The theoretical power density spectrum G(f) of fluctuations in the steady-state squid axon K+ current in the 103 Hz region has been derived assuming that these are fluctuations in the number of open K+ channels in the Hodgkin-Huxley (HH) model. Various modifications of the HH model were also studied. The results were negative in all cases when compared with experiment. This confirms the generally held view that the observed G(f) ∼ 1/f is associated primarily with K+ current through open K+ channels and not with the open-close kinetics of these channels
The solutions, n(t), of the differential equation dn/dt = α (1 - n) n (4 - 6n + 4n2 - n3) - βn2 (4 -...
One of the most celebrated successes in computational biology is the Hodgkin-Huxley framework for mo...
We have measured the fluctuations in the current through gramicidin A (GA) channels in symmetrical s...
The theoretical power density spectrum G(f) of fluctuations in the steady-state squid axon K+ curren...
We consider the equilibrium or steady-state noise power density spectrum in the quantity N = Σxi=0ai...
We consider the equilibrium or steady-state noise power density spectrum in the quantity N = Σxi=0ai...
A model is presented for the ionic mechanism of low frequency 1/f electrical noise which has been ob...
A quantitative study of the steady-state behavior of the sodium and potassium conductance for the Ho...
Differentiation of membrane channel models based on fluctuation (or noise) analysis is discussed. Th...
A model is presented for the ionic mechanism of low frequency 1/f electrical noise which has been ob...
Threshold fluctuations in axon firing can arise as a result of electrical noise in the excitable mem...
We have developed a novel technique for simulating the influence of the effects of single channel ki...
A standard membrane model, based on the continuous deterministic Hodgkin-Huxley equations, is compar...
Random fluctuations in the steady-state current of neural membrane were measured in the giant lobste...
Voltage-gated ion channels in neuronal membranes fluctuate randomly between different conformational...
The solutions, n(t), of the differential equation dn/dt = α (1 - n) n (4 - 6n + 4n2 - n3) - βn2 (4 -...
One of the most celebrated successes in computational biology is the Hodgkin-Huxley framework for mo...
We have measured the fluctuations in the current through gramicidin A (GA) channels in symmetrical s...
The theoretical power density spectrum G(f) of fluctuations in the steady-state squid axon K+ curren...
We consider the equilibrium or steady-state noise power density spectrum in the quantity N = Σxi=0ai...
We consider the equilibrium or steady-state noise power density spectrum in the quantity N = Σxi=0ai...
A model is presented for the ionic mechanism of low frequency 1/f electrical noise which has been ob...
A quantitative study of the steady-state behavior of the sodium and potassium conductance for the Ho...
Differentiation of membrane channel models based on fluctuation (or noise) analysis is discussed. Th...
A model is presented for the ionic mechanism of low frequency 1/f electrical noise which has been ob...
Threshold fluctuations in axon firing can arise as a result of electrical noise in the excitable mem...
We have developed a novel technique for simulating the influence of the effects of single channel ki...
A standard membrane model, based on the continuous deterministic Hodgkin-Huxley equations, is compar...
Random fluctuations in the steady-state current of neural membrane were measured in the giant lobste...
Voltage-gated ion channels in neuronal membranes fluctuate randomly between different conformational...
The solutions, n(t), of the differential equation dn/dt = α (1 - n) n (4 - 6n + 4n2 - n3) - βn2 (4 -...
One of the most celebrated successes in computational biology is the Hodgkin-Huxley framework for mo...
We have measured the fluctuations in the current through gramicidin A (GA) channels in symmetrical s...