ライフサイエンスコーパス: Tc

1 Tc toxin complexes are virulence factors of many bacteri

2 Tc toxins are composed of three subunits that act togeth

3 Tc toxins are modular toxin systems of insect and human

4 ygen at pH 6.00 +/- 0.07 and 10.00 +/- 0.04, Tc was neither reoxidized nor redissolved.

5 trated for the first time that non-TcO(4)(-) Tc present in the AN-102 tank waste is composed of sever

6 the uptake process is slower, leading to 98% Tc removal (log K(d) = 4.5 +/- 0.1) after 35 days.

7 Technetium-99 (Tc), a high yield fission product generated in nuclear r

8 (99) Tc contamination at legacy nuclear sites is a serious an

9 (99)Tc originating from nuclear energy production and global

10 (99)Tc(VII) uptake by synthetic pure pyrite at 21 degrees C

11 ent and immobilization of technetium-99 ((99)Tc) contained in reprocessed nuclear waste and present i

12 A fully automated and rapid system for (99)Tc monitoring is introduced with the aim to improve hosp

13 l preparation procedure, measurements of (99)Tc concentrations at the fg/g levels with a sensitivity

14 e GAMS setup is used for the analysis of (99)Tc in samples of the seawater reference material IAEA-44

15 determination of environmental levels of (99)Tc in small samples.

16 ty of the mass spectrometric analysis of (99)Tc is the background of its stable isobar (99)Ru.

17 for the treatment and immobilization of (99)Tc present in reprocessed nuclear waste streams and cont

18 pected in groundwater after diffusion of (99)Tc through the bentonite constituting the technical barr

19 understanding the migration behavior of (99)Tc.

20 l composition and speciation of Tc using (99)Tc nuclear magnetic resonance spectroscopy and X-ray abs

21 These tracers in their (99g)Tc version were assessed in vitro on a set of human meta

22 (99m)Tc activity was also used to calculate the amount of dye

23 (99m)Tc-ADAPT6 cleared rapidly from the blood and most other

24 (99m)Tc-AGA-2 displayed faster blood clearance in mice and be

25 (99m)Tc-AGA-2 uptake detected by autoradiography was signific

26 (99m)Tc-C2Am and (111)In-C2Am generated tumor-to-muscle ratio

27 (99m)Tc-duramycin holds promise as a noninvasive imaging radi

28 (99m)Tc-FAPI-34 accumulated in the tumor lesions, as also sho

29 (99m)Tc-NOET therefore traps in myocardium independently of t

30 (99m)Tc-PHC-102 has previously shown favorable in vivo biodis

31 (99m)Tc-PHC-102 is a (99m)Tc-labeled derivative of acetazolam

32 (99m)Tc-PHC-102 might also serve as a companion diagnostic ag

33 (99m)Tc-PHC-102 SPECT/CT allowed the identification of 4 prev

34 (99m)Tc-PSMA I&S is a prostate-specific membrane antigen (PSM

35 (99m)Tc-PSMA I&S SPECT/CT showed high TBR in PCa patients.

36 (99m)Tc-sestamibi is used clinically to image cardiac perfusi

37 (99m)Tc-SP is a valid radiotracer alternative to (99m)Tc-SC f

38 (99m)Tc-tilmanocept is a novel radiopharmaceutical for sentin

39 (99m)Tc-trofolastat SPECT/CT detected LNI with a sensitivity

40 dose was computed using technetium 99m ((99m)Tc) macroaggregated human albumin (MAA) SPECT/CT.

41 (99m)Tc-PHC-102 is a (99m)Tc-labeled derivative of acetazolamide, a high-affinity

42 conventional imaging (CT or MRI, and a (99m)Tc-methylene diphosphonate bone scan) before enrollment.

43 phosphono-1,2-propanodicarboxylic acid ((99m)Tc-DPD) typically show intense uptake in skeletal metast

44 set (n = 20), we used the imaging agent (99m)Tc-cAbVCAM1-5 to evaluate expression of an inflammatory

45 (99m)Tc(V)) ((99m)Tc-NOET) could allow (99m)Tc-sestamibi to be repurposed to specifically report on

46 The cross-talk and (99m)Tc dose required was evaluated in 2 lead-in studies.

47 dism and inconclusive results at US and (99m)Tc sestamibi scintigraphy were prospectively enrolled.

48 contrast-enhanced mammography (CEM) and (99m)Tc sestamibi-based molecular breast imaging (MBI) in thi

49 (99m)Tc-radiotracers, (99m)Tc-AGA-1 and (99m)Tc-AGA-2, derived from AGA.

50 enhanced magnetic resonance imaging and (99m)Tc-diethylene-triamine-pentacetic acid-single-photon emi

51 cs of (99m)Tc-MAS3-y-nal-k(Sub-KuE) and (99m)Tc-mas3-y-nal-k(Sub-KuE) ((99m)Tc-PSMA-I&S for imaging a

52 ate between ICG-(99m)Tc-nanocolloid and (99m)Tc-nanocolloid.

53 armacokinetics of (99m)Tc-sestamibi and (99m)Tc-NOET in response to mitochondrial perturbation by hyp

54 adiotracers (68)Ga/(177)Lu-PSMA-I&T and (99m)Tc-PSMA-I&S (for i maging and s urgery) are currently su

55 on of (99m)Tc-MAS3-y-nal-k(Sub-KuE) and (99m)Tc-PSMA-I&S in consistently high radiochemical yield and

56 c meal retention between (99m)Tc-SP and (99m)Tc-SC, was found to be comparable at all measured time p

57 /pertechnetate subtraction imaging, and (99m)Tc-sestamibi dual-phase imaging.

58 embrane potential of (18)F-MitoPhos and (99m)Tc-sestamibi were tested in isolated perfused rat hearts

59 Radiolabeled bisphosphonates such as (99m)Tc-3,3-diphosphono-1,2-propanodicarboxylic acid ((99m)Tc

60 for carbon monoxide (DLCO), as well as (99m)Tc-macroaggregated albumin PS and SPECT/CT quantificatio

61 found a significant correlation between (99m)Tc-DTPA content in brain and both the discrimination ind

62 as total gastric meal retention between (99m)Tc-SP and (99m)Tc-SC, was found to be comparable at all

63 Both (99m)Tc and Re complexes were prepared from the corresponding

64 0 men, 60.1 +/- 12.7 y old) detected by (99m)Tc-pertechnetate or (123)I scintigraphy.

65 olus of phenol red or independently by [(99m)Tc]-diethylenetriamine pentaacetic acid scintigraphy, wa

66 The lead candidate (99m)Tc-FAPI-34 was applied for diagnostic scintigraphy and S

67 Cardiac (99m)Tc-NOET retention (34.0 +/- 8.0% ID) was unaffected in a

68 re was a dose-dependent loss of cardiac (99m)Tc-sestamibi retention (from 2.3 +/- 0.3 to 0.9 +/- 0.2

69 e gold-standard (99m)Tc-sulfur colloid ((99m)Tc-SC) for gastric emptying scintigraphy (GES).

70 ation of three novel (99m)Tc complexes ((99m)Tc-1-3) and their corresponding Re complexes (Re-1-3), i

71 Conclusion: (99m)Tc-FAPI-34 represents a powerful tracer for diagnostic s

72 Conclusion: (99m)Tc-PHC-102 is a promising SPECT tracer for the imaging o

73 by the cyclopentadienyl tricarbonyl [Cp(99m)Tc(CO)(3)] core, are reported.

74 Visual agreement among CT, (99m)Tc-MAA SPECT/CT, and yttrium 90 ((90)Y) SPECT/CT or PET/

75 nsisting of (99m)Tc-sestamibi SPECT/CT, (99m)Tc-sestamibi/pertechnetate subtraction imaging, and (99m

76 mission computed tomography diagnostic ((99m)Tc complexes) and antiamyloid therapeutic (Re complexes)

77 A dynamic (99m)Tc tracer experiment was performed to investigate the ca

78 ipants were randomly assigned to either (99m)Tc-SP or (99m)Tc-SC on the first GES session before cros

79 quivalent to that with generator-eluted (99m)Tc and had no particular features allowing discriminatio

80 e on the indole moiety adjacent to EuK ((99m)Tc-EuK-(SO(3))Cy5-mas(3)) yielded the most promising tra

81 MA)-targeted radiotracers, for example, (99m)Tc-labeled PSMA tracer analogs for radioguided surgery.

82 and kits) were reported, especially for (99m)Tc/(99)Mo generators and (131)I, particularly in Africa,

83 Baseline and furosemide (99m)Tc-MAG3 imaging examinations in 50 patients suspected of

84 tudy was to develop a second-generation (99m)Tc-labeled PSMA-targeted tracer incorporating a fluoresc

85 es for SN biopsy with indocyanine green-(99m)Tc-nanocolloid or (99m)Tc-nanocolloid with free indocyan

86 iopsy procedure using indocyanine green-(99m)Tc-nanocolloid.

87 Preoperative SPECT/CT showed a high (99m)Tc-PSMA-I&S uptake in all suspect lesions identified in

88 led succinimidyl-hydrazinonicotinamide ((99m)Tc-S-HYNIC)-conjugated anti-FAP antibody 28H1 at 2, 5, a

89 ation of either indocyanine green (ICG)-(99m)Tc-nanocolloid (hybrid-tracer group) or (99m)Tc-nanocoll

90 ode (SN) tracer indocyanine green (ICG)-(99m)Tc-nanocolloid generates temporary tattoolike markings a

91 onal superficial 3 or 4 deposits of ICG-(99m)Tc-nanocolloid (0.1 mL each), and in 12 patients additio

92 tic tracer administration of either ICG-(99m)Tc-nanocolloid (hybrid tracer group) or (99m)Tc-nanocoll

93 the SN identification rate between ICG-(99m)Tc-nanocolloid and (99m)Tc-nanocolloid.

94 The fluorescent nature of ICG-(99m)Tc-nanocolloid supported in vivo and ex vivo identificat

95 e 25 patients and the hybrid tracer ICG-(99m)Tc-nanocolloid was shown to outperform "free" ICG.

96 25 patients, and the hybrid tracer ICG-(99m)Tc-nanocolloid was shown to outperform free ICG.

97 on with SPECT and fluorescence imaging, (99m)Tc-EuK-(SO(3))Cy5-mas(3) had the most promising properti

98 No change in (99m)Tc-linear duramycin uptake could be detected in COLO205

99 mitochondrial perturbations that induce (99m)Tc-sestamibi washout, demonstrating proof-of-concept for

100 All interventions induced (99m)Tc-sestamibi washout; hypoxia from 24.9 +/- 2.6% ID to 0

101 KuE) and (99m)Tc-mas3-y-nal-k(Sub-KuE) ((99m)Tc-PSMA-I&S for imaging and surgery) were determined usi

102 tients with stenoocclusion and negative (99m)Tc-HMPAO SPECT.

103 N-ethoxy-N-ethyldithiocarbamato)nitrido (99m)Tc(V)) ((99m)Tc-NOET) could allow (99m)Tc-sestamibi to b

104 synthesis and evaluation of three novel (99m)Tc complexes ((99m)Tc-1-3) and their corresponding Re co

105 Here we report four novel (99m)Tc-labeled radiotracers derived from a highly selective

106 The obtained (99m)Tc complexes were investigated in vitro by binding and c

107 ined by the ex vivo gamma-well assay of (99m)Tc activity were detected by fluorescence mode imaging.

108 ancer (MBC) by (18)F-FDG PET instead of (99m)Tc bone scintigraphy (BS) supports clinically relevant c

109 Immobilization of (99m)Tc was highest where continuous acetate amendment had re

110 ual- and triple-isotope combinations of (99m)Tc, (111)In, (123)I, (177)Lu, and (201)Tl were performed

111 he favorable biodistribution profile of (99m)Tc- and (111)In-labeled C2Am, and their ability to produ

112 Conclusion: Injections of (99m)Tc-ADAPT6 are safe and associated with low absorbed and

113 avenous injection of 385 +/- 125 MBq of (99m)Tc-ADAPT6 was performed, randomized to an injected prote

114 Results: Injections of (99m)Tc-ADAPT6 were well tolerated at all mass levels and not

115 by SPECT/CT imaging after injection of (99m)Tc-DTPA, an imaging marker of blood-brain barrier permea

116 determine the diagnostic performance of (99m)Tc-labeled SPECT MPI compared with (18)F-flurpiridaz PET

117 s were acquired 24 h after injection of (99m)Tc-labeled succinimidyl-hydrazinonicotinamide ((99m)Tc-S

118 Conclusion Administered doses of (99m)Tc-MAG3 in the range of 300-370 MBq (approximately 8-10

119 (IC50) and internalization kinetics of (99m)Tc-MAS3-y-nal-k(Sub-KuE) and (99m)Tc-mas3-y-nal-k(Sub-Ku

120 stablished, allowing the preparation of (99m)Tc-MAS3-y-nal-k(Sub-KuE) and (99m)Tc-PSMA-I&S in consist

121 il/valsartan induced an early uptake of (99m)Tc-NC100692 (a radiotracer of angiogenesis) and improved

122 s used to measure the in vivo uptake of (99m)Tc-pertechnetate and (123)I in 2 NIS-expressing mouse ti

123 to explore the targeting performance of (99m)Tc-PHC-102 in SPECT in patients with renal cell carcinom

124 total of CAIX ligand and 600-800 MBq of (99m)Tc-PHC-102.

125 ed data for translation and approval of (99m)Tc-PSMA I&S by regulatory agencies.

126 study was to estimate the dosimetry of (99m)Tc-PSMA I&S using a hybrid method (sequential gamma-plan

127 Results: The mean injected activity of (99m)Tc-PSMA I&S was 717 MBq (range: 562-828 MBq).

128 Biodistribution of (99m)Tc-PSMA I&S was assessed in 10 patients with PCa on SPEC

129 Methods: Dosimetry of (99m)Tc-PSMA I&S was investigated in 4 healthy volunteers.

130 Conclusion: Effective doses of (99m)Tc-PSMA I&S were comparable to those known for most of t

131 erse events related to the injection of (99m)Tc-PSMA I&S were reported.

132 hint toward the unexpected potential of (99m)Tc-PSMA-I&S as a SPECT imaging agent.

133 The pharmacokinetics of (99m)Tc-PSMA-I&S in humans were investigated in a patient wit

134 this first (to our knowledge) study of (99m)Tc-pyrophosphate cardiac imaging using a novel cadmium-z

135 ID measured by absolute quantitation of (99m)Tc-pyrophosphate were moderately correlated with LVMI an

136 The ischemic to nonischemic ratio of (99m)Tc-RP805 was significantly increased following I/R in sa

137 Finally, aortic uptake of (99m)Tc-RYM1 in vivo correlated with aortic MMP activity and

138 The uptake of (99m)Tc-S-HYNIC-28H1 in all joints was quantified and correla

139 Moreover, the uptake of (99m)Tc-S-HYNIC-28H1 was slightly increased at 9 d after ther

140 to characterize the pharmacokinetics of (99m)Tc-sestamibi and (99m)Tc-NOET in response to mitochondri

141 F-MitoPhos was more than double that of (99m)Tc-sestamibi in isolated perfused rat hearts.

142 igraphic imaging methods, consisting of (99m)Tc-sestamibi SPECT/CT, (99m)Tc-sestamibi/pertechnetate s

143 Methods: For the preparation of (99m)Tc-tricarbonyl complexes, a chelator was selected whose

144 aves the way for further evaluation of [(99m)Tc]-1 for imaging AAA and other MMP-12-associated diseas

145 postinjection revealed high uptake of [(99m)Tc]-1 in AAA relative to adjacent aorta.

146 Tc-nanocolloid (hybrid-tracer group) or (99m)Tc-nanocolloid to create a road map that depicted all SN

147 Tc-nanocolloid (hybrid tracer group) or (99m)Tc-nanocolloid to create a roadmap that depicted all sen

148 ndocyanine green-(99m)Tc-nanocolloid or (99m)Tc-nanocolloid with free indocyanine green used as trace

149 scintigraphy with either radioiodine or (99m)Tc-pertechnetate is useful to characterize different for

150 ndomly assigned to either (99m)Tc-SP or (99m)Tc-SC on the first GES session before crossed over to th

151 labeled hexamethylpropyleneamine oxime ((99m)Tc-HMPAO) or PET with (15)O-water.

152 f LN involvement (LNI) underwent pelvic (99m)Tc-trofolastat SPECT/CT before radical prostatectomy wit

153 the basis of its in vivo performance, [(99m)Tc]-1 was selected for evaluation in murine AAA, where M

154 re widely available alternative to PET, (99m)Tc-labeled FAPIs represent attractive tracers for imagin

155 unclear if the (99m)Tc-sodium phytate ((99m)Tc-SP) is as reliable as the gold-standard (99m)Tc-sulfu

156 eing the highest recorded for potential (99m)Tc Abeta plaque imaging probes in mice.

157 d-energy window with cyclotron-produced (99m)Tc was equivalent to that with generator-eluted (99m)Tc

158 n +/- SD) MBq of the cyclotron-produced (99m)Tc-NaTcO4, whereas the age- and sex-matched controls rec

159 Conclusion: Whatever the protocol, (99m)Tc-tilmanocept showed good results in a heterogeneous br

160 The aim of this study was to quantify (99m)Tc-DPD uptake by means of SPECT/CT before (223)Ra and co

161 rrelation between absolute quantitative (99m)Tc-pyrophosphate metrics and traditional measures of car

162 so, we report two (99m)Tc-radiotracers, (99m)Tc-AGA-1 and (99m)Tc-AGA-2, derived from AGA.

163 Patients who received (99m)Tc-nanocolloid were injected with "free" ICG immediately

164 Patients who received (99m)Tc-nanocolloid were injected with "free" ICG immediately

165 ds: Patients referred for a stress-rest (99m)Tc-sestamibi protocol and positioned in the biker positi

166 The resulting (99m)Tc-labeled FAPI tracers revealed excellent binding prope

167 Results: (99m)Tc-FAPI-19 showed specific binding to recombinant FAP-ex

168 imetry, and safety of the HER2-specific (99m)Tc-ADAPT6.

169 SP) is as reliable as the gold-standard (99m)Tc-sulfur colloid ((99m)Tc-SC) for gastric emptying scin

170 ultaneously with the solid standardized (99m)Tc egg-substitute meal.

171 te 1 acquired its standard 300-s static (99m)Tc-DMSA studies as 5-frame dynamic studies in 29 childre

172 Patients underwent stress (99m)Tc-sestamibi MPI with new-generation solid-state SPECT s

173 Results: In the 5 patients studied, (99m)Tc-PHC-102 was well tolerated and no study drug-related

174 Compared with (111)In-PSMA-I&T, (99m)Tc-PSMA-I&S showed delayed clearance kinetics but identi

175 We have demonstrated that (99m)Tc-duramycin specifically accumulates in apoptotic tumor

176 We conclude, therefore that (99m)Tc-rCR2 imaging can be used for non-invasive detection o

177 The brain uptake of the (99m)Tc complexes ranges between 7.94 and 3.99% ID/g at 2 min

178 res allowing discrimination between the (99m)Tc production methods.

179 mparable to those known for most of the (99m)Tc tracers and was lower than for the (68)Ga-labeled and

180 reatment, indicating specificity of the (99m)Tc-duramycin tumor signal.

181 It is unclear if the (99m)Tc-sodium phytate ((99m)Tc-SP) is as reliable as the gol

182 2% of participating sites limited their (99m)Tc/(99)Mo generator purchases, and 12% of them temporari

183 Based on this, (99m)Tc-AGA-2 was chosen as the lead tracer and tested in mur

184 ter radiochemical stability compared to (99m)Tc-AGA-1.

185 P is a valid radiotracer alternative to (99m)Tc-SC for routine GES examination.

186 Results: Total (99m)Tc-DPD uptake of the central skeleton varied between 11%

187 eveloped pan-MMP inhibitor-based tracer (99m)Tc-RYM1 displays favorable pharmacokinetics for early va

188 Also, we report two (99m)Tc-radiotracers, (99m)Tc-AGA-1 and (99m)Tc-AGA-2, derive

189 s: We studied 72 patients who underwent (99m)Tc-pyrophosphate SPECT/CT using a novel general-purpose

190 In this work, renal imaging using (99m)Tc-dimercaptosuccinic acid (DMSA) projects are presented

191 ported for renal cortical imaging using (99m)Tc-DMSA, leading to significant reductions in administer

192 ctive power of cell death imaging using (99m)Tc-duramycin with the current gold standard (18)F-FDG fo

193 ing tubular extraction rate (TER) using (99m)Tc-mercaptoacetyltriglycine renal scintigraphy.

194 ecision of SPECT MBF measurements using (99m)Tc-tetrofosmin and a solid-state cardiac camera.

195 y, SPECT measurements of MBF made using (99m)Tc-tetrofosmin were compared with PET in the same patien

196 dy, tumor perfusion was accessed using [(99m)Tc]NaTcO(4) and BB2r-targeted uptake evaluated by utiliz

197 hyldithiocarbamato)nitrido (99m)Tc(V)) ((99m)Tc-NOET) could allow (99m)Tc-sestamibi to be repurposed

198 udies are justified to evaluate whether (99m)Tc-ADAPT6 can be used as an imaging probe to stratify pa

199 2 ID/g with 10 mg/kg (p < 0.05)), while (99m)Tc-NOET retention (0.93 +/- 0.16 ID/g) was unaffected.

200 Their radiolabeling with (99m)Tc was shown to be efficient and stable in both buffer a

201 After radiolabeling with (99m)Tc, we performed in vivo SPECT imaging, biodistribution,

202 his expression correlated strongly with (99m)Tc-cAbVCAM1-5 uptake (r = 0.75; P < 0.05).

203 al cerebral blood flow using SPECT with (99m)Tc-labeled hexamethylpropyleneamine oxime ((99m)Tc-HMPAO

204 dual isotope imaging was performed with (99m)Tc-RP805 and (201)Tl along with contrast cineCT to asses

205 regional myocardial MMP activation with (99m)Tc-RP805 and dynamic (201)Tl for determination of myocar

206 Scintigraphy with (99m)Tc-sestamibi allows differentiation of type 1 from type

207 Our aim was to describe results with (99m)Tc-tilmanocept in a heterogeneous group of breast cancer

208 5 days when they were again imaged with (99m)Tc.

209 RYM1, was synthesized and labeled with (99m)Tc.

210 tform, we report herein the development of a Tc goat system expressing human polyclonal antibodies in

211 ounterparts), Ce (an actinide analog), Re (a Tc analog), bentonite particles, and fluorescent dye tra

212 oxide like hematite at pH 6.00 +/- 0.07, and Tc(IV) incorporation into magnetite via Fe(III) substitu

213 library of the Tc(I) [fac-Tc(CO)(3)](+) and Tc(II, IV, V, VII) compounds was generated and applied t

214 , including the Tc(I) [fac-Tc(CO)(3)](+) and Tc(IV) compounds.

215 Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc-fez1.

216 tudy, we compared the distribution of Th and Tc cell subsets between blood and RM compartments in 62

217 erved similar tissue distributions of Th and Tc cell subsets, although Tc17 cell frequencies in both

218 n neutron reflectivity, both above and below Tc.

219 g to give a magnetically ordered phase below Tc = 105 K, one of the highest reported ordering tempera

220 ium obtained from CD3 bead-isolated T cells (Tc CM) but not from those isolated without CD3 beads.

221 CMV-Tc and/or Th became (-) in 50% to 70% of these sero (+)

222 CMV-specific CD8+ (CMV-Tc), CD4+ (CMV-Th) T cell activity, and natural killer (

223 Toxin complex (Tc) toxins are virulence factors of pathogenic bacteria.

224 ty of CD4 T helper (Th) and CD8 T cytotoxic (Tc) cell subsets in the rectal mucosa (RM), a major site

225 xplaining the formation of the two different Tc species depending on the pH.

226 atment technologies effective for dissimilar Tc species.

227 chnetium-labeled cardiac scintigraphy (i.e., Tc-PYP scan) has been repurposed for the diagnosis of tr

228 Designing strategies for effective Tc management, including separation and immobilization,

229 Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc-fez1.

230 e, a spectroscopic library of the Tc(I) [fac-Tc(CO)(3)](+) and Tc(II, IV, V, VII) compounds was gener

231 -valent Tc species, including the Tc(I) [fac-Tc(CO)(3)](+) and Tc(IV) compounds.

232 ollowed by somatic cell nuclear transfer for Tc goat production.

233 uptake mechanism involves the reduction from Tc(VII) to Tc(IV) and subsequent inner-sphere complexati

234 ive vaccines, passive countermeasures (e.g., Tc bovine), and as a means to produce more potent DNA-la

235 s been subject to strong controversy in high-Tc copper oxides.

236 e recent discovery of a second class of high-Tc materials, Fe-based superconductors, may provide anot

237 More surprisingly, the highest Tc that occurs at lower decompression pressures is 8.2 K

238 lution in the form of poorly soluble hydrous Tc(IV)-oxides or Tc(IV)-sulfides during the development

239 tion due to rapid reoxidation of immobilized Tc, and competing comingled contaminants, e.g., Cr(VI),

240 ng revealed that the costimulatory factor in Tc CM was glycoprotein Ib alpha (GPIbalpha).

241 Strikingly, in Tc-foxQ2 RNAi knock-down embryos the primary brain commi

242 led contaminants, e.g., Cr(VI), that inhibit Tc(VII) reduction and incorporation into stable mineral

243 obile pertechnetate (TcO(4)(-)) to insoluble Tc(IV) species.

244 2, moderate Hc2 anisotropy, and intermediate Tc.

245 bsequent inner-sphere complexation of Tc(IV)-Tc(IV) dimers onto a Fe oxide like hematite at pH 6.00 +

246 gnet applications are still dominated by low-Tc Nb3Sn due probably to cost and processing issues.

247 cer trap line built by genome editing marked Tc-foxQ2 positive neurons, which projected through the p

248 w in atomic detail a fully assembled 1.7-MDa Tc holotoxin complex from Photorhabdus luminescens in th

249 etion of PGE(2), IL-1beta, and IL-6 in MDP + Tc CM-activated monocytes, whereas recombinant GPIbalpha

250 jor components of the noble metal phase (Mo, Tc, Ru, Rh, Pd).

251 In a nontoxic Tc toxin variant, we can visualize part of the transloca

252 ing insights into the mechanism of action of Tc toxins.

253 Binding of Tc toxins to target cells and a pH shift trigger the con

254 and subsequent inner-sphere complexation of Tc(IV)-Tc(IV) dimers onto a Fe oxide like hematite at pH

255 onons are responsible for the enhancement of Tc over other FeSe-based superconductors.

256 we compare the architecture and function of Tc toxins with those of anthrax toxin and vertebrate ten

257 Furthermore, immunization of Tc caprine with inactivated influenza A (H7N9) viruses f

258 These findings emphasize the importance of Tc cattle in the production of nonimmunogenic MAbs and h

259 Incorporation of Tc(IV) has little effect on the spinel lattice structure

260 red over other lipids for the integration of Tc toxins.

261 a glycan dependent association mechanism of Tc toxins on the host cell surface.

262 cells (PBMC) and the sera, respectively, of Tc caprine demonstrated the successful expression of hum

263 d for chemical composition and speciation of Tc using (99)Tc nuclear magnetic resonance spectroscopy

264 We characterized four distinct types of Tc-foxQ2 positive neural progenitor cells based on diffe

265 confirm that SCU-102 represents the optimal Tc scavenger with the highest reported clean-up efficien

266 fferential co-expression with Tc-six3/optix, Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc

267 m of poorly soluble hydrous Tc(IV)-oxides or Tc(IV)-sulfides during the development of reducing condi

268 A positive Tc-99m pyrophosphate study was defined by the presence o

269 biostimulation and the stability of reduced Tc(IV) phases under oxic conditions.

270 We found that pyrite removes Tc quantitatively from solution (log K(d) = 5.0 +/- 0.1)

271 /optix, Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc-fez1.

272 l co-expression with Tc-six3/optix, Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc-fez1.

273 The slower Tc uptake was explained by higher pyrite solubility unde

274 flurpiridaz PET and 1- or 2-day rest-stress Tc-99m-labeled SPECT and ICA.

275 the lack of CATC's binding to triplexes Ta, Tc, and Tf in HHV-6B.

276 Technetium (Tc) remains a priority remediation concern due to persis

277 also increased phase transition temperature (Tc) of nanoliposomes (2.01-7.24 degrees C).

278 us and possibly high-transition-temperature (Tc) superconductivity.

279 remobilization and were more resistant than Tc(IV) produced via biostimulation with an acetate/lacta

280 Results showed that Tc was removed from solution in the form of poorly solub

281 shment of herds, therefore complementing the Tc cattle platform in responses to a range of medical ne

282 old while utilizing 10 times less DNA in the Tc bovine.

283 In the Tc goat system, a human artificial chromosome (HAC) comp

284 several low-valent Tc species, including the Tc(I) [fac-Tc(CO)(3)](+) and Tc(IV) compounds.

285 The architecture of the Tc toxin complex allows TcB-TcC to bind to an already me

286 is objective, a spectroscopic library of the Tc(I) [fac-Tc(CO)(3)](+) and Tc(II, IV, V, VII) compound

287 Here, we study the function of the Tc-foxQ2 forkhead transcription factor, a key regulator

288 m based on the singlet fission material TIPS-Tc combined with PbS QDs.

289 anism involves the reduction from Tc(VII) to Tc(IV) and subsequent inner-sphere complexation of Tc(IV

290 utralizing antibodies in a transchromosomic (Tc) bovine for use as a passive immunoprophylactic.

291 our previously established transchromosomic (Tc) cattle platform, we report herein the development of

292 MAb), 53C10, isolated from transchromosomic (Tc) cattle exhibits potent neutralization and hemaggluti

293 In the present study, transchromosomic (Tc) cattle were used for the generation of nonimmunogeni

294 As a small ungulate, Tc caprine offers the advantages of low cost and quick e

295 tank waste is composed of several low-valent Tc species, including the Tc(I) [fac-Tc(CO)(3)](+) and T

296 ion with Tc-six3/optix, Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc-fez1.

297 line solutions typifying Hanford tank waste, Tc exists as pertechnetate (TcO(4)(-)) (oxidation state

298 lls based on differential co-expression with Tc-six3/optix, Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-e

299 While for X = Tc the CI phase is further stabilized under tensile stra

300 high electronegativities for Mn, Co, Ni, Zn, Tc, Cd, Hg (affected by choice of valence state), and Gd