over the dendrites in an activity-dependen

73 eport cross-modal dendritic interactions via backpropagating postsynaptic potentials.

74 This backpropagating SD current flow resembles that of activi

75 mitochondria, the coincidence of EPSP with a backpropagating spike produced prominent, highly localiz

76 Backpropagating spikes caused increases in [Ca2+]i at al

77 oltage-dependent calcium conductances by the backpropagating spikes during sharp wave bursts may be c

78 Therefore, backpropagating spikes in these cells can only influence

79 ML model determines the trainable weights by backpropagating the loss function.

80 al synaptic stimulation rapidly and actively backpropagated throughout the entire dendritic arbor and

81 siological conditions in rat nerve terminals backpropagated up the axon ( approximately 400-800 micro

82 ikely in the axon initial segment, that then backpropagate with high fidelity into the dendrites, res