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1                                              LNA (locked nucleic acids, i.e. oligonucleotides with a
2                                              LNA finds small highly conserved network regions and pro
3                                              LNA modified ASOs can cause hepatotoxicity, and this ris
4                                              LNA was used in three positional patterns: near the 5' e
5                                              LNA-5' increased the average Phred Q30 score by 60% and
6                                              LNA-92a exerts cell-protective, proangiogenic, and anti-
7                                              LNA-92a significantly (P<0.01) reduced miR-92a expressio
8                                              LNA-anti-miR-192 significantly reduced levels of miR-192
9                                              LNA-antimiR-34 (8-mer) efficiently silenced all three mi
10                                              LNA-CTGs produced rapid and sustained improvement of mot
11                                              LNA-FISH requires 5 h, or between 10 and 36 h when combi
12                                              LNA-modified chemistries can effectively silence miR-15
13                                              LNA-modified TFOs form more stable triplexes than alpha-
14                                              LNAs targeting sequences at or near transcription start
15                          The RNA with the 5'-LNA-modified cap was found to be approximately 1.61- and
16 rotein decreased activity of PS-ASOs with 5'-LNA or 5'-cEt wings, but not with 5'-MOE wing.
17                  The RNA capped with the m(7(LNA))G[5']ppp[5']G 3 cap analogue was translated the mos
18                Molecular modeling of the m(7(LNA))G[5']ppp[5']G 3 cap analogue with the cap binding p
19 st that the new antireverse cap analogue m(7(LNA))G[5']ppp[5']G 3 is a potential candidate for RNA-ba
20 leic acid (LNA)-modified cap analogue 3, m(7(LNA))G[5']ppp[5']G, has been synthesized and its biologi
21 ked nucleic acid-modified antisense miR-92a (LNA-92a) was applied either regionally (antegrade or ret
22 NAs) to the beacon structure, resulting in a LNA molecular beacon (LMB) with robust stability after s
23 ulation of MOR by let-7 was revealed using a LNA-let-7 inhibitor to knockdown let-7 in SH-SY5Y cells.
24 sized from a precursor alpha-linolenic acid (LNA) or obtained preformed in the diet.
25 studies in vitro and by locked nuclear acid (LNA) modified inhibitors in vitro and in vivo.
26 ed by direct sequencing, locked nuclei acid (LNA)-based PCR, and immunohistochemistry.
27                         Locked nucleic acid (LNA) and its diastereomer alpha-L-LNA are two interestin
28 ted nucleotides such as locked nucleic acid (LNA) are very popular as affinity-, specificity-, and st
29  take full advantage of locked nucleic acid (LNA) based molecular beacons (LNA-MBs) for a variety of
30 tor capped hairpin with locked nucleic acid (LNA) bases on the dynamics and efficiency of hole transp
31                  First, locked nucleic acid (LNA) bases were incorporated into the probes to normaliz
32                         Locked Nucleic Acid (LNA) can enhance oligonucleotide affinity and specificit
33 hococcus, Prochlorococcus, low nucleic acid (LNA) content bacterioplankton and small plastidic protis
34 fications (BNA) such as locked nucleic acid (LNA) designed to induce target RNA cleavage have been sh
35  vivo administration of locked nucleic acid (LNA) inhibitors that suppression of endogenous miR-29 lo
36                         Locked nucleic acid (LNA) microarrays were used to investigate the miRNA tran
37 oxyethylribose (MOE) or locked nucleic acid (LNA) modifications were designed to investigate whether
38 A-BCA system contains a locked nucleic acid (LNA) modified DNA probe for improving hybridization effi
39 -1-yl)carbonyl-2'-amino locked nucleic acid (LNA) monomer X is a highly versatile building block for
40 d by affinity-enhancing locked nucleic acid (LNA) monomers and additional regulatory strands.
41 ted nucleotides such as locked nucleic acid (LNA) monomers are used extensively in molecular biology
42 fied with six different locked nucleic acid (LNA) monomers, i.e. conventional and C5-alkynyl-function
43 -methoxyethyl (MOE) and locked nucleic acid (LNA) nucleosides yielded a series of nucleoside modifica
44 e use of functionalized locked nucleic acid (LNA) oligomers as biomolecular handles that permit seque
45 RNAs in plants by using locked nucleic acid (LNA) oligonucleotide probes.
46 petitively blocked by a locked nucleic acid (LNA) oligonucleotide.
47 ates containing DNA and locked nucleic acid (LNA) oligonucleotides are active, and oligospermine conj
48         Transfection of locked nucleic acid (LNA) oligonucleotides designed to block the function of
49 ults were obtained with locked nucleic acid (LNA) phosphorothioate gap-mers.
50  also demonstrated that locked nucleic acid (LNA) probes improved sensitivity approximately 4-fold co
51  the targeted loci, and locked nucleic acid (LNA) probes were used to enhance the detection of strain
52 goxigenin (DIG) RNA and locked nucleic acid (LNA) probes, respectively.
53                  Use of locked nucleic acid (LNA) residues in the DNA probes resulted in greater disc
54                         Locked nucleic acid (LNA), a conformationally restricted DNA analogue, is pot
55 es comprising DNA, RNA, locked nucleic acid (LNA), or 2'O-methyl-DNA.
56 the let-7 family with a locked nucleic acid (LNA)-anti-miR has the opposite effect.
57         With the use of locked nucleic acid (LNA)-antimiR-21 oligonucleotides, bimodal imaging vector
58                         Locked nucleic acid (LNA)-based miRNA array was employed to profile miRNAs us
59 h DNA, RNA and combined locked nucleic acid (LNA)-DNA backbones can all detect miRNAs of low (<1 nM)
60 iac tissues and whether locked nucleic acid (LNA)-modified anti-miR chemistries can target cardiac ex
61 of 8-mer seed-targeting locked nucleic acid (LNA)-modified anti-miR oligonucleotides, termed tiny LNA
62 ed seed-targeting 8-mer locked nucleic acid (LNA)-modified antimiR (LNA-antimiR-34) can provide thera
63 sed miRNA-122 using the locked nucleic acid (LNA)-modified antisense oligonucleotide miravirsen.
64  the present study, the locked nucleic acid (LNA)-modified cap analogue 3, m(7(LNA))G[5']ppp[5']G, ha
65 uated the efficacy of a locked nucleic acid (LNA)-modified inhibitor of miR-192, designated LNA-anti-
66 cted chimpanzees with a locked nucleic acid (LNA)-modified oligonucleotide (SPC3649) complementary to
67 n suspended cells using locked nucleic acid (LNA)-modified oligonucleotide probes.
68 d cultured cells, using locked nucleic acid (LNA)-modified oligonucleotides.
69 L-6((-)/(-))) mice with locked nucleic acid (LNA)-modified phosphorothioate oligonucleotide complemen
70 delivery using a simple locked nucleic acid (LNA)-polymer conjugate that assembles into spherical mic
71 building blocks such as locked nucleic acid (LNA).
72 inds PS-ASOs containing locked-nucleic-acid (LNA) or constrained-ethyl-bicyclic-nucleic-acid ((S)-cEt
73                    DNA/locked nucleic acids (LNA) AMOs synthesized with a phosphorothioate backbone a
74 tide probes containing locked nucleic acids (LNA) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide
75 rected mutagenesis and locked nucleic acids (LNA) complementary to defined domains of SL9266 and its
76 with modification with locked nucleic acids (LNA) increased conformational stability and nuclease res
77                        Locked nucleic acids (LNA) show remarkable affinity and specificity against na
78           We have used locked nucleic acids (LNA) to engineer novel molecular beacons (MBs) for long-
79 dies, using anti-sense locked-nucleic acids (LNAs) and synthetic RNA mimetics, respectively, revealed
80 el antigens containing locked nucleic acids (LNAs) as targets for antibodies.
81 Me ribonucleotides and locked nucleic acids (LNAs) at selected sites.
82 scribe a unique use of locked nucleic acids (LNAs) for studying nuclear long noncoding RNA, an RNA su
83 ucleotides (ASOs) with locked nucleic acids (LNAs) improve target affinity, RNase H activation and st
84        The presence of locked nucleic acids (LNAs) in the ssODNs at mismatching bases, or also at dir
85 herapeutic delivery of locked nucleic acids (LNAs) targeting BCAR4 attenuated YAP-dependent glycolysi
86 herapeutic delivery of locked nucleic acids (LNAs) targeting BCAR4 strongly suppresses breast cancer
87 reatment of cells with locked nucleic acids (LNAs) targeting these miRNAs inhibits metastasis to mult
88  we introduced Invader locked nucleic acids (LNAs), i.e., double-stranded probes that are activated f
89 ence signal intensity between the beta-actin LNA probe and a biotinylated, nonspecific control LNA we
90 se-tolerability studies in mice administered LNA-modified ASOs.
91 uences with DNA/LNA alternating bases or all LNA bases were able to resist nonspecific protein bindin
92                           Some, but not all, LNA containing oligonucleotides increased potency for re
93 sed exclusively of locked nucleic acids (all-LNAs) complementary to CUG repeats, as potential therape
94    Our data strongly indicate that short all-LNAs complementary to CUG repeats are a promising therap
95                                      The all-LNAs had low impact on the cellular level of CUG(exp)-co
96  skeletal muscles of DM1 mouse model the all-LNAs induced the reduction of the number and size of CUG
97 onstrated that very short, 8- or 10-unit all-LNAs effectively bound the CUG repeat RNA and prevented
98 othesized that enhanced affinity might allow LNAs to recognize chromosomal DNA inside human cells and
99 general, and the N2'-functionalized 2'-amino-LNA derivatives in particular, showed improved duplex th
100  hydrocarbon (PAH) dyes attached to 2'-amino-LNA monomers are incorporated at four stations of the sy
101                    In addition, the 2'-amino-LNA-T derivatives induced remarkable 3'-exonuclease resi
102 tose-modified thymidine, LNA-T, and 2'-amino-LNA-T nucleosides were synthesized, converted into the c
103 ionalized thymine and 5-methylcytosine amino-LNA phosphoramidites from these key intermediates, respe
104                      In contrast, LNA-3' and LNA-Even did not improve read lengths or C(T).
105                                These DNA and LNA/DNA sequences showed improved binding in enzyme-link
106                The structures of the DNA and LNA:DNA hybrids are tentatively assigned to B- or A-type
107  range of backbone structures (RNA, DNA, and LNA templates and RNA and DNA primers) and two types of
108 y to completion on short homopolymer RNA and LNA templates, which favor an A-type duplex geometry.
109 est this hypothesis, we synthesized antigene LNAs (agLNAs) complementary to sequences within the prom
110  locked nucleic acid (LNA)-modified antimiR (LNA-antimiR-34) can provide therapeutic benefit in mice
111  of the standard Linear Noise Approximation (LNA) to remain uniformly accurate for long times, still
112 roperties for complementary nucleic acids as LNA.
113 ntaining high affinity modifications such as LNA, hepatotoxicity can occur as a result of unintended
114 otides containing locked nucleic acid bases (LNAs) have increased affinity for complementary DNA sequ
115 s new design adds locked nucleic acid bases (LNAs) to the beacon structure, resulting in a LNA molecu
116  nucleic acid (LNA) based molecular beacons (LNA-MBs) for a variety of applications including analysi
117  a DNA stretch less than three bases between LNA bases was able to block RNase H function.
118 alized to high affinity modifications beyond LNA.
119  cells by hybridization with a biotinylated, LNA-modified probe.
120 AE residues, the conformationally locked BNA/LNA ribose with a 2'-O,4'-C-methylene bridge, or the 2'-
121 hen loaded in a shear orientation, the bound LNA oligomers were measured to be two orders of magnitud
122                      Inhibition of miR-34 by LNA-34a significantly reduced miR-34a expression and blo
123 perature; binding of SSB was not affected by LNA bases.
124                  Decreasing uc.173 levels by LNA-anti-uc.173 in mice reduced renewal of the intestina
125 e purine or pyrimidine bases are replaced by LNA bases.
126                 This combined method, called LNA flow-FISH, can be used for detection and quantificat
127 ity and biological activity with carbocyclic LNA (cLNA) analogs by replacing the 2'-oxygen atom in LN
128                     So, which one to choose, LNA or GNA?
129 ionally, in MMR-proficient Escherichia coli, LNA modification of the ssODNs enabled effective single-
130 scrimination ability of the surface-confined LNA probes could be controlled by ionic modulations.
131 ce thermal stability of the surface-confined LNA-DNA duplexes, the nature of concentration dependence
132 tion of melting behavior of surface-confined LNA-DNA duplexes.
133 r non-clamp, or nucleotide-linker containing LNA-constructs.
134                    Further, when we contrast LNA and GNA in the application of learning novel protein
135                                 In contrast, LNA-3' and LNA-Even did not improve read lengths or C(T)
136 robe and a biotinylated, nonspecific control LNA were used to determine optimal conditions for this t
137 detected and differentiated from the control LNA with high confidence (< 14% overlap between curves).
138 duced the infarct size compared with control LNA-treated pigs, which correlated with an improved ejec
139           Our method, called phase-corrected LNA (pcLNA) overcomes the main limitations of the standa
140  of microRNA-155 by a systemically delivered LNA-anti-miR attenuated cardiac infiltration by monocyte
141 A)-modified inhibitor of miR-192, designated LNA-anti-miR-192, in mouse models of diabetic nephropath
142 t allow for fair comparison of the different LNA and GNA outputs, as such measures do not exist.
143  with a 4 base-pair stem and alternating DNA/LNA bases is desirable for intracellular applications as
144           A highly specific biotinylated DNA/LNA molecular beacon (MB) probe was conjugated with gold
145 e systematically synthesized a series of DNA/LNA chimeric MBs and studied the effect of DNA/LNA ratio
146 A chimeric MBs and studied the effect of DNA/LNA ratio in MBs on their thermodynamics, hybridization
147 e significantly improved by lowering the DNA/LNA ratio in the probe, and most significantly, by havin
148 It was found that only MB sequences with DNA/LNA alternating bases or all LNA bases were able to resi
149 aperitoneal injections of a plasmid encoding LNA-anti-uc.173, to knock down endogenous uc.173.
150 : near the 5' end (LNA-5'), near the 3' end (LNA-3') and distributed throughout (LNA-Even).
151  three positional patterns: near the 5' end (LNA-5'), near the 3' end (LNA-3') and distributed throug
152      Herein we introduce a novel fluorescent LNA/DNA machine, a nanocrawler, which reversibly moves a
153 to inhibit miR-34a alone as a comparison for LNA-antimiR-34.
154  further suggest a therapeutic potential for LNA-CTG in polyglutamine disorders.
155 Histopathological evaluation of tissues from LNA treated animals confirmed the hepatocellular involve
156 . conventional and C5-alkynyl-functionalized LNA and alpha-L-LNA pyrimidine monomers.
157 t, these properties render C5-functionalized LNA as a promising class of building blocks for RNA-targ
158 dified with four different C5-functionalized LNA cytidine and C8-functionalized LNA adenosine monomer
159 welve structurally diverse C5-functionalized LNA uridine (U) phosphoramidites were synthesized and in
160 ionalized LNA cytidine and C8-functionalized LNA adenosine monomers.
161  modified with C5-fluorophore-functionalized LNA-U monomers enable fluorescent discrimination of targ
162                                 Furthermore, LNA-anti-miR-192 attenuated proteinuria in these diabeti
163 nal cohort of mice subjected to MI was given LNA-antimiR-34a (15-mer) to inhibit miR-34a alone as a c
164 tilabeled quencher-free MBs based on Glowing LNA monomers is demonstrated (a) using in vitro transcri
165                These features render Glowing LNA as promising diagnostic probes for biomedical applic
166 and fluorescence properties of these Glowing LNA probes are efficiently modulated and optimized by ch
167 ined by substituting LNA with 2'-glycylamino-LNA, contributing a positive charge.
168 ockdown in mice treated with non-hepatotoxic LNA ASOs, while the levels of many unintended transcript
169 y efficacious hepatotoxic or non-hepatotoxic LNA ASOs.
170 ere reduced in mice treated with hepatotoxic LNA ASOs.
171 acids) 0.07% of LNA; "Low LNA" (0.4%); "High LNA" (4.8%); and a "DHA + EPA" diet, containing 0.4% of
172  results differentiate the effects of a High LNA diet from one with added EPA and DHA even though the
173 ared to the DHA + EPA diet, whereas the High LNA diet induced a less pronounced, but significant redu
174 r between 10 and 36 h when combined with IF; LNA-CISH requires 2 d.
175 ) analogs by replacing the 2'-oxygen atom in LNA with an exocyclic methylene group.
176                          Improved outcome in LNA-antimiR-34-treated MI and TAC mice was accompanied b
177                        Disease prevention in LNA-antimiR-34a treated DCM female mice was characterize
178  with similar efficiency as original Invader LNAs.
179  RNA, but less stabilizing than both alpha-L-LNA (2) and alpha-L-TriNA 1 (4).
180  A constrained tricyclic analogue of alpha-L-LNA (2), which contains dual modes of conformational res
181 ubstitution converts 8 into 2'-amino-alpha-L-LNA adenine intermediate 9, which after a series of nont
182 eotides (ONs) modified with 2'-amino-alpha-L-LNA adenine monomers W-Z.
183  with pyrene-functionalized 2'-amino-alpha-L-LNA adenine monomers X-Z display greatly increased affin
184  sequences containing this tricyclic alpha-L-LNA analogue (alpha-L-TriNA 2, 5) indicate that this mod
185 leic acid (LNA) and its diastereomer alpha-L-LNA are two interesting examples thereof.
186 her target specificity than 2'-amino-alpha-L-LNA benchmark probes.
187  of 2'-N-(pyren-1-yl)methyl-2'-amino-alpha-l-LNA monomers.
188 nd C5-alkynyl-functionalized LNA and alpha-L-LNA pyrimidine monomers.
189                                      alpha-L-LNA uridine monomers that are conjugated to small C5-alk
190 ionalized monomers based on 2'-amino-alpha-l-LNA, 2'-N-methyl-2'-amino-DNA, and RNA scaffolds.
191 TFOs form more stable triplexes than alpha-L-LNA-modified counterparts owing to slower triplex dissoc
192 c stability relative to conventional alpha-L-LNA.
193  article, we extend this strategy to alpha-L-LNA: i.e., one of the most interesting diastereomers of
194   N2'-Pyrene-functionalized 2'-amino-alpha-L-LNAs (locked nucleic acids) display extraordinary affini
195 r N2'-pyrene-functionalized 2'-amino-alpha-L-LNAs of considerable interest for DNA-targeting applicat
196 f N2'-pyrene-functionalized 2'-amino-alpha-L-LNAs.
197        There exist two NA categories: local (LNA) and global (GNA).
198                    The n-3 Deficient and Low LNA diets caused a substantial deficit in PPI compared t
199  (as % total fatty acids) 0.07% of LNA; "Low LNA" (0.4%); "High LNA" (4.8%); and a "DHA + EPA" diet,
200 bases, was readily accessible to tiled 8-mer LNA and 15-mer DNA probes, whereas an unmodified version
201 dulloblastoma cells) passively took up 8-mer LNA-anti-miRs and specifically inhibited targeted microR
202 ion of the miR-17~92 cluster family by 8-mer LNA-anti-miRs might be considered for the treatment of S
203 derscore the utility of seed-targeting 8-mer LNA-antimiRs in the development of new therapeutic appro
204                   Furthermore, in R6/2 mice, LNA-CTG blocked several pathogenic mechanisms caused by
205 , and 9 healthy controls (HCs) using miRCURY LNA Universal RT microRNA polymerase chain reaction pane
206 ssion of miR-183-96-182 cluster with miRCURY LNA miR inhibitors decreases the proliferation and migra
207             The LNA-MBs were made of a mixed LNA and DNA bases to have extremely high biostability.
208  delivery of a locked nucleic acid-modified (LNA-modified) antimiR oligonucleotide also failed to blo
209 ng 2'-methoxyethyl bases or noncomplementary LNAs.
210 onvergent synthesis of bicyclic nucleosides (LNA monomers) T, U, A, and C.
211 the first time that it is possible to obtain LNA-like (Locked Nucleic Acid 1) binding affinity and bi
212 containing (as % total fatty acids) 0.07% of LNA; "Low LNA" (0.4%); "High LNA" (4.8%); and a "DHA + E
213 ; and a "DHA + EPA" diet, containing 0.4% of LNA, 2% DHA, and 2% EPA.
214 that was paralleled by persistent binding of LNA-CTG to the expanded HTT exon 1 transgene.
215 r efforts have been devoted to the design of LNA derivatives that induce even higher binding affinity
216  findings have implications on the design of LNA molecular probes for intracellular monitoring applic
217   New guidelines are suggested for design of LNA probes, which significantly improve mismatch discrim
218 one of the most interesting diastereomers of LNA.
219 is effort we have investigated the effect of LNA on the performance of sequencing and PCR primers in
220                                   Effects of LNA modifications on mismatch discrimination were studie
221 vivo, as we observed complete eradication of LNA-antimiR-21-treated gliomas subjected to the presence
222 odified ONs, whereas C8-functionalization of LNA adenosines is detrimental to binding affinity and sp
223 s of LNA: i.e., through functionalization of LNA nucleobases.
224 trongly suggest that C5-functionalization of LNA pyrimidines is indeed a viable approach for improvin
225  recently introduced C5-functionalization of LNA uridines as an alternative and synthetically more st
226 ward this end, i.e., C5-functionalization of LNA uridines.
227 d delivery, but not intravenous infusion, of LNA-92a significantly (P<0.05) reduced the infarct size
228  on the length of the agLNA, the location of LNA bases, the number of LNA substitutions, and the loca
229 of this work has focused on modifications of LNA's oxymethylene bridge.
230 NA, the location of LNA bases, the number of LNA substitutions, and the location of the target sequen
231               Given the different outputs of LNA and GNA, when a new NA method is proposed, it is com
232 rs to optimize the biophysical properties of LNA through additional modification of the sugar skeleto
233 ach to improve the biophysical properties of LNA.
234 approach for modulation of the properties of LNA: i.e., through functionalization of LNA nucleobases.
235                   The hybridization rates of LNA-MBs were significantly improved by lowering the DNA/
236 stablish structure-toxicity relationships of LNA-modified ASOs and decrease the likelihood of hepatot
237 t specificity, and/or enzymatic stability of LNA-modified ONs, whereas C8-functionalization of LNA ad
238 proved therapeutic index relative to that of LNA antisense oligonucleotides.
239 iscrimination attributes similar to those of LNA but greatly improved resistance to exonuclease diges
240                                 A triplet of LNA residues centered on the mismatch was generally foun
241     These data suggest that the mechanism of LNAs involves recognition of chromosomal DNA and that LN
242 ocked nucleic acid-modified oligonucleotide (LNA-antimiR-34a) at 6-7 weeks of age when the models dis
243  acids (also known as locked nucleic acid or LNA, and 2',4'-constrained ethyl [cET]).
244 ydrophobic 2' modifications, e.g. (S)-cEt or LNA, in the 5'-wing of the ASO.
245      In mice subjected to pressure overload, LNA-antimiR-34 improved systolic function and attenuated
246 tive, chemically stable, and photostable PAH LNA interstrand communication systems, including pyrene
247                        We evaluate prominent LNA and GNA methods on synthetic and real-world biologic
248 ng screening of fully phosphorothioated (PS)-LNA gapmer ASOs designed against the BACH1 transcript.
249 te Hsp90 protein enhances the activity of PS/LNA or PS/(S)-cEt ASOs, and imply that altering protein
250                                     Regional LNA-92a delivery reduces miR-92a levels and infarct size
251  against 3'-exonucleases relative to regular LNA.
252 onucleotide complementary to the CAG repeat (LNA-CTG) preferentially binds to mutant HTT without affe
253                      Cellular uptake of soft LNA nanoparticles occurs rapidly within minutes as evide
254 m behind the hepatoxicity observed with some LNA-modified gapmers.
255 r improvements were obtained by substituting LNA with 2'-glycylamino-LNA, contributing a positive cha
256                                    We target LNAs at Xist RNA and show displacement from the X chromo
257 ly improved by applying the surface-tethered LNA probes, in comparison to the corresponding DNA probe
258 n start sites yielded better inhibition than LNAs targeting transcription factor binding sites or an
259                In vivo studies revealed that LNA(TM) anti-miR-130a could up-regulate the AQP4 M1 tran
260                 Histochemistry revealed that LNA-92a increased capillary density but decreased leukoc
261                        Our results show that LNA provides a simple, stable means to functionalize dsD
262 experiments using 2-aminopurine suggest that LNA modifications enhance base stacking of perfectly mat
263                   These results suggest that LNA-CTGs promote neuroprotection by blocking the detrime
264 lves recognition of chromosomal DNA and that LNAs are bona fide antigene molecules.
265                          We demonstrate that LNAs which block formation of the closed conformation in
266                                          The LNA bound to beta-actin was then stained using phycoeryt
267                                          The LNA-let-7 inhibitor decreased brain let-7 levels and par
268                                          The LNA-MBs were made of a mixed LNA and DNA bases to have e
269                                          The LNA-modified cap analogue was an efficient substrate for
270          After 24 h inside living cells, the LNA-MBs were still functional, demonstrating a greatly e
271 ing 50% formamide allow cells containing the LNA-bound mRNA to be detected and differentiated from th
272 ntly, by having a shared-stem design for the LNA-MB to prevent sticky-end pairing.
273 e speed and analytically tractability of the LNA.
274 nce to the increased A-form character of the LNA:RNA hybrid.
275                      In the second step, the LNA-blocking approach is combined with a mutant-specific
276                        It was found that the LNA bases in a MB stem sequence had a significant effect
277  analytical HPLC assay to determine that the LNA-modified 3 cap analogue was incorporated solely into
278 ing protein elF4E complex indicates that the LNA-modified cap-protein complex is more stable by 47.28
279                           Importantly, these LNA nanoparticles knockdown survivin mRNA, an establishe
280 le organs, and therapeutic delivery of these LNAs strongly suppresses melanoma metastasis.
281                                       Though LNA has been used in many applications, formal design ru
282  3' end (LNA-3') and distributed throughout (LNA-Even).
283                                        Thus, LNAs provide a tool for studying an emerging class of re
284                Galactose-modified thymidine, LNA-T, and 2'-amino-LNA-T nucleosides were synthesized,
285 ified anti-miR oligonucleotides, termed tiny LNAs, that inhibit microRNA seed families expressed by m
286 activity but reduced toxicity as compared to LNA ASOs.
287 sts of magnetic nanoparticles, conjugated to LNA-based miR-10b antagomirs.
288 e mRNA transcripts commonly reduced by toxic LNA ASOs were generally not strongly associated with any
289 tion temperature is required for each unique LNA probe.
290        Oligonucleotide-based therapies using LNA-modified chemistries for modulating cardiac miRNAs i
291                                    In vitro, LNA modification of mismatches precluded binding of puri
292                                    In vitro, LNA-92a protected against hypoxia/reoxygenation-induced
293 cations were designed to investigate whether LNA antisense oligonucleotides (ASOs) have the potential
294 n contrast, inhibition of miR-34a alone with LNA-antimiR-34a (15-mer) provided no benefit in the MI m
295                   Pre-treatment of BMCs with LNA-34a ex vivo significantly increased the therapeutic
296  the G-block of the diblock DNA hairpin with LNA bases results in a modest decrease in the base-to-ba
297 properties of oligonucleotides modified with LNA or other conformationally restricted monomers.
298 amer 2'-O-methyl oligonucleotide probes with LNA (locked nucleic acid) and 2,6-diaminopurine substitu
299 aco-2 and IEC-6 lines) were transfected with LNA-anti-uc.173 or uc.173 transgene.
300 plexes modified with C5-(3-aminopropyn-1-yl)-LNA-U monomer Z are particularly stable.

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