ライフサイエンスコーパス: scaffolding

1 drug delivery combined with transient vessel scaffolding.

2 ion of laminin trimers and basement membrane scaffolding.

3 lished findings and a refined model of IQGAP scaffolding.

4 in compared to control mice that received no scaffolding.

5 desensitization is directed by PKA via AKAP scaffolding.

6 omosome conformation capture data for genome scaffolding.

7 hanisms, including sporadic mutations in its scaffolding A and regulatory B subunits or more frequent

8 ind that ARPP-16 interacts directly with the scaffolding A subunit of the serine/threonine protein ph

9 ugh epigenetic modifications of postsynaptic scaffolding A-kinase anchoring protein 79/150 (AKAP79/15

10 ntains a catalytic (C) subunit, a structural/scaffolding (A) subunit, and a regulatory (B) subunit.

11 PP2A comprises catalytic (C), scaffolding (A), and regulatory (B) subunits that determ

12 However, allosteric modulation of their scaffolding abilities and direct targeting of their inte

13 urther suggest co-targeting of enzymatic and scaffolding activities within Ras-MAPK signalling comple

14 Arrestin2 (Arr2) is a ubiquitous scaffolding/adaptor protein first characterized as a reg

15 tailored torques to specific environments by scaffolding alternative stator placement and number.

16 Within MLRs are the scaffolding and cholesterol binding proteins named caveo

17 esults indicate that the respective roles of scaffolding and coat proteins may have been redistribute

18 potentiates sequence assembly of genomes via scaffolding and comparisons that globally validate or co

19 read sequencing technology by assisting with scaffolding and detecting large and complex structural v

20 which CAV1 phosphorylation facilitates CAV1 scaffolding and GRK2-CAV1 interaction, thus clustering e

21 -forming connexin proteins and also multiple scaffolding and regulatory protein components, which wer

22 g the kinase arm, PI3Kgamma inhibits PP2A by scaffolding and sequestering, playing a key parallel syn

23 y a significant role in postsynaptic protein scaffolding and synaptic strength and plasticity.

24 applications, including diagnostics, tissue scaffolding and targeted drug release.

25 neered for molecular recognition and modular scaffolding applications.

26 We then investigated a "multivalent scaffolding" approach by displaying 24 copies of an epit

27 Scaffolding approaches have been powerfully applied to c

28 eir conserved reticulon homology domain, and scaffolding, arising from the ability of RTNs to form lo

29 Rab3-interacting molecules (RIMs) provide scaffolding at presynaptic active zones and are involved

30 a previously unnoticed link between membrane scaffolding by endoA2 and pulling-force-driven dynamic s

31 n, short reads for consensus validation, and scaffolding by optical and chromatin interaction mapping

32 epair systems and components, e.g. potential scaffolding cofactors (Rot/TROVE and SPFH/Band-7 modules

33 We also identify the endocytic scaffolding complex that includes Dap160 as a regulator

34 heterotypic association is used to assemble scaffolding complexes with distinct binding properties a

35 ds to finishing assemblies through tools for scaffolding contigs and close gaps.

36 Cullin neddylation is modulated by a scaffolding DCN protein through interactions with both t

37 highly conserved membrane-proximal caveolin scaffolding domain (CSD; amino acids 82-101).

38 inversely regulated by endothelin-1 and CAV1 scaffolding domain after liver injury.

39 CAV1 function was modified using a CAV1 scaffolding domain construct and cDNAs encoding wild-typ

40 ner of Sirt1, as shown by the binding of the scaffolding domain of caveolin-1 (amino acids 82-101) to

41 The N-terminal scaffolding domain of PAQR11 was associated with key reg

42 Treatment with the caveolin-1 scaffolding domain peptide (CSP) reversed these effects.

43 blocked CAV1 phosphorylation induced by CAV1 scaffolding domain, indicating that CAV1 interaction wit

44 ed in cardiovascular procedures primarily as scaffolding during surgery.

45 promote enzyme-mediated ligand hydrolysis by scaffolding effects.

46 the Hsp70 co-chaperone, BAG3, is a modular, scaffolding factor to bring together sHsps and Hsp70s.

47 BAG3 does not appear to be a passive scaffolding factor; rather, its binding promoted de-olig

48 ected by the giant protein titin, which is a scaffolding filament, signaling platform, and provider o

49 onomic details of diversity are an essential scaffolding for biology education, yet outdated methods

50 extracellular matrix (ECM) provides physical scaffolding for cellular constituents and initiates bioc

51 f coordinated activities between wedging and scaffolding for endophilin to produce stable membrane tu

52 t this topographic organization provides the scaffolding for the subsequent development of visual cor

53 a, we discuss the insights obtained from the scaffolding function and how this non-canonical role cou

54 Our findings support a kinase-independent scaffolding function of CK2alpha that promotes resistanc

55 dence from recent studies implicate that the scaffolding function of enzymes could be as important in

56 osphorylation, we have demonstrated that the scaffolding function of receptor interacting protein kin

57 RAC1/PAK1 and promoted a kinase-independent scaffolding function that led to recruitment and phospho

58 suppressor homologs 1/2 (LATS1/2), uses its scaffolding function to link MST1/2 with MARK3, and inhi

59 isoforms are emerging with localizations and scaffolding functions at sites away from the NE, suggest

60 hese findings, we propose that Brc1 provides scaffolding functions linking gammaH2A, Rhp18, and Smc5/

61 pletion suggest that OGT's glycosylation and scaffolding functions play distinct roles in the replica

62 rotein depletion, indicative of catalytic or scaffolding functions, respectively.

63 While Tum/RacGAP has well-documented scaffolding functions, whether it influences Pav/kinesin

64 inase catalytic functions from the protein's scaffolding functions.

65 In this scaffolding hypothesis, a shifting balance between the t

66 trates an unexpected level of autoregulatory scaffolding in mammalian stress-activated MAP kinase sig

67 AJ formation and aberrant radial glial fiber scaffolding in the embryonic mouse cortex.

68 hly resolved assembly graphs with long-range scaffolding information promises the complete and automa

69 d to calculate the effective kon and koff of scaffolding interactions such as those that immobilize r

70 nases is kept at a minimum in the absence of scaffolding interactions, which position the enzymes for

71 ric reads, and genome repeats the problem of scaffolding is a challenging task.

72 otic genomes; however, at present additional scaffolding is needed to achieve chromosome-level assemb

73 ury (SCI), we demonstrated that the tailored scaffolding maintained hMSC stemness, engraftment, and l

74 ombining the programming ability of DNA as a scaffolding material with a one-step lithographic proces

75 A similar scaffolding mechanism may underlie FER function in other

76 e observations elevate the importance of the scaffolding mechanism, rather than H0 insertion, for the

77 ted thus far using whole-genome assembly and scaffolding methods.

78 in SZ cohorts is the duplication of Synaptic Scaffolding Molecule (S-SCAM, also called MAGI-2), which

79 , a gene encoding a protein kinase A-binding scaffolding molecule, were significantly associated with

80 ing involvement of additional factors like a scaffolding molecule.

81 nding proteins (RBPs) as central active-zone scaffolding molecules.

82 as curvature sensors, membrane benders, and scaffolding molecules.

83 ions by binding to cytoplasmic signaling and scaffolding molecules.

84 e, all known functions of Raptor involve its scaffolding mTOR kinase with substrate.

85 rve as important hubs in signaling networks, scaffolding multivalent interactions.

86 truct a highly accurate de novo assembly and scaffolding of a human genome with scaffold N50 of 20 Mb

87 for the systematic sequencing, assembly and scaffolding of large genomes.

88 atal experiences may shape the somatosensory scaffolding of later perceptual, cognitive, and social d

89 nity reagents based upon single-stranded DNA scaffolding of peptide fragments.

90 issociated, suggesting that laminins mediate scaffolding of post-synaptic components.

91 s of agarose-derived hydrogels depend on the scaffolding of the polysaccharide network.

92 -eluting stents, while providing a transient scaffolding of the vessel to prevent acute vessel closur

93 non-canonical role of class IIa HDACs in the scaffolding of transcriptional regulatory complexes, whi

94 ike structures possibly providing additional scaffolding opportunities for NEC.

95 eins, Ras guanine exchange factors, kinases, scaffolding or adaptor proteins, ubiquitin ligases, phos

96 Rather than simply being scaffolding or extracellular matrix-secreting cells on w

97 h one characterized by an interaction with a scaffolding or structural protein.

98 Multisensory processes are fundamental in scaffolding perception, cognition, learning, and behavio

99 eric structures have been examined for their scaffolding potential.

100 uitination, which markedly modifies PSD-95's scaffolding potentials, enables its synaptic targeting,

101 euse theory, empirical tests of the related "scaffolding" principle of abstract concept development s

102 MeDuSa formalizes the scaffolding problem by means of a combinatorial optimiza

103 provide a novel mechanism that exploits the scaffolding properties of the N terminus of p120RasGAP t

104 and show that CpmB competes with the 80alpha scaffolding protein (SP) for a binding site on the capsi

105 through interaction with thioredoxin and the scaffolding protein 14-3-3.

106 in (Pdc-ND) followed by association with the scaffolding protein 14-3-3.

107 d G protein-coupled receptors coupled by the scaffolding protein A-kinase-anchoring protein (AKAP)79/

108 During varphiX174 assembly, the external scaffolding protein acts like a coat protein, self-assoc

109 We show that loss of the scaffolding protein Afadin disrupts de novo lumenogenesi

110 The scaffolding protein AKAP350A is known to localize to the

111 smaller than a Golgi subdomain positive for scaffolding protein AKAP450, which is thought to recruit

112 Dishevelled (DVL) is a key scaffolding protein and a branching point in Wnt signali

113 ite for the dynamic functions of IQGAP1 as a scaffolding protein and a critical mechanism in temporal

114 apsid') built by multiple copies of coat and scaffolding protein and by one dodecameric portal protei

115 dditionally, we explored the function of the scaffolding protein and main component of caveolae, cave

116 One residue in the internal scaffolding protein and three in the coat protein consti

117 The cytoskeletal scaffolding protein ankyrin G (AnkG) has been thought to

118 The scaffolding protein ankyrin-G is the master-organizer of

119 ting that DNA packaging and expulsion of the scaffolding protein are coupled processes.

120 at appears to contain substantial amounts of scaffolding protein as well as DNA, suggesting that DNA

121 ule dynamics at both locations, but how this scaffolding protein assembles microtubule nucleation mac

122 ne-associated guanylate kinase, is the major scaffolding protein at excitatory postsynaptic densities

123 ose assembly depends on the polymeric master scaffolding protein AXIN.

124 bstitutions ranged from inefficient internal scaffolding protein B binding to faulty procapsid elonga

125 The internal scaffolding protein B mediates the formation of pentamer

126 a interaction protein (GSKIP) is a cytosolic scaffolding protein binding protein kinase A (PKA) and g

127 te receptor fields that lack the active zone scaffolding protein Bruchpilot.

128 called MAGI-2), which encodes a postsynaptic scaffolding protein controlling synaptic AMPA receptor l

129 Thus, the scaffolding protein controls fidelity.

130 74 morphogenesis, 240 copies of the external scaffolding protein D organize 12 pentameric assembly in

131 assembly intermediates, whereas the external scaffolding protein D organizes 12 of these intermediate

132 id elongation reactions mediated by external scaffolding protein D.

133 neuromuscular junction (NMJ), the endocytic scaffolding protein Dap160 colocalizes during the SV cyc

134 -CDF) of CaV1.3 channels that depends on the scaffolding protein densin and CaMKII and that outlasts

135 orted interaction among CaV1.3 channels, the scaffolding protein densin, and CaMKII could generate a

136 HTT forms a ternary protein complex with the scaffolding protein DISC1 and cAMP-degrading phosphodies

137 with each other and simultaneously with the scaffolding protein eIF4G.

138 te 1/5 receptor function and Homer2 receptor-scaffolding protein expression.

139 gene encodes MAPKBP1, a poorly characterized scaffolding protein for JNK signaling.

140 As a scaffolding protein for Protein Kinases A and C (PKA and

141 tein likely acting as a dynamic cell surface scaffolding protein for the assembly of different signal

142 basolateral amygdala, the clustering of the scaffolding protein Gephyrin and of gamma-aminobutyric a

143 otein collybistin (CB) recruits the receptor-scaffolding protein gephyrin to mammalian inhibitory gly

144 ere we show that the conserved signaling and scaffolding protein Girdin localizes to the proximal reg

145 Keratin 16 (K16) is a cytoskeletal scaffolding protein highly expressed at pressure-bearing

146 The scaffolding protein Homer assembles SOC complexes, but i

147 mGlu5 is less associated with its scaffolding protein Homer in Fmr1 KO mice, and restorati

148 xpression of the AMPAR subunit GluA1 and the scaffolding protein Homer.

149 rtant new insights into the role of FAK as a scaffolding protein in molecular complexes that regulate

150 omplementation group A (XPA) is an essential scaffolding protein in the multiprotein nucleotide excis

151 RLTPR encodes a recently described scaffolding protein in the T-cell receptor signaling pat

152 We further show that the CPC scaffolding protein INCENP (inner centromere protein) bi

153 acid side chains mediate most coat-internal scaffolding protein interactions.

154 STATEMENT: Integrin-linked kinase (ILK) is a scaffolding protein involved in integrating signals from

155 ozygous mutations in CARD11, which encodes a scaffolding protein involved in lymphocyte receptor sign

156 1; also known as p62) encodes a multidomain scaffolding protein involved in various key cellular pro

157 our capsids, aided by the discovery that the scaffolding protein is exceptionally prone to radiation-

158 c capsomers afford the pathway via which the scaffolding protein is expelled.

159 Here we show that Scribble, a scaffolding protein known primarily for its role as a ce

160 es, MAP17 is known to interact with PDZK1, a scaffolding protein linked to other transporters, includ

161 also called AKAP450/CG-NAP/AKAP9) is a large scaffolding protein located at both the centrosome and G

162 Here, we show that loss of function of a scaffolding protein Mask, also known as ANKHD1 (Ankyrin

163 sis of human metastatic genes identified the scaffolding protein metastasis suppressor 1 (MTSS1) as a

164 Mutations in NBEAL2, the gene encoding the scaffolding protein Nbeal2, are causal of gray platelet

165 nsically disordered tail of the multi-domain scaffolding protein NHERF1, which affects the intracellu

166 milar to mice overexpressing PSD-95, a major scaffolding protein of postsynaptic density involved in

167 Disrupted in Schizophrenia 1 (DISC1) is a scaffolding protein of significant importance for neurod

168 teins BAZ2A and BAZ2B constitute the central scaffolding protein of the nucleolar remodeling complex

169 , we show the utility of tandem GFP11-tag in scaffolding protein oligomerization.

170 The Cas family scaffolding protein p130Cas is a Src substrate localized

171 ed microRNA-mediated repression of the Golgi scaffolding protein PAQR11.

172 lation of GluN2B Y1472, whereas the synaptic scaffolding protein postsynaptic density protein 95 (PSD

173 s a dual-binding partner of the postsynaptic scaffolding protein PSD-95 and AMPA glutamate receptors

174 where it associates with and stabilizes the scaffolding protein PSD95, promoting dendritic spine mat

175 abnormalities were noted in the postsynaptic scaffolding protein PSD95.

176 We have previously shown that the scaffolding protein Ran-binding protein 9 (RanBP9), whic

177 ogene required for development, and DCAF7, a scaffolding protein required for craniofacial developmen

178 with poor patient prognosis, and BRPF1 is a scaffolding protein required for the assembly of histone

179 me through direct interaction with the large scaffolding protein RPN2 within the 19S regulatory parti

180 roteins 1 and 2 and with the multifunctional scaffolding protein sequestosome-1 (SQSTM1/p62) confirme

181 The postsynaptic scaffolding protein SH3 and multiple ankyrin repeat doma

182 Sds3 engages the scaffolding protein Sin3A, via a bipartite motif within

183 ises the NAD-dependent deacetylase Sir2, the scaffolding protein Sir4, and the nucleosome-binding pro

184 The chromatin scaffolding protein SMCHD1 (structural maintenance of ch

185 We examined whether the scaffolding protein sodium-hydrogen exchanger regulatory

186 rrent study, we identify the multifunctional scaffolding protein spinophilin as a novel Group I mGluR

187 cultured astrocytes, suggesting that the DLG scaffolding protein stabilizes EAAT2b at the surface.

188 The Drosophila melanogaster scaffolding protein Stardust (Sdt) stabilizes the transm

189 y reported that the immunophilin FKBP51 is a scaffolding protein that can enhance PHLPP-AKT interacti

190 ation of the Mdm2 pathway degrades PSD-95, a scaffolding protein that clusters NMDARs at the synapse

191 s sigma-1 receptor) is a unique chaperone or scaffolding protein that contributes to cellular protein

192 signaling is negatively regulated by Axin, a scaffolding protein that controls a rate-limiting step i

193 Filamin is a scaffolding protein that functions in many cells as an a

194 chizophrenia 1 (DISC1) is a multi-functional scaffolding protein that has been associated with neurop

195 Shank is a post-synaptic scaffolding protein that has many binding partners.

196 SHANK3 is a ubiquitously expressed scaffolding protein that is enriched in postsynaptic exc

197 Zonula occludens-1 (ZO-1) is a submembrane scaffolding protein that may display proinvasive functio

198 SgK269/PEAK1 is a pseudokinase and scaffolding protein that plays a critical role in regula

199 ptic density 95 (PSD-95) is a major synaptic scaffolding protein that plays a key role in bidirection

200 cells by knocking down ANLN, a cytoskeletal scaffolding protein that regulates cytokinesis and might

201 associated with its binding partner Homer, a scaffolding protein that regulates mGlu5 localization to

202 exclusively to wag31, a gene that encodes a scaffolding protein thought to orchestrate cell elongati

203 t RA T cells abundantly express the podosome scaffolding protein TKS5, which enables them to form tis

204 Caveolin-1 acts as a scaffolding protein to functionally regulate signaling m

205 igher-order protein complexes containing K-H scaffolding protein to gain insight into its cellular fu

206 mplex comprising DNA ligase IIIalpha and the scaffolding protein X-ray repair cross-complementing pro

207 ng of DNA from the histone octamer; that the scaffolding protein XRCC1 enhances the ligation; that th

208 9 (AC9) is found tightly associated with the scaffolding protein Yotiao and the IKs ion channel in he

209 y a novel functional complex of the junction scaffolding protein ZO-1 and the F-BAR-domain protein TO

210 nding of CCCTC-binding factor, a chromosomal scaffolding protein, and increases histone and DNA methy

211 r components of the node is the cytoskeletal scaffolding protein, ankyrin G (AnkG), which interacts w

212 multiple ankyrin repeat domains 3 (SHANK3B) scaffolding protein, defective expression of which has b

213 ighly conserved double-PDZ domain-containing scaffolding protein, is robustly expressed in human-deri

214 which otoferlin acts as a calcium-sensitive scaffolding protein, localizing SNARE proteins proximal

215 rangement of the coat protein and release of scaffolding protein, resulting in dramatic procapsid lat

216 nhibitor, pointed to a mechanism involving a scaffolding protein, Wag31, involved in polar elongation

217 The scaffolding protein, which forms inner shells in the pro

218 PNKP and LigIV require the NHEJ scaffolding protein, XRCC4.

219 ng cycle, featuring two enzymes and a single scaffolding protein.

220 tial for tumor growth through one individual scaffolding protein.

221 interaction with Ajuba, an actin binding and scaffolding protein.

222 redistributed during the evolution of a two-scaffolding-protein system.

223 In one-scaffolding-protein virus assembly systems, coat protein

224 guanylate kinase (MAGUK) family of synaptic scaffolding proteins anchor glutamate receptors at CNS s

225 ion, we observed marked loss of postsynaptic scaffolding proteins and reduced complexity of the sub-s

226 as associated with reduced recruitment of TZ scaffolding proteins and reduced Smoothened levels at ci

227 d kinesins have also been reported to act as scaffolding proteins and signaling molecules.

228 taining for PSD-95 and gephyrin postsynaptic scaffolding proteins as proxies for excitatory and inhib

229 ediated by heterotrimeric G proteins and the scaffolding proteins beta-arrestin 1/2.

230 nalling domain interacts with the chemotaxis scaffolding proteins CheV and CheW, and comparative geno

231 eodomain finger-containing (BRPF) family are scaffolding proteins important for the recruitment of hi

232 domain and PHD finger-containing) family are scaffolding proteins important for the recruitment of hi

233 f the Dscams and multi-PDZ domain-containing scaffolding proteins in mouse.

234 termined T number, although the influence of scaffolding proteins is also important.

235 guanylate kinase (MAGUK) family of synaptic scaffolding proteins is critical for localization of glu

236 ts suggest that enzyme sequestration through scaffolding proteins is exploited by evolution to genera

237 DZ-binding motif allowing for binding of the scaffolding proteins Na(+)/H(+) exchanger regulatory fac

238 MAGUK (membrane-associated guanylate kinase) scaffolding proteins or NMDA receptors, it is necessary

239 Two scaffolding proteins orchestrate varphiX174 morphogenesi

240 Scaffolding proteins organize the information flow from

241 m increase in the expression of the synaptic scaffolding proteins PSD-95 and SAP90/PSD-95-associated

242 Prosap/Shank scaffolding proteins regulate the formation, organizatio

243 We show that removal of scaffolding proteins RIM1/2 from rod photoreceptor ribbo

244 isoform was recruited to nascent AZs by the scaffolding proteins Syd-1 and Liprin-alpha, and Unc13A

245 ) exchanger regulatory factor (NHERF) family scaffolding proteins that are required for many aspects

246 Talins, scaffolding proteins that bind to the membrane proximal

247 regulatory proteins (TARPs) are a family of scaffolding proteins that regulate AMPA receptor traffic

248 4-3-3 proteins, a family of highly conserved scaffolding proteins ubiquitously expressed in all eukar

249 al cellulosome assembly, including conserved scaffolding proteins unique to the Neocallimastigomycota

250 se disorders are those encoding postsynaptic scaffolding proteins with roles in synaptic transmission

251 ins constitute a highly conserved network of scaffolding proteins, adaptors and enzymes that form and

252 olytic metabolon is dependent on presynaptic scaffolding proteins, and disruption of the glycolytic m

253 depend on interactions between claudins, ZO scaffolding proteins, and the cytoskeleton.

254 es, including transcription factors, adaptor/scaffolding proteins, and uncharacterized proteins.

255 ned with RNA-induced phase separation of key scaffolding proteins, may be a general mechanism for con

256 Internalization seems to involve scaffolding proteins, such as beta-arrestin and clathrin

257 ignal through Gi/o-coupled G-proteins and/or scaffolding proteins, such as beta-arrestin, we find tha

258 hogen effectors by partnering with different scaffolding proteins, which can each recognize distinct

259 n of G protein-coupled receptor signaling by scaffolding proteins.

260 ibitory, and experimentally evolved coat and scaffolding proteins.

261 natorial interactions among many enzymes and scaffolding proteins.

262 ion, triggered by limited proteolysis of the scaffolding proteins.

263 ytic enzymes with regulatory, accessory, and scaffolding proteins.

264 eneous aberrant structures in the absence of scaffolding proteins.

265 s enriched in sphingolipids, cholesterol and scaffolding proteins; they serve as a platform for signa

266 deficiency of Shank3 can impair mGluR5-Homer scaffolding, resulting in cortico-striatal circuit abnor

267 ciliary function revealing that FAK plays a scaffolding role in multiciliated cells.

268 3 channels and self-associates, suggesting a scaffolding role in organizing nodal proteins.

269 BRPF1 plays a scaffolding role in transcription.

270 psids are empty, B capsids retain a shrunken scaffolding shell, and C capsids-which develop into infe

271 ed with DNA and ostensibly have expelled the scaffolding shell.

272 oassembly of the surface shell with an inner scaffolding shell; then the procapsid matures via a majo

273 ts indicated that impaired AKAP-mediated PKA scaffolding significantly reduces DOR-GRK2 association a

274 Current scaffolding software packages widely vary in their quali

275 shed yet constantly evolving multifunctional scaffolding strategies as well as in the emerging on-dem

276 ripotent stem cells, which bioengineering or scaffolding strategies have the most potential for kidne

277 tly far more candidate antigens than antigen scaffolding strategies.

278 We are convinced that the presented scaffolding strategy and the improved characteristics of

279 cleation, serving as an excellent biomimetic scaffolding strategy to rebuild natural bone integrity.

280 The APC/C assembly comprises two scaffolding subcomplexes: the platform and the TPR lobe

281 Although the role of Apc1 as an APC/C scaffolding subunit has been characterized, its specific

282 ort the biological importance of PSMD12 as a scaffolding subunit in proteasome function during develo

283 NF-kappaB essential modulator (NEMO) is the scaffolding subunit of the inhibitor of kappaB kinase (I

284 -binding protein), whose binding to eIF4G (a scaffolding subunit) and eIF4A (an ATP-dependent RNA hel

285 r integration with complementary phasing and scaffolding techniques.

286 The scaffolding that holds chromosome pairs together plays a

287 ilaments thus serve an important function in scaffolding the axon/myelin-unit, evidently a late stage

288 Scaffolding the calcium/calmodulin-dependent phosphatase

289 ving existing assemblies by reassembling and scaffolding the genome of the American alligator.

290 nsic role that developmental vision plays in scaffolding the neural implementation of touch perceptio

291 ution, providing insights into their role in scaffolding the nuclear lamina.

292 ilin are thought to bend lipid membranes via scaffolding (the molding of membranes through the cresce

293 on laser lithography is employed for LC cell scaffolding to accurately verify theoretical predictions

294 A variety of assembly and scaffolding tools are available, but it is not always ob

295 iable vocal behavior of human infants is the scaffolding upon which speech and social interactions de

296 oolsets into two paradigms: "multifunctional scaffolding" versus "on-demand targeting".

297 Chromosome-level scaffolding was achieved by combining reference-guided w

298 ough several different mechanisms, including scaffolding, wedging, oligomerization, and crowding.

299 it of the COPII coat contributes to membrane scaffolding, which enforces curvature on the nascent ves

300 These networks are built upon a structural scaffolding with intrinsic neuroplasticity that changes