ライフサイエンスコーパス: Ch

1 Ch drastically reduced the water vapour permeability (WV

2 Ch-loading decreased the incorporation of [14C]Ar into t

3 logarithm of the odds (LOD) scores >or=2.0: Ch. 3q29, LOD 2.61 (P = 0.0003); Ch. 4q31.3, LOD 2.13 (P

4 es >or=2.0: Ch. 3q29, LOD 2.61 (P = 0.0003); Ch. 4q31.3, LOD 2.13 (P = 0.0009); and Ch. 7q31.31, LOD

5 [14C]Ch-labeled L1210 cells also accumulated ChOX when incuba

6 [Me-14C]Ch placed in the superfusion medium for 30 min during a

7 palmitoyl-2-oleoyl-phosphatidylcholine, [14C]Ch, and 3beta-hydroxy-5alpha-cholest-6-ene-5-hydroperoxi

8 d the critical RyR1 residues were 1924-2446 (Ch-21) and 2644-3223 (Ch-19).

9 sidues were 1924-2446 (Ch-21) and 2644-3223 (Ch-19).

10 e layered oxychalcogenides Sr4Mn3O7.5Cu2Ch2 (Ch=S, Se) is described.

11 (ChOx) and ascorbic acid oxidase (AAO) for a Ch sensor or ChOx, acetylcholinesterase (AChE), and AAO

12 ity of imaged cells responded only once to A Ch presentations.

13 studies have shown that chondroitinase ABC (Ch'ase ABC) digestion of inhibitory chondroitin sulfate

14 etylcholinesterase (AChE), and AAO for a ACh/Ch sensor was immobilized with bovine serum albumin by c

15 Studies on different ratio (ACh/Ch) revealed that 10:1, gave best overall response.

16 se of Carboxydothermus hydrogenoformans (ACS(Ch)), and truncated ACS(Ch) lacking its 317-amino acid N

17 ydrogenoformans (ACS(Ch)), and truncated ACS(Ch) lacking its 317-amino acid N-terminal domain.

18 HC3), a selective inhibitor of high affinity Ch uptake.

19 morphometric analysis demonstrates that all Ch. stipae stipae populations are one very variable subs

20 003); Ch. 4q31.3, LOD 2.13 (P = 0.0009); and Ch. 7q31.31, LOD 3.08 (P = 0.00008).

21 ely related KAS III clones (Ch KAS III-1 and Ch KAS III-2) from Cuphea hookeriana.

22 ions of RyR1 (chimera Ch-10 aa 1681-2641 and Ch-9 aa 2642-3770), were independently able to restore s

23 The limit of detection for ACh and Ch at the PB/AChE-ChO electrode was 5 microM or 9.5 fmol

24 f physiologically relevant levels of ACh and Ch in vivo.

25 In either AD and Ch, the incidence of TUNEL- or Klenow-positive nuclei di

26 In both AD and Ch, the individual positive nuclei were labeled with bot

27 ate [NA]/creatine [Cr], NA/choline [Ch], and Ch/Cr) and the presence of a characteristic lactate doub

28 inly 5alpha-OOH, transferred total ChOOH and Ch to liposomes in apparent first-order fashion, the rat

29 a clear interaction between fish gelatin and Ch, forming a new material with enhanced mechanical prop

30 g stimuli all produce elevated CS levels and Ch-ST activity and that CS levels and Ch-ST activity wer

31 ls and Ch-ST activity and that CS levels and Ch-ST activity were constitutively elevated in both papi

32 sterol-peptides without histidine (Ch-R5 and Ch-R3), and the luciferase expression level was comparab

33 tide conjugates (Ch-R5H5, Ch-R3H3, Ch-R5 and Ch-R5) were designed and synthesized, and their properti

34 BM/Ch mounted in the chamber exhibited no obvious damage ev

35 M/Ch, and that we can measure flux across BM/Ch preparations with an exposed surface area as small as

36 diffusion of a mixture of tracers across BM/Ch, and that we can measure flux across BM/Ch preparatio

37 Porcine BM/choroid (BM/Ch) was mounted in a modified Ussing chamber.

38 Both Ch KAS IIIs are expressed constitutively in all tissues

39 M and 10-2000 microM, respectively, for both Ch and ACh.

40 BrM/Ch cholesteryl esters respond to long-term storage diffe

41 BrM/Ch LLP do not resemble plasma lipoproteins in density pr

42 Peaks 1 and 2, native RPE, and fresh BrM/Ch were cholesteryl linoleate enriched and contained lit

43 A pooled fraction of LLP released from BrM/Ch (concentrated total LLP, density [d] < 1.24 g/mL frac

44 From BrM/Ch of 20 eyes of 10 donors aged >60 years, LLPs were rel

45 onors), cholesteryl ester composition of BrM/Ch, cornea, and sclera was determined by ESI/MS.

46 Preserved BrM/Ch was cholesteryl oleate-enriched, unlike sclera and co

47 spholipid repair metabolism in spur cells by Ch-loading, we compared the Ar metabolism of RBCs loaded

48 trand breaks was detected in AD, followed by Ch, and controls (C).

49 ChOOH transfer, 0.5 unit/mL (based on [(14)C]Ch transfer) increasing the first-order rate constant (k

50 These species were generated in [(14)C]Ch-labeled donor membranes [erythrocyte ghosts or unilam

51 However, in addition to binding C4b, Ch E binds C3b.

52 ed superinfection by sheep-derived Chandler (Ch) and 22L scrapie agents.

53 ains with Alzheimer neurofibrillary changes (Ch) from non-demented individuals, and controls (C) were

54 arboxydothermus hydrogenoformans chaperonin (Ch-CPN), is able to refold denatured proteins in an ATP-

55 stages in T-cell homing involve chemokines (Ch) and lymphocyte chemokine receptors (ChR) for vascula

56 uman (Hu), mouse (Mo), rabbit (Ra), chicken (Ch), and pig (P) and different cultured rabbit keratocyt

57 data show that two regions of RyR1 (chimera Ch-10 aa 1681-2641 and Ch-9 aa 2642-3770), were independ

58 The chimpanzee (Ch) E complement receptor type 1 (CR177) appears to be a

59 with increasing concentrations of chitosan (Ch) (100G:0Ch, 80G:20Ch, 70G:30Ch, 60G:40Ch and 0G:100Ch

60 friendly to the environment and (Li2Fe)ChO (Ch = S, Se) melt congruently; the latter is advantageous

61 (Li2Fe)ChO (Ch = S, Se) possess cubic anti-perovskite crystal struct

62 Both compounds (Li2Fe)ChO (Ch = S, Se) were tested as cathode materials against gra

63 des with the general composition (Li2Fe)ChO (Ch = S, Se, Te) are successfully synthesized.

64 ylcholine with the bile salts (BSs) cholate (Ch), glycocholate (GC), chenodeoxycholate (CDC), and gly

65 phosphatidylcholine (EYPC) +/- cholesterol (Ch) or rat liver microsomal membranes by monitoring self

66 phosphatidylcholine (EYPC) +/- cholesterol (Ch) vesicles under conditions in which one or both hemil

67 r protein-2 (SCP-2) facilitates cholesterol (Ch) and phospholipid (PL) transfer/exchange between memb

68 ich involves use of 14C-labeled cholesterol (Ch) as a "reporter" lipid.

69 an increased ratio of membrane cholesterol (Ch) to phospholipid, evidence of oxidative damage, and s

70 n-mediated transfer/exchange of cholesterol (Ch) between membranes has been widely studied, relativel

71 e implicated in the delivery of cholesterol (Ch) from internal or external sources to mitochondria (M

72 To accurately determine the cholesterol (Ch) distribution between mixed micelles and vesicles in

73 Acetylcholine (ACh) and choline (Ch) are important neuroactive molecules, yet detection o

74 We assessed acetylcholine (ACh) and choline (Ch) dynamics 2.5 h, 1, 4 and 14 days after cerebral cort

75 etection of acetylcholine (ACh) and choline (Ch) were realized at an applied potential of +750 mV vs

76 ed after an injection of deuterated choline (Ch) for determination of the rate of ACh synthesis.

77 nd-column amperometric detectors of choline (Ch) and acetylcholine (ACh) following separation by capi

78 of brain cells regulate the flux of choline (Ch) into membrane or neurotransmitter biosynthesis was i

79 e oxidase (ChOx) in the presence of choline (Ch).

80 E hydrolyzes acetylcholine (ACh) to choline (Ch) which in turn interacts with AuQC@BSA-AChE and quenc

81 tylaspartate [NA]/creatine [Cr], NA/choline [Ch], and Ch/Cr) and the presence of a characteristic lac

82 (including N-acetylaspartate [NAA], choline [Ch], creatine and phosphocreatine [Cr]) were obtained in

83 of the mechanosensory cilium of chordotonal (Ch) neurons.

84 rived from mono- and disubstituted chrysenes Ch (5- methyl- 3, 2-methoxy- 19, 2-methoxy-11-methyl- 20

85 isolate two closely related KAS III clones (Ch KAS III-1 and Ch KAS III-2) from Cuphea hookeriana.

86 ow that the notion of executive competition (Ch.

87 tine (Cr) plus choline-containing compounds (Ch) (NAA/[Cr + Ch]) ratios were determined.

88 rtate (NAA) to choline-containing compounds (Ch) and creatine plus phosphocreatine (CR) (NAA/[Cr + Ch

89 amphiphilic cholesterol-peptide conjugates (Ch-R5H5, Ch-R3H3, Ch-R5 and Ch-R5) were designed and syn

90 emically and periodontally healthy controls (Ch).

91 the control subjects, ipsilateral NAA/(Cr + Ch) levels were reduced in every part of hippocampal tis

92 The NAA/(Cr + Ch) ratio in the ipsilateral hippocampus was significant

93 In patients, whole-brain NAA/(Cr + Ch) ratio outside the hippocampus was significantly lowe

94 psilateral hemisphere in patients, NAA/(Cr + Ch) ratio was significantly lower than that in control s

95 gions revealed trends toward lower NAA/(Cr + Ch) ratios in many areas of the ipsilateral and, to a le

96 anteroposterior (AP) difference in NAA/(Cr + Ch) values was found in both ipsilateral and contralater

97 portional reduction in ipsilateral NAA/(Cr + Ch) was greatest in voxels from anterior hippocampal reg

98 eduction of 17%, and contralateral NAA/(Cr + Ch) was reduced by about 10%.

99 reatine plus phosphocreatine (CR) (NAA/[Cr + Ch]) in the anterior as compared with the posterior part

100 choline-containing compounds (Ch) (NAA/[Cr + Ch]) ratios were determined.

101 esterase cDNA from C. hookeriana, designated Ch FatB2, has been identified, which, when expressed in

102 In the disubstituted Ch derivatives 20 and 21, the 2-methoxy overrides the 5-

103 anes [erythrocyte ghosts or unilamellar DMPC/Ch (1.0:0.8 mol/mol) liposomes] by means of dye-sensitiz

104 ariable region exon from Cmu to a downstream Ch (for example, Cgamma, Cepsilon or Calpha), thereby sw

105 itch regions that flank Cmu and a downstream Ch, followed by fusion of the broken switch regions.

106 sed in conjunction with different downstream Ch genes, each having a unique biological activity.

107 2.10 and 2.25 for the trihydroxy BSs, i.e., Ch and GC, and 2.85 and 2.75 for the dihydroxy BSs, i.e.

108 investigate the mechanism of these effects, Ch uptake studies were performed with and without hemich

109 One element (Ch-M16) showed 99.1% sequence identity with the SINE-R.C

110 the chicken beta-globin insulator element, (Ch beta GI)(2), in mice.

111 Exogenous and endogenous Ch and ACh were measured in the rat brain in vivo.

112 CS) and activity of its biosynthetic enzyme, Ch-ST, during multistage carcinogenesis in mouse skin.

113 Epidermal Ch-ST activity was also elevated during wound healing.

114 anges the heavy chain constant region exons (Ch) expressed with a given variable region exon from Cmu

115 s did not significantly alter Pf of EYPC +/- Ch or rat liver microsomal membranes.

116 2 mM TDC) did not alter Pf of equimolar EYPC/Ch membranes.

117 ocholate and tauroursodeoxycholate, for EYPC/Ch vesicles, and at lower temperatures.

118 Finally, Ch-ST activity was significantly elevated in the epiderm

119 3 mM) and ACh (K(M)=0.59+/-0.07 mM), and for Ch the highest ascorbic acid blocking capacity (97.2+/-2

120 fd3F regulates genes for Ch-specific axonemal dyneins and TRPV ion channels, whic

121 fit the observed data and yielded a K(m) for Ch uptake of 5 microM into cholinergic structures and 72

122 ACh (5.8+/-0.3 muA mM(-1)), linear range for Ch (K(M)=0.52+/-0.03 mM) and ACh (K(M)=0.59+/-0.07 mM),

123 Selectivity for Ch and ACh relative to potential interferences and pharm

124 ical endogenous ACh (D0ACh), endogenous free Ch (D0Ch), deuterium-labeled Ch (D4Ch), and ACh synthesi

125 The Ch FatB2 differs from Ch FatB1, another Cuphea hookeriana thioesterase reporte

126 We assayed LAT in RBC membranes from Ch-loaded RBCs, using [14C]arachidonoyl CoA as precursor

127 pe reversal has been restricted to the GeCh (Ch=S, Se, Te) family of glasses, with very high Bi or Pb

128 Ch, 70G:30Ch, 60G:40Ch and 0G:100Ch, gelatin:Ch), and some of their main physical and functional prop

129 The other gene (Ch-Tbx6L), together with chick T, appears to mark primit

130 We have isolated an en gene, Ch-en, from a Chaetopterus cDNA library.

131 One of these novel genes (Ch-TbxT) becomes restricted to the axial mesoderm lineag

132 with cholesterol-peptides without histidine (Ch-R5 and Ch-R3), and the luciferase expression level wa

133 collagenases from Clostridium histolyticum (Ch), and neutral protease (NP) from Bacillus thermoprote

134 entified including, LDH (Ra, Ch), G3PDH (Hu, Ch), pyruvate kinase (Ch), Annexin II (Ch), and protein

135 bacterium Carboxydothermus hydrogenoformans (Ch-CooA).

136 (Hu, Ch), pyruvate kinase (Ch), Annexin II (Ch), and protein disulfide isomerase (Ch).

137 The model also predicts that an increase in Ch uptake within cholinergic neurons, reported to be ass

138 cating that a larger number of RN neurons in Ch'ase ABC-treated cats had axons below the lesion level

139 idine ring with respect to the heme plane in Ch-CooA.

140 unt for the inhibited phospholipid repair in Ch-loaded intact RBCs in vitro and in spur cell anemia R

141 mized) red nucleus (RN) neurons were seen in Ch'ase ABC-treated (23%) compared with control-treated c

142 ation [4,27,32], would significantly inhibit Ch uptake into all other cells, and would account for th

143 trong tendency to display acute interligand, Ch-M-Ch, bond angles that are often well below 90 degree

144 in II (Ch), and protein disulfide isomerase (Ch).

145 H (Ra, Ch), G3PDH (Hu, Ch), pyruvate kinase (Ch), Annexin II (Ch), and protein disulfide isomerase (C

146 endogenous free Ch (D0Ch), deuterium-labeled Ch (D4Ch), and ACh synthesized from D4Ch (D4ACh) were me

147 Seventeen different plants from Tai Lake (Ch: Taihu), China were heated to 600 degrees C at a rate

148 .8 nM in the presence of Na(+), K(+), Li(+), Ch(+), and Tris(+) and that the catalytic efficiency of

149 Like Ch desorption, ChOOH desorption from donor membranes was

150 These findings support the notion that like Ch itself, 7alpha-OOH can be transported to/into Mito of

151 incorporation of [14C]Ar into total lipids (Ch-loaded, 1,113 +/- 48 pmol/10(10) RBCs; control, 1,525

152 tendency to display acute interligand, Ch-M-Ch, bond angles that are often well below 90 degrees .

153 The 2-methoxy-Ch 19 is protonated at C-1 to give two conformationally

154 +/- 0.46 microM ACh and 0.33 +/- 0.09 microM Ch, and response times were <1 s.

155 Ch fluctuations, on top of which micromolar Ch increases occurred during periods of theta activity i

156 ssion, using a non-essential minichromosome, Ch(16), in fission yeast.

157 generated in a non-essential minichromosome, Ch(16), using the Saccharomyces cerevisiae HO-endonuclea

158 (P = .006) and children (P < .001), and NAA/Ch ratios were significantly lower in infants (P = .001)

159 strate measurements of spontaneous nanomolar Ch fluctuations, on top of which micromolar Ch increases

160 However, only 22L and not Ch prevented FU-CJD infection, even though both scrapie

161 g SENCAR mice, we determined the activity of Ch-ST in normal epidermis, in tumor promoter-treated epi

162 The increased levels of CS and activity of Ch-ST in tumor promoter-treated epidermis were accompani

163 ncreases in CS levels and in the activity of Ch-ST were found in nearly all of the papillomas and squ

164 The results indicated that the addition of Ch caused significant increase (p<0.05) in the tensile s

165 to determine whether intraspinal delivery of Ch'ase ABC, following T10 hemisections in adult cats, en

166 re accurately represents the distribution of Ch in biliary lipid aggregates.

167 is proposed that the amplified expression of Ch FatB2 in the embryo provides the hydrolytic enzyme sp

168 a segment polarity pattern of expression of Ch-en in the ectoderm, as is observed in arthropods.

169 mode near ~90 cm(-1) in the ferrous form of Ch-CooA is suggested to contain a large component of hem

170 y coherence spectrum of the CO-bound form of Ch-CooA shows a strong vibration at ~230 cm(-1) that is

171 specific DNA binding to the CO-bound form of Ch-CooA was also investigated, and although the CO rebin

172 f the ferric, ferrous, and CO-bound forms of Ch-CooA in order to compare the protein-induced heme dis

173 1) in both the ferrous and CO-bound forms of Ch-CooA is consistent with coupling of the heme doming d

174 ters led to significantly elevated levels of Ch-ST activity and of CS.

175 with Ch relative to phospholipid by means of Ch-rich, phospholipid-Ch sonicates.

176 ATP levels nor in the kinetic properties of Ch kinase (E.C. 2.7.1.32) or Ch acetyltransferase (ChAT)

177 combination with efficient CE separation of Ch and ACh provides a new sensitive and selective strate

178 t higher N/P ratios, and the minimum size of Ch-R5H5/DNA complexes was 180 nm with zeta potential of

179 related to the enhanced thermal stability of Ch-CooA and that there is a smaller (time dependent) til

180 y little is known about the translocation of Ch oxidation products, particularly hydroperoxide specie

181 also suggest a mechanism for upregulation of Ch-ST in skin tumors involving activation/upregulation o

182 eurons account for 60% of observed uptake of Ch at physiologic Ch concentrations, even though they re

183 c properties of Ch kinase (E.C. 2.7.1.32) or Ch acetyltransferase (ChAT) (E.C.2.3.1.7).

184 response was linear up to 100 microM ACh or Ch.

185 s thermoproteolyticus rokko (thermolysin) or Ch (ChNP).

186 Whereas parent Ch 1 is protonated at C-6/C-12, 3 is protonated at C-6 (

187 f total (unresolved) ChOOH along with parent Ch, whereas the latter allowed measurement of individual

188 In particular, Ch-R5H5 condensed DNA into smaller nanoparticles than Ch

189 tes of formula M(ChAr)2 (M = Si, Ge, Sn, Pb; Ch = O, S, or Se; Ar = bulky m-terphenyl ligand, includi

190 the PY-Ch E/M ratio during fusion of DOPC/PE/Ch small unilamellar vesicles showed a transient increas

191 rated model biles [3-10 g/dL, 10 mol percent Ch, taurocholate (TC)]/([TC + egg yolk phosphatidylcholi

192 romatography, only 19 percent +/- 2 percent (Ch/EYPC = 1.0) and 22 percent +/- 2 percent (Ch/EYPC = 1

193 Ch/EYPC = 1.0) and 22 percent +/- 2 percent (Ch/EYPC = 1.5) of total Ch were found in the correspondi

194 ospholipid by means of Ch-rich, phospholipid-Ch sonicates.

195 60% of observed uptake of Ch at physiologic Ch concentrations, even though they represent fewer than

196 derived from autoxidation of optically pure Ch-15-HpETE by atmospheric pressure chemical ionization-

197 esumably resulting from redistribution of PY-Ch from the curved lamellar leaflets to coexisting HMs t

198 ability of cholesterol 1-pyrenebutyrate (PY-Ch) and other pyrene-containing fluorescent probes to re

199 Our results suggest that PY-Ch provides a tool for monitoring fusion intermediates t

200 und a significant (>150%) increase in the PY-Ch E/M in the hexagonal phase relative to the lamellar p

201 The time course of the PY-Ch E/M ratio during fusion of DOPC/PE/Ch small unilamell

202 sterol-peptide conjugates (Ch-R5H5, Ch-R3H3, Ch-R5 and Ch-R5) were designed and synthesized, and thei

203 lic cholesterol-peptide conjugates (Ch-R5H5, Ch-R3H3, Ch-R5 and Ch-R5) were designed and synthesized,

204 ssed proteins identified including, LDH (Ra, Ch), G3PDH (Hu, Ch), pyruvate kinase (Ch), Annexin II (C

205 control AcylCn, 169 +/- 31 pmol/10(10) RBCs; Ch-loaded AcylCn, 196 +/- 35 pmol/10(10) RBCs; P = .0012

206 immunoglobulin heavy-chain constant region (Ch) gene with another.

207 In the A region, Ch-en is also expressed in a small group of mesodermal c

208 In the B region, Ch-en is initially expressed broadly in the mesoderm tha

209 Thus, following SCI, Ch'ase ABC may facilitate axonal growth at the spinal le

210 In all segments, Ch-en is expressed in a small set of segmentally iterate

211 sDNA oligonucleotides having a Chi sequence (Ch+) or a single base change that abolishes the Chi sequ

212 At later stages, Ch-en is expressed in distinct patterns in the three seg

213 As cells leave the primitive streak, Ch-Tbx6L becomes restricted to the early paraxial mesode

214 ty that we see today in the aphid subspecies Ch. stipae stipae may in the future lead to speciation a

215 he activity of cholesterol sulfotransferase (Ch-ST) is increased during squamous differentiation of k

216 xidation caused by the oxidant chloramine-T (Ch-T) without altering other functional characteristics.

217 ondensed DNA into smaller nanoparticles than Ch-R3H3 at higher N/P ratios, and the minimum size of Ch

218 We conclude that Ch-loading of RBC membranes results in inhibition of LAT

219 ole-mount in situ hybridization reveals that Ch-en is expressed throughout larval life in a complex s

220 Here, we show that Ch'ase ABC enhanced crossing of a peg walkway post-SCI a

221 The Ch FatB1 has a broad substrate specificity with strong p

222 The Ch FatB2 differs from Ch FatB1, another Cuphea hookerian

223 The Ch-en transcript is initially detected in a small number

224 The Ch-T effect is mediated specifically by M536, M712 and M

225 break (DSB) repair, form nuclear foci at the Ch region in the G1 phase of the cell cycle in cells und

226 r in the BM to Ch direction than that in the Ch to BM direction for only two of the tracers: cytosine

227 o be an alternatively spliced product of the Ch CR1 gene transcript.

228 t membranes in which approximately 4% of the Ch had been peroxidized, giving mainly 5alpha-OOH, trans

229 ca napus) seeds overexpressing either of the Ch KAS IIIs driven by napin.

230 igh [Ca2+]i and biophysical modelling of the Ch-T effect on steady-state activation implicates a decr

231 g with substitution of bulkier groups on the Ch atom of the adsorbate.

232 n of the channel and essentially removes the Ch-T sensitivity, suggesting that M712 and M739 may be p

233 On paternal inheritance, the (Ch beta GI)(2) was also hypomethylated and displayed str

234 On maternal inheritance, the (Ch beta GI)(2) was hypomethylated and displayed full chr

235 Thus, Ch E CR177, one-third of the size and with only a single

236 ignificantly (P < 0.05) greater in the BM to Ch direction than that in the Ch to BM direction for onl

237 rcent +/- 2 percent (Ch/EYPC = 1.5) of total Ch were found in the corresponding biles.

238 /- 5 percent (TC/(TC + EYPC) = 0.7) of total Ch were found in vesicles (Ch/EYPC molar ratios = 1.0 an

239 as observed to have high sensitivity towards Ch (6.3+/-0.3 muA mM(-1)) and ACh (5.8+/-0.3 muA mM(-1))

240 marker of trauma, while 14 days after trauma Ch uptake from blood was enhanced in and around the trau

241 ed formation of vesicles in ultracentrifuged Ch-unsaturated model bile (cholesterol saturation index

242 Unconjugated Ch and CDC (pKa values of approximately 5.0) showed pron

243 ely 8 times greater than that for unoxidized Ch.

244 Moreover, using Ch. stipae stipae and Stipa species occurrences, as well

245 ) = 0.7) of total Ch were found in vesicles (Ch/EYPC molar ratios = 1.0 and 1.3, respectively).

246 ystems containing only micelles or vesicles, Ch-supersaturated model biles [3-10 g/dL, 10 mol percent

247 rifugation systematically elevates vesicular Ch, possibly because of induced shifts in lipids between

248 s showed a progressive increase in vesicular Ch to 41 percent after 13 hours.

249 5 hours after ultracentrifugation, vesicular Ch decreased to 31 percent, thus approaching the initial

250 that ethanol and ethanethiol both adsorb via Ch-H dissociation at 310 K, where Ch (chalcogen) is eith

251 adsorb via Ch-H dissociation at 310 K, where Ch (chalcogen) is either S or O.

252 d is expressed throughout the plant; whereas Ch FatB2 is specific for 8:0/10:0-ACP and its expression

253 lutaminase I activity did not correlate with Ch-ST activity in these mice.

254 mpared the Ar metabolism of RBCs loaded with Ch in vitro with that of control cells incubated in auto

255 odel system that loads the RBC membrane with Ch relative to phospholipid by means of Ch-rich, phospho