ライフサイエンスコーパス: tail

1 tion treatments (intact, 'short tail', 'long tail').

2 alpha-tocopherol analogue lacking the phytyl tail).

3 while they crawl forward when touched on the tail.

4 c perturbations within the carboxyl-terminal tail.

5 ning physiological cargo interactions in the tail.

6 ) for Ser in the integrin alphaM cytoplasmic tail.

7 ding domains within the cadherin cytoplasmic tail.

8 diating the sequential assembly of the phage tail.

9 tained only one tyrosine in their C-terminal tail.

10 versibly cross-linked through the histone H4 tail.

11 apped into a half-cylinder with a meandering tail.

12 f several Ser/Thr residues in the N-terminal tail.

13 nd the Ser65 loop and shorten the C-terminal tail.

14 rylation, often at the receptor's C-terminal tail.

15 of E. coli TatC involving both its N- and C-tails.

16 brane proteins toward the chemistry of lipid tails.

17 mplexes and the length of transcript poly(A) tails.

18 related to noncontractile Siphoviridae phage tails.

19 ons (PTMs), such as glutamylation of tubulin tails.

20 with the aforementioned orientations of the tails.

21 the latter into heads, brandy, secondes, and tails.

22 emporal thickness and amygdalar volume (Pone-tailed=0.026, 0.019 and 0.003, respectively).

23 ing events with low probabilities (unbounded tails), 82% are tide-dominated, and almost 49% are highl

24 importance, the cleavage of the VE-cadherin tail alters the postendocytic trafficking itinerary of t

25 Mislocalized tail-anchored (TA) proteins of the outer mitochondrial m

26 With few exceptions, SNAREs are tail-anchored (TA) proteins, bearing a C-terminal hydrop

27 rane targeting and ubiquitination of nascent tail-anchored membrane proteins to understand how their

28 nsertion pathways fail to effectively engage tail-anchored membrane proteins with moderately hydropho

29 ion for the conserved ATPase guided entry of tail-anchored protein 3 (Get3), which targets the essent

30 ed by monitoring the membrane insertion of a tail-anchored protein, SYP72, a syntaxin.

31 Recently, the Guided Entry of Tail-anchored proteins (GET) pathway was described in ma

32 (Get3), which targets the essential class of tail-anchored proteins (TAs) to the endoplasmic reticulu

33 We found that one candidate, the tail-anchored, PDZ-domain-containing OMM protein SYNJ2BP

34 f the Het-s fibril comprising the N-terminal tail and a loop connecting beta-strands 4 and 5, consist

35 with other East African and western Asia fat-tail and European sheep, reveal at least two phylogeogra

36 enous sheep are classified as fat-tail, thin-tail and fat-rump hair sheep.

37 in binding to the beta3-integrin cytoplasmic tail and inducing a kink in the transmembrane domain of

38 ); ultimately these drive contraction of the tail and limb muscles.

39 a soluble TCR construct to a CAR-signalling tail and named the final product TCR-CAR.

40 ytic subunit, selective for the unmethylated tail and perturbing/inactivating the phosphatase active

41 ciations, secondary interactions between the tail and regions of the adapter proteins outside of the

42 erized by different angles between the phage tail and the cell surface.

43 , binds directly to the E-cadherin cytosolic tail and thereby localizes at cell-cell adhesions.

44 thionine (SAM) to lysine residues in histone tails and core histones.

45 ind to acetylated lysine residues on histone tails and thereby facilitate the reading of the histone

46 oth the early phase (r = 0.363, P = 0.03 one-tailed) and the late phase (r = 0.538, P = 0.004).

47 ane-proximal region of the GluA2 cytoplasmic tail, and suggest a distinct model for the regulation of

48 CPF cleaves pre-mRNAs, adds a polyadenylate tail, and triggers transcription termination, but it is

49 ave mild histologic defects, shorter poly(A) tails, and evidence of mitochondrial damage.

50 are related to contractile Myoviridae phage tails, and the F-type PTLBs, which are related to noncon

51 The fat-tail are well adapted to dryland environments, but littl

52 Tails are an intricate component of the locomotor system

53 ble tool to probe the mechanisms by which H3 tails are read out by effector proteins in the cell.

54 Aortas and tail arteries were isolated from young (3-4 months) and

55 y and aortic trifurcation into the iliac and tail arteries.

56 cle function were diminished in uterine (and tail) arteries from aged mice and post-menopausal women.

57 ized phosphorylation target site in the Hec1 tail, as a critical Aurora A substrate for this regulati

58 In the assembled ribosome, uL23(tail) associates with Domain III of the rRNA and a subdo

59 carrying driver mutations had a heavy right tail at the time of tumor detection, with only 1 to 4 do

60 tments similar to those that occur following tail autotomy, characterized by more flexed hind limb jo

61 ar-spherical (icosahedral) and nonspherical (tailed) bacterial viruses were experimentally determined

62 to a preformed protein capsid exemplified by tailed bacteriophages and herpesviruses.IMPORTANCE Adeno

63 Unlike tailed bacteriophages, which use a preformed tail for tr

64 We uncover a poly(A) tail-based regulatory mechanism that dynamically control

65 ion data showed that stroke rates, including tail beat and whole-body movements during feeding, were

66 ach individual in a school, as well as their tail-beating kinematics.

67 Here we mapped the H4-tail binding pocket of ISWI.

68 iation factor 4E (eIF4E), eIF4G, and poly(A) tail-binding protein (PABP) that circularizes mRNAs, pro

69 ad of Uso1 binds to Ypt1 and its coiled-coil tail binds to the Golgi-associated SNARE, Sed5.

70 hematoma expansion was tested by an in vivo tail bleeding cessation method and an ex vivo coagulatio

71 Tail bleeding time was prolonged in DREAM KO control mic

72 The tail bleeding time was significantly lower in laropipran

73 by Ypt1-SW1(Sec4), the extended coiled-coil tail blocks docking to the plasma membrane.

74 ires hydrophobic interactions with the lipid tails but not charged interactions with the lipid headgr

75 s of the absolute configuration of the lipid tail carbinols at pH 4.0 and 8.0.

76 athways originating from the primate caudate tail (CDt).

77 timer-based models of size control and heavy-tailed cell-size distributions.

78 ete normalization of bleeding after a severe tail clip injury in these mice.

79 Tail coating on the back of developments in other fields

80 4, GCL, ML and both sides of the hippocampal tail, compared with healthy subjects and patients with M

81 rcing statistics are non-Gaussian, with long tails corresponding to rare intermittent forcing that pr

82 ns with host cell machinery, the cytoplasmic tail (CT) of F is a likely interactive domain.

83 Tail cuff blood pressure and uterine artery Doppler ultr

84 l(-) with gluconate(-) diminishes the inward tail current (Cl(-) efflux) at a membrane potential of -

85 chronic wasting disease (CWD)-infected white-tailed deer brain homogenates and found that lipid extra

86 from codon 96 glycine/glycine, captive white-tailed deer that were analyzed for prion infection post-

87 in early CWD pathogenesis, we exposed white-tailed deer to CWD prions by mucosal routes and performe

88 WD infection in natural populations of white-tailed deer.

89 with activation of HSP1; looping is lost in tail-deleted TFAM.

90 eins directly recruit PABP, in a non-poly(A) tail-dependent manner, to stimulate the small subunit re

91 developed a pseudoaneurysm of the pancreatic tail, diagnosed as a splenic artery pseudoaneurysm by CT

92 otide-binding domains (NBDs) form a "head-to-tail" dimer upon binding ATP; and the cytoplasmic pathwa

93 davirus (MrNV), the causative agent of white tail disease (WTD) are associated with up to 100% mortal

94 The WD40-containing KIF21B tail displays preference for a GTP-type over a GDP-type

95 This C-terminal tail displays the binding site for partner proteins and

96 These anomalously large values follow a fat-tailed distribution, with a universal exponent related t

97 bly scheme revealed here may be common among tailed DNA phages and herpesviruses.

98 Thus, CAT-tails do not serve as a degron, but rather provide a fai

99 mulation shows the essential role of Kif15's tail domain for load storage within the Kif15-microtubul

100 found that the non-motor microtubule-binding tail domain interacts with the microtubule's E-hook tail

101 ependent catch bond with F-actin through its tail domain, but with lifetimes that depend strongly on

102 ity and includes the MyoA light chain myosin tail domain-interacting protein (MTIP) and several glide

103 osphorylated on two residues at its unfolded tail domain.

104 itical target of Aurora B is the N-terminal "tail" domain of Hec1, which is a component of the NDC80

105 e structure and interactions of the head and tail domains of epidermal keratins 1 and 10, based on al

106 affect the interactions of the core histone tail domains with nucleosomal DNA, redirecting the tails

107 inst phages from all three major families of tailed double-stranded DNA phages.

108 We suggest modelers consider heavy-tailed, downward-skewed probability distributions, such

109 ses are best known for degrading the poly(A) tail during mRNA decay.

110 Carboxy-terminal Alanine and Threonine (CAT) tail elongation-can be recapitulated in vitro with a yea

111 ct observation for the first time of a heavy-tail emissions distribution from flares suggests the nee

112 tially and fully edited mRNAs, while the A/U-tail enables mRNA binding to the ribosome.

113 ng arms, drumstick-shaped legs and a slender tail, features that were probably widespread among parav

114 urthermore, different conformations of phage tail fibers correlated with the aforementioned orientati

115 nd tens of genomes from zebra finch and long-tailed finch populations in Australia.

116 A 2-tailed Fisher exact test was used to assess for differen

117 tailed bacteriophages, which use a preformed tail for transporting their genomes into a host bacteriu

118 lular motility and spreading via actin comet tail formation.

119 FtsZ monomers polymerize head to tail forming tubulin-like dynamic protofilaments, whose

120 in how basal paravians utilized arm, leg and tail function for aerodynamic benefit.

121 ctures, termed tailocins, derived from phage-tail gene assemblies and hypothesized to be the settleme

122 ological traits relevant to fitness in black-tailed godwits Limosa limosa limosa on their northward m

123 al for the isotopic ratio analysis of cattle tail hair in determining the geographical origin of raw

124 Tail handled mice showed little willingness to explore a

125 The beta1 cytoplasmic tail has two NPxY motifs that mediate functions by bindi

126 sules has been synthesized by connecting the tailed hydroxyl groups of C-propan-3-ol pyrogallol[4]are

127 region of the protein, and carboxyl-terminal tail identity both contribute to MLO activity during PT

128 t functional decoupling between the legs and tail in at least some basal paravians.

129 igh-resolution structure of DISC1 C-terminal tail in complex with its binding domain of Ndel1.

130 the lack of an acidic, disordered C-terminal tail in human mtSSB protein.

131 oteoforms of ADAM8 that lack the cytoplasmic tail in the supernatant.

132 The replacement tail includes a regenerated spinal cord with a simple mo

133 interaction of RecQ with the SSB C-terminal tail increases the on-rate of RecQ-DNA binding and has a

134 In addition to the known light chain myosin tail interacting protein (MTIP), we identified an essent

135 tramerization of RXRalpha, owing to the head-tail interaction that is absent in tRXRalpha.

136 mbly of the dodecamer occurs through head-to-tail interactions of the bipolar monomers.

137 substantial destabilization of the main head-tail interface, which is rigid and undergoes very limite

138 a BRafV600E-driven melanomagenic program in tail interfollicular melanocytes.

139 dpq absorption with a maximum at 546 nm that tails into the near-IR and is significantly red-shifted

140 We show that the TubZ C-terminal tail is an unstructured domain that fulfills multiple fu

141 Picking up mice by the tail is aversive, stimulating stress and anxiety.

142 nucleobase is conjugated to a phenyldiazene tail is studied in view of its ability to form triply H-

143 ycloaddition of TrFE: the cis and trans head-tail isomers and the trans head-head isomer, where the C

144 of the steroid ring (LKM38) or the aliphatic tail (KK174), we mapped a binding pocket in mVDAC1 local

145 We demonstrate that the aliphatic tail length (i) can be used as a handle to systematicall

146 e heart, where controlled changes in poly(A) tail length influence mRNA translation.

147 Phage tail-like bacteriocins (PTLBs) are widespread in bacteri

148 the length of the intrinsically disordered C-tail linker modifies the interfilament spacing.

149 e starting oxoacids, many of which are multi-tailed lipids.

150 nt tail-resection treatments (intact, 'short tail', 'long tail').

151 Prior to tail loss, we performed a bromodeoxyuridine pulse-chase

152 leucine zipper at the C-terminal end of the tail (M10(Full)LZ) and the tail-truncated myosin-X witho

153 e obtained a 2.24-A crystal structure of pig-tailed macaque APOBEC3H with bound RNA.

154 tool-assisted foraging on shellfish by long-tailed macaques (Macaca fascicularis) in Khao Sam Roi Yo

155 Our findings further support female pig-tailed macaques as a model of M. genitalium infection, p

156 The unique requirement of HSP1 for the TFAM tail may enable its regulation by post-translational mod

157 n of the Thr(567) in the MT1-MMP cytoplasmic tail may function as a regulatory mechanism to impact ov

158 olar FtsZ protofilaments through their the C-tails may facilitate the coherent treadmilling dynamics

159 rane phenotype that is not observed in flaky tail mice or in newborn individuals with ichthyosis vulg

160 s of A17-PABPN1 and detected shorter poly(A) tails, modest changes in poly(A) signal (PAS) usage, and

161 ively and significantly enriched for histone-tail modifications and transcription factor binding with

162 that connects the Mediator head, middle and tail modules.

163 sing neurons that are sufficient to initiate tail movements.

164 B end contains a 3' protruding nonhomologous tail, Msh2 promotes the rejection of mismatched substrat

165 ty function (pdf) of strength, including its tail, must be determined.

166 synaptic integrity through binding the ColQ tail of acetylcholine esterase.

167 volved in ATP binding and that the phosphate tail of ATP in this structure is in an outward-facing po

168 XXLL-motif sequence DISLL in the cytoplasmic tail of BACE1.

169 es with talin for binding to the cytoplasmic tail of beta3-integrin, whereas it cooperates with talin

170 find evidence of power-law statistics in the tail of C. crescentus cell-size distribution, although t

171 led that a conserved motif in the C-terminal tail of DC2 is critical for assembly into the STT3A comp

172 ientation machinery that binds the cytosolic tail of E-cadherin.

173 ealed a partial truncation in the C-terminal tail of Env that had emerged in the sort; however, itera

174 on, Gbetagamma interacts with the C-terminal tail of GPR124 and promotes the formation of a GPR124-El

175 ot influence H2A.Z occupancy, the C-terminal tail of H2A.Z is one important mediator to recruit PWWP2

176 Proteins binding to the cytoplasmic tail of L-selectin regulate L-selectin functions.

177 in cells and dephosphorylate the C-terminal tail of Lck, which prevents its adoption of an active op

178 phosphorylation of the inhibitory C-terminal tail of Lck.

179 xa (Synechococcus and Cyanobium) with a long tail of low abundance representatives, and local peaks o

180 lysine residue (Lys(1112)) at the C-terminal tail of mGluR1 (a member of the group I mGluR family) pl

181 mphipathic helix in the C-terminal cytosolic tail of RHD3 has a membrane anchoring ability that is re

182 t luminal loop of Glut4, and the cytoplasmic tail of sortilin binds to retromer.

183 y occurring protease sites in the C-terminal tail of SUMO proteins.

184 ive effect on EFW, particularly in the lower tail of the distribution, of the order of 2% to 3% for e

185 cal activity resided in the phytosphingosine tail of the ligand.

186 nd interventions targeting the extreme right tail of the pesticide distribution near human habitation

187 nding site, whereas the conserved C-terminal tail of the second monomer provides residues essential f

188 l striatum ('VS dopamine') and the posterior tail of the striatum ('TS dopamine').

189 The p-aminobenzoyl-l-glutamate tail of THF remains weakly bound in a widened binding cl

190 ludes carrier relaxation into an exponential tail of trap states extending up to 1.5 eV into the band

191 inides was investigated over 8 months in the tailing of the breakthrough curve of run 13-05 as well a

192 his microarray to interrogate the C-terminal tails of a small group of candidate proteins and identif

193 show that DPF2 interacts with the acetylated tails of both histones 3 and 4 via bipartite binding poc

194 decreased the acetylation of the N-terminal tails of cytosolic histones.

195 ognition of sorting signals in the cytosolic tails of the cargos by adaptor proteins, leading to carg

196 are found on the N-terminal histone domains (tails) of approximately 50 residues protruding from the

197 on in eutherian mammals using the gray short-tailed opossum (Monodelphis domestica) as a model.

198 The shape of the tailed organisms was incorporated into two modeling appr

199 .9 x 10(-8)) was replicated among females (1-tailed P = 0.002), as well as replicated in meta-analysi

200 s ( P = 2.6 x 10(6)) and replicated (i.e., 1-tailed P = 0.016) in the Brazilian cohort.

201 replicated in meta-analysis of both sexes (1-tailed P = 0.021).

202 icated among females in the meta-analysis (1-tailed P = 0.052).

203 overall performance (AUC, 0.930 vs. 0.891; 2-tailed P value for difference, 0.31).

204 Because the 1-tailed P value from the Fisher exact test was <.001, whi

205 confidence interval [CI], 0.32 to 0.95 [two-tailed P=0.04 for superiority]).

206 RNA function is controlled by the 3' poly(A) tail (PAT) and poly(A)-binding protein (PABP).

207 rosines (Y24 and Y48) bind to a Kme3-histone tail peptide via cation-pi interactions, but linear free

208 is first reported crystal structure of a two-tailed peptidic bilayer reveals similarities in thicknes

209 The truncated tail phospholipids, 1-palmitoyl-2-(5-oxovaleroyl)-sn-gly

210 We show that Hec1 tail phosphorylation tunes friction along polymerizing m

211 1) and Asn-236 (equivalent to Asn-563 in the tail piece of IgM).

212 The resulting head and tail pieces regenerate within about a week, forming two

213 om passenger pigeons and 2 genomes from band-tailed pigeons, which are passenger pigeons' closest liv

214 pO2 (15 +/- 4% from baseline) in response to tail pinch stress paradigm.

215 han unexpected increases, and ignoring heavy-tailed process noise leads to an underestimate in the ma

216 S81 cleavage of regressed forks with a ssDNA tail promotes POLD3-dependent fork rescue.

217 cetyl groups from lysine residues on histone tails, promoting transcriptional repression via condensa

218 chimeric phages, we show that specific phage tail proteins allow for infection of strains with glycos

219 y to those obtained from conventional poly-A tail purification methods, indicating both enumerate the

220 ion of these cells before, during, and after tail regeneration.

221 and reveal a critical role of the C-terminal tail region of IN in higher order oligomerization of int

222 Mutations in the distal cytoplasmic tail region of M2, and in particular a tyrosine-to-alani

223 For the tail region of the protein, folding requires rRNA, and a

224 hat the last 18 residues of the C terminus ("tail" region) of IN (residues 1-286) determined whether

225 The globular and tail regions of rProtein uL23 are distinctive in their f

226 fusion proteins (IFPs) with the cytoplasmic tail replaced by the signaling domain of the costimulato

227 also evaluated by comparing three different tail-resection treatments (intact, 'short tail', 'long t

228 is, preventing Aurora phosphorylation of the tail results in prematurely stable attachments that rest

229 ribosome profiling and mitochondrial poly(A)-tail RNA sequencing (MPAT-Seq) assay, we identify the po

230 The mutation is located in the tail segment and is predicted to disrupt STAT1 sumoylati

231 cterized motif, termed AcidicN, to confer H4-tail sensitivity and discriminate between DNA and nucleo

232 en by elastic energy stored in a contractile tail sheath.

233 hylogeographically distinct genepools of fat-tail sheep in Africa that differ from the European genep

234 he CCR4-NOT complex function in mRNA poly(A) tail shortening.

235 The A-tail stabilizes partially and fully edited mRNAs, while

236 nanoparticles (MSNs) with controllable head-tail structures have been successfully synthesized.

237 The sophisticated tail structures of DNA bacteriophages play essential rol

238 al viruses (bacteriophages/phages) have long tail structures that serve as organelles for DNA deliver

239 dds ratio (OR)=1.23) and COLQ (collagen-like tail subunit of asymmetric acetylcholinesterase; rs76098

240 duced immobility time in the forced swim and tail suspension tasks, as well as reduced latency to fee

241 ty relative to wild-type (WT) littermates in tail suspension, an antidepressant-predictive assay, and

242 he nematic feature that arises from the head-tail symmetry of cell-to-cell interaction).

243 A 2-tailed t test with a significance level of .05 was used

244 Differences were evaluated using paired 2-tailed t tests.

245 unveils a region of the N-terminal cytosolic tail targeted by the Art1 alpha-arrestin, which is activ

246 nuclear translocation of the PC1 C-terminal tail/TAZ (PC1-CTT/TAZ) complex, leading to increased run

247 tion across the inner membrane of the COX2 C-tail that contains the apo-CuA site.

248 We identify a mutant of the Ndc80 tail that is deficient in Ska recruitment to kinetochore

249 For M. smegmatis TopoI-CTD, a 27-amino-acid tail that is rich in basic residues at the C-terminal en

250 que, structurally uncharacterized C-terminal tail that plays an important role in autophosphorylation

251 ivities for the highly basic Rrp6 C-terminal tail that we term the 'lasso' because it binds RNA and s

252 a negative charge to residues of the histone tails that interact with the negatively charged DNA, is

253 breaks are resected to form 3' single-strand tails that participate in a homology search, ultimately

254 occurs without a protruding nonhomologous 3' tail, the mismatch repair protein Msh2 does not discoura

255 rican indigenous sheep are classified as fat-tail, thin-tail and fat-rump hair sheep.

256 m in which its transmembrane and cytoplasmic tail (TMCT) domains were replaced with those of the HPIV

257 O3) with a nanostructured organic functional tail to create a platform capable of monitoring biospeci

258 liposomes by reengineering the polyhistidine tail to include a free cysteine on each protomer of mode

259 eling enzymes need the histone H4 N-terminal tail to mobilize nucleosomes.

260 omains with nucleosomal DNA, redirecting the tails to more interior positions within the nucleosome.

261 e) were successfully obtained with over 99 % tail-to-head content and high molecular weight (up to 92

262 how how Pxn binding to the CD103 cytoplasmic tail triggers alphaEbeta7 integrin outside-in signaling

263 rminal end of the tail (M10(Full)LZ) and the tail-truncated myosin-X without artificial dimerization

264 o couples to a model of the viral capsid and tail tube.

265 H)CBCANH spectra of the 20 kDa bacteriophage tail-tube protein gp17.1 in a total time of two and a ha

266 e rRNA interactions of rProtein uL23 and its tail, uL23(tail), which is a beta-hairpin that penetrate

267 Restricting tail undulations resulted in kinematic adjustments simil

268 gher cholesterol concentration and increased tail unsaturation in brain PM) appear to have opposite,

269 mble in a domino-like mechanism from head-to-tail upon a triggering event induced by an external stim

270 ied upon for food consumption and prehensile tail usage.

271 yte number in living mice was assessed after tail vein injection (150 mug of each conjugate per mouse

272 pecific gene transfer following hydrodynamic tail vein injection using the kidney-specific podocin an

273 by administering an insulin stimulation via tail vein injection.

274 ration of 42.1 +/- 3.9 MBq of (18)F-FMISO by tail vein injection.

275 HepG2 colonization into lung and liver after tail vein injection.

276 Tracer was injected via the tail vein, and dynamic PET scans were acquired for 90 mi

277 lowing injection of carcinoma cells into the tail vein.

278 injected them into FIX knockout mice via the tail vein.

279 tal metastasis assay we detail here includes tail-vein injection of cancer cells into the mouse and d

280 Hydrodynamic tail-vein injection of MAN2A1-FER resulted in rapid deve

281 bitor RNAs against PPP1R1, injected into the tail veins of immune-compromised mice, and followed by n

282 comparing TLN versus HLL (without cytotopic tail) versus negative control.

283 ticle-wrapping polymer are mobile (loops and tails) versus immobile (trains).

284 ins recognize histone H3 lysine 9 methylated tails via their chromodomain and recruit additional liga

285 However, when the tailed viruses were approximated as spheres, poor agreem

286 Hippocampal tail volume is proposed as a potentially useful biomarke

287 for age and total brain volume, hippocampal tail volume was larger in the MDD cohort compared to con

288 Larger hippocampal tail volume was positively related to clinical remission

289 rated after a method to remove decorrelation tails was applied to the DRL images.

290 The Fisher exact test (2-tailed) was used to compare proportions, Student t test

291 ractions of rProtein uL23 and its tail, uL23(tail), which is a beta-hairpin that penetrates deep into

292 rs of FtsZ constructs lacking the C-terminal tail, which is known to provide a flexible tether essent

293 step included the cut into heads, heart and tails, while the latter into heads, brandy, secondes, an

294 main interacts with the microtubule's E-hook tail with a rupture force higher than the stall force of

295 Incubation of the L-selectin tail with cell extracts from phorbol 12-myristate 13-ace

296 te the interactions of rProtein uL23 and its tail with Domain III and with DIII(core) rRNA.

297 single-stranded RNAs that are joined head to tail with largely unknown functions.

298 engthening electrostatic interactions of the tail with the microtubule lattice.

299 ractions of one hydrophobic palmitoleic acid tail with two CRD palmitoleoyl-binding grooves oriented

300 tracellular half constructs and compared the tails with the ordered kinase domains.