ライフサイエンスコーパス: uncoupling

1 of the carrier to adrenergic activation and uncoupling.

2 fatty acid and glucose oxidation, as well as uncoupling.

3 NAFLD is via salicylate-driven mitochondrial uncoupling.

4 is by dissipating energy through thermogenic uncoupling.

5 brain show a high level of palmitate-induced uncoupling.

6 ions for Asn in DIII-S6 showed somewhat less uncoupling.

7 educed antioxidant capacity of cells and NOS uncoupling.

8 e), that produces mild hepatic mitochondrial uncoupling.

9 ding with matrix alkalinization, followed by uncoupling.

10 susceptibility on pharmacological electrical uncoupling.

11 ring, which could lead to significant future uncoupling.

12 blasts during pharmacological gap junctional uncoupling.

13 l membrane potential following mitochondrial uncoupling.

14 ncoupling protein 3 (UCP3) and mitochondrial uncoupling.

15 ance to halothane- and acidification-induced uncoupling, absence of voltage-dependent fast inactivati

16 be a direct consequence of its mitochondrial uncoupling activity.

17 ss the mitochondrial inner membrane, thereby uncoupling adenosine diphosphate phosphorylation from nu

18 tathionylation as the main mechanism for NOS uncoupling after reperfusion.

19 tes, as well as in those treated with TNF or uncoupling agent carbonyl cyanide m-chlorophenyl hydrazo

20 tion were detected with blunted responses to uncoupling agents and reduced membrane potentials.

21 development of liver-targeted mitochondrial uncoupling agents as a potential novel therapy for lipod

22 mapping in the absence of electromechanical uncoupling agents, the method relieves a long-standing l

23 is results in ventricular-pulmonary vascular uncoupling and acute RV dilation.

24 H4, which resulted in nitric oxide synthases uncoupling and augmented radiation-induced ROS.

25 ligomycin resistant, suggesting ATP synthase uncoupling and bypass of the normal Fo-A6-subunit requir

26 RATIONALE: Intercellular uncoupling and Ca(2+) (Ca) mishandling can initiate trig

27 Endothelial nitric-oxide synthase (eNOS) uncoupling and increased inducible NOS (iNOS) activity a

28 o limit the reduction in stroke volume, with uncoupling and increased wall stress as a consequence.

29 specifically with regard to the substantial uncoupling and limited stabilization of the C4a-hydroper

30 s deregulation can explain the mitochondrial uncoupling and lower ATP levels in VCP mutation-bearing

31 rgy in the form of heat, using mitochondrial uncoupling and perhaps other pathways.

32 Our data identify replication fork uncoupling and reversal as global responses to genotoxic

33 Respiratory uncoupling and ROS excess occurred at PCoA > 600 nmol/mg

34 clusively by combined application of contact uncoupling and TGFbeta.

35 in perfusate temperature, electromechanical uncoupling, and acute ischemia/reperfusion injury.

36 sed AMP kinase activity, beta-oxidation and -uncoupling, and decreased triglyceride content).

37 and consequent mechanical stiffness, myocyte uncoupling, and ischemia, are key contributors to heart

38 metabolic substrate usage and mitochondrial uncoupling, and protects against ischaemia/reperfusion.

39 dothelial caveolae, which contributes to NOS uncoupling, and, hence, reduced NO-mediated coronary vas

40 on in apoptotic cells and inhibits CPS, thus uncoupling apoptosis from CPS.

41 ative stress and nitric oxide synthase (NOS) uncoupling are thought to contribute to Fabry cardiovasc

42 but decreased ATP, suggesting mitochondrial uncoupling as its mechanism of action.

43 infections could protect against allergy by uncoupling asIgE from its effector mechanisms.

44 TP turnover and DNA interaction, effectively uncoupling ATP hydrolysis from DNA movement.

45 leration of basal respiration by genetically uncoupling ATP synthesis from electron transport resulte

46 This temporal uncoupling became larger in short photoperiods and may r

47 This uncoupling between association and causation may result

48 ained 40% of the ATPase activity, suggesting uncoupling between ATP hydrolysis and activation of the

49 ine-bound closed conformation, revealing the uncoupling between ATP-PRT open and closed conformations

50 plies a selection for aerobic glycolysis and uncoupling biosynthesis from NADH generation.

51 an imbalance in glucose carbon allocation by uncoupling biosynthetic pathway activity, which could di

52 ore bone density, structure, and strength by uncoupling bone formation from resorption.

53 Dysregulation of TGF-beta alters MSC fate, uncoupling bone remodeling and causing skeletal disorder

54 Due to uncoupling, brown adipose tissue (BAT) dissipates energy

55 Neurovascular uncoupling by cocaine during stimulation but not during

56 examine the mechanism behind lipid-dependent uncoupling by comparing the propensities of two prokaryo

57 V or caCaMKIV, respectively, suggesting that uncoupling CaMKIV activation from activity generates an

58 Neurovascular uncoupling could contribute to cocaine's neurotoxicity,

59 t produces mild liver-targeted mitochondrial uncoupling could decrease hypertriglyceridemia and rever

60 are differentially regulated in response to uncoupling Crkl from its signaling pathways in the devel

61 at S384 by the PP2A-B56 phosphatase, thereby uncoupling cyclin E degradation from cyclin E-CDK2 activ

62 Uncoupling discovery from genotyping thus allows for the

63 This uncoupling effect is tightly correlated with the suppres

64 on levels increased in the tumor cell lines (uncoupling effect), resulting in a DeltaPsi(m) decrease

65 oA oxidation and its concentration-dependent uncoupling effect, together with a partial lipid-depende

66 ed by NTZ in real time by virtue of its mild uncoupling effect.

67 e fuel role of lipids is influenced by their uncoupling effects, and how this affects mitochondrial e

68 n adipose tissue, where it generates heat by uncoupling electron transport from ATP production.

69 t a statistically significant reversal after uncoupling electron transport from ATP synthesis, consis

70 ediated arginase activation, endothelial NOS uncoupling, endothelial dysfunction, and atherogenesis.

71 adation, but increases chromosomal breakage, uncoupling fork protection, and chromosome stability.

72 ed cellulose synthesis enabled by regulatory uncoupling from primary wall synthesis.

73 s lacking these residues results in complete uncoupling from the cell cycle.

74 yofilament Ca(2+) sensitivity and, moreover, uncoupling from the impact of phosphorylation of cTnI me

75 minal residues (2)ERSTQ leads to loss of the uncoupling function even though the truncated peptide ca

76 ssue activates the canonical thermogenic and uncoupling gene expression program.

77 acterize a unique pharmacological target for uncoupling GIV-dependent signaling downstream of multipl

78 l looping combustion with and without oxygen uncoupling have received considerable attention of resea

79 K activator, had no effect on proliferation, uncoupling high AMPK activity from inhibition of prolife

80 EPO prevented IL-2-induced proliferation by uncoupling IL-2 receptor signaling, inhibiting phosphory

81 In this model, uncoupling impaired K(+) buffering and temporally preced

82 Mitochondrial uncoupling in HepG2 cells by SR4 results in the reductio

83 Our results validate a prevalence of uncoupling in the evolution of tadpole and adult phenoty

84 , and nitro-oxidative stress as well as eNOS uncoupling in the vessel wall, which can be prevented by

85 Mechanistic studies reveal that uncoupling increases fatty acid oxidation and membrane p

86 stimulate its ubiquitination function, thus uncoupling increases in p53 binding from its E3 ubiquiti

87 Mitochondrial uncoupling induced by NE in brown adipocytes was reduced

88 epidermis, we show that forced mitochondrial uncoupling inhibits skin carcinogenesis by blocking Akt

89 Uncoupling innate and adaptive functions of cDCs reveale

90 hese findings demonstrate that mitochondrial uncoupling is an effective strategy to limit proliferati

91 oterenol, evidence of excitation-contraction uncoupling is indicated by an elevation in diastolic cal

92 by endothelial nitric oxide synthase (eNOS) uncoupling, is an initial step in atherosclerosis.

93 C-1 activity slows reproductive development, uncoupling it from its typical progression relative to t

94 ing the remodelling and turnover of K16, and uncoupling it from K6, iRHOM2 regulates the epithelial r

95 -p38 MAPK-CMA pathway in the mouse brain and uncoupling it results in a greater loss of SNc dopaminer

96 Finally, the uncoupling led to an accumulation of apoptotic newborn c

97 adipogenic, insulin sensitivity, and energy uncoupling machinery, while limiting inflammation in WAT

98 f of concept that mild hepatic mitochondrial uncoupling may be a safe and effective therapy for the r

99 hetic anion transporters and potentially the uncoupling mechanism of naturally occurring membrane pro

100 By uncoupling membrane binding from internalization, we fou

101 Blocking ROS production with rotenone by uncoupling mitochondria or by expressing the alternative

102 y transition pores (mPTP) causes respiratory uncoupling, mitochondrial injury, and cell death.

103 Thus, NBP is a conserved uncoupling motif of the ecto-TM domain transition and th

104 wever, regulated their mRNA concentration by uncoupling mRNA stability from the transcription rate.

105 We also conclude that, by uncoupling mRNA synthesis from decay, cells control the

106 Uncoupling MTFP1 levels from the mTORC1/4E-BP pathway up

107 hondrial matrix independent of ATP synthase, uncoupling nutrient metabolism from ATP generation.

108 ies used in this study but also displayed an uncoupling of A and gs in most of the species.

109 therapeutic efficacy through pharmacological uncoupling of a convergence point of NF-kappaB-mediated

110 ent in IBA and 4OGlcI3F, and allele-specific uncoupling of a subset of PEN3 functions suggest that PE

111 ediated downregulation, desensitization, and uncoupling of beta-adrenoreceptors.

112 associated with enhanced downregulation and uncoupling of beta2-receptors.

113 The uncoupling of C fixation from dissolved inorganic nitrog

114 CA throughout its kinetic cycle and promotes uncoupling of Ca(2+) transport from ATP hydrolysis.

115 halamic inflammatory pathways results in the uncoupling of caloric intake and energy expenditure, fos

116 Our results indicate an uncoupling of cellular, tissue, and organismal aging thr

117 ssion of Esco1-proximal genes and functional uncoupling of cohesion from Smc3 acetylation.

118 The uncoupling of complex II's electron transport function f

119 has no effect on work output, indicating an uncoupling of disassembly speed from protofilament strai

120 ventricular dysfunction was associated with uncoupling of endothelial nitric oxide synthase (NOS) ac

121 The mutagenic uncoupling of femtosecond motions between catalytic site

122 A at supersaturating concentrations to cause uncoupling of H1 receptors from phospholipase C.

123 HFS throughout the light-dark cycle suggests uncoupling of hypothalamic responses involving appetite-

124 tro via tyrosine phosphatase SHP-1-dependent uncoupling of IL-2Rbeta signaling.

125 3K27me3 at the Zbtb16/PLZF promoter leads to uncoupling of iNKT cell development from TCR specificity

126 act epithelia; the other prerequisite is the uncoupling of intercellular contacts, which induces Rho-

127 dent impaired autophagic flux after chemical uncoupling of mitochondria, increased mitochondrial-prot

128 Nitrite exhibited an uncoupling of mitochondrial respiration and a decrease i

129 propose that ethanol-induced inhibition and uncoupling of mRNA and protein synthesis through direct

130 This manifest uncoupling of negative element turnover from circadian p

131 We propose that the uncoupling of neurogenesis and differentiation could pro

132 ignificantly stunted dendrites-suggesting an uncoupling of neuron survival and dendritogenesis.

133 Reduced bioavailability or uncoupling of nitric oxide in the kidney, leading to dec

134 Inadequate availability of BH4 leads to uncoupling of nitric oxide synthases and production of h

135 49%; p=0.002 and p=0.0002, respectively) and uncoupling of NOS activity.

136 mbrane transfer of protons, resulting in the uncoupling of oxidative phosphorylation from ATP product

137 a highly phase-specific pattern, suggesting uncoupling of phenotypic evolution across life-history p

138 ate testable predictions for coupling versus uncoupling of phenotypic evolution of tadpole and adult

139 Here, we show that uncoupling of polymerized TUBB3 with netrin-1-repulsive

140 We propose a model whereby the uncoupling of protein levels of biogenesis-related genes

141 NPQ recovery in the dark requires uncoupling of PsbS.

142 The uncoupling of safety from other xylem functions allowed

143 ute PI3K activation and provide evidence for uncoupling of Ser(473) and Thr(308) phosphorylation, as

144 e the structural regions of SLN that mediate uncoupling of SERCA, we employed mutagenesis and generat

145 Uncoupling of SV40 from BAP31 traps the virus in ER subd

146 Our results demonstrate uncoupling of symbiosis and the symbiotic root developme

147 tion of GC responses was, in part, caused by uncoupling of Tfh-B cell interactions, as evidenced by r

148 These findings indicate an uncoupling of the canonical Akt/FoxO1 pathway in HCV pro

149 the cell in response to spatially controlled uncoupling of the cell interior.

150 The similarities include regulatory uncoupling of the CESAs that synthesize primary and seco

151 n, pharmacologically induced neuromechanical uncoupling of the diaphragm should facilitate lung-prote

152 hat has little constitutive activity reveals uncoupling of the ligand-binding domain from conserved c

153 ia TSC1 gene deletion in chondrocytes causes uncoupling of the normal proliferation and differentiati

154 substitutions for Asn in both S6s result in uncoupling of the pore domains from their voltage-sensor

155 Here we show partial uncoupling of the replication, release, and cell-to-cell

156 in avian DT40 cells, indicative of extensive uncoupling of the replicative helicase and polymerase.

157 ural features within the S4-S5 linker permit uncoupling of the voltage sensor from the pore in the ab

158 sor-competent and -incompetent molecules and uncoupling of the VSR and particle assembly capacities.

159 ation of aperiodic decidual gene expression; uncoupling of these events may cause recurrent pregnancy

160 The uncoupling of tissue growth and neurogenesis is shown to

161 enigmatic outcomes are due to a biochemical uncoupling of tolerogenic signaling, or simply a quantit

162 The mechanism of iRAPs involves active uncoupling of transcription and translation, making nasc

163 Strategies aimed at preventing the uncoupling of TRPM2-S from TRPM2 and subsequent Ca2+ gat

164 Finally, our data reveal a striking uncoupling of Vangl1 and Dvl1 asymmetry.

165 Structure-guided mutagenesis enabled uncoupling of virulence from I-2-mediated recognition.

166 e and inhibited by IL-4R-signaling in vitro, uncoupling parasite killing from expulsion mechanisms.

167 retains the ability to flux cations in this uncoupling PC membrane environment.

168 ansion of brown adipose tissues that express uncoupling protein (UCP) 1 and thus can uncouple mitocho

169 The mitochondrial carrier uncoupling protein (UCP) 2 belongs to the family of the

170 pathetic stimulation, activate mitochondrial uncoupling protein (UCP)-1 and oxidize fatty acids to ge

171 expression of the brown fat signature genes uncoupling protein (UCP)-1 and peroxisome proliferator-a

172 on of caloric excess through the activity of uncoupling protein (UCP)-1.

173 Indeed, BAT dissipates energy as heat via uncoupling protein (UCP)1.

174 In uncoupling protein 1 (UCP-1) knockout mice, the middle a

175 wn AT showed reduced activity with decreased uncoupling protein 1 (ucp-1), cell death-inducing DFFA-l

176 dipocytes are specialized cells that express uncoupling protein 1 (UCP1) and dissipate chemical energ

177 (GADD45gamma) as a cold-induced activator of uncoupling protein 1 (UCP1) and oxidative capacity in BA

178 m promoters of BAT-specific genes, including uncoupling protein 1 (Ucp1) and peroxisome proliferator-

179 Both uncoupling protein 1 (UCP1) and UCP3 are important for m

180 h was accompanied by increased expression of uncoupling protein 1 (UCP1) and UCP3 in brown adipose ti

181 Uncoupling protein 1 (UCP1) catalyzes fatty acid-activat

182 s previously reported, HFD feeding increased uncoupling protein 1 (UCP1) expression (fold increase: 3

183 eling of white adipose tissue and increasing uncoupling protein 1 (UCP1) expression in both white and

184 nduces mitochondrial dysfunction and reduces uncoupling protein 1 (UCP1) expression.

185 ed to the enhancer of the brown fat-specific uncoupling protein 1 (Ucp1) gene through this interactio

186 ses expression of the brown adipocyte marker uncoupling protein 1 (UCP1) in both adipose tissue depot

187 t production and decreased the expression of uncoupling protein 1 (UCP1) in brown adipose tissue (BAT

188 is is primarily accomplished by induction of uncoupling protein 1 (UCP1) in brown and beige adipocyte

189 LPS abolished cAMP-induced up-regulation of uncoupling protein 1 (UCP1) in primary human adipocytes,

190 Uncoupling protein 1 (UCP1) is highly expressed in brown

191 Uncoupling protein 1 (UCP1) is nearly absent in brown ad

192 Uncoupling protein 1 (UCP1) is the established mediator

193 nts of heat through activation of the unique uncoupling protein 1 (UCP1) located within the inner mit

194 Uncoupling protein 1 (UCP1) mediates nonshivering thermo

195 Uncoupling protein 1 (UCP1) plays a central role in nons

196 We combined an uncoupling protein 1 (UCP1) reporter system and expressi

197 This was associated with recruitment of uncoupling protein 1 (UCP1)(+) beige adipocytes in WAT,

198 al analysis revealed extensive expression of uncoupling protein 1 (UCP1), a definitive marker of brow

199 n browning of WAT and elevated expression of uncoupling protein 1 (Ucp1), a key regulator of thermoge

200 t of glucose homeostasis were independent of uncoupling protein 1 (UCP1), but required expression of

201 protein restriction increases adipose tissue uncoupling protein 1 (UCP1), energy expenditure and food

202 ssue (BAT), characterized by the presence of uncoupling protein 1 (UCP1), has been described as metab

203 uce expression of thermogenic genes, such as uncoupling protein 1 (Ucp1), in adipocytes cultured with

204 Both brown adipose tissue (BAT) (i.e. uncoupling protein 1 (UCP1)-based) and skeletal muscle (

205 attributed to its role in fuel oxidation and uncoupling protein 1 (UCP1)-mediated thermogenesis.

206 sion analyses and found that a population of uncoupling protein 1 (UCP1)-positive human adipocytes po

207 ough thermogenic respiration, which requires uncoupling protein 1 (UCP1).

208 thermogenesis, which requires mitochondrial uncoupling protein 1 (UCP1).

209 omys tridecemlineatus) express mitochondrial uncoupling protein 1 (UCP1).

210 both electron transport chain components and uncoupling protein 1 (UCP1).

211 on the principal effector of thermogenesis: uncoupling protein 1 (UCP1).

212 temperature as a result of higher levels of uncoupling protein 1 and a low abundance of the proinfla

213 press markers of brown and beige fat such as uncoupling protein 1 and transmembrane protein 26.

214 Moreover, the abundance of uncoupling protein 1 competent brite cells in white adip

215 loss was significantly associated with less uncoupling protein 1 expression (P = 0.006, R(2) = 0.09)

216 Cytochrome c oxidase activity, uncoupling protein 1 expression and maximal norepinephri

217 Pep19 induced uncoupling protein 1 expression in both white adipose ti

218 Uncoupling protein 1 expression induced by Pep19 in 3T3-

219 nterscapular region of neonates was lower in uncoupling protein 1 knockout pups employed as a positiv

220 Uncoupling protein 1(+) beige adipocytes are dynamically

221 neither presence nor thermogenic function of uncoupling protein 1(+) beige adipocytes contributed to

222 ined as multilocular adipocytes that express uncoupling protein 1, rose from undetectable to 30% of t

223 ramembraneous segments and the mitochondrial uncoupling protein 1, which is a transmembrane protein e

224 d body weight gain, induced the formation of uncoupling protein 1-positive beige adipocytes in white

225 wn adipose tissue respiration independent of uncoupling protein 1.

226 tissue-derived AAMs expressed high levels of uncoupling protein 1.

227 Additionally, intracellular glutathione and uncoupling protein 2 (UCP2) gene expressions were quanti

228 Uncoupling protein 2 (UCP2) is involved in various physi

229 atty acids (FFAs) and elevated expression of uncoupling protein 2 (UCP2) without concomitant increase

230 elated peptide 1 (DRP1) under the control of uncoupling protein 2 (UCP2).

231 ty from inflammation via upregulation of the uncoupling protein 2 (UCP2).

232 is increased the expression of mitochondrial uncoupling protein 2 and raised the AMP-to-ATP ratio, th

233 They also exhibit decreased uncoupling protein 3 (UCP3) and mitochondrial uncoupling

234 ers have shown previously that mitochondrial uncoupling protein 3 (UCP3) improves functional recovery

235 Uncoupling protein 3 (UCP3) is highly selectively expres

236 ion, fatty acid oxidation, and mitochondrial uncoupling protein 3 (UCP3) levels, while increasing gly

237 lex IV subunit 1 (COX1) was tightly bound to uncoupling protein 3 (UCP3), but this complex was disrup

238 Conversely, restoration of uncoupling protein 3 expression attenuated reactive oxyg

239 Uncoupling protein 3 was markedly downregulated in Gq or

240 me proliferator-activated receptor alpha and uncoupling protein 3, increases in mitochondrial protein

241 d cell death were abrogated by knock down of uncoupling protein 3.

242 mics signature in mice overexpressing muscle uncoupling protein 3.

243 y mouse neurons and test the hypothesis that uncoupling protein 4 (UCP4) and F0F1-ATP synthase are sp

244 lity of yeast ADP/ATP carrier AAC2 and ovine uncoupling protein UCP1 allow optimal conditions for sta

245 the well-known betaAR-dependent increase of uncoupling protein UCP1 expression and expansion of beig

246 a the unique expression of the mitochondrial uncoupling protein UCP1.

247 gy in the form of heat via the mitochondrial uncoupling protein UCP1.

248 ediated by beige adipocytes that express the uncoupling protein UCP1.

249 issipates nutritional energy as heat via the uncoupling protein-1 (UCP1) and BAT activity correlates

250 ous finding that LXRs serve as repressors of uncoupling protein-1 (UCP1) in classic brown adipose tis

251 enic fat cell that express the mitochondrial uncoupling protein-1 and thus represent a powerful targe

252 dipose tissue (WAT) were stained for CB1 and uncoupling protein-1 by immunofluorescent staining.

253 We found that CB1 was colocalized with uncoupling protein-1 in BAT, but neither protein was fou

254 t is on the splicing of transcripts encoding uncoupling protein-1, resulting in uncoupled respiration

255 ch encodes the key thermogenic mitochondrial uncoupling protein-1.

256 nscription factor-3 (Atf3) and mitochondrial uncoupling protein-2 (Ucp2) are highly induced in Tsc2-d

257 our group showed an increased expression of uncoupling protein-2 (UCP2) in pancreas from rats with B

258 Here, we demonstrated that the mitochondrial uncoupling protein-2 (UCP2) regulates NLRP3-mediated cas

259 ation in the TCA cycle, and independently of uncoupling protein-2 (UCP2), sirtuin-2 (SIRT2), the G pr

260 Uncoupling proteins (UCPs) oppose this phenotype by indu

261 Uncoupling proteins (UCPs) regulate energy expenditure i

262 s superoxide generation through induction of uncoupling proteins (UCPs), and transgenic overexpressio

263 he aim of this study was to evaluate whether uncoupling proteins (UCPs), located in the inner membran

264 2(+/-)) mice leads to increased expresson of uncoupling proteins (UCPs).

265 the transcriptional and protein abundance of uncoupling proteins that mediates thermogenesis, and it

266 Mitochondrial carriers, including uncoupling proteins, are unstable in detergents, which h

267 endent of adenine nucleotide translocase and uncoupling proteins, decreased mitochondrial membrane po

268 of mitochondrial biogenesis or activation of uncoupling proteins.

269 neuronal stimuli, resulting in neurovascular uncoupling, reduced oxygen supply to the brain and metab

270 controls to evaluate: (i) ADMA-mediated NOS uncoupling reduces epithelial production of NO and incre

271 ed to play a role in apoptotic cell death by uncoupling regions important for IP3 binding from the ch

272 Uncoupling RIG-I deamidation from HSV-1 infection, by en

273 ect of DeltarodZ without restoring rotation, uncoupling rotation from rod-like growth.

274 ssary for the initiation of sexual behavior, uncoupling sexual behavior from reproductive status.

275 Thus, uncoupling SPB growth from NE insertion unmasks function

276 , Pten is not effectively repressed, thereby uncoupling STAT5 phosphorylation and phosphoinositide-3-

277 Uncoupling synergistic interactions between physio-chemi

278 Uncoupling SYS-1 from the centrosome by RSA-2 depletion

279 e); end-systolic peak (peak ); and diastolic uncoupling (systolic -diastolic at same volume) during e

280 heterodimer, with beta2AR activation rapidly uncoupling TAS2R14 function ( approximately 65% desensit

281 e without affecting stress behavior, thereby uncoupling the contribution of a specific OXT cluster to

282 the perceived intention of others which, by uncoupling the dynamics of sensorimotor facilitation, co

283 t binds directly to the dynein motor domain, uncoupling the enzymatic and mechanical cycles of the mo

284 FC from its cognitive functions by partially uncoupling the mPFC from experience-induced inputs.

285 and androgen receptor signaling, effectively uncoupling the normal negative feedback between these tw

286 However, uncoupling the Shaker K(+) channel's pore domain (PD) fr

287 Divergent mechanisms of uncoupling the two steps of splicing argue for multiple

288 godendrocyte differentiation and maturation, uncoupling them at a transcriptional level and highlight

289 n by binding active phosphorylated GPCRs and uncoupling them from heterotrimeric G proteins.

290 mplex can activate developmental pathways by uncoupling them from upstream control.

291 brown adipocytes (BA) induces mitochondrial uncoupling, thereby increasing energy expenditure by shi

292 m fibrils, thus providing powerful tools for uncoupling these processes and investigating the role of

293 Uncoupling these processes through genome duplications l

294 The present work offers two strategies for uncoupling these two processes and converting concerted

295 diated mechanism that activates mitochondria uncoupling to reduce ROS production, which precedes the

296 esses the underlying basis for mitochondrial uncoupling using VCP knockdown neuroblastoma cell lines,

297 s to ventricular dysfunction by electrically uncoupling viable cardiomyocytes in the infarct region.

298 Uncoupling was induced through intraperitoneal injection

299 Mitochondrial uncoupling, which reduces cellular energy efficiency and

300 balance leads to nitric oxide synthase (NOS) uncoupling with reduced nitric oxide (NO) formation and