ライフサイエンスコーパス: anchoring of

1 This genetic map enabled the anchoring of 100 Mb of WGS and 420 Mb of BAC sequences,

2 We report the anchoring of 3D-DNA-cholesterol labeled cages on spheric

3 t C-Au coupling compared to the coordinative anchoring of 7-9, endorsing C-Au coupled organometallic

4 These findings indicate that the anchoring of a chromatin-modifying complex to its produc

5 polypeptide-micelle interaction include the anchoring of a hydrophobic residue cluster into gaps in

6 e of the cell wall and alters processing and anchoring of a major Isd system component, IsdC.

7 ng at postsynaptic sites, both regarding the anchoring of a single receptor (the AMPA receptor) in py

8 n Staphylococcus aureus that is required for anchoring of a surface protein with a NPQTN motif.

9 matic guide-tree construction, protein-based anchoring of ab-initio gene predictions, and constraints

10 Anchoring of AC to the complex also sensitizes the chann

11 The anchoring of AC to this complex generates local pools of

12 in-activated MuSK to regulate clustering and anchoring of AChRs in skeletal muscle.

13 e, agrin-induced clustering and cytoskeletal anchoring of AChRs was dependent on Src-family kinases.

14 ls in vivo: increased functional expression, anchoring of AKAP15 and PKA, and initiation of excitatio

15 ults call into question the role of membrane anchoring of alpha(2)delta subunits for calcium current

16 ings support a role for GRIP in the synaptic anchoring of AMPA receptors but also suggest that GRIP h

17 for the first time a model for a multivalent anchoring of AmpDh3 onto the cell wall, which lends itse

18 of the host farnesylation machinery and its anchoring of an F-box effector to the LCV membrane, and

19 PDZ domain protein is required, in vivo, for anchoring of an ion channel to a signaling complex.

20 Although co-inoculating with, temporary anchoring of and transgenic expression of exogenous PAMP

21 bacteria followed by rapid farnesylation and anchoring of AnkB to the cytosolic side of the plasma me

22 led-DNA strands and hybrids on paper via the anchoring of antibodies with a fusion protein that combi

23 onolayer to serve as a template for chemical anchoring of antibodies.

24 lignment of the core-module, reveal that the anchoring of apical non-centrosomal MTs at apical juncti

25 is study aimed to determine the mechanism of anchoring of APS to the surface of P. gingivalis.

26 Because anchoring of AQP4 to the perivascular astrocyte endfoot

27 results are consistent with a model whereby anchoring of ASH1 mRNA requires molecular remodeling of

28 Cell wall anchoring of assembled BcpA pili requires sortase A, whi

29 We also have shown that anchoring of AtFH1 in the cell wall promotes actin bundl

30 n the Tubby domains that are required for PM anchoring of AtTLPs.

31 iation hybrid (RH) mapping, will aid precise anchoring of BAC contigs in the large regions of suppres

32 We show that CP110 is required for anchoring of basal bodies to the membrane during cilia f

33 her, these results implicate EF1alpha in the anchoring of beta-actin mRNA to the protrusion in crawli

34 to the posterior of the oocyte, the anterior anchoring of bicoid mRNA and the basal localization of p

35 The entry and anchoring of blocking-peptides is facilitated by the pre

36 The plots thus reveal details of the anchoring of bonds to the cell and provide a better unde

37 Thus, the direct anchoring of both PKA and AC to TRPV1 by AKAP79/150 faci

38 ligand-dependent manner to provide critical anchoring of both proteins to the membrane.

39 at the source of this fidelity is due to the anchoring of both the SPase I enzyme (by way of its tran

40 ormation of oligomeric clusters controls the anchoring of cadherin to actin and cell-cell contact flu

41 results support a model whereby subcellular anchoring of CaN by AKAP150 is a key molecular determina

42 is critical for intracellular signalling and anchoring of carbohydrates and proteins to outer cellula

43 face and further suggest that preventing GPI anchoring of CaValpha2delta1 averts its cell-surface exp

44 nch extension into the synaptic neuropil and anchoring of cell bodies at the neuropil border.

45 l step in glycosylphosphatidylinositol (GPI) anchoring of cell surface proteins consists of a transam

46 vides for glycosylphosphatidylinositol (GPI) anchoring of cell-surface proteins occurs in the lumen o

47 HYLS-1 is required for the apical targeting/anchoring of centrioles at the plasma membrane but not f

48 development through physical interaction and anchoring of circulating tumor cells to endothelium.

49 ish that the CTD mutations indeed compromise anchoring of ColQ and that both HSBD and CTD are essenti

50 f AChE, suggesting that CTD mutations affect anchoring of ColQ to the synaptic basal lamina.

51 is not required for targeting but rather for anchoring of complexes, because INAD and TRP can be targ

52 Anchoring of complexing ligand on the gold surface aboli

53 eostasis require both component turnover and anchoring of components to the plasma membrane.

54 ward the cortex during oocyte maturation and anchoring of cortical granules in the cortex.

55 nd that sensory dendrites form by stationary anchoring of dendritic tips during cell-body migration.

56 e biosynthetic processing, transport, and/or anchoring of DHPRs, with residues 1543-1620 being partic

57 sus GABAergic interneurons and regarding the anchoring of different receptors (AMPA vs NMDA receptors

58 inct mechanisms to regulate the movement and anchoring of different transcripts.

59 he closed active center), His(221) (covalent anchoring of dihydroxyacetone to K), Asp(401) and Asp(40

60 This methodology allows for the anchoring of DNA cages on supported lipid bilayers, the

61 mid DNA by T7 RNA polymerase did not require anchoring of DNA to the bacterial cytoplasmic membrane.

62 ssible basis for this difference is the dual anchoring of doubly phosphorylated AANAT via one 14-3-3z

63 target epitopes determines accessibility for anchoring of drug conjugates and bulkier drug carriers,

64 that facilitates BICD2- and CENP-F-mediated anchoring of dynein to nuclear pore complexes.

65 affinity of the FYVE domain, reinforcing the anchoring of early endosome antigen 1 (EEA1) to endosoma

66 sing knockin mice that are deficient in AKAP-anchoring of either PKA or the opposing phosphatase calc

67 Such a modification allows anchoring of even highly hydrophilic proteins to the mem

68 Restoring LARGE expression repaired anchoring of exogenous and endogenous laminin and modula

69 In vitro data suggest that membrane anchoring of FKN, and the existence of a shed, soluble F

70 ly-Gly-Ala-Arg-Pro-Asp-Phe): (i). side-chain anchoring of Fmoc-Asp-OAl via its free beta-carboxyl as

71 as responsible for the quantitative membrane anchoring of FR-alpha and the production of soluble FR-b

72 ggests a role for Vangl2 in the targeting or anchoring of Fz3, a hypothesis strengthened by the exist

73 yrin is a key scaffold protein mediating the anchoring of GABAA receptors at inhibitory synapses.

74 Accordingly, the anchoring of GAD65 to exosome-mimetic liposomes strongly

75 ating the N-terminus is not required for the anchoring of GAD65 to SV.

76 sphorylation status does not affect membrane anchoring of GAD65, nor its Km or Vmax for glutamate.

77 does not affect the GAD65-dependent membrane anchoring of GAD67.

78 We conclude that pericentrin anchoring of gamma tubulin complexes at centrosomes in m

79 We show that the anchoring of GAUT1 in the Golgi requires association wit

80 ur strategy uses a combination of phenotypic anchoring of gene expression profiles and loss-of-functi

81 ell membranes and that constitutive membrane anchoring of GIV in yeast cells or rapid membrane transl

82 By exploiting DNA hybridization-directed anchoring of gold nanoparticles (AuNPs) on substrates, a

83 sphatidylinositol addition site for membrane anchoring of gp63.

84 n nucleoskeleton provides a scaffold for the anchoring of highly condensed heterochromatic DNA to the

85 ene glycol maleimide labelling revealed that anchoring of HMW1 requires the C-terminal 20 amino acids

86 In this study, we simulated the membrane anchoring of human immunodeficiency virus-1 myristoylate

87 nal motif in eukaryotic proteins facilitates anchoring of hydrophilic proteins, such as Ras and Rab,

88 napse to nucleus involves activity-dependent anchoring of importins at the synapse.

89 tation of the host prenylation machinery for anchoring of injected effectors to host membranes.

90 ynthesized by direct nucleation, growth, and anchoring of inorganic nanomaterials on the functional g

91 Covalent anchoring of intact PV3 molecules on Co(3)O(4) nanoparti

92 ns, their cytoplasmic plaques are sparse and anchoring of intermediate filaments is defective.

93 d desmoplakin to the plaque, and ending with anchoring of intermediate filaments, which represents th

94 The strong anchoring of intermediates is widely accepted to retard

95 In mutant OSNs, cilia base-anchoring of intraflagellar transport components IFT88,

96 Selective concentration and anchoring of ionotropic receptors at the synapse is esse

97 The proposed method allowed anchoring of iron oxyhydroxides nanoparticles on AC, whi

98 Anchoring of IsdC to the cell wall envelopes of vegetati

99 nding of its extracellular domain and by the anchoring of its intracellular domain to actin cytoskele

100 Anchoring of laminins at the cell surface enables assemb

101 These striking differences in the anchoring of LCs on surfaces presenting chiral versus ac

102 the cytoskeleton and RNA may function in the anchoring of localized RNAs at the vegetal cortex of Xen

103 Glycolipid anchoring of LTA appears to play an important role durin

104 Beyond anchoring of LTMRs to the surrounding dermis and epiderm

105 tead, Lys 116 participates in the structural anchoring of Lys 115 in a long, hydrophobic funnel provi

106 positive membrane enzyme which catalyzes the anchoring of many cell surface proteins conserved with t

107 residue was required for efficient cell wall anchoring of mature Ebp pili.

108 in cell signaling, membrane trafficking, and anchoring of membrane proteins in addition to membrane s

109 tin network dynamics and participates in the anchoring of membrane proteins to the actin cytoskeleton

110 falciparum because of their role in membrane anchoring of merozoite surface proteins involved in para

111 of distinct cadherin profiles on peritoneal anchoring of metastatic lesions remains poorly understoo

112 rch and capture" model posits that selective anchoring of microtubule plus ends at the cell cortex ma

113 not promote nucleation but were required for anchoring of microtubules, a previously uncharacterized

114 suggest general principles for cytoskeletal anchoring of mitochondria in all tissues, reveal potenti

115 Furthermore, anchoring of MPER peptides to the membrane via a hydroph

116 We propose that anchoring of mtDNA within the organelle is linked to an

117 Nucleation and anchoring of MTs required the same number of gamma-tubul

118 universal avian BAC clones that permit rapid anchoring of multiple scaffolds to chromosomes on all av

119 gnificant importance for all work related to anchoring of nanoparticles on nanocarbon-based supports,

120 Anchoring of nanos depends on integrity of the actin cyt

121 Actin-dependent anchoring of nanos RNA complexed to the germ plasm at th

122 lusters, suggesting a modulatory role in the anchoring of NMDA receptor at spines.

123 vel physiologic NO effector and suggest that anchoring of nNOS to specific targets is a mechanism by

124 Accordingly, anchoring of not only PKA but also AC by AKAP5 is import

125 amino acid residues play a role in membrane anchoring of NS5B and replication, to determine whether

126 Even distribution and anchoring of nuclei at the embryo cortex are crucial for

127 unc-84 mutants are also defective in the anchoring of nuclei within the hypodermal syncytium and

128 lf-assembles by means of reversible covalent anchoring of nucleobase recognition units onto simple ol

129 dure, for efficient and selectively oriented anchoring of oligosaccharide probes via their reducing e

130 r cells following bacterial division and for anchoring of one of the major S-layer proteins.

131 multicomponent systems involves the lateral anchoring of organic heteromolecules to graphene.

132 er from the oocyte cortex, severely disrupts anchoring of osk gene products only when Homer (not Bifo

133 Transport, translation, and anchoring of osk mRNA and proteins are essential for pos

134 Pho-like and Pho may not participate in the anchoring of PcG complexes, but may be necessary for tra

135 HCII complexes are stabilized by hydrophobic anchoring of peptide side chains to pockets in the MHCII

136 icentrin complex is required for centrosomal anchoring of pericentrin/gamma-tubulin and for centrosom

137 This activity is necessary for anchoring of PI(4)P-binding effectors to bacterial phago

138 rmeability, suggesting a role for the proper anchoring of pili in retaining OM integrity.

139 B (srtB) or C (srtC), is required for proper anchoring of pili to the bacterial envelope, suggesting

140 alled housekeeping sortase, in the cell wall anchoring of pili.

141 Therefore, SrtF can catalyse the cell wall anchoring of pilin monomers as well as pili, but it does

142 e data support a model in which ERM-mediated anchoring of PKA activity to DCC is required for proper

143 tein that participates in both mitochondrial anchoring of PKA and mitochondrial dynamics.

144 tal muscle Ca2+ channel by PKA also required anchoring of PKA by A-Kinase Anchoring Proteins because

145 rpose of this study was to determine whether anchoring of PKA by mAKAP regulates RyR function.

146 ssion of RI and RII and consequently reduced anchoring of PKA holoenzyme.

147 Anchoring of PKA in proximity to certain adenylyl cyclas

148 Anchoring of PKA near the channel by an AKAP, which bind

149 These data indicate that synaptic anchoring of PKA through association with AKAPs plays an

150 kinase (PKA) may be mediated in part by the anchoring of PKA to a family of A-kinase anchor proteins

151 The anchoring of PKA to AKAPs (A kinase-anchoring proteins)

152 Our results reveal a novel mechanism whereby anchoring of PKA to Ca(2+) channels via LZ interactions

153 Thus, the anchoring of PKA to mitochondria represents a focused su

154 using the peptide Ht31 known to disrupt the anchoring of PKA, inhibited both basal and hormone-induc

155 provides potential mechanisms for regulating anchoring of PKAII and targeting of cAMP signals to effe

156 Thus, anchoring of PKAII in actin cortical cytoskeleton increa

157 Our results suggest that anchoring of PKG to NPRA is a key event after ligand bin

158 a, these physiological results indicate that anchoring of PP2A at this site of Ca(v)1.2 in the heart

159 has been shown to be required for cell wall anchoring of protein A as well as virulence in the patho

160 merging paradigm in matrix biology involving anchoring of proteinases to the cell surface to regulate

161 Glycosylphosphatidylinositol (GPI) anchoring of proteins is catalyzed by GPI transamidase (

162 Glycosylphosphatidylinositol (GPI) anchoring of proteins provides a potential mechanism for

163 Further, sortase A-mediated anchoring of proteins to peptidoglycan, which also invol

164 Glycosylphosphatidylinositol (GPI) anchoring of proteins to the cell surface is important f

165 Here, we investigated the role of the anchoring of PrP on prion neuroinvasion by studying vari

166 Direct anchoring of quinone to the protein backbone permits sec

167 formation of RAG-DNA complexes that involves anchoring of RAG1 at the recombination signal nonamer an

168 : the interaction with switch 2 mediates the anchoring of Ras to Sos, whereas the interaction with sw

169 potential role for MAPs in the cytoskeletal anchoring of receptor-ion channels at specific subcellul

170 thought to be important in the targeting and anchoring of receptors to specific synapses.

171 Importantly, no anchoring of reentrant rotors was visibly identifiable i

172 we developed a system to mimic the membrane anchoring of Rho GTPases by creating liposomes containin

173 as used to map the sequence requirements for anchoring of RIalpha to D-AKAP1.

174 dependent pathways that are regulated by the anchoring of RIIbeta to BIG2 via AKAP domains B and C.

175 density for capsid stability and intracapsid anchoring of RNA templates.

176 and fistulas, but newer indications such as anchoring of self-expandable metal stents and bariatric

177 Electronic anchoring of sets of amplification primers in distinct a

178 lipid rafts, trafficking of cholesterol, and anchoring of signaling molecules.

179 porulation in Bacillus subtilis involves the anchoring of sister chromosomes to opposite ends of the

180 l steps includes the process of cytoskeletal anchoring of SK2 channel by its interacting protein, alp

181 dfeet are required for the basement-membrane anchoring of Slit.

182 Given that S-acylation facilitates anchoring of soluble proteins to cell membranes, our fin

183 Sortase enzymes are responsible for covalent anchoring of specific proteins to the peptidoglycan of t

184 ly induce BPL cell apoptosis due to membrane anchoring of sTRAIL and simultaneous activation of the C

185 ns suggest a mechanism by which LC2 provides anchoring of surface Ca(v)2.2 to the actin cytoskeleton,

186 n assembled cell wall as a substrate for the anchoring of surface protein.

187 These results reveal that the cell wall anchoring of surface proteins in Gram-positive bacteria

188 Cell wall anchoring of surface proteins in Staphylococcus aureus r

189 a nucleophilic acceptor in sortase-catalyzed anchoring of surface proteins in Staphylococcus aureus.

190 taphylococcus aureus mutant defective in the anchoring of surface proteins was isolated and shown to

191 f is required for the secretion or cell wall anchoring of surface proteins, we analyzed variants of s

192 wall synthesis inhibitors interfere with the anchoring of surface proteins.

193 SdpI in the trafficking and/or cytoskeletal anchoring of synaptic GlyRs.

194 tions in the nicking complex are assisted by anchoring of terminase to cosB.

195 ane repair and vesicular trafficking system, anchoring of the actin and tubulin cytoskeleton to the p

196 Thus, anchoring of the adenosine 2'-phosphate of NADPH by Arg

197 e absence of a beta subunit, plasma membrane anchoring of the alpha1C N terminus or its deletion inhi

198 Here we report that transient anchoring of the alpha1C subunit C-tail in the plasma me

199 ignal showed a lower value implying that the anchoring of the aptamer on the Au surface enhanced its

200 in the fluorescence assay, implying that the anchoring of the aptamer on the Au surface improved its

201 ellular matrix receptor that is required for anchoring of the basement membrane to the cell surface a

202 track detector indicated fairly homogeneous anchoring of the bifunctional polymer on the surface of

203 Anchoring of the C-terminal tail to the plasma membrane

204 one-subunit complex formation depends on the anchoring of the carboxylate group of the subunit into t

205 nstrate a unique role for PIP5KIgamma in the anchoring of the cell membrane to the cytoskeleton in me

206 se-mediated mechanism for covalent cell-wall anchoring of the cellulosome in R. flavefaciens differs

207 of handling, long-term culture in vitro and anchoring of the central collagen gel to avoid shrinkage

208 ila fusome that that is probably involved in anchoring of the centrioles and organization of the prim

209 Glu60, Glu61, and Glu64 provide the anchoring of the cluster to the protein cage.

210 herent advantages, the main being the strong anchoring of the coating to the capillary wall resulting

211 sting that it may be involved in the tighter anchoring of the corneal epithelium to the underlying ti

212 sites within the first few atomic planes, an anchoring of the Cr film to the substrate, charge transf

213 eptide with neutral bilayers was promoted by anchoring of the cysteamine moiety.

214 We discuss how FtsA and ZipA provide anchoring of the cytoplasmic FtsZ to the membrane and ho

215 of the enzyme-substrate interaction involves anchoring of the desosamine residue in two alternative b

216 , suggesting that CSB may participate in the anchoring of the DNA repair complex.

217 Here, we show that membrane anchoring of the ENTH and ANTH domains is regulated by t

218 3' to 5' "scanning" mechanism and imply that anchoring of the enzyme to the 5'-monophosphorylated end

219 11-mercaptoundecanoic acid for the covalent anchoring of the enzyme.

220 ausible that yet-unknown proteins facilitate anchoring of the ER membrane with the cytoskeleton.

221 sapentaenoic acids involves charge-dependent anchoring of the fatty acids at the mouth of the access

222 rotein (YqxM) required for the formation and anchoring of the fibers to the cell.

223 ponent of all musculoskeletal systems is the anchoring of the force-generating muscles to the solid s

224 mechanistic functions that go beyond passive anchoring of the force-generating SNAREpin to the fusing

225 hat the intracellular domain interfered with anchoring of the full-length CD44 to the cytoskeleton an

226 me localization domains leads to the loss of anchoring of the gamma-tubulin ring complex and of nucle

227 elasticity strongly relies on the mechanical anchoring of the giant protein titin to both the sarcome

228 gue of vertebrate band 4.1, functions in the anchoring of the glutamate receptor IIA subunit (GluRIIA

229 This mutation affects anchoring of the GPIb alpha polypeptide in platelets and

230 nce that this propionate participates in the anchoring of the heme within the heme pocket.

231 Crystal structures showed anchoring of the hits in the nicotinamide pocket.

232 operties of the holdfast, as well as for the anchoring of the holdfast to the cell envelope.

233 xport of the holdfast polysaccharide and the anchoring of the holdfast to the cell were previously di

234 agation and selection can be affected by GPI anchoring of the host's PrP(C).

235 The anchoring of the ionomer-based plastic antibody on the c

236 -cell adhesion in the paracellular space and anchoring of the junctional complex to the cytoskeleton.

237 ey implicate a role for SNAREs in positional anchoring of the K(+) channel protein.

238 cell line (RINm5F), suggesting that membrane anchoring of the kinase participates in physiologically

239 defects in the direction of movement and/or anchoring of the kinocilium within each hair cell.

240 ng into PVA solution that facilitates planar anchoring of the liquid-crystal molecules at the droplet

241 alanines is required for efficient membrane-anchoring of the M13 procoat protein that inserts by a h

242 This asymmetry results from the anchoring of the meiotic spindle to the oocyte cortex an

243 receptor is not present in lipid rafts, and anchoring of the MHV receptor to lipid rafts did not enh

244 f centrioles are involved in the docking and anchoring of the mother centriole to the cellular membra

245 role of dynein at the synapse, in which the anchoring of the motor to the cortex via binding to an a

246 Anchoring of the myonuclei to the core acto-myosin fibri

247 mbrane association appears to also depend on anchoring of the N terminus by myristoylation.

248 temperatures, which can be explained by the anchoring of the N-terminal domain to the C-terminal cor

249 restricting axons to the brain, providing an anchoring of the neuroepithelial cells to the pial surfa

250 sion, DNA replication, and exocyst-dependent anchoring of the nuclear envelope to the bud affect nucl

251 d for the localization of oskar mRNA and the anchoring of the nucleus in the Drosophila oocyte.

252 n of bicoid (bcd) and gurken (grk) mRNAs and anchoring of the oocyte nucleus to the cell cortex.

253 Bifocal act redundantly to promote posterior anchoring of the osk gene products.

254 in, may act redundantly to mediate posterior anchoring of the osk gene products.

255 e suggested that in contrast to the membrane anchoring of the PBP4 and PBP6b C-terminal alpha-helices

256 Tethering also required proximate membrane anchoring of the PDZ domain, suggesting a mechanism that

257 e charging of the interface also facilitates anchoring of the peptide near the surface via one of its

258 from the bulk phase toward the surface; (2) anchoring of the peptide to the water/solid interface vi

259 pilus-specific sortase followed by cell wall anchoring of the pilus that is promoted by the housekeep

260 ownstream cytokinesis factors and for stable anchoring of the plasma membrane at the midbody.

261 ed-forward signal amplification by promoting anchoring of the PLCgamma2 C2 domain to phospho-SLP65.

262 Glycosylphosphatidylinositol (GPI) membrane anchoring of the prion protein (PrP(C)) directs it to sp

263 Glycosylphosphatidylinositol (GPI) anchoring of the prion protein (PrP(C)) influences PrP(C

264 membrane domain by L39Stop mutation prevents anchoring of the protein in the membrane, greatly reduci

265 We examined the possibility of GPI anchoring of the protein in three ways: (i) Phosphatidyl

266 her the predicted periplasmic domain nor the anchoring of the protein to the inner membrane is necess

267 f (class B), which is important for membrane anchoring of the protein; the presence of such subunits

268 choline receptor beta and delta subunits and anchoring of the receptor to the cytoskeleton.

269 horylation of rhotekin by PKD2 modulates the anchoring of the RhoA in the plasma membrane.

270 Cell wall anchoring of the SpaA polymers is triggered when SrtA in

271 rylation of spinophilin by PKA modulates the anchoring of the spinophilin-PP1 complex within dendriti

272 h the lateral wall either to give additional anchoring of the stereocilia or to provide a route for i

273 cificity is achieved through recognition and anchoring of the sugar-amide headgroup to the GLTP recog

274 endocytosis, revealing that GluN2B-mediated anchoring of the synaptic proteasome is responsible for

275 We found that anchoring of the termini at the cell centre and proper s

276 generated in a tetA-bearing DNA ring through anchoring of the tetA transcripts to cell membrane, thes

277 sterol, which is important to facilitate the anchoring of the virus at the mammalian cell membrane.

278 clear platinum-DNA interactions and a novel "anchoring" of the polyamine by Pt-DNA bond formation all

279 activation and actin dynamics, but impaired anchoring of their integrins to the cytoskeleton.

280 PIP5KIgamma-null platelets do have impaired anchoring of their integrins to the underlying cytoskele

281 s leading to the transport, localization and anchoring of their RNAs to the cortical ER.

282 We report the uniform planar anchoring of thermotropic liquid crystals on films of bo

283 in kinase C family may be helped by specific anchoring of these enzymes to scaffold proteins that loc

284 mutant proteins are only compatible with the anchoring of these surface lipoproteins in the outer lea

285 Anchoring of these two structured TFIIF domains at separ

286 d glucose at 0.6 V vs SCE, demonstrating the anchoring of this enzyme via two coordination systems.

287 while SrtF facilitated the optimal cell wall anchoring of this heterodimer.

288 Heterobifunctional anchoring of this polyprotein construct and DNA via copp

289 that the QVPTGV sequence is a substrate for anchoring of this protein by SrtC.

290 Anchoring of this protein segment to the endoplasmic ret

291 t palmitoylation of Cys30 and Cys34 leads to anchoring of this region of the cytoplasmic tail to the

292 Stable anchoring of titin within the muscle Z-disk is essential

293 Supramolecular anchoring of transition metal complexes to a protein sca

294 The strength of anchoring of transmembrane receptors to cytoskeleton and

295 conclude, we suggest that Tyr(511)-mediated anchoring of vanilloids in their binding pocket is pivot

296 Since the anchoring of Vg1 mRNA to the vegetal cortex is actin dep

297 We show the anchoring of well-defined amounts of lipid-DNA onto the

298 g critically involved in the plasma membrane anchoring of XLalphas.

299 Anchoring of xnf7 was not dependent on association with

300 We demonstrated that cytoplasmic anchoring of xnf7 was regulated by changes in the phosph