ライフサイエンスコーパス: polyamide

1 incorporation of bromine and iodine into the polyamide.

2 h trimesoyl chloride, one of the monomers of polyamide.

3 eight, size, and color with the exception of polyamide.

4 pleting a closed loop cycle for recycling of polyamides.

5 hway may also be involved in the response to polyamides.

6 culties synthesizing these tandem hairpin PI polyamides.

7 ys and compared to the corresponding hairpin polyamides.

8 g liver toxicity was only observed for three polyamides.

9 nker affects on the cellular permeability of polyamides.

10 d (alpha-amino-gamma-turn)-linked eight-ring polyamides.

11 inting data of DNA binding pyrrole-imidazole polyamides.

12 tractive C5 building block of polyesters and polyamides.

13 In this study we introduce the Py-Im polyamide 1 that binds preferentially to the sequences 5

14 abeled radioactive pyrrole-imidazole (Py-Im) polyamide 1, targeted to the 5'-WGWWCW-3' DNA sequence,

15 An 8-ring hairpin polyamide 1, which targets the DNA sequence 5'-WGWWCW-3'

16 We find that cyclic Py-Im polyamides 1-3 bind DNA with exceptionally high affiniti

17 Cyclic 8-ring Py-Im polyamides 1-3 target the DNA sequence 5'-WGWWCW-3', whi

18 s that cause animal toxicity, we synthesized polyamides 1-4 with variations at the alpha- and beta-po

19 A focused library of cyclic polyamides 1-7 targeted to the androgen response element

20 A hairpin pyrrole-imidazole polyamide (1) targeted to the androgen receptor consensu

21 or the largest proportion (38%), followed by polyamide (22%) and polypropylene (16%).

22 Polyamide 3, with an alpha-acetamide, caused no signific

23 ing with automated data analysis showed that polyamide (39%) and ethylene-propylene-diene rubber (23%

24 -clay nanocomposites: polypropylene (PP) and polyamide 6 (PA6) with O-MMT.

25 th positively charged polymeric beads, e.g., polyamide 6/6 (Nylon) and polyoxymethylene (Delrin), and

26 ease of the nanofiller and transformation of polyamide-6 (PA6), a thermoplastic polymer widely used i

27 sited via atomic layer deposition (ALD) onto polyamide-6 nanofibers enable the formation of conformal

28 Bio-based unsaturated nylon-6,6 (unsaturated polyamide-6,6) was finally obtained by polymerization of

29 y developed novel porous nano-hydroxyapatite/polyamide 66 (nHP66)-based nanoscaffold materials contai

30 rpin with a second turn unit yields a cyclic polyamide, a lesser-studied architecture mainly attribut

31 To directly identify the binding sites of polyamides across the genome, we designed, synthesized,

32 The fully aromatic polyamide active layer of a commercial nanofiltration me

33 averaged amide link scission in the aromatic polyamide active layer of a reverse osmosis membrane upo

34 uptake into the bulk region of the aromatic polyamide active layer of a reverse osmosis membrane upo

35 he partition coefficient of solutes into the polyamide active layer of reverse osmosis (RO) membranes

36 nterfacial polymerization, thereby forming a polyamide active layer with more uniform sub-nanometre p

37 s, and measurements of charge density in the polyamide active layers of reverse osmosis (RO) and nano

38 rmine solute partition coefficients into the polyamide active layers of RO membranes.

39 istic understanding of Cl uptake by aromatic polyamide active layers.

40 o measure solute partition coefficients into polyamide active layers.

41 Small animal PET imaging of radiolabeled polyamides administered to mice revealed distinct differ

42 serum concentration was similar for all four polyamides after injection, dose-limiting liver toxicity

43 on between maleimides and resin-linked diene-polyamides allows the latter to be used in the preparati

44 quence specificity and binding affinity, six polyamide analogues containing the core triheterocyclic

45 The use of an oxime linkage between the polyamide and an aromatic functionality on the C-terminu

46 the carbon nanotubes are embedded within the polyamide and form ester bonds with trimesoyl chloride,

47 Polyamide and polyurethane were found to exhibit the hig

48 ation by fractionation on Amberlite(R) XAD16 polyamide and semi-preparative reverse-phase HPLC column

49 tructed from a DNA-binding pyrrole-imidazole polyamide and the peptide FYPWMK facilitates binding of

50 DNA dimerizer constructed from a DNA-binding polyamide and the peptide FYPWMKG facilitates the bindin

51 The high affinity of phenols toward polyamide and their high uptake may change membrane char

52 anscripts are affected by treatment with the polyamide and with bicalutamide.

53 In this study, the isolation with polyamide and XAD resin allowed detection of the presenc

54 s will influence the further design of Py-Im polyamides and facilitate their study in animal models.

55 ts point to a new design principle to deploy polyamides and perhaps other synthetic molecules to effe

56 des could bridge the gap between traditional polyamides and polyethylenes.

57 ensile deformation has been applied to these polyamides and significantly enhances tensile strength t

58 ine colors, composed mostly of polyurethane, polyamide, and polyethylene.

59 expanded to a wide range of other polyester, polyamide, and polyurethane platform materials.

60 ing oligonucleotides, peptide nucleic acids, polyamides, and other approaches, recognition of mixed-s

61 e nucleic acids (PNAs), minor groove binding polyamides, and--more recently--engineered proteins such

62 upramolecular polymers based on a multiblock polyamide architecture.

63 Hairpin pyrrole-imidazole (Py-Im) polyamides are a class of cell-permeable DNA-binding sma

64 Pyrrole-imidazole (Py-Im) hairpin polyamides are a class of programmable, sequence-specifi

65 Pyrrole-imidazole (Py-Im) hairpin polyamides are a class of small molecule DNA minor groov

66 Pyrrole-imidazole polyamides are a class of small molecules that can be pr

67 Pyrrole-imidazole (Py-Im) polyamides are a group of chemicals that are able to bin

68 Pyrrole-imidazole polyamides are DNA minor-groove binding molecules that a

69 Pyrrole-imidazole polyamides are DNA-binding molecules that are programmab

70 These chromophore-free polyamides are observed with strong luminescence ascribe

71 Polyamides are one of the most important polymers.

72 Polyesters and polyamides are very suitable to be depolymerised to othe

73 Groove specificity: pyrrole-imidazole polyamides are well-known for their specific interaction

74 Overall, our results identify Py-Im polyamide as a promising therapeutic strategy in enzalut

75 A polyamide backbone is used for tuning the proteolytic st

76 ar equivalents of DNA with a neutral acyclic polyamide backbone that has nucleobases attached via ter

77 minimum first step toward the translation of polyamide-based gene regulation from cell culture to sma

78 ability and mechanical rigidity, compared to polyamide-based molecules, limit their application.

79 enome-wide view from live cells reveals that polyamide-based synthetic genome readers bind cognate si

80 ofiles, including hydrogen, of NaOCl-treated polyamide-based thin-film composite (TFC) membranes.

81 served results in which polyester fibers and polyamide beads triggered the most pronounced impacts on

82 x different microplastics (polyester fibers, polyamide beads, and four fragment types: polyethylene,

83 Pyrrole-imidazole polyamides bind to a P.Z-containing DNA duplex to form a

84 Pyrrole-imidazole (PI) polyamides bind to the minor groove of DNA in a sequence

85 Pyrrole-imidazole (Py-Im) polyamides bind to the minor groove of DNA with programm

86 the impact of different chromatin states on polyamide binding in live cells remains an unresolved qu

87 the major groove to those induced by cyclic polyamide binding in the minor groove.

88 sembling ARE half-sites that match the Py-Im polyamide binding preferences determined in vitro.

89 ing single or double mismatches to the Py-Im polyamide binding sequence are not enriched.

90 Comparison of polyamide biological activity in two cell lines revealed

91 crystal structure of an 8-ring cyclic Py/Im polyamide bound to the central 6 bp of the sequence d(5'

92 ta-amino turn-linked eight-ring cyclic Py-Im polyamide bound to the central six base pairs of the seq

93 The kinetics of polyamide bromination were first order with respect to t

94 oligonucleotides, peptide nucleic acids, and polyamides, but substantial efforts are currently devote

95 In vivo imaging of pyrrole-imidazole polyamides by PET is a minimum first step toward the tra

96 g elastomers from biomass-derived long-chain polyamides by thiol-ene addition copolymerization with d

97 nzaldehyde and a hydroxylamine moiety at the polyamide C terminus.

98 constructed by attaching the peptide to the polyamide C-terminus expand the range of protein-DNA dim

99 thesis and characterization of a macrocyclic polyamide cage that incorporates redox-active 1,4-dithii

100 An FITC-labeled analogue of this polyamide can be detected in tumor-derived cells by conf

101 Polyamides can access cognate sites within repressive he

102 Pyrrole/imidazole-based polyamides can be rationally designed to target specific

103 Previous studies suggest that Py-Im polyamides can prevent transcription factor binding, as

104 ute to the creation and application of these polyamide-carbon nanotube thin films is also reported.

105 A final clean up via SPE on polyamide cartridges was also employed.

106 o group on imidazole- and pyrrole-containing polyamides causes stacked polyamides to bind in the mino

107 Amberlite XAD 16 HP, polyamide, chitosan, and lignosulfonate were used as ads

108 the latter exhibiting 50% higher adhesion to polyamide coated crystals (mimicking an RO membrane surf

109 resent study, we synthesized tandem tetramer polyamides composed of four hairpin moieties, targeting

110 Polyamides, composed of N-methylpyrrole and N-methylimid

111 ze telomeres specifically, tandem hairpin PI polyamides conjugated with a fluorescent dye have been s

112 ractive alternative for constructing hairpin polyamide conjugates.

113 binding sites in the reverse orientation for polyamides containing beta/Im pairs.

114 Cyclic Py-Im polyamides containing two GABA turn units exhibit enhanc

115 bation pattern caused by a sequence specific polyamide correlates with its in vitro binding preferenc

116 The occupancy patterns suggest that polyamides could be harnessed to target loci within regi

117 Long-chain aliphatic polyamides could bridge the gap between traditional poly

118 micrometre-sized, few-layer two-dimensional polyamide crystals were grown.

119 Long-term treatment with Py-Im polyamide demonstrated a global decrease in RNA levels c

120 This polyamide demonstrates antitumor activity in a prostate

121 These self-terminated polyamide dendrimers are enzymatically and hydrolyticall

122 genome, we designed, synthesized, and tested polyamide derivatives that enabled covalent crosslinking

123 previously that a pyrrole-imidazole (Py-Im) polyamide designed to bind the consensus androgen respon

124 reached a maximum of approximately 25%, (iv) polyamide disintegration occurs when high free chlorine

125 the biological activity of pyrrole-imidazole polyamide DNA-binding molecules, we characterized the ag

126 igh-throughput analysis of pyrrole-imidazole polyamide DNA-binding specificity in a 10(12)-member DNA

127 l pairing rules are remarkably predictive of polyamide DNA-binding specificity.

128 ed covalent crosslinking and localization of polyamide-DNA interaction sites in live human cells.

129 However, polyamides do not show similar binding to duplex RNA, an

130 A series of monodisperse polyamide "drag-tags" was created using both chemical an

131 Influence of cell line grafted on systemic polyamide elimination was established.

132 All the foams were crosslinked with a polyamide-epichlorohydrin crosslinker (Polycup) to impar

133 reatment with this pyrrole-imidazole (Py-Im) polyamide exhibits sequence selectivity in its repressio

134 We used a technique with double polyamide experimental bags (1-mum mesh) to study the in

135 f a modified UiO-66-NH(2) MOF with a growing polyamide fiber (PA-66) during an interfacial polymeriza

136 ined velocities ranged between 0.39 cm/s for polyamide fibers (settling) and 31.4 cm/s for expanded p

137 g diffusivities of several alcohols within a polyamide film of commercial RO membrane using attenuate

138 ependent ionization of carboxyl groups in NF polyamide films.

139 To further optimize Py-Im polyamides for enhanced potency in cell culture, a focus

140 amides more easily, we have developed new PI polyamide fragments and have used them as units in Fmoc

141 of one PBD unit attached to tri-heterocyclic polyamide fragments was designed and synthesized.

142 n of dsDNA sequences using pyrrole-imidazole polyamide-GNP (PA-GNP) conjugates.

143 This study reveals that the combination of polyamide groups, open metal sites, appropriate pore geo

144 A facile modular approach toward cyclic polyamides has been developed via microwave-assisted sol

145 d, but the study of telomeres using these PI polyamides has not been reported because of difficulties

146 odeoxynucleotide decoys or pyrrole-imidazole polyamides) has demonstrated antitumor responses with mi

147 Fluorescein-labeled cyclic polyamides have been synthesized and imaged via confocal

148 Various polyimides and polyamides have recently been prepared via hydrothermal

149 Three hosts were studied: (1) two polyamide hosts, one with isophthaloyl spacers and the o

150 , e.g., polytetrafluoroethylene (Teflon) and polyamide-imide (Torlon), discharge when the like-charge

151 These polyamide-immobilized substrates selectively detected a

152 equent investigations of the availability of polyamides in mouse plasma to human cells.

153 to form composite products with unprotected polyamides in parallel.

154 tion of conventional, widely used nylons and polyamides, in general.

155 ynthetic alkylating agent (pyrrole-imidazole polyamide indole-seco-CBI conjugate; KR12) that selectiv

156 Hairpin polyamides induce a higher melting stabilization of a DN

157 This suggests that polyamides induce replication stress that ATR can counte

158 In biochemical assays, polyamides inhibit DNA helicases, providing a plausible

159 In enzalutamide-resistant LREX' cells, Py-Im polyamide interfered with both AR- and GR-driven gene ex

160 ve binding hairpin pyrrole-imidazole (Py-Im) polyamide interferes with RNA polymerase II (RNAP2) acti

161 The cyclic polyamide is an allosteric modulator that perturbs the D

162 Polyamide is the key material in modern membrane desalin

163 minor groove recognition of a P.Z pair by a polyamide is the reduced level of allosteric distortion

164 tic information by hairpin pyrrole-imidazole polyamides is described.

165 the mechanism of pol II inhibition by Py-Im polyamides is unclear.

166 ased monomers and polymers, and particularly polyamides, it should be noticed that very few natural a

167 membranes consist of a functional selective polyamide layer formed by highly reproducible interfacia

168 oscale nonuniformities inherently present in polyamide layer may reduce selectivity, e.g., for boron

169 The top polyamide layer of composite reverse osmosis (RO) membra

170 the mechanism of phenol transport across the polyamide layer of RO membranes is studied using model p

171 Smoked meat sausages were packed into o-polyamide/low density polyethylene laminated film and co

172 Polyamide material had a moderate reflectivity with subt

173 Here, we combine the advantages of polyamide materials and the structural patterns inspired

174 a was centrifuged and passed over a 0.45-mum polyamide membrane filter, after which the extract was s

175 The polyamide membrane formed by SARIP exhibits highly size-

176 m that mimics the surface chemistry of an RO polyamide membrane was synthesized stepwise on gold-coat

177 As reverse osmosis (RO) and nanofiltration polyamide membranes become increasingly used for water p

178 ive to the long-existing thin-film composite polyamide membranes for water separation applications.

179 lute-solute separation can be achieved using polyamide membranes formed via surfactant-assembly regul

180 ar dynamic simulations, however, reveal that polyamide membranes have a distinctly different structur

181 osure and guidance on how chlorine-resistant polyamide membranes should be designed.

182 d by reverse osmosis (RO) and nanofiltration polyamide membranes that are widely used for water purif

183 ine and chlorine-treated thin-film composite polyamide membranes with either MgCl2 or CaCl2 draw solu

184 anes compared to control thin-film composite polyamide membranes, in both reverse and forward osmosis

185 important tool to enhance the selectivity of polyamide membranes.

186 compared to the control thin-film composite polyamide membranes.

187 ative carboxyl groups of thin-film composite polyamide membranes.

188 ctions between uncharged organic solutes and polyamide membranes.

189 Spike recoveries for 63-90 mum polyamide microplastics demonstrated 101% (standard devi

190 nderstand this effect, the reactivity of the polyamide monomer (benzanilide (BA)) with free chlorine

191 ndings provide a predictive model of how the polyamide monomer degrades during chlorine exposure and

192 igh-yielding routes to commercially valuable polyamide monomers using a single catalyst, telescopic w

193 To synthesize tandem hairpin PI polyamides more easily, we have developed new PI polyami

194 s necessary for efficacy studies in animals, polyamides must be readily synthesized in solution.

195 rfacial polymerization to form free-standing polyamide nanofilms less than 10 nanometers in thickness

196 works (CAFs) by devitrification of amorphous polyamide network polymers using high-temperature and hi

197 ving a variable effect on the upper limit of polyamide nuclear accumulation.

198 utoxide) reacts with surface amide groups of polyamide nylon 6/6 to give (eta(2)-amidate)zirconium co

199 f 65 vol% isotropic NdFeB powder and 35 vol% polyamide (Nylon-12).

200 Our findings indicate that hairpin polyamide of sequence PyImbetaIm-gamma-PyImbetaIm (1), p

201 roperties of three pyrrole-imidazole (Py-Im) polyamides of similar size and Py-Im content but differe

202 e expression analysis of the effects of this polyamide on a set of glucocorticoid-induced and -repres

203 y stage therapeutic investigations involving polyamides or histone deacetylase inhibitors are being p

204 Analysis of polyamide (PA) 6, 46, 66, and 12 pellets and PA 6, 66, p

205 mers (G1-NH2) was covalently attached to the polyamide (PA) active layer of a commercially available

206 ormance of a RO membrane with fully aromatic polyamide (PA) active layer.

207 ng of the structure-property relationship of polyamide (PA) active layers in thin-film-composite memb

208 Two fabrics [polyamide (PA) and polyester/cotton (PES/CO)] were selec

209 curring dsDNA-ssDNA telomere interface using polyamide (PA) and pyridostatin (PDS) conjugates (PA-PDS

210 ed the interactions of an eight-ring hairpin polyamide (PA) and two beta derivatives as well as a six

211 standing the effects of chlorine exposure on polyamide (PA) based membranes is essential in membrane

212 process between an Al foil and a finite size polyamide (PA) film.

213 ouling performance comparable with that of a polyamide (PA) membrane.

214 The degradation of polyamide (PA) nanofiltration and reverse osmosis membra

215 53(Al), NH2-MIL-53(Al) and MIL-101(Cr)] in a polyamide (PA) thin film layer were synthesized via in s

216 walled carbon nanotubes (MWCNT) and aromatic polyamide (PA), was successfully prepared by interfacial

217 Polyamides (PAs) are distamycin-type ligands of DNA that

218 ere the most abundant compounds, followed by polyamides, plastic-based paints, polyvinyl chloride, po

219 conformation in the densely charged aromatic polyamide poly(2,2'-disulfonyl-4,4'-benzidine terephthal

220 Polyamide-polyamine hybrid macrobicycle L is explored wi

221 llular biopolymers, such as polysaccharides, polyamides, polyesters, polyphosphates, extracellular DN

222 increases in MC, aw and DB, when compared to polyamide/polyethylene.

223 terials: aluminum laminated polyethylene and polyamide/polyethylene.

224 into a single low molecular weight precision polyamide polymer.

225 , they are key monomers for the synthesis of polyamides, polyureas, polyepoxydes, which are all of gr

226 , and degradability of long-chain polyester, polyamides, polyurethanes, polyureas, polyacetals, and p

227 otency in cell culture, a focused library of polyamides possessing various modifications at the C-ter

228 d down by the biotin-labeled tandem tetramer polyamide probe confirmed its effective binding to telom

229 synthetic method of fluorescent tandem dimer polyamide probes composed of two hairpin moieties with a

230 Fluorescently labeled tandem tetramer polyamide probes could visualize human telomeres in chem

231 new method, we synthesized four fluorescent polyamide probes for the human telomeric repeat TTAGGG,

232 xed cells with lower background signals than polyamide probes reported previously, suggesting that th

233 and fluorescence spectra of the fluorescent polyamide probes, and telomere staining in mouse MC12 an

234 A linear beta-linked polyamide programmed to target a (GAA)3 repeat yielded a

235 An eight-ring hairpin polyamide programmed to target the 5 bp sequence 5'-TACG

236 owed by an acidic treatment that removes the polyamide protecting groups with no harm to the cycloadd

237 icro-spectroscopy to be mineralized, natural polyamide proteins, or nonplastic shell pieces.

238 ma-turn increase the DNA-binding affinity of polyamides relative to the ( R)-alpha-amino-gamma-turn.

239 Gene regulation by polyamides requires efficient cellular uptake and nuclea

240 osaccharide purification uses a normal-phase polyamide resin (DPA-6S) in custom-made pipette tips.

241 robial modification of a thin-film composite polyamide reverse osmosis (RO) membrane.

242 n the surface of a thin-film composite (TFC) polyamide RO membrane.

243 assess the ionization behavior of nanoporous polyamide selective layers in state-of-the-art nanofiltr

244 ped TFC PRO membranes consist of a selective polyamide skin formed on the lumen side of well-construc

245 general purpose and specialty polyesters and polyamides; some of them are currently derived from oil,

246 urn unit affords the classical hairpin Py-Im polyamide structure.

247 e instruments included forceps, metallic and polyamide subretinal needles, and soft silicone-tipped i

248 but had no effect on the EPS adhesion to the polyamide surface.

249 e applied our methodology for solution-phase polyamide synthesis to cyclic polyamides with an improve

250 The former dense skin is a polyamide synthesized via interfacial polymerization, wh

251 The polyamides synthesized using the new method successfully

252 nce-specific agents, and it is the first non-polyamide, synthetic compound to specifically recognize

253 stigation of a DNA-binding pyrrole-imidazole polyamide targeted to bind the DNA sequence 5'-WGGWWW-3'

254 oximately 20-fold increase in the potency of polyamides targeted to the androgen response element (AR

255 Pyrrole-imidazole polyamides targeted to the androgen response element wer

256 A specific pyrrole-imidazole polyamide targeting GAA.TTC triplet-repeat DNA partially

257 turn potentiates the biological effects of a polyamide targeting the sequence 5'-WGWWCW-3' (W =A/T) b

258 a small library of hairpin pyrrole-imidazole polyamides targeting the sequence 5'-CGCG-3' and assesse

259 turn modifications enhance the uptake of all polyamides tested, while having a variable effect on the

260 ion, we designed a DNA minor groove-targeted polyamide that inhibits NES with low micromolar efficacy

261 A DNA-binding polyamide that targets the consensus androgen response e

262 We show that a DNA-binding polyamide that targets the consensus GRE sequence binds

263 king on the development of pyrrole-imidazole polyamides that bind to the minor groove of DNA in a seq

264 ctivity in N-methylpyrrole/N-methylimidazole polyamides that helps explain how these molecules locate

265 ing the intracellular concentration of Py-Im polyamides that will prove valuable for future applicati

266 s and specificities of the tandem hairpin PI polyamides, the UV-vis absorption and fluorescence spect

267 eriments with cellulose triacetate (CTA) and polyamide thin-film composite (TFC) FO membranes demonst

268 Aromatic polyamide thin-film composite membranes are widely used

269 Conventional polyamide thin-film composite membranes with a ridge-and

270 be reduced to a dipeptide WM attached to the polyamide through an epsilon-aminohexanoic acid linker w

271 llosteric distortion induced by binding of a polyamide to a DNA duplex.

272 a foundation for design of DNA binding Py-Im polyamides to be tested in vivo.

273 pyrrole-containing polyamides causes stacked polyamides to bind in the minor groove of DNA in the sta

274 e N-terminus is important for the binding of polyamides to DNA in a stacked and staggered motif.

275 g of two bioactive and structurally distinct polyamides to genomes directly within live H1 human embr

276 Polyamide treatment activates p53 signaling in LNCaP pro

277 Polyamide treatment also induced accumulation of monoubi

278 Polyamide treatment induced accumulation of S-phase cell

279 Polyamide treatment results in a time- and dose-dependen

280 probes have been proposed as alternatives to polyamides, triplex-forming oligonucleotides, and peptid

281 the biodistribution of a 5-ring beta-linked polyamide versus an 8-ring hairpin, which exhibited bett

282 The polyamide was active against two enzalutamide-resistant

283 Down-regulation of PSA by this polyamide was comparable to that produced by the synthet

284 New antioxidant polyamide was prepared by total immersion in active extr

285 The solubility of both hairpin and cyclic polyamides was increased upon addition of carbohydrate s

286 , we found that the cellular permeability of polyamides was size-dependent.

287 lutes and the membrane phase (fully aromatic polyamide) was computed from molecular dynamics (MD) sim

288 Using the fluorescent polyamides, we demonstrated that the telomere length at

289 he presence of site-specifically bound Py-Im polyamides, we find that the pol II elongation complex b

290 on profiles in mice of two pyrrole-imidazole polyamides were determined by PET.

291 Nearly all studied polyamides were found to form measurable particles 50-50

292 Cyclooctyne-derivatized pyrrole-imidazole polyamides were immobilized on azide-modified glass subs

293 NA binding affinities of a library of cyclic polyamides were measured by DNA thermal denaturation ass

294 The (18)F-radiolabeled polyamides were prepared by oxime ligation between 4-[(1

295 In the same study, a polyamide with an acetamide at the beta-position of the

296 analysis by RNA-seq compares the DNA-binding polyamide with the well-characterized NF-kappaB inhibito

297 solution-phase polyamide synthesis to cyclic polyamides with an improved high-yield cyclization step.

298 of a new class of pyrrole-imidazole hairpin polyamides with beta-amino-gamma-turn units for recognit

299 These insights allow the redesign of hairpin polyamides with different turn units capable of distingu

300 ere, we report a class of easily processable polyamides with stereocontrolled mechanical properties a