ライフサイエンスコーパス: iso-

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

2 nergic receptor activation by isoproterenol (ISO).

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

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

5 rved betaAR responsiveness to isoproterenol (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 s induced by the beta-agonist isoproterenol (ISO).

11 ignals emanating from the isthmus organizer (IsO).

12 energic agonist isoproterenol (isoprenaline; ISO).

13 11 > delta22 > delta33) and associated delta(iso).

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

15 uring adrenergic stimulation (isoproterenol, ISO).

16 timulation with isoproterenol (isoprenaline; ISO).

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

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

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

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

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

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

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

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

25 ; 0.3 to 3 micromol/L) and/or isoproterenol (Iso; 0.2 to 1 micromol/L).

26 Isoprenaline (Iso, 1 mg/kg, sc., 10 days) was administered 5 weeks aft

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

28 prototypical general anesthetic, isoflurane (ISO, 1.5% for 3 hr), at three early postnatal ages (P3,

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

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

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

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

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

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

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

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

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

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

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

40 0 minutes) pretreatment were stimulated with ISO (10 minutes).

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

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

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

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

45 diagnostic for the distally bound H atom ( a(iso) = 16.5 MHz).

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

47 les were prepared using the standard method (ISO, 18593:2018) in sensor vials, which were then incuba

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

49 er adopts an S = (1)/(2) ground state with g(iso) > 2.

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

51 /-1%)>ALB (2+/-1%); 10 mcmol/L: NE (35+/-2%)>ISO (23+/-1%)>ALB (3+/-1%); 100 mcmol/L: NE (50+/-2%)>IS

52 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,

53 -1%)>ALB (3+/-1%); 100 mcmol/L: NE (50+/-2%)>ISO (29+/-2%)>ALB (14+/-1%), P<0.0001 except for NE vers

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

55 3 (48 hours) or isoproterenol hydrochloride (ISO; 30 minutes) pretreatment were stimulated with ISO (

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

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

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

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

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

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

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

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

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

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

66 3+/-22% versus eIF2Bepsilon only; P<0.05) or ISO (+84+/-33% versus eIF2Bepsilon only; P<0.05) enhance

67 eous action potentials (APs) when exposed to ISO (9.99 +/- 4.2 vs. 0.16 +/- 0.05 APs/min, p = 0.004);

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

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

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

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

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

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

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

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

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

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

78 ontrast to these regional distinctions under ISO, alterations in Ca(2+) handling at baseline and myoc

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

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

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

82 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

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

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

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

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

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

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

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

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

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

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

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

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

95 We report that isoproterenol (ISO) and related beta2-adrenergic agonists reacidify lys

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

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

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

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

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

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

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

103 A concise synthesis of iso- and 9-dechlorochrysophaentin A enabled by a Z-selec

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

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

106 Natto major BCFA are C14-17 iso- and anteiso-BCFA similar to fluid milk.

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

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

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

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

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

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

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

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

115 -1,15-quinquecyclopropanedimethanol (4) with iso- and terephthaloyl chlorides and 4,4'-methanediyl-di

116 ng membrane-inner segment outer segment (ELM-ISOS); and inner segment outer segment-retinal pigment e

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

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

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

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

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

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

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

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

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

126 , 5-HT reduced the standing outward current (ISO) at -20 mV by 106+/-17 pA, inhibiting a conductance

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

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

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

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

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

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

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

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

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

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

137 5F and 3R4F research cigarettes smoked under ISO (Cambridge Filter or FTC) and Intense (Health Canada

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 ve effects of canagliflozin in isoprenaline (ISO)-induced cardiac oxidative damage-a model mimicking

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

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

177 d if canagliflozin can reverse isoprenaline (ISO)-induced renal oxidative damage in rats, a model tha

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

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

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

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

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

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

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

185 ernational Organization for Standardization (ISO) is designing a new solution for the representation,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 for 120 min with either 0.9% NaCl [isotonic (ISO)] or 3.0% NaCl [hypertonic (HYPER)].

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

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

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

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

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

222 er, distinguishing local oxidation levels in iso- or mixed-valent materials can be dramatically obscu

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

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

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

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

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

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

229 NHERF1 knockdown fully abrogated the ISO-, PGE(2)-, and FSK-induced IL-6 gene expression and

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

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

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

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

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

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

236 veal that the betaAR agonist, isoproterenol (ISO), promotes enhanced Ca(V) 1.2-Ca(V) 1.2 physical int

237 ed phosphoprotein (p-VASP) by isoproterenol (ISO), prostaglandin E(2) (PGE(2)), or forskolin (FSK) as

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

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

240 ernational Organization for Standardization (ISO) protocols.

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

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

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

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

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

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

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

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

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

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

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

252 80)) between groups; however, isoproterenol (ISO) significantly shortened APD(80) in DBH-Sap but not

253 A) and International Standards Organization (ISO) standard ISO 20776-2 criteria using Clinical and La

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 some transport pathways and reversibility by ISO, thus accounting for lysosomal Cl(-) deficits that c

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

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

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

273 nhibition by siRNA to Ces3 on isoproterenol (ISO)-treated 3T3-L1 and brown adipocyte cells.

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

275 receptor stimulation (through isoproterenol (ISO) treatment) on heart metabolism.

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

277 ed ethers sevoflurane (SEVO) and isoflurane (ISO), using UV-Vis spectroscopy, time dependent-density

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

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

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

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

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

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

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

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

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

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

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

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

290 free water fraction (isotropic compartment (ISO)) were derived.

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

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

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

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

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

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

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

298 ivity to circulating adrenergic stimulation (ISO), while having blunted responses to SNS, providing i

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

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