ライフサイエンスコーパス: Da

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

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

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

4 1355 Da) and proteins ( approximately 14 000 Da) are demonstrated, with approximately 1-2 orders of m

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

6 0-100 ppm) and molecular weight (1550-20,000 Da).

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

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

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

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

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

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

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

14 n of individual peaks at a spacing of 0.0034 Da at m/z 597 from a complex mixture of Canadian bitumen

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

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

17 y precisions of < s(Lab)> <= (0.15 +/- 0.01) Da (1sigma(x)).

18 with equal intensity and differing by 6.018 Da.

19 acJ1 had an exact molecular mass of 1881.036 Da.

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

21 rocessed heavy chain lysine residues (+128.1 Da), and loss of N-acetylglucosamine (GlcNAc; -203.1 Da)

22 tion post-translational modification (+162.1 Da), partially processed heavy chain lysine residues (+1

23 loss of N-acetylglucosamine (GlcNAc; -203.1 Da).

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

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

26 sting a deamidation at a NN motif for a LC+1 Da species, and inconclusive information for a LC+40 Da

27 ith quadrupole isolation at nominal mass (~1 Da).

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

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

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

31 spectrometers and a set of 9 reagents with 1 Da spacing between reporter ions for single dalton analy

32 clusters using optimized narrow windows (~10 Da) in scan mode, and standard full scan methods using h

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

34 on is notable both in its size (e.g., at 100 Da, it is one of the larger chemical PTMs) and in its ab

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

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

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

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

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

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

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

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

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

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

45 tides that mimic biomolecules upward of 1000 Da.

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

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

48 previously unreported protein of mass 10433 Da.

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

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

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

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

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

54 this, the use of a wide-isolation window (12 Da) to encompass the target analyte and the isotope stan

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

56 llows a ready overview of metabolites (<1200 Da) and potentially molecular routes to monitor food aut

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

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

59 -87% for four proteins (MW 42 287 to 162 134 Da), and 56% for one protein (MW 51 358 Da).

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

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

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

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

64 diagnostic pairs of fragment ions spaced 14 Da apart, thus enabling cyclopropane localization.

65 mass of (protonated) legiobactin is 437.140 Da.

66 glycans appear modified with a group of 144 Da, whose identity has yet to be confirmed.

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

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

69 sequencing of oligoporphyrans of up to 1500 Da and included the positioning of the methyl ether and

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

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

72 An increase in molecular weight from 1569 Da to 3740 Da resulted in a fivefold decrease in ET tran

73 er of high molecular weight compounds (>1569 Da) to purees ranged from 56% to 87%.

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

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

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

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

78 Moreover, diagnostic ion pair with 16 Da mass difference indicated localization of carbon-carb

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 hallenging, since the mass difference of -17 Da or -18 Da, when formed from Gln or Glu, respectively,

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

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

84 , since the mass difference of -17 Da or -18 Da, when formed from Gln or Glu, respectively, is not un

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

86 This 1899 Da molecule, termed FXII900, efficiently blocks FXIIa in

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 tion of N-hexanoyl-L-homoserine lactone (199 Da), a gram-negative bacterial infection biomarker.

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

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

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

100 cover a range of MWs (25 000-50 000 vs <200 Da) as well as carboxyl content (polygalacturonic acid (

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

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

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

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

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

106 ting equipment, a large search space of 2000 Da was constructed, and assignment performance was evalu

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 docyanine green (ICG) conjugated with a 2100 Da PEG molecule (ICG-PEG45) as a renal-tubule-secreted n

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

118 of bisphenol A, a low molecular weight (228 Da) target usually detectable only by indirect detection

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 Ls yields diagnostic fragment ions spaced 24 Da apart.

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 the PSE-like defect, and a mass shift of 27 Da suggested a possible connection with oxidation.

135 5 Da), retrorsine (351 Da), and estrone (270 Da), to demonstrate some important aspects of the workfl

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

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

138 the loss of the GlcNAcPHN unit (311 and 295 Da), and fucose cleavage followed the loss of the chitob

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

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

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

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

145 n be difficult especially for molecules >300 Da.

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

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

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

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

150 Ile residues and molecular masses up to 3000 Da.

151 s, WAFAPA (661.3224 Da) and MYPGLA (650.3098 Da).

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

153 cing produced two peptides, WAFAPA (661.3224 Da) and MYPGLA (650.3098 Da).

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

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

156 olecular-weight cutoff of approximately 3500 Da.

157 cryptospirolepine (505 Da), retrorsine (351 Da), and estrone (270 Da), to demonstrate some important

158 134 Da), and 56% for one protein (MW 51 358 Da).

159 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

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

161 ase in molecular weight from 1569 Da to 3740 Da resulted in a fivefold decrease in ET transfer for ra

162 BBB permeability of sodium fluorescein (376 Da), Alexa Fluor (643 Da), and fluorescent albumin (45 k

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

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

165 All laboratories achieved <s(Lab)> <= 0.4 Da.

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

167 98 (Ser198) was detected as parent ion 966.4 Da.

168 es, and inconclusive information for a LC+40 Da species.

169 a proline-to-histidine sequence variant (+40 Da) missed by classical MD analysis.

170 We define a metabolic range of 100-400 Da with 143 m/z features.

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

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

173 he inhibitors possess molecular weights <400 Da, log D(7.4) < 2.5, topological polar surface area < 7

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

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

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

177 II variant having an additional size of 420 Da.

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

179 92% for three proteins (MW 15 971 to 36 431 Da), 80-87% for four proteins (MW 42 287 to 162 134 Da),

180 6-98% for five proteins (MW 11 458 to 36 431 Da), 92% for three proteins (MW 15 971 to 36 431 Da), 80

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

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

183 FucGlcNAcPHN residue with a mass 457 and 441 Da from the parent ions.

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

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

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

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

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

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

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

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

192 ces two labeled peak clusters separated by 5 Da in MS(1) spectra that are detected as five isotopic p

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

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

195 ge, but in this work, membranes with 100-500 Da MWCO were evaluated for feasibility in concentrating

196 ely wide range of molecular weights (150-500 Da), polarities, and structural diversity were selected

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

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

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

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

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

202 occus pyogenes Cas9 (SpCas9) that weigh <500 Da and are cell permeable, reversible, and stable under

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

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

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

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

207 n for the ionization of small molecules <500 Da.

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

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

210 gether with the small molecular weight (~500 Da), the water solubility, the ease of functionalization

211 ple compounds, namely cryptospirolepine (505 Da), retrorsine (351 Da), and estrone (270 Da), to demon

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

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

214 The MA4 fraction (centered at ~550 Da) increased by 47%, and MA5 and MA7 fractions with hig

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

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

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

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

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

220 e-C47 product (molecular weight: 7.3 x 10(6) Da) was composed of the following monosaccharides: gluco

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

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

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

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

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

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

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

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

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

230 odium fluorescein (376 Da), Alexa Fluor (643 Da), and fluorescent albumin (45 kDA).

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

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

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

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

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

236 cules with molecular weight smaller than 700 Da.

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

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

239 med molecules by which dehydrodimers (MW 706 Da) are included.

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

241 etect the protein brazzein (his-tagged, 7445 Da) in all but two droplets.

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

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

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

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

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

247 species with apparent masses of 600 and 800 Da for WT and vma2Delta, respectively.

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

249 This analysis revealed that PAHs of 239-838 Da, containing few oxygenated species, comprise the soot

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

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

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

253 loss of 2-fluoro-1,3,2-dioxaborale (MW of 88 Da) only in the case of deprotonated, migrated acyl-gluc

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

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

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

257 meable membrane pore for molecules up to 900 Da.

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

259 it is confirmed that fennel nsLTP1 is a 9433 Da single polypeptide chain consisting of 91 amino acids

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

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

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

263 red for the synergistic activation by Ey and Da.

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

265 ic Health of the People's Republic of China, Da Qing First Hospital, China-Japan Friendship Hospital,

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

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

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

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

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

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

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

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

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

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

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

277 rexpression of each single orthologous gene (Da, Mef2, Ube3a, Zfh1, XNP) and in pairwise combinations

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

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

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

281 ial, started in 1986, in which 33 clinics in Da Qing, China, were randomly assigned to either be a co

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

283 015, 54 researchers from 10 countries met in Da Lat, Vietnam, to discuss advances in TBM.

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

285 0 or more times, a molecular mass >8 million Da, and a length >20 mum.

286 ith masses of ~500 (major) and ~1300 (minor) Da.

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

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

289 d monoisotopic mass to handle the off-by-one-Da prediction error.

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

291 g a nanomolar inhibitor ([Formula: see text] Da).

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

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

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

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

296 pneumonia (per clinician assessment) to the Da Nang Hospital for Women and Children were prospective

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