ライフサイエンスコーパス: lipid

1 s are formed from their corresponding diacyl lipids.

2 he integrated roles of ATP6AP1, glycans, and lipids.

3 on precursor for polyphosphoinositide (PPIn) lipids.

4 rst time among the minor components of these lipids.

5 s, constituting up to 50% of plasma membrane lipids.

6 intestinal tract to aid in the absorption of lipids.

7 r levels of alpha-tocopherol (6.7 mg/100 g), lipids (23.11 g/100 g, manly oleic and linoleic acids),

8 e-glycine dipeptide lipid classes, including lipid 430 and lipid 654, are produced by the periodontal

9 ptide lipid classes, including lipid 430 and lipid 654, are produced by the periodontal pathogen Porp

10 Of the 5024 detected lipids, 95% showed significant age-dependent concentrati

11 stis mutant synthesizing an adjuvant form of lipid A (monophosphoryl lipid A, MPLA) displayed increas

12 rocrystalline tyrosine (MCT), monophosphoryl lipid A (MPLA) and calcium phosphate (CaP) used less fre

13 Addition of a C16 fatty acid (palmitate) to lipid A by the outer membrane acyltransferase enzyme Pag

14 e death as a result of septic shock, and its lipid A core is the target of polymyxin antibiotics(3,4)

15 phism to the sequence present in Ypt and Ye, lipid A isolated from a Yp pagP+ strain synthesized two

16 an adjuvant form of lipid A (monophosphoryl lipid A, MPLA) displayed increased biogenesis of bacteri

17 is asymmetry by regulating the biogenesis of lipid A, the conserved and essential anchor of LPS.

18 In addition, 7j prevents oleic acid-induced lipid accumulation in hepatoma cells.

19 mediators of ER stress pathway in promoting lipid accumulation remain poorly understood.

20 multisubunit protein machines extract these lipids after their synthesis is completed at the inner m

21 For lipids, an increase in milk (total and low-fat) or yogur

22 Analysis of total body lipid and cholesterol levels were also investigated, wit

23 n measures of lipoprotein subclasses; and 81 lipid and fatty acids ratios.

24 brosis and inflammation, as well as improved lipid and glucose metabolism.

25 aque phenotype characterized by an increased lipid and macrophage content, plaque size, and pro-infla

26 me had no effect (P > 0.05) on dry-aged beef lipid and protein oxidative stabilities and proteolysis

27 The high lipid and protein oxidative stability of long-term froze

28 's lipid phosphatase activity or both PTEN's lipid and protein phosphatase activities.

29 eriority of COOH-NHMe (IV) in detecting more lipid and protein species compared to commercially avail

30 lyses revealed a marked reduction in storage lipids and an increase in membrane phospholipids, sugges

31 he process of migration to metabolize stored lipids and fuel invasive migration.

32 fuse across cell envelopes and interact with lipids and intracellular nucleic acids.

33 ts were observed, elevated levels of neutral lipids and phospholipids resemble previously reported ef

34 The higher oxygenation altered methionine, lipid, and purine metabolism, and inhibited quiescence,

35 nelline, formic acid, hydroxymethylfurfural, lipids, and gamma-butyrolactone also contributed to scor

36 case that spectral measurements of proteins, lipids, and glucose in the short-wavelength IR region, p

37 of the scavenger receptor CD36, accumulated lipids, and used fatty acid oxidation (FAO) instead of g

38 A myriad of transient, nanoscopic lipid- and protein-based interactions confer a steady-st

39 A hallmark of AMD is the overproduction of lipid- and protein-rich extracellular deposits that accu

40 natural variability range for most meibomian lipids (app. +/- 15% of the Mean), these differences in

41 Specific species of these lipids appear to be more negative toward insulin sensiti

42 Lipids are basic cellular constituents playing essential

43 Ionizable cationic lipids are critical components involved in nanoparticle

44 These lipids are endogenous ligands for the nuclear receptor P

45 Water and lipids are key participants in many biological processes

46 s a key process utilized to catabolize these lipids as an energy source.

47 lted in the increased oxidative stability of lipids as confirmed by low PV, TBARS and FFA.

48 The functional roles of the lipid asymmetry of biomembranes are attracting increasin

49 detergent-based protocol for scrambling the lipid asymmetry of liposomes and maybe cells without com

50 e a very valuable tool to study functions of lipid asymmetry.

51 large unilamellar liposomes showing a stable lipid asymmetry.

52 oscopy, the 3D configuration of proteins and lipids at intermediate steps can only be resolved with c

53 Lipids at wheat and rye DL stabilized A-W interfaces imp

54 tions to maximise protein integration into a lipid bilayer and the oligomerisation of the protein int

55 w insertion of hydrophobic moieties into the lipid bilayer core.

56 e BsYetJ (or TMBIM6) structure embedded in a lipid bilayer is uncharacterized, let alone the molecula

57 (4)) or greigite (Fe(3)S(4)), enveloped by a lipid bilayer membrane, produced by magnetotactic bacter

58 ies effect originates from a looser swelling lipid bilayer structure due to the adsorption and electr

59 eptor SpA was attached to BioPE-DOTAP binary lipid bilayer tethered on alkane thiol molecular cushion

60 ristics of transient pores on a patch of the lipid bilayer that is strengthened by an elastic meshwor

61 ts of the bulky transport domain through the lipid bilayer.

62 nd exhibit selective proton transport across lipid bilayers at a rate similar to those of natural pro

63 ingle-channel electrical recording in planar lipid bilayers in conjunction with protein engineering,

64 MBP-mediated assembling of lipid bilayers proceeds in two steps, with a slow second

65 ractions contribute to lateral clustering on lipid bilayers.

66 equire the presence of cholesterol to pierce lipid bilayers.

67 A lipid binding groove and clusters of conserved residues

68 re we report that, in mammalian cells, NF2's lipid-binding ability is critical for its function in ac

69 we suggest how changes in the association of lipid-binding caveolar proteins upon flattening of caveo

70 e demonstrate that SWG directly binds to the lipid-binding cavity of OSBP.

71 by interacting with lipid membranes (termed lipid-binding loop [LBL]).

72 scovered that Fabp5, an abundant cytoplasmic lipid-binding protein found in brain endothelial cells,

73 ting BAR surfaces are sequestered and the PX lipid-binding sites are occluded.

74 suggesting changes in the Kennedy pathway of lipid bioassembly.

75 led means and prevalences were estimated for lipid biomarkers from >=2005.

76 mic reticulum (ER), the main cellular hub of lipid biosynthesis and the entry site for the secretory

77 A), 2-monoacylglycerol (2-MAG), and membrane lipid biosynthesis and transport during nodule developme

78 il composition involve the overexpression of lipid biosynthetic enzymes, but how these enzymes are as

79 hese measurements suggest that Zn(2+) caused lipid blebbing by decreasing the area per lipid on the s

80 onformational properties of the protein when lipid bound.

81 l tissues using quantitative results of both lipid C=C location and sn-position isomers.

82 t, we demonstrated that genetic induction of lipid cacostasis in the CNS of normal mice was associate

83 on of a 1:1 protein-lipid complex, where the lipid cannot be displaced by detergent from the highly p

84 The transfer of WTA from lipid carriers to PG, catalyzed by the LytR-CpsA-Psr (LC

85 re downregulated while those associated with lipid catabolism and chitin turnover were significantly

86 These results indicate that AHL4 suppresses lipid catabolism by repressing the expression of specifi

87 Thus, the autophagic process participates in lipid catabolism that supports OxPHOS in AML cells.

88 a substrate buffer or reservoir to modulate lipid, catecholamine, and iron availability.

89 h protonated ions of the species of the same lipid class with two additional CH(2) and three double b

90 ation of authentic standards belonging to 12 lipid classes and helps to assign 133/58 lipid features

91 hingolipids (notably GM(3) gangliosides) and lipid classes previously associated with cardiometabolic

92 The serine-glycine dipeptide lipid classes, including lipid 430 and lipid 654, are pr

93 r CCS and HILIC retention time for 22 and 23 lipid classes, respectively, were trained using the larg

94 y assembles with lipid vesicles into peptide/lipid coaggregates that resemble amyloid fibrils in some

95 II results in the formation of a 1:1 protein-lipid complex, where the lipid cannot be displaced by de

96 Coenzyme Q (Q (n) ) is a vital lipid component of the electron transport chain that fun

97 ds, and low-molecular-weight metabolites; 98 lipid composition and particle concentration measures of

98 The lipid composition of arteries in lung tissue samples fro

99 However, the influence of lipid composition on caveolae surface stability is not w

100 fspring, with a positive correlation between lipid concentrations and survival under OA.

101 ososomes were constructed by rosmarinic acid-lipid conjugates which not only work synergistically wit

102 enriched batches or affect the moisture and lipid content during processing and/or culinary cooking.

103 The results show that while total neutral lipid content was unchanged relative to age-matched cont

104 copy was used to probe de novo intracellular lipid content.

105 er self, even though their diets had similar lipid contents.

106 enabled the generation of a large predicted lipid database with 145,388 entries.

107 mmation and remarkably blocked the increased lipid deposition and the atherogenic gene expression in

108 V1 worms with low levels of phosphoinositide lipids display an enhanced response to capsaicin, wherea

109 mitochondrial alanine metabolism to membrane lipid diversity, which further sensitizes tumours to met

110 the MS/MS(ALL) lipidomic dataset, identified lipids driving the clustering of the groups.

111 Lipid droplet (LD) formation from the endoplasmic reticu

112 ablation of EHD2 in mice leads to increased lipid droplet size in fat tissue.

113 rotein expression and redistributed PLIN2 to lipid droplet stores in type I fibres.

114 Lipid droplets (LDs) are neutral lipid storage organelle

115 Selective breakdown of lipid droplets (LDs) by autophagy (also called lipophagy

116 ol-loaded macrophages-including in cytosolic lipid droplets of SMCs.

117 ct that TGs and SEs are the typical cargo of lipid droplets suggests that these organelles could be c

118 In Caco-2/TC7 cells, the number of lipid droplets was identical for both milk types, while

119 Here, we addressed the role of lipids during morphogenesis of the rhabdomere, the micro

120 dynamics of lipid-lipid, lipid-protein, and lipid-dye interactions with single-molecule, nanoscale r

121 These results indicate that lipids engage in specific, trimer-stabilizing interactio

122 ty to RAS and with RBD causing local anionic lipid enrichment that enhances the overall affinity betw

123 The local lipid environment is known to affect the structure, stab

124 The lipid extraction step is time consuming and often employ

125 phyromonas gingivalis and can be detected in lipid extracts of diseased periodontal tissues and teeth

126 id vesicles produced from the individual HIE-lipid extracts.

127 latform provided 230 metabolite measures: 51 lipids, fatty acids, and low-molecular-weight metabolite

128 12 lipid classes and helps to assign 133/58 lipid features in positive-/negative-ion mode from mouse

129 Turning to the lipid flippase MurJ, we find that addition of the natura

130 e analysis of organic residues, particularly lipids, from archaeological contexts.

131 by using summary-level data from the Global Lipid Genetics Consortium (n = 188,577) and UK Biobank C

132 , height, weight, waist circumference, blood lipids, glucose, insulin, and blood pressure were measur

133 Whereas the enzymes that attach lipid groups are known, the enzymes mediating lipid remo

134 strated fluctuations in correlations between lipid groups at M1, M3, and CB, signifying differences i

135 ABHD17a and ABHD17c, that excise BK channel lipid groups with remarkable precision.

136 These lipids have potential applications in food, feed and pha

137 interaction between the fluorophores and the lipid headgroups facilitates the initial, fast membrane

138 Maintaining ER lipid homeostasis despite these fluctuations is crucial

139 ve SHs, and thus for deciphering the role of lipid homeostasis during rice seed germination.

140 Lipid homeostasis in animal cells is maintained by stero

141 pids resemble previously reported effects on lipid homeostasis in other species.

142 ential role in the regulation of glucose and lipid homeostasis.

143 or their inhibition against the formation of lipid hydroperoxides and carbonyl compounds in a strippe

144 erry press cake remarkably reduced levels of lipid hydroperoxides, malondialdehyde (MDA) and 4-hydrox

145 find that addition of the natural substrate lipid-II results in the formation of a 1:1 protein-lipid

146 eviously identified B. burgdorferi proteins, lipid immunogens, and live mutants lead the design of ca

147 Dietary lipids impact development, homeostasis, and disease, but

148 as found to dramatically reduce the area per lipid in lipid monolayers, while Mg(2+) and Cu(2+) did n

149 Accumulation of lipid in skeletal muscle is thought to be related to the

150 atidylcholine and anionic phosphatidylserine lipids in mixed lipid membranes.

151 To enhance our understanding of the role of lipids in regulation of lifespan and healthspan addition

152 vivo, and none that can isolate and quantify lipids in the blood.

153 By contrast, it accounts for only 5% of lipids in the endoplasmic reticulum (ER)(1).

154 traightforward derivatization of unsaturated lipids in tissue sections.

155 erved transporter of mycolic acid-containing lipids including monomeromycolyl diacylglycerol (MMDAG),

156 trol bacteria and had alterations in hepatic lipids, including oxylipins.

157 uctural characterization by CryoEM reveals a lipid-induced stabilization to the channel, resulting in

158 acids are rapidly incorporated into membrane lipids, inducing a reduction in membrane packing.

159 establish a mechanistic understanding of LBL-lipid interactions and create a modified BoNT/B with imp

160 The segregation of lipids into lateral membrane domains has been extensivel

161 of caveolae could allow release of specific lipids into the bulk PM.

162 dence that a metabolic shift from glucose to lipid is a key mechanism in neurodegeneration.

163 f concept, in situ separation and imaging of lipid isomers with distinct spatial distributions were p

164 PI3K lipid kinases signal through the PI3K/Akt pathway, regul

165 al benefits of statin use in PWH with normal lipid levels requires further clinical outcome research.

166 Alcohol intake influences plasma lipid levels, and such effects may be moderated by genet

167 strong enrichment with typical mitochondrial lipids like cardiolipins and demonstrated the presence o

168 A lipid-like density-possibly representing an acyl-accepto

169 development of synthetic membranes to study lipid-lipid interactions in vitro, alongside optical mic

170 he organizational and functional dynamics of lipid-lipid, lipid-protein, and lipid-dye interactions w

171 aphy and quantitatively analyzed periprotein lipids located within the diameter defined by one SMALP.

172 Bempedoic acid is a first-in-class lipid-lowering drug recommended by guidelines for the tr

173 eventive pharmacotherapies, such as aspirin, lipid-lowering mediations, and cardiometabolic agents.

174 criteria for intensive secondary prevention lipid-lowering therapy (28.3% vs. 40.0% vs. 81.4%, respe

175 e the receipt of maximum doses of background lipid-lowering therapy.

176 hat they are induced in the periphery during lipid-lowering therapy.

177 0 to 17 years of age who had received stable lipid-lowering treatment for at least 4 weeks before scr

178 er, our results establish that the bioactive lipid LPA drives the expression of TNF-alpha to regulate

179 Prostaglandin E2 (PGE2) is a lipid mediator of inflammation, and its tissue concentra

180 and upregulation of specialized proresolving lipid mediators.

181 lethanolamines (NAEs), a family of bioactive lipid mediators.

182 l characterization, structures of TRPV3 in a lipid membrane environment provide unique insights into

183 toxin binding to neurons by interacting with lipid membranes (termed lipid-binding loop [LBL]).

184 d step occurring over many days where native lipid membranes assemble into well-defined multilayer st

185 ined multilayer structures, whereas diseased lipid membranes form folded assemblies with high local c

186 Human Nuclear Lipid Membranes were at least two orders of magnitude mo

187 ") of lipophilic probes transiently bound to lipid membranes, revealing that Nile red's (NR) orientat

188 es in Lewy bodies rich in vesicles and other lipid membranes.

189 enes strain EGD-e while bound to native-like lipid membranes.

190 on of transmembrane proteins in cell-derived lipid membranes.

191 types of anions, rather than cations, across lipid membranes.

192 d anionic phosphatidylserine lipids in mixed lipid membranes.

193 MDD was associated with disorders of lipid metabolism (OR 1.22, 95% CI 1.12-1.34) and ischaem

194 odimer partner (Shp) plays a complex role in lipid metabolism and inflammation.

195 The relationship between lipid metabolism and longevity remains unclear.

196 a large number of molecules associated with lipid metabolism are known to be implicated in MNDs, the

197 genome sequences reveals photosynthesis and lipid metabolism are preferentially retained after a rec

198 estigate the role of fructose in glucose and lipid metabolism in the liver, heart, skeletal muscle, a

199 This study demonstrates that lipid metabolism is a sensitive endpoint for the interac

200 Oncogenic transformation alters lipid metabolism to sustain tumor growth.

201 s have the potential to rebalance disordered lipid metabolism, leading to improvements in nonalcoholi

202 meostasis and metabolic activities involving lipid metabolism, specifically the synthesis of pigments

203 This signaling pathway regulates lipid metabolism, unfolded protein responses, secretion

204 at M1, M3, and CB, signifying differences in lipid metabolism.

205 ribosome biogenesis and function, as well as lipid metabolism.

206 kinases to the control of cell survival and lipid metabolism.

207 MTG content while minimising accumulation of lipid metabolites known to disrupt skeletal muscle insul

208 rt IMTG storage and minimise accumulation of lipid metabolites to protect skeletal muscle insulin sig

209 e profile highlighted by the upregulation of lipid metabolites.

210 rticle IAV lipid mixing, whereas the rate of lipid mixing is independent of cholesterol composition.

211 pids within the membrane, yet the effects of lipid mixing on the membrane biophysical properties rema

212 hances the efficiency of single-particle IAV lipid mixing, whereas the rate of lipid mixing is indepe

213 A lipid-mixing assay with confocal imaging reveals that bo

214 ng nuclear localized (AHL) protein regulates lipid mobilization and fatty acid beta-oxidation during

215 ired food restriction-induced adipose tissue lipid mobilization in CT-1 null mice.

216 toylation is a reversible post-translational lipid modification that dynamically regulates protein fu

217 containing an NGL consisting of the optimal lipid moiety and the GM1 ganglioside pentasaccharide yie

218 Lipid molecules referred to as specialized proresolving

219 to dramatically reduce the area per lipid in lipid monolayers, while Mg(2+) and Cu(2+) did not.

220 ized SthK and in channels reconstituted into lipid nanodiscs.

221 RS-CoV-2 spike protein encapsulated within a lipid nanoparticle (LNP) as a vaccine.

222 in (lacking AD-3) with squalene adjuvant, or lipid nanoparticle (LNP)-encapsulated nucleoside-modifie

223 Lung-, spleen- and liver-targeted SORT lipid nanoparticles were designed to selectively edit th

224 ngly, many combinations resulted in distinct lipid nanostructures.

225 um and the chloroplast to lower 16:0 in leaf lipids of fab1 plants.

226 ed lipid blebbing by decreasing the area per lipid on the side of the bilayer to which the salt was e

227 ch weaker when either the background anionic lipids or PIP(2) is removed.

228 ce of the identified compounds and indicated lipid oxidation and the Maillard were the reaction pathw

229 ry press cake (called "helpers") to minimize lipid oxidation during acid/alkaline pH-shift protein is

230 Treatment with 3P10 reverses excessive lipid oxidation in tumor-bearing mice and prevents cance

231 Understanding how PLA2 inhibits lipid oxidation promoted by hemoglobin (Hb) is important

232 for microbial count, chemical stability (pH, lipid oxidation, lipolysis), and optical properties.

233 Concomitantly, membrane morphology and lipid packing became disrupted.

234 he membrane diffusivity drops with increased lipid packing order when comparing the endoplasmic retic

235 A significant change in the lipid-packing order takes place during assembly of pre-p

236 Changes from baseline in most lipid parameters also favored DOR.

237 of normal mice was associated with ALS-like lipid pathology, astrogliosis, neurodegeneration, and cl

238 es associated with prevalent AD arising from lipid pathways including; ether lipids, sphingolipids (n

239 ung IR increased the tissue iron content and lipid peroxidation accumulation, along with key protein

240 al, we found high consistency in measures of lipid peroxidation and circulating non-enzymatic antioxi

241 d by 4-hydroxynonenal ([4HNE] a byproduct of lipid peroxidation) on mitochondrial function and struct

242 The role of lipid peroxidation, a potent form of oxidative stress, i

243 ve summary of fundamental concepts regarding lipid peroxidation, experimental tools for the study of

244 The mechanism of the effect of lipid peroxidation, mediated by 4-hydroxynonenal ([4HNE]

245 dies with PTEN mutants that lack only PTEN's lipid phosphatase activity or both PTEN's lipid and prot

246 s multiple interactions with plasma membrane lipids: Phosphatidylinositol (4, 5)-bisphosphate (PIP(2)

247 an MLA was 2.9 mm(2), and the median maximum lipid plaque content was 33.4%.

248 erogeneity can differentiate metastases from lipid-poor adenomas.

249 to explore the associations between maternal lipid profile and small-for-gestational-age neonates.

250 population, the effect of Adv36 infection on lipid profile varied between healthy individuals and ind

251 We demonstrate that bioactive lipid profiles can be readily detected from three-dimens

252 We purified SMALP-lipid-protein complexes by chromatography and quantitati

253 lecular dynamics simulations, we explore the lipid-protein interaction profiles of 28 different GPCRs

254 onal and functional dynamics of lipid-lipid, lipid-protein, and lipid-dye interactions with single-mo

255 ulted in the defective expression of over 60 lipid-raft-associated surface receptors, and impaired BC

256 n of neuronal cholesterol trafficking and of lipid rafts by Nef may contribute to early stages of neu

257 In Ifitm3(-/-) B cells, lipid rafts were depleted of PIP3, which resulted in the

258 Galpha(s), when ensconced in lipid rafts, couples less effectively with adenylyl cycl

259 attachment of carbohydrates to proteins and lipids, regulates nearly all cellular processes and is c

260 rrow-derived macrophages, heme induced HO-1, lipid regulatory genes including LXR (lipid X receptor),

261 ipid groups are known, the enzymes mediating lipid removal (i.e. deacylation) are largely unknown.

262 s is regulated is crucial to revealing these lipids' role in health and disease.

263 rves as the measured variable for regulating lipid saturation.

264 TIPE proteins are carriers of lipid second messengers.

265 on, including heat, force, osmotic pressure, lipid shortage, and starvation.

266 results are consistent with NAE 18:3 being a lipid signaling molecule in plants with a requirement fo

267 ) activates the channel; a secondary anionic lipid site has been identified, which augments the activ

268 These lipids slow Ras' translational and orientational diffusi

269 aracterized by an asymmetric distribution of lipid species across the exofacial and cytofacial aspect

270 arising from lipid pathways including; ether lipids, sphingolipids (notably GM(3) gangliosides) and l

271 Our results show that lipid sponge droplets permit the facile integration of m

272 ce nutritional quality, but to decrease beef lipid stability.

273 Abeta oligomers, which reveal how they form lipid-stabilized pores that might disrupt neuronal membr

274 ic medium induced a significant increment of lipid storage in ccRCC cells that had a low 36-kDa AnxA3

275 The mechanisms coordinating lipid storage in LDs with cellular metabolism are unclea

276 Lipid droplets (LDs) are neutral lipid storage organelles assembled at the endoplasmic re

277 as dynamic organelles with functions beyond lipid storage.

278 e bound to MlaFEDB, suggesting that multiple lipid substrates may be transported each cycle.

279 A decrease in the total levels of complex lipids such as phosphatidylethanolamines (PE), lactosylc

280 esicles that also contain background anionic lipids such as phosphatidylserine but much weaker when e

281 ponse to capsaicin, whereas phosphoinositide lipid supplementation reduces TRPV1-mediated responses.

282 oth C. elegans and human cancer cells, ether-lipid synthesis protects against ferroptosis.

283 of terminal differentiation (FLG and FLG2), lipid synthesis/metabolism (ELOVL3 and FA2H), and tight

284 embrane led to a local enrichment of anionic lipids that could potentially enhance the membrane affin

285 f phosphatidylinositol 4,5-bisphosphate-like lipids that induce a directional membrane-mediated inter

286 e phosphatidylinositol 4,5-bisphosphate-like lipids that preferentially interact with the charged end

287 lexes and noncovalent binding of ligands and lipids to membrane proteins.

288 ic variation in the maternal provisioning of lipids to offspring, with a positive correlation between

289 low for the separation and identification of lipids to the underlying structures of tissues.

290 to construct genetic instruments for plasma lipid traits.

291 ial challenge, as exemplified by the case of lipid transfer polyproteins, which are common pollen all

292 enotypic switch to oxidative metabolism with lipid utilization to fuel invasion and metastasis occurs

293 AP(248-286) much more readily assembles with lipid vesicles into peptide/lipid coaggregates that rese

294 nity of HuNoV virus-like particles (VLPs) to lipid vesicles produced from the individual HIE-lipid ex

295 low nanomolar apparent affinity to PIP(2) in lipid vesicles that also contain background anionic lipi

296 luding oligomers and microfilaments bound to lipid vesicles.

297 slet amyloid polypeptide (hIAPP), with giant lipid vesicles.

298 (ATCC 33277) was grown in broth culture, and lipids were extracted and fractionated by high-performan

299 edged to depend on the unique composition of lipids within the membrane, yet the effects of lipid mix

300 HO-1, lipid regulatory genes including LXR (lipid X receptor), the growth factor IGF1 (insulin-like