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 ation with semivolatile organic carbon (OC1) subfraction.

3 e negative than the intermediate density LDL subfraction.

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

5 trolled vesiculation caused by the cytosolic subfraction.

6 17e relative to the intermediate density LDL subfraction.

7 activity manifested by the cytosolic protein subfraction.

8 raction rather than in the caveolae of the B 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 ontrol CETP-facilitated lipid flux among HDL subfractions.

13 in response to copper exceeded that of other subfractions.

14 located state in Western blots of neutrophil subfractions.

15 by measurement of cholesterol in lipoprotein subfractions.

16 eins from two entire proteome pools or their subfractions.

17 recovered from gels of membrane and content subfractions.

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

19 one concentrations in plasma and lipoprotein subfractions.

20 ctions but not for ion mobility-measured HDL 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 negligible role in efflux to HDL3b and HDL3c subfractions.

25 and protein content of liver plasma membrane subfractions.

26 Rab1a was detected in the immunoadsorbed subfractions.

27 l and vanadyl porphyrins into polarity-based subfractions.

28 about the metabolism and composition of LDL subfractions.

29 ano-clay complexes were separated into humic subfractions.

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

31 negatively correlated with total HDL and HDL subfractions.

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

33 9 +/- 2.1 mg/dl, P < 0.0001; delta bilirubin subfraction 16.7 +/- 4.0% versus 9.2 +/- 1.8%; P < 0.002

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

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

36 elease by exogenous high density lipoprotein subfraction 3.

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

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

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

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

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

42 00 proteins identified in different cellular subfractions and cell cycle stages of MCF7/MCF10A cells,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

64 The A1c1 subfraction contained both stable and unstable hemoglobi

65 The A1c2 subfraction contained only unstable hemoglobin complexes

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

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

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

69 Subfractions containing only the purified phospholipids

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

71 Subfraction content of membrane and cytosolic subunits o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 Specific subfractions made superoxide in the presence of NADPH by

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

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

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

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

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

114 The contact site subfraction morphology is consistent with the biochemica

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

116 A membrane subfraction obtained from secretion granules isolated fr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 A subfraction of particulate PIKfyve resisted nonionic det

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 Subfractions of LDL and HDL defined by differences in pa

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

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

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

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

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

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

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

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

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

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

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

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

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

169 ain distinguishable from caveolin-containing subfraction or caveolae.

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

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

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

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

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

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

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

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

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

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

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

181 Both subfractions quantitatively increased in the presence of

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

183 These subfractions resemble, in low buoyant density, structure

184 giocytes and isolated cholangiocyte membrane subfractions, respectively.

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

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

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

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

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

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

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

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

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

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

195 We found three subfractions that possessed different expression pattern

196 5-93% of all peptides are unique to a single subfraction, the combination of TAPEG and FASP offers an

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

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

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

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

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

202 303 +/- 116 nM) and realignment of LDL lipid subfractions toward a less atherogenic profile [decrease

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

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

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

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

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

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

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

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

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

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

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

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

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

216 Other LDL subfractions were generally not associated with cardiova

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

218 Four subfractions were separated from BCSP100 by anion-exchan

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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