ライフサイエンスコーパス: homopolymer

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

2 ne block copolymers from nanocrystals of the homopolymer.

3 interesting case of a biologically relevant homopolymer.

4 also lectins that bind fibrils of the GalNAc homopolymer.

5 t representation of a protein: a hydrophobic homopolymer.

6 estigate the conformational behavior of this homopolymer.

7 of T homopolymers directly followed by an A homopolymer.

8 ontrast to the natural poly(hydroxybutyrate) homopolymer.

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

10 d with suitable molecular weight polystyrene homopolymers.

11 s of the diblock copolymer compared to their homopolymers.

12 minus greatly enhance the formation of SEPT2 homopolymers.

13 ts can be designed as block copolymers or as homopolymers.

14 xtures of diblock copolymers and hydrophobic homopolymers.

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

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

17 rs were prepared without the presence of any homopolymers.

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

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

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

21 mopolymers differ significantly from G and C homopolymers.

22 C-mass spectrometry with non-labeled glucose homopolymers.

23 al), in contrast to the case for random walk homopolymers.

24 urs, Juhua, 3F, 3M/Dyneon, etc., produce TFE homopolymers.

25 rch constituents amylose and amylopectin are homopolymers.

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

27 st naturally as symmetrical homooligomers or homopolymers(1).

28 4 A homopolymers immediately followed by a T homopolymer (5' to 3') and only 8 instances of T homopol

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

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

31 The homopolymer (A)(n), consisting of cyanostar-stabilized a

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

33 outcomes such as self-sorted supramolecular homopolymers, a random (statistical) supramolecular copo

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

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

36 es the interfaces observed in the individual homopolymers, albeit exhibiting a slight rearrangement o

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

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

39 upramolecular polymer by synthesizing both a homopolymer and an alternating copolymer from the same g

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

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

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

43 The D homopolymer and its diblock copolymer poly(ethylene glyc

44 the variant, even in repeat regions, such as homopolymer and other sequence repeats.

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

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

47 is polymerization of benzoladderenes yielded homopolymers and block copolymers with controlled molecu

48 Both homopolymers and block copolymers with controlled molecu

49 ate libraries of polyester and polycarbonate homopolymers and block copolymers with exquisite efficie

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

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

60 n number X of the cross-links for two new 2D homopolymers and one (of three) new 2D copolymers.

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 known to correlate with real variation, like homopolymers and short tandem repeats (STR).

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 of the specific methods of synthesis of the homopolymer, and the relationships between synthesis con

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

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

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

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

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

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

75 with low charge, hydroxyl-rich proteins and homopolymers as growth additives, we show that extremely

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

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

78 olvents like dimethylsulfoxide, controls the homopolymer assembly into crystalline frameworks or unif

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

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

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

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

83 ustrates an ability to classify an erroneous homopolymer call.

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

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

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

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

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

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

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

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

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

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

94 everage the full potential of HiFi reads via homopolymer compression, overlap-based error correction,

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

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

97 Surprisingly, the DNA homopolymers containing as few as 10 tandem hairpins dis

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

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

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

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

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

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

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

105 IVIS imaging of rhodamine labeled homopolymer depots showed that degradation and release o

106 The homopolymer depots with p(Alkyl-TAFMA) exhibited sustain

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

108 Next, the homopolymer design with a high TAF drug wt% of 73% was c

109 The homopolymer designs have a drug reservoir potential of w

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

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

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

113 ominantly in regions of homopolymers, with G homopolymers displaying the largest number of errors and

114 isplaying the largest number of errors and C homopolymers displaying the least.

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 For example, cyclic homopolymers exhibit a reduced hydrodynamic volume and a

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 prone to systematic biases, including large homopolymer flanks (odds ratio = 23.29-33.69) and the NI

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 s a result, 2-aminobenzamide-labeled glucose homopolymer (Glcs) was effectively separated by both C60

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

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

134 46 deletions and two insertions, occurred in homopolymer (HP) tracts [i.e., 47 poly(A) or (T) tracts,

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

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

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

138 to C15) upon the addition of minority-block homopolymer in the dry-brush regime, accompanied by the

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

147 y determination by using single-molecule DNA homopolymers, in which up to 473 identical sensing eleme

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

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

150 which resulted in greater mutational loads, homopolymer instabilities, and higher fractions of mutat

151 ced R-loop, while others are associated with homopolymer instability or translesion DNA synthesis.

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

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

157 nylenes and pre-functionalized polyphenylene homopolymers is demonstrated.

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

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

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

161 was assigned based on analysis of 114 intron homopolymer loci.

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

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

164 unable hysteresis not previously observed in homopolymer materials.

165 when they are dispersed in the corresponding homopolymer matrix.

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

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

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

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

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

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

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

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

174 this acid-sensitive polysaccharide, a linear homopolymer of alpha(2 -> 9)-linked sialic acid, to the

175 Vi polysaccharide is a homopolymer of alpha-1,4-N-acetylgalactosaminouronic aci

176 Polysialic acid (polySia), a homopolymer of alpha2,8-linked glycans, is a posttransla

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 le and diphosphate produces a supramolecular homopolymer of general formula (A)(n) comprised of repea

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

184 hich the genomic RNA is sequestered within a homopolymer of nucleocapsid protein (N).

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

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

187 We also demonstrated that a guanosine homopolymer of various lengths located between the -10 a

188 Homopolymers of 3-acrylamidophenylboronic acid (APBA) fo

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

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

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

192 We show in particular that homopolymers of RNA-polyribouridylic acid and polyriboad

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

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

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

196 monomers are synthetically incorporated into homopolymer or block designs that exhibit high drug weig

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 talyst control allows for the preparation of homopolymers or diblock copolymers with perfect stereose

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 P3HT, and the dibenzo[b,d]thiophene sulfone homopolymer P10, we demonstrate how differences in the t

204 A particle-by-particle analysis of homopolymer partitioning furnishes a basis for understan

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

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

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

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

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

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

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

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

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

214 bly and subsequent collapse of the synthetic homopolymer poly(propylene sulfone).

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

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

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

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 heath layer, contrasting with flagellin-only homopolymers previously observed in exoflagellated bacte

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 y toward systematic errors, in particular in homopolymer regions, which present additional challenges

233 mproved signal and base-calling accuracy for homopolymer regions.

234 nION reads were error-prone, particularly in homopolymer regions.

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

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

237 latforms, having limited ability to sequence homopolymers, repeated motifs or long-range structural v

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

239 ion composition and atmospheres around each homopolymer, revealing a complex interplay of base, ion,

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

241 Homopolymer run enrichment outside of genes causes inser

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

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

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

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

246 roblematic because of the poor resolution of homopolymer runs.

247 creased sequencing error indel rates in long homopolymer runs.

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

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

250 Mimicry of this homopolymer self-assembly using synthetic systems has re

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

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

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

254 el molecular discrimination of the 70 unique homopolymer spots on the array while also identifying in

255 he unique structural and ionic signatures of homopolymer ssRNAs explains their role(s) in folding str

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

257 hes of cylindrical micelles on a crystalline homopolymer substrate.

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

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

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

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

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

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

264 protein in human urine and forms filamentous homopolymers that encapsulate and aggregate uropathogens

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

266 Amphiphilic homopolymers that self-assemble into reverse micelles in

267 ctron-rich monomer inherently forms toroidal homopolymers, the additional electrostatic interaction t

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

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

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

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

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

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

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

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

276 The indels affect short homopolymer tracts of A/T and increase affinity for FOX

277 ivity of the enzyme eliminates stuttering at homopolymer tracts.

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

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

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

281 mproved single-read accuracy by 25 to 70% in homopolymers up to 9 nucleotides long.

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

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

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

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

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

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

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

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

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

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

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

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

297 nctionalized poly(oxanorborneneimide) (PONI) homopolymers with varying molecular weights to stabilize

298 cing errors were predominantly in regions of homopolymers, with G homopolymers displaying the largest

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