ライフサイエンスコーパス: nA

1 2.1-20.6 mM and a sensitivity of 7.8 +/- 1.0 nA/mM (n = 6).

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 todetectors (EQE < 5%, dark current > 10,000 nA cm(-2)).

6 , with a high sensitivity of 0.097 +/- 0.001 nA/muM and one-week storage stability.

7 2) sensor showed a slope of -0.052 +/- 0.002 nA/muM H(2)O(2) at pH 7.2 and a detection limit of 1.0 +

8 n potential (AP) generation (0.012 +/- 0.004 nA); (iv) firing of APs throughout a depolarizing pulse

9 dition to a high sensitivity (-0.16 +/- 0.02 nA muM(-1)) and a low limit of detection (0.33 +/- 0.20

10 ectrode is achieved at a sensitivity of 0.02 nA/spot.

11 nM for cysteine with sensitivities of 0.023 nA/microM and 4.71 nA/microM, respectively.

12 evation (from 0.22 +/- 0.04 to 0.30 +/- 0.03 nA, P < .05) of the threshold current amplitude required

13 , increased dramatically from -0.14 +/- 0.04 nA at P1 to -6.71 +/- 0.65 nA at P4 with sharp jumps bet

14 rent amplitudes to pH 6.0 were 0.84 +/- 0.06 nA (oxidative muscle) versus 1.36 +/- 0.07 nA (glycolyti

15 6 nA (oxidative muscle) versus 1.36 +/- 0.07 nA (glycolytic muscle, P < 0.05).

16 range with a resulting sensitivity of 0.096 nA muM(-1).

17 Muller cells (1.3 +/- 0.1 versus 1.2 +/- 0.1 nA at -160 mV) or in inwardly rectifying current-voltage

18 an be focused to less than 3 microm with 0.1 nA currents.

19 ectric field, a field-emission current (<0.1 nA in our device) switches the mesoscopic superconductor

20 ar response above 20 microm with approx. 0.1 nA/microM slope.

21 Nonmass selective currents up to 1.1 nA and mass-selected currents of up to 500 pA have been

22 d 0.1-5 mM for glucose, sensitivities of 4.1 nA/mM.mm(2) for lactate and 56 nA/mM.mm(2) for glucose,

23 /- 3 mU/min; and LCL was 4 +/- 1 and 5 +/- 1 nA in steatotic and nonsteatotic hepatocytes, respective

24 g the aptamer surface coverage, was 67 +/- 1 nA muM(-1) cm(-2), and the dopamine LOD was 62 nM.

25 imally activated currents (Imax) of around 1 nA.

26 ourse similar to the PF sEPSP, peaking at -1 nA in 700 ms.

27 GHz, at which the pumping current exceeds 1 nA.

28 -14 mice, light-evoked EPSCs were large (> 1 nA at -70 mV).

29 ted Cl(-) currents in HEK cells that were >1 nA in amplitude.

30 toresistance of 1100% at a bias current of 1 nA and a giant anomalous zero-bias spin voltage effect i

31 or example, a mean outward K(+) current of 1 nA for 2 s could decrease [K(+)](i) from 10 mM to 3 mM i

32 N cells of several hundred pA to more than 1 nA.

33 ane potential, firing rate in response to +1 nA of injected current, slope of the frequency-current c

34 Lower sensitivities (1.13 x 10(-1) nA/mM glucose) are observed when immobilization method i

35 y increased in amplitude from -0.76 +/- 0.10 nA at 25 degrees C to -1.11 +/- 0.19 nA 35 degrees C.

36 was attenuated by application of Mg2+ (1-10 nA) in sixteen of seventeen neurones or Cd2+ (2-10 nA) i

37 sixteen of seventeen neurones or Cd2+ (2-10 nA) in seven of eight neurones tested.

38 Ionophoresis of AP5 (2-10 nA), at currents which selectively inhibited NMDA-evoked

39 h was evident at low ejection currents (5-10 nA), had relatively short onset (4-12 s) and offset (6-2

40 of approximately 0.1 V and approximately 10 nA cm(-2) .

41 outward potassium current ( approximately 10 nA), decreased muscle input resistance (50-fold), and a

42 samples yielding mass 44 ion currents of 10 nA.

43 ials of +/-2 VDC and gains of 1, 10, and 100 nA/V.

44 as highly selective and sensitive (LRS>/=100 nA/mM) for each analyte and within an adequate range for

45 is kept below a certain critical level (<100 nA at positive potential and <25 nA at negative potentia

46 t can be tuned from zero to greater than 100 nA.

47 from approximately 14.5 to approximately 103 nA by combining the pyro-phototronic and piezo-phototron

48 ble, albeit at a decreased sensitivity (0.11 nA muM(-1)).

49 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+/-

50 rease in hSlo1 current density from 20 to 12 nA*M ohm.

51 eurones tested, ionophoresis of Mg2+ (10-120 nA) attenuated the PBG-evoked increases in synaptic nois

52 (40 nA) and excitation at high currents (120 nA).

53 of 8.25 nmol L(-1) and a sensitivity of 120 nA L micromol(-1).

54 response time (<4 s), high sensitivity (1200 nA/mM x cm2), low interference from endogenous electroac

55 g DNA concentration and a sensitivity of 122 nA decade(-1) was achieved.

56 king electrode yields a sensitivity of 0.127 nA/muM and a limit of quantitation (LOQ) of 9 muM.

57 reased sensitivity to dopamine, at 46 +/- 13 nA/muM, compared to 26 +/- 6 nA/muM for the electrodes c

58 culture medium (pH 7.3), a sensitivity of 13 nA/mM was obtained and the response was linear up to 5 m

59 L(-1), with a sensitivity of (5.56 +/- 0.13) nA L mg(-1) and a limit of detection of (0.5 +/- 0.3) mg

60 Three-terminal memory devices produced 14 nA read currents at an operating voltage of 5 V, and ope

61 induced current amplitudes were 2.3 +/- 0.15 nA (oxidative muscle) versus 3.1 +/- 0.21 nA (glycolytic

62 also permits sensitive tactile sensing (0.15 nA kPa(-1)).

63 the energy spread of the electron beam at 15 nA is 100 meV or better.

64 4-fold beta-saturated porphynoids are 13-17 nA/T, showing that the inner-cross 18pi [16]annulene pat

65 ch would deny coherent superpositions of 170 nA currents over a approximately 10 ns timescale.

66 /- 0.10 nA at 25 degrees C to -1.11 +/- 0.19 nA 35 degrees C.

67 tegrated NG device reaches up to 3 V and 195 nA under human walking conditions.

68 SP produced an outward current of 3 +/- 0.2 nA (n = 10).

69 8 +/- 0.2 nA in control cells to 0.9 +/- 0.2 nA in cells expressing the epsilon subunit (P < 0.05).

70 de activated by GABA (1 mM) from 1.8 +/- 0.2 nA in control cells to 0.9 +/- 0.2 nA in cells expressin

71 mit of detection for glucose of 19.4 +/- 0.2 nA mM(-1) and 13.1 +/- 0.7 muM, respectively.

72 njected or uninjected) oocytes (-1.0 +/- 0.2 nA); the Na+-dependent histidine transport showed a stoi

73 Na+-independent outward current (11 +/- 1.2 nA) in NBAT-expressing oocytes.

74 ectrodes coated in 200 muM EDOT and 13 +/- 2 nA/muM for an uncoated fiber.

75 10 nM and 220 microM, a sensitivity of 14.2 nA x microM(-1), and good selectivity against ascorbic a

76 pA pF(-1); cutaneous Aalpha/beta LTMs: -2.2 nA, -20 pA pF(-1); Abeta-nociceptors: -2.6 nA, -21 pA pF

77 n limit of 0.05 muM and a sensitivity of 3.2 nA.muM(-1) in a pH = 7.4 phosphate buffer solution.

78 tailoring of the glucose electrodes for > 2 nA/mM sensitivity; 0-30 mM dynamic range; drift of < or

79 l initiation required currents of at least 2 nA for their generation and never occurred repetitively.

80 te voltages (<1 V) with low gate leakage (<2 nA), highlighting the defect-free and conformal nature o

81 In most cells, short (2 ms), strong (2 nA) current injections elicited a single spike followed

82 Prolonged GABA application (0-20 nA, 2-4 min) reduced basal impulse activity, but was les

83 DNQX (5-20 nA), at currents which selectively inhibited AMPA-evoked

84 ively high AMPH ejection currents (> or = 20 nA).

85 ones ionophoretic application of PBG (10-200 nA) depolarized the membrane and increased firing rate w

86 ound to be generated at a current of 150-200 nA in detectable quantities: with a yield of 0.5-1 H2O2

87 ug/mL was electrosprayed at a current of 200 nA.

88 15 nA (oxidative muscle) versus 3.1 +/- 0.21 nA (glycolytic muscle, P < 0.05).

89 and 100 muM, sensitivity of 275, 500 and 217 nA muM(-1) cm(-2), and detection limits of 0.4, 0.2 and

90 sitivities were determined to be 205 and 222 nA/microM, respectively.

91 mic range, 6 nM-0.4 microM; sensitivity, 225 nA microM(-1); detection limit (k = 3 criterion), 2 nM.

92 11.7, with average NO sensitivities of 1.24 nA/muM and a limit of detection (LOD) of <1 nM.

93 the chlorins and bacteriochlorins are 19-24 nA/T depending on whether the ring current is forced to

94 level (<100 nA at positive potential and <25 nA at negative potential for 96% ethanol; < 40 nA at pos

95 An electron beam of 250 nA could be obtained through the 0.45-mm diameter openin

96 nA, -7.6 pA pF(-1); and C-nociceptors: -0.26 nA, -5 pApF(-1).

97 microm)-stimulated K+ currents of 308 +/-26 nA and 298 +/-29 nA, respectively, which were both Ba2+-

98 ns have the strongest ring current of ca. 27 nA/T among the investigated porphynoids.

99 ed K+ currents of 308 +/-26 nA and 298 +/-29 nA, respectively, which were both Ba2+- and pertussis to

100 Current was injected (+/-0.1-3 nA) at site 1 while recording membrane potential (V(m))

101 biosensor shows a sensitivity of 4.7 +/- 1.3 nA mM(-1)mm(-2) and a detection limit of 1.4mM (S/N = 3s

102 (-1); both Adelta-LTMs and nociceptors: -1.3 nA, approximately -14 pA pF(-1); C-LTMs: -0.4 nA, -7.6 p

103 sensitivity of the biosensor was 110 +/- 1.3 nA/(mM mm(2)) with the apparent Michaelis-Menten constan

104 to 500 muM, with a sensitivity of about 1.3 nA/muM.

105 100 nm gave the highest sensitivity of 19.3 nA mL (pg IL-6)(-1) cm(-2) and the best detection limit

106 0.1 to 100 muM, and high sensitivity of 76.3 nA muM(-)(1) were achieved for the detection of methylgl

107 to 26 GHz frequency with current values 8.3 nA and limited by the present set-up bandwidth.

108 strated a sensor with high sensitivity (82.3 nA/[mumol L(-1).cm(-2)]), low limit of detection (LOD, 8

109 in UHV with high ion beam intensity (up to 3 nA) limiting contaminations and deposition time, and (iv

110 Prolonged AMPH iontophoresis (2-3 min; 5-30 nA) inhibited both spontaneous impulse activity and Glu-

111 active neurons known to respond to ACh (5-30 nA) when the animals rested quietly with no overt moveme

112 10+/-9 microM), and 3-deazauridine (506+/-30 nA, 50.8+/-9.90 microM).

113 at coherent structures is typically above 30 nA/m(2).

114 sivity of 0.31 A/W), 3 GHz bandwidth, and 30 nA dark current at a reverse bias of 30 V.

115 deposition at 0 V led to a sensitivity of 34 nA nM(-1) min(-1), a 4-fold improvement over previous me

116 r produced an inward current of 1.6 +/- 0.35 nA (n = 27) in approximately 80% of the neurones.

117 red the current by 29% versus WT (243 +/- 35 nA, n=13, p<0.05).

118 .31 +/- 0.55 nA/muM for DA and 9.47 +/- 0.36 nA/muM for E2.

119 ction limit of 6.4 muM and sensitivity of 36 nA mM(-1).

120 nsitivity were calculated as 0.229 mM, 42.37 nA, 3.3 x 10(-4)nM and 6.4 nA/mM cm(2), respectively.

121 nA, 59.7+/-17.5 microM), ribavirin (546+/-37 nA, 61.0+/-13.2 microM), AZT (420+/-4 nA, 310+/-9 microM

122 ielded sensitivities of 0.38, 0.41, and 0.38 nA/ppmv for measurements at 9%, 33%, and 76% humidity, r

123 The sensitivity of 2.38 nA ppb(-1) obtained in the present work for As(III) quan

124 roM (five points) had slopes of 35.2 +/- 0.4 nA microM(-1) and correlation coefficients of 0.999.

125 A, approximately -14 pA pF(-1); C-LTMs: -0.4 nA, -7.6 pA pF(-1); and C-nociceptors: -0.26 nA, -5 pApF

126 ith sensitivities of 9 +/- 9 and 1.2 +/- 0.4 nA/muM, respectively.

127 /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

128 buffer solutions with a sensitivity of 26.4 nA/mM and a linear range of 0.45 to 9.0 mM.

129 tential of 0.15 V with a sensitivity of 42.4 nA/muM and a detection limit of 2.4 nM.

130 6+/-37 nA, 61.0+/-13.2 microM), AZT (420+/-4 nA, 310+/-9 microM), and 3-deazauridine (506+/-30 nA, 50

131 s 0.229 mM, 42.37 nA, 3.3 x 10(-4)nM and 6.4 nA/mM cm(2), respectively.

132 accelerate a deuteron beam (> 100 keV and >4 nA), which, upon striking a deuterated target, produces

133 single large input, typically larger than 4 nA, emerged from P3-P4.

134 tracellular recording experiments, PBG (0-40 nA) increased the firing rate of thirty-five of the thir

135 Iontophoretically applied GLU (0-40 nA, 20 s) excited all spontaneously active neurons in do

136 neurons were highly sensitive to GABA (0-40 nA, 20 s); most showed short-latency inhibitions during

137 AMPH dose-dependently (5-40 nA) inhibited the vast majority of spontaneously active

138 nded to cause inhibition at low currents (40 nA) and excitation at high currents (120 nA).

139 ut relatively high AA ejection currents (>40 nA) often inhibited fast-firing units.

140 at negative potential for 96% ethanol; < 40 nA at positive potential for water).

141 35% (>1 mum) and dark current density < 400 nA cm(-2), a >25% increase in EQE and >90% reduced dark

142 on limit of 2.8 nM and a sensitivity of 9.46 nA microM-1.

143 reatment from 0.55 +/- 0.32 to 3.25 +/- 0.47 nA (n=6, P < .01).

144 e and excellent selectivity to glucose (0.47 nA/mM) against interferants such as ascorbic acid, uric

145 tion of the M3 receptor produced 2382 +/-478 nA of current which was insensitive to Ba2+ and pertussi

146 le L-type currents were measured (469 +/- 48 nA in 10 mM Ba2+).

147 The sensitivity is 49 nA nM(-1) min(-1) with 30 s deposition time and the LOD

148 higher sensitivity of -2.496 nA/mmHg (-1.495 nA/muM) when comparing with its bare counterpart.

149 cally showing a higher sensitivity of -2.496 nA/mmHg (-1.495 nA/muM) when comparing with its bare cou

150 round 5 nA (: 40-50 ms) at P10/11 to 0.3-0.5 nA (: 10-15 ms) by P18.

151 ons had smaller-amplitude responses (0.2-1.5 nA when all inputs were activated) that appeared to cont

152 1 mM) evoked current (I(His) = -14.7 +/- 1.5 nA) in NBAT-expressing oocytes compared with native (wat

153 nitude of the Jy(0) in the CSFI is about 5.5 nA/m(2).

154 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

155 iostat with a large dynamic current range (5 nA to 1.2 mA) and short conversion time (10 ms) were fab

156 intracellular current injection (+/-0.5 to 5 nA, 20 s pulses) while V(m) changed linearly between app

157 Microiontophoresis of ACh (500 ms, 500 nA) onto the distal end of a feed artery evoked hyperpol

158 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

159 uantify ALT with increased sensitivity (1.53 nA/(U/L*mm(2)) and over a wide, linear concentration ran

160 w 30 nM and high sensitivity: 11.31 +/- 0.55 nA/muM for DA and 9.47 +/- 0.36 nA/muM for E2.

161 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

162 t of 200 nM and sensitivity of 84.5 +/- 1.56 nA microM(-1)cm(-2).

163 Enhanced sensitivity (up to 1.56 nA muM(-1)) and lowered theoretical detection limits (do

164 vities of 4.1 nA/mM.mm(2) for lactate and 56 nA/mM.mm(2) for glucose, and limit of detections of 0.41

165 ucleoside analog drugs gemcitabine (638+/-58 nA, 59.7+/-17.5 microM), ribavirin (546+/-37 nA, 61.0+/-

166 with sensitivity of 2.84 nA muM(-1) and 3.59 nA muM(-1) for liquid-liquid and liquid-organogel interf

167 in AMPA-mediated current amplitude (0.3-0.6 nA) in the range of CA1 apical dendrites that receive a

168 iration a large magnitude (approximately 0.6 nA) outward current generated by Na(+)/K(+) ATPase that

169 from -9 +/- 0.8 nA at pH 7.5 to -19 +/- 2.6 nA at pH 6.5, at which histidine is predominantly cation

170 2 nA, -20 pA pF(-1); Abeta-nociceptors: -2.6 nA, -21 pA pF(-1); both Adelta-LTMs and nociceptors: -1.

171 e, at 46 +/- 13 nA/muM, compared to 26 +/- 6 nA/muM for the electrodes coated in 200 muM EDOT and 13

172 ectively:muscle spindle afferents(MSAs):-4.6 nA,-33 pA pF(-1); cutaneous Aalpha/beta LTMs: -2.2 nA, -

173 ifetime of 188 h with average current of 8.6 nA under continuous illumination, and no decrease of QE

174 n large inward 'AD current' (approximately 6 nA) which was largely prevented by blocking AMPA recepto

175 iezoelectric generator that produces up to 6 nA of current and 400 mV of potential and use it to oper

176 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

177 integrity of increased ion currents up to 60 nA during bulk milling of thicker planar samples, showin

178 that of CDPG (maximal amplitude, 272 +/- 62 nA).

179 <1 s, and the sensitivity of analysis was 62 nA muM(-1) cm(-2).

180 om -0.14 +/- 0.04 nA at P1 to -6.71 +/- 0.65 nA at P4 with sharp jumps between P2 and P4.

181 opores have unusually high sensitivity (0.65 nA/A) to extremely small changes in the translocating mo

182 een 5 and 200 nM, and a sensitivity of 83.65 nA x microM(-1) were recorded.

183 can be detected with the sensitivity of 0.7 nA muM(-1) and the limit of detection of 0.5 muM (3 sB/m

184 currents had a mean amplitude of 2.6 +/- 0.7 nA with activation and fast inactivation V(50) values of

185 mit of 50 nM and sensitivity of 98.5 +/- 1.7 nA microM(-1)cm(-2).

186 GLU-induced excitations (mean threshold 19.7 nA) were dose-dependent, inversely correlated with rate

187 biosensor that offers a sensitivity of 22.7 nA/(muM.cm(2)), a limit of detection (LOD) of 9.4 muM, a

188 ion from 6.2 mV and 9 nA to 24.2 mV and 34.7 nA for [Formula: see text] nm.

189 previous IR model, and from 24.2 mV and 34.7 nA to 38.8 mV and 80.9 nA for the improved IR model.

190 steps for frequencies up to 24 GHz (I = 7.7 nA).

191 osensor exhibits high sensitivity (1.9x10(7) nA(-1)), low limit of detection (1.7x10(-7) M), high sto

192 th sensitivities of 0.023 nA/microM and 4.71 nA/microM, respectively.

193 age sensitivity of the microsensors was 1.72 nA/muM and the limit of detection was 25 nM.

194 00 ng/muL with improved sensitivity of 36.72 nA/ng/cm(2), faster response time of 3s and high stabili

195 reased from -3.14 +/- 0.59 to -4.15 +/- 0.73 nA with the fast decay time constant accelerating from 0

196 rrent were similar (approximately 365 +/- 75 nA at 1 microM CDPG) to those of InsP3.

197 uced a current similar to the WT (369 +/- 76 nA (mean +/- SEM), n=13 versus 342 +/- 55 nA in WT, n=13

198 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

199 In a reciprocal manner, +0.8 nA caused depolarization ( approximately 2 mV) of SMCs w

200 Injection of -0.8 nA into an EC caused hyperpolarization ( approximately 5

201 3) was 8-130 muM and the sensitivity was 1.8 nA muM(-1) (RSD=5.0%) for substrate of Baeyer-Villiger o

202 performance with a sensitivity of 2.4+/-1.8 nA/microM, a response time of 20+/-13 s and a lower dete

203 r exhibited excellent sensitivity (G = 178.8 nA/mug mL(-1), A = 92.9 nA/mug mL(-1), T = 1.4 nA/mug mL

204 ing from 6.2 mV and 9 nA to 11.7 mV and 18.8 nA for the previous IR model, and from 24.2 mV and 34.7

205 te biosensor the sensitivity is 12.2 +/- 3.8 nA mM(-1)mm(-2) and the detection limit is 0.3mM.

206 Current injection (up to 8 nA) into a single CM cell elicited electrotonic potentia

207 nnels with 0.33 +/- 0.14 versus 2.5 +/- 0.80 nA of amiloridesensitive inward current at -80 mV.

208 onophoretic application of ATP (0.2 M, 20-80 nA for 40 s) increased the activity of approximately 80

209 Brief applications of AA (20 s, 5-80 nA) elicited few changes in either basal activity or act

210 vity toward the oxidation of oxalic acid (80 nA/nM) achieved by the amperometry method.

211 the P2 receptor blocker suramin (0.02 M, 80 nA), which also reduced the baseline firing in some expi

212 at the sensitivity increased (1840 to 25 800 nA muM(-1)) and the limit of detection decreased (11.10

213 97 muM and 0.71 muM with sensitivity of 2.84 nA muM(-1) and 3.59 nA muM(-1) for liquid-liquid and liq

214 ose, characterized by a sensitivity of 45.85 nA muM(-1)cm(-2) and a detection limit (S/N=3) of 0.9 mu

215 cal aptamer-based sensor (292 muA/dec vs. 85 nA/dec).

216 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

217 equivalent current dipole source was 38+/-9 nA-m (n=17).

218 from 24.2 mV and 34.7 nA to 38.8 mV and 80.9 nA for the improved IR model.

219 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/

220 2.5nm to 10nm, increasing from 6.2 mV and 9 nA to 11.7 mV and 18.8 nA for the previous IR model, and

221 reasing standard deviation from 6.2 mV and 9 nA to 24.2 mV and 34.7 nA for [Formula: see text] nm.

222 Sensitivities in the range of 9.97 nA/mM glucose are observed when the enzyme is immobilize

223 imum amplitude of reduction peak current (A, nA), a reduction peak area (S, nA x V), and a peak poten

224 ary A-T couple consisting of 2-aminoadenine (nA) and 2-thiothymine (sT) bases.

225 one that could be used with 2-aminoadenine (nA) and 2-thiothymine (sT) to generate structure-free DN

226 nucleoside triphosphates of 2-aminoadenine (nA) and 2-thiouracil (sU) are taken up by T7 RNA polymer

227 Bicoid (Bcd) morphogen gradient's amplitude nA.

228 , or both, Hmx2/HMX2 and Hmx3/HMX3 in B- and nA/nB ICs.

229 In contrast, 300 microgram ml-1 Co nA (a specific kainate receptor desensitization blocker)

230 DNA-RNA hybrids that contained nA and sU in the RNA strand exhibited enhanced specifici

231 RNA hairpins that contained nA and sU were able to hybridize to DNA probes under con

232 r protein heterointeractions of the type D + nA<-->DA(n).

233 es generate A-ICs, the former also generates nA/nB-ICs and the latter B-ICs.

234 NonA-nonB-ICs (nA/nB-ICs) also produce Slc26a4 though their function is

235 high resistance, small switching currents in nA range, low power generated, and signals that can be d

236 implied by classic nucleation theory and its nA right harpoon over left harpoon An, "critical nucleus

237 1.8 currents that even 99% inhibition leaves nA-level Nav1.8 current that could help drive repetitive

238 These results suggest that incorporation of nA and sU during in vitro transcription is a promising s

239 The high stability of nA-T and A-sU base pairs in DNA-RNA hybrids, combined wi

240 life cycle, stemming from a finite value of nA~3, underscores a key feature of developmental systems

241 n permitted high gain (1 V/nA) to measure pA-nA level currents in the detection cell.

242 k current (A, nA), a reduction peak area (S, nA x V), and a peak potential (P, V), were measured for

243 ction at gate voltages < 1 V, respond to sub-nA gate currents, and offer ion current amplification wi

244 The nA-sT couple is a mismatch even though nA-T and A-sT are

245 e biosensor measurement with currents in the nA range and a resolution of 54 pA.

246 ombined with the destabilizing effect of the nA-sU couple in RNA targets, accounts for the improved h

247 The nA-sT couple is a mismatch even though nA-T and A-sT are stable base pairs.

248 No A(U)nA mRNA instability motifs were present.

249 dance configuration permitted high gain (1 V/nA) to measure pA-nA level currents in the detection cel

250 yl or ethyl) can be used in conjunction with nA and sT to render DNA largely structure-free and pseud

251 Either analog could be used with nA and sT to generate DNA that was nearly structure-free