ライフサイエンスコーパス: TMR

1 TMR and TMR genetic risk scores are significantly associ

2 TMR causes decreased myocardial HED uptake in most patie

3 TMR did not significantly affect resting or stress myoca

4 TMR is a nerve transfer procedure developed for prosthes

5 TMR is an alternative surgical technique for the treatme

6 TMR provide key ecosystem services to hundreds of millio

7 TMR studies hypothesize that this method taps into norma

8 TMR was used to measure ventricular repolarization dynam

9 TMR with CO(2) laser as sole therapy for severe disablin

10 TMR(rec) was also associated with all-cause mortality (h

11 TMR-D readily diffused transsclerally and dispersed thro

12 TMR-D was also observed in the retinal and optic nerve v

13 MR (Galbeta1-4GlcNAcbeta(CH2)8CONH(CH2)2NHCO-TMR)), a fluorescently labeled model substrate for glyca

14 nalogs LacdiNAc-TMR (GalNAcbeta1-4GlcNAcbeta-TMR), LacNAc-TMR, and LacNAcbeta1-6LacNAcbeta-TMR.

15 the beta1-6 bond in LacNAcbeta1-6LacNAcbeta-TMR, an activity that is of potential importance in rela

16 MR), LacNAc-TMR, and LacNAcbeta1-6LacNAcbeta-TMR.

17 redefines mechanisms of ERK2 regulation by 7-TMR signaling in Dictyostelium and establishes new impli

18 controlling seven-transmembrane receptor (7-TMR) ERK2 activation/deactivation function independently

19 Seven-transmembrane receptor (7-TMR)-G protein networks are molecular sensors of extrace

20 nanoparticles, estimated to contain 700-900 TMRs per ca. 23 nm particle, were surface modified with

21 ible MTJs are fully functional, exhibiting a TMR ratio as high as 190% under bending radii as small a

22 acids adjacent to acylation sites or with a TMR cysteine shifted to a cytoplasmic location to identi

23 nctionalized azidobutyl-Q7 and NHS-activated TMR.

24 In addition, TMR patients used the same control system to operate adv

25 hedrine (HED) was performed before and after TMR in 8 patients with class IV angina ineligible for CA

26 Six months after TMR, there was a significant increase over baseline in r

27 ciation with regional ischemia is seen after TMR with a holmium:YAG laser.

28 e 6 h post-CO2 TMR, p = 0.03) was seen after TMR with both lasers.

29 prospectively collected up to 7 years after TMR.

30 of the patients had no angina 5 years after TMR.

31 postamputation pain in major limb amputees, TMR improved PLP and trended toward improved residual li

32 (16.9+/-6.5 U to 25.9+/-14.4 U, P=0.002) and TMR (0.51+/-0.14 to 0.79+/-0.32 mm Hg x mL(-1) x min(-1)

33 well as the % change in IMR (147+/-66%) and TMR (159+/-105%, P=NS versus IMR % change), increased si

34 Overall mortality rates for TMR-alone and TMR + CABG were 6.4% and 4.2%, respectively.

35 stress test had a cardiovascular event, and TMR(rec) was significantly associated with cardiovascula

36 ome-wide association studies for TMR(ex) and TMR(rec) were performed, and genetic risk scores were de

37 ied 12 genetic loci in total for TMR(ex) and TMR(rec), of which 9 are associated with another ECG mar

38 logistic regression model combining GTV and TMR(max), were assessed and compared with a previous tra

39 poxic volume, and the combination of GTV and TMR(max), were not able to stratify patient groups accor

40 significant correlation between mean IMR and TMR values, as well as between the % change in IMR and %

41 Such high values of spin polarization and TMR in readily manufactureable and highly thermally stab

42 TMR and TMR genetic risk scores are significantly associated wit

43 In the aortic arch, TMR-D labeled large and small vagal afferent axons (axon

44 All other investigated parameters, such as TMR(max), GTV, relative hypoxic volume, and the combinat

45 eptor dye pairs (TMR-ATTO647N, Cy3-ATTO647N, TMR-Cy5, and Cy3-Cy5), we find that this phenomenon depe

46 vary (CHO) cells were pulse-labeled with BAC-TMR-dextran by fluid-phase endocytosis.

47 On-bead TMR-labeled alpha-synuclein and aggregated Cy5-labeled a

48 ing perfusion defects in all patients before TMR (34.6+/-27.3% for HED versus 9.4+/-10.8% for NH3, P=

49 t upon photoconversion, the distance between TMR (donor) bound to a cysteine in the C-terminal domain

50 An intricate connection exists between TMR ratio, RA value and the bandgap and crystal structur

51 We microinjected micelles of Bodipy TMR-PIP(2) into cells, and we measured D on the inner le

52 led with BODIPY-tetramethylrhodamine (BODIPY(TMR)).

53 -tetramethylrhodamine-(+/-)CGP 12177 (BODIPY-TMR-CGP)] at the human beta1-adrenoceptor expressed in C

54 scence resonance energy transfer from Bodipy-TMR-PIP2 to Texas Red MARCKS(151-175) adsorbed to large

55 olipid substrates, GM3-BODIPY-FL, GM1-BODIPY-TMR, and lactosylceramide-BODIPY-650/665.

56 The dissociation rate of 3 nM BODIPY-TMR-CGP was 0.09 +/- 0.01 min(-1) in the absence of comp

57 Second, we detect quenching of Bodipy-TMR-PIP2 in large unilamellar vesicles when unlabeled MA

58 e-resolved fluorescence spectroscopy, Bodipy-TMR-X-labeled 4R1, 4BB, and 4alphaE quenched fluorescenc

59 These effects on the BODIPY-TMR-CGP dissociation rate were markedly enhanced in beta

60 cleavage lies relatively far from the bound TMR ( approximately 15 A).

61 Beads with bound TMR-labeled alpha-synuclein are then incubated with a re

62 hanges in this cleavage, are not affected by TMR-labeling of actin.

63 C2A-TMR assembled into oligomers via a novel N-terminal olig

64 es the membrane-spanning and C2A domain (C2A-TMR) into proteoliposomes.

65 uced disturbances, including climate change, TMR can be used as natural model systems to examine the

66 = 0.05; 206+/-36.7% of baseline 6 h post-CO2 TMR, p = 0.03) was seen after TMR with both lasers.

67 y underway to assess the results of combined TMR and CABG [4].

68 Filaments of cofilin-decorated TMR-actin and unlabeled actin are indistinguishable, as

69 374) with tethramethylrhodamine derivatives (TMR-actin) has been widely used for direct observation o

70 loads, e.g., tetramethyl rhodamine-dextran (TMR-D) and CdSe/ZnS quantum dots (QDs), are loaded in th

71 of the tracer tetramethylrhodamine dextran (TMR-D) into the nodose ganglion to label vagal aortic af

72 f 0.25% 70-kDa tetramethylrhodamine-dextran (TMR-D).

73 oads (tetramethylrhodamine-modified dextran, TMR-D; microperoxidase-11, MP-11; CdSe/ZnS quantum dots;

74 TAC-Lime-dextran-TMR fluorescence was K(+)-selective, increasing >4-fold

75 tran to measure ASL [K(+)], TAC-Lime-dextran-TMR, consisting of a green-fluorescing triazacryptand K(

76 Efficient TMR trafficking is critical for regulation of several pr

77 Silica-embedded TMR retains very high quantum yield, is resistant to que

78 ynamics, exposed in this cohort by exercise (TMR during exercise, TMR(ex)) and recovery from exercise

79 ercise, TMR(ex)) and recovery from exercise (TMR during recovery, TMR(rec)).

80 his cohort by exercise (TMR during exercise, TMR(ex)) and recovery from exercise (TMR during recovery

81 tunnel barriers and CoFe electrodes, exhibit TMR values of up to approximately 220% at room temperatu

82 luding 3 crossover patients, results favored TMR over standard treatment.

83 e increased severing of copolymer filaments, TMR-actin accelerates the polymerization of unlabeled ac

84 cal improvement in angina pectoris following TMR.

85 For TMR patients, the mean motion selection and motion compl

86 al (aCI) -0.1 to 6.9, adjusted P = 0.06) for TMR and standard treatment, respectively.

87 isk-adjusted mortality was also compared for TMR + CABG relative to CABG only in patients not amenabl

88 e also identified important risk factors for TMR and compared outcomes of TMR combined with coronary

89 tion in residual limb pain was favorable for TMR (P = 0.10).

90 Overall mortality rates for TMR-alone and TMR + CABG were 6.4% and 4.2%, respectivel

91 Genome-wide association studies for TMR(ex) and TMR(rec) were performed, and genetic risk sc

92 We identified 12 genetic loci in total for TMR(ex) and TMR(rec), of which 9 are associated with ano

93 dels are consistent with the requirement for TMRs in viral fusion proteins.

94 protein conformation and the distances from TMR to the carotenoid throughout the photocycle.

95 binding to DNA, the total fluorescence from TMR-Tc3 increases by three- to fourfold.

96 Moreover, we also show that functional TMR-cytochrome c undergoes a response of identical magni

97 by the metabolic products produced from GM1-TMR and the other monitored the metabolic products produ

98 thylrhodamine-labeled glycosphingolipid (GM1-TMR) was used as a substrate.

99 olipid tetramethylrhodamine labeled GM1 (GM1-TMR) produced by single cells isolated from the rat cere

100 n with tetramethylrhodamine-labeled GM1 (GM1-TMR).

101 ntrol in eight transhumeral amputees who had TMR in a balanced randomized cross-over study.

102 l virus-host model, we show that herpesvirus TMRs facilitate viral genome integration into host telom

103 Consistent with these high TMR values, superconducting tunnelling spectroscopy expe

104 Much higher TMR values have been theoretically predicted for perfect

105 Homologous TMR motifs are often found as multiple repeats in quite

106 F-actin that substitute for disrupted (as in TMR-actin and mutant actin) or weakened (as in ADP-actin

107 between the % change in IMR and % change in TMR.

108 tCS) during sleep can also be used to induce TMR, resulting in the facilitation of high-level cogniti

109 rescently labeled substrate analogs LacdiNAc-TMR (GalNAcbeta1-4GlcNAcbeta-TMR), LacNAc-TMR, and LacNA

110 1 and lipid-anchored synaptobrevin-2 lacking TMRs efficiently promoted spontaneous and Ca(2+)-trigger

111 al. show that lipid-anchored SNAREs lacking TMRs can support neurotransmitter release, suggesting th

112 ta1-4GlcNAcbeta-tetramethylrhodamine (LacNAc-TMR (Galbeta1-4GlcNAcbeta(CH2)8CONH(CH2)2NHCO-TMR)), a f

113 Ac-TMR (GalNAcbeta1-4GlcNAcbeta-TMR), LacNAc-TMR, and LacNAcbeta1-6LacNAcbeta-TMR.

114 whereas they were less active toward LacNAc-TMR conjugates.

115 = 12) or carbon dioxide (CO2) (n = 12) laser TMR.

116 These changes were not seen after CO2 laser TMR.

117 stimulated nostril) was improved after local TMR during sleep.

118 Moreover, local TMR improved phase-amplitude coupling (PAC) between slow

119 lateral stimulus processing to perform local TMR in one brain hemisphere.

120 tion switching and tunnel magnetoresistance (TMR) in perpendicularly magnetized CoFeB/MgO/CoFeB MTJs

121 interplay between tunnel magnetoresistance (TMR) ratio and the product of resistance and junction ar

122 nal bias-dependent tunnel magnetoresistance (TMR) response is observed in Sm0.75 Sr0.25 MnO3 -based n

123 om-temperature tunnelling magnetoresistance (TMR) of technologically relevant MTJs.

124 teine with tetramethylrhodamine-5-maleimide (TMR), a fluorophore with specific brightnesses that we a

125 ocystis with tetramethylrhodamine-maleimide (TMR) and obtained a photoactive OCP-TMR complex, the flu

126 and by transverse digital microradiography (TMR) for mineral content.

127 eased markedly, driven predominately by more TMR + CABG cases.

128 Immobilized ribosome.mRNA.TMR-Met-tRNAMetf complexes form peptide bonds with purom

129 ual assumption of complete quenching for NBD-TMR pairs in the dimer could not be quantitatively recon

130 leimide (TMR) and obtained a photoactive OCP-TMR complex, the fluorescence of which was highly sensit

131 The OCP-TMR complex was sensitive to the light intensity, temper

132 nal insights into the mechanism of action of TMR, which remains the Achilles' heel of this procedure.

133 The advantage of TMR-actin is that it does not lock actin in filaments (a

134 MgZnO barriers allow effective balancing of TMR ratio and RA value.

135 The challenge of TMR is related to improvement in perioperative outcomes,

136 The destabilizing and severing effect of TMR-actin is countered by filament stabilizing factors,

137 The effects of TMR may be enhanced when paired with pattern recognition

138 lts show an absence of allosteric effects of TMR on subdomain 2, while confirming ATP/ADP-dependent c

139 s point to an analogy between the effects of TMR-actin and severing proteins on F-actin, and imply th

140 The long-term efficacy of TMR persists for >/=5 years.

141 The fluorescence of TMR covalently linked to Y290C, T287C, and H83C decrease

142 e specificity constant within the library of TMR analogues.

143 Single molecule measurements of TMR-Tc3 bound to DNA shows that this complex also fluctu

144 ring as a function of the average number of TMR molecules per ring.

145 us to compute the number and orientation of TMR dimers per ring as a function of the average number

146 isk factors for TMR and compared outcomes of TMR combined with coronary artery bypass graft surgery (

147 ponses depend strongly on the molar ratio of TMR used to label cytochrome c.

148 In the recently solved structure of TMR-modified ADP-G-actin, the nucleotide cleft is in a c

149 Further studies of TMR + CABG are needed given its growing use and unclear

150 Clinical studies of TMR have noted a significant incidence of cardiac compli

151 ies, the FDA granted approval for the use of TMR as a sole therapy.

152 The use of TMR, and in particular, TMR + CABG, is expanding in comm

153 for cardiovascular risk and the validity of TMR as a cardiovascular risk predictor.

154 luate the cardiovascular prognostic value of TMR in a UK middle-aged population and identify any gene

155 ration is poorly understood, the presence of TMRs in a number of herpesviruses suggests it is their d

156 Our results and the presence of TMRs in many herpesviruses suggest that integration medi

157 , there are limited data on the outcomes of (TMR + CABG).

158 HCF145 represents the only TMR protein found in vascular plants.

159 l mixed ration (TMR) (Control, C; n = 40) or TMR + alfalfa green feed (30% of diet) (Treated, T; n =

160 pain were assigned to standard treatment or TMR.

161 rogrammed ribosomes with TMR-Met-tRNAMetf or TMR-Met-Phe-tRNAPhe are immobilized on mica and observed

162 While the overall TMR is slower than predicted based on concurrent regiona

163 ing four different donor-acceptor dye pairs (TMR-ATTO647N, Cy3-ATTO647N, TMR-Cy5, and Cy3-Cy5), we fi

164 The use of TMR, and in particular, TMR + CABG, is expanding in community practice.

165 2001, the number of STS hospitals performing TMR and total procedural counts increased markedly, driv

166 er equimolar mismatch DNA for each polyamide-TMR conjugate.

167 ned from 2.4+/-1.6 pre-TMR to 1.7+/-2.0 post-TMR (P=0.01).

168 at 1 h, p = 0.02; 18.4% decrease at 6 h post-TMR, p = 0.01).

169 01)Tl imaging at any temporal end point post-TMR.

170 an anginal class improved from 3.5+/-0.5 pre-TMR to 2.8+/-0.7 and 2.5+/-0.7 at 3 and 6 months, respec

171 unstable angina declined from 2.4+/-1.6 pre-TMR to 1.7+/-2.0 post-TMR (P=0.01).

172 Their average pre-TMR angina class was 3.7+/-0.4.

173 with nitrilotriacetic acid (NTA), producing TMR-SiO2-NTA-Ni2+.

174 red with those from six published randomized TMR trials.

175 orresponds to a mean thermal migration rate (TMR) of 0.0065 degrees C yr(-1) (95% CI = 0.0005-0.0132

176 f thermophilization [thermal migration rate (TMR), degrees C y(-1)] across all censuses were 0.011 de

177 8)F-FMISO and maximum tumor-to-muscle ratio (TMR(max)) at 4 h after injection, gross tumor volume (GT

178 Buffaloes received a total mixed ration (TMR) (Control, C; n = 40) or TMR + alfalfa green feed (3

179 Targeted memory reactivation (TMR) allows the manipulation of sleep-dependent consolid

180 method called targeted memory reactivation (TMR) for selectively strengthening memories during sleep

181 ved to rely on targeted memory reactivation (TMR) induced by the sensory stimulation.

182 ermine whether targeted memory reactivation (TMR) of specific memory traces during slow-wave sleep pr

183 e promoted via targeted memory reactivation (TMR) that re-presents training cues or context during sl

184 his technique, targeted memory reactivation (TMR), selectively enhances memory consolidation.

185 performance in a control group who received TMR before sleep.

186 We identified 3,717 patients receiving TMR at 173 U.S. hospitals participating in the Society o

187 er internalization, transmembrane receptors (TMRs) are typically recycled back to the cell surface or

188 recovery from exercise (TMR during recovery, TMR(rec)).

189 rane helices forming a transmembrane region (TMR), a large periplasmic (PP) domain, and a cytoplasmic

190 oned at the end of the transmembrane region (TMR).

191 otif, and a C-terminal transmembrane region (TMR).

192 hat each contains six transmembrane regions (TMRs) localized near the carboxyl terminus.

193 fusion by pulling the transmembrane regions (TMRs) of SNARE proteins together, thus allowing their TM

194 been proposed for the transmembrane regions (TMRs) of SNARE proteins, including formation of channel-

195 repeats, four central transmembrane regions (TMRs), and a cytoplasmic tail.

196 Targeted Muscle Reinnervation (TMR) is a nerve transfer procedure that creates addition

197 hnique called targeted muscle reinnervation (TMR) transfers residual arm nerves to alternative muscle

198 ignated the transcript binding motif repeat (TMR) domains, confer sequence-specific RNA binding capab

199 her herpesviruses, harbor telomeric repeats (TMRs) identical to host telomeres at either end of their

200 her herpesviruses harbors telomeric repeats (TMRs) that are identical to host telomere sequences (TTA

201 hy that when compared to previously reported TMR analogues, subtle modification of the TMR scaffold c

202 we examined whether synaptic SNAREs require TMRs for catalysis of synaptic vesicle fusion, which was

203 istance (TER) and tunnel magneto resistance (TMR) states in the junction.

204 elate with true microcirculatory resistance (TMR), defined as the distal left anterior descending (LA

205 The T-wave morphology restitution (TMR), an ECG marker quantifying ventricular repolarizati

206 Transmyocardial revascularisation (TMR) is an operative treatment for refractory angina pec

207 ter transmyocardial laser revascularization (TMR) and to identify predictors of these adverse clinica

208 ing transmyocardial laser revascularization (TMR) as the sole operative therapy for patients with sev

209 ith transmyocardial laser revascularization (TMR) at our institution.

210 ith transmyocardial laser revascularization (TMR) for induction of therapeutic angiogenesis and arter

211 ugh transmyocardial laser revascularization (TMR) has provided symptomatic relief of angina over the

212 of transmyocardial laser revascularization (TMR) on regional left ventricular systolic and diastolic

213 ter transmyocardial laser revascularization (TMR).

214 tcomes of transmyocardial revascularization (TMR) in community practice.

215 ents receiving incomplete revascularization, TMR + CABG was not associated with decreased mortality r

216 assembly incompetent tethramethyl rhodamine (TMR)-actin and T203C/C374S yeast mutant actin.

217 irpin polyamides with tetramethyl rhodamine (TMR) attached to an internal pyrrole ring were synthesiz

218 cent signal, only the tetramethyl rhodamine (TMR) HALO ligand provides sufficient signal for detectio

219 e in target tissue, a tetramethyl rhodamine (TMR)-labeled ribozyme was administered as a single SC or

220 Tropical montane rivers (TMR) are born in tropical mountains, descend through mon

221 not be accurately determined, yet these same TMR analogues promoted ATP occlusion at relatively low c

222 Herein, we characterize several TMR analogues that elicit modest turnover ( k cat <or= 1

223 The fifth and sixth TMRs contain numerous beta-branched amino acids that may

224 However, the role of the SNARE TMRs in synaptic vesicle fusion has not yet been tested

225 d with coronary artery bypass graft surgery (TMR + CABG) versus bypass alone in patients receiving in

226 Tetramethylrhodamine (TMR)-doped silica nanoparticles, estimated to contain 70

227 nsensitive chromophore tetramethylrhodamine (TMR).

228 The fluorescent dye tetramethylrhodamine (TMR) was conjugated to a synthetic peptide containing th

229 to the fluorescent dye tetramethylrhodamine (TMR), and the characterization of its optical and guest-

230 arger fluorescent dye, tetramethylrhodamine (TMR).

231 N-termini with either tetramethylrhodamine (TMR) or 7-nitrobenz-2-oxa-1,3-diazole (NBD) also indicat

232 s with the fluorophore tetramethylrhodamine (TMR).

233 cent rhodamines [e.g., tetramethylrhodamine (TMR)-thiols].

234 olecular weight marker tetramethylrhodamine (TMR)-dextran and its blockage by the Na(+)/H(+) exchange

235 oncovalently "stacked" tetramethylrhodamine (TMR) dimers have been used to both report and perturb th

236 ling with a green dye (tetramethylrhodamine, TMR) and attachment to microbeads.

237 a synthetic library of tetramethylrosamine ( TMR) analogues, we observed significant variation in ATP

238 Tetramethylrosamine (TMR) displays a relatively high affinity for Pgp when co

239 of the aptamer bound to tetramethylrosamine (TMR), a high-affinity MG analog.

240 arge corpus of studies now demonstrates that TMR is both reliable and effective.

241 ed by several new studies demonstrating that TMR upregulates the reactivation of cued memories, and t

242 Although it is established that TMR-actin alone is polymerization incompetent, the impac

243 ow-oscillation upstate, we hypothesized that TMR stimulation effects would depend on the phase of the

244 severing proteins on F-actin, and imply that TMR-actin may be inappropriate for investigations of act

245 In this study, we show that TMR-actin perturbs the filaments structure when copolyme

246 binding site in the apical domain, such that TMR molecules on adjacent subunits are able to form dime

247 These findings suggest that TMR during sleep can alter memory representations and pr

248 The TMR dimers also serve as a surrogate for substrate prote

249 The TMR dimers thus serve as quantitative reporter of the al

250 The TMR modification inhibits nucleotide exchange, but has n

251 The TMR patients were able to repeatedly perform 10 differen

252 his review, background information about the TMR procedure will be discussed along with an analysis o

253 ise distance between the SNARE motif and the TMR was critical for fusion.

254 ssential for fusion, the SNARE motif and the TMR, and these domains have to be closely coupled to fun

255 e the folding of loop nucleotides around the TMR.

256 by substrate protein is also mimicked by the TMR dimers.

257 Finally, the TMR analogues facilitated uptake of calcein-AM into CR1R

258 inases examined hydrolyzed LacdiNAc from the TMR aglycone to various degrees, whereas they were less

259 t CCSA score was II or lower in 47.8% in the TMR group compared with 14.3% in the medication-only gro

260 res for PLP was significantly greater in the TMR group compared with standard treatment [mean (aCI) =

261 In the TMR group, the entire LCx region was treated with transm

262 l vascular density was increased only in the TMR-treated regions six months postoperatively.

263 Moreover, the TMR analogues competitively inhibited VER-dependent ATPa

264 within the first transmembrane helix of the TMR and deletions within the PP domain both resulted in

265 netics were identical in the presence of the TMR derivatives, VER, or in the absence of drug, suggest

266 The free energy of unstacking of the TMR dimers was estimated at 2.6 +/- 1.0 kJ/mol dimer.

267 ng sites, with concomitant unstacking of the TMR dimers.

268 re raised regarding the possible role of the TMR label on Cys(374) in determining these aspects of G-

269 ed TMR analogues, subtle modification of the TMR scaffold can confer large differences in ATP turnove

270 Individuals in the top 20% of the TMR(rec) genetic risk score were significantly more like

271 Our reanalysis of the TMR-modified actin structures suggests that the nucleoti

272 In contrast, shifting the TMR cysteine to a cytoplasmic location virtually elimina

273 Evidence is presented to show that the TMR-Tc3 conjugate exists in at least two conformational

274 however, for larger barrier thicknesses, the TMR-bias dependence is more complex and reverses sign at

275 ion of a library of compounds based upon the TMR scaffold and use this set to assess the determinants

276 most stable conformation is one in which the TMR fluorescence is quenched.

277 tom magnetic layers is observed in which the TMR ratio of the MTJs is almost unmeasurable.

278 to the membrane and/or sequences within the TMR and PP domain.

279 The conservation of the TMRs in all SCAMPs with the variable presence of N-termi

280 se-related motifs support association of the TMRs to the psaA RNA, presumably pointing to a regulator

281 SNARE proteins together, thus allowing their TMRs to form a fusion pore.

282 nction in membrane traffic mediated by their TMRs.

283 Thus, TMR in human sleep transcends global action by selective

284 ERalpha, bound to TMR-SiO2-NTA-Ni++ beads in a site-specific manner, exhib

285 This dual-mode type TMR-SiO2-NTA-Ni2+ system represents a powerful combinati

286 retained excellent performance and unaltered TMR ratio after over 1000 bending cycles.

287 Animals then underwent TMR with a holmium:yttrium-aluminum-garnet (holmium:YAG)

288 on or transhumeral amputations who underwent TMR surgery between February 2002 and October 2006 and 5

289 s suggest that integration mediated by viral TMRs is a conserved mechanism, which ensures faithful vi

290 At least in the case of MDV, viral TMRs facilitate integration into host telomeres.

291 We observe weak TMR fluorescence in the absence of DNA.

292 efficient of extremely high molecular weight TMR-Dextran (MW 2 000 000), which rises linearly with th

293 Whether TMR acts locally or globally on cortical sleep oscillati

294 Mice treated SC or IV with TMR-labeled ribozyme had positive fluorescence in the li

295 A GroEL mutant (K242C) has been labeled with TMR, close to the peptide-binding site in the apical dom

296 ify clinical risk factors for mortality with TMR.

297 complexes of mRNA-programmed ribosomes with TMR-Met-tRNAMetf or TMR-Met-Phe-tRNAPhe are immobilized

298 0 cells were used that had been treated with TMR-G(M1).

299 7.4+/-44.2% of baseline 6 h post-holmium:YAG TMR, p = 0.05; 206+/-36.7% of baseline 6 h post-CO2 TMR,

300 .4% of baseline, p = 0.02) after holmium:YAG TMR.