ライフサイエンスコーパス: homopolymer

1 ne block copolymers from nanocrystals of the homopolymer.

2 interesting case of a biologically relevant homopolymer.

3 also lectins that bind fibrils of the GalNAc homopolymer.

4 t representation of a protein: a hydrophobic homopolymer.

5 estigate the conformational behavior of this homopolymer.

6 of T homopolymers directly followed by an A homopolymer.

7 s or less) more potent chaperone than alphaA homopolymer.

8 ted gradient copolymer, and a non-segregated homopolymer.

9 n a nucleocapsid made of a nucleoprotein (N) homopolymer.

10 minus greatly enhance the formation of SEPT2 homopolymers.

11 xtures of diblock copolymers and hydrophobic homopolymers.

12 TAR and molecules approximating A.U and G.C homopolymers.

13 formed in vitro with calf thymus DNA and DNA homopolymers.

14 rch constituents amylose and amylopectin are homopolymers.

15 rs were prepared without the presence of any homopolymers.

16 ic DNAs but is inactive with single-stranded homopolymers.

17 -fold more slowly than mitochondrial A and T homopolymers.

18 for G and C homopolymers compared to A and T homopolymers.

19 mopolymers differ significantly from G and C homopolymers.

20 ne) block copolymers blended with resins and homopolymers.

21 e constituents, and the distributions of the homopolymers.

22 sistently exceeded those of TAT and arginine homopolymers.

23 ficantly less fragmentation of polyadenylate homopolymers.

24 rs but induce fragmentation in polyadenylate homopolymers.

25 ies for short (</=50 bp) double-stranded DNA homopolymers.

26 ta-fibril formation on the part of glutamine homopolymers.

27 M13 DNA, but only poorly to single-stranded homopolymers.

28 ine- and phospholysine-containing amino acid homopolymers.

29 d with suitable molecular weight polystyrene homopolymers.

30 s of the diblock copolymer compared to their homopolymers.

31 d by laminarin [a beta(1-->3)-linked glucose homopolymer].

32 4 A homopolymers immediately followed by a T homopolymer (5' to 3') and only 8 instances of T homopol

33 ry (ESI-MS), and 8a, together with insoluble homopolymer 8d, was also characterized by (11)B and (1)H

34 We show that homopolymer A/T tracts within the human beta-globin CoTC

35 We find that, compared with a related homopolymer, a four times higher dopant/polymer molar ra

36 ave now identified readily prepared cationic homopolymers active against strains of C. albicans that

37 to be and to behave more like a random coil homopolymer, after passing through a 250 kg mol(-1)-broa

38 r polystyrene or the poly(thioether) network homopolymers alone.

39 c changes in the secondary structure of both homopolymers, alphaA- and alphaB-crystallins markedly di

40 sts are more active and selective than their homopolymer analogues, providing further proof that cata

41 CPEs with cationic polythiophenes, in both homopolymer and block copolymer configurations, were use

42 offset by interactions between the inserted homopolymer and flanking heteropolymer portions of the u

43 neralization in recombinant H- and L-subunit homopolymer and heteropolymer ferritins and several site

44 can immediately accommodate the use of both homopolymer and heteropolymer RNA templates lacking urid

45 esented here suggest that both these models (homopolymer and heteropolymer) could be applicable depen

46 ce MS(2) spectra obtained from a polystyrene homopolymer and polystyrene end-capped with a p-DMSS blo

47 Studies with RNA homopolymers and a variety of oligoribonucleotides revea

48 A family of 10 homopolymers and bithiophene copolymers is then synthesi

49 Both homopolymers and block copolymers with controlled molecu

50 ymer architectures, such as monodisperse PFS homopolymers and block copolymers.

51 ith single- and double-stranded nucleic acid homopolymers and calf thymus DNA.

52 hniques are prone to sequence erroneously at homopolymers and can, therefore, raise indels in reads.

53 hods that have been applied to the resulting homopolymers and copolymers and the application of the m

54 phene-3,3'-dicarboximide-based pi-conjugated homopolymers and copolymers containing the 2,2'-bithioph

55 te coupling steps allowed rapid synthesis of homopolymers and copolymers.

56 en peptides are extracted by the amphiphilic homopolymers and detected on the Anchorchip MALDI target

57 e in situ generation of chain-end functional homopolymers and diblock copolymers, providing facile ac

58 he central domain and native eIFiso4F to RNA homopolymers and double- and single-stranded DNAs was st

59 nthocyanidins contained predominantly B-type homopolymers and heteropolymers up to 12-mers (3400 Da).

60 anges localized at the 4-fold pore of MT-FTL homopolymers and imply that the C terminus of the MT-FTL

61 Poly(tert-butyl ester norbornene imide) homopolymers and poly(tert-butyl ester norbornene imide-

62 his study, we investigate the ability of RNA homopolymers and polyP to bind the primary constituents

63 Homopolymers and pure block copolymers were successfully

64 ier-crossing kinetics, while the collapse of homopolymers and random heteropolymers is continuous and

65 tides by reverse micelle-forming amphiphilic homopolymers and subsequent matrix-assisted laser desorp

66 es with various sequences indicated that DNA homopolymers and those lacking 8-oxopurines were less re

67 We focus especially on mixtures of glucose homopolymers and water.

68 led 2D materials derived from nanoparticles, homopolymers, and block copolymers.

69 leen, human liver, recombinant human H and L homopolymers, and mixtures of the two- and the single-su

70 s and deletions associated with abundant DNA homopolymers, and occasional larger deletions.

71 ologically relevant temperatures, the alphaB homopolymer appears to be modestly (two times or less) m

72 rease in temperature, the activity of alphaB homopolymer appears to change very little upon heating.

73 ted state dynamics of a conjugated tetracene homopolymer are studied.

74 erent DNA sequences, where complementary DNA homopolymers are adsorbed faster than other sequences.

75 Nuclear A and T homopolymers are also found to mutate approximately 100-

76 To overcome this challenge, short linear homopolymers are used to swell the arrays to approximate

77 ned using a fluorometric assay and a poly(A) homopolymer as a template.

78 epare functional redox-active and conjugated homopolymers as well as the construction of covalently l

79 structure with a narrower diameter than Drp1 homopolymers assembled in isolation.

80 Torrent PGM and 454 GS Junior both produced homopolymer-associated indel errors (1.5 and 0.38 errors

81 theoretical prediction that symmetric mixed homopolymer brushes undergo lateral rather than vertical

82 ed by pustulan [a beta(1-->6)-linked glucose homopolymer] but was not inhibited by laminarin [a beta(

83 on of gradient samples, by the addition of a homopolymer, by the combination with micro-fluidics and

84 evidence of an unanticipated catechyl lignin homopolymer (C lignin) derived solely from caffeyl alcoh

85 ustrates an ability to classify an erroneous homopolymer call.

86 The iron-loaded homopolymer can be detected on non-denaturing gels by ei

87 We found that long (>1 Kb) ssDNA homopolymer can be grown by SIEP, and that the length of

88 Depending on the substituents, PFS homopolymers can be amorphous or crystalline, and solubl

89 Generally, common homopolymers cannot self-assemble into multiple nanostru

90 Each cyst wall contains a sugar homopolymer: chitin in Entamoeba and a unique N-acetylga

91 A scanning window analysis of homopolymer chromosomal distribution reveals distinct cl

92 could as well be observed by a homopolymer (homopolymer collapse).

93 wer than is predicted by Langevin models for homopolymer collapse.

94 osa contains two different sugar chains, the homopolymer common antigen (A band) and the heteropolyme

95 ely 20-fold higher mutation rate for G and C homopolymers compared to A and T homopolymers.

96 A commercial RNA homopolymer complementary to the RNA product is included

97 Both alphaA and alphaB homopolymer complexes, as well as a reconstituted 3:1 he

98 The various monomer and homopolymer components have been examined in turn and th

99 pressure ranges within which highly compact homopolymer configurations are thermodynamically stable.

100 We report an extraordinarily long homopolymer consisting of 306 tandem serine repeats from

101 gel filtration and electron microscopy, the homopolymer consists of globular particles of approximat

102 ngal beta-glucans are comprised of d-glucose homopolymers containing beta-1,3-linked glucose backbone

103 The O9a and O8 antigens are linear mannose homopolymers containing conserved reducing termini (the

104 eats (particularly Alu elements) and guanine homopolymer content as parameters that significantly aff

105 Here we first introduce a homopolymer decomposition method which estimates error b

106 on but has a high error rate and was rich in homopolymer deletions.

107 relative methods based on calibrations with homopolymers delivered inaccurate results for all invest

108 by the cell type tested, although polylysine homopolymers demonstrate levels of internalization that

109 Competition experiments with different RNA homopolymers demonstrate that C114 preferentially binds

110 al distribution reveals distinct clusters of homopolymer density in autosome arms that are regions of

111 least 90% of the rigidity of the dT(n)-dA(n) homopolymer derives from base pair stacking effects, wit

112 This method provides well-defined homopolymers, diblock copolymers, and biohybrids under a

113 and the run-length distributions of A and T homopolymers differ significantly from G and C homopolym

114 polymer (5' to 3') and only 8 instances of T homopolymers directly followed by an A homopolymer.

115 sly proposed hidden Markov model that models homopolymer errors and then merges these pairwise alignm

116 f the existing mapping programs do not model homopolymer errors when aligning reads against the refer

117 tanding of the forces that shape patterns of homopolymer evolution, however, is lacking.

118 ions, two frameshift mutations, and one tRNA homopolymer expansion.

119 Redistribution of homopolymer facilitates the defect-free assembly in loca

120 ss the same capsular polysaccharide (CPS), a homopolymer featuring an unusual [-->3)-2-O-acetyl-6-deo

121 Previous kinetics studies with homopolymer ferritins (bullfrog M-chain, human H-chain a

122 y statistics calculation, quality filtering, homopolymer filtering, length and nucleotide filtering,

123 show that monomeric VP39's affinity for RNA homopolymers follows the hierarchy poly(I) >poly(U) >>po

124 that BH3 peptides, modified with an arginine homopolymer for membrane transduction (called r8-BidBH3

125 tic biases are detected among closely spaced homopolymers; for instance, we observe 994 A homopolymer

126 tended range of salt concentration following homopolymer formalism.

127 of the novel C-type only, which we show is a homopolymer formed by endwise beta-O-4-coupling of caffe

128 re and report functional studies of ferritin homopolymers formed from the mutant FTL polypeptide p.Ph

129 the poly(A) tail is necessary to protect the homopolymer from degradation by deadenylating enzymes.

130 quired to remove single-stranded DNA (ssDNA) homopolymers from single-walled carbon nanotubes (SWCNTs

131 sequence causes inclusion of low-complexity homopolymers from the ends of sequence runs.

132 C) binding, while single-stranded RNA homopolymers have no effect.

133 adjusting the azulene density, ranging from homopolymers (having one azulene group per repeat unit)

134 action, which could as well be observed by a homopolymer (homopolymer collapse).

135 46 deletions and two insertions, occurred in homopolymer (HP) tracts [i.e., 47 poly(A) or (T) tracts,

136 nce of PsaA, the subunit of the Psa fimbrial homopolymer, identified residues that abolish galactosyl

137 homopolymers; for instance, we observe 994 A homopolymers immediately followed by a T homopolymer (5'

138 and a unique N-acetylgalactosamine (GalNAc) homopolymer in Giardia.

139 urther expands the repertoire of amphiphilic homopolymers in a variety of areas.

140 A survey of other very long amino-acid homopolymers in eukaryotes shows that high codon diversi

141 rate block copolymers from both their parent homopolymers in one single run.

142 range of glycans in general and fragments of homopolymers in particular.

143 he precise border of poly(A) tails and other homopolymers in raw mRNA sequence reads.

144 ealed iron mishandling by soluble mutant FTL homopolymers in that only wild type incorporated iron wh

145 d mutation rate for single base deletions in homopolymers in the Buchnera genome, implying a strong s

146 in-like GTPase that forms protofilament-like homopolymers in vitro.

147 2) and LUCA15 specifically bound poly(G) RNA homopolymers in vitro.

148 n shown by us in a recent communication that homopolymers, in which each repeat unit contains a hydro

149 se activity, with specificity toward uridine homopolymers, including the 3' oligo(U) tails of guide R

150 orms sequence clustering in the order of (i) homopolymer indel patterns only, (ii) indel patterns onl

151 nt block ratios and to incorporate different homopolymers into the polymersomes will allow the tuning

152 calculated specificity constants that the AT homopolymer is by far the most effective coenzyme and ra

153 This is because the serine homopolymer is conserved despite much DNA sequence chang

154 cture and protein sequences suggest that the homopolymer is functional.

155 The described homopolymer is hypervariable in length, varying from 12

156 Compared with alphaB-crystallin, the alphaA-homopolymer is markedly less active at low temperatures,

157 ximately 60 degrees C), even though this RNA homopolymer is single-stranded in the absence of a ligan

158 ier-crossing kinetics, while the collapse of homopolymers is continuous and multi-phasic.

159 nylenes and pre-functionalized polyphenylene homopolymers is demonstrated.

160 Increased iron incorporation into the FtH homopolymer leads to reduced cellular iron availability,

161 light increase in f(PS), by blending with PS homopolymer, led to a dramatic change in the BCP morphol

162 ide component was recognized as the fructose homopolymer levan, and a glucosylated lipoteichoic acid

163 r at the insert site and thus closure of the homopolymer loops, possibly as an aspect of the folding

164 selectivity of these reverse micelle-forming homopolymers makes these materials promising tools for s

165 unable hysteresis not previously observed in homopolymer materials.

166 when they are dispersed in the corresponding homopolymer matrix.

167 The persistence length of poly(U) RNA homopolymer, modeled as a worm-like chain, was found to

168 same as those reported earlier for vimentin homopolymer molecules and, by implication, are also the

169 Empirical homopolymer mutation assays in a set of C. elegans mutat

170 approach yields a total nuclear genome-wide homopolymer mutation rate estimate of approximately 1.6

171 Despite the functional importance of its homopolymers, no structural information is available on

172 ch is synthesized at the inner membrane as a homopolymer of 1-4-linked beta-D-mannuronate.

173 MtF), unlike other mammalian ferritins, is a homopolymer of 24 subunits that has a high degree of seq

174 tibody titers against the OPS, an unbranched homopolymer of 4,6-dideoxy-4-formamido-D-mannopyranosyl

175 lids using a unique FTACP determined to be a homopolymer of 8:2 fluorotelomer acrylate (8:2 FTAC).

176 ningitidis group B polysaccharide capsule, a homopolymer of alpha(2-->8) sialic acid, has been attrib

177 Polysialic acid, a homopolymer of alpha2,8-linked sialic acid expressed on

178 Polysialic acid (PSA) is a unique linear homopolymer of alpha2,8-linked sialic acid that has been

179 Polysialic acid is a linear homopolymer of alpha2-8-linked sialic acids attached mai

180 Chitin, a homopolymer of beta1,4-linked N-acetylglucosamine (GlcNA

181 We report here the presence of a homopolymer of caffeyl alcohol in the seed coats of both

182 lar matrix of the biofilm seems to contain a homopolymer of N-acetyl-d-glucosamine, which is a consti

183 template is entirely embedded into a helical homopolymer of nucleoproteins that constitutes the nucle

184 psular polysaccharide (CPS) is composed of a homopolymer of O-acetylated, alpha1-->6-linked ManNAc 1-

185 Exposure of SSB and a homopolymer of radiolabeled thymidine (dT(40)) to HOCl r

186 Homopolymers of 3-acrylamidophenylboronic acid (APBA) fo

187 hiol-ene and thiol-Michael reactions to form homopolymers of a single nucleobase (e.g., poly(A)n ) or

188 alic acid (PSA) capsules are cell-associated homopolymers of alpha2,8-, alpha2,9-, or alternating alp

189 Homopolymers of dT (40- and 60mer), dA (40mer), and dC (

190 eslundii to convert sucrose to extracellular homopolymers of fructose and to catabolize these types o

191 beta-Glucans, homopolymers of glucose, are widespread in many microorg

192 filament; this repulsive force is absent in homopolymers of neurofilament L or trypsinized native fi

193 s, purified from bovine spinal cord, to form homopolymers of NF-L or filaments composed of NF-L and N

194 of a single nucleobase (e.g., poly(A)n ) or homopolymers of specific repeating nucleobase sequences

195 ccharides of pathogenic Brucella species are homopolymers of the rare sugar 4,6-dideoxy-4-formamido-a

196 pendent, and the ability of phosphorothioate homopolymers of thymidine of variable lengths to cause t

197 served in a hydroxyethyl methacrylate (HEMA) homopolymer or in networks formed from nanogels copolyme

198 ion of either a like charged polyelectrolyte homopolymer or through careful control of ionic strength

199 y in a cylinder-on-Si geometry of conjugated homopolymers or all-conjugated diblock copolymer (P3BHT)

200 o observed upon the addition of linear ssDNA homopolymers or hydrolyzed M13 ssDNA.

201 i-biofouling properties of both polymers, as homopolymers or nanoparticle-decorating shell, in compar

202 For example, addition of PS homopolymer, or a PS-PEO copolymer of different composit

203 In DMSO with small amounts of water, the homopolymer PBA shows a tunable upper critical solution

204 xy-functional low-fouling coatings including homopolymer pCB brushes and OEG-SAMs.

205 QM calculations, polyguanidine-oxanorbornene homopolymers (PGONs) showed that curvature generation is

206 s, poly(N-(3-guanidinopropyl)methacrylamide) homopolymer (PGPMA) and malathion specific aptamer.

207 s to LPS, lipoteichoic acid (LTA), thymidine homopolymer phosphorothioate oligonucleotide [Poly(dT)],

208 lles by using seeds of the charge-terminated homopolymer PLLA24[PPh2Me]I to initiate the sequential g

209 on of N-HA-N triblock comicelles with the HD homopolymer PMVSOH, and second, the interaction of N-HD-

210 he short-chain (n approximately equal to 50) homopolymer poly(L-cysteine) (PLC) has been previously s

211 processable in common organic solvents: the homopolymer poly(N-(2-octyldodecyl)-2,2'-bithiophene-3,3

212 The linear homopolymer poly-beta-1,6-N-acetyl-D-glucosamine (beta-1

213 fically, we probe the melting of a synthetic homopolymer, poly(dA) . poly(dT), in the presence of exc

214 the dithienosilole- and dibenzosilole-based homopolymers, poly(4,4-di-n-hexyldithienosilole) (TS6) a

215 hown that the polypeptides copurify with two homopolymers, poly[(R)-3-hydroxybutyrate] (PHB) and inor

216 e vesicles were spontaneously assembled from homopolymer polyamine polyelectrolytes and water-soluble

217 between the positively charged amines of the homopolymer polyelectrolytes and the negatively charged

218 TBX5 can bind to RNA homopolymers (polyribonucleotides) and to the 5'-splice

219 and urea on the unfolding of the hydrophobic homopolymer polystyrene.

220 Separation of parent homopolymers, polystyrene and poly(ethylene oxide), from

221 high time-of-flight charge transport of the homopolymer polythiophene (mu(h) ~10(-4) cm(2) V(-1) s(-

222 strongly linked to the presence and size of homopolymers, position in the sequence and length of the

223 In contrast to wild type, MT-FTL homopolymers precipitated at much lower iron loading, ha

224 cleotide nucleic acid segments, and that its homopolymer preference for polyadenylylation priming is

225 f low-melting temperature (Tm) solid-surface homopolymer primers and a low-Tm solution phase primer.

226 ein conjugated with a horseradish peroxidase homopolymer (ProtA-HRP40).

227 ated by the addition of L-arginine, arginine homopolymers (R2, R6, R10), and protamine, all of which

228 In both settings, frequent homopolymer read errors inflate the estimation of microb

229 tk mutations were detected in a seven-G homopolymer region in 11 of 12 ganglia tested, with clon

230 DNA templates consisting of homopolymer regions were accurately sequenced by using t

231 Various DNA templates, including those with homopolymer regions, were accurately sequenced with a re

232 ersible termination (CRT) experiment using a homopolymer repeat of ten complementary template bases w

233 g the exquisite, stepwise addition through a homopolymer repeat, demonstrates the applicability of th

234 it readily protonate upon MALDI, whereas PES homopolymers require alkali metal ion addition to become

235 of the weight fractions of a blend of three homopolymers, respectively.

236 tions proceed rapidly to completion on short homopolymer RNA and LNA templates, which favor an A-type

237 preincubation was assessed using NS5B and a homopolymer RNA template and a time-dependent increase o

238 on was used in an RT processivity assay with homopolymer RNA template-primer, poly(A), and oligo(dT),

239 Homopolymer run enrichment outside of genes causes inser

240 ough there was no direct correlation between homopolymer run length and frameshift accumulation in th

241 er with the Best Overlap Graph) is robust to homopolymer run length uncertainty, high read coverage a

242 Nonetheless, long genomic homopolymer runs are overrepresented relative to random

243 noise including insertion/deletion errors in homopolymer runs by addressing the bidirectional aspect

244 ows facile inactivation of genes with coding homopolymer runs including FRR1, which encodes the targe

245 roblematic because of the poor resolution of homopolymer runs.

246 creased sequencing error indel rates in long homopolymer runs.

247 s, and a larger increase in genes containing homopolymer runs.

248 y 65% corresponding to incorrectly recovered homopolymer segments, and 35% to carry-forward-incomplet

249 Anion-dipole interactions can make homopolymers self-assemble like an amphiphilic block cop

250 s error bias toward insertion or deletion in homopolymer sequence runs.

251 oach, SCOPE++ accurately identifies specific homopolymer sequences in error-prone EST/cDNA data or RN

252 lute/concentrated poly(ethylene oxide) (PEO) homopolymer solutions.

253 marked preference for poly(G) among the four homopolymers studied.

254 A homopolymer substituted with GRGDS peptides was signific

255 hes of cylindrical micelles on a crystalline homopolymer substrate.

256 fundamentally different from those based on homopolymers such as P3HT (poly-3-hexylthiophene).

257 R and RNase II are most active on synthetic homopolymers such as poly(A), but their substrate specif

258 hydrophobicity properties of the individual homopolymers supports the view that the chaperone activi

259 51-mer with 2'-O-methylribonucleotides and a homopolymer tail are reported in this study.

260 fied high-throughput technique called methyl homopolymer tail mediated sequencing (methyl HTM-seq) to

261 t transformation to test the effects of mRNA homopolymer tails in vivo, with either the endogenous at

262 and efficient nonenzymatic copying of a DNA homopolymer template (dC(15)) encapsulated within fatty

263 ver, synthesis of RNA on poly(C) and poly(U) homopolymer templates by 1b-42 NS5B did not require the

264 es, which are the least efficient of the RNA homopolymer templates.

265 We report here on a new amphiphilic homopolymer that binds noncovalently to proteins.

266 rm of human frataxin assembles into a stable homopolymer that can bind approximately 10 atoms of iron

267 c protein sequences often contain amino-acid homopolymers that consist of a single amino acid repeate

268 ted ternary blends of diblock copolymers and homopolymers that naturally form periodic arrays to asse

269 Amphiphilic homopolymers that self-assemble into reverse micelles in

270 electric charge on graphene can force a DNA homopolymer to adopt a range of strikingly different con

271 copolymers and the corresponding crystalline homopolymer to cylindrical micelle seeds.

272 n-dipole interactions can enable a number of homopolymers to achieve a variety of self-assembly behav

273 yacrylamide and poly(N,N-dimethylacrylamide) homopolymers to quantitate their molar mass, solution co

274 copolymers by merely mixing the constituent homopolymers together under ambient conditions, using no

275 ethylase with unusual site specificity and a homopolymer tract that functions as a hotspot for frames

276 was determined and consists of interspersed homopolymer tracts and an HCV-like 3'-terminal poly(U)-X

277 DNA misalignment occurs in homopolymer tracts during replication and can lead to fr

278 ivity of the enzyme eliminates stuttering at homopolymer tracts.

279 mutation spectra of the four strand-specific homopolymer types (A, T, G, C) >or=8 bp in the genome of

280 ng brain development and its ability to form homopolymers, unlike the triplet, which are obligate het

281 ng brain development and its ability to form homopolymers, unlike the triplet, which are obligate het

282 A and T homopolymers vastly outnumber G and C HPs, and the run-l

283 ut serogroup C polysaccharide (a sialic acid homopolymer) was separable from sialic acid monosacchari

284 data obtained for the whole class of glucose homopolymer, we show that these theories predict the moi

285 ed arginine-rich PTDs, including TAT, lysine homopolymers were able to mediate transduction of a wide

286 a selected radiolabeled RNA, single-stranded homopolymers were not effective competitors.

287 grafted) blends of the same graft and matrix homopolymers, where the wetting-dewetting is a sharp tra

288 s demonstrated by comparison with the parent homopolymer, which provides only paramagnetic materials,

289 he packing features of the ionic groups in a homopolymer, which results in a vesicle-like structure t

290 Interrupting the U homopolymer with C residues was deleterious, implicating

291 important source of beta-d-glucan, a glucose homopolymer with many functional, nutritional and human

292 Addition of crystallizable homopolymers with charged end-groups to seeds generated

293 nd a series of new brush-type DNA side-chain homopolymers with high DNA grafting density are produced

294 The synthesis of homopolymers with molecular weights ranging from 1000 to

295 ramolecular assemblies formed by amphiphilic homopolymers with negatively charged groups in the hydro

296 However, very long homopolymers with over a hundred repeats are very rare.

297 Here, reverse micelle-forming amphiphilic homopolymers with positively charged interiors are synth

298 amic properties of small single-stranded RNA homopolymers with three and six nucleotides in free solu

299 e arises through a single base deletion in a homopolymer within the promoter of ibpA, which encodes a

300 ystallizable blends of a block copolymer and homopolymer yields well-defined, low area dispersity exa