ライフサイエンスコーパス: Tm

1 Tm deletion library in the presence of metergoline revea

2 Tm growing in macrophage-mimicking media and within macr

3 Tm measurements of modified oligodeoxynucleotides with c

4 Tm measurements of oligonucleotides with single and doub

5 Tm replication by conducting parallel chemical screens a

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

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

8 Tm) establishes systemic infection in susceptible hosts

9 dation under NIR illumination using SrYbF:1 %Tm(3+) @CaF(2) , highlighting the efficiency of these UC

10 In 10.9 nm SrYbF:1 %Tm(3+) @CaF(2) particles, UV emission increased to 9.9 %

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

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

13 3+), Gd(3+), Tb(3+), Dy(3+), Ho(3+), Er(3+), Tm(3+), Yb(3+)) and linear amino-functionalized dicarbox

14 The use of NIR excitable NaYF(4):Yb(3+),Tm(3+) UCNPs enables background free read-out.

15 version luminescence (UCL) of NaYF(4):Yb(3+),Tm(3+) UCNPs excited at 980 nm, that overlaps with the a

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

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

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

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

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

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

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

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

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

25 0-nm luminescence intensity of (A) Er(3+)(8%)Tm(3+)(0.5%):telluride glass was approximately 4.4 to 19

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

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

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

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

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

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

32 hlight the surface feature's role in F-actin-Tm interactions and contractile regulation.

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

34 Cr, Mo, Co(II), Mg, Nd, Li, Ti, Ca, Cs, Ag, Tm, Er(III), La(III), Yb(III), Eu(III), Pr(III), Gd(III)

35 5.93 vs. 6.00 in the control fibers) against Tm(H276N), but not against Tm(WT) background.

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

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

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

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

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

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

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

43 e-earth host materials doped with Yb(3+) and Tm(3+) , with alkaline-earth (M) spanning Ca, Sr, and Ba

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

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

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

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

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

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

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

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

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

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

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

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

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

57 45-74 enhanced pCa50 in both alpha- and beta-Tm fibres, with beta-Tm having a bigger effect.

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

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

60 Both Tm-stabilizing substitutions strongly decreased the slac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 of Ca(2+) , Tn binds to actin and constrains Tm to an azimuthal location where it sterically occludes

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

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

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

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

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

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

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

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

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

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

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

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

91 La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) and trace elements (Li, Mg, Mn, Ni, Co, Cu,

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

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

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

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

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

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

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

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

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

101 changes observed in vitro of TnT mutants for Tm.

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

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

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

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

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

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

108 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.

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

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

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

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

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

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

115 ds are the reasons for these alternations in Tm.

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

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

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

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

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

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

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

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

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

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

126 functions and the structural instability in Tm is unknown.

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

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

129 ddition to Tn-actin interactions, inhibitory Tm positioning requires associations between other thin

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

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

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

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

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

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

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

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

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

139 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

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

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

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

143 Td and the thermophile Thermotoga maritima (Tm) in the Fe[III](2)-O(2) (2-), Zn[II], and apo states

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

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

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

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

148 ecedented cases, where the rare earth metals Tm and Lu partially substitute Al atoms in the structure

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

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

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

152 ng the drug-like attributes of the molecule (Tm = 75 degrees C and intrinsic stability DeltaGu = 63.5

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

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

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

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

157 mum inner-shell clock transition in neutral Tm atoms to BBR.

158 which is another remarkable trait of the new Tm- and Lu-substituted compounds.

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

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

161 e and passive components forming cavities of Tm-doped all-fibre lasers.

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

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

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

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

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

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

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

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

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

171 2 results in an exchange in localizations of Tm forms on actin polymers.

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

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

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

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

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

177 powders showed characteristic transitions of Tm(3+) and Eu(3+), respectively.

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

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

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

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

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

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

184 der Waals interactions with H2 than precious Tm.

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

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

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

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

189 ulted in compromised biophysical properties (Tm = 61 degrees C and intrinsic stability DeltaGu = 24.3

190 port a numerical model of a stretched-pulsed Tm-doped fibre laser with hybrid mode-locking and compar

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

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

193 dye's fluorescence and the analyte-inert red Tm(3+) UCL correlate directly with pH, which was success

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

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

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

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

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

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

200 +2 oxidation states, i.e., Ln = Eu, Yb, Sm, Tm, Dy, and Nd, to allow direct structural and spectrosc

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

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

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

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

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

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

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

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

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

210 0 degrees C drop in the melting temperature (Tm ) was observed at pH 2.5: DeltaDeltaGF >/=11.3 kJ mol

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

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

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

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

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

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

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

218 rall sequence-dependent melting temperature (Tm).

219 t, satisfying the properties of temperature (Tm) and entropy (DeltaG), while minimizing the formation

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

221 the same manner as the melting temperature, Tm.

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

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

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

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

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

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

228 The Tm mapping method is therefore useful for identifying in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 the spin-label phase memory relaxation time Tm .

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

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

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

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

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

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

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

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

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

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

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

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

260 c myosin binding protein-C in FTY720-treated Tm-E180G mice and reduction in oxidative stress by downr

261 ompared with vehicle-treated, FTY720-treated Tm-E180G mice had a significant reduction in left atrial

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

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

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

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

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

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

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

269 with an HCM-linked mutation in tropomyosin (Tm-E180G) and nontransgenic littermates with FTY720 or v

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

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

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

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

274 the thin filament troponin (Tn)-tropomyosin (Tm) complex.

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

276 ression was induced by salt and tunicamycin (Tm).

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

278 Ultrafast Tm-doped fibre lasers have been actively studied for the

279 and can be used for development of ultrafast Tm-doped fibre laser systems.

280 tress-responsive genes BiP1/2 and BiP3 under Tm treatment and sensitivity to salt stress.

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

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

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

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

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

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

287 ighly favourable electrostatic contacts with Tm that are critical for establishing its inhibitory azi

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

289 structure of TNT1 and its interactions with Tm.

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

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

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

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

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

295 ons of rare earth ions (RE(3+) = Gd, Eu, Yb, Tm) to achieve a synergy among their magnetic and optica

296 version nanoparticles (UCNP, type NaYF(4):Yb,Tm) served as background-free optical label for the dete

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

298 Cell viability tests of HAp:Gd/Yb/Tm and HAp:Gd/Eu powders in human dental pulp stem cell

299 d the "down"-conversion spectra of HAp:Gd/Yb/Tm and HAp:Gd/Eu powders showed characteristic transitio

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