ライフサイエンスコーパス: MFI

1 MFI for CD18 was decreased in both CD4+ and CD8+ T cells

2 MFI varied according to manufacturer, kit, bead type and

3 ning for anti-HLA antibodies using the 3,000 MFI threshold may be important in managing transplant ca

4 hout leakage (PPV, 88.1% vs 90.6% [P = .01]; MFI, 2.1 vs 2.4 [P = .007]), most markedly during the cr

5 arkers in a diverse cohort, baseline sICAM-1 MFI is associated with HCC incidence.

6 e age, antiviral treatment, and high sICAM-1 MFI; on multivariate analysis, sICAM-1 remained associat

7 The growth mechanism of silicalite-1 (MFI zeolite) is juxtaposed between classical models that

8 intercellular adhesion molecule 1 (sICAM-1) MFI.

9 suggested optimal cutoffs from 1000 to 1500 MFI.

10 ly in recipients with DSAs greater than 2000 MFI in the second run.

11 ph nodes had reduced Foxp3 expression (> 25% MFI loss) and increased IL-17A expression (> 15%), compa

12 he formation of functional membranes from 2D MFI nanosheets.

13 High-quality 2D MFI nanosheet coatings were prepared on alpha-alumina ho

14 nsity (MFI), 7/19 were between 1000 and 3000 MFI, and one was >3000 MFI.

15 between 1000 and 3000 MFI, and one was >3000 MFI.

16 fluorescence intensity (MFI) versus 42 +/- 4 MFI for stimulated GP IIb/IIIa expression (p < 0.001).

17 an increase in the inducibility of pSTAT-4 (MFI 157 vs 173; P=0.0002).

18 ients, an increase in nCD64 expression >/=40 MFI predicted intensive care unit (ICU)-acquired infecti

19 sAMR were MFI of immunodominant DSA > 4000, MFI of the sum of DSA > 6300, age of the recipient < 45

20 e sAMR were MFI of immunodominant DSA >4000, MFI of the sum of DSA >6300, age of the recipient <45 ye

21 ter therapy (mean decrease of 1916 [SE, 425] MFI, P < 0.01).

22 1.38-3.43; P = 0.0008), DSA greater than 500 MFI at transplant (HR, 1.64; 95% CI, 1.05-2.57; P = 0.03

23 threshold was increased to greater than 8000 MFI, because no matches were found with standard allocat

24 roup, one patient developed de novo DSA (A24-MFI 970; biopsy for cause did not show biopsy-proven acu

25 bindings of l- and d-lysine (Lys) in achiral MFI zeolites.

26 dissociation inhibitor 2 (ARHGDIB) (adjusted MFI [aMFI]>=1000), a minor histocompatibility antigen, a

27 ntibodies (sensitization) were defined by an MFI of more than 1000.

28 If the thresholds were increased to an MFI of 2000 or less and 5000 or less, an extra 6.4 and 6

29 Increasing the threshold to an MFI of 2000 or less may provide an acceptable balance fo

30 as background) cutoff of 15 combined with an MFI cutoff of 500, resulting in 8% and 21% lower 1- and

31 group, mean peak panel reactive antibody and MFI at transplant were 51% +/- 7% and 960 +/- 136, respe

32 etween platelets count and both of CD62P and MFI.

33 nstrate that wNMR outperformed SEC, DLS, and MFI in that it was most consistently sensitive to increa

34 y a single conformer was found (BEA, LTA and MFI).

35 Using Luminex and MFI quantification, anti-HLA antibodies are common befor

36 ine nanosheets of zeolite frameworks MWW and MFI.

37 PPV and MFI were correlated with the endothelial activation mark

38 e bis-imidazolium cation with n = 4, TON and MFI were also obtained, and again two (19)F MAS NMR reso

39 munodominant, but not the sum, of antibodies MFI.

40 3,000 (group III), and 24% had antibodies at MFI 1,000 to 3,000 (group II).

41 e cases with a posttransplant DSA peaking at MFI >2000 U on microbead assay, rejection did not occur.

42 a CNN for muscle segmentation and automatic MFI calculation using high-resolution fat-water images f

43 Single antigen flow bead MFI thresholds allowing XM positivity to be predicted we

44 of predominantly amorphous aggregates before MFI crystallization.

45 There is no association between MFI levels and development of complications after LT.

46 iled consideration of the structures of both MFI, and a closely related material MEL, lead to the pro

47 ts contract upon calcination similar to bulk MFI crystals.

48 iated with AAD, but the quantity assessed by MFI levels may play a role.

49 he pronounced increase in particle count (by MFI).

50 proved all other fatigue aspects measured by MFI, including Physical Fatigue and Mental Fatigue (acup

51 CD63 MFI expression was reduced from 68 248 (29 336-92 001) t

52 Additionally, CNN MFI was higher in participants with persisting pain and

53 relationships between CNN muscle volume, CNN MFI, and clinical measures of pain and neck-related disa

54 isability (R = -0.286, p = 0.045), while CNN MFI tended to be positively correlated to disability (R

55 verted to C1q - when diluted to a comparable MFI level as the C1q - DSA from AMR- patients, and some

56 examining interaction effects, and comparing MFI distribution between groups.

57 Manganese-containing MFI-type Mn-ZSM-5 zeolite was synthesized by a facile on

58 o those of other mesoporous and conventional MFI zeolites.

59 A highly crystalline MFI zeolite structure was formed under pH = 11 in 2 days

60 ered silicate moieties and the crystallizing MFI zeolite nanosheet framework.

61 hter structures of higher framework density (MFI) under hydrothermal conditions.

62 sk of AMR is higher in patients with a dnDSA MFI level that is greater than 3,000.

63 on at 1 year was 30% in the group with dnDSA MFI level of 3,000 or greater but only 4% for the group

64 DSA MFI greater than 10 000 versus MFI 1000 to 10 000 at 1 y

65 DSA MFI values increased at the time of AAD and returned to

66 d significantly higher IgG, C1q, and C3d DSA MFI than nonrejecting or C4d-negative patients, respecti

67 m of mean fluorescence intensity of DSA (DSA MFI-Sum) of 6,000 or higher (OR, 18; 95% CI, 7.0-47; P <

68 as 2.03 (95%CI, 1.05-3.92; P = 0.04) for DSA MFI-Sum of 6,000 or higher and 2.23 (95% CI, 1.04-4.80;

69 1.73 m(2) per log10 increase in Class II DSA MFI (p < 0.01).

70 t class II DSA, those with IgG4 class II DSA MFI sum >2000 exhibited an odds ratio (OR) of 20.79 (95%

71 protocols based on their immunodominant DSA MFI pretransplant (D1: 100-500, D2: 501-1000, and D3: 10

72 ter evaluated through the immunodominant DSA MFI than through the sum of DSA MFI.

73 High-dose IVIG resulted in modest DSA MFI reductions in patients with previous graft damage, w

74 dominant DSA MFI than through the sum of DSA MFI.

75 red with 4 of 7 (57%) patients with peak DSA MFI 2000 to 7000U, and 2 of 12 (17%) patients with peak

76 0U, and 2 of 12 (17%) patients with peak DSA MFI less than 2000U (P<0.02).

77 Our data suggest that DSA MFI and presence of intragraft DSA might provide prognos

78 Our study suggests that DSA MFI-Sum and HLA class of DSA are characteristics predict

79 on from January 2000 to April 2009, had DSA (MFI >/=1000) in serum 10 to 14 months postliver transpla

80 riable regression analysis that included DSA-MFI-Sum or HLA DSA class.

81 nts are indeed due to significantly enhanced MFI-polymer adhesion and distribution of MFI crystals.

82 th MFI structure reveals that the exfoliated MFI nanosheet is 1.5 unit cells (3.0 nm) thick and wrink

83 h other MFI membranes prepared from existing MFI materials (such as exfoliated nanosheets or nanocrys

84 for MFI >/=100 vs. 4.7[2.4-8.8], P<0.001 for MFI >/= 800).

85 from MFI 100 to 800 (1.7[0.8-3.2], P=0.1 for MFI >/=100 vs. 4.7[2.4-8.8], P<0.001 for MFI >/= 800).

86 eactivity and selectivity, also inferred for MFI from titration of OH groups by Na(+), have not been

87 rely at the pH and temperatures required for MFI synthesis.

88 The obtained OSDA-free MFI nanosheets disperse well in water and can be used fo

89 eased linearly with higher class II DSA from MFI 100 to 800 (1.7[0.8-3.2], P=0.1 for MFI >/=100 vs. 4

90 s of high-quality, mesoporous zeolite (e.g., MFI-type) nanocrystals is presented, based on a biomass-

91 Between groups, MFI trends were analyzed.

92 lites without 8-MR channels (H-BEA, H-FAU, H-MFI).

93 genation and cracking are examined over Ga/H-MFI catalysts prepared via vapor-phase exchange of H-MFI

94 action conditions, [GaH](2+) cations in Ga/H-MFI exhibit a turnover frequency for C(3)H(8) dehydrogen

95 rogenation to the rate of cracking over Ga/H-MFI is independent of C(3)H(8) and H(2) partial pressure

96 tions exhibit first-order kinetics over Ga/H-MFI only at very low C(3)H(8) partial pressures and zero

97 both dehydrogenation and cracking over Ga/H-MFI via reaction with [GaH](2+) cations to form [GaH(2)]

98 n and cracking of C(3)H(8) proceed over Ga/H-MFI via reversible, heterolytic dissociation of C(3)H(8)

99 H(2) inhibits both reactions over Ga/H-MFI.

100 n the locations of exchangeable cations in H-MFI and on the monomolecular cracking and dehydrogenatio

101 lysts prepared via vapor-phase exchange of H-MFI with GaCl(3).

102 der kinetics with respect to C(3)H(8) over H-MFI, but both reactions exhibit first-order kinetics ove

103 he corresponding turnover frequencies over H-MFI.

104 g zeolites with varying channel structure (H-MFI, H-FER, H-MOR) and between OH groups within eight-me

105 tivity of alkane cracking catalysis in the H-MFI zeolite is investigated using both static and dynami

106 panol (0.075-4 kPa) was studied on zeolite H-MFI (Si/Al = 26, containing minimal amounts of extra fra

107 s follows: 66% had MFI 1000 to 4999, 14% had MFI 5000 to 10 000, and 20% had MFI greater than 10 000.

108 999, 14% had MFI 5000 to 10 000, and 20% had MFI greater than 10 000.

109 of DSA+ recipients were as follows: 66% had MFI 1000 to 4999, 14% had MFI 5000 to 10 000, and 20% ha

110 presence of anti-HLA antibodies at the high MFI threshold (>3,000) was associated with lower transpl

111 ggest that DSA-sensitized patients with high MFI levels can receive transplantation across the HLA-ba

112 HLA class II Ab show a higher MFI (median: 5.300) compared to HLA class I Ab (median:

113 DSA+ patients regardless of MFI, and higher MFI at 1 year predicts DSA persistence at 5 years.

114 C1q + DSA exhibited significantly higher MFI values regardless of whether they were from AMR+ or

115 dominant DSA (iDSA, the DSA with the highest MFI level) was 6724+/-464, and 41.6% of patients had iDS

116 nvestigate water infiltration in hydrophobic MFI zeolites with different concentration of hydrophilic

117 IgG MFI was analyzed after elimination of prozone effect, an

118 cipients and conclude that assessment of IgG MFI may add predictive accuracy, without an independent

119 e highest accuracy was computed for peak IgG MFI (AMR, 0.73; C4d + AMR, 0.71).

120 IgGpan MFI alone showed a very strong association with standard

121 IgGpan MFI greater than 14,154 predicted standard C1q positivit

122 Combining all IgG subclass MFI and IgGpan MFI only marginally improved the prediction of standard

123 standard C1q positivity compared with IgGpan MFI alone (Deltar=0.02).

124 ssociation of AHG C1q positivity with IgGpan MFI was less strong (r=0.51).

125 ng on SAB is strongly associated with IgGpan MFI.

126 vival was detected in patients with class II MFI more than or equal to 1000 (75% vs. 91.9%, P=0.055).

127 were only evident in patients with class II MFI more than or equal to 500 (estimated glomerular filt

128 al), was investigated by micro-flow imaging (MFI) during freeze-thaw cycling in phosphate buffered so

129 ion chromatography (SEC), microflow imaging (MFI), and dynamic light scattering (DLS), and water NMR

130 ion chromatography (SEC), microflow imaging (MFI), and dynamic light scattering (DLS).

131 ex 2200 MMRV IgG multiplex flow immunoassay (MFI; Bio-Rad Laboratories, Hercules, CA) and matched imm

132 rate structure-direction effect for n = 4 in MFI, with each imidazolium ring, in two different orient

133 LF compared with blood (median difference in MFI 1337, p=0.0020) and that of CXCR2, CCR1, CCR2, and C

134 Periodic DFT calculations suggest that F in MFI resides always in the [4(1)5(2)6(2)] cages, with the

135 gely dissimilar intensities were observed in MFI.

136 The higher activity in BEA than in MFI for dehydration of a tertiary alkanol, 2-methyl-2-he

137 fused vessels (PPV) and the mean flow index (MFI) were lower in patients with dengue with plasma than

138 istribution of neck muscle fat infiltration (MFI) in the deep cervical extensor muscles (multifidus a

139 Muscle fat infiltration (MFI) of the deep cervical spine extensors has been obser

140 tation, class I/II distribution, and initial MFI).

141 rrelate with success of treatment if initial MFI values were >10 000, likely due to single antigen be

142 e single-line manifold micro flow injection (MFI) systems.

143 antibodies (DSA) mean florescence intensity (MFI) greater than 10 000 and requires confirmation in pa

144 Cytokine mean florescence intensity (MFI) was the primary predictor and HCC development the p

145 b is measured as mean florescence intensity (MFI).

146 el of DSA had median fluorescence intensity (MFI) >2000 U, in 6 of 10 when the microbead MFI >4000 U.

147 ears) and lower mean fluorescence intensity (MFI) (2658, 1573-3819 vs. 7820, 5166-11 990).

148 ion between SAB mean fluorescence intensity (MFI) and complement assays positivity, presence of gDSA,

149 haracterized by mean fluorescence intensity (MFI) and normalized subclass composition (>5%).

150 ) more than 100 mean fluorescence intensity (MFI) at the time of transplant is associated with a sign

151 ession of 230 median fluorescence intensity (MFI) identified sepsis with a sensitivity of 89% (81%-94

152 esults with the mean fluorescence intensity (MFI) in Luminex class I single antigen flow beads (SAFB)

153 s with DSA at median fluorescence intensity (MFI) more than 7000U experienced rejection, compared wit

154 munologic risk, mean fluorescence intensity (MFI) more than or equal to 100 for class I and more than

155 lanted with DSA mean fluorescence intensity (MFI) of 500 to 1000 and greater than 1000, respectively.

156 Mean fluorescence intensity (MFI) of 70 total DSA decreased by 12%at the end of treat

157 measured by the mean fluorescence intensity (MFI) of antibodies stored with known stabilizers.

158 nly DSAs with a mean fluorescence intensity (MFI) of greater 999 were included.

159 The dnDSA mean fluorescence intensity (MFI) of the stable function patient group (n=8; eGFR dec

160 reases in CD11a mean fluorescence intensity (MFI) on naive, central memory, and effector memory CD4+

161 Comparing median fluorescence intensity (MFI) signals for the influenza A virus and hemagglutinin

162 Change in mean fluorescence intensity (MFI) value did not correlate with success of treatment i

163 A or with a DSA mean fluorescence intensity (MFI) value of 500 or less, screening by bead-based assay

164 d sera, Luminex mean fluorescence intensity (MFI) values for IgG-SAB and C1q-SAB correlated poorly (r

165 -HLA antibodies mean fluorescence intensity (MFI) values were stable prior to BTZ (P = 0.96) but decr

166 nce of AMR, DSA mean fluorescence intensity (MFI) values, and immunoglobulin G isotype was determined

167 VLA-4 mean fluorescence intensity (MFI) varied 35-fold (range, 30 to 1,110; median, 219.5).

168 and 138 +/- 19 mean fluorescence intensity (MFI) versus 42 +/- 4 MFI for stimulated GP IIb/IIIa expr

169 onders, bAb net mean fluorescence intensity (MFI) was significantly higher with the DNA-primed regime

170 expression and mean fluorescence intensity (MFI) were highly correlated with increases in HIV-specif

171 ally from nevi [mean fluorescence intensity (MFI), 48.1; interquartile range, 41.7 to 59.6] to primar

172 1/19 were <1000 mean fluorescence intensity (MFI), 7/19 were between 1000 and 3000 MFI, and one was >

173 parallel to IgG mean fluorescence intensity (MFI), allows for improved prediction of AMR.

174 ss specificity, mean fluorescence intensity (MFI), C1q-binding, and IgG subclass, and graft injury ph

175 uantified using mean fluorescence intensity (MFI).

176 eater than 2000 mean fluorescence intensity (MFI).

177 LA antibodies at mean fluorescent intensity (MFI) greater than or equal to 3,000 (group III), and 24%

178 Peak DSA mean fluorescent intensity (MFI) levels were significantly higher at baseline (class

179 tins) and higher mean fluorescent intensity (MFI) positivity.

180 y 0 DSA levels (mean fluorescence intensity [MFI] > 3000) with a complement-dependent cytotoxicity-ne

181 n difference in mean fluorescence intensity [MFI] 703 arbitrary units [p=0.0699] for CXCR1 and 658.7

182 xpression (Deltamean fluorescence intensity [MFI] of 118.5 +/- 16.8), followed by CD11b(+)Gr-1(int) (

183 IgGpan results (mean fluorescence intensity [MFI]>500), strong complement-binding IgG1 and IgG3 subcl

184 [SFI]/10,000 median fluorescence intensity [MFI]) were determined to be unacceptable and entered int

185 SA (One Lambda, mean fluorescence intensity [MFI], >1000).

186 nding strength (mean fluorescence intensity [MFI]_max).

187 change in log median fluorescence intensity(MFI-BG) values was -0.15 overall (p < .001).

188 l infection at the maternal-fetal interface (MFI) in the early gestational stages.

189 hannels comprising a microfluidic interface (MFI) that prevents media leakage between the two dimensi

190 by in-plane XRD, indicating well-intergrown MFI films that are strongly attached to the substrate.

191 Encapsulation into MFI via direct hydrothermal syntheses was unsuccessful b

192 ctroscopic analysis of Co(II) exchanged into MFI, it was inferred that the fraction of Co(II) (and, b

193 sentially unchanged upon transformation into MFI.

194 with the Multidimensional Fatigue Inventory (MFI).

195 of the presence of de novo DSA (One Lambda, MFI > 1000).

196 approach based on the exfoliation of layered MFI, followed by centrifugation to remove non-exfoliated

197 The recovered group had significantly less MFI in Q1 compared to the two symptomatic groups.

198 requires confirmation in patients with lower MFI (1000-10 000).

199 g the bead of the same HLA-locus with lowest MFI as background) cutoff of 15 combined with an MFI cut

200 r the bead of the same HLA locus with lowest MFI taken as background.

201 Seven patients still had DSA with a mean MFI of 1298 +/- 930 at the last follow-up.

202 High VLA-4 expression (> median MFI), compared with low expression, was associated with

203 The median MFI of the immunodominant class I or II DSA in the peak

204 nge, 58.4 to 77.0) and metastatic melanomas (MFI, 87.5; interquartile range, 77.1 to 114.5) (P < 0.00

205 e range, 41.7 to 59.6] to primary melanomas (MFI, 68.8; interquartile range, 58.4 to 77.0) and metast

206 Mesostructured MFI zeolite nanosheets are established to crystallize no

207 (MFI) >2000 U, in 6 of 10 when the microbead MFI >4000 U.

208 In 8 of 10 cases, the microbead MFI at the time of resolution was greater than at the on

209 ype Pg381 or isogenic major (DPG-3)-, minor (MFI)-, or double fimbriae (MFB)-deficient mutant P. ging

210 ML-MFI was first exfoliated by melt compounding and then de

211 s were prepared from a multilamellar MFI (ML-MFI) zeolite.

212 ing up to 35 wt % of solvothermally modified MFI crystals.

213 sing first year peak MFI (pMFI), eight month MFI change (DeltaMFI), and eighteen month MFI trend (MFI

214 th MFI change (DeltaMFI), and eighteen month MFI trend (MFI slope).

215 ng agents were prepared from a multilamellar MFI (ML-MFI) zeolite.

216 m (Mo) atoms into the framework of nanosized MFI zeolite is demonstrated for the first time.

217 tion enthalpy in the tighter confinements of MFI that offsets a less positive activation entropy.

218 ced MFI-polymer adhesion and distribution of MFI crystals.

219 ted in preferentially oriented thin films of MFI, which had sub-12-nm thickness in certain cases.

220 neous distribution of Mo in the framework of MFI nanozeolite, and the presence of Lewis acidity.

221 rdless of WAD recovery, but the magnitude of MFI in the medial portions of the muscles is significant

222 Bilateral measures of MFI in four quartiles (Q1-Q4; medial to lateral) at cerv

223 MDA has a small effect on reduction of MFI-BG.

224 graft survival was 96% to 100% regardless of MFI (P = NS).

225 graft failure in DSA+ patients regardless of MFI, and higher MFI at 1 year predicts DSA persistence a

226 if transplantation occurs at a threshold of MFI of 500 or less or in those without preformed DSA.

227 alculated panel-reactive antibodies based on MFI of 2000, 4000, and 8000 was unchanged in all patient

228 risk to develop graft damage independent on MFI and requires an individualized risk management.

229 ibenzyl ketone and dibenzyl ketone sorbed on MFI zeolites is examined.

230 membranes that compare favourably with other MFI membranes prepared from existing MFI materials (such

231 nstrating the approach for l- and d-Lys over MFI zeolites at an atomistic resolution, the differentia

232 Highly b-oriented, closely packed, MFI zeolite films are prepared on seeded stainless-steel

233 ctive method was developed to convert parent MFI zeolites with tetrahedral extra-framework Al into Al

234 The parent MFI zeolite was prepared by rapid ageing of the zeolite

235 =16; eGFR decline>25%) using first year peak MFI (pMFI), eight month MFI change (DeltaMFI), and eight

236 ee survival was worse in patients with pfDSA MFI >1000, evidenced by a fourfold increase in the risk

237 ctions for specimens with very low positive (MFI < 1,000) or "no-call" H1 results reliably distinguis

238 We show significantly decreased Bio-Rad MFI sensitivity for detection of anti-measles and anti-m

239 easles, mumps, rubella, and VZV, the Bio-Rad MFI was positive in 77.3, 85.4, 84.3, and 91.1% of HCWs,

240 The Bio-Rad MFI was positive in 83.7% of HCWs fully vaccinated again

241 ted against measles, mumps, and VZV, Bio-Rad MFI/Bion IFA positivity rates were 77.4%/93%, 84.8%/90.7

242 intergrowth to synthesize high-aspect-ratio MFI nanosheets with a thickness of 5 nanometres (2.5 uni

243 Global normalization further reduced MFI variation to levels near 20%.

244 ardized) operating procedure greatly reduced MFI variation from 62% to 25%.

245 These transformations required MFI seeds or organic templates for FAU parent zeolites,

246 g 39 patients with a lower immunologic risk (MFI between 500 and 3000 at day 0) who received the same

247 correlation between IgG-SAB MFI and C1q-SAB MFI was lowest using undiluted sera and SAB with greater

248 onsequently, the correlation between IgG-SAB MFI and C1q-SAB MFI was lowest using undiluted sera and

249 Prediction and sensitivity SAFB MFI thresholds were determined, respectively, assessing

250 XM results were tightly associated with SAFB MFI values.

251 own to produce high-flux and ultra-selective MFI membranes that compare favourably with other MFI mem

252 thylenediaminetetraacetic acid-treated serum MFI was considered.

253 orthorhombic ( Pnma), typical of high silica MFI, to monoclinic ( P21/ n), as well as an expansion of

254 However, until now, single MFI nanosheets have been prepared using a multi-step app

255 Single-unit-cell Sn-MFI, with the detectable Sn uniformly distributed and ex

256 Integrating iDSA HLA class specificity, MFI level, C1q-binding status, and IgG subclasses in a C

257 perior to a model including all IgG subclass MFI (r=0.62).

258 Combining all IgG subclass MFI and IgGpan MFI only marginally improved the predicti

259 035) compared with treatment initiation (T0) MFI.

260 with the preliminary study, indicating that MFI is spatially concentrated in the medial portions of

261 The MFI distribution of DSA+ recipients were as follows: 66%

262 The MFI of the immunodominant DSA (iDSA, the DSA with the hi

263 The MFI structure offers inherent geometric and internal con

264 nderstanding of HCV-specific immunity at the MFI as well as novel insights into mechanisms that limit

265 and activation of innate immune cells at the MFI.

266 different crystallographic positions in the MFI framework.

267 In addition, the insertion of Mo into the MFI structure induces a symmetry lowering, from orthorho

268 sites in the zeolite HZSM-5, a member of the MFI family of zeolite structures, contradicts the tradit

269 The feasibility of the use of the MFI membranes as an explosive preconcentrator is examine

270 luable chemical intermediates, and therefore MFI-type zeolites are widely used in the chemical indust

271 Nanometre-thick MFI crystals (nanosheets) have been introduced in pillar

272 uspensions of zeolite nanosheets (3 nm thick MFI layers) were prepared in ethanol following acid trea

273 In this MFI zeolite, two distinct (19)F MAS NMR resonances with

274 nd Ti sites become tighter, and is >10 on Ti-MFI.

275 Ti sites are confined within 10-MR pores (Ti-MFI, Ti-CON), likely because of intrapore reactant diffu

276 dies converted to C1q + when concentrated to MFI levels comparable to those observed for AMR+/C1q + s

277 ge (DeltaMFI), and eighteen month MFI trend (MFI slope).

278 A zeolite with structure type MFI is an aluminosilicate or silicate material that has

279 on membranes containing nonporous uncalcined MFI revealed that the performance enhancements are indee

280 e determined pretransplant DSA using various MFI cutoffs, signal-to-background ratios, and combinatio

281 DSA MFI greater than 10 000 versus MFI 1000 to 10 000 at 1 year was also more likely to per

282 iated with the diagnosis of active sAMR were MFI of immunodominant DSA > 4000, MFI of the sum of DSA

283 iated with the diagnosis of active sAMR were MFI of immunodominant DSA >4000, MFI of the sum of DSA >

284 While MFI was reported to be concentrated in the medial portio

285 er but only 4% for the group with dnDSA with MFI less than 3,000.

286 For the dnDSA group with MFI of 3,000 or greater (compared with the group with MF

287 000 or greater (compared with the group with MFI<3,000), the hazard ratio for AMR was 10.6 (95% confi

288 er than 13 (P = 0.004) in DSA+ patients with MFI 1000 to 10 000.

289 y putative chronic AMR in DSA+ patients with MFI from 1000 to 10 000.

290 plication of the method to a 2D zeolite with MFI structure reveals that the exfoliated MFI nanosheet

291 lation of metal clusters (Pt, Ru, Rh) within MFI was achieved by exchanging cationic metal precursors

292 with n = 4 was able to produce also zeolite MFI at highly concentrated conditions.

293 ure and function for aluminosilicate zeolite MFI two-dimensional nanosheets before and after superhea

294 For a medium-pore zeolite, such as zeolite MFI, hydrated hydronium ions consist of eight water mole

295 The higher activity in zeolite MFI with pores smaller than BEA and FAU is caused by a l

296 crystal-thick b-oriented pure silica zeolite MFI films produced by in situ crystallization.

297 surface-treated nanoparticles of the zeolite MFI can be incorporated in situ during growth of a polyc

298 Highly selective thin zeolite MFI membranes are synthesized on porous stainless steel

299 The higher rates with zeolite MFI having pores smaller than those of zeolite BEA for d

300 organic Mg(OH)(2) nanostructures on zeolite (MFI) crystal surfaces in a controlled manner.