ライフサイエンスコーパス: SMT

1 SMT can provide real-time information for the investigat

2 SMT decreased both left ventricular end-systolic volume

3 SMT detoxifies selenocysteine by methylating it to methy

4 SMT is, on average, 1 mm in patients seeking sinus augme

5 SMT meets the criteria of a practical typing method: it

6 SMT transgenic seedlings tolerated Se, particularly sele

7 In addition, 23 patients (MARS: 19; SMT: 4) were excluded from per-protocol (PP) analysis (P

8 ncode an S-adenosylmethionine-dependent C-24 SMT that catalyzes a single methyl addition.

9 SMT2 and SMT3, which also encodes a C-24 SMT, catalyze the reaction that distinguishes the synthe

10 nhibition of recombinant Leishmania major 24-SMT and the effect of compounds on sterol composition an

11 f the enzyme sterol 24-methyltransferase (24-SMT), which is a vital enzyme in the biosynthesis of erg

12 sterols which were not good inhibitors of 24-SMT also showed antiproliferative activity, suggesting t

13 ting patient-related factors that may affect SMT.

14 es in the Neoproterozoic, but that the algal SMT duplication event occurred later in the Phanerozoic.

15 (130% +/- 44% vs. 61% +/- 25%; p < .001) and SMT groups (130% vs. 97% +/- 80%; p < .007).

16 CPA was abrogated by DPCPX (29.3+/-3.4%) and SMT (32.3+/-2.6%) and was absent in mice with targeted a

17 product, which was also blocked by DPCPX and SMT.

18 The implementation of FRAP and SMT measurements in identical areas provides complementa

19 y two selective NOS II inhibitors, L-NIL and SMT.

20 o 10(4), depending on biochar properties and SMT concentration.

21 ing soil contaminated with compounds such as SMT.

22 d biochemically compare it with an authentic SMT enzyme from the Se-hyperaccumulator Astragalus bisul

23 Groups of DBA/2 mice bearing SMT-F mammary tumors were placed on a diet containing 0-

24 isolated from 105 (4.0%) of 2640 FSWs before SMT and from 43 (1.6%) 1 week later (P < .001).

25 As a secondary goal, the association between SMT and membrane perforation rate was studied.

26 rtant differences in pain were found between SMT and HEA at any time point.

27 Both SMT and PE corrected LPS-induced gastric mucosal acidosi

28 For patients with BRLP, SMT plus HEA was more effective than HEA alone after 12

29 CR enhanced by SMT produced significant reductions in stress and greate

30 In some cases, SMT offered smaller diffusion coefficients than FRAP, po

31 Live-cell SMT of Cbx7 mutants demonstrates that Cbx7 is targeted t

32 of FSWs found infected or named as contacts, SMT of FSWs (without increasing condom use or treating r

33 samples contaminated with SMX also contained SMT, indicating that more than one antibiotic was used f

34 nclusive data were obtained when correlating SMT and perforation rate, although it seems that thicker

35 CR or comprehensive CR combined with SMT (CR+SMT), with assessments of stress and coronary heart dise

36 Participants in the CR+SMT group exhibited lower rates of clinical events compa

37 Patients randomized to CR+SMT exhibited greater reductions in composite stress lev

38 d in dystrophin-deficient mdx studies, daily SMT C1100 treatment significantly reduced muscle degener

39 Patients were randomized to ECAD + SMT (n = 39) or SMT alone (n = 31).

40 trointestinal cancers for mutations in eight SMT loci with the highest reported frequencies.

41 SPICER is easy to implement with existing SMT analysis routines and should find broad applications

42 s found were 10.97ng/g for SMD, 6.23ng/g for SMT, 11.13ng/g for SDZ and 245.91ng/g for SMX, which was

43 within the range of KOC values reported for SMT in 19 soils.

44 ficial effects on left ventricular function, SMT was not superior to PE.

45 utines and should find broad applications in SMT analysis.

46 Optimal pH to stabilize TPs in SMT was ca. 5.7, which reduced total TP loss by ca. 40%

47 The selective iNOS inhibitors SMT and 1400W, given 24 hours after PC, abrogated the in

48 ever, current data were inconclusive to link SMT to the rate of membrane damage.

49 NOS inhibitors LNNA, SMT, and 7NI significantly attenuated the stimulatory re

50 Furthermore, for similar increases in MAP, SMT improved gastric mucosal acidosis, had less adverse

51 Thirty-one studies that reported maxillary SMT were considered for qualitative analysis.

52 Although mean SMT for the three-dimensional radiography (3DR) group wa

53 systematic review aims at studying the mean SMT and further investigating patient-related factors th

54 e inclusion criteria to investigate the mean SMT, its contributing factors, and the influence on memb

55 R and RBF with those of S-methylisothiourea (SMT), a selective NOS inhibitor, and those of saline.

56 d this hypothesis using S-methylisothiourea (SMT), one of the specific pharmacological inhibitors of

57 d by the iNOS inhibitor S-methylisothiourea (SMT).

58 PCPX; 0.1 mg/kg IP) and S-methylisothiourea (SMT; 3 mg/kg IP) were used to block A(1)ARs and iNOS, re

59 a putative selenocysteine methyltransferase (SMT) enzyme from the non-accumulator Astragalus drummond

60 e encoding selenocysteine methyltransferase (SMT) from the selenium (Se) hyperaccumulator Astragalus

61 as well as selenocysteine methyltransferase (SMT), in eight Astragalus species with varying abilities

62 Sterol methyltransferase (SMT) from Saccharomyces cerevisiae was purified from Esc

63 Sterol methyltransferase (SMT) plays a key role in sterol biosynthesis in differen

64 Sterol methyltransferase (SMT), the enzyme from Saccharomyces cerevisiae that cata

65 Moreover, SMT plants had significantly increased Se accumulation a

66 ly; the other groups received either L-NAME, SMT, or PE.

67 nosylmethionine was bound only to the native SMT, K(d) of about 2 microm.

68 The new SMT gene was isolated from Trypanosoma brucei genomic DN

69 decanetetraacetic acid-Phe1-Tyr3-octreotide (SMT 487) is an SSTR radiopharmaceutical currently under

70 of replication was reversed upon addition of SMT to the culture medium of cytokine-treated cells.

71 erent conclusions about the effectiveness of SMT.

72 The expression of SMT transcript was suppressed in soybean cell suspension

73 ew studies of the effectiveness and harms of SMT for acute (</=6 weeks) low back pain.

74 teine (MeSeCys), in addition to the level of SMT enzymatic activity.

75 bean vegetative tissues had higher levels of SMT transcript than mature vegetative tissues.

76 The transcriptional regulation of SMT in phytosterol biosynthesis is discussed.

77 stablishing the evolutionary relationship of SMT and homocysteine methyltransferase enzymes in plants

78 12 weeks of SMT, medication, or HEA.

79 l therapy (SMT) (FPSA group, n = 77) or only SMT (SMT group, n = 68).

80 ts were randomized to ECAD + SMT (n = 39) or SMT alone (n = 31).

81 e (carbon-24/28 sterol methyltransferase, or SMT) responsible for 24-ipc production.

82 o ECAD and standard medical therapy (SMT) or SMT alone.

83 For pain, SMT had a statistically significant advantage over medic

84 For leg pain, SMT plus HEA had a clinically important advantage over H

85 ticipants with acute and subacute neck pain, SMT was more effective than medication in both the short

86 ot explained by type of clinician performing SMT, type of manipulation, study quality, or whether SMT

87 ein in Escherichia coli and shown to possess SMT activity.

88 much shallower burial depth than the present SMT around 30 meters below seafloor.

89 acceptor strongly suggest that the protozoan SMT has an active site topography combining properties o

90 equence of the yeast ERG6 gene, the putative SMT structural gene.

91 Another group of MLA350 mice received SMT 3 mg/kg IP 30 minutes before heart perfusion.

92 The recombinant SMT was purified to homogeneity to give a band at 40.0 k

93 ression of Arabidopsis SMT1 in erg6 restores SMT activity to the yeast mutant.

94 Thus, the P. carinii SAM:SMT catalysed the transfer of both the first and the sec

95 o be a unique property of the P. carinii SAM:SMT.

96 servations, together with the absence of SAM:SMT among mammals, further support the identification of

97 Unlike SAM:SMT from other organisms, the P. carinii enzyme had high

98 Overall mean +/- SE SMT was 1.17 +/- 0.1 mm (95% confidence interval [CI] =

99 rapy (SMT) (FPSA group, n = 77) or only SMT (SMT group, n = 68).

100 A cDNA clone (SMT1) encoding soybean SMT was isolated from an etiolated hypocotyl cDNA librar

101 0 sterol biosynthesis through clade-specific SMT duplications.

102 ach, we demonstrate that the relevant sponge SMT duplication event overlapped with the appearance of

103 pore water concentration of sulfamethazine (SMT).

104 f sulfamethoxydiazine (SMD), sulfamethazine (SMT), sulfamethoxazole (SMX) and sulfadiazine (SDZ) in i

105 iNOS) inhibitor S-methylisothiourea sulfate (SMT) restored LV contractility.

106 ces by exploiting this near-room-temperature SMT.

107 We conclude that SMT is beneficial to myocardial contractility in this mo

108 We demonstrate that SMT is localized predominantly within the chloroplast in

109 nts) produced moderate-quality evidence that SMT has a statistically significant association with imp

110 nts) provided moderate-quality evidence that SMT has a statistically significant association with imp

111 Our findings indicate that SMT may provide incremental benefit when combined with c

112 We postulated that SMT, by maintaining constitutive NO, would be more benef

113 bined with comprehensive CR and suggest that SMT should be incorporated routinely into CR.

114 The SMT data exhibited one-dimensional diffusion of individu

115 The SMT transcript was highly expressed in flowers.

116 differential impacts on how they altered the SMT.

117 Using new procedures to analyze the SMT data and to guide the FRAP and FCS analysis, we show

118 d characterized were shown to complement the SMT deficient cvp1 mutant Arabidopsis plants, consistent

119 It also decreases the SMT of the VO2 thin film by approximately 5-10 degrees C

120 28 were 66% in the FPSA group and 63% in the SMT group (P = .70); on day 90, they were 47% and 38%, r

121 ached faster and more frequently than in the SMT group (P = 0.045).

122 gnificantly in the FPSA group but not in the SMT group.

123 Myocardial NO content in the SMT was lower than that of the LPS only group, but highe

124 This detailed evaluation of the SMT C1100 drug series strongly endorses the therapeutic

125 tuned to facilitate the fine control of the SMT of the VO2 thin film and its associated properties.

126 nd immature seeds had very low levels of the SMT transcript.

127 f sediments that may lead to shoaling of the SMT.

128 found that the impact of SK channels on the SMT critically depended on the voltage dependence and ki

129 that the impact of different channels on the SMT was variable and differential.

130 are several nonunique routes to regulate the SMT, and call for a systematic analysis of the variabili

131 Taken together, our studies suggest that the SMT active center is composed of a set of acidic amino a

132 s of dissolved sulfate also suggest that the SMT is highly sensitive to variations in organic carbon

133 in ECAD (mean, 34%; median, 30%) versus the SMT group (mean, 18.9%; median, 0%) (P = 0.044) and was

134 n is common and spinal manipulative therapy (SMT) is a treatment option.

135 nation of FPSA and standard medical therapy (SMT) (FPSA group, n = 77) or only SMT (SMT group, n = 68

136 omized to ECAD and standard medical therapy (SMT) or SMT alone.

137 ither to MARS (n=95) or to standard therapy (SMT) (n=94).

138 that, although there is a trend for thicker SMT as determined using 3DR compared with histologic ana

139 0.13) and smoking (P = 0.11) showed thicker SMT.

140 oration rate, although it seems that thicker SMT might be more prone to perforation (P = 0.14).

141 Schneiderian membrane thickness (SMT) has been regarded as a key factor for influencing m

142 gulating the sliding modification threshold (SMT).

143 ologies overestimate approximately 2.5 times SMT when compared with histologic analysis.

144 ombining live-cell single-molecule tracking (SMT) and genetic engineering, we reveal that H3K27me3 co

145 s and experimental single-molecule tracking (SMT) data of RNA polymerase in live Escherichia coli cel

146 eaching (FRAP) and single-molecule tracking (SMT).

147 troscopy (FCS) and single-molecule tracking (SMT).

148 Frameshifts in short mononucleotide tracts (SMT) in genes, such as TGFbetaRII and BAX, are common in

149 health outcomes, stress management training (SMT) is not included routinely as a component of CR.

150 ionine (SAM):C-24 sterol methyl transferase (SMT), suggesting high activity of this enzyme in the org

151 onine: delta 24-sterol-C-methyl-transferase (SMT), a rate-limiting enzyme for phytosterol biosynthesi

152 o induce its semiconductor-metal transition (SMT).

153 ally form at the sulfate-methane transition (SMT), occur at much shallower burial depth than the pres

154 Selective mass treatment (SMT) with oral ampicillin-probenecid or tetracycline was

155 dependence of log kcat/Km for the wild-type SMT indicated a pH optimum for activity between 6 and 9.

156 d multiplex PCR (SmaI-multiplex PCR) typing (SMT) with respect to pulsed-field gel electrophoresis (P

157 individual SRB molecules was explored using SMT in the identical area ( approximately 16 x 16 mum(2)

158 e of manipulation, study quality, or whether SMT was given alone or as part of a package of therapies

159 hensive CR or comprehensive CR combined with SMT (CR+SMT), with assessments of stress and coronary he

160 hr 3) and was larger than the decrease with SMT at hrs 3 and 5 and larger than the decrease with sal

161 ut, but the increase in MPAP was higher with SMT.

162 ly all secondary outcomes improved more with SMT plus HEA at 12 weeks, but only global improvement, s

163 ack pain treated in ambulatory settings with SMT compared with sham or alternative treatments, and th

164 vivo studies (DBA/2 mice, transplanted with SMT/F tumors), ketobacteriochlorins were found to be mor

165 n large case series of patients treated with SMT.

166 icantly, to 22.2+/-2.8% after treatment with SMT in the MLA350 group.

167 Using this scoring method, (90)Y-SMT 487 appears effective in improving the clinical stat

168 d assess the clinical effectiveness of (90)Y-SMT 487 therapy in patients with neuroendocrine tumors.

169 reotide being used after completion of (90)Y-SMT 487 therapy in the 20 patients who were on this medi

170 had completed 3 cycles of therapy with (90)Y-SMT 487.