ライフサイエンスコーパス: Ch

1 Ch drastically reduced the water vapour permeability (WV

2 Ch(2)Cl(2)-extracts of B. loyo, C. lebre, L. edodes, M.

3 Ch(2)Cl(2)-extracts were more active against bacteria an

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

5 Ch-ZnO@gal films possess significant antibacterial poten

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

7 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

8 [14C]Ch-labeled L1210 cells also accumulated ChOX when incuba

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

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

11 ed oxychalcogenides Sr(2)MnO(2)Cu(1.5)Ch(2) (Ch = S, Se) into Cu-deintercalated phases where antifluo

12 ol-2-ylidene); Tipp=2,4,6-iPr(3) C(6) H(2) ; Ch=Se, Te) by treatment of NHC-stabilized aluminum dihyd

13 e fabrication of highly conductive Au@MoS(2)/Ch nanocomposite for sensitive electrochemical detection

14 n the present detection technique, Au@MoS(2)/Ch was used as a conductive matrix and anti-glutamate an

15 n a molybdenum disulfide/chitosan (Au@MoS(2)/Ch) nanocomposite.

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

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

18 f layered oxychalcogenides Sr(2)MnO(2)Cu(1.5)Ch(2) (Ch = S, Se) into Cu-deintercalated phases where a

19 lated phases where antifluorite type [Cu(1.5)Ch(2)](2.5-) slabs collapsed into two-dimensional arrays

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

21 We have designed a Ch derivative where a benzophenone moiety is linked to C

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

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

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

25 s/ECM in the LHAad using chondroitinase ABC (Ch-ABC) blocked the expression of cue-induced reinstatem

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

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

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

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

30 Additionally, Ch. vulgaris also showed a higher micronutrient content.

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

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

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

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

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

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

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

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

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

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

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

42 nclude Chromosome (Ch.) 1p loss/1q gain, and Ch.

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

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

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

46 By combining biomass from A. maxima and Ch. vulgaris in a ratio of 6:1, we can fulfill the recom

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

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

49 terial obtained from persons with the APOE3 (Ch) and PSEN1 (E280A) variants showed fewer vascular amy

50 persons who were heterozygous for the APOE3 (Ch) variant in a kindred with a high prevalence of autos

51 of PSEN1 (E280A) carriers without the APOE3 (Ch) variant, among whom the median age at the onset was

52 (E280A) who were heterozygous for the APOE3 (Ch) variant, the median age at the onset of cognitive im

53 the PSEN1 (E280A) variant but not the APOE3 (Ch) variant.

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

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

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

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

58 Both Ch KAS IIIs are expressed constitutively in all tissues

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

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

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

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

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

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

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

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

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

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

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

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

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

72 interactions in isochalcogenourea catalysis (Ch=O, S, Se) is investigated.

73 The importance of 1,5-O...chalcogen (Ch) interactions in isochalcogenourea catalysis (Ch=O, S

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

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

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

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

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

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

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

81 Chitosan (Ch) and zinc oxide nanoparticles loaded gallic-acid film

82 arabic, sodium alginate (Alg) and chitosan (Ch).

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

84 The mass ratios of chitosan (Ch) to tripolyphosphate (TPP), 1:1, for unloaded ChNPs a

85 perties of DES integrated into the chitosan (Ch) matrix.

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

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

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

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

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

91 Cholesterol (Ch) is an integral part of cell membrane, where it is pr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Chromophobe (Ch) renal cell carcinoma (RCC) arises from the intercala

112 copy-number alterations include Chromosome (Ch.) 1p loss/1q gain, and Ch.

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

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

115 ow that the notion of executive competition (Ch.

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

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

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

119 emically and periodontally healthy controls (Ch).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 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.

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

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

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

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

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

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

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

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

145 2 mM TDC) did not alter Pf of equimolar EYPC/Ch membranes.

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

147 ide nanoparticles loaded gallic-acid films, (Ch-ZnO@gal) have been prepared aiming for their exploita

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

149 (TPP), 1:1, for unloaded ChNPs and 1:1:1 for Ch to TPP to CEO, for CEO-loaded ChNPs (CEO-ChNPs), were

150 3 mM) and ACh (K(M)=0.59+/-0.07 mM), and for Ch the highest ascorbic acid blocking capacity (97.2+/-2

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

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

153 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),

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

155 of solid-liquid equilibrium (SLE) data for [Ch]Cl + acetic acid, SLE, and DES density and viscosity

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

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

158 established that the most efficient HA from Ch occurs at C7, although HA from C4 by peroxyl radicals

159 Conversely, HA from Ch positions other than the thermodynamically preferred

160 er begin with hydrogen abstraction (HA) from Ch by a reactive free radical.

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

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

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

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

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

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

167 r dechlorophyllization using chloroform (GLE-Ch) were prepared.

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

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

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

171 bacterium Carboxydothermus hydrogenoformans (Ch-CooA).

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

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

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

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

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

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

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

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

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

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

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

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

184 .8 nM in the presence of Na(+), K(+), Li(+), Ch(+), and Tris(+) and that the catalytic efficiency of

185 Like Ch desorption, ChOOH desorption from donor membranes was

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

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

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

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

190 +/- 0.46 microM ACh and 0.33 +/- 0.09 microM Ch, and response times were <1 s.

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

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

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

194 ier aluminum chalcogenides [(NHC)Al(Tipp)-mu-Ch](2) (NHC=IiPr (1,3-diisopropyl-4,5-dimethylimidazol-2

195 ctions and synaptic pruning (decreasing NAA, Ch, Cr, Glx) in posterior regions, support age-related i

196 aturation (increasing FA and increasing NAA, Ch, Cr concentrations accompanying advancing age) in fro

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

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

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

200 data demonstrate the significance of 1,5-O...Ch interactions in enantioselective catalysis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 This mirrors a specific orientation of Ch within a confined environment.

217 In humans, oxidation of Ch is commonly linked to various pathologies like Alzhei

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

219 f reactants is crucial for the reactivity of Ch.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

238 60% of observed uptake of Ch at physiologic Ch concentrations, even though they represent fewer than

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

258 trointestinal levels of cholesterol sulfate (Ch-S) compared with wild-type B. thetaiotaomicron-coloni

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

282 /- 5 percent (TC/(TC + EYPC) = 0.7) of total Ch were found in vesicles (Ch/EYPC molar ratios = 1.0 an

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

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

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

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

287 ely 8 times greater than that for unoxidized Ch.

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

289 ) = 0.7) of total Ch were found in vesicles (Ch/EYPC molar ratios = 1.0 and 1.3, respectively).

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

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

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

293 5 hours after ultracentrifugation, vesicular Ch decreased to 31 percent, thus approaching the initial

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

295 ) maxima (A. maxima) and Chlorella vulgaris (Ch. vulgaris) are among the approved microalgae and cyan

296 of oil globules in the W/O/W(Alg) and W/O/W(Ch) was d(23) = 6.56 +/- 0.09 and d(23) = 5.33 +/- 0.01

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

298 o be relevant in biological membranes, where Ch, polyunsaturated fatty acids, and numerous oxidizing

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

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

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

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