ライフサイエンスコーパス: ft

1 ZATION1 (VRN1), VRN2, and FLOWERING LOCUS T (FT).

2 2,4-dinitrotoluene (DNT), and fenitrothion (FT).

3 ues of the floral inducer FLOWERING LOCUS T (FT).

4 d more than 50% of those above 6000 m (19700 ft).

5 wainson's Thrushes' arrival and departure at Ft.

6 d, which is several times finer than that of FT.

7 g only exon 4 of the C terminus of AcMFT and FT.

8 nd fewer than half have any abnormalities on FT.

9 ingly, a similar partial compensation of the ft-1 late flowering phenotype was observed in Arabidopsi

10 :TOE1(R) ) and mutant (flowering locus T-10 (ft-10)) lines were used for functional analysis of nemat

11 modulate photoperiodic flowering by changing FT accumulation patterns.

12 iring more computational power than standard FT algorithms, PhiSDM runs in a quasilinear time.

13 -ft) increase in altitude above 2500 m (8200 ft), AMS prevalence increased 13% (95% CI, 9.5%-17%).

14 Nine of 16 (56.2%) patients who received FT and 5 of 12 (41.7%) in the vancomycin taper group exp

15 dopsis FD proteins interact with full-length FT and AcMFT, as well as peptides encoded by 1-3 exon fr

16 that FD could form the similar complex with FT and AcMFT.

17 LOCUS C (FLC) genes which directly regulate FT and are key to LD and vernalisation responses in Arab

18 results was significantly different between FT and CAC (FT: normal, n=3588 [78.0%]; mild, n=432 [9.4

19 better prognostic information compared with FT and CAC testing (C index, 0.72).

20 In our model, the binding affinity of Ft and Ds depends on phosphorylation by Fj.

21 Fj), which affects the binding affinities of Ft and Ds.

22 rnal temperature changes combine to modulate FT and flowering time.

23 167780 and Marker139469 were associated with FT and HD at the same location (Ya'an) over two differen

24 tensities (steady-state fluorescence yields, Ft ) and saturation pulses (maximal fluorescence yields,

25 ion of bonds between the protocadherins Fat (Ft) and Dachsous (Ds), which form heterodimers between a

26 5% of individuals ascending to 3500 m (11500 ft) and more than 50% of those above 6000 m (19700 ft).

27 ssion tomography, gait speed over 4.57 m (15 ft), and cognition on the Mini-Mental State Examination

28 stigated the contribution of symptomatic TS+/FT- and TS+/FT+ patients in C. difficile transmission in

29 sources for each TS+/FT+ case, including TS+/FT- and TS+/FT+ patients, were determined using WGS, wit

30 -predominant subgroups (frontal/temporal [SN-FT] and frontal [SN-F]), a semantic appraisal network-pr

31 studies suggested that the roles of VRN1 and FT are conserved in Brachypodium distachyon yet identifi

32 ants are young, cooler temperatures suppress FT at dusk through SHORT VEGETATIVE PHASE (SVP) function

33 tly demonstrated performance superior to the FT-based methodologies, be it across the entire mass ran

34 an acute episode of recurrent CDI, a single FT by enema was not significantly different from oral va

35 days of oral vancomycin followed by a single FT by enema with oral vancomycin taper (standard of care

36 omycin treatment followed by a single 500-mL FT by enema, or a 6-week taper of oral vancomycin.

37 zation was similar and fair for both CAC and FT (C statistic, 0.67 versus 0.64).

38 the basic principles of wide-field detected FT-CARS microscopy and demonstrate how it can be used as

39 Intrinsic to FT-CARS microscopy, the ability to control the range of

40 This is made possible by an integration of a FT-CARS system and a rapid-scanning retro-reflective opt

41 Our rapid-scanning FT-CARS technique holds great promise for studying chemi

42 Stokes Raman scattering (wide-field detected FT-CARS) microscopy capable of acquiring high-contrast l

43 sform coherent anti-Stokes Raman scattering (FT-CARS) spectroscopy technique that achieves broadband

44 cleotide polymorphisms) to >/=1 previous TS+/FT+ case or TS+/FT- patient: 27 (10%) to only TS+/FT+ ca

45 to be plausibly acquired from a previous TS+/FT+ case than a TS+/FT- patient.

46 Plausible sources for each TS+/FT+ case, including TS+/FT- and TS+/FT+ patients, were d

47 Fifty-one of 265 (19%) TS+/FT+ cases diagnosed >3 months into the study were geneti

48 TS+/FT+ cases were 3 times more likely to be plausibly acqui

49 ase or TS+/FT- patient: 27 (10%) to only TS+/FT+ cases, 9 (3%) to only TS+/FT- patients, and 15 (6%)

50 ounted for less onward transmission than TS+/FT+ cases.

51 ), representing 235 Leeds and 191 Oxford TS+/FT+ cases.

52 ollected for 214 VPT children (95.5%) and 46 FT children (100%), while 126 VPT children (56.3%) and 3

53 100%), while 126 VPT children (56.3%) and 31 FT children (67.4%) had usable magnetic resonance imagin

54 nm to 400 nm possess fmax 31-41% higher than fT, closely resembling Si n-channel MOSFETs at comparabl

55 feature tracking-cardiac magnetic resonance (FT-CMR) is emerging as a novel, simple and robust method

56 We assume that the asymmetry of the Ft-Ds bond distribution around the cell periphery define

57 metry after division by rapidly replenishing Ft-Ds bonds at new cell-cell interfaces.

58 both of which can alter the distribution of Ft-Ds heterodimers around the cell periphery.

59 hich reduces the expression levels of CO and FT during the morning for seasonal flowering.

60 For this reason, the FT-ELIT MS approach is most appropriate for wide m/z ran

61 omain data via Fourier transformation (i.e., FT-ELIT MS).

62 Excellent predictive capability of FT-EoS was observed with an overall relative absolute av

63 on Theory-based Tait-like Equation of State (FT-EoS).

64 e coronary artery disease were randomized to FT (exercise electrocardiography, nuclear stress, or str

65 (SPL3/4/5) potentiate the FLOWERING LOCUS T (FT)-FD module in photoperiodic flowering.

66 Furthermore, similar FRET efficiencies for FT-FD and AcMFT-FD heterodimer in nucleus were observed.

67 er we assemble a range of methods (including FT-FIR using synchrotron radiation, nanoindentation and

68 gated using Fourier transform far infra-red (FT-FIR) with synchrotron radiation.

69 A 200-nm-gate-length GFET achieves fT/fmax = 35.4/50 GHz.

70 expression of the main photoperiod-regulated FT gene, FTb2, implying that it plays a primary role in

71 FLOWERING LOCUS T (FT) genes, first identified in Arabidopsis thaliana (Ara

72 c ratio would not differ between the BPD and FT groups.

73 One of four FT homologues present in the narrow-leafed lupin genome,

74 ches to determine whether Flowering Locus T (FT) homologues are associated with the Ku locus.

75 .14; 95% confidence interval, 1.81-5.44; and FT: HR, 2.65; 95% confidence interval, 1.46-4.83; severe

76 .56; 95% confidence interval, 1.99-6.36; and FT: HR, 3.88; 95% confidence interval, 2.58-5.85).

77 m ion cyclotron resonance mass spectrometry (FT ICR MS), can resolve thousands of molecular ions in c

78 igned and successfully installed in a hybrid FT-ICR instrument in place of the standard gas collision

79 eptide and proteins within the ICR cell of a FT-ICR mass spectrometer are accomplished through approp

80 ing power of 90-220) to ultrahigh resolution FT-ICR MS (resolving power over 400k) permitted the iden

81 The TIMS-FT-ICR MS analysis provided, in addition to the heteroat

82 In the present study, the capabilities of 2D FT-ICR MS are explored with a tryptic digest of cytochro

83 2D FT-ICR MS has been optimized as a data-independent metho

84 resolution FT-ICR MS/MS analysis, but the 2D FT-ICR MS method required only one experimental scan.

85 rrelate with DOM composition, the ability of FT-ICR MS to characterize DOM subpopulations provides un

86 ections (<1%) can be measured using OSA-TIMS-FT-ICR MS with high mobility resolving powers (RIMS up t

87 on cyclotron resonance mass spectrometry (2D FT-ICR MS) allows the correlation between precursor and

88 m-ion cyclotron resonance mass spectrometry (FT-ICR MS) and quantify DOM photochemical activity using

89 cyclotron resonance mass spectrometry (MALDI-FT-ICR MS) and single cell imaging flow cytometry to det

90 m ion cyclotron resonance mass spectrometry (FT-ICR MS) is applied to the analysis of the low energy

91 m ion cyclotron resonance mass spectrometry (FT-ICR MS) provides ultrahigh resolution and ultrahigh m

92 n cyclotron resonance mass spectrometry (21T FT-ICR MS).

93 o ultrahigh resolution mass analyzers (e.g., FT-ICR MS).

94 In the case of OSA-TIMS-FT-ICR MS, the TIMS operation sequence, trapping conditi

95 ide 3 KRGRGRPRK [M + 2H](+2) during OSA-TIMS-FT-ICR MS.

96 ost matched data provided by high-resolution FT-ICR MS/MS analysis, but the 2D FT-ICR MS method requi

97 The SID-FT-ICR platform has been tested with several protein com

98 lly intact, demonstrating the ability of the FT-ICR to maintain the noncovalent interactions and effi

99 ignificantly reduced by tandem-MS (Q-ToF and FT-ICR) followed by mild collisional or continuous IRMPD

100 a Fourier transform-ion cyclotron resonance (FT-ICR) mass spectrometer.

101 lglucoside-micelle by collisional (Q-ToF and FT-ICR) or continuous IRMPD activation (FT-ICR).

102 and FT-ICR) or continuous IRMPD activation (FT-ICR).

103 Insights generated using FT-ICR-MS analysis can be confirmed and further explored

104 Metabolic fingerprints from FT-ICR-MS data could discriminate wines according to the

105 earing organic formulas were identified with FT-ICR-MS in the stormwater runoff and pond outflow wate

106 d by ultrahigh resolution mass spectrometry (FT-ICR-MS) and excitation emission matrix fluorescence (

107 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) as a nontargeted technique to assign unambigu

108 PPI) ultrahigh resolution mass spectrometry (FT-ICR-MS) revealed a strong interaction between DOM and

109 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) to determine the biodegradability and molecul

110 m ion cyclotron resonance mass spectrometry (FT-ICR-MS), combined with chromatographic prefractionati

111 m-Ion Cyclotron Resonance-Mass Spectrometry (FT-ICR-MS), which delivered the molecular formulae and i

112 ARAFAC)) and the exact mass information from FT-ICR-MS, and thus revealing the extent of sulfur-conta

113 nd the level of identification possible with FT-ICR-MS.

114 h the ultrahigh mass resolution available in FT-ICR.

115 s previously implicated in the activation of FT in Arabidopsis.

116 this interaction and shown that COL3 targets FT in the presence of BBX32 to regulate the flowering pa

117 such as CONSTANS (CO) and FLOWERING LOCUS T (FT) in Arabidopsis.

118 to how CAC compares with functional testing (FT) in estimating prognosis in symptomatic patients.

119 ain positive (TS+) but fecal toxin negative (FT-) in transmission of Clostridium difficile is current

120 For each 1000-m (3300-ft) increase in altitude above 2500 m (8200 ft), AMS pre

121 e 6 months, as well as in parents of healthy FT infants (>/=37 weeks' gestational age; birth weight >

122 e at birth, 35.9 [5.3] years) of 151 healthy FT infants (50% male; 149 singletons, 2 multiples; mean

123 Compared with parents of FT infants, parents of VPT infants had higher rates of d

124 Of 224 VPT infants and 46 full-term (FT) infants, usable magnetic resonance imaging data at e

125 nd delta(18)O on the VPDB scale, with either FT-IR (in this case a Vertex 70 V (Bruker)) or an isotop

126 In the case of FT-IR a novel methodology using only two standards of CO

127 ected in our samples were identified through FT-IR analysis (n = 4050 particles), shedding for the fi

128 ferential scanning calorimetry (DSC) & novel FT-IR analysis based on peak symmetry measurements confi

129 The application of FT-IR analysis is inexpensive, easy to use, and portable

130 FT-IR analysis of plasma-exposed AHLs highlighted the ap

131 FT-IR analysis of the dry material combined with chemome

132 DSC and FT-IR analysis of the flours evidenced a "stabilizing" e

133 FT-IR analysis revealed ingestion of a range of polymers

134 SEM and FT-IR analysis were studied to characterize the biosorbe

135 tion of (f)Si NP with cells was confirmed by FT-IR analysis.

136 both imine COFs is complete, as assessed by FT-IR and (13)C CP-MAS NMR spectroscopy and demonstrates

137 A excipient can be studied simultaneously by FT-IR and 2D IR correlation spectroscopies.

138 ing data, comparing classifiers developed on FT-IR and DFIR imaging modalities and identifying specif

139 ated results is complementary to established FT-IR and Raman methods providing particle counts of ind

140 Moreover, FT-IR and Raman spectroscopies are useful complementary

141 tructure of CPCMs were characterized by SEM, FT-IR and XRD.

142 roscopy in attenuated total reflection mode (FT-IR ATR) and identified successfully with the new meth

143 However, FT-IR failed to discriminate between the same species.

144 as at least 16 times faster than the fastest FT-IR imaging instrument.

145 Despite recent technological advances in FT-IR microscopy, sample throughput and speed of acquisi

146 FT-IR monitoring and HR-ESI-MS spectra point to a stable

147 Notably, the FT-IR peak at 947cm(-1) and XRD peaks at 2theta approxim

148 The FT-IR spectra confirmed the formation of new peptide bon

149 s were constructed and cross-validated using FT-IR spectra from 18 types of chocolate and correspondi

150 and cheap method based on the acquisition of FT-IR spectra of 3g/L hydroalcoholic tannin solutions, o

151 tool to compare and describe similarities of FT-IR spectra of microplastics, which may improve furthe

152 d long FeN-N2 (1.246 A) distances, while the FT-IR spectra show an unusually low N-N stretching frequ

153 d Artificial Neural Networks were applied to FT-IR spectra to investigate the possibility of differen

154 skin and grape seed) were collected and the FT-IR spectra were acquired in the region 926-5011cm(-1)

155 and the effect of gum were manifested in the FT-IR spectra.

156 ounds were characterized by (1)H, (13)C NMR, FT-IR spectral analyses and XRD data.

157 FT-IR spectral analysis revealed electrostatic interacti

158 Principal component analysis applied on FT-IR spectral data in the region between 4000 and 650cm

159 osition of dietary fibre from fruit based on FT-IR spectral information in combination with chemometr

160 tudy micro-attenuated total reflection (ATR)-FT-IR spectroscopic imaging was required for the investi

161 Micro-ATR-FT-IR spectroscopic imaging, thanks to a very high chemi

162 rode was characterized by X-ray diffraction, FT-IR spectroscopy and scanning electron microscopy.

163 capacity, transmission electron microscopy, FT-IR spectroscopy and thermal properties of chia seed o

164 ATR-FT-IR spectroscopy can be used for rapid prediction of a

165 iency (82.8%), loading capacity (35.38%) and FT-IR spectroscopy demonstrated the interaction between

166 FT-IR spectroscopy showed increase in the ratio of inten

167 ated using chromatographic, fluorescence and FT-IR spectroscopy techniques and degradation kinetics.

168 py, Viscometry, Dynamic light scattering and FT-IR spectroscopy techniques.

169 Biochemical and FT-IR studies indicated differences between SB6 and comm

170 The FT-IR technique confirmed that SGs maintained their chem

171 of Fourier transform-infrared spectroscopy (FT-IR) analysis, X-ray diffractometry (XRD) and gas chro

172 vestigated using Fourier transform infrared (FT-IR) and Raman spectroscopies.

173 oorganic materials by infrared spectroscopy (FT-IR) is frequently limited due to overlapping of diagn

174 Fourier transform infrared (FT-IR) microscopy coupled with machine learning approach

175 ain tissue using Fourier-transform infrared (FT-IR) microspectroscopy, confocal Raman microspectrosco

176 Fourier transform-IR (FT-IR) spectra of clusters of electromagnetically couple

177 Fourier transform infrared (FT-IR) spectroscopic imaging has been widely tested as a

178 lectance (ATR)-Fourier transformed-infrared (FT-IR) spectroscopy (4000-550cm(-1)).

179 l reflection Fourier transform infrared (ATR-FT-IR) spectroscopy and developed a spectrochemical tool

180 (SEM and TEM), Fourier transformed infrared (FT-IR) spectroscopy and fluorescence microscopy for char

181 l reflection Fourier transform infrared (ATR-FT-IR) spectroscopy and multivariate modeling methods to

182 Fourier transform infrared (FT-IR) spectroscopy can be used to ascertain the presenc

183 Fourier transform infrared (FT-IR) spectroscopy of microcapsules showed peaks in the

184 sition analysis, Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM)

185 l reflection Fourier-transform infrared (ATR FT-IR) spectroscopy, time-resolved luminescence spectros

186 and Fourier transform infrared spectroscopy (FT-IR) studies.

187 D), Fourier transform infrared spectroscopy (FT-IR), sorption isotherms and antifungal activity were

188 iques (Raman and Fourier transform infrared, FT-IR).

189 and Fourier transform-infrared spectroscopy (FT-IR).

190 UV, FT-IR, (1)H NMR in addition to HPLC were applied to cons

191 PdBPI) were synthesized and characterized by FT-IR, (1)H NMR, (13)C NMR, UV-Vis spectroscopies and vi

192 UV-vis, photoluminescence (PL) spectroscopy, FT-IR, and cyclic voltammetry techniques.

193 poly-alpha-truxillates were analyzed by NMR, FT-IR, and HRMS.

194 kes (po-Gr-NR) were characterized by UV-vis, FT-IR, and Raman spectroscopies and FE-SEM, which indica

195 are characterized by light scattering, NMR, FT-IR, and TEM.

196 oscopic techniques (CP/MAS (13)C NMR, Raman, FT-IR, and XPS) and high-resolution transmission electro

197 uded sugar estimation, SDS-PAGE, GPC, color, FT-IR, DSC, thermal stability, solubility, emulsifying,

198 nt characterization was investigated by SEM, FT-IR, EDX and VSM.

199 sing thermogravimetric analysis coupled with FT-IR, gas chromatography, and mass spectrometry (TGA/FT

200 The material was characterized by FT-IR, NMR, high resolution mass spectrometry and dynami

201 ally and characterized by using UV-Vis, TGA, FT-IR, Raman Spectroscopy and SEM techniques.

202 XRS constitutes a powerful complement to FT-IR, Raman, and conventional XANES spectroscopy, overc

203 nalysis of the functionalized precursors and FT-IR, Raman, and XPS analyses of the resulting GNRs.

204 by using different spectroscopic techniques (FT-IR, Raman, UV-vis), TGA and Kaiser test.

205 repared nanobiocatalyst was characterized by FT-IR, SEM and XRD.

206 have been synthesized and characterized with FT-IR, SEM, EDX, TEM, UV-Visible, XRD and TG/DTA techniq

207 icles (NPs) were physically analyzed by TEM, FT-IR, TGA and DTG to characterize the nanoencapsulation

208 CMO NPs were characterized in details using FT-IR, UV/vis., FESEM, XEDS, XPS, TEM, and XRD technique

209 was carefully characterized by the SEM, TEM, FT-IR, XRD and so on.

210 mori samples were characterized by SEM-EDX, FT-IR, XRD and TGA-DSC techniques.

211 ices was synthesized and characterized using FT-IR, XRD, SEM and VSM techniques.

212 re irradiated with UV light and monitored by FT-IR.

213 s chromatography, and mass spectrometry (TGA/FT-IR/GC/MS).

214 etection of dimeric cleavage products by TGA/FT-IR/GC/MS.

215 ay and qPCR indicated that the expression of FT is down-regulated in both OsbHLH068-overexpressing Ar

216 tbhlh112 mutant plants, whereas SOC1 but not FT is highly expressed in AtbHLH112-overexpressing Arabi

217 tochemical characterization reveals that the FT is mitotically active and its cells express similar m

218 JQ-FT is recognized by folate receptors on the plasma membr

219 Fecal transplantation (FT) is a promising treatment for recurrent Clostridium d

220 2 factorial, cluster-randomized trial in 467 FT-LBW infants during 2 periods: from 0 to 5 mo postpart

221 hanced MNP significantly reduced stunting in FT-LBW infants in this high-risk setting.

222 FT-LBW infants who received the MNP (with or without the

223 mprove nutrient intake to reduce stunting in FT-LBW infants.

224 ries are at full term with low birth weight (FT-LBW).

225 FT levels correlated strongly with flowering time across

226 elevated expression of the floral activator, FT-like gene FTa1.

227 d phospho-STAT3 proteins in the skin of Flg (ft) mice, suggesting that macrophages to change from the

228 ncreased in the skin of IMQ-treated and Flg (ft) mice.

229 like skin inflammation, and flaky-tail (Flg (ft) ) mice, a model for IL-17A-induced chronic atopic de

230 (NIR) and attenuated total reflection (ATR) FT mid-infrared (MIR) spectroscopy were used to qualitat

231 Interestingly, ATR FT-MIR spectra from fresh homogenized berry samples prov

232 FT-NIR and ATR FT-MIR spectroscopy, coupled with spectral preprocessing

233 In addition, the organization of the FT most closely resembles that of the adult spinal cord

234 nsity-independent noise filtering in shotgun FT MS and FT MS/MS spectra that capitalizes on a stable

235 roduces several hundred of densely populated FT MS and FT MS/MS spectra, each of which might comprise

236 nts in the spectral quality and the speed of FT MS instruments.

237 ned for Fourier transform mass spectrometry (FT MS).

238 pendent noise filtering in shotgun FT MS and FT MS/MS spectra that capitalizes on a stable compositio

239 veral hundred of densely populated FT MS and FT MS/MS spectra, each of which might comprise thousands

240 olution Fourier transform mass spectrometry (FT-MS); (b) high-resolution chromatography such as compr

241 n (n=4209) and compared that with results of FT (n=4602).

242 ith mildly, moderately, or severely abnormal FT (n=57 of 132, 43%; P<0.001).

243 Fourier transform (FT) near-infrared (NIR) and attenuated total reflection

244 FT-NIR and ATR FT-MIR spectroscopy, coupled with spectra

245 hose of haddock (n=90), in comparison with a FT-NIR benchtop spectrometer.

246 lyzed using Fourier transform near infrared (FT-NIR) transmission spectroscopy in the range of 5435cm

247 tandard three-dimensional Fourier transform (FT) NMR experiments of molecular systems often involve p

248 , 100-400 AS, and >400 AS, respectively; for FT: normal, mild=late positive treadmill, moderate=early

249 significantly different between FT and CAC (FT: normal, n=3588 [78.0%]; mild, n=432 [9.4%]; moderate

250 cle we report a histological analysis of the FT NSC niche in postnatal rats and humans.

251 ) were genetically related to a previous TS+/FT+ or TS+/FT- patient and shared the same ward simultan

252 tically related to a previous TS+/FT+ or TS+/FT- patient and shared the same ward simultaneously or w

253 ired from a previous TS+/FT+ case than a TS+/FT- patient.

254 phisms) to >/=1 previous TS+/FT+ case or TS+/FT- patient: 27 (10%) to only TS+/FT+ cases, 9 (3%) to o

255 contribution of symptomatic TS+/FT- and TS+/FT+ patients in C. difficile transmission in 2 UK region

256 each TS+/FT+ case, including TS+/FT- and TS+/FT+ patients, were determined using WGS, with and withou

257 Symptomatic TS+/FT- patients were a source of C. difficile transmission,

258 %) to only TS+/FT+ cases, 9 (3%) to only TS+/FT- patients, and 15 (6%) to both.

259 indicated that the fourth exon of AcMFT and FT plays a similar and important role in promoting flowe

260 wed that the regulatory module miRNA172/TOE1/FT plays an important role in correct GCs and gall devel

261 s needed to explore optimal donor selection, FT preparation, route, timing, and number of administrat

262 f the Re promoter does not change during the FT process.

263 re present on specific regions of the CO and FT promoters where CDF1 binds during the morning.

264 FT-Raman analysis highlighted the structural changes tha

265 on partial least squares (PLS) treatment of FT-Raman data is described.

266 Within single FT-Raman experiment carbohydrates, carotenoids, and poly

267 FT-Raman spectra were again obtained at the same 12 poin

268 FT-Raman spectra were obtained from samples of whole lac

269 In contrast, application of FT-Raman spectroscopy for quantification of two laserine

270 Application of FT-Raman spectroscopy for simultaneous quantification of

271 FT-Raman spectroscopy has been explored as a quick scree

272 These results demonstrate the utility of FT-Raman spectroscopy in combination with chemometrics t

273 In this work, FT-Raman spectroscopy was explored to evaluate spreadabl

274 FT-Raman spectroscopy, thermogravimetry and differential

275 Fecal microbiota analysis of 3 successful FT recipients demonstrated increased diversity.

276 filtrate from donors and stool samples from FT recipients, as available.

277 We stratified CAC and FT results as normal or mildly, moderately, or severely

278 ded initial fast, high-energy HCD (Orbitrap, FT) scans, which produced intense ADP-ribose fragmentati

279 with altered expression of miRNA172, TOE1 or FT showed lower susceptibility to the RKNs and smaller g

280 spectra are lower than those of the original FT spectra.

281 reserved, the method deconvolves an observed FT spectrum into a distribution of harmonic components b

282 BPD had significantly lower D(M) and Vc than FT subjects after adjustment for race, sex, body length,

283 and did not differ for infants with BPD and FT subjects.

284 ition of mass spectra via Fourier transform (FT) techniques (frequency measurement) and via time-of-f

285 eam of FT, was up-regulated more strongly by FT than AcMFT in transgenic Arabidopsis.

286 onstrated that NSCs can be isolated from the FT, the in vivo architecture of this tissue and its rela

287 veral CDFs (CDF1, CDF3, CDF5) and increasing FT transcript levels, indicating both cis and trans func

288 FLOWERING LOCUS T (FT) transcript levels were reduced at dusk, but increase

289 the mechanism by which CDF1 represses CO and FT transcription remained elusive.

290 tein delays flowering by directly repressing FT transcription, FLORE promotes it by repressing severa

291 ith resolution beyond the Fourier transform (FT) uncertainty limit.

292 regulated by photoperiod similar to that for FT under both long day and short day conditions.

293 re specific for predicting events (78.6% for FT versus 35.2% for CAC; P<0.001).

294 However, an abnormal FT was more specific for cardiovascular events, leading

295 In contrast, any abnormality on FT was significantly more specific for predicting events

296 the expression of AP1, a gene downstream of FT, was up-regulated more strongly by FT than AcMFT in t

297 traits-heading date (HD) and flowering time (FT)-were identified and positioned on linkage groups LG1

298 f the major flowering pathway genes VRN2 and FT, whereas no linkage was observed at VRN1 Characteriza

299 has been identified in the filum terminale (FT), which is a thin band of tissue at the caudal end of

300 induces the expression of FLOWERING LOCUS T (FT), which promotes flowering.