ライフサイエンスコーパス: Da

1 or molecule with a mass less than 1,000,000 Da.

2 surveyed >3,700 plasma metabolites (50-1,000 Da) for differential expression in XOR wildtype vs. mice

3 bute to their relatively large size (>10,000 Da).

4 ctionalized molecules with a mass m = 10,000 Da.

5 AA is synthesized as a precursor of ~110,000 Da that is N-glycosylated and targeted to the lysosome v

6 1355 Da) and proteins ( approximately 14 000 Da) are demonstrated, with approximately 1-2 orders of m

7 complex that eluted at approximately 151,000 Da upon Superdex 200 size-exclusion chromatography (SEC)

8 0-100 ppm) and molecular weight (1550-20,000 Da).

9 P enzymes, whose large mass (160,000-250,000 Da) precludes solution NMR approaches.

10 oroid or sclera had an apparent Mr of 27,000 Da.

11 l (PEG, molecular weight approximately 8,000 Da, 10(-7)-10(-4) M) increase the half-life of a green f

12 molecular weights from 27,000 < Mn < 80,000 Da (1.4 < Mw/Mn < 2.2) within 30 min at room temp.

13 ) with a molecular weight as high as 900 000 Da was successfully detected using the carbon nanofibrou

14 C) with molecular weights up to Mn = 940,000 Da (Mw/Mn = 3.2).

15 m 500-Da targeted polar molecules to 150,000-Da tagged immunoglobulins into the brain of living mice.

16 including L4 proteins of 22,000- and 33,000-Da apparent molecular mass (L4-22K and -33K proteins) th

17 The C3 vs SH4 (0.0034 Da) mass split is considered to be one of the most criti

18 aks of (15)N labeled lipids (Deltam = 0.0063 Da).

19 with equal intensity and differing by 6.018 Da.

20 acJ1 had an exact molecular mass of 1881.036 Da.

21 sor and fragment ions differing by -116.0473 Da, attributed to the neutral loss of deoxyribose.

22 re isolated for tandem MS analysis using a 1 Da mass isolation window, followed by collision-induced

23 ecision, and accuracy of quantification as 1 Da spaced reporter ions.

24 or the 10 LC-MS(2) DDA data sets with > +/-1 Da isolation windows, the median precursor purity score

25 results in a molecular weight increase of 1 Da.

26 n II-2 which differed in mass by less than 1 Da, the determination of a sequence for protein IB8a tha

27 nd lipids from 92 selected m/z windows (+/-1 Da) with a spatial resolution of better than 150 mum.

28 r the realization of 16-plex reagents with 1 Da spacing between reporter ions and up to 28-plex at 6

29 low molecular weight ( approximately 30-100 Da) contaminants representative of those detected in wat

30 served that three molecules ranging from 100 Da to 70 kDa permeated into a preclinical glioblastoma m

31 reby circumventing the mass limitation (~100 Da) of conventional SPR measurement.

32 tes are driven by enzyme kinetics (Pe = 100, Da = 7000).

33 d poor selectivity, especially in the 0-1000 Da molecular weight cut-off range.

34 a for 20 Da wide mass segments across a 1000 Da range, stitched into a single composite mass spectrum

35 permeability at molecular weights above 1000 Da and it appears likely that this cutoff constitutes an

36 0), compounds of molecular masses above 1000 Da were observed in the plasma air purifier.

37 d small cyclic peptides ( approximately 1000 Da) with more than 100 naturally occurring analogs.

38 mately 30% are protein-ligand (MW below 1000 Da) complexes.

39 ct, matrix-free analysis of small (MW < 1000 Da) lipid compounds, without interferences in the result

40 in the low molecular weight fractions (<1000 Da).

41 Catalysis by small molecules (</=1000 Da, 10(-9) m) that are capable of binding and activating

42 However, chemical space from 500 to 1000 Da remains virtually unexplored and represents a vast op

43 another intermediate with a [M-H](-) at 102 Da, identified as ONNHCH(2)NHCHO (NO-NDAB), were detecte

44 previously unreported protein of mass 10433 Da.

45 An approximately 11,109-Da MS peak corresponding to a gene product of the bla(KP

46 t pKpQIL_p019 (p019)-an approximately 11,109-Da protein associated with certain blaKPC-containing pla

47 iaceae spectra found an approximately 11,109-Da signal in nine spectra (1.3%), including seven from p

48 acteristic neutral losses of 98, 80, and 116 Da.

49 molecules, are shifted by + 4, + 8 and + 12 Da, which expose signals across areas of the previously

50 ty is used to detect small molecules (60-120 Da) printed on a dextran-modified sensor surface.

51 Methanobactin (Mb), a 1217-Da copper chelator produced by the methanotroph Methylos

52 es to accurately determine the mass (202.126 Da) of a compound that is specifically present in this p

53 the gas phase, evident from +64 Da and +128 Da signals that can be assigned to Hb carrying two and f

54 aminal (+148 Da) or Schiff base (imine, +130 Da) products.

55 -87% for four proteins (MW 42 287 to 162 134 Da), and 56% for one protein (MW 51 358 Da).

56 depleted human plasma had an additional 1347 Da over the native albumin extracted from human plasma,

57 all model molecules ( approximately 200-1355 Da) and proteins ( approximately 14 000 Da) are demonstr

58 utral loss chromatograms for 78, 98, and 136 Da allowed the identification of long-chain fatty acids

59 Neutral losses of 78, 98, and 136 Da were consistently observed for fatty acids with five

60 periodicity of the oscillations is about 14 Da which is the most common difference between the masse

61 We show that the intact mass of Rpl1ab is 14 Da larger than its calculated mass with the previously d

62 final adduct with a net mass increase of 14 Da.

63 heavy chain, with a net mass increase of 14 Da.

64 ltransferase, results in the loss of the +14-Da modification.

65 mass of (protonated) legiobactin is 437.140 Da.

66 lion molecular structures between 0 and 1450 Da, which correspond to about 27000 distinct elemental f

67 p202-220, 2127 Da), and 12-mer (p57-68, 1453 Da)] in duodenal biopsy specimens mounted in Ussing cham

68 le lysines), forming either hemiaminal (+148 Da) or Schiff base (imine, +130 Da) products.

69 or a few N-methyl groups (molecular mass 15 Da).

70 weight (LMW) molecules (molecular mass < 150 Da) that differ from each other by one or a few N-methyl

71 s" that showed mass increases of 174 and 156 Da, respectively.

72 oiety corresponding to a neutral loss of 156 Da per cysteine.

73 on reaction pathways: hydroxyl addition (+16 Da), alcoholic oxidation or dehydrogenation (-2 Da), and

74 hich contain the radical moiety with more 16 Da units than sulfaquinoxaline.

75 ns with a peak-to-peak mass difference of 16 Da consistent with the repeating unit of the beta-(1-->3

76 and a mass consistent with ritonavir plus 16 Da, in agreement with the whole-protein mass spectrometr

77 ozide (N-(dimethylamino)succinamic acid, 160 Da), a plant growth regulator, selectively inhibits the

78 n provided insufficient mass resolution (162 Da) to observe porosity on the experimental time scale;

79 well as a low molecular weight anatoxin (165 Da, 10(-14) m) are detected selectively and reproducibly

80 (110.18 Da) and 4-fluorobenzenethiol (128.17 Da), or large macromolecules such as anti-mouse IgG (~15

81 ptide FGES198AGAAS with an added mass of 170 Da from cresyl phosphate on serine 198 (Ser198) was dete

82 eights, including small benzenethiol (110.18 Da) and 4-fluorobenzenethiol (128.17 Da), or large macro

83 results were corroborated with glucose (180 Da) and inulin (5000 Da) transdermal flux experiments, w

84 rom pure bis-SorbPC was equivalent to a 1800 Da linear dextran, corresponding to a maximum pore diame

85 arkers [ionic conductance (G), mannitol, 182 Da; horseradish peroxidase, 40 kDa] and gliadin peptides

86 ides, dyes, drugs, lipids, and proteins (186 Da to 8.5 kDa) from various materials including urine, b

87 tic neutral loss pattern of 98, 178, and 196 Da, which enables the distinction between isobaric pyro-

88 on of three precursor ions: [M - H](+) = 197 Da, [M(*)](+) = 198 Da, and [M + H](+) = 199 Da.

89 r ions: [M - H](+) = 197 Da, [M(*)](+) = 198 Da, and [M + H](+) = 199 Da.

90 isomers formed single unique [M + H](+) (199 Da) parent ions, whereas in MALDI each isomer shows sign

91 Da, [M(*)](+) = 198 Da, and [M + H](+) = 199 Da.

92 The identified glycan of mass 450.2 Da is composed of a monoacetylated nonulosonic acid (Non

93 idate will appear as doublets separated by 2 Da.

94 , alcoholic oxidation or dehydrogenation (-2 Da), and elimination of sulfate (-80 Da).

95 idation product with the loss of hydrogen (2 Da mass decrease) for Trp-107 of the heavy chain was ide

96 The molecular weight difference of 2 Da between Met sulfoxide with the (16)O atom and Met sul

97 h (18)O at isoAsp leads to a mass shift of 2 Da, which can be automatically and unambiguously recogni

98 Therefore, the 2 Da molecular weight difference at the deamidation sites

99 repeatedly cycles through 28 consecutive 20 Da precursor isolation windows detecting all precursor i

100 anic asphalt sample by acquiring data for 20 Da wide mass segments across a 1000 Da range, stitched i

101 ted by Orbitrap MS were found in the 100-200 Da mass range.

102 ecular weight target molecule (less than 200 Da) by aptamer-based sensors.

103 between 375 and 525 Da, which was 150 to 200 Da higher than for an average DOM molecule.

104 molecular weight cutoff (MWCO) of 1000-2000 Da but also have a high pure water permeability (PWP) of

105 reening low-molecular weight analytes (<2000 Da) having many variants.

106 seful for analysis of small molecules (<2000 Da) such as those present in petroleum crude oil and pet

107 d iptycenes with molecular weights over 2000 Da.

108 peptides from these fractions were 800-2100 Da. and consisted of 6-21 amino acid residues.

109 19-mer (p31-49, 2245 Da; and p202-220, 2127 Da), and 12-mer (p57-68, 1453 Da)] in duodenal biopsy sp

110 MW) 216 Da (most likely C10H16O5) and MW 214 Da (C10H14O5) was confirmed with LC-ESI/MS/MS.

111 boxylic acids with molecular weight (MW) 216 Da (most likely C10H16O5) and MW 214 Da (C10H14O5) was c

112 saccharides were identified using 73 and 217 Da mass and the Wiley Online Library search.

113 saccharides were identified using 73 and 217 Da mass and the Wiley Online Library search.

114 an increase in mass of the apo-CYP2B4 by 218 Da as determined by electrospray ionization liquid chrom

115 ALDI-TOF revealed a molecular mass of 13,221 Da, and 12-23 aa sequences of OIF had homology with huma

116 ith a relatively small molecular weight (221 Da), provides an optimal building block for developing a

117 -mer (p56-88, 3900 Da), 19-mer (p31-49, 2245 Da; and p202-220, 2127 Da), and 12-mer (p57-68, 1453 Da)

118 ducing compound has an estimated mass of 226 Da, as determined by mass spectrometry, and is referred

119 Neutral loss (NL of 176, 194, 211, and 229 Da) and precursor ion (PI of m/z 141, 159, and 177, in p

120 Wt, 165.23 Da) were selected and identified in vitro using the syst

121 and covered a broad m/z scan range (67-2300 Da).

122 was observed with MW 188, 200, 204, and 232 Da.

123 provides a diagnostic mass difference of 24 Da and enables differentiation of double-bond positional

124 el with a fitted molar mass of 40180 +/- 240 Da (without Mg(2+) ions) or 41290 +/- 330 Da (with Mg(2+

125 e assays for the herbicide clomazone (MW 240 Da).

126 orm to detect ultralow-molecular-weight (244 Da) biomolecules at picomolar concentrations using a sta

127 With the Q1 window set to 20-25 Da, several precursors pass Q1 at the same time and are

128 olites (SigmaLMWP <250 Da and SigmaHMWP >250 Da) were calculated.

129 weight phthalate metabolites (SigmaLMWP <250 Da and SigmaHMWP >250 Da) were calculated.

130 unchanged low molecular weight cut off (~250 Da).

131 eight hyaluronan (LMW-HA, approximately 2500 Da) promotes endothelial cell (EC) barrier disruption an

132 of 0.50 nm, a molecular weight cutoff of 255 Da, and a reasonably high pure water permeability (A) of

133 chains provide the solubility of the 25 260 Da compound in common organic solvents.

134 educing the size of this analog by about 274 Da resulted in the resumption of the transport activity

135 For large peptides such as melittin (2845 Da), CID of the [M + 3H](3+), [M + 4H](4+), and [M + 5H]

136 ic and multimeric, ranging in mass from 2846 Da (melittin) to 150 kDa (Immunoglobulin G), and we cons

137 haracterized by the presence of a dimer (286 Da) proposed to be formed through the self-reaction of n

138 re modified with a glycan with a mass of 291 Da, while B. thailandensis flagellin protein was modifie

139 de ions have masses ranging from 231 to 2969 Da, Omega(He) of 89-616 A(2), and Omega(N(2)) of 151-801

140 The small molecule (<2k Da) sensitivity was found to increase with increased por

141 A peak at 703.3 Da was assigned as a sphingomyelin.

142 results in a molecular weight increase of 3 Da due to the incorporation of the (18)O atom to the sid

143 confirmed the protein mass and revealed a 30 Da mass difference between proteins from the two species

144 etween the two species that explained the 30 Da mass difference.

145 limit of EcChiP to be approximately 200-300 Da for small permeants that pass through by general diff

146 as drugs and metabolites ( approximately 300 Da) to intact proteins (25.6 kDa).

147 n be difficult especially for molecules >300 Da.

148 of small molecule fragment disulfides (< 300 Da) that could either activate or inhibit PDK1 by conjug

149 The adsorption and transport of a 300-Da molecular-mass hydrophobic ion at the Escherichia col

150 high pressures associated with using the 300-Da membrane, calibration in this small size range, accou

151 lest size range using AF4-ICPMS with the 300-Da membrane.

152 ear lossless transmission of ions up to 3000 Da in mass.

153 Ile residues and molecular masses up to 3000 Da.

154 in mobility and an increase in mass of 3145 Da.

155 LC-TOF/MS) revealed adducts of +162 and +324 Da to both the light and heavy chains, suggesting the pr

156 40 Da (without Mg(2+) ions) or 41290 +/- 330 Da (with Mg(2+) ions).

157 ymers and heteropolymers up to 12-mers (3400 Da).

158 th related glycans with a mass of 300 or 342 Da.

159 ctra (SWATH), which uses Q1 windows of 20-35 Da for data-independent fragmentation, was systematicall

160 the mass of the protein by approximately 350 Da.

161 Increasing PEG chain lengths from 350 Da-30 kDa in DSPE-PEG micelles, or increasing DSPE-PEG c

162 olecular-weight cutoff of approximately 3500 Da.

163 134 Da), and 56% for one protein (MW 51 358 Da).

164 f ca. 1.8 S and a molecular weight of 14 363 Da were determined for HD5(ox) at pH 7.0, supporting a t

165 ), probably as a result of its lower MW (366 Da) and favorable hydrophobicity (log P = 1.5).

166 linkage, with a single monosaccharide of 376 Da, which we show to be a pseudaminic acid derivative.

167 heptasaccharide, linked through the same 376-Da sugar to the protein backbone, also in O-linkage.

168 olecules (molecular weight approximately 380 Da) that compete with the peptide docking motif for bind

169 ] and gliadin peptides [33-mer (p56-88, 3900 Da), 19-mer (p31-49, 2245 Da; and p202-220, 2127 Da), an

170 g a 62-nucleotide (molecular weight = 20,395 Da) RNA-based aptamer, highly specific to the human IL-2

171 tural diversity, which ranges from the 803.4 Da thalassospiramide C to the 1291.7 Da thalassospiramid

172 98 (Ser198) was detected as parent ion 966.4 Da.

173 ecular mass varied considerably (4400-34,400 Da).

174 4-10 kDa), low molecular weight (LMW; 50-400 Da), and retained (R) fraction.

175 d on several mass ranges between 100 and 400 Da to characterize the functional groups of AOM species.

176 olar and higher molecular weight (HMW; > 400 Da) components abundant in crude and heavy fuel oils (HF

177 o detect low molecular weight (less than 400 Da) chemical and biological analytes under extremely dil

178 from more recent lots are roughly 200 to 400 Da lower than initial measurements made in the early 199

179 apparent diameter of about 1.4 nm with a 400-Da molecular mass cut-off.

180 II variant having an additional size of 420 Da.

181 of 100% for six proteins (MW 8759 to 68 425 Da), 96-98% for five proteins (MW 11 458 to 36 431 Da),

182 92% for three proteins (MW 15 971 to 36 431 Da), 80-87% for four proteins (MW 42 287 to 162 134 Da),

183 6-98% for five proteins (MW 11 458 to 36 431 Da), 92% for three proteins (MW 15 971 to 36 431 Da), 80

184 lycones (anthocyanidins) at 449, 419 and 433 Da.

185 tion of diagnostic neutral molecules CO2 (44 Da) and C2H6O2Si (90 Da) for aromatic carboxylic acids.

186 The 4467 Da peptide was identified as the C-terminal fragment of

187 h-molecular weight (molecular weight of >450 Da) products were observed under dry conditions with ind

188 d systematic iron coagulation of large (>450 Da), oxygen-rich, and highly aromatic DOM molecules of t

189 he development of low molecular weight (<450 Da) and nonpeptidic, single-digit micromolar mechanism-b

190 f 40 poly(8:2 FTAC-co-HDA) signals (911-4612 Da) were normalized to the signal intensity of a matrix-

191 ve and apparent permeabilities to TAMRA (467 Da), dextran (70 kDa), and LDL (2000 kDa), as well as hy

192 s specific to the antibiotic tobramycin (467 Da).

193 with a molecular weight cutoff (MWCO) of 470 Da.

194 d glycopeptides, producing an abundant Y1-48 Da ion instead (the nominal mass difference is given rel

195 ed for an anticipated DDA experiment (+/-0.5 Da).

196 m approximately 10(6) to approximately 10(5) Da).

197 Small molecules (<1,500 Da) were measured in urine collected from 469 patients w

198 s of structures in the mass range of 120-500 Da and correctly predicted approximately 70% of the indi

199 o the low molecular weight peptides (300-500 Da) recovered.

200 wed concentration of the 300-400 and 400-500 Da molecular weight range peptides in the KCl-F1 and KCl

201 nge of molecular weights from 4200 to 49 500 Da was obtained.

202 of peptides with molecular weights above 500 Da are needed to identify parameters that influence oral

203 imited to the mass range between 200 and 500 Da.

204 ecular weight (typically < approximately 500 Da) drugs can effectively permeate through intact stratu

205 rity of absorption was due to molecules >500 Da, and these contributed an increasing fraction of abso

206 he detection of lower-molecular-weight (<500 Da) biomolecules in highly diluted solutions is still a

207 low background in the low mass region (<500 Da), contrary to citrate stabilized AuNPs (citrate-AuNPs

208 QS is mediated through a small (<500 Da), non-proteinaceous, stable but unidentified 'stumpy

209 ects the pattern at lower masses (i.e., <500 Da).

210 unts of low molecular weight compounds (<500 Da).

211 thetically feasible organic molecules of 500 Da molecular weight or less, is estimated to contain ove

212 odifications of unknown masses up to +/- 500 Da.

213 orophores of a wide range of sizes: from 500-Da targeted polar molecules to 150,000-Da tagged immunog

214 rated with glucose (180 Da) and inulin (5000 Da) transdermal flux experiments, which showed greater p

215 ced cell-to-cell transport of the small (524 Da) fluorescent tracer 8-hydroxypyrene-1,3,6-trisulfonic

216 and had a molecular mass between 375 and 525 Da, which was 150 to 200 Da higher than for an average D

217 increases of molecular weights of 72 and 54 Da, respectively.

218 A 5447 Da antifungal peptide with an N-terminal sequence highly

219 ules with molecular weights ranging from 560 Da to 150 kDa.

220 re detected, including acetylation and a +57 Da species that could be the addition of a glyoxal moiet

221 ncentrate low molecular weight SMPs (MW< 580 Da) from effluents were optimized.

222 ified major product with a mass change of +6 Da.

223 he ratios of doublet signals with a static 6 Da mass difference in MALDI-MS and the change in relativ

224 ed glycerol clusters ( greater, similar10(6) Da, greater, similar +/- 100 charges) have been used to

225 accharide with molecular weight of 1.35x10(6)Da and a specific optical rotation of +64 degrees (c 1.0

226 ecular masses of more than approximately 600 Da is thought to be mediated by TonB-dependent, active t

227 ent mPTP, as neither Rhod-2 nor calcein (600 Da) were lost.

228 cular formulas of compounds with masses <600 Da in a complex mixture, such as SRFA.

229 tic WEOM molecules that are greater than 600 Da and the reduced binding force of orthophosphate to WE

230 Hs were found at molecular weights up to 600 Da.

231 ar weights of 4,062, 5,919, 7,777, and 9,634 Da, respectively.

232 rage monoisotopic molecular mass of 40074.64 Da was determined for pegfilgrastim.

233 nsition into the gas phase, evident from +64 Da and +128 Da signals that can be assigned to Hb carryi

234 al intensity of a matrix-sodium cluster (659 Da).

235 ins and even molecules the size of NADH (663 Da) will be retained during these tPTP.

236 exploits either generation of a signature 69 Da ion from Ile or formation of unique w-ions employing

237 l, co-oligomers with molar masses up to 6901 Da, ultralow molar mass dispersities (D </= 1.00002), an

238 e 803.4 Da thalassospiramide C to the 1291.7 Da thalassospiramide F, results from a complex sequence

239 cules with molecular weight smaller than 700 Da.

240 The E3B 14,700-Da protein (E3B-14.7K) inhibits STAT1 function by preven

241 les of intermediate size (approximately 7000 Da), which possess both the targeting and effector funct

242 of ca. 1.0 S and a molecular weight of 7079 Da, corresponding to a HD5(ox) dimer, were obtained.

243 tal ion current) chromatograms, using the 74 Da fragment ion, which originated from McLafferty rearra

244 spectrometrically obtained ion peaks at 760 Da for the PC standard.

245 l protein containing 71 amino acids (MW 7821 Da) with a reported analgesic potency greater than morph

246 t (R(2) = 0.98), varying from 163.9 to 923.8 Da.

247 can isotopologues with a mass increment of 8 Da over the natural products.

248 ion (-2 Da), and elimination of sulfate (-80 Da).

249 and the concomitant increase in the (n x 80 Da)-shifted phosphorylated peptide.

250 maximum peak widths of 1.19, 1.26, and 0.82 Da, respectively.

251 ealed the binding modes of these large (~850 Da) compounds in detail and explained the observed SAR,

252 of its inability to stabilize the large 854-Da substrate.

253 r large biomolecules such as ubiquitin (8565 Da), the amino acid sequence coverage increases from 39%

254 ed protein with a molecular weight of 25,897 Da, very near the observed molecular weight of the purif

255 utral molecules CO2 (44 Da) and C2H6O2Si (90 Da) for aromatic carboxylic acids.

256 Small marine molecules (500-900 Da) were also enriched in sulfate groups that appeared b

257 I, compounds with masses between 300 and 900 Da were detected by LDI.

258 gh molecular mass (e.g., between 400 and 900 Da) to less than 10 and in some cases, it was possible t

259 eable membrane pore for molecules up to 900 Da.

260 y identical fluorine atoms with a MW of 9082 Da.

261 on mutant has a molecular weight that is 919 Da less than that of the wild-type.

262 idneys within 24 h) based on a synthetic 970-Da organic molecule (CH1055).

263 ing studies, we also demonstrate that the 98 Da neutral loss occurs via gas-phase phosphoryl transfer

264 c acid (E) results in a mass shift of +0.984 Da.

265 ly we show that mammalian homologs of Ey and Da can functionally replace their Drosophila counterpart

266 red for the synergistic activation by Ey and Da.

267 ristic Df approximately 2.6, Dm > 1 mum, and Da </= 300 nm that form via the cluster-dense aggregatio

268 on characteristic image parameters: Daisne (Da) modified, based on signal-to-background ratio; Nestl

269 we show that a linked dimer of Daughterless (Da), the only Drosophila class I bHLH protein, activates

270 ks expression of the E protein Daughterless (Da), which heterodimerizes with bHLH proteins to activat

271 f the bHLH DNA-binding protein Daughterless (Da).

272 T2h, the complex T2h with HIE had decreased Da, increased De, perpendicular in both premyelination a

273 meter Dm </= 1 mum, and aerodynamic diameter Da </= 300 nm.

274 The apparent diffusivities (Da) of Rhodamine WT and bromide in sediments containing

275 extra-axonal axial and radial diffusivities (Da, De,// and De, perpendicular), to compare WM differen

276 Where extracellular signals repress emc, Da expression can increase.

277 mc lacks a basic DNA-binding domain, the Emc-Da heterodimer cannot bind to and regulate genomic targe

278 d by measuring dialyzable mineral fraction (%Da) resulting from in vitro gastrointestinal digestion.

279 antagonizes the synergistic activation from Da but not the Da-Da linked dimer with Ey.

280 d bromide in sediments containing 8-18% gas (Da,YE) were suppressed by 7-39% compared to the control

281 n, WHO, the China-Japan Friendship Hospital, Da Qing First Hospital.

282 In this issue of Immunity, Da Ros et al. (2017) report that, in experimental aortic

283 perpendicular, but no significant change in Da in multiple premyelination regions, indicative of exp

284 ster randomised trial in which 33 clinics in Da Qing, China-serving 577 adults with impaired glucose

285 015, 54 researchers from 10 countries met in Da Lat, Vietnam, to discuss advances in TBM.

286 In this issue, Da Silva and Kempenaers take on this task using an impor

287 Eli Lilly, Da Costa Family Foundation for Research in Breast Cancer

288 lar species show a size range of 2-6 million Da and have other similarities to hIAPP protofibrils, bu

289 One effect of Da sequestration is to relieve the repression on growth.

290 The measured ratios of Da,YE:Da,C were well within the range of ratios predicte

291 the widespread Emc expression that restrains Da expression, opposing bHLH-dependent differentiation w

292 compared to the control (no gas) sediments (Da,C).

293 We show that Da directly interacts with Ey and promotes Ey binding to

294 ed glucose tolerance who participated in the Da Qing Diabetes Prevention Study.

295 e synergistic activation from Da but not the Da-Da linked dimer with Ey.

296 Whereas gas voids in sediments reduce the Da for soluble species, they represent a shortcut for lo

297 41 resident physicians performing the Tubes (Da Vinci Intuitive Surgical, Sunnyvale, CA) simulator ex

298 turn, then forms a biochemical complex with Da.

299 rocheate (Emc), which forms heterodimer with Da, antagonizes the synergistic activation from Da but n

300 The measured ratios of Da,YE:Da,C were well within the range of ratios predicted by a