ライフサイエンスコーパス: subfraction

1 re concentrated in the HDL3 than in the HDL2 subfraction.

2 e negative than the intermediate density LDL subfraction.

3 h slightly more in the HDL2 than in the HDL3 subfraction.

4 trolled vesiculation caused by the cytosolic subfraction.

5 17e relative to the intermediate density LDL subfraction.

6 activity manifested by the cytosolic protein subfraction.

7 raction rather than in the caveolae of the B subfraction.

8 ation with semivolatile organic carbon (OC1) subfraction.

9 gulates TRAF2 abundance in the mitochondrial subfraction.

10 d (PhiF) were subsequently measured for each subfraction.

11 d almost completely absent in the CD114(pos) subfraction.

12 negatively correlated with total HDL and HDL subfractions.

13 ontrol CETP-facilitated lipid flux among HDL subfractions.

14 in response to copper exceeded that of other subfractions.

15 located state in Western blots of neutrophil subfractions.

16 by measurement of cholesterol in lipoprotein subfractions.

17 eins from two entire proteome pools or their subfractions.

18 recovered from gels of membrane and content subfractions.

19 +-ATPase [ATPase]) were used to identify the subfractions.

20 one concentrations in plasma and lipoprotein subfractions.

21 s but also including dendritic cells in both subfractions.

22 lowest density (chylomicrons and Sf 100-400) subfractions.

23 presenilin-1, and it is found in particulate subfractions.

24 and protein content of liver plasma membrane subfractions.

25 Rab1a was detected in the immunoadsorbed subfractions.

26 phospholipid, apolipoprotein and cholesterol subfractions.

27 ming (CLA(+) ) and non-skin-homing (CLA(-) ) subfractions.

28 ctions but not for ion mobility-measured HDL subfractions.

29 negligible role in efflux to HDL3b and HDL3c subfractions.

30 l and vanadyl porphyrins into polarity-based subfractions.

31 about the metabolism and composition of LDL subfractions.

32 ano-clay complexes were separated into humic subfractions.

33 , as the major components of the most active subfractions.

34 The large HDL subfraction (10.5-14.5 nm) increased at 8 wk (+346 +/- 1

35 9 +/- 2.1 mg/dl, P < 0.0001; delta bilirubin subfraction 16.7 +/- 4.0% versus 9.2 +/- 1.8%; P < 0.002

36 terol (HDL-C), apolipoprotein A-I, and HDL-C subfractions 2 (HDL2-C) and 3 (HDL3-C).

37 ) parameters from SPC(1), SPC(2), and SPC(3) subfractions; 2 N-acetyl signals from alpha-1-acid glyco

38 his effect was limited to changes in the HDL subfraction 3 (HDL3) (P for interaction=0.04).

39 elease by exogenous high density lipoprotein subfraction 3.

40 l) and high density lipoprotein2 cholesterol subfraction (3.2 mg/dl) at follow-up.

41 re high-density lipoprotein particle (HDL-P) subfractions across groups, and Cox proportional hazards

42 e not determined whether any measures of LDL subfractions add incremental benefit to traditional risk

43 ived CD45(-)Lin(-) nonhematopoietic cellular subfraction after a reperfused myocardial infarction in

44 several LDL and very-low-density lipoprotein subfractions, albeit with a pattern of association that

45 to accumulate plutonium (Pu) in a colloidal subfraction and is hypothesized to contain cutin-like ch

46 proteins distribute unevenly between the two subfractions and antigens involved in signal transductio

47 00 proteins identified in different cellular subfractions and cell cycle stages of MCF7/MCF10A cells,

48 tested for association with response of LDL subfractions and non-HDL-C to rosuvastatin or placebo fo

49 ants influence statin-induced changes in LDL subfractions and non-HDL-C.

50 nvestigated whether detailed measures of LDL subfractions and other lipoproteins can be used to asses

51 rtant insights into the roles of lipoprotein subfractions and particle sizes in preventing coronary a

52 n by immunoblotting of liver plasma membrane subfractions and the morphological demonstration at both

53 ling to determine associations between HDL-P subfractions and time to death or major adverse cardiac

54 and determine the relationship between TRLP subfractions and whole-body insulin sensitivity, hepatic

55 ze, fractionated into cytosolic and membrane subfractions, and analyzed by sucrose gradient, SDS-PAGE

56 ein B, lipoprotein(a), glucose, insulin, HDL subfractions, and indicators of lipoprotein metabolism (

57 Arsenite and total inorganic arsenic in each subfraction are converted to arsine sequentially by hydr

58 Lipoprotein subfractions are biomarkers for the early diagnosis of c

59 re stable for metabolites, while lipoprotein subfractions are equally stable for both types of matric

60 ur aims were to determine which HDL particle subfractions are most efficient in mediating cellular ch

61 Small, dense HDL subfractions are the most efficient mediators of cholest

62 l likely controls a discrete PtdIns(3,5)P(2) subfraction as the high pressure liquid chromatography-m

63 transport of plasma apoB within 21 distinct subfractions as separated by anti-apoC-III and anti-apoE

64 and increased rates of oxidation in both LDL subfractions, as measured by the conjugated diene format

65 n particle concentration was the most likely subfraction associated with CAD risk (marginal inclusion

66 centration was identified as the most likely subfraction associated with PAD risk (marginal inclusion

67 lerotic cardiovascular disease, and distinct subfraction-associated genes suggest possible difference

68 oncentrations of apoB-containing lipoprotein subfractions; at either A3GALT2 or NRG4, with markedly r

69 e fraction, is thereby resolved into a bound subfraction (B), which consists primarily of PVs or cave

70 with (a) total phospholipids in lipoprotein subfractions; (b) apolipoproteins B100, A1, and A2 in di

71 G responses induced by BCSP70, BCSP100, and subfraction BCSP100-B vaccines only.

72 to identify key differences in plasma HDL-P subfractions between patients with HF with reduced eject

73 study evaluated the incremental value of LDL subfractions beyond traditional cardiovascular risk fact

74 several LDL and very-low-density lipoprotein subfractions but not for ion mobility-measured HDL subfr

75 (E(0)) and concentrations of the asphaltene subfractions (C) are used to calculate adsorption dynami

76 Certain tumor cell subfractions can self-renew and repopulate the heterogen

77 e turnover or distribution of an active STAR subfraction cannot be excluded.

78 0.001), small low-density lipoprotein (LDL) subfraction cholesterol (-13.9%; 95% CI: -23.2%, -3.49%;

79 We investigated differences in lipoprotein subfraction cholesterol distribution and insulin resista

80 Myoglobin, creatine kinase-MB subfraction (CK-MB) and troponin I (cTnI) were measured

81 holesterol, E-selectin (P < 0.0001), and LDL subfraction composition (cholesterol [LDL-I and LDL-II],

82 ein particle (TRL-P, HDL-P, LDL-P) sizes and subfraction concentrations (large/very large TRL-P, larg

83 The A1c1 subfraction contained both stable and unstable hemoglobi

84 The A1c2 subfraction contained only unstable hemoglobin complexes

85 detected in an inner mitochondrial membrane subfraction containing components of the mtBER complex.

86 of subfractions, of which only one, a small subfraction containing only 10% of the entire membrane,

87 Up to 1000 mug L(-1) of an OSPW subfraction containing only alicyclic NA, and considered

88 Subfractions containing only the purified phospholipids

89 mpared for chromatographically purified CLSE subfractions containing the complete mix of phospholipid

90 Subfraction content of membrane and cytosolic subunits o

91 Additional analyses of mitochondrial subfractions demonstrated that the PET309-c-myc fusion p

92 The subfractions designated BCSP100-A through BCSP100-D puri

93 (HDL) profile, whereas humans have two major subfractions designated HDL(2) and HDL(3).

94 ation of lower fasting and postprandial TRLP subfractions despite insulin resistance in black compare

95 nd CD133- cells, but tumorigenicity of these subfractions did not differ significantly and aCGH revea

96 ent in response to TKI therapy compared with subfractions displaying primitive and quiescent signatur

97 The increase in this lipoprotein affects the subfraction distribution, with a specific increase in al

98 ons, whereas others are restricted to the NB subfraction (e.g., angiotensin converting enzyme, podoca

99 short tubules of 40 x 60 nm, segregating in subfractions either positive for active zone or synaptic

100 One circulating subfraction, electronegative LDL (LDL(-)), which is incr

101 file of proteins in the postsynaptic density subfraction elicited by a cocaine challenge in daily coc

102 ity measurements revealed that the light LDL subfractions exhibit a surface charge at pH 8.6 that is

103 ollection of a given number of its aliquots (subfractions) exposed to the solid sample.

104 t, fetal liver CFU-C was CD45(+), and only a subfraction expressed CD41, demonstrating down-regulatio

105 The 2D system separated hemoglobin into five subfractions, four of which contained glycated hemoglobi

106 our laboratory, we have isolated a caveolar subfraction from rat lung endothelium and we have partia

107 Homogenates and subfractions from macaque parotid glands were able to ph

108 s but instead eluted intact in A1c1 and A1c2 subfractions from nonglycated affinity fractions.

109 drug targets and ApoB-containing lipoprotein subfractions had diverse associations with atherosclerot

110 and ABCA1-dependent efflux to individual HDL subfractions has not been systematically studied.

111 Measures of low-density lipoprotein (LDL) subfractions have been proposed as an independent risk f

112 The alpha and beta heavy chain subfractions have binding parameters similar to those of

113 etary protein source on lipoprotein particle subfractions, have not been extensively evaluated.

114 most marked efficiency with small, dense HDL subfractions (HDL3b and HDL3c).

115 c focusing separated hemoglobin A1c into two subfractions identified as A1c1 and A1c2.

116 ng high-density lipoprotein particle (HDL-P) subfractions impact atherogenesis, inflammation, and end

117 as capable of substituting for the cytosolic subfraction in promoting the scission of coated buds fro

118 ycated apolipoprotein B across different LDL subfractions in healthy controls, patients with type 2 d

119 In the largest analysis of HDL-P subfractions in HF to date, derangements in HDL-P subfra

120 uncontrolled activity in a cytosolic protein subfraction, in which it is separated from regulatory co

121 tribution of L5-the most electronegative LDL subfraction-in total LDL (i.e. L5%).

122 icrons, very-low-density-lipoproteins (VLDL) subfractions, intermediate-density lipoproteins (IDLs),

123 The i.v. transplantation of these subfractions into immune-deficient mice established that

124 Thus, the GM3-enriched subfraction, involved in cell adhesion and capable of se

125 Hb is not involved; rather a membrane-bound subfraction is responsible for channel activation.

126 d (4) pretreatment of an electronegative LDL subfraction isolated from hypercholesterolemic human pla

127 matic, hypercholesterolemic patients yielded subfractions L1-L5 in increasing electronegativity.

128 emia patients undergoing hemodialysis into 5 subfractions (L1-L5) according to charge by using fast-p

129 30) was chromatographically resolved into 5 subfractions (L1-L5) with increasing electronegativity.

130 (versus placebo control) on lipid and lipid subfraction levels in the Diabetes Prevention Program ra

131 ining self-renewing leukemia-initiating cell subfractions (LICs).

132 onated heparin (UFH), its 16-, 8-, and 6-mer subfractions, low-molecular-weight heparin (LMWH), and t

133 Specific subfractions made superoxide in the presence of NADPH by

134 ride-rich lipoproteins, IDL and specific LDL subfractions may have a role in atherogenesis disproport

135 idence as to the extent to which LDL and HDL subfraction measurements improve clinical assessment of

136 omponent analysis was used to group multiple subfraction measurements into three distinct and statist

137 These novel kinetic studies of HDL subfraction metabolism are compelling in-vivo data that

138 k of) the majority component of the membrane subfraction (mol wt approximately 40,000).

139 The contact site subfraction morphology is consistent with the biochemica

140 primarily of PVs or caveolae, and a nonbound subfraction (NB) enriched in vesicles derived from the p

141 A membrane subfraction obtained from secretion granules isolated fr

142 two unknown spectra detected in a mutagenic subfraction of a water sample from the Elbe River using

143 mouse embryonic stem cells (ESCs) exhibit a subfraction of cells expressing uncharacteristically low

144 ifferentiated EpiSC cultures contain a major subfraction of cells with reversible early primitive str

145 ree screen and included a small but discrete subfraction of cellular ATP-binding cassette family E1 (

146 Furthermore, a subfraction of cellular HDAC1 is acetylated after associ

147 al hDna2 revealed that it colocalized with a subfraction of DNA-containing mitochondrial nucleoids in

148 The unique ability of a subfraction of E46K and wild type alpha-synuclein protof

149 Remarkably, a subfraction of fibrils showed immunoreactivity to PrPSc-

150 Activity is provided by a subfraction of h2, h2B, that is structurally constrained

151 port the hypothesis that apoC-III may mark a subfraction of HDL that is associated with higher risk o

152 indicative of a selective process in which a subfraction of HMG-14 is preferentially acetylated.

153 sed on these observations, we suggest that a subfraction of hnRNP U, as a component of the Pol II hol

154 We demonstrated that a subfraction of human hnRNP U is associated with the Pol

155 Here we report that at least a subfraction of human telomerase RNA and individual resid

156 AF2 abundance increases in the mitochondrial subfraction of ischemia/reperfusion-modeled hearts; and

157 Similarly, a subfraction of KSHV-positive cultured PEL cells and of K

158 to examine whether the most electronegative subfraction of low-density lipoprotein (LDL), L5, is cor

159 tiating component is L5, the electronegative subfraction of low-density lipoproteins (LDLs), which wa

160 eta protein is constitutively expressed in a subfraction of melanoma cell lines, and around 30% of al

161 A subfraction of oligo(dT) (15%) moved over 10-fold more s

162 ized to the basolateral plasma membrane of a subfraction of outer medullary collecting duct cells.

163 A subfraction of particulate PIKfyve resisted nonionic det

164 as a defined in vivo organization in which a subfraction of proteins and LPS are embedded in stable d

165 hat actin filaments may spatially organize a subfraction of synaptic vesicles with respect to the cal

166 ation signals result in the maintenance of a subfraction of Tax as "active" protein.

167 ins in a postsynaptic density (PSD)-enriched subfraction of the NAc from cocaine-trained animals were

168 ate that plastochromanol-8 originates from a subfraction of the non-photoactive pool of plastoquinone

169 ough 20-2000 mug L(-1) of an esterifiable NA subfraction of the OSPW NA concentrate did induce expres

170 lar kinases or is simply binding a misfolded subfraction of the proteins.

171 regation of a metastable, disease-associated subfraction of the proteome.

172 ria-associated particles represented a small subfraction of the SR.

173 s suggested that the tracer binds a distinct subfraction of the total Hsp90 pool, which is significan

174 ency-associated nuclear protein LANA1, and a subfraction of these cells undergo spontaneous lytic cyc

175 A low density subfraction of these vesicles (MV1), highly enriched in

176 given chronic exposure to nPM, a nano-sized subfraction of urban air pollution.

177 and brain regional responses to a nanosized subfraction of urban traffic ultrafine particulate matte

178 The relatively small subfraction of virions that carry both functional and no

179 of apo C-III in ultracentrifugally isolated subfractions of apo B-containing lipoproteins.

180 Two subfractions of asphaltenes having contrasting affinitie

181 ined the risk of VTE in relation to baseline subfractions of HDL (HDL(2) and HDL(3)) and apolipoprote

182 es of defined size and composition, isolated subfractions of human plasma HDL, cell lines stably expr

183 ow-density lipoprotein (LDL) cholesterol and subfractions of IDL and LDL in group B.

184 tical to enrich the sample to be analyzed in subfractions of interest.

185 Subfractions of LDL and HDL defined by differences in pa

186 lysates, cytosolic, microsomal, and nuclear subfractions of MLE cells.

187 The most immature subfractions of PHPs, CD34++CD38- and CD34+2CD38+ FL cel

188 l cyclase activity is present in low-density subfractions of plasma membrane from a cell type (S49 ly

189 we examined the channel-forming activity of subfractions of Pseudomonas aeruginosa OprF, which was s

190 Employing antisera against various subfractions of rat liver mitochondria (mitoplast, inner

191 Molecular subfractions of raw (UP), blanched (BP) and roasted (RP)

192 ll-length and several C-terminally truncated subfractions of RBP4 among 468 women who developed CHD a

193 PCs, purified grafts of CD62L(-) or CD49e(+) subfractions of Sca-1(+)lin(-) cells, previously shown t

194 These subfractions of the classic collector efficiency were up

195 he myofibrillar, mitochondrial and cytosolic subfractions of the soleus.

196 non-HDL particles, LDL particles, and select subfractions of very-low-density lipoprotein particles a

197 the women (n = 7), plasma chylomicrons and 3 subfractions of VLDLs were separated by cumulative rate

198 separate the inner membrane into a number of subfractions, of which only one, a small subfraction con

199 Two membrane subfractions, one enriched in GM3 ganglioside and the ot

200 gradient separation, two predominant culture subfractions, one with potent suppressor function and an

201 ain distinguishable from caveolin-containing subfraction or caveolae.

202 Prediction was not enhanced by HDL-C density subfractions or apolipoproteins (apo) A-I or B.

203 ed with statin response for >/= 1 of the LDL subfractions or non-HDL-C, 20 single-nucleotide polymorp

204 nthin in plasma, chylomicrons, and each VLDL subfraction (P < 0.05), but did not significantly affect

205 e variables were HDL2-C (P<0.001), large HDL subfraction (P<0.001), or HDL size (P=0.001).

206 re analyzed by (1)H NMR, and 112 lipoprotein subfraction parameters; 3 supramolecular phospholipid co

207 lesterol, and triglycerides) and lipoprotein subfraction particle concentrations and size in 2993 par

208 exercise-induced improvements in lipoprotein subfraction particle size, and reduction in visceral adi

209 Of the leukocyte subfractions, PlGF stimulated monocyte chemotaxis (P <.0

210 highly electronegative, mildly oxidized LDL subfraction present in human hypercholesterolemic but no

211 neous containing dynamically interconverting subfractions primed for either of the two ICM lineages,

212 d-frequency questionnaire) and a lipoprotein subfraction profile (nuclear magnetic resonance spectros

213 The lipoprotein subfraction profile was evaluated in relation to diet in

214 e intervention to measure cumulative RNA and subfraction protein synthesis.

215 without additional apolipoproteins or lipid subfractions, provide substantial CHD prediction, with m

216 Both subfractions quantitatively increased in the presence of

217 ated in the NB (plasmalemma proper-enriched) subfraction rather than in the caveolae of the B subfrac

218 These subfractions resemble, in low buoyant density, structure

219 giocytes and isolated cholangiocyte membrane subfractions, respectively.

220 the most likely causal major lipoprotein and subfraction risk factors for PAD and CAD.

221 Markers for mitochondrial subfractions ruled out the possibility of eNOS associati

222 Extra-large HDL subfractions seem to be drivers in the relationship with

223 In contrast, the caveolin-containing subfraction, separated by anti-caveolin antibody, contai

224 The GM3-enriched subfraction, separated by anti-GM3 monoclonal antibody D

225 enera with very-low-density and high-density subfractions, serum lipid measures, glycolysis-related m

226 noanalysis of mitochondria and mitochondrial subfractions shows that a membrane-bound protein is pres

227 om phospholipids in high-density lipoprotein subfractions (SPC-A) together with a phospholipid compon

228 ing of the composition and metabolism of LDL subfractions strengthens the association between sdLDL a

229 resistance exercise mediates muscle protein subfraction synthesis.

230 Routine use of clinically available LDL subfraction tests to estimate cardiovascular disease ris

231 Furthermore, the heparin subfraction that binds to the HIP peptide with high affi

232 ring further segregated into a TNFRSF12A(hi) subfraction that comprised about ten per cent of KRT5(+)

233 munofluorescence analyses identified a small subfraction that escapes loss and relocalizes to splicin

234 tein[a]) is a highly atherogenic lipoprotein subfraction that may contribute to polygenic risk of cor

235 This is the same subfraction that was also found to bind oriV and TrfA to

236 er-soluble matrix and KCl-insoluble membrane subfractions that contained respectively 47- and 54-kDa

237 We found three subfractions that possessed different expression pattern

238 5-93% of all peptides are unique to a single subfraction, the combination of TAPEG and FASP offers an

239 Regarding lipid subfractions, the concentration of extra-large HDL parti

240 thods are available for quantitation of this subfraction, there is considerable room for improvement.

241 Z mitochondria and plastids, and of plastid subfractions (thylakoids and envelopes), using HPLC high

242 o E-selectin, calcium-dependent binding of a subfraction to L-selectin and to P-selectin, and calcium

243 ty of HDL, and a demonstrated ability of HDL subfractions to bind LTIP, we examined whether LTIP migh

244 Differences in the capacities of HDL subfractions to remove cellular cholesterol may explain

245 compounds and their hydrophobic/hydrophilic subfractions to the ROS (reactive oxygen species)-genera

246 303 +/- 116 nM) and realignment of LDL lipid subfractions toward a less atherogenic profile [decrease

247 on to estimate the genetic correlation of 77 subfraction traits with traditional lipid profile and id

248 on downstream of Rac, and the phosphorylated subfraction translocates to endothelial cell-cell juncti

249 sity lipoprotein and low-density lipoprotein subfractions), triglycerides, hemoglobin and albumin wer

250 further characterizes this high Pu affinity subfraction using electrospray ionization Fourier transf

251 30.0+/-5.6 kg/m(2), we measured lipoprotein subfractions using nuclear magnetic resonance.

252 g the plastic adherent stroma-vascular (aSV) subfraction (using 3 h culture) that contains mostly adi

253 we compared the action of the CD34+KDR+ cell subfraction vs. the CD34+KDR- subset.

254 The GM3/c-Src-enriched membrane subfraction was characterized by (i) maintenance of GM3-

255 ta-carotene in chylomicrons and in each VLDL subfraction was lower after ingestion with the meal cont

256 d a fraction of these peptides; only another subfraction was targeted by effector/memory T cells that

257 eir G(0) (G(0)CD34(+)) or G(1) (G(1)CD34(+)) subfractions, was detected in the BM of recipient mice,

258 ations, and on concentrations of lipoprotein subfractions, was investigated.

259 centrations in the LDL fraction and the HDL2 subfraction were higher in the late follicular than in t

260 ion, and proteins of the bound and non-bound subfractions were analyzed by Western blotting.

261 change chromatography (SCX), selected sample subfractions were analyzed with conventional and microfl

262 However, two subfractions were associated with significant (P < 0.05)

263 nerve terminals and nerve terminal membrane subfractions were examined by EM after incubations with

264 Other LDL subfractions were generally not associated with cardiova

265 Differences from placebo in lipoprotein subfractions were greatest for the lutein + DHA group (4

266 In a subgroup of the Rotterdam Study, lipid subfractions were identified by the Nightingale biomarke

267 actions in HF to date, derangements in HDL-P subfractions were identified that were more severe in HF

268 Genes relevant to prioritized lipoprotein subfractions were identified with transcriptome-wide ass

269 Lipid subfractions were measured by NMR.

270 A total of 65 lipoprotein main and subfractions were predictable with high accuracy, Q(2) o

271 Four subfractions were separated from BCSP100 by anion-exchan

272 e primary assays and in all four glycated 2D subfractions were significantly different between HGI gr

273 las relatively more abundant in the purified subfraction where Pu had been observed than in the crude

274 ing, there was a shift in the light membrane subfractions where ROS production was highest.

275 istributed about evenly between the B and NB subfractions, whereas others are restricted to the NB su

276 APAF may represent a small polyreactive IgG subfraction which also contains antinuclear and anti-DNA

277 ool of Raf-1 constitute a membrane-localized subfraction which could also be inactivated with PTP-1B.

278 partially characterized the proteins of this subfraction which include an apparently caveolae-specifi

279 tography, we identified a conditioned medium subfraction, which specifically displays these highly pr

280 and cell cloning, we could not obtain a male subfraction with a regeneration capacity similar to that

281 nd SLE patients represents a polyreactive Ig subfraction with concomitant anti-DNA, anti-Sm, and anti

282 es as well as the strong correlations of the subfractions with each other and with standard lipid and

283 obing protein blots of endoplasmic reticulum subfractions with radio-iodinated calreticulin showed sp

284 nd transfer from HDL to water vary among HDL subfractions with the larger and more buoyant species ex

285 Fractionation of X2C gave a subfraction, with enhanced alpha-glucosidase inhibitory

286 the factors that control the distribution of subfractions within the spectrum of apolipoprotein B-con