1 cells and subjected them to a computational
noise analysis.
2 ics criteria with incorporation of signal-to-
noise analysis among Texas Children's Hospital cases.
3 k that extends classical extrinsic-intrinsic
noise analysis and enables mapping of noise within upstr
4 We combined nonstationary
noise analysis and modeling techniques to estimate the c
5 By a combination of signal-to-
noise analysis and numerical simulations, we demonstrate
6 R2A channels using single-channel recording,
noise analysis and spectral analysis.
7 gh numerous control experiments, conductance
noise analysis and transport calculations based on densi
8 rge single-channel conductance, derived from
noise analysis,
and previous immunolocalization studies
9 We present a signal-to-
noise analysis based on a new data set of soil cation he
10 are and equation-generated data; 2) a system
noise analysis combined with Monte Carlo simulations; an
11 Non-stationary
noise analysis demonstrated that GLT-1c and EAAT5 also d
12 We integrate a discriminative
noise analysis for ds and ss DNA topologies into the thr
13 Kinetic modeling and nonstationary
noise analysis for gamma(2)R43Q reveal that these effect
14 We report here a detailed
noise analysis for oligonuleotide-based microarray exper
15 present an updated framework and a signal-to-
noise analysis for using soil-based mass balance approac
16 mal analysis of these data in the equivalent
noise analysis framework showed that the most parsimonio
17 ransporters show single-channel behavior and
noise analysis in native cells strongly suggests channel
18 on cross-correlational techniques and white-
noise analysis in spherical auditory space.
19 Non-stationary
noise analysis indicated that enhanced Ca(2+) channel cu
20 properties of the chemotaxis network from a
noise analysis of behavioural variations in individual b
21 Results from macroscopic current
noise analysis of both wild-type CFTR and K1250A-CFTR ch
22 Furthermore, a peak-scaled nonstationary
noise analysis of mEPSCs revealed a larger estimated sin
23 e Wiener kernels derived from standard white-
noise analysis of noise-driven discharge in neurones act
24 Non-stationary
noise analysis of Rb+ currents in cell-attached apical m
25 Non-stationary
noise analysis of Rb+ currents in cell-attached patches
26 clamp technique in conjunction with current
noise analysis of recordings containing multiple channel
27 ctuations decrease during acidification, but
noise analysis of single-vesicle data confirms our findi
28 Quasi-stationary
noise analysis of the AMPH-induced hDAT currents reveale
29 Using non-stationary
noise analysis of the mIPSCs, I estimate that GABA(A) re
30 The b1 bipolar cell is known from
noise analysis of the On-alpha ganglion cell to have a n
31 Noise analysis of the SiNW array with and without the Ag
32 Noise analysis of the system is presented.
33 From
noise analysis of the tonic current, GABA(C) receptor ga
34 Using
noise analysis of the whole-cell MC current, the single
35 Noise analysis of whole-cell currents indicates that app
36 otoreceptors from the tiger salamander using
noise analysis on whole-cell patch-clamp recordings.
37 The detailed
noise analysis presented here uses an experimental desig
38 te permeant in L46P EAAT2, and nonstationary
noise analysis revealed slightly increased unitary curre
39 Nonstationary
noise analysis revealed that GoF effects observed for bo
40 Noise analysis revealed that I domain mutations introduc
41 In addition, our seismic
noise analysis reveals an asymmetry and a high coherence
42 Noise analysis showed that protons regulate TMEM16A by t
43 However,
noise analysis showed that the apparent unitary conducta
44 In this study, using
noise analysis,
statistics of time-resolved single-chann
45 Noise analysis suggested that blocking Na+ channels with
46 From
noise analysis the estimated single channel conductance
47 From
noise analysis the single channel conductance (gamma) wa
48 Here we use white-
noise analysis to measure tuning functions of V2 neurons
49 mammalian cells, patch-clamp recordings and
noise analysis to study and compare glutamate transport
50 Noise analysis,
using Wiener kernels, indicates that cli
51 System
noise analysis was also carried out and the different no
52 Stationary and nonstationary
noise analysis was consistent with a sub-femtosiemen Cl-
53 Amino acid-level signal-to-
noise analysis was performed.
54 Using
noise analysis,
we demonstrate that alkaline block is me
55 ing single-molecular conductance and Flicker
noise analysis,
we have probed the interfacial electric
56 Noise analysis (
with the assumption of independent gatin