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1 nto oligomeric strands that are analogous to peptide nucleic acid.
2 -(2-aminoethyl)glycine (AEG), a backbone for peptide nucleic acids.
3 very of conventional and chemically-modified peptides nucleic acids.
4 sed by reduction in the cytoplasm, including peptide nucleic acids, a cyclic peptide (phalloidin), an
5 mobilized anthraquinone-labeled pyrrolidinyl peptide nucleic acid (acpcPNA) probe was successfully de
7 ssay for DNA detection based on pyrrolidinyl peptide nucleic acid (acpcPNA)-induced nanoparticle aggr
8 sensor was developed based on a pyrrolidinyl peptide nucleic acid (acpcPNA)/polypyrrole (PPy)/silver
9 ethylenediamine portion of aminoethylglycine peptide nucleic acids (aegPNAs) with one or more (S,S)-t
15 itions adjacent to the lambda operators with peptide nucleic acids and monitored their movement by te
16 here is a brief introduction to the field of peptide nucleic acids and their potential benefits as pr
17 y method is described based on surface-bound peptide nucleic acids and water-soluble cationic conjuga
19 made with triplex-forming oligonucleotides, peptide nucleic acids, and polyamides, but substantial e
20 biomimetics, molecular imprinting polymers, peptide nucleic acids, and ribozymes were encompassed as
23 ments using two triplex-forming molecules, a peptide nucleic acid-antennapedia (PNA-Antp), and a TFO
29 s, stemless and stem-containing DNA and PNA (peptide nucleic acid) beacons, in Tris-buffer solutions
32 emplated chemical transformation of bifacial peptide nucleic acid (bPNA) fragments directed by an abi
34 operties of bPNA+, a new variant of bifacial peptide nucleic acid (bPNA) that binds oligo T/U nucleic
35 tative NMR spectral parameters for proteins, peptides, nucleic acids, carbohydrates and ligands or co
37 hanism and kinetic specificity of binding of peptide nucleic acid clamps (bis-PNAs) to double-strande
39 ces, followed by highlights of ways by which peptide nucleic acids could benefit a number of establis
42 We show that systemic delivery of antisense peptide nucleic acids encapsulated in unique polymer nan
43 ever, "ligand" molecules, included proteins, peptides, nucleic acids, etc. are expensive and vulnerab
44 diffusivity between a free ferrocene-labeled peptide nucleic acid (Fc-PNA) and a Fc-PNA hybridized wi
45 ates or anti-GFP nanobodies, interfaced with peptide nucleic acids, flipper force probes, or fluoresc
48 valuate the performance of a new three-color peptide nucleic acid fluorescence in situ hybridization
52 carensis and C. nivariensis species-specific peptide nucleic acid fluorescence in situ hybridization
53 cation of Candida albicans blood isolates by peptide nucleic acid fluorescence in situ hybridization
54 in blood culture bottles within 2.5 h using peptide nucleic acid fluorescence in situ hybridization.
58 ichment broths by the use of subculture, GBS peptide nucleic acid fluorescent in situ hybridization (
59 selective Streptococcus agar (SSA), and by a peptide nucleic acid fluorescent in situ hybridization (
60 nce of the Candida albicans/Candida glabrata peptide nucleic acid fluorescent in situ hybridization (
61 on of a biofilm in vivo was visualized using peptide nucleic acid fluorescent in situ hybridization (
62 ch probes could be used as an alternative to peptide nucleic acids for investigating the dynamics of
63 mides, triplex-forming oligonucleotides, and peptide nucleic acids for recognition of chromosomal DNA
64 ntly, we have considered the use of DNAs and peptide nucleic acids for this purpose because oligomers
65 how that conformationally preorganized gamma-peptide nucleic acid (gamma-PNA) containing an acridine
66 opipette and an assay of complementary gamma-peptide nucleic acid (gamma-PNA) probes conjugated to po
67 eparing optically pure guanidine-based gamma-peptide nucleic acid (gammaGPNA) monomers for all four n
68 the mRNA and a complementary gamma-modified peptide nucleic acid (gammaPNA) sequence with a noncompl
74 ansfer (FRET) between fluorescently labelled peptide nucleic acids, hybridized to defined single stra
75 midate (MO) 20mer or hydroxyprolyl-phosphono peptide nucleic acid (HypNA-pPNA) 16mer antisense oligon
77 tment of established PNFs using anti-miR-155 peptide nucleic acid-loaded nanoparticles marginally dec
78 eukaryotic histones, synthetic peptides, or peptide nucleic acids may be limited by high production
81 from 97 baseline blood samples by our novel peptide nucleic acid-mediated 5 nuclease real-time polym
82 rference with these lncRNAs using complement peptide nucleic acid molecules down-regulated the active
85 sequences are superior to those of analogous peptide nucleic acid oligomers, emphasizing the value of
86 ring probe) is threaded, with the aid of two peptide nucleic acid openers, between the two strands of
88 e, we report the use of pseudo-complementary peptide nucleic acids (pcPNAs) for intracellular gene ta
89 aluates the potential of pseudocomplementary peptide nucleic acids (pcPNAs) for sequence-specific mod
90 ere, we demonstrate that pseudocomplementary peptide nucleic acids (pcPNAs) represent a class of vers
92 ore stably bound to plasmid DNA than similar peptide nucleic acid (PNA) 'clamps' for procedures such
95 etrating peptide (CPP) conjugates of a 16mer peptide nucleic acid (PNA) analogue targeted to the apic
96 lly cationic and chiral C(gamma)-substituted peptide nucleic acid (PNA) analogues have been synthesiz
97 Here, we test the hypothesis that antisense peptide nucleic acid (PNA) and locked nucleic acid (LNA)
98 based on the strand replacement of dsDNA by peptide nucleic acid (PNA) and the in situ growth of ele
99 G12D and ~100-fold increased sensitivity of Peptide Nucleic Acid (PNA) and Xenonucleic Acid (XNA) cl
100 systemic barriers for in vivo application of peptide nucleic acid (PNA) anti-microRNA therapeutics.
102 sociated CD40 protein expression by use of a peptide nucleic acid (PNA) antisense inhibitor, ISIS 208
106 engineered with a novel and highly specific peptide nucleic acid (PNA) as the recognition element.
107 (2'-O-MOE) phosphorothioate, morpholino and peptide nucleic acid (PNA) backbones was investigated us
111 lo domain partitioning of the palmitoylated peptide nucleic acid (PNA) can be influenced by formatio
113 a gold electrode coated with charge neutral peptide nucleic acid (PNA) capture probes (CPs) is first
114 itoneal injection of an unmodified antisense peptide nucleic acid (PNA) complementary to mRNA of the
116 id fluorenylmethyloxycarbonyl (Fmoc)-guanine peptide nucleic acid (PNA) conjugate with diverse morpho
117 ense imaging agent comprised of an iodinated peptide nucleic acid (PNA) conjugated to a monoclonal an
118 sonant mechanism of charge transfer in short peptide nucleic acid (PNA) duplexes obtained through ele
119 hroughput microarray screening process using peptide nucleic acid (PNA) encoding technology, allowing
120 e tube coagulase test (TCT) read at 4 h, and peptide nucleic acid (PNA) fluorescence in situ hybridiz
121 easts on Gram stain using a Candida albicans peptide nucleic acid (PNA) fluorescent in situ hybridiza
123 "reporter and miRNA" and "reporter and miRNA-peptide nucleic acid (PNA) hybrid", which yields two sig
124 esized that scintigraphic detection of CCND1 peptide nucleic acid (PNA) hybridization probes with a (
125 ations, using allele-specific, mass-labeled, peptide nucleic acid (PNA) hybridization probes, and dir
128 the zein gene from maize using pyrrolidinyl peptide nucleic acid (PNA) immobilized on a magnetic sol
137 s of molecular dynamics simulations of small peptide nucleic acid (PNA) molecules, synthetic analogs
138 uration of the target plasmid sample using a peptide nucleic acid (PNA) oligomer as the probe is desc
141 nes in two mutually complementary mixed-base peptide nucleic acid (PNA) oligomers are substituted wit
146 ere, we show that a short antisense chimeric peptide nucleic acid (PNA) oligonucleotide conjugated to
148 led telomeric repeat complementing (CCCTAA)3 peptide nucleic acid (PNA) probe coupled with cardiac-sp
149 va telomeric sequence d(G(4)T(4)G(4)) with a peptide nucleic acid (PNA) probe having a homologous rat
150 iameter polystyrene beads to which uncharged peptide nucleic acid (PNA) probe molecules have been con
151 cribed were internally functionalized with a peptide nucleic acid (PNA) probe specific for a gene tra
154 n situ hybridization (FISH) method that uses peptide nucleic acid (PNA) probes for identification of
155 nce in situ hybridization (FISH) method with peptide nucleic acid (PNA) probes for identification of
157 report demonstrates the use of high-affinity peptide nucleic acid (PNA) probes in labeling mRNA trans
158 Comparison with published data for DNA and peptide nucleic acid (PNA) probes is carried out to look
160 orescence in situ hybridization (FISH) using peptide nucleic acid (PNA) probes targeting Staphylococc
163 on by using cationic conjugated polymers and peptide nucleic acid (PNA) probes with ultrafast pump-du
165 nologies: rapid cycling PCR thermal cyclers, peptide nucleic acid (PNA) probes, and a new double-stra
166 zation biosensor, based on thiol-derivatized peptide nucleic acid (PNA) probes, offers unusual in sit
167 acid and nucleobase sequences into a single peptide nucleic acid (PNA) scaffold to enable tunable st
168 ochemically active molecular probes based on peptide nucleic acid (PNA) scaffolds for the detection o
170 ensitize the emission of a dye on a specific peptide nucleic acid (PNA) sequence for the purpose of h
174 mycin B (ring II) was conjugated to a 16-mer peptide nucleic acid (PNA) targeting HIV-1 TAR RNA.
175 ew DNA diagnostic is based on combination of peptide nucleic acid (PNA) technology, rolling circle am
176 tic approach to develop an embedded chimeric peptide nucleic acid (PNA) that effectively enters the c
177 nt studies describe the production of 16-mer peptide nucleic acid (PNA) that is antisense around the
178 n 3D nucleic acid-amino acid complexes using peptide nucleic acid (PNA) to assemble peptides inside a
182 A modified M918 peptide conjugated to a peptide nucleic acid (PNA) was shown to silence lucifera
184 We show here that the hybridization of a peptide nucleic acid (PNA) within or adjacent to the pro
186 C locked nucleic acid (LNA) residues, and a peptide nucleic acid (PNA), inhibit Tat-dependent in vit
187 molecules, each linked to a short strand of peptide nucleic acid (PNA), synthetic polymers that use
188 o acid is used as a building block for a new peptide nucleic acid (PNA), which exhibits excellent DNA
197 was to synthesize and evaluate radiolabeled peptide nucleic acid (PNA)-peptide conjugates targeting
205 screening with less flexible, self-assembled peptide nucleic acid (PNA).DNA complexes uncovered a wel
206 An approach is described for predicting peptide nucleic acid (PNA):DNA duplex stability from bas
207 ying lengths by hybridization of n-alkylated peptide nucleic acids (PNA amphiphiles) to the products,
209 d whether tunable-surface bead chemistry and peptide nucleic acids (PNA) could enhance the recovery a
213 logues, which also include compounds such as peptide nucleic acids (PNA), in surface hybridization ap
219 obes: anneal-inhibiting blocking primers and peptide-nucleic acid (PNA) oligonucleotide blockers.
220 equently, molecularly-imprinted polymers and Peptide nucleic acid (PNAs) were developed as an attract
221 is based on two ligands functionalized with peptide nucleic acids (PNAs) (templating strand and cata
222 the field - locked nucleic acids (LNAs) and peptide nucleic acids (PNAs) - significantly increase th
229 lamide (HPMA) polymers grafted with multiple peptide nucleic acids (PNAs) are crosslinked upon additi
237 es for a successful and broad application of peptide nucleic acids (PNAs) as antisense therapeutics.
238 eport the development of chemically modified peptide nucleic acids (PNAs) as probes for qualitative a
241 assembled monolayers of single-stranded (ss) peptide nucleic acids (PNAs) containing seven nucleotide
245 forming oligonucleotides and triplex-forming peptide nucleic acids (PNAs) have been shown to stimulat
246 plex-forming DNA oligonucleotides (TFOs) and peptide nucleic acids (PNAs) have been shown to stimulat
250 st attempt to overcome this problem by using peptide nucleic acids (PNAs) modified with extended nucl
254 e imaged in a mouse by PET with 64Cu-labeled Peptide nucleic acids (PNAs) tethered to the permeation
255 induce G-quadruplex formation, we used short peptide nucleic acids (PNAs) that bind to the complement
256 use high-affinity recognition by overlapping peptide nucleic acids (PNAs) to identify nucleotides wit
260 triplex-forming oligonucleotides (TFOs) and peptide nucleic acids (PNAs), can be utilized to introdu
261 rapeutic (FAST) platform to create antisense peptide nucleic acids (PNAs), gene-specific molecules de
262 ergence of triplex-forming oligonucleotides, peptide nucleic acids (PNAs), minor groove binding polya
263 sical properties, we explore the assembly of peptide nucleic acids (PNAs), which are short DNA mimics
270 gress with triplex-forming oligonucleotides, peptide nucleic acids, polyamides, and other approaches,
272 erstand how the addition of mutations to the peptide nucleic acid probe could enhance the selectivity
273 In each case, fluorescence intensity of a peptide nucleic acid probe specific for telomeric sequen
274 ocked by electrophoretically mobilized bead-(peptide nucleic acid probe) conjugates upon hybridizatio
275 rt 21 base-long RNA target to an immobilized peptide nucleic acid probe, while fragmented mRNA target
278 es, fluorescence in situ hybridization using peptide nucleic acid probes (PNA-FISH) and matrix-assist
280 al nucleic acid sensors based on fluorogenic peptide nucleic acid probes embedded in permeable, physi
281 oligonucleotide-templated reactions between peptide nucleic acid probes embedded within permeable ag
282 lization, hybridization of cellular DNA with peptide nucleic acid probes with cells intact, and analy
284 at provide small molecular mimics to explore peptide-nucleic acid recognition have been prepared.
287 so delivered a biotinylated 18-mer antisense peptide-nucleic acid specific for the rev gene of HIV-1
288 ransfer (CT) properties are compared between peptide nucleic acid structures with an aminoethylglycin
289 f the net increase in negative charge at the peptide nucleic acid surface that occurs upon single-str
294 n of isotopomer tandem nucleic acid mass tag-peptide nucleic acid (TNT-PNA) conjugates is described a
297 have designed FIT-PNAs (forced-intercalation-peptide nucleic acids) to detect two RNA cancer biomarke
298 simple oligo-dipeptide backbones [thioester peptide nucleic acids (tPNAs)] and undergoes dynamic seq
299 A-norbornyl monomers to yield poly-PNA (poly(peptide nucleic acid)) via ring-opening metathesis polym
300 -MOE)-phosphorothioate and PNA-4K oligomers (peptide nucleic acid with four lysines linked at the C t