ライフサイエンスコーパス: iso-

1 nergic receptor activation by isoproterenol (ISO).

2 protein powder containing 3 mg isoflavones; -ISO).

3 o signals produced by the isthmic organizer (IsO).

4 rved betaAR responsiveness to isoproterenol (ISO).

5 11 > delta22 > delta33) and associated delta(iso).

6 NP and at a site dilated with isoproterenol (ISO).

7 mal beta1-AR activation using isoproterenol (Iso).

8 mulated ex vivo by insulin or isoproterenol (ISO).

9 esence of activated PKA (with Isoproterenol, ISO).

10 the chemical shift tensor and thereby delta(iso).

11 s induced by the beta-agonist isoproterenol (ISO).

12 ignals emanating from the isthmus organizer (IsO).

13 energic agonist isoproterenol (isoprenaline; ISO).

14 d presence of the beta-agonist isoprenaline (Iso).

15 the beta2-adrenergic agonist isoproterenol (ISO).

16 by the beta-adrenergic agonist isoprenaline (Iso).

17 ose (HG) and the beta-agonist isoproterenol (ISO).

18 nhancing electron transfer (ET) from W400 to ISO*.

19 weakly coupled (2)H has r(eff) = 3.8 A and A(iso) = 0 MHz.

20 At the azeotrope, x(iso) = 0.68, one of the methyl groups aligned approximat

21 ues in transgenic mice during isoproterenol (ISO, 0.02 micrograms/kg per minute) infusion were higher

22 asal I(Ba) by 40.5+/-7.4% and isoproterenol (ISO, 0.1 micromol/L)-stimulated I(Ba) by 48.9+/-7.8%.

23 between sites prior to (SNP: 0.42 +/- 0.11; ISO: 0.46 +/- 0.11 AU mmHg(-1) (AU, arbitrary units), P

24 Isoproterenol (isoprenaline; ISO; 0.01 microM), a non-selective beta-AR agonist, elic

25 When isoproterenol (ISO; 0.1 microM) plus the beta(2)-AR antagonist ICI 118,

26 Specifically, isoproterenol (ISO; 0.1 micromol/L) induces a 3-fold increase in the nu

27 or a beta-adrenergic agonist, isoproterenol (ISO; 0.2 mg/kg BW) alone or in combination with 500 micr

28 ; 0.3 to 3 micromol/L) and/or isoproterenol (Iso; 0.2 to 1 micromol/L).

29 presence of a subthreshold concentration of Iso (0.001 microM).

30 ld constant, LV dP/dt rose by 33 +/- 2% with ISO (0.02 micrograms/kg per minute) and by only 13 +/- 2

31 rrents were also activated by isoproterenol (ISO, 1 microM, 6.9 +/- 2.4 pA/pF, n = 6).

32 d the beta-adrenergic agonist isoproterenol (ISO, 1 mumol/L)-stimulated increase in ICa-L.

33 following drug infusion (SNP: 1.36 +/- 0.21; ISO: 1.27 +/- 0.23 AU mmHg(-1), P > 0.05).

34 icroM), NE (0.1-10 microM) or isoproterenol (ISO; 1 microM) or in combinations of CCH, NE, or ISO wit

35 The beta-adrenergic agonist isoproterenol (ISO; 1 muM) increased [Ca(2+)](SR) well above the contro

36 However, the highest concentration of ISO (1 x 10(-5) M) rescued cardiac function.

37 f submaximally stimulating concentrations of Iso (1-3 nM) resulted in a transient rebound stimulation

38 After pretreatment with isoproterenol (ISO) (1 mumol/L), PDBu still increased the NKA V(max) an

39 mM K+o, noradrenaline (NA) and isoprenaline (Iso) (1-50 microM) stimulated Ip by 40-45%.

40 the experimental ENDOR data, for complex 1 A(iso) = -1 MHz.

41 prazosin (0.1 micromol/L), or isoproterenol (ISO, 10 micromol/L) for 24 hours.

42 's solution with or without a combination of iso (10 microM) and roli (2 microM).

43 In contrast, in the presence of IL-13 plus ISO (10 minutes), binding of GRK2 to PEBP1 decreased, wh

44 0 minutes) pretreatment were stimulated with ISO (10 minutes).

45 d 64% decreases in the ability of subsequent ISO (10(-6) M) stimulation to reduce HASM cell stiffness

46 , whereas LiCl (10 mmol/L) or isoproterenol (ISO) (10 micromol/L), a treatment known to inhibit GSK-3

47 However, ISO (100 micromol/L) elicited less relaxation after mode

48 osed of 92% 2-(+/-)-[13C]JA and 8% 2-(+/-)-7-iso-[13C]JA.

49 The isotropic hyperfine constant (((17)O)A(iso) = -16.8 MHz) was derived from the experimental valu

50 esonance spectroscopy in toluene solution: g(iso) = 2.007; A(53Cr) = 125 MHz; A(13CO) = 22.5 MHz; A(O

51 gle subcutaneous injection of isoproterenol (ISO; 200 mg/kg) in mice causes acute myocyte death (8%-1

52 /-1%)>ALB (2+/-1%); 10 mcmol/L: NE (35+/-2%)>ISO (23+/-1%)>ALB (3+/-1%); 100 mcmol/L: NE (50+/-2%)>IS

53 dip) tensor of (+5.6, +5.3, -10.9) MHz and A(iso) = -25.9 MHz for the [Fe(IV)H(3)buea(O)](-) complex,

54 -1%)>ALB (3+/-1%); 100 mcmol/L: NE (50+/-2%)>ISO (29+/-2%)>ALB (14+/-1%), P<0.0001 except for NE vers

55 ut the PARP inhibitors 1,5-isoquinolinediol (ISO; 3 mg kg(-1) d(-1) intraperitoneally) and 10-(4-meth

56 (150 nl) of the beta-agonist isoproterenol (ISO) (3.75 microg, 17 nmol) into MS, but not SI (150-450

57 3 (48 hours) or isoproterenol hydrochloride (ISO; 30 minutes) pretreatment were stimulated with ISO (

58 in-diabetic rats treated with/without ABA or ISO (30 and 3 mg x kg(-1) x day(-1), intraperitoneally,

59 uct radical (isotropic hyperfine coupling, A(iso) = 4.7 MHz), and (d) a second type of C1 beta-(2)H c

60 e Wistar rats received a single injection of ISO (5 mg kg-1) and were sacrificed 1, 3, and 6 days lat

61 (P<0.05) for MB(p) (12+/-2 U) than either MB(iso) (6+/-3 U) or MB (5+/-3 U).

62 tions of both the hyperfine tensor ((14)N, A(iso) = -6.25 MHz, T = -0.94 MHz) and the quadrupolar ten

63 trant activity during ACh (49+/-39%) and ACh/Iso (62+/-25%) (P=0.38).

64 d) a second type of C1 beta-(2)H coupling (A(iso) = 7.7 MHz).

65 d relaxation in cTnI S23/24D myocytes (delta Iso: 7.2 ms) relative to the maximum Iso effect (31.2 ms

66 aining [1 mcmol/L: NE (8+/-2%) approximately ISO (7+/-1%)>ALB (2+/-1%); 10 mcmol/L: NE (35+/-2%)>ISO

67 yperfine coupling to the bridging hydride (A(iso) = -75.8 MHz).

68 3+/-22% versus eIF2Bepsilon only; P<0.05) or ISO (+84+/-33% versus eIF2Bepsilon only; P<0.05) enhance

69 nificantly more than in F-HVMs (NF >LVAD> F: ISO: 90+/-15% versus 77+/-19% versus 24+/-12%; db-cAMP:

70 reased cell size (+107+/-35%) as strongly as ISO (+95+/-25%), and abolished antihypertrophic effects

71 is induced by stimulation of isoproterenol (ISO), a beta-adrenergic agonist with a peak at approxima

72 ed whether small infusions of isoproterenol (ISO), a beta-adrenergic agonist, into MS alter behaviora

73 action after stimulation with isoproterenol (ISO), a beta-adrenergic receptor (betaAR) agonist.

74 In HF myocytes and muscle, isoproterenol (ISO), a beta-AR agonist, led to small inotropic and lusi

75 renergic receptor activation [isoproterenol (ISO)], a protocol that may be particularly relevant to n

76 Here, we describe mzMatch-ISO, a new extension to the metabolomics analysis pipeli

77 d in two, temporally distinct ways after TPS-ISO: a transient rise in the fraction of phosphorylated

78 bition of the R(-)-isoproterenol bitartrate (Iso)-activated Cl- current was also reversed by the cGMP

79 om Bacillus subtilis to synthesize branched (iso-) alkanes.

80 a-adrenergic receptor agonist isoproterenol (ISO) also induced persistent PDE3A down-regulation and c

81 factor (ANF) transcription by isoproterenol (ISO), an agonist for the beta-adrenergic receptor (betaA

82 ed Fgf8 expression in the isthmus organiser (IsO), an embryonic signalling centre that directs early

83 activity upstream of CRTISO, which we term Z-ISO, an activity that catalyzes the cis- to trans-conver

84 hes Ar(iPr(4))Ga(C(8)H(8))GaAr(iPr(4)) (3, 3(iso)), and polycyclic compounds Ar(iPr(4))Ga(C(5)H(6))Ga

85 risingly low downfield chemical shift (delta(iso)) and large chemical shift anisotropy.

86 rostaglandin E(2) (PGE(2)), 8-isoprostane (8-iso), and IL-6, and serum levels of IL-6, soluble interc

87 )-adrenergic receptor agonist isoproterenol (iso), and rolipram (roli), a phosphodiesterase (type IV)

88 by the beta-adrenergic agonist isoprenaline (Iso), and washout of ACh revealed a stimulatory response

89 marker and to measure 15-isoprostane F2t (F2-Iso) and 8-hydroxydeoxyguanosine (8-OHdG) as biomarkers

90 eta1-AR) by the catecholamines isoprenaline (Iso) and adrenaline (Adr) is regulated by V(M).

91 the beta-adrenoceptor agonist isoproterenol (ISO) and by varying afterload pressures.

92 the nonselective beta-agonist isoprenaline (ISO) and compared this with cold-activated BAT activity.

93 alized after stimulation with isoproterenol (ISO) and fully recycled at 4 h upon ISO removal.

94 Azi-propofol (AziPm) and Azi-isoflurane (Azi-iso) and molecular docking were also used.

95 eral brain regions from neonatally isolated (ISO) and nonhandled (NH) adult male and female rats.

96 pe increased the potencies of isoproterenol (ISO) and other agonists in stimulating cAMP accumulation

97 ted in International Standards Organization (ISO) and other international or regional standards.

98 a-adrenergic receptor agonist isoproterenol (ISO) and the cholinergic receptor agonist carbachol had

99 Isoxyl (ISO) and thiacetazone (TAC), two prodrugs once used in t

100 ed by nonspecific NOS inhibition at low dose Iso, and by preferential neuronal NOS inhibition at high

101 thologs, lmx1b.1 and lmx1b.2, in the rostral IsO, and demonstrate that these genes are necessary for

102 ist, did not decrease the percentage of NE-, ISO-, and ALB-induced apoptosis.

103 inase 2, or beta-arrestin1, attenuates LPA-, ISO-, and EGF-mediated internalization of EGFR.

104 he diastereomers of (-)-sparteine, (-)-alpha-iso- and (+)-beta-isosparteine, in the kinetic resolutio

105 function of intraportally administered islet iso- and allografts by treating recipients with anti-asi

106 ch was expressed at equivalent levels in all iso- and allografts for the first 4-5 days posttransplan

107 s of young adult white and Taiwanese-Chinese iso- and anisomyopes (N = 56), from measured keratometry

108 bFabH1 and bFabH2 also utilized iso- and anteiso-branched-chain acyl-CoA primers as subs

109 Surround modulation at iso- and cross-orientations showed distinct contrast dep

110 In addition, both iso- and cross-oriented half-images produced less dichop

111 m, as witnessed by the singular formation of iso- and heterochiral associations composed of regular,

112 ary lumen opacification can be achieved with iso- and low-osmolar contrast media when it is injected

113 rexpression of ICER significantly attenuated ISO- and phenylephrine-induced cardiac hypertrophy but d

114 nse mutation in the hadA gene of spontaneous ISO- and TAC-resistant mutants was sufficient to confer

115 re also found in M. tuberculosis spontaneous ISO- and TAC-resistant mutants.

116 -1,15-quinquecyclopropanedimethanol (4) with iso- and terephthaloyl chlorides and 4,4'-methanediyl-di

117 ocal inflammatory response occurred and both iso- and xenogeneic tissues were destroyed within 5 week

118 serve at the same time as fluorescence-based ISOs, and apply it specifically to potassium (K(+)).

119 ated with the beta-AR agonist isoproterenol (ISO) (anxA4a(+/+) vs. anxA4a(-/-): 5.1 +/- 0.3 vs. 6.7 +

120 have large isotropic hyperfine couplings, A(iso)( )() approximately 23 MHz, which shows they are bou

121 t protein subunit(s) prior to RNA binding (k(iso) approximately 0.23 s(-1)).

122 ropic (95)Mo hyperfine coupling in E(4) is a(iso) approximately 4 MHz, less than that for the resting

123 -proton isotropic EPR hyperfine splitting, A(iso), are theta(1) = 21 to 30 degrees and theta(2) = -99

124 tein (hsCRP), d-8-iso prostaglandin F2a (d-8-iso) as a marker of oxidative stress, and matrix metallo

125 increased flexibility or isomerization in {N(iso)} as predicted in recent theoretical work.

126 he-77 to Leu, Lys-101 to Glu, and Val-106 to Iso) associated with antiretroviral resistance were iden

127 , 5-HT reduced the standing outward current (ISO) at -20 mV by 106+/-17 pA, inhibiting a conductance

128 o genotype, pretreatment with Isoproterenol (ISO) at 10(-7) M for 1 h or 24 h caused approximately 25

129 +) release was approximately 50% faster with ISO (at most loads and I(Ca) levels).

130 beta(2)-selective AR agonists isoproterenol (ISO) (beta(1) approximately beta(2)) and albuterol (ALB)

131 ith estrogen receptor alpha, although ACTN4 (Iso) binds ERalpha more strongly.

132 However, under isoprenaline (ISO), both the application of JNJ-303 and additional E-4

133 nked beta-adrenergic agonist, isoproterenol (ISO), but in a transient manner.

134 of Na(+), and (3) K(suc), a solution using K(iso) but with the addition of sucrose to obtain a hypert

135 hat weight loss decreased water intake after Iso, but had no effect on PRA.

136 endent reduction in subsequent relaxation to ISO, but not to forskolin.

137 for IMTSL, g iso correlates linearly with A iso, but the slopes are different for the neutral and ch

138 was subsequently lowered in the presence of ISO (by lowering [Ca(2+)](o) to 1 mM and partially inhib

139 5F and 3R4F research cigarettes smoked under ISO (Cambridge Filter or FTC) and Intense (Health Canada

140 tion of beta-receptor agonist isoproterenol (Iso) caused a long-term enhancement of ICa.

141 preparations with 1.0 microM isoproterenol (ISO) caused a rapid maximal 10-15-fold increase in GRK s

142 incubation with EGF, LPA, or isoproterenol (ISO) causes the time-dependent loss of cell surface EGFR

143 Isolated sulfite oxidase deficiency (ISOD) causes severe intellectual disability, epilepsy, a

144 mice in response to 10(-8) M isoproterenol (ISO) compared with WT mice.

145 inobenzamide (ABA) and 1,5-isoquinolinediol (ISO), counteract overexpression of endothelin-1 (ET-1) a

146 kening variance of its low-frequency ISO (LF-ISO) cycle.

147 ) as well as midbrain and rostral hindbrain (IsO) development.

148 itions and in the presence of isoproterenol (ISO), dibutyryl-cAMP (db-cAMP), Bay K 8644 (BayK), Okada

149 The ED50 of ISO (dose of ISO resulting in 50% of the maximal respons

150 with 10 microM isoprenaline (isoproterenol, ISO) enhanced INa by 68.4 +/- 9.6 % (mean +/- s.e.m.; n

151 caused 7-13-fold increases in the potency of ISO, epinephrine, and zinterol, but not of norepinephrin

152 E's effect on ET-1-induced [Ca2+]i (1 microM ISO + ET-1; 254 +/- 56 nM).

153 The decrease in a(iso) for (95)Mo of E(4) from the already small value in

154 dult feline heart by infusing isoproterenol (ISO) for 10 days via minipumps, and then animals were al

155 onic beta-AR stimulation with isoproterenol (ISO) for 48 h reduced Ito,f along with mRNA expression o

156 l), treated with 10 nmol/L of isoproterenol (ISO) for 5 min followed by 5 min washout, or preconditio

157 were examined in response to isoproterenol (ISO), forskolin (FSK), and dibutyryl-cAMP (DB), coupled

158 cient 10,20-bis(perfluoroalkyl)porphyrin (Rf-Iso) frameworks.

159 of the beta-agonist isoproterenol (0.1 mum; ISO), from 0% to 64% (P < 0.05).

160 Rats isolated (ISO) from their mother and each other for 1 h daily from

161 ISO, FSK, or DB rapidly increased oxidative and glycolyt

162 f the beta-adrenergic agonist isoproterenol (Iso), genistein caused a near-maximal activation of this

163 After ISO, graded I(Na) was associated with small amounts of S

164 The K(iso) group was not affected by L-NAME at any K(+) concen

165 to controls, and isoproterenol stimulation (Iso) had only a small effect to further speed relaxation

166 ble seizures are invariable in children with ISOD; however, to our knowledge, infantile spasms with a

167 In the absence of ISO, I(Na) was associated with SR Ca release in human bu

168 were exposed to high doses of isoproterenol (ISO), in vivo and in vitro.

169 cardiac damage responding to isoproterenol (ISO) in adult offspring that underwent maternal inflamma

170 The higher value of carbon-13 delta(iso) in alkylidene complexes relative to ethylene is thu

171 ta-adrenergic receptor agonist isoprenaline (Iso) in CA1 pyramidal cells, suggesting that mGluRs coup

172 Isoproterenol (ISO) increased Ca2+ transient amplitude during systole,

173 beta-AR stimulation with isoprenaline (ISO) increased Ca2+ transient amplitude, ICa-L and SRCa2

174 Terbutaline (TERB) and isoproterenol (ISO) increased lung edema clearance in control nonventil

175 In WT myocytes, 1 micromol/L isoproterenol (ISO) increased PLM phosphorylation and stimulated NKA ac

176 Isoproterenol (isoprenaline; ISO) increased the amplitude of the inward Ca(2+) curren

177 a-adrenergic receptor agonist isoproterenol (ISO) increased the Na,K-ATPase protein abundance at the

178 ic receptor (beta-AR) agonist isoproterenol (ISO)-induced contractile response was measured in isolat

179 weight loss to isoproterenol (isoprenaline; Iso)-induced Fos immunoreactivity (IR) and to angiotensi

180 pe and IL-10 knockout mice by isoproterenol (ISO) infusion.

181 rformance was examined during isoproterenol (ISO) infusions (1x10(-10) to 1x10(-7) mol/L) and pacing

182 und that both ACTN4 (full length) and ACTN4 (Iso) interact with the ligand-independent and the ligand

183 Although ACTN4 (Iso) interacts efficiently with transcriptional co-activ

184 ernational Organization for Standardization (ISO) International Workshop Agreement on tiered cookstov

185 ne signaling mechanism distinct from that of ISO, involving G(i)-coupled betagamma subunits of hetero

186 o) to the reverse rate of isomerization (kr, iso), is 2-6-fold lower for the mutants at position 214

187 also explains why the highest value of delta(iso) is observed for Mo and the lowest for Ta, the value

188 tric acid extraction (0.43 M) was adopted by ISO (ISO-17586:2016) as standard for extraction of geoch

189 ISO (ISO-beta(1)/beta(2)-AR stimulation) increased I(Ca,

190 ernational Organization for Standardization (ISO) (ISO/TS 17728, ISO 18593:2004 and ISO 17604:2003) s

191 R Ca(2+) release +/- 1 microm isoproterenol (ISO; isoprenaline) in voltage-clamped ventricular myocyt

192 ly 20%) at 21 mM K(+) in all three groups (K(iso), K(hyper), and K(suc)).

193 t3a, wnt10b, pax8 and fgf8 expression at the IsO, leading ultimately to programmed cell death and the

194 nd a weakening variance of its low-frequency ISO (LF-ISO) cycle.

195 To prove the existence of Z-ISO, maize (Zea mays) and Arabidopsis (Arabidopsis thali

196 s quasi-rhythmic intraseasonal oscillations (ISO) manifested as alternate 'active' phases of copious

197 ue-light excitation, the isoalloxazine ring (ISO) may undergo an ultrafast reduction by a nearby tryp

198 ibition by dGMP and 8-oxo-dGMP indicates an "iso" mechanism in which the nucleotide product leaves an

199 Consistent with an "iso" mechanism, single-turnover studies with dGTP and 8-

200 , using right-side-out (RSO) and inside-out (ISO) membrane vesicles.

201 acheal grafts from B10.A (allo) or C57BL/6J (iso) mice were transplanted into cyclosporine-treated wi

202 ically significant improvement in hsCRP, d-8-iso, MMP-2, and MMP-9 levels.

203 um glycated hemoglobin A1c (A1c), hsCRP, d-8-iso, MMP-2, and MMP-9.

204 e of maximally stimulating concentrations of Iso, nor was it observed in the absence of Iso.

205 of 2.2 A, and isotropic coupling constant (A(iso)) of -0.35 MHz.

206 ith an equilibrium isomerization constant, K(iso), of 2.1.

207 rototypical volatile anesthetic, isoflurane (Iso), on recombinant human Ca(V)3.1 and Ca(V)3.2 isoform

208 effects of the PKA activator Isoproterenol (Iso) on L-type Ca(2+) current (I(CaL)), contractions, an

209 dy effects of the beta agonist isoprenaline (Iso) on the current-voltage (I-V) relationship of the Na

210 he beta-adrenoceptor agonist, isoproterenol (ISO), or the beta-adrenoceptor antagonist, propranolol.

211 llowing intravenous infusion of either 0.9% (ISO) or 3.0% (HYPER) NaCl saline, 12 subjects were passi

212 in powder/d containing 83 mg isoflavones/d; +ISO) or a control group (ethanol-extracted soy-protein p

213 ial remodeling in response to isoproterenol (Iso) or Angiotensin II (Ang II).

214 her electron-rich 10,20-diaryl porphyrin (Ar-Iso) or electron-deficient 10,20-bis(perfluoroalkyl)porp

215 of the cAMP-producing agonists isoprenaline (Iso) or histamine.

216 r (P<0.01) retention of MB(p) than either MB(iso) or MB.

217 perpolarization (sAHP) such as isoprenaline (ISO) or noradrenaline (NA) reduced the hyperpolarization

218 Isoproterenol (ISO) or PKA activation results in strong nuclear accumul

219 ngle injections of vehicle, 200 or 300 mg/kg ISO, or 2 daily doses of 200 mg/kg ISO for 6 days.

220 Rate of iso- or hyperintense HCA on HPB phase gadoxetic acid-enh

221 series were included to analyze the rate of iso- or hyperintense HCAs on HPB phase MR images.

222 Mammograms showed well-defined, iso- or hypodense masses; most were not calcified.

223 APAs (mean size, 20 x 16 mm) were iso- or hypointense relative to the liver on T1-weighted

224 were hypointense to the MTG and were either iso- or hypointense to the STG.

225 We incubated defined mixtures of iso- or n-alkanes with mature fine tailings from two tai

226 (Asn) deamidation, isoaspartic acid (isoAsp, isoD, or beta-Asp) is a ubiquitous nonenzymatic modifica

227 onal modification, isoaspartic acid (isoAsp, isoD, or beta-Asp), generated via the deamidation of asp

228 in which right-side-out (RSO) or inside-out (ISO) orientations could be analyzed independently to ask

229 D showed the greatest lusitropic response to ISO (P<0.05) and offset the pacing-induced increase in L

230 hat chronic administration of isoproterenol (ISO) persistently increases the frequency of mPTP openin

231 pertrophic stimuli, including isoproterenol (ISO), phenylephrine (PE), and endothelin-1 (ET-1).

232 (full length) and its spliced isoform ACTN4 (Iso) possess an unusual LXXLL nuclear receptor interacti

233 Both ACTN4 (full length) and ACTN4 (Iso) potentiate basal transcription activity and directl

234 osely folded isomerized native-like state {N(iso)} predicted in simulation.

235 and contractile amplitude in isoproterenol (ISO)-prestimulated ventricular myocytes isolated from ad

236 Isoprenaline (ISO) prolonged APDs and triggered EADs in LQT1 myocytes

237 Oxidative stress was assessed by urinary 8-iso- prostaglandin F2alpha and serum soluble NOX2-derive

238 wise, Ca(2+) current augmentation induced by iso- proterenol and forskolin was markedly depressed in

239 ernational Organization for Standardization (ISO) protocols.

240 es (DNICs) [((R)DDB)Fe(NO)2](+) (R = Me, Et, Iso; (R)DDB = N,N'-bis(2,6-dialkylphenyl)-1,4-diaza-2,3-

241 e of D396 determine the preferred pathway of ISO* relaxation.

242 ural ridge (ANR), and the isthmic organiser (IsO) represent two signalling centres possessing organis

243 to be confidently analyzed (IsoA, IsoC, and IsoD) require Gln3 and UASGATA promoter elements, both r

244 and Ar(iPr(4))Ga(C(7)H(8))GaAr(iPr(4)) (5, 5(iso)), respectively, under ambient conditions.

245 shifts when the native-like intermediate {N(iso)} responsible for GFP's hysteretic folding behavior

246 beta-adrenergic receptors by isoproterenol (ISO) resulted in an impaired contractile response of TG

247 Thus we avoid use of the prefix "iso".) Selective S-acylations of serine peptide 3k and t

248 t-side-out (RSO) (resistant) and inside-out (ISO) (sensitive) orientations after reconstitution.

249 Perfusion with isoproterenol (ISO) significantly increased the peak amplitude of fura-

250 We infer from complex 1 that an A(iso) significantly larger than 1.2 MHz for a Mn-coordina

251 Both basal and isoproterenol (ISO)-stimulated AC activities were decreased by 30% to 4

252 L sildenafil (SIL) suppressed isoproterenol (ISO)-stimulated contractility, whereas 10 micromol/L atr

253 ysophosphatidic acid (LPA) or isoproterenol (ISO)-stimulated MAP kinase phosphorylation.

254 More prominently, isoproterenol (ISO)-stimulated systolic and diastolic function in WT wa

255 ebrafish embryos demonstrated isoproterenol (ISO)-stimulated, propranolol-sensitive calcium transient

256 er basal conditions and after isoproterenol (Iso) stimulation.

257 ysiological HR increases with isoproterenol (ISO), suggesting that other I(f)-independent pathways ar

258 genous eIF2Bepsilon was decreased by LiCl or ISO, suggesting that GSK-3beta is the predominant kinase

259 of a number of other genes expressed at the IsO, suggesting that it does not generate a new signalin

260 the effects of ACh on Ip in the presence of Iso, suggesting that these effects are also mediated by

261 In contrast, an ACTN4 isoform, ACTN4 (Iso), that loses its actin-binding domain is still capab

262 the beta-adrenoceptor agonist isoproterenol (ISO), the adenylate cyclase activator forskolin, and the

263 Ion-selective optodes (ISOs), the optical analog of ion-selective electrodes, h

264 ed similar increases in ICa-L in response to ISO, there was no measurable suppression of ICa-L by CCh

265 However, in the presence of ISO, there were no differences in the peak amplitude of

266 n of Frizzled-2 chimera and stimulation with ISO, they were subject to depletion of G protein subunit

267 dition of the beta-AR agonist isoproterenol (ISO) to serum-starved cells induced DNA synthesis in a d

268 dictated stomatal sensitivity and hence the iso- to anisohydric spectrum of regulation.

269 ecies' operating ranges along a continuum of iso- to anisohydry have been elusive.

270 n T1-weighted images in all six patients and iso- to hyperintense on T2-weighted images in five patie

271 ypo- to isointense on T1-weighted images and iso- to slightly hyperintense on proton-density- and T2-

272 Isoproterenol (ISO) treatment in concert with stretch in parallel with

273 sistent with a di-iso ping-pong bi-bi and an iso (two-site) ping-pong mechanism for the reduction of

274 ln-241 --> Leu; Phe-261 --> Val; Thr-266 --> Iso; Val-367 --> Glu; and Ala-369 --> Pro).

275 imulations of the experimental data led to A(iso) values of 1.2, 1, and 2 MHz, respectively.

276 formation of isoaspartyl residues (isoAsp or isoD) via either aspartyl isomerization or asparaginyl d

277 The concept of iso- vs. anisohydry has been used to describe the string

278 s could serve as proxies for their degree of iso- vs. anisohydry.

279 tive of stilbene compound, isorhapontigenin (ISO), was isolated from this Chinese herb.

280 The value for A(iso) was determined based on simulation of the experimen

281 icited by isoproterenol (10 microg/kg, i.v.; ISO) was diminished in AV3V-lesion rats treated with bet

282 nse to phenylephrine (PE) and isoproterenol (ISO) was measured in a dorsal hand vein using the linear

283 taAR agonist stimulation with isoproterenol (ISO) was shifted leftward by approximately 1.5 orders of

284 to the beta-adrenergic agonist isoprenaline (Iso) was studied in both WT and NOS3-KO mouse myocytes.

285 This step, mediated by a putative Z-ISO, was predicted to occur in the sequence of redox rea

286 dy (MB) or with isotype control antibody (MB(iso)) were assessed by intravital microscopy of cremaste

287 n (CDF) and I(Ca) response to isoproterenol (ISO) were significantly reduced.

288 n of 0.5 microM isoproterenol (isoprenaline; ISO) when measured using the whole-cell patch clamp meth

289 using three paradigms: (1) isotonic K(+) (K(iso)) where increases in K(+) were offset by decreases i

290 n factor Lmx1b is expressed within the chick IsO, where it is sufficient to maintain expression of th

291 etic rats and this increase was corrected by ISO, whereas ABA had a weaker effect.

292 ctive beta-adrenergic agonist isoproterenol (Iso), which indicates that the PTX treatment increases t

293 naling center, termed the isthmic organizer (IsO), which is localized at the boundary between them.

294 tivated serum had no effect on relaxation to ISO, while 2 hours of exposure of vessels to ISO caused

295 ILI raised HPC numbers, further increased by ISO, with attenuation of liver injury.

296 pically exhibits intraseasonal oscillations (ISOs) with periods from approximately 15 to 40 days, as