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2 k exhibited high sensitivity (465.9 +/- 48.0 nA/mM), a low detection limit of 1 muM, a linear respons
3 ciliary neurons had large-amplitude (1.5-8.0 nA) EPSCs that could be classified according to the kine
4 ns during GABA diffusion from the pipette (0 nA) and the response quickly progressed to complete sile
5 n potential (AP) generation (0.012 +/- 0.004 nA); (iv) firing of APs throughout a depolarizing pulse
6 dition to a high sensitivity (-0.16 +/- 0.02 nA muM(-1)) and a low limit of detection (0.33 +/- 0.20
9 evation (from 0.22 +/- 0.04 to 0.30 +/- 0.03 nA, P < .05) of the threshold current amplitude required
10 , increased dramatically from -0.14 +/- 0.04 nA at P1 to -6.71 +/- 0.65 nA at P4 with sharp jumps bet
11 rent amplitudes to pH 6.0 were 0.84 +/- 0.06 nA (oxidative muscle) versus 1.36 +/- 0.07 nA (glycolyti
14 Muller cells (1.3 +/- 0.1 versus 1.2 +/- 0.1 nA at -160 mV) or in inwardly rectifying current-voltage
18 /- 3 mU/min; and LCL was 4 +/- 1 and 5 +/- 1 nA in steatotic and nonsteatotic hepatocytes, respective
25 or example, a mean outward K(+) current of 1 nA for 2 s could decrease [K(+)](i) from 10 mM to 3 mM i
27 ane potential, firing rate in response to +1 nA of injected current, slope of the frequency-current c
29 y increased in amplitude from -0.76 +/- 0.10 nA at 25 degrees C to -1.11 +/- 0.19 nA 35 degrees C.
30 was attenuated by application of Mg2+ (1-10 nA) in sixteen of seventeen neurones or Cd2+ (2-10 nA) i
33 h was evident at low ejection currents (5-10 nA), had relatively short onset (4-12 s) and offset (6-2
35 outward potassium current ( approximately 10 nA), decreased muscle input resistance (50-fold), and a
38 as highly selective and sensitive (LRS>/=100 nA/mM) for each analyte and within an adequate range for
39 is kept below a certain critical level (<100 nA at positive potential and <25 nA at negative potentia
41 from approximately 14.5 to approximately 103 nA by combining the pyro-phototronic and piezo-phototron
43 creased Im (-0.249+/-0.038 to -0.571+/-0.111 nA, P<0.05) at -100 mV and reduced Rm (151+/-21 to 77+/-
45 eurones tested, ionophoresis of Mg2+ (10-120 nA) attenuated the PBG-evoked increases in synaptic nois
48 response time (<4 s), high sensitivity (1200 nA/mM x cm2), low interference from endogenous electroac
50 reased sensitivity to dopamine, at 46 +/- 13 nA/muM, compared to 26 +/- 6 nA/muM for the electrodes c
51 culture medium (pH 7.3), a sensitivity of 13 nA/mM was obtained and the response was linear up to 5 m
52 Three-terminal memory devices produced 14 nA read currents at an operating voltage of 5 V, and ope
53 induced current amplitudes were 2.3 +/- 0.15 nA (oxidative muscle) versus 3.1 +/- 0.21 nA (glycolytic
55 4-fold beta-saturated porphynoids are 13-17 nA/T, showing that the inner-cross 18pi [16]annulene pat
60 8 +/- 0.2 nA in control cells to 0.9 +/- 0.2 nA in cells expressing the epsilon subunit (P < 0.05).
61 de activated by GABA (1 mM) from 1.8 +/- 0.2 nA in control cells to 0.9 +/- 0.2 nA in cells expressin
63 njected or uninjected) oocytes (-1.0 +/- 0.2 nA); the Na+-dependent histidine transport showed a stoi
66 10 nM and 220 microM, a sensitivity of 14.2 nA x microM(-1), and good selectivity against ascorbic a
67 pA pF(-1); cutaneous Aalpha/beta LTMs: -2.2 nA, -20 pA pF(-1); Abeta-nociceptors: -2.6 nA, -21 pA pF
68 tailoring of the glucose electrodes for > 2 nA/mM sensitivity; 0-30 mM dynamic range; drift of < or
69 l initiation required currents of at least 2 nA for their generation and never occurred repetitively.
70 te voltages (<1 V) with low gate leakage (<2 nA), highlighting the defect-free and conformal nature o
75 ones ionophoretic application of PBG (10-200 nA) depolarized the membrane and increased firing rate w
76 ound to be generated at a current of 150-200 nA in detectable quantities: with a yield of 0.5-1 H2O2
79 and 100 muM, sensitivity of 275, 500 and 217 nA muM(-1) cm(-2), and detection limits of 0.4, 0.2 and
81 mic range, 6 nM-0.4 microM; sensitivity, 225 nA microM(-1); detection limit (k = 3 criterion), 2 nM.
83 the chlorins and bacteriochlorins are 19-24 nA/T depending on whether the ring current is forced to
84 level (<100 nA at positive potential and <25 nA at negative potential for 96% ethanol; < 40 nA at pos
87 microm)-stimulated K+ currents of 308 +/-26 nA and 298 +/-29 nA, respectively, which were both Ba2+-
89 ed K+ currents of 308 +/-26 nA and 298 +/-29 nA, respectively, which were both Ba2+- and pertussis to
91 biosensor shows a sensitivity of 4.7 +/- 1.3 nA mM(-1)mm(-2) and a detection limit of 1.4mM (S/N = 3s
92 (-1); both Adelta-LTMs and nociceptors: -1.3 nA, approximately -14 pA pF(-1); C-LTMs: -0.4 nA, -7.6 p
93 sensitivity of the biosensor was 110 +/- 1.3 nA/(mM mm(2)) with the apparent Michaelis-Menten constan
94 100 nm gave the highest sensitivity of 19.3 nA mL (pg IL-6)(-1) cm(-2) and the best detection limit
95 0.1 to 100 muM, and high sensitivity of 76.3 nA muM(-)(1) were achieved for the detection of methylgl
96 Prolonged AMPH iontophoresis (2-3 min; 5-30 nA) inhibited both spontaneous impulse activity and Glu-
97 active neurons known to respond to ACh (5-30 nA) when the animals rested quietly with no overt moveme
100 deposition at 0 V led to a sensitivity of 34 nA nM(-1) min(-1), a 4-fold improvement over previous me
104 nsitivity were calculated as 0.229 mM, 42.37 nA, 3.3 x 10(-4)nM and 6.4 nA/mM cm(2), respectively.
105 nA, 59.7+/-17.5 microM), ribavirin (546+/-37 nA, 61.0+/-13.2 microM), AZT (420+/-4 nA, 310+/-9 microM
106 ielded sensitivities of 0.38, 0.41, and 0.38 nA/ppmv for measurements at 9%, 33%, and 76% humidity, r
108 roM (five points) had slopes of 35.2 +/- 0.4 nA microM(-1) and correlation coefficients of 0.999.
109 A, approximately -14 pA pF(-1); C-LTMs: -0.4 nA, -7.6 pA pF(-1); and C-nociceptors: -0.26 nA, -5 pApF
111 /mug mL(-1), A = 92.9 nA/mug mL(-1), T = 1.4 nA/mug mL(-1), and C = 15.1 9 nA/mug mL(-1)), low limit
113 6+/-37 nA, 61.0+/-13.2 microM), AZT (420+/-4 nA, 310+/-9 microM), and 3-deazauridine (506+/-30 nA, 50
115 accelerate a deuteron beam (> 100 keV and >4 nA), which, upon striking a deuterated target, produces
117 tracellular recording experiments, PBG (0-40 nA) increased the firing rate of thirty-five of the thir
119 neurons were highly sensitive to GABA (0-40 nA, 20 s); most showed short-latency inhibitions during
126 e and excellent selectivity to glucose (0.47 nA/mM) against interferants such as ascorbic acid, uric
127 tion of the M3 receptor produced 2382 +/-478 nA of current which was insensitive to Ba2+ and pertussi
131 ons had smaller-amplitude responses (0.2-1.5 nA when all inputs were activated) that appeared to cont
132 1 mM) evoked current (I(His) = -14.7 +/- 1.5 nA) in NBAT-expressing oocytes compared with native (wat
133 ude (and dominant decay ) fell from around 5 nA (: 40-50 ms) at P10/11 to 0.3-0.5 nA (: 10-15 ms) by
134 iostat with a large dynamic current range (5 nA to 1.2 mA) and short conversion time (10 ms) were fab
135 intracellular current injection (+/-0.5 to 5 nA, 20 s pulses) while V(m) changed linearly between app
137 of the SAMN-BMIM-PF6-CP electrode was 206.51 nA muM(-1)cm(-2), with a detection limit (S/N=3) of 0.8
138 76 nA (mean +/- SEM), n=13 versus 342 +/- 55 nA in WT, n=13), while the co-expression of 1/2 WT+1/2 R
141 ucleoside analog drugs gemcitabine (638+/-58 nA, 59.7+/-17.5 microM), ribavirin (546+/-37 nA, 61.0+/-
142 in AMPA-mediated current amplitude (0.3-0.6 nA) in the range of CA1 apical dendrites that receive a
143 iration a large magnitude (approximately 0.6 nA) outward current generated by Na(+)/K(+) ATPase that
144 from -9 +/- 0.8 nA at pH 7.5 to -19 +/- 2.6 nA at pH 6.5, at which histidine is predominantly cation
145 2 nA, -20 pA pF(-1); Abeta-nociceptors: -2.6 nA, -21 pA pF(-1); both Adelta-LTMs and nociceptors: -1.
146 e, at 46 +/- 13 nA/muM, compared to 26 +/- 6 nA/muM for the electrodes coated in 200 muM EDOT and 13
147 ectively:muscle spindle afferents(MSAs):-4.6 nA,-33 pA pF(-1); cutaneous Aalpha/beta LTMs: -2.2 nA, -
148 n large inward 'AD current' (approximately 6 nA) which was largely prevented by blocking AMPA recepto
149 iezoelectric generator that produces up to 6 nA of current and 400 mV of potential and use it to oper
150 from 0.2 to 3.0 nM (R (2) = 0.9947) and 7.60 nA x microM (-1) from 0.5 to 4.0 microM ( R (2) = 0.9999
154 opores have unusually high sensitivity (0.65 nA/A) to extremely small changes in the translocating mo
156 can be detected with the sensitivity of 0.7 nA muM(-1) and the limit of detection of 0.5 muM (3 sB/m
158 GLU-induced excitations (mean threshold 19.7 nA) were dose-dependent, inversely correlated with rate
159 osensor exhibits high sensitivity (1.9x10(7) nA(-1)), low limit of detection (1.7x10(-7) M), high sto
162 00 ng/muL with improved sensitivity of 36.72 nA/ng/cm(2), faster response time of 3s and high stabili
163 reased from -3.14 +/- 0.59 to -4.15 +/- 0.73 nA with the fast decay time constant accelerating from 0
165 uced a current similar to the WT (369 +/- 76 nA (mean +/- SEM), n=13 versus 342 +/- 55 nA in WT, n=13
166 ward 0.1 mM I(His) increased from -9 +/- 0.8 nA at pH 7.5 to -19 +/- 2.6 nA at pH 6.5, at which histi
169 3) was 8-130 muM and the sensitivity was 1.8 nA muM(-1) (RSD=5.0%) for substrate of Baeyer-Villiger o
170 performance with a sensitivity of 2.4+/-1.8 nA/microM, a response time of 20+/-13 s and a lower dete
171 r exhibited excellent sensitivity (G = 178.8 nA/mug mL(-1), A = 92.9 nA/mug mL(-1), T = 1.4 nA/mug mL
175 onophoretic application of ATP (0.2 M, 20-80 nA for 40 s) increased the activity of approximately 80
178 the P2 receptor blocker suramin (0.02 M, 80 nA), which also reduced the baseline firing in some expi
179 at the sensitivity increased (1840 to 25 800 nA muM(-1)) and the limit of detection decreased (11.10
180 ose, characterized by a sensitivity of 45.85 nA muM(-1)cm(-2) and a detection limit (S/N=3) of 0.9 mu
181 L(-1), T = 1.4 nA/mug mL(-1), and C = 15.1 9 nA/mug mL(-1)), low limit of detection (G, A = 0.5 mug m
183 nsitivity (G = 178.8 nA/mug mL(-1), A = 92.9 nA/mug mL(-1), T = 1.4 nA/mug mL(-1), and C = 15.1 9 nA/
185 imum amplitude of reduction peak current (A, nA), a reduction peak area (S, nA x V), and a peak poten
187 one that could be used with 2-aminoadenine (nA) and 2-thiothymine (sT) to generate structure-free DN
188 nucleoside triphosphates of 2-aminoadenine (nA) and 2-thiouracil (sU) are taken up by T7 RNA polymer
194 implied by classic nucleation theory and its nA right harpoon over left harpoon An, "critical nucleus
195 These results suggest that incorporation of nA and sU during in vitro transcription is a promising s
197 life cycle, stemming from a finite value of nA~3, underscores a key feature of developmental systems
199 k current (A, nA), a reduction peak area (S, nA x V), and a peak potential (P, V), were measured for
201 ombined with the destabilizing effect of the nA-sU couple in RNA targets, accounts for the improved h
204 dance configuration permitted high gain (1 V/nA) to measure pA-nA level currents in the detection cel
205 yl or ethyl) can be used in conjunction with nA and sT to render DNA largely structure-free and pseud
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