ライフサイエンスコーパス: tail

1 the acidic residues destabilized GFP::SpxA1(tail) .

2 at 3 or 11 weeks (P < .000l, Barnard test, 2-tailed).

3 d UBL domains (UBL1-2) within the C-terminal tail.

4 g the last 19 amino acids of the cytoplasmic tail.

5 cone because of mobility of its unsaturated tail.

6 reassociated with the alpha-subunit carboxyl tail.

7 NA-binding domains (dsRBDs) and a C-terminal tail.

8 which revealed loss of the pancreas body and tail.

9 ntributed by nonmuscle structures within the tail.

10 DNA translocation into bacteria through the tail.

11 r of perturbed interactions with the mutated tail.

12 rcentage of the atoms without the attractive tail.

13 rlinked by three loops and a long C-terminal tail.

14 ures with a characteristic hypertransmission tail.

15 mmodated by the oligomers as an unstructured tail.

16 f macrocystic/unilocular lesions of the body-tail.

17 tabilized by the centrally positioned MTF1 C-tail.

18 l, telescope-eye, albinism, and heart-shaped tail.

19 olutionarily extended N-terminal cytoplasmic tail.

20 hich account for the extended n -> pai* band tails.

21 oligonucleotides and 3'-terminal transferase tailing.

22 idine insertion/deletion editing, and 3' A/U-tailing.

23 ni of these RNAs (designated poly(UG) or pUG tails)(5).

24 This study shows that tail anatomy is not universal in avians, and suggests se

25 including an independent paleognathous long-tailed ancestor.

26 Type II tail-anchored (TA) membrane proteins are involved in div

27 d proteins (GET) pathway targets and inserts tail-anchored (TA) proteins into the endoplasmic reticul

28 is well known for extraction of mislocalized tail-anchored ER proteins from the mitochondrial outer m

29 e EMC activities, as an insertase regulating tail-anchored protein levels and a broader role in polyt

30 The guided entry of tail-anchored proteins (GET) pathway targets and inserts

31 so responsible for inserting the TMH of some tail-anchored proteins(1-3).

32 rtion and integrity of diverse clients, from tail-anchored to polytopic transmembrane proteins.

33 ing cDNA synthesis by aiming at the poly(A)+-tail and (2) introduced a pre-amplification of human RNA

34 ticle (clubSP), which contains a cylindrical tail and a disc-like head.

35 s autoregulatory role for the mammalian CRY1 tail and conservation of PHR-tail interactions in both m

36 this role is independent of its cytoplasmic tail and of its catalytic activity.

37 kable similarities in the functions of the C-tail and sigma3.2 finger of the bacterial factor suggest

38 ls and binds directly to both the N-terminal tail and the histone fold domain of non-nucleosomal CenH

39 During TDMD, miRNAs undergo tailing and trimming, suggesting that this is an importa

40 The lipid tails and other hydrophobic fragments form the core, wit

41 However, the relative role of histone tails and regulatory proteins in the simultaneous coordi

42 ht on the roles played by disordered tubulin tails and tail modifications in the molecular mechanism

43 substrates with TTGT or UUGU single-stranded tails and that the KH domain is critically important for

44 domain of the measles virus nucleoprotein (N(TAIL)) and the X domain (XD) of the measles virus phosph

45 ills and mouse skin) and appendages (Xenopus tail), and provide recommendations on how to adapt the a

46 terferon-gamma(-/-) malignancies of the ear, tail, and foot comprised poorly differentiated, round to

47 ne regulatory light chain interacts with the tail, and the other with the partner head, revealing how

48 For 10 groups of rhesus, long-tailed, and bonnet macaques, we collected social behavio

49 ugh curves show early arrivals and very long tails, and this type of transport is usually referred to

50 nds to generate long, 3' single-stranded DNA tails, annealing of complementary sequence segments (mic

51 Here, a six-arginine-tailed anti-epidermal growth factor receptor (EGFR) affi

52 The "tail approach" has become a milestone in human carbonic

53 lar muscle cell populations in the post-anal tail are generated from tailbud, declining Fgf signallin

54 inor effects in tryptophan fluorescence peak tailing are observed over a large pH range (5.5-9.0).

55 hospholipids with polyunsaturated fatty acyl tails are oxidized in an iron-dependent manner.

56 embranes where both glycerophospholipid acyl tails are predominantly 16-18 carbons long, S. japonicus

57 c ordering, including a tendency for head-to-tail association into polar, chain-like assemblies havin

58 overlap via tropomyosin-tropomyosin head-to-tail associations, forming a continuous strand along the

59 r cassette to bind hypo-acetylated histone 4 tails at promoters, guaranteeing continuous progression

60 of a central "body", with a "pincer" and a "tail" at the respective ends.

61 The portal proteins of tailed bacteriophage and Herpesvirus capsids form dodeca

62 The genome packaging motor of tailed bacteriophages and herpesviruses is a powerful na

63 eme contractile speeds required to swim with tail-beat frequencies of 80-100 Hz.

64 stance, at higher speed and performed larger tail bends, indicating that Somatostatin 1.1 inhibits sp

65 This establishes multivalent, synergistic H3-tail binding causing distinct cellular localization and

66 AD2, KDM5B, NSD2, FOXP1, MED13L, DYRK1A; one-tailed binomial test P <= 4.08E-05) contributed to the c

67 rst genetic assessment of the Australian red-tailed black-cockatoo (Calyptorhynchus banksii), a wides

68 ted in vivo by reducing blood loss in a mice tail bleeding assay.

69 e anticoagulant effects ex vivo and in vivo (tail-bleeding assay and FeCl(3)-induced thrombosis).

70 ein sigma1 is a trimeric molecule containing tail, body, and head domains.

71 w glycolysis regulates WNT signalling in the tail bud is currently unknown.

72 nd specification of the paraxial mesoderm in tail bud precursors.

73 In the neuromesodermal precursors of the tail bud(4), WNT signalling promotes the mesodermal fate

74 Here we used chicken embryos and human tail bud-like cells differentiated in vitro from induced

75 ks, most particularly the presence of a long-tailed but monotone decline in the probability of intera

76 a-hairpin loop, and interconnected along the tail by the splayed beta-hairpins.

77 be measured rapidly in whole, intact larval tails by adapting protocols developed for ex vivo muscle

78 which involves reading of acetylated histone tails by the bromodomain-containing proteins SMARCA2 (BR

79 dius of gyration decreases linearly with the tail charge q, the trend is explained using a simple pol

80 tion of acidic amino acids to the GFP::SpxA2(tail) chimera stabilized GFP, while deletion of the acid

81 mice received IV emicizumab 24 hours before tail-clip bleeding was performed.

82 Possible effects of the H4 tail compaction on chromatin structure are discussed wit

83 In this picture, phospholipid acyl tail composition naturally adapts to added molecules suc

84 DOPC because mobilities of both unsaturated tails confer a cone shape to DOPC, and PGPC separates fo

85 CD2 numbers and motifs in its cytoplasmic tail controlled corolla formation.

86 mall molecule compatibility with 3HM's alkyl tail core.

87 e transmembrane domain (TMD) and cytoplasmic tail (CT), can reshape the antigenic structure of the En

88 TM) protein with a 97-residue-long cytosolic tail (CT).

89 gnaling, serine 365 (S365) in the C-terminal tail (CTT) of STING is phosphorylated, leading to induct

90 Most SecA proteins contain a long C-terminal tail (CTT).

91 Using dorsal tail curvature as the assay readout, three major chemica

92 erent synthetic strategies including head-to-tail cyclization (C1), side-chain-to-tail cyclization (C

93 head-to-tail cyclization (C1), side-chain-to-tail cyclization (C2), and a disulfide bond cross-linkag

94 s of cyclic peptides that are small, head-to-tail cyclized, composed of proteinogenic amino acids and

95 Kinesin-5 tails decrease microtubule-stimulated ATP-hydrolysis by

96 oylated cysteine residues in the cytoplasmic tail decreased the efficiency of these processes.

97 The white-tailed deer (Odocoileus virginianus), a popular ruminant

98 The first examination of MHC-DOB in white-tailed deer found significantly less polymorphism (11 al

99 region in ruminants, and suggests that white-tailed deer may have a recombination hotspot between the

100 amples from heterozygous (G(96)/S(96)) white-tailed deer orally dosed with CWD from homozygous (G(96)

101 While studying C-terminal (C-tail) deletion mutants of Mtf1 and TFB2M, we stumbled up

102 and C-terminal regions of Abeta, which bear "tails" derived from the N-terminus of Abeta.

103 asymmetrical" glycerophospholipids where the tails differ in length by 6-8 carbons.

104 an undergo self-assembly either as a tail-to-tail dimer, showing monomer-dimer sigmoidal transitions,

105 The heavy-tailed distribution of gene expression violates the assu

106 scribing the transition from light- to heavy-tailed distributions along a continuum of behavior as pa

107 While the thiolate tails do not significantly affect the rate of the supram

108 otein-protein contact with the cytoplasmic C-tail domain of Canx.

109 only the second AR (AR2) binds to the cargo/tail domain of Klp64D.

110 easing the microtubule affinity of the XCTK2 tail domain.

111 otor domain fused to the MYO7B cargo-binding tail domain.

112 acement of its transmembrane and cytoplasmic tail domains with their counterparts from bovine parainf

113 ll division cycle 25), and PR (proline-rich) tail domains.

114 en the eutherian mouse and the marsupial fat-tailed dunnart.

115 the ossifying hypochord-induced loss of the tail during metamorphosis has enabled the evolution of t

116 While disorder in the histone tails enables a large variation of inter-nucleosome arra

117 hlight the complex interplay between histone tails, epigenetic enzymes, and modulators of enzymatic a

118 wnt1 was required for tail expansion after mob4 inhibition and dynamically ree

119 es may also use sequential processes of acyl tail exposure, followed by membrane curvature and distal

120 e the targets of interventions that minimize tail exposure.

121 entially lost in incomplete prophages, while tail fiber, transposase and integrase genes are signific

122 equence of events during pyocin contraction: tail fibres trigger lateral dissociation of baseplate tr

123 icropipette perfusion to unwounded zebrafish tail fins.

124 The 2-tailed Fisher exact test was used to compare outcomes be

125 es gene transfection and the length of alkyl tail, flexibility of sterol ring and polarity due to -OH

126 ly active potent antinociceptive activity in tail-flick assay in mice, with diminished tolerance, dep

127 n driven by a migratory drop-off in the fork-tailed flycatcher (Tyrannus savana) resulting in reprodu

128 sequence segments (microhomologies) in these tails, followed by microhomology-primed synthesis suffic

129 poly(A) binding KPAF4 shields the nascent A-tail from uridylation and decay thereby protecting pre-m

130 n of clpC and clpE stabilized the GFP::SpxA2(tail) fusion protein.

131 eat over large surface areas, and automotive tail gas converters.

132 error signals are early and phasic in the PH tail, global value maximum signals are delayed and susta

133 as no affinity for DNA but deletion of the C-tail greatly increases Mtf1's DNA binding affinity.

134 verse array of neurons responding to head-to-tail (h-t) flow, tail-to-head (t-h) flow, or both.

135 early developmental boundary between the two tail halves in the chicken, then followed major developm

136 ty-related behaviour in tunnel compared with tail handled BALB/c mice.

137 Thus, our data suggest that C-terminal tails harbor crucial signals for both the insertion and

138 trations revealed that Mtf1 with an intact C-tail has no affinity for DNA but deletion of the C-tail

139 probability distributions which have lighter tails (higher settling rates) than the inverse Gaussian.

140 of wild-caught, juvenile American alligator tails identifies a distinct pattern of wound repair in m

141 or the determination of the lipid fatty acyl tail identities and positions, which is not possible via

142 secondary cases is consistent with being fat-tailed, implying that large superspreading events are ex

143 The importance of the tail in cofactor handover from ATR to MCM is revealed by

144 1 variant alters an intrinsically disordered tail in CRY1 downstream of the PHR.

145 important role for the dimethylbenzimidazole tail in moving the cobalamin cofactor between active sit

146 Here we discover extensive mixed tailing in transcripts of hepatitis B virus (HBV) and hu

147 dation pressure and no record of autotomized tails in articulated specimens.

148 ple architecture, synthesize such C-terminal tails in the absence of a small ribosomal subunit and mR

149 ore histone H2A C-terminal and H3 N-terminal tails in the chromatosomes.

150 10) of the human CD300f receptor cytoplasmic tail inhibits the protein kinase C phosphorylation of a

151 In both zebrafish tail injury and murine acute lung injury models of neutr

152 The fully saturated tails, instead, self-assemble into a combination of eith

153 ment is absolutely dependent on the arrestin tail interaction, and in one of the cellular backgrounds

154 restin 2, strongly dependent on the arrestin tail interaction.

155 t, with reference to the current "core" and "tail" interaction model for arrestin-GPCR interaction.

156 Moreover, PHR-tail interactions are conserved in the paralog CRY2 and

157 mammalian CRY1 tail and conservation of PHR-tail interactions in both mammalian cryptochromes highli

158 insect cryptochromes, which also utilize PHR-tail interactions to reversibly control their activity.

159 While this heavy tail is less dramatic than previous observations of meth

160 asts with lepidosaurs, where the regenerated tail is radially organized around a central endoskeleton

161 A Gly13 in the histone H3 tail is responsible for a sharp reduction in deacetylase

162 ently having the ability to autotomize their tail, it is unlikely that they actually made use of this

163 glaucous gulls, rough-legged hawks and long-tailed jaegers) feeding on a pulsed resource (brown and

164 isrupts the four-helix bundle at the head-to-tail junction, leading to weaker tropomyosin-tropomyosin

165 glutamylation and polyglycylation of tubulin tails lead to slower protein diffusion along MTs, althou

166 ke motif sequence (RLLRLLR) and polyarginine tail length (R(7)) for cargo delivery.

167 omplex (MHC) class I-binding epitopes in the tail length tape measure protein (TMP) of a prophage fou

168 Most mRNA molecules degrade only after their tail lengths fall below 25 nt.

169 ave almost no effect on steady-state poly(A)-tail lengths of their targets in mouse fibroblasts, whic

170 approaches steady state, whereas effects on tail lengths peak for recently transcribed target mRNAs

171 ate measurements of the effects of miRNAs on tail lengths, mRNA levels, and translational efficiencie

172 of binary mixtures of lipids with different tail lengths.

173 es whose backbones are cyclized from head to tail, like the membrane permeable and orally bioavailabl

174 on in serum was correlated with radiological tail-like patterns, characteristic of the infiltrative M

175 s frequently stalled, triggering RQC and CAT-tailing-like C-terminal extension (CTE).

176 st, C-TMDs with sufficient hydrophobicity or tails longer than ~80 residues are quickly released from

177 the lognormal distribution which has heavier tails (lower settling rates) than the inverse Gaussian;

178 and macroH2A1/2 at the divergent N-terminal tail lysine residue.

179 te colobus), Macaca nemestrina (southern pig-tailed macaque), and Mandrillus leucophaeus (the drill).

180 mong bonnet macaques, but not rhesus or long-tailed macaques, individuals who were more well-connecte

181 l approaches to show that two molecules with tails made of alkyl carbon, alkylphosphocholines (APCs)

182 cessibility, nucleosome positioning, histone tail modifications and enhancer-promoter interactions in

183 roles played by disordered tubulin tails and tail modifications in the molecular mechanism of protein

184 broadly (1000-fold) and are larger for short-tailed mRNAs that have previously undergone more rapid d

185 Decay rate constants of short-tailed mRNAs vary broadly (1000-fold) and are larger for

186 dimer sigmoidal transitions, or as a head-to-tail noncentrosymmetric columnar polymer, exhibiting a n

187 xponential function in the bulk, while their tail obeys the Pareto power law.

188 nsory peripheral nervous system (PNS) in the tail of a cephalochordate, Asymmetron lucayanum.

189 imental pancreatic sutures in the pancreatic tail of C57/Bl6 mice.

190 The C-terminal tail of CENH3 is confirmed to be responsible for the int

191 ly, we provided evidence that the C-terminal tail of DHHC5 can be palmitoylated in response to stimul

192 wn to interact with the conserved C-terminal tail of FtsZ.

193 vely, our results reveal that the N-terminal tail of GiKIN14a is a de facto dual regulator of motilit

194 holesterol-recognition motif and cytoplasmic tail of gp41.

195 tructure also implicates a unique C-terminal tail of MlaF in self-dimerization.

196 levant interactions with both the C-terminal tail of Na(v)1.6 and FGF14.

197 There is also evidence that the C-terminal tail of PC2 is also cleaved in ELVs.

198 d stable when fused to the C-terminal acidic tail of SpxA1.

199 r RV-A16 replication, nor was the C-terminal tail of STING that mediates IRF3 signaling.

200 ntent ratios between the head, midpiece, and tail of the cells can predict the percentages of success

201 rating linker, which connects the dimerizing tail of the motor to the AAA+ ring.

202 synthesize 5' methylated cap and 3' poly(A) tail of the transcribed viral mRNAs.

203 omplex with only a phosphorylated C-terminal tail of the vasopressin 2 receptor activates Src as effi

204 lata (SNr), ~30% in the VTA, and ~70% in the tail of the VTA (also called the rostromedial tegmental

205 We show that the flexible C-terminal tails of Mtf1 and TFB2M play a crucial role in RNA primi

206 rd high predictive quality while having long tails of poor predictions.

207 likely causal gene for fat deposition in the tails of sheep through transcriptome, RT-PCR, qPCR, and

208 To handle long plateaus in the tails of survival curves, we also exploited "cure models

209 arge-amplitude motions, including the phytol tails of two chlorophylls.

210 Although the endodomain (cytoplasmic tail) of the S2 subunit was not absolutely required for

211 e conducted independent samples t-tests (two-tailed) on pre-post change scores.

212 embrane helix, and a short carboxyl-terminal tail, or as a soluble ectodomain that acts as a decoy re

213 t these can not deal with multi-modal, heavy-tailed, or discrete distributions.

214 DOX promoted crystalline alkyl tail ordering, which significantly increased (+63%) the

215 n actin dominated by stereo-specific head-to-tail overlap linkage.

216 om zero were judged significant when the two-tailed P value was less than .05.

217 -injection effects of FA were evaluated by 2-tailed paired t test comparison of mean 5-minute preinje

218 over 1 year (mean change 2.24 +/- 3.09; two-tailed paired t-test P = 0.009) and over 2 years (mean c

219 over 2 years (mean change 4.00 +/- 3.79; two-tailed paired t-test P = 0.031) with respective standard

220 minant CMT2A (mean change 0.84 +/- 2.42; two-tailed paired t-test P = 0.039).

221 LARP4 was shown to promote poly(A) tail (PAT) lengthening and stabilization of individual m

222 at form the rigid inner tubes of contractile tail phages, such as T4, and its C-terminal domain adopt

223 in and kinase domain, which is relieved by C-tail phosphorylation, but the precise molecular mechanis

224 ) CFU/cm(2) counts were higher in p-trap and tail pipe biofilm samples from HCP compared to PR sinks

225 ansitions in cells is the reversible head-to-tail polymerization of hub proteins into filaments that

226 Ph SAM forms helical head to tail polymers, and SAM-SAM interactions between chromati

227 ributed to the buckling of the subfragment 2 tail portion.

228 t acts within the membrane to increase lipid tail protrusion and promote stalk formation and then act

229 nce in an alpine-obligate species, the white-tailed ptarmigan (Lagopus leucura), a species distribute

230 usion on MTs is mediated primarily by the MT tails rather than the MT body.

231 ture and contemporary gene flow in the thorn-tailed rayadito (Aphrastura spinicauda), a passerine bir

232 ify Pbx3 and Meis1 as critical regulators of tail regeneration and axon organization.

233 he essential role of the myeloid lineage for tail regeneration in the regeneration-competent tadpoles

234 re, we took advantage of naturally occurring tail regeneration-competent and -incompetent development

235 a finding that suggested that the flexible C-tail region of these factors autoregulates their DNA bin

236 It forms as the tail regresses during metamorphosis, when locomotion cha

237 irst anatomical and histological evidence of tail repair with regrowth in an archosaur, the American

238 steps of dimeric tubulin, the removal of the tails results in a step of monomeric tubulin.

239 the experimentally observed increase in acyl tail saturation with added cholesterol.

240 bearing different tpy "heads" and thiolate "tails" scrambles to afford up to 10 ternary assemblies v

241 fic via the incorporation of a SNP at the 3' tail, sequences other than the target sequence will also

242 Here, we introduce single cell RNA Cap And Tail sequencing (scRCAT-seq), a method to demarcate the

243 Poly(A) tail shortening, also termed deadenylation, is the rate-

244 ant of large whole-tail skins, but not small tail skins (0.8 cm x 0.8 cm), led to exhaustion of anti-

245 Transplant of large whole-tail skins, but not small tail skins (0.8 cm x 0.8 cm),

246 )alamin binds with its dimethylbenzimidazole tail splayed into a side pocket and its corrin ring buri

247 icrotubule-sliding model, in which kinesin-5 tails stabilize motor domains in the microtubule-bound s

248 ead stacking geometry (orange) for a head-to-tail stacking geometry (yellow).

249 ut the distillation process (head, heart and tail stages), FT-RAMAN spectroscopy was applied.

250 We model residual errors with a heavy-tailed Student's t-distribution to estimate a manifold t

251 eightened; immobility times decreased on the tail suspension and forced swim tests; and sucrose prefe

252 a second IQ domain to the Ca(V)1.3 carboxyl tail switched the apparent functional stoichiometry, per

253 post-drug CPTs separately using paired, two-tailed t tests.

254 phenotypes, including dorsal fin loss, long-tail, telescope-eye, albinism, and heart-shaped tail.

255 upports a model in which a single C-terminal tail tethers XLF to Ku, while allowing XLF to form inter

256 e dictated by a conserved kleisin N-terminal tail that guides the DNA through the kleisin gate.

257 rcylaldehyde headgroup linked to a 15-carbon tail that harbors two conjugated all-trans trienes separ

258 by a conformational change in the C-terminal tail that leads to creation of an enlarged binding cavit

259 Ala tailing thus follows mechanistic principles surprisingly

260 ttle or no protection was conferred by mouse tail tip or human skin fibroblasts.

261 The reconstructed region extends from the tail tip to the origin of the most posterior peripheral

262 n convert mouse embryonic fibroblasts, adult tail-tip fibroblasts and postnatal supporting cells into

263 of woodland areas, accurately captures long-tailed tit home range patterns.

264 Here we show that, in long-tailed tits (Aegithalos caudatus), a cooperative breeder

265 Here, we apply MHRA to a population of long-tailed tits Aegithalos caudatus, a non-territorial passe

266 Long-tailed tits are known to discriminate between the calls

267 operative contexts, so we conclude that long-tailed tits use the same kin discrimination rule to avoi

268 hydrophobic complementarity between the TnT tail (TnT1) and tropomyosin, which is difficult to recon

269 that uses its N-terminal microtubule-binding tail to achieve minus-end-directed processivity on singl

270 RM and ankyrin motifs within its cytoplasmic tail to bind actin, LYVE-1 displays little if any direct

271 ra - that in many extant squamates allow the tail to separate and the animal to escape predation.

272 in the 5' region, KPAF1/2 dimer induces A/U-tailing to activate translation.

273 (LNA)-containing oligo(dT) probes to poly(A) tails to maximize RNA capture selectivity and efficiency

274 e of 5'-deoxyadenosylcobinamide, lacking the tail, to transfer.

275 urons responding to head-to-tail (h-t) flow, tail-to-head (t-h) flow, or both.

276 nine 1 can undergo self-assembly either as a tail-to-tail dimer, showing monomer-dimer sigmoidal tran

277 Dyads of acidic residues inside the tail-tube present regularly-spaced motifs well suited to

278 Hexameric rings of the tail-tube protein are braced by the N-terminus and a bet

279 = - 0.88) and Contact (r = - 0.91), but not Tail Twining or infant carrying.

280 partner affiliation (Proximity, Contact, and Tail Twining) and infant carrying were determined from l

281 activation of the cytoplasmic immunoglobulin tail tyrosine (ITT) motif in transmembrane IgE (mIgE) im

282 kidneys and spleen after inoculation via the tail vein in a bacteremia mouse model.

283 ted with mismatch or H2HR vivo-morpholino by tail vein injection for 1 week.

284 etent mice with HCC, induced by hydrodynamic tail vein injection of proto-oncogenes, enhanced HCC dev

285 Mice were given hydrodynamic tail vein injections of clustered regularly interspaced

286 coccus aureus (MRSA) was inoculated into the tail vein of rats.

287 ormation and hepatosplenic infiltration in a tail-vein-injected mouse model.

288 bolaamphiphiles self-assemble into "head-to-tail" versus "stacked" arrangements, respectively.

289 We further show that tail vertebrae also arise through resegmentation, though

290 Modification of the lipid tail was generally well tolerated, with longer alkyl cha

291 ecific acetylated lysine residues on histone tails where they facilitate the assembly of transcriptio

292 n the first capillary bed encountered in the tail, whereas cells overexpressing constitutively active

293 berrant translation products with C-terminal tails which assist with RQC-mediated protein degradation

294 conserved N-linked glycan within the IgG-Fc tail, which is essential for IgG function, shows variabl

295 tal regulatory role, apart from the histone "tails," which modulate gene activity.

296 splays incipient rigidity at the base of the tail with a flexible lumbar region.

297 -1BB IFP that replaces the Fas intracellular tail with costimulatory 4-1BB.

298 Initially, steric clashes of the Mtf1 C-tail with short RNA-DNA hybrids cause abortive synthesis

299 RNA fragments attached to pUG tails with more than 16 perfectly alternating 3' U and G

300 ve impaired neutrophil directed migration to tail wounds with an initial lag in recruitment early aft