ライフサイエンスコーパス: raft

1 olution of ordered microdomains (i.e., lipid rafts).

2 in (APP) and gamma-secretase levels in lipid rafts.

3 ting amyloidogenic pathway proteins in lipid rafts.

4 7 rafts compared to their levels in parental rafts.

5 rt of galactosylceramide from Golgi to lipid rafts.

6 some and its proteolytic activation in lipid rafts.

7 archical morphologies resembling bicomponent rafts.

8 little to no replication in HPV-immortalized rafts.

9 f cervical, foreskin, and tonsil organotypic rafts.

10 controlled by their complexation with other rafts.

11 as a cell-signaling receptor system in lipid rafts.

12 h the beta-glucan receptor dectin-1 in lipid rafts.

13 ll as on their lateral accumulation in lipid rafts.

14 how that soluble klotho binds membrane lipid rafts.

15 membrane sequence redirects PrP(C) away from rafts.

16 ral membrane proteins and formation of lipid rafts.

17 ral domains, including lipid-driven membrane rafts.

18 ing high concentrations of sterol-rich lipid rafts.

19 nd sphingolipid-rich membrane regions called rafts.

20 aturally occurring nanodomains such as lipid rafts.

21 aching the Antarctic continent alive on kelp rafts.

22 cyclodextrin (MbetaCD), which disrupts lipid rafts.

23 and cholesterol binding in the cell membrane rafts.

24 membrane anchoring and trafficking to lipid rafts.

25 n with cholesterol present in membrane lipid rafts.

26 survival and dispersal of coastal species by rafting.

27 duces cell surface gangliosides, a metric of raft abundance, as well as expression and surface displa

28 d find that, in the achiral limit, colloidal rafts acquire complex structural properties and interact

29 raft association, here we directly quantify raft affinity for dozens of TMDs.

30 ls that plasma membrane proteins have higher raft affinity than those of intracellular membranes, con

31 normal human epidermal keratinocytes and 3D rafts after topical application, affirming a role for SR

32 hain polymers to be grafted from the pendant RAFT agent by a radical-mediated RAFT polymerization of

33 Selective consumption of the first RAFT agent is used to control the cationic RAFT polymeri

34 yl ether monomer bearing a secondary dormant RAFT agent, which subsequently allows side-chain polymer

35 size bottlebrush polymers using two distinct RAFT agents.

36 sible addition-fragmentation chain-transfer (RAFT) agents.

37 yl ether, xenon, and propofol, disrupt lipid rafts and activate PLD2.

38 Importantly, LMP1 trafficking to lipid rafts and activation of NF-kappaB and PI3K/Akt pathways

39 e HIV-1 Gag polyprotein, retains it in lipid rafts and blocks HIV-1 virion production and spread.

40 In addition, the interplay between lipid rafts and different modes of cancer cell death, includin

41 oid precursor protein (APP) and Tau to lipid rafts and increased the abundance of these proteins, as

42 ialyllactose moiety of gangliosides in lipid rafts and inhibition of raft-dependent signaling underli

43 on of normal prion protein (PrP(C)) in lipid rafts and lipid cofactors generating infectious prions i

44 tudy exploits the correspondence of cellular rafts and liquid ordered (L(o)) phases of three-componen

45 twist promotes the formation of finite-sized rafts and mediates a repulsion that distributes them eve

46 We observed that SFK and FAK in the lipid rafts and nonrafts are differently regulated by fluid fl

47 he whole brain of flies, anesthesia disrupts rafts and PLD(null) flies resist anesthesia.

48 y, elucidation of the complex roles of lipid rafts and raft components within the metastatic cascade

49 hospholipase D2 (PLD2) localization to lipid rafts and subsequent production of signaling lipid phosp

50 ated that tubulin anchors Galpha(s) to lipid rafts and that increased tubulin acetylation (due to HDA

51 stinct adaptors, Flot-1 in noncaveolar lipid rafts and the AP2A1/2 complex in clathrin vesicles.

52 moving beyond questions of the existence of rafts and towards understanding their physiological sign

53 ce of PrP(res) not associated with host cell rafts and without the potential influence of endogenous

54 rganization into more ordered (L(o) or lipid raft) and more disordered (L(d)) domains.

55 anscriptomes of natural lesions, organotypic rafts, and human papillomavirus (HPV)-immortalized kerat

56 pical application to psoriatic 3-dimensional rafts, anti-human IL17RA L-SNAs reduced the expression o

57 In the present study, the RAFT aqueous emulsion polymerization of 2-methoxyethyl m

58 r understanding of the PISA mechanism during RAFT aqueous emulsion polymerization.

59 ng the analogous in situ SAXS studies during RAFT aqueous emulsion polymerizations poses a formidable

60 ding to the literature, over 70 million kelp rafts are afloat in the Southern Ocean at any one time.

61 Nanoscale rafts are believed to play an important functional role,

62 anchoring and the localization of PrP(C) to rafts are crucial to the ability of PrP(C) to propagate

63 Lipid rafts are hypothesized to facilitate protein interaction

64 Rafts are involved in most plasma membrane functions by

65 the notion that sialogangliosides and lipid rafts are membrane receptors for sKlotho and that the KL

66 ms towards the coast of the continent, these rafts are often cited as theoretical vectors for the int

67 Lipid rafts are tightly packed, cholesterol- and sphingolipid-

68 nt membrane nanodomains, also known as lipid rafts, are the primary response element in EF sensing.

69 nce that this is through regulation of lipid rafts as Lrch4 silencing reduces cell surface gangliosid

70 ntaining a cholesterol binding motif, is not raft associated.

71 To identify novel lipid-raft-associated CXCR4 regulators supporting invasion/met

72 Sulfatides and gangliosides are raft-associated glycolipids essential for maintaining my

73 S2 with Core and endoplasmic reticulum lipid raft-associated protein 2 (Erlin-2).

74 affinity purification, we detected the lipid raft-associated proteins flotillin-1 and flotillin-2 and

75 -down suppresses the expression of the lipid raft-associated proteins VE-cadherin and caveolin-1.

76 ant membrane phase changes together with the raft-associated receptor-ligand binding through the surf

77 nary conserved, ubiquitously expressed lipid raft-associated scaffolding protein.

78 in the defective expression of over 60 lipid-raft-associated surface receptors, and impaired BCR sign

79 otein transmembrane domains (TMDs) determine raft association, here we directly quantify raft affinit

80 of BACE1 S-palmitoylation and reduced lipid raft association.

81 sible addition fragmentation chain transfer (RAFT)-based dynamic covalent chemistry is incorporated i

82 The RAFT-based bond exchange process, which leads to stress

83 nimal-borne GPS data can be used to identify rafting behaviour outside of the breeding colonies and,

84 uid flow, while inhibition of SFK in the non-rafts blocked FAK activation by the cytokines.

85 Inhibition of FAK in the lipid rafts blocked SFK response to fluid flow, while inhibiti

86 sulted in the exclusion of D(1) R from lipid rafts, blunted cAMP response, impaired sodium transport,

87 In addition, CXCR4 is present on membrane rafts but can go into the nucleus during cancer progress

88 howed robust EBV replication in HPV-negative rafts but little to no replication in HPV-immortalized r

89 Kidney-restricted disruption of lipid rafts by beta-MCD jettisoned the D(1) R from the brush b

90 euronal cholesterol trafficking and of lipid rafts by Nef may contribute to early stages of neurodege

91 The results show how cellular rafts can be structurally rigid signaling platforms whil

92 In particular, rafts can switch between 2 chiral states of opposite han

93 Well-defined RAFT-capped polymers are synthesized and the kinetics ar

94 Lipid raft/caveolae disruptors (methyl-beta-cyclodextrin (MCD)

95 osomes was dominantly mediated via the lipid raft/caveolae endocytic pathway.

96 xidant and signaling molecule, through lipid raft/caveolae-dependent processes.

97 ompartmentalization of Nox isoforms in lipid rafts/caveolae and assessed the role of these microdomai

98 on induced trafficking into and out of lipid rafts/caveolae for Nox1 and Nox5 respectively.

99 We identify an important role for lipid rafts/caveolae that act as signaling platforms for Nox1

100 Whether cholesterol-rich microdomains (lipid rafts/caveolae) are involved in these processes is uncle

101 ble addition - fragmentation chain transfer (RAFT) chain transfer agent, with and without pre-conjuga

102 ction in uninfected cells to fine-tune lipid raft cholesterol that regulates innate immunity to adeno

103 These rafts closely mimic persistent HPV16 infection, long bef

104 tightly regulated by cholesterol-rich "lipid rafts." Collectively, these data show that RIDalpha util

105 ation markers, were reduced in HPV E6 and E7 rafts compared to their levels in parental rafts.

106 tors of signal transduction in cancer, where raft compartmentalization can promote transmembrane rece

107 early increased cell-surface levels of lipid raft components in detached fibroblasts, which might ind

108 tion of the complex roles of lipid rafts and raft components within the metastatic cascade may be ins

109 f CD1d accompanied by an alteration in lipid raft content on the plasma membrane of thymocytes and an

110 assemblies in cell membranes known as lipid rafts, coself-assembly of 1-decanol into cetyltrimethyla

111 Galpha(s), when ensconced in lipid rafts, couples less effectively with adenylyl cyclase to

112 thermodynamic properties in physically aged RAFT-CuAAC networks that undergo bond exchange in the gl

113 talized tonsillar cells grown in organotypic raft culture, we showed robust EBV replication in HPV-ne

114 ng date, and concentrations of UV filters in raft cultured mussel ( Mytilus galloprovincialis) of the

115 cell invasion was studied using organotypic raft cultures and in vivo significance was assessed via

116 When grown as organotypic raft cultures, keratinocytes infected with wild-type but

117 s in the HPV16 life cycle using organotypic (raft) cultures as a model.

118 s are in phase with peaks in Cordilleran ice-rafted debris delivery, and both consistently precede ic

119 high-temporal-resolution records of iceberg-rafted debris derived from the Antarctic Ice Sheet, and

120 , a Southern Ocean (Atlantic-sector) iceberg rafted debris event appears to have occurred synchronous

121 nt of key climate data sets spanning iceberg-rafted debris event Heinrich 3 and Greenland Interstadia

122 Ocean, leaving behind distinct layers of ice-rafted debris in the ocean sediments.

123 Sedimentation rates, ice-rafted debris, and microfossil and biogeochemical proxie

124 aminiferal assemblages, the abundance of ice-rafted debris, and sortable silt grain size data.

125 rsal of UV filters from potential sources to rafts decreases 5-fold over 5 km.

126 ic leukemia (APL), NTAL depletion from lipid rafts decreases cell viability through regulation of the

127 In vivo, raft-dependent PI3K signaling is up-regulated in klotho-

128 gliosides enriched in lipid rafts to inhibit raft-dependent PI3K signaling.

129 angliosides in lipid rafts and inhibition of raft-dependent signaling underlies the mechanism.

130 viously identified in natural lesions and in rafts derived from immortalized keratinocytes.

131 sed quantitative proteomic analysis of lipid-rafts derived from PC3 stable cell lines with overexpres

132 and warming, reduced sedimentary coastal ice rafted detritus contents indicate less severe winters.

133 in which it can likely survive long-distance rafting dispersal due to its varying lifecycle stages; e

134 Diblock copolymer vesicles are prepared via RAFT dispersion polymerization directly in mineral oil.

135 sible addition-fragmentation chain transfer (RAFT) dispersion polymerization have previously provided

136 ll-contact dependent and unaffected by lipid raft disruption of donor TEC.

137 lesterol release from cells, increased lipid-raft disruption, decreased phosphatidylserine (PS) flip

138 complex formation and changes the NHE3 lipid raft distribution, which cause changes in specific aspec

139 de brain showed increased Galpha(s) in lipid-raft domains compared with normal subjects.

140 increased localization of Galpha(s) in lipid-raft domains responsible for attenuated cAMP signaling.

141 min, which translocated Galpha(s) from lipid raft domains to non-raft domains.

142 ncreased sequestration of Galpha(s) in lipid-raft domains, where it is less likely to couple to adeny

143 be concentrated in cholesterol-rich membrane raft domains, whereas M2, although containing a choleste

144 esulted in D(1) R partitioning solely to non-raft domains, while silencing of SNX19 impaired D(1) R f

145 translocate Galpha(s) from lipid raft to non-raft domains.

146 ted Galpha(s) from lipid raft domains to non-raft domains.

147 nts and physical properties of membranes and raft domains.

148 ly associates with cholesterol to form lipid raft domains.

149 with TLR4 and translocates to membrane lipid raft domains.

150 s and other molecules and summarize work on "raft" domains in model and cell membranes, as determined

151 le stages possess chemically different lipid rafts due to different sterol utilization.

152 In situ activation of RAFT during mechanical loading results in a 50% improvem

153 the same network without light-activation of RAFT during the tensile testing.

154 g and hence allows in situ monitoring during RAFT emulsion polymerization for the first time.

155 In order to test the importance of the raft environment on prion propagation, we developed a no

156 surface, while the saturated chains face the raft environment, thus minimizing perturbations therein.

157 diesterase acid-like 3b (SMPDL3b) is a lipid raft enzyme that regulates plasma membrane (PM) fluidity

158 Reports of contradictory ice-rafted erratics and cold water glendonites in the higher

159 ed during fracturing, drifting, ridging, and rafting events.

160 dal monolayers with thermodynamically stable rafts exhibiting chiral structure and repulsive interact

161 The use of human foreskin keratinocyte rafts expressing the HPV16 E6 and/or E7 oncogene(s) (HPV

162 esults highlight the essential role of lipid rafts for effective D(1) R signaling.

163 al features that allow it to reside in lipid rafts for its activity.

164 various niche signaling molecules into lipid rafts for promoting neuronal differentiation of NSCs, an

165 amics of the lipid-lipid interactions during raft formation and resultant membrane phase changes toge

166 The forces that drive lipid raft formation are poorly understood.

167 itch-activated protein 70 (SWAP-70) in lipid raft formation of dendritic cells.

168 ipid asymmetry impacts ordered lipid domain (raft) formation may yield important clues to how ordered

169 e demonstrated the underlying mechanisms for raft formations that the infiltration of cholesterols in

170 blocked its LPS-induced accumulation in the raft fraction of RAW264 cells.

171 GM3, a lipid raft ganglioside synthesized by GM3 synthase (GM3S), reg

172 Rafts have been strongly implicated as master regulators

173 red to the original spherical structure, the rafts have rotated relative to each other.

174 e review the conceptual underpinnings of the raft hypothesis and critically discuss the supporting an

175 The lipid raft hypothesis postulates that lipid-lipid interactions

176 solvus annealing is rendered possible by the rafting (i.e., directional coarsening) of gamma ' partic

177 n animals suspended from a commercial mussel raft in the urban Bronx River Estuary, NY, in waters clo

178 resembles the assembly process of the lipid rafts in cell membranes and triggers orders of magnitude

179 showed that S. aureus colocalized with lipid rafts in HMEECs.

180 t spontaneous correlated motions, similar to rafts in many bacterial communities.

181 l role for SR-A complexes in epidermal lipid rafts in mediating the uptake of nucleic acid-laden nano

182 ning of TMDs and support the central role of rafts in membrane traffic.

183 increasing the abundance and modifying lipid rafts in neuronal plasma membranes.

184 in detergent-resistant outer membrane lipid rafts in which conversion to the pathogenic misfolded fo

185 onal significance of ordered nanodomains (or rafts) in cholesterol rich eukaryotic cell membranes has

186 tudy of naturally occurring domains, such as rafts, in biological membranes.

187 E3 complex size, reduced expression in lipid rafts, increased BB mobile fraction, and reduced binding

188 regulates TRPC6 calcium signaling via lipid rafts, independent of the FGFR-FGF23 pathway.

189 esters, and vinyl amides were polymerized by RAFT/iniferter and ATRP methods using Gel-PTH and a read

190 sible addition-fragmentation chain-transfer (RAFT) initiator complex.

191 le interactions enable assembly of colloidal rafts into intricate higher-order architectures, includi

192 sible addition fragmentation chain transfer (RAFT) into photoinitiated copper(I)-catalyzed azide-alky

193 nce of caveolae, which are specialized lipid raft invaginations of the plasma membrane associated wit

194 at the translocation of Galpha(s) from lipid rafts is a reliable hallmark of antidepressant action th

195 how that clustering of gangliosides in lipid rafts is important.

196 pic, fusiform (tufts), spherical (puffs) and raft-like colonies that provide a pseudobenthic habitat

197 The MAM region of the ER is a lipid raft-like domain closely apposed to mitochondria in such

198 , we observed the formation of low-polarity, raft-like nanodomains upon cholesterol addition or chole

199 Lamellar "raft-like" nanomorphologies on the surface of glycodendr

200 lement-independent manner and required lipid raft localization for CSC maintenance and cisplatin resi

201 their molecular properties obtained through RAFT/MADIX polymerization.

202 he membrane region of cholesterol-rich lipid raft markedly weakens the membrane association of VAMP2

203 l electrosensing and provide a role in lipid raft mechanotransduction.

204 e that MCPyV enters cells via caveolar/lipid raft-mediated endocytosis but not macropinocytosis, clat

205 ion proceeds via clathrin-independent, lipid raft-mediated endocytosis.

206 of intracellular membranes, consistent with raft-mediated plasma membrane sorting.

207 Furthermore, macropinocytosis and lipid raft-mediated were shown here as mechanisms of MkMP upta

208 issue homogenate, plasma membrane, and lipid-raft membrane domains in tissue from normal control subj

209 rch4 promotes proper docking of LPS in lipid raft membrane microdomains.

210 n-T cell activation linker (NTAL) is a lipid raft-membrane protein expressed by normal and leukemic c

211 duces both VEGFR2 and cholesterol in buoyant raft membranes.

212 the MAGUK family, recruits Kv1.3 into lipid-raft microdomains and protects the channel against ubiqu

213 persistent PrP(res) propagation, implicating raft microdomains as a location for conversion.

214 or, recruits the BMP receptor complexes into raft microdomains, and positively modulates signaling po

215 ranslocate Galpha(s) from lipid rafts to non-raft microdomains, similarly to other antidepressants bu

216 The rafted microstructure is removed in subsequent solution

217 and predicts AC frequency-dependent cell and raft migration.

218 ignaling microdomains, termed membrane/lipid rafts (MLRs).

219 iazole linkages with enhanced toughness, the RAFT moieties undergo bond exchange leading to stress re

220 cholesterol distribution and aberrant lipid raft morphology, supporting an unrecognized role for PMP

221 pithecoidea and indicates that transatlantic rafting of the lineage leading to Ucayalipithecus likely

222 findings illuminate differences in the lipid rafts of an organism employing life cycle-specific stero

223 extracellular space and typically form large rafts of clustered channels, called plaques, at cell app

224 hroughout the epidermis and CAV-1-containing rafts only in the upper epidermis.

225 The material may also act as a substrate for rafting organisms while being exposed to elevated concen

226 impse at the structural factors that promote raft partitioning for multispan helical membrane protein

227 d physical model establish general rules for raft partitioning of TMDs and support the central role o

228 physical features that independently affect raft partitioning, namely TMD surface area, length, and

229 Four rafting patterns were identified according to the prevai

230 irming a role for SR-As in SNA uptake and 3D raft penetration.

231 By developing cytocompatible PET-RAFT (photoinduced electron transfer-reversible addition

232 ous nature of our system, we also report PET-RAFT polymerization at the microliter scale in a mammali

233 the pendant RAFT agent by a radical-mediated RAFT polymerization of a different monomer, thus complet

234 t RAFT agent is used to control the cationic RAFT polymerization of a vinyl ether monomer bearing a s

235 RAFT polymerization was exploited to copolymerize these

236 ROAMP followed by RAFT polymerization yields hybrid poly-(o-phenylene ethy

237 he bioconjugation of polymers synthesized by RAFT polymerization, bearing no specific functional end

238 sible addition-fragmentation chain transfer (RAFT) polymerization and permits the synthesis of block

239 sible addition fragmentation chain transfer (RAFT) polymerization from styrene and 2-vinyl pyridine i

240 e addition-fragmentation chain transfer (PET-RAFT) polymerization is particularly versatile owing to

241 sible addition-fragmentation chain transfer (RAFT) polymerization of 2-hydroxethyl methacrylate (HEMA

242 sible addition-fragmentation chain transfer (RAFT) polymerization offers a platform technology for th

243 and selectivity of the cationic and radical RAFT polymerizations allow both polymerizations to be co

244 thogonal combination of cationic and radical RAFT polymerizations is used to synthesize bottlebrush p

245 the absence of subsequent triggering of the RAFT process, the (dis)order in the LCN and its associat

246 sible addition-fragmentation chain transfer (RAFT) process without compromising the polymerization ki

247 e addition-fragmentation chain-transfer (PET-RAFT) process, after which the deprotection and click re

248 in the miRNA-rich-EVs, suggesting the lipid raft protein as a biomarker of EV-miRNA enrichment.

249 Notably, caveolin-1, a lipid raft protein, is exclusively detected in the miRNA-rich-

250 ESPCs and PSC-derived epidermal organotypic rafts (PSC-EORs).

251 h alters the nature of the membrane-mediated raft-raft interactions.

252 s proposed, in which CYP46A1-dependent lipid raft rearrangement and subsequent decrease of protein ph

253 er ones often called lipid domains or "lipid rafts." Recent findings highlight the dynamic nature of

254 In contrast to the non-raft region, the membrane region of cholesterol-rich lip

255 erties, and even the very existence of lipid rafts remain unresolved.

256 Despite both proteins being raft resident, HA and NA occupy distinct but adjacent me

257 as expression and surface display of CD14, a raft-resident LPS co-receptor.

258 translocation of the TRAF2 complex to lipid rafts, resulting in its degradation and activation of th

259 The RAFT (Resynchronization in Ambulatory Heart Failure Tria

260 surface of silica microparticles following a RAFT (reversible addition-fragmentation chain transfer)

261 nd HER2 within specific actin-rich and lipid raft-rich membrane signaling domains.

262 PV16 E6 and/or E7 oncogene(s) (HPV E6 and E7 rafts) showed that E7 was sufficient to reduce EBV repli

263 The clinical role of lipid raft-specific proteins, caveolin and flotillin, in asses

264 lin and signaling proteins further stabilize raft structure and feed-forward downstream signaling eve

265 IKV complex shows Fabs locking the E protein raft structure containing three E dimers.

266 ETHODS AND All ventricular arrhythmias among RAFT study participants were downloaded and adjudicated

267 Furthermore, the properties of individual rafts, such as their sizes, are controlled by their comp

268 sible addition-fragmentation chain transfer (RAFT) system, thereby promoting polymerization of variou

269 nconsistent with the unmodified forms of the raft, tether, and fence models.

270 We have designed a system of DNA origami rafts that exponentially replicates a seed pattern, doub

271 is very much resembles the role of the lipid rafts that sharply increases the reaction rate of biomol

272 functional SR-As to FLOT-1-containing lipid rafts throughout the epidermis and CAV-1-containing raft

273 ist did not translocate Galpha(s) from lipid raft to non-raft domains.

274 Historic records tell of rats rafting to the southern island of Suouroy in 1768 follow

275 t HCV could induce the localization of lipid rafts to autophagosomes to mediate its RNA replication.

276 results identify ganglioside-enriched lipid rafts to be receptors that mediate soluble klotho regula

277 se-containing gangliosides enriched in lipid rafts to inhibit raft-dependent PI3K signaling.

278 amine would translocate Galpha(s) from lipid rafts to non-raft microdomains, similarly to other antid

279 relocalization of gamma-secretase from lipid rafts to nonlipid rafts where it cleaved Notch.

280 mal LMP1 release that is distinct from lipid raft trafficking.

281 Normal human epidermal keratinocytes and 3D raft treatment with SR-A inhibitors reduced SNA uptake b

282 sor was further targeted in or outside lipid rafts via different lipid modification signals.

283 h HAND was lower, and the abundance of lipid rafts was higher compared with HIV-negative individuals.

284 lain why klotho preferentially targets lipid rafts we show that clustering of gangliosides in lipid r

285 quid-ordered (l(o)) domain formation, called rafts, we developed a method of reconstituting continuou

286 ing is dependent on CD44 clustering in lipid rafts, we pretreated animals with methyl-beta-cyclodextr

287 Rafts were created using uninfected human foreskin kerat

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

289 A2, which are proteins associated with lipid rafts, were also identified.

290 gamma-secretase from lipid rafts to nonlipid rafts where it cleaved Notch.

291 opposite handedness assemble into colloidal rafts, which are finite-sized reconfigurable droplets co

292 ential localization of the receptor in lipid rafts, which are plasma membrane platforms replete with

293 er depends heavily on the integrity of lipid rafts, which include sphingolipids as key components.

294 e expression and receptor signaling on lipid rafts, which induces protease expression and cancer cell

295 ancer cells form a complex in membrane lipid raft with caveolin-1 (CAV1) and focal adhesion kinase (F

296 specifically induce the association of lipid rafts with autophagosomes for its RNA replication.IMPORT

297 Disruption of lipid rafts with cyclodextrin reversed the phenotype.

298 The association of lipid rafts with HCV-induced autophagosomes was confirmed by W

299 Rafts with the same chirality have long-ranged repulsion

300 This review highlights the roles of lipid rafts within the metastatic cascade, specifically within