ライフサイエンスコーパス: Tm

1 Tm measurements of modified oligodeoxynucleotides with c

2 Tm measurements of oligonucleotides with single and doub

3 Tm values of single-layer and multilayer samples do not

4 Tm was, however, well tolerated by all patients providin

5 ximately temperature independent values of 1/Tm for 1 and 2 up to about 160 K and modest temperature

6 f a series of lanthanide activators (Er(3+), Tm(3+), and Ho(3+)) at a biocompatible excitation wavele

7 3+), Gd(3+), Tb(3+), Dy(3+), Ho(3+), Er(3+), Tm(3+), Yb(3+)) and linear amino-functionalized dicarbox

8 an IgG and blue emitting UCNPs (NaYF4:Yb(3+),Tm(3+)) coated with antihuman IgM were used to detect hu

9 cence phenomenon that occurs in novel Er(3+)-Tm(3+) ion pairs.

10 ared, quantum cutting luminescence in Er(3+)/Tm(3+) co-doped telluride glass was studied.

11 crystals doped with Yb(3+)/Er(3+) and Yb(3+)/Tm(3+).

12 UV-Vis-NIR UCNPs consisting of LiYF4:Yb(3+)/Tm(3+)@SiO2 individually coated with a 10 +/- 2 nm layer

13 it from the transmembrane isoform of CTLA-4, Tm-CTLA-4.

14 of strongly bound XBs in McTnT(1-44Delta) + Tm(H276N) fibers, whereas diminished thin-filament coope

15 t decreased (17%) only in McTnT(1-44Delta) + Tm(H276N) fibers.

16 strains > 12), elevated temperatures (> 0.45 Tm of a constituent), and irradiation (light ion).

17 room temperature and at 2300 degrees C (~0.7 Tm) showed increased plasticity response with temperatur

18 ty attenuated tension in McTnT(45-74Delta) + Tm(H276N) fibers.

19 nm and 652 nm luminescence, of (A) Er(3+)(8%)Tm(3+)(0.5%):telluride glass are very similar to those o

20 0-nm luminescence intensity of (A) Er(3+)(8%)Tm(3+)(0.5%):telluride glass was approximately 4.4 to 19

21 t 65 degrees C, 1.3-fold improved kcat and a Tm increased by 5 degrees C above that of wild type.

22 gle modification in a 12-mer duplex causes a Tm increase of 36.0 degrees C relative to the metal-free

23 und; and (3) highly stable duplexes having a Tm of 64(2) degrees C form if 18.5-19.0 Mg(2+) ions are

24 ane properties of unsaturated systems with a Tm below 0 degrees C were not influenced by encapsulatio

25 eins and thermostabilize the proteins with a Tm increase of more than 10 degrees C.

26 to the wild type enzyme, and unfolds with a Tm of 53 degrees C.

27 hal repositioning of Tm along the actin (Ac):Tm:troponin (Tn) thin filament to block or expose myosin

28 lpha-tetramethyl-1,4,7,1 0-tetraacetic acid (Tm(DOTMA)).

29 rties of the ASO including binding affinity (Tm), nuclease stability, activity in vitro and in vivo,

30 5.93 vs. 6.00 in the control fibers) against Tm(H276N), but not against Tm(WT) background.

31 l fibers) against Tm(H276N), but not against Tm(WT) background.

32 and Tm(H276N) (38%), but sped g only against Tm(H276N) by 35%.

33 ted Ca(2+)-activated maximal tension against Tm(WT) (36%) and Tm(H276N) (38%), but sped g only agains

34 l activation), decreased in McTnT1-44 (alpha-Tm) fibres.

35 utilizing a mouse model expressing an alpha-Tm protein that cannot be phosphorylated (S283A) shows a

36 sults, we hypothesized that decreasing alpha-Tm phosphorylation may be beneficial in the context of a

37 ) mouse hearts that expressed a mutant alpha-Tm (Tm(H276N)).

38 mice (Tm(DM)) that expressed a mutant alpha-Tm in the heart; S229E and H276N substitutions induce st

39 an Ser-16 and Thr-17 compared with the alpha-Tm E180G mice.

40 Although Tm-1 homologs are widely present in bacteria, archaea an

41 figurations like Eu(2+), Yb(2+), Sm(2+), and Tm(2+).

42 erms were defined, using Dy(3+), Tb(3+), and Tm(3+).

43 ted maximal tension against Tm(WT) (36%) and Tm(H276N) (38%), but sped g only against Tm(H276N) by 35

44 r dynamics simulations for both Tm alone and Tm-F-actin complex in the presence of explicit solvent (

45 assive small bowel resection, tuft cells and Tm were diminished due to the diet used postoperatively.

46 rithm-based matching of melt curve shape and Tm to a database of known sequence-specific melt curves.

47 lmost all amplicons with different sizes and Tm values under identical PCR conditions.

48 l template contained known amounts of Tb and Tm ions, allowing us to estimate via atomic mass spectro

49 cobacterium tuberculosis ThyX (Mtb-ThyX) and Tm-ThyX, our crystal structure paves the way for a struc

50 tachment (g) decreased in Tm(DM)+TnT(WT) and Tm(H276N)+TnT(WT) fibers but increased in Tm(DM)+TnT(45-

51 scores the primers based on factors such as Tm, GC content and secondary structure allowing for simp

52 or the more commonly studied cell-associated Tm-CTLA-4.

53 roles of sCTLA-4 and microvesicle-associated Tm-CTLA-4 warrant further investigation, especially as t

54 with low duplex stability having an average Tm of 31(3) degrees C, if an average of 17.5-18.0 Mg(2+)

55 ly 4.4 to 19.5 times larger than that of (B) Tm(3+)(0.5%):telluride glass, and approximately 5.0 time

56 45-74 enhanced pCa50 in both alpha- and beta-Tm fibres, with beta-Tm having a bigger effect.

57 t of XBs was attenuated by McTnT1-44 in beta-Tm fibres.

58 ct of McTnT1-44 on pCa50 was ablated in beta-Tm fibres.

59 in both alpha- and beta-Tm fibres, with beta-Tm having a bigger effect.

60 The relationship between Tm and the inverse thickness follows the linear scaling

61 Both Tm-stabilizing substitutions strongly decreased the slac

62 sive molecular dynamics simulations for both Tm alone and Tm-F-actin complex in the presence of expli

63 hnique, centimetre long gold nanowires (bulk Tm = 1064 degrees C) embedded in silicate glass fibres (

64 e mesenchyme were significantly reduced, but Tm burden was not affected.

65 ed to type 2 immune response only in WT, but Tm colonization in both WT and Raptor deficient mice.

66 esponses, and apoptosis in reactivated CD4(+)Tm cells during T-cell receptor stimulation.

67 ce in the proliferation of reactivated CD4(+)Tm cells.

68 In T1D patients and siblings, CD4(+)Tm cells easily acquired the activated CD25(+) phenotype

69 CD4-Tm generation of IL-2, IL-4, and IFN-gamma and, for youn

70 Abs significantly increased all CD4-Tm ex-mRNAs, but only IL-2 and IL-6 ex-mRNAs were increa

71 cts, but only narrow and age-independent CD4-Tm responses.

72 signals by integrating multiple cholinergic Tm inputs using nicotinic and muscarinic cholinoceptors.

73 from over 90% of all four types of chromatic Tm neurons, whereas LT11 is postsynaptic to the chromati

74 d to probe connections between the chromatic Tm neurons and 28 known and novel types of lobula neuron

75 The synaptic targets of the chromatic Tm neurons in the lobula are not known, however.

76 hereas LT11 is postsynaptic to the chromatic Tm neurons, with only modest selectivity and at a lower

77 and Li4 as synaptic targets of the chromatic Tm neurons.

78 These chromatic Tm neurons project axons to a deeper optic neuropil, the

79 appeared at -9.2 ppm after TGase conjugated Tm-DO3A-cadaverine to albumin, which also caused a decre

80 nction of the overlapping ends of contiguous Tm dimers, we used transgenic mice (Tm(DM)) that express

81 cTnT and the overlapping ends of contiguous Tm effectuates different states of Tm on the actin filam

82 effect on the overlapping ends of contiguous Tm.

83 ncy using islets from Isl-1(L/L); Pdx1-CreER(Tm) mice and betaTC3 insulinoma cells, respectively.

84 Rather, islets from Isl-1(L/L); Pdx1-CreER(Tm) mice showed impaired insulin secretion.

85 ss-of-function mouse: Isl-1(L/L); Pdx1-CreER(Tm).

86 xation: myofibrils with D137L/G126R or D137L Tm showed prolonged durations of the slow phase of relax

87 Cells possess different Tm isoforms, each capable of differentially regulating t

88 Yb) but also in the visible (Sm, Eu, Tb, Dy, Tm).

89 discriminating, exhibiting markedly elevated Tm values only in the presence of Cu(2+) and only when c

90 The infrared-excited, ultraviolet-emitting, Tm(III)-doped upconverting nanoparticles were used as do

91 skeletal myofibrils by replacing endogenous Tm and troponin (Tn) with recombinant Tm mutants and pur

92 ingle mutation L110A destabilizes the entire Tm(1-131) molecule, showing that the effect of this muta

93 s, namely [LnL(1)] (Ln = Eu, Tb, Dy, Ho, Er, Tm, and Yb; L(1): 1,4,7-tris[(6-carboxypyridin-2-yl)meth

94 ios of Ti with Al, V, Ga, Y, Nb, Eu, Ho, Er, Tm, Yb, and Ta as determined by ICPMS and ICPOES, in com

95 La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) detected in sludges showed enrichment factor

96 p(ttt))2](+) cations (1-Ln; Ln = Gd, Ho, Er, Tm, Yb, Lu), synthesized by halide abstraction of [Ln(Cp

97 f [Ln(Cp(ttt))2(Cl)] (2-Ln; Ln = Gd, Ho, Er, Tm, Yb, Lu).

98 La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm; Cp' = C5H4SiMe3) and the analogous trivalent complex

99 of a 4f(n+1) configuration for Ln = Sm, Eu, Tm and a 4f(n)5d(1) configuration for Ln = Y, La, Gd, Tb

100 erature of native Cu2,Zn2-SOD1 (e.g., fibril Tm = 84.49 degrees C for acetylated D90A apo-SOD1 fibril

101 Adverse gastrointestinal events were 8 for Tm, Vs 11 for rice (p = 0.6321) and Vs 31 for Amygluten

102 itric acid, malic acid, or NTA, the Jint for Tm was more than 1 order of magnitude higher than that p

103 finity of some, but not all, TnT mutants for Tm relative to WT TnT.

104 changes observed in vitro of TnT mutants for Tm.

105 is possible to identify samples suitable for Tm mapping identification.

106 pathy is by changing the affinity of TnT for Tm within the TNT1 region.

107 the widest spectral width demonstrated from Tm-doped all-fiber lasers based on 1 or 2 dimensional na

108 d McTnT(45-74Delta), into muscle fibers from Tm(H276N).

109 e Tomato mosaic virus (ToMV) resistance gene Tm-1 encodes a direct inhibitor of ToMV RNA replication

110 For T=43 degrees C>Tm, the milk-SM molecules were in a LE phase regardless

111 holesterol in a Lo phase for both T<Tm and T>Tm and (ii) of high Tm lipids in a gel phase for T<Tm.

112 h some differences were significant (hairpin Tm values increased 0.7 degrees C by the quantum method

113 ed into hyperstable collagen triple helices (Tm approximately 80 degrees C).

114 FGM with the lateral segregation (i) of high Tm lipids and cholesterol in a Lo phase for both T<Tm an

115 hase for both T<Tm and T>Tm and (ii) of high Tm lipids in a gel phase for T<Tm.

116 mposed of various mixtures containing a high-Tm lipid (brain sphingomyelin (SM)) or dipalmitoyl phosp

117 sordered domains in vesicles containing high-Tm and low-Tm lipids plus 1:1 (mol/mol) coprostanol/epic

118 However, Tm shifts cannot be readily transformed into binding aff

119 ds are the reasons for these alternations in Tm.

120 ied oligonucleotides, no relevant changes in Tm were detected, attributing the fluorine substituent a

121 owed a consistent ~3.1 degrees C decrease in Tm per 2'-O-acetyl group.

122 of cross-bridge detachment (g) decreased in Tm(DM)+TnT(WT) and Tm(H276N)+TnT(WT) fibers but increase

123 DNA backbone and showed no discrimination in Tm with complementary RNA, demonstrating that 6'-F subst

124 he ecRNH lineage exhibited an abrupt drop in Tm followed by relatively little change.

125 which exhibited a 10.4 degrees C increase in Tm and a 44-fold greater half-life compared with the wil

126 was accompanied by a significant increase in Tm and effectively abolished the P(r) dependence on T.

127 nd Tm(H276N)+TnT(WT) fibers but increased in Tm(DM)+TnT(45-74Delta) fibers; however, TnT(45-74Delta)

128 Increases in Tm were in the range of +1-2 degrees C compared to thymi

129 Nanocalorimetry shows stepwise increases in Tm, as the lamella thickness increases by integer increm

130 functions and the structural instability in Tm is unknown.

131 did not alter g, demonstrating that S229E in Tm(DM) had divergent effects on g.

132 ization of myofilament Ca(2+) sensitivity in Tm(DM)+TnT(1-44Delta) fibers.

133 The S229E substitution in Tm(DM) ablated the H276N-induced desensitization of myof

134 s showed variable fluctuations of individual Tm periods from the closed position toward the open posi

135 DEX inhibited Tm-induced MUC2 precursor accumulation, promoted product

136 ers strongly stabilizes gp12, increasing its Tm to 54 degrees C.

137 to the formation of a ternary Tm complex {L-Tm-R} at the metal transport site.

138 nd methyl groups is effective in lengthening Tm at T > 70 K.

139 The plant Tm-1-like (Tm-1L) protein is predicted to contain an uncharacterize

140 spin label has been prepared that has longer Tm between 80 and 295 K in immobilized samples than conv

141 solid-surface homopolymer primers and a low-Tm solution phase primer.

142 mains in vesicles containing high-Tm and low-Tm lipids plus 1:1 (mol/mol) coprostanol/epicholesterol.

143 domains in vesicles containing high and low-Tm lipids plus cholesterol or 1:1 (mol/mol) cholesterol/

144 dipalmitoyl phosphatidylcholine (DPPC)), low-Tm lipid (dioleoylphosphatidylcholine (DOPC) or 1-palmit

145 The same packing features that lower Tm in the odd acids lead to easy accommodation of the de

146 For T=15 degrees C<Tm, the liquid expanded (LE) to liquid condensed (LC) ph

147 ids and cholesterol in a Lo phase for both T<Tm and T>Tm and (ii) of high Tm lipids in a gel phase fo

148 (ii) of high Tm lipids in a gel phase for T<Tm.

149 en algae were exposed to a constant 10(-9) M Tm(3+).

150 ay crystal structure of Thermatoga maritima (Tm) ThyX in complex with a nonsubstrate analog inhibitor

151 f complexes between the Thermotoga maritima (Tm) NadA K219R/Y107F variant and (i) the first intermedi

152 saturable absorber and a single gain medium (Tm(3+):ZBLAN fiber) to implement (1) a dual-band fiber r

153 sing a combination of STD-NMR, thermal melt (Tm), and biochemical assays to identify compounds that b

154 in-lattice relaxation (T1) and phase memory (Tm) times are found to be independent of the nuclei bear

155 helated with 11 different transition metals (Tm), including abundant first-row Tm (Sc through Cu), to

156 ntiguous Tm dimers, we used transgenic mice (Tm(DM)) that expressed a mutant alpha-Tm in the heart; S

157 nt, which increased the transition midpoint (Tm) for the N-terminal domain by 8 and 12 degrees C; tog

158 A series of structurally modified Tm(3+) DOTAM-alkyl complexes as potential PARACEST MRI c

159 Tamoxifen injection in Tritrichomonas muris (Tm) infected mice, tuft cells, IL-25 in epithelium and I

160 ed and visualized cardiac and gizzard muscle Tm on filamentous Ac in the position that corresponds to

161 state of Tn and the binding state of myosin, Tm can occupy the blocked, closed, or open position on A

162 ears that reducing the flexibility of native Tm coiled-coil structure decreases the optimum interacti

163 These NMR binding data and the negative Tm shifts are very similar to those previously reported

164 +) donor ions and the infrared absorption of Tm(3+) acceptor ions.

165 hages were labeled with different amounts of Tm-DOTMA.

166 To elucidate the molecular details of Tm flexibility in relation to its binding to F-actin, we

167 The systemic distribution of Tm(DOTMA) of both cell types was investigated by means o

168 Er(3+) doped Y2O3 microtubes by co-doping of Tm(3+) or Ho(3+) ion and controlling excitation power.

169 The elimination of Tm and subsequent re-infection of mice with Tm led to ty

170 divergent effect on the overlapping ends of Tm were employed.

171 e central region and the overlapping ends of Tm, respectively.

172 administration of a single dose of gluten of Tm in patients with CD on GFD.

173 d proton three-dimensional UTE MR imaging of Tm-DOTMA-labeled cells is a highly specific and sensitiv

174 The influence of Tm(3+) or Ho(3+) ion on optical temperature behavior of

175 A detection limit of about 25 micromol/L of Tm-DOTMA was calculated from in vitro MR measurements.

176 The strongly shifted MR lines of Tm- and Dy-DOTMA can be separated from the tissue water

177 2 results in an exchange in localizations of Tm forms on actin polymers.

178 and (10.1 +/- 3.0) x 10(10) (macrophages) of Tm-DOTMA molecules per cell was achieved.

179 h resolution of 25 mum, distribution maps of Tm in different tissues such as tumor, liver, lung, and

180 rystal field splitting between d orbitals of Tm and p orbitals of B.

181 optimum interactions of the central part of Tm with the C-terminal region of TnI.

182 uctural instability in the central region of Tm modifies cardiac contractile function via its effect

183 uctural instability in the central region of Tm modulates the function of the overlapping ends of con

184 s achieved by the azimuthal repositioning of Tm along the actin (Ac):Tm:troponin (Tn) thin filament t

185 We identified key residues of Tm involved in its dynamic interactions with F-actin, ma

186 ite conclusion can be drawn on the safety of Tm, based on no change in urinary L/R because even Amygl

187 ontiguous Tm effectuates different states of Tm on the actin filament.

188 g transition having a melting temperature of Tm = 71 +/- 2 degrees C, in agreement with prior measure

189 the principle that the shifted resonances on Tm and dysprosium (Dy)-DOTMA can be detected separately

190 However, the mechanism by which a particular Tm localizes to a specific actin polymer is unknown.

191 The plant Tm-1-like (Tm-1L) protein is predicted to contain an unc

192 ong the plateau and above the melting point (Tm = 280 degrees C) initially results in the formation o

193 having a well-spaced discrete melting point, Tm, distribution.

194 m temperature, produced linear polyethylene (Tm =135 degrees C) at -20 degrees C, and, most important

195 der Waals interactions with H2 than precious Tm.

196 e 1,180,416 member interactome for predicted Tm values and (iii) used predicted Tm cutoff points to i

197 predicted Tm values and (iii) used predicted Tm cutoff points to isolate eight peptides that form fou

198 show that three types of medulla projection (Tm) neurons extend their dendrites in stereotyped direct

199 R8 and their downstream medulla projection (Tm) neurons Tm5a, Tm5b, Tm5c, and Tm20 in the second opt

200 We prepared three recombinant (rat) Tm(1-131) proteins, including the wild type sequence, a

201 genous Tm and troponin (Tn) with recombinant Tm mutants and purified skeletal Tn.

202 on metals (Tm), including abundant first-row Tm (Sc through Cu), totaling 60 molecular compounds with

203 It was found that first-row Tm gave similar and sometimes superior van der Waals int

204 electron to the methyl protons that shorten Tm at T > 70 K in currently used labels.

205 e gel to Lalpha phase transition of milk-SM (Tm approximately 34 degrees C).

206 ound in a few compounds [RRh4B4 (R = Nd, Sm, Tm, Er), R'Mo6X8 (R' = Tb, Dy, Er, Ho, and X = S, Se), U

207 The Eu, Yb, Sm, Tm, Dy, and Nd complexes were expected to show much larg

208 +2 oxidation states, i.e., Ln = Eu, Yb, Sm, Tm, Dy, and Nd, to allow direct structural and spectrosc

209 role for formins in dictating which specific Tm variant will associate with a growing actin filament

210 ing only marginal thermodynamic stabilities (Tm < 40 degrees C) can still pose large kinetic barriers

211 e involved in its extreme thermal stability (Tm = 128 degrees C).

212 small size (7 kDa), high thermal stability (Tm of 98 degrees C), and absence of cysteines and glycos

213 cterial or mammalian host to produce stable (Tm of 81 degrees C), predominantly monomeric (>90%) anti

214 Because temperatures range from T/Tm = 1 at the inner-outer core boundary to T/Tm approxim

215 Tm = 1 at the inner-outer core boundary to T/Tm approximately 0.99 at the center, this strong nonline

216 60 gigapascals up to its melting temperature Tm.

217 e shift in protein denaturation temperature (Tm shift) has become a popular approach to identify pote

218 rmostable with its denaturation temperature (Tm) increased to 60 degrees C.

219 e that spanned the denaturation temperature (Tm) of hybrids by applying a spatial temperature gradien

220 0 degrees C drop in the melting temperature (Tm ) was observed at pH 2.5: DeltaDeltaGF >/=11.3 kJ mol

221 ve little effect on the melting temperature (Tm) although some differences were significant (hairpin

222 monstrate that both the melting temperature (Tm) in a subsection of siRNA non-seed region, and the GC

223 erein report the novel "melting temperature (Tm) mapping method" for rapidly identifying the dominant

224 ly-Pro-Hyp)4-NH2] had a melting temperature (Tm) of 36.2 degrees C and was hydrolyzed efficiently by

225 owed by analysis of the melting temperature (Tm) of the amplicons on qPCR platforms (the Mx3000P qPCR

226 ism using a pair of low-melting temperature (Tm) solid-surface homopolymer primers and a low-Tm solut

227 e shift in NBD1 thermal melting temperature (Tm), pointing to direct VX-809 interaction shifting the

228 rall sequence-dependent melting temperature (Tm).

229 eduction in the lipids' melting temperature (Tm).

230 mplifiable beta-globin (melting temperature [Tm], 87.2 degrees C +/- 0.2 degrees C) occurred in 99.1%

231 the same manner as the melting temperature, Tm.

232 ng a range of phase transition temperatures (Tm).

233 was attributed to the formation of a ternary Tm complex {L-Tm-R} at the metal transport site.

234 ted human CD4(+) T cells, we discovered that Tm-CTLA-4 is associated with microvesicles produced by t

235 a variety of extant bacteria and found that Tm correlates with the species' growth temperatures, con

236 egrees C) at saturating [Ca(2+)] showed that Tm-stabilizing substitutions did not significantly affec

237 The Tm internalization flux (Jint) followed first-order (Mic

238 The Tm mapping method is therefore useful for identifying in

239 ired, the amount of 4-hydroxyproline and the Tm of collagen II were reduced, and the extracellular ma

240 tructure form at temperatures well below the Tm, with a melting transition that is distinctly less co

241 ction of fdG into a DNA duplex decreases the Tm by approximately 1.6 degrees C/modification.

242 ontrol region (SCR), residues 97-118, in the Tm sequence that controls overall protein stability but

243 C; together the substitutions increased the Tm by 21 degrees C.

244 In a glassy trehalose matrix the Tm for the doubly labeled T4 lysozyme was long enough to

245 ically analyzed the local flexibility of the Tm coiled coil using multiple parameters.

246 On the basis of the Tm values of the LSG-qPCR amplicons from reference and c

247 ired genes and resulted in the origin of the Tm-1L gene in streptophytes.

248 e use destabilizing mutations that shift the Tm and Cm.

249 We tested the Tm mapping method using 200 whole blood samples obtained

250 d ligand exchange studies, we found that the Tm of the membrane controls optical and chemical propert

251 f 130 samples were negative according to the Tm mapping method, 98% (128/130) of which were also nega

252 e, 70 samples were positive according to the Tm mapping method, and of the 59 suitable for identifica

253 ession levels (up 60%), and thermostability (Tm, 12 degrees C higher).

254 trimers as being appropriately thermostable (Tm of 63.4 degrees C and 62.7 degrees C, respectively) a

255 n complex generation in mode-locked thulium (Tm)-doped fibre laser, using double-wall carbon nanotube

256 TP(8-)) complexed with paramagnetic thulium (Tm(3+)), to generate pHe maps in rat brains bearing U251

257 the spin-label phase memory relaxation time Tm .

258 nitroxides causes spin echo dephasing times (Tm) to be too short to perform DEER measurements at temp

259 e sufficiently long quantum coherence times, Tm, to perform quantum operations, but their use in real

260 Mn, Na, Nd, Ni, Pb, Pr, Rb, Sc, Se, Sr, Tl, Tm, V, Y, Yb, Zn) and variables selected by means of ste

261 Mn, Mo, Nb, Nd, Ni, Pr, Rb, Sm, Te, Ti, Tl, Tm, U, V, Y, Zn and Zr).

262 use hearts that expressed a mutant alpha-Tm (Tm(H276N)).

263 perhard transition metal tetraborides (TmB4, Tm = Cr, Mn and Fe) evoked recently much attention from

264 on effects, indicating the importance of TnI-Tm interactions in maintaining the blocked state.

265 dral binary quasicrystals, i-R-Cd (R = Gd to Tm, Y), six of which bear localized magnetic moments.

266 In contrast to the acutely toxic Tm(3+) DOTAM-alkyl complexes, the structurally modified

267 periment with macrophages for cell tracking, Tm was detected in the explanted biogell pellet with rel

268 d the native-to-unfolded thermal transition (Tm), quite different to the large increases in DeltaTm s

269 report that multiple types of transmedulla (Tm) neurons provide unexpectedly complex inputs to T5 at

270 that C1 directly interacts with Tm and traps Tm in the open position on the surface of F-actin.

271 TRV120067- treated Tm-E54K mice showed improved cardiac structure and funct

272 Myofilaments of TRV120067-treated Tm-E54K mice had significantly improved myofilament-Ca(2

273 Tropomyosin (Tm) is a coiled-coil protein that binds to filamentous a

274 Tropomyosin (Tm) is a key factor in the molecular mechanisms that reg

275 Tropomyosin (Tm) is an actin-binding, thin filament, two-stranded alp

276 the functional impact of alpha-tropomyosin (Tm) substituted with one (D137L) or two (D137L/G126R) st

277 genic mice that expressed alpha-tropomyosin (Tm).

278 e causal link between disparate tropomyosin (Tm) functions and the structural instability in Tm is un

279 mouse model expressing a mutant tropomyosin (Tm-E54K) for 3 months with either TRV120067, a beta-arre

280 actin-binding protein nonmuscle tropomyosin (Tm) provides spatially specific regulation of interactio

281 to activate the TF by shifting tropomyosin (Tm) to the "open" structural state.

282 Studies indicate that tropomyosin (Tm) phosphorylation status varies in different mouse mod

283 mutations are clustered in the tropomyosin (Tm) binding region of TnT, TNT1 (residues 80-180).

284 to the ER-stress-inducing agent tunicamycin (Tm).

285 the N-glycosylation inhibitor, tunicamycin (Tm).

286 onsiveness, which was depressed in untreated Tm-E54K mice.

287 plore the mechanism for the enhanced uptake, Tm internalization was carefully evaluated.

288 In vivo, Tm-DOTMA signal was detectable for 1 week in both tumors

289 When Tm infected mice were treated with rapamycin, DCLK1 and

290 diagram characterized with dTm/dP < 0, where Tm is the melting temperature and P is pressure, above a

291 specific formin family members dictate which Tm isoform will associate with a particular actin filame

292 +) microtubes is inhibited by co-doping with Tm(3+) or Ho(3+) ion, moreover the maximum sensitivity v

293 structure of TNT1 and its interactions with Tm.

294 further show that C1 directly interacts with Tm and traps Tm in the open position on the surface of F

295 ly, tumor cells and macrophages labeled with Tm(DOTMA), were performed.

296 Tm and subsequent re-infection of mice with Tm led to type 2 immune response only in WT, but Tm colo

297 P and ceh1 plants treated with Tm display similar UPR transcript profiles, suggesting t

298 ered quantum material RFe2O4 (R = Y, Er, Yb, Tm, and Lu) system.

299 shell heterostructure consisting of NaYF4:Yb,Tm upconversion nanoparticle (UCN) as the core and ZnO s

300 siRNA is complexed onto a NaYF4:Yb/Tm/Er UCNP through an azobenzene (Azo)-cyclodextrin (CD)