ライフサイエンスコーパス: ss

1 ss-catenin activation level was assessed in tumors by qu

2 ss-CyFaP is detected through 12 cm of chicken breast tis

3 ss-CyFaP is imaged through whole compressed human breast

4 ss-HBCD was biotransformed to two mercapturic acid pathw

5 ABAA-R PAMs can increase significantly INS-1 ss-cell replication, which is enhanced by exogenous GABA

6 ancer drug and modified into a dimer (CPT)2 -ss-Mal, in which two CPT molecules are connected by a re

7 local subspace Ca(2+) concentration ([Ca(2+)]ss).

8 d dsDNA, and interact with the 5' arm and 3' ss/dsDNA respectively.

9 he resection of the 5' strand to generate 3' ss-DNA.

10 s 3'->5' helicase activity and DNA2's 5'->3' ss-DNA exonuclease activity.

11 3-angstrom resolution, revealing that the 3' ss is mainly recognized through non-Watson-Crick base pa

12 BaPif1 bound to the 3' ss/dsDNA junction impacts duplex unwinding by stabilizin

13 arching spliced sequences against 5'ss and 3'ss sequences from the well-known orthologous U12-type sp

14 last intron processing, alternative 5 and 3'ss usage and exon skipping are marked by distinct patter

15 ese results reveal important links between 3'ss control and ATM-dependent responses to double-strand

16 rrelated with significant usage of cryptic 3'ss known to be utilized in mutant SF3B1 expressing cells

17 nclear how widespread this type of cryptic 3'ss usage is in cancers and what is the full spectrum of

18 e molecular defect responsible for cryptic 3'ss usage.

19 tility of intronic SSOs that target pseudo-3'ss to modify gene expression.

20 ts without widespread failure to recognize 3'ss or constitutive exons.

21 e-mRNA segments upstream of U2AF-repressed 3'ss.

22 ine at rs609621 in the NSE 3' splice-site (3'ss), which is predominant in high cancer risk population

23 nd AG dinucleotides at the 3' splice site (3'ss).

24 ons induce use of cryptic 3' splice sites (3'ss), and these splicing errors contribute to tumorigenes

25 ectrum of pathogenic mutations at both the 3'ss and 5'ss of the exon 7.

26 completely or partially recapitulated the 3'ss defects.

27 exons in a 3' to 5' direction to achieve 3'-ss proofreading or exon release, respectively.

28 intron release, but lacked information on 3'-ss recognition, exon ligation, and exon release.

29 19% in eyes with PDR (0.020 +/- 0.005 mm(3), ss = -0.01, P = .01) compared to controls (0.025 +/- 0.0

30 gh non-Watson-Crick base pairing with the 5' ss and branch point.

31 to the 5' arm causes a sharp bend in the 5' ss/dsDNA junction, consequently breaking the first base-

32 med by searching spliced sequences against 5'ss and 3'ss sequences from the well-known orthologous U1

33 pathogenic mutations at both the 3'ss and 5'ss of the exon 7.

34 modulation through activation of a cryptic 5'ss (Cr1).

35 ODE samples indicated that the presence of 5'ss with U12-type signature is more frequent than U2-type

36 located downstream of the 5' splice site (5'ss) of exon 7.

37 ic step of splicing at the 5' splice site (5'ss).

38 tion, despite its distal position from the 5'ss (85 bp downstream), induces cis alterations in pre-mR

39 perimental evidence that strengthening the 5'ss and increasing the T content in PPT significantly enh

40 This hairpin sequesters the 5'ss residues involved in U1 small nuclear RNA interaction

41 n the formation of a stable hairpin at the 5'ss.

42 m to be directly involved in regulating U1/5'ss unwinding.

43 cing efficiency positively correlates with 5'ss strength while no such correlation was identified for

44 to generate three constructs ((ss)DFO-5B1, (ss)FL-5B1, and (ss)dual-5B1) in which the immunoreactivi

45 vity when unwinding a DNA fork compared to a ss/ds DNA junction substrate.

46 Diminished hepatic fatty acid ss-oxidation was associated with decreased mRNA expressi

47 ovo lipogenesis (DNL), 45% slower fatty acid ss-oxidation, and 40% decreased VLDL-triglyceride export

48 y augmented by the addition of a long-acting ss-agonist.

49 CTNNB1 mutations activating ss-catenin are frequent somatic events in hepatocellular

50 edicted based on pretreatment visual acuity (ss coefficient = -0.621, P < .01, R(2) = 0.45).

51 Following intravenous administration, ss-CyFaP accumulates in neoplastic tissues of mice and r

52 ygous for the long (ll) or the short allele (ss).

53 PARs and NMDARs, as well as alpha7 and alpha*ss* nAChRs, but no evidence was found for mEPSCs associa

54 c alpha7 receptors and the heteromeric alpha*ss* receptors) as well as the two types of glutamate rec

55 otin operons bioH is replaced by other alpha/ss hydrolases of diverse sequence.

56 licated in AD pathology triggered by amyloid-ss oligomers (Asso) and propagated by Tau.

57 onmelanoma cancers may involve some ss-1 and ss-2 HPV types, but the biology of most ss-HPV types and

58 e a discriminative noise analysis for ds and ss DNA topologies into the threshold detection, resultin

59 rrestin 1 and 2 binding, internalization and ss-arrestin-mediated proliferation and adipogenesis.

60 ee constructs ((ss)DFO-5B1, (ss)FL-5B1, and (ss)dual-5B1) in which the immunoreactivity was not affec

61 otransporters, functionalized with antibody, ss-DNA, aptamer or lectin receptors, are particularly us

62 Aqueous ss-CyFaP dispersions exhibit intense NIR-II optical abso

63 arkers p21(CIP1/WAF1), senescence-associated ss-galactosidase (SA-ss-gal), and p16(INK4a) were increa

64 poptotic but displayed senescence associated-ss-galactosidase activity and upregulated p16, indicatin

65 In the female MTBI group, average ss values at both initial and follow-up studies were low

66 The hybridization between ss DNA probe and target ss DNA was detected by reduction

67 ssDNA gate that enables transitions between ss and dsDNA.

68 response behaviour of the DNA bioelectrode (ss th-DNA/ZNF/Pt/Si) has been studied by both differenti

69 is a prodrug converted into Daunorubicin by ss-galactosidase.

70 or not (hen egg lysozyme; HEL) expressed by ss-cells have proven useful in dissecting the developmen

71 .g., occludin-ZO-1, CAR-ZO-1, and N-cadherin-ss-catenin), through a down-regulation of p-Akt1-S473 an

72 on proteins (e.g., occluden-ZO-1, N-cadherin-ss-catenin).

73 oids such lutein, zeaxanthin, canthaxanthin, ss-carotene and beta-apocarotenoic ester.

74 ulin (Ig) molecules that efficiently capture ss-cell antigens allows autoreactive B-lymphocytes bypas

75 of change were associated with baseline CCT (ss = -0.1 to -0.09 and -0.011, respectively, all P < .00

76 I restriction enzymes, single-stranded cDNA (ss-cDNA) ligation using T4 polynucleotide kinase and Cir

77 rences in the biologic properties of certain ss-type HPV that affect their impact on carcinogenesis i

78 systematic or significant offsets in coeval ss-sl delta(18)O, and delta(13)C.

79 igase, Escherichia coli FadD, in the E. coli ss-oxidation pathway and deletion of RpfB from the Xcc g

80 Eosinophil receptors for IL-5 share a common ss-chain with IL-3 and GM-CSF receptors.

81 g methodology to generate three constructs ((ss)DFO-5B1, (ss)FL-5B1, and (ss)dual-5B1) in which the i

82 volved in GC differentiation including CREB, ss-catenin, AKT, p42/44 MAPK, GAB2, GSK-3ss, FOXO1, and

83 D presented a statistically thinner mean CT (ss = -21.9, P = .006) and CT in all the individual ETDRS

84 Coenzyme Q10 into surfactant-stripped CyFaP (ss-CyFaP) micelles improves yield, storage stability, an

85 lved in L-cysteine metabolism: cystathionine-ss-synthase (CBS) and cystathionine-gamma-lyase (CSE).

86 ncreasing the number of helix-destabilizing, ss-branched valine or isoleucine residues within the TMD

87 e implications for the mechanism of diabetic ss-cell apoptosis and cancer cell chemoresistance.

88 CK5, vimentin) and lineage differentiation (ss-tubulin IV+ ciliated cells, MUC5AC+ goblet cells, p63

89 lly immobilization of the single strand DNA (ss-DNA) probe and hybridization with the target miRNA se

90 de aerogel labeled with a single strand DNA (ss-HSDNA/rGOae) modified on a rotating disk electrode (R

91 using responsiveness of single-stranded DNA (ss-DNA), far less work has been done for the manipulatio

92 y immobilized single stranded thiolated DNA (ss th-DNA) probe of N. meningitides onto the nanostructu

93 the FTIR analysis of extracted RNA, ds-DNA, ss-cDNA and isolated nuclei, we verified that the spectr

94 Decreasing [(3)DOM]ss with molecular weight is shown to derive from elevate

95 moter and a single-stranded overhang domain (ss-dsDNA), can unlock dynamic DNA-based information stor

96 uplex DNA at the double-/single-stranded (ds-ss) junction.

97 oportion of duplex nucleic acids in mixed ds/ss nucleic acid solutions, demonstrating significant adv

98 to express ss is made intrinsically by each ss locus.

99 Stochastic on or off expression of each ss allele is determined by combinatorial inputs from one

100 range regulation does not require endogenous ss chromosomal positioning or pairing.

101 tein (WRN) and the heterotrimeric eukaryotic ss-DNA binding protein RPA.

102 chastic, cell-autonomous decision to express ss is made intrinsically by each ss locus.

103 th Daun02 in the dlBST previously expressing ss-galactosidase under control of the FosB/DeltaFosB pro

104 ) and CT in all the individual ETDRS fields (ss </= -18.79, P </= .026).

105 w that variation in the abundance of the FLM-ss splice form strictly correlate (R(2) = 0.94) with flo

106 sure per 1-week increment and change in FLZ (ss = .00; P = .51) or change in HLZ (ss = .00; P = .40).

107 ting for 13% of dose for alpha-HBCD, 30% for ss-HBCD, and 21% for gamma-HBCD.

108 ting for 42% of dose for alpha-HBCD, 59% for ss-HBCD, and 53% for gamma-HBCD.

109 ce to develop surrogate phosphate analog for ss-siRNA and demonstrates that ss-siRNA provides an alte

110 of the 5'-phosphate analog was critical for ss-siRNA activity.

111 Thr(350) and Ser(349) are not necessary for ss-arrestin recruitment, but are involved in the stabili

112 terminal tail were primarily responsible for ss-arrestin 1 and 2 binding, internalization and ss-arre

113 o enhance the ability of GABA, secreted from ss-cells, or exogenously administered, to promote ss-cel

114 involved in the stabilization of the GHSR1a-ss-arrestin complex in a manner that determines the ulti

115 1, respectively, all P < .001) and glaucoma (ss = -6.8 to -5.6, P </= .009, and -0.75 to -0.69, P </=

116 as significantly associated with the global (ss = 0.026, P < .01) and temporal sector coefficient of

117 High ss-catenin activity driven by specific CTNNB1 mutations

118 s were duplicated, resulting in a final high ss-catenin activity.

119 in FLZ (ss = .00; P = .51) or change in HLZ (ss = .00; P = .40).

120 ith attributes intermediate to the holotypic ss and sl morphologies.

121 e tested: conventional liposomes (CL) and HP-ss-CD-loaded liposomes (CDL).

122 ated using hydroxypropyl-ss-cyclodextrin (HP-ss-CD) as membrane protectant.

123 physically stable upon reconstitution in HP-ss-CD solutions, and are able to retain anethole after 6

124 Moreover, the presence of HP-ss-CD in the aqueous phase of CDL protected them during

125 Results demonstrated that HP-ss-CD protected only the hydrogenated batches (CL and CD

126 ntiviral vector (LV) that incorporates human ss-interferon scaffold/matrix-associated region sequence

127 o develop treatments to safely promote human ss-cell replication.

128 posomes was investigated using hydroxypropyl-ss-cyclodextrin (HP-ss-CD) as membrane protectant.

129 ers (H3N2 swine IAV-alpha and H3N2 swine IAV-ss) with a sensitivity of 84.9% and a specificity of 100

130 Moreover, ApoC III ss-siRNAs were able to reduce the triglyceride and LDL c

131 ging ) and single-shot echo-planar imaging ( ss-EPI single-shot echo-planar imaging ) with or without

132 e, there is no evidence for discrepancies in ss-sl calcifying depth habitat or seasonality in the Gul

133 ing insertion in a regulatory DNA element in ss that lowers the ratio of Ss(ON) to Ss(OFF) cells.

134 Therefore, although individual ss alleles make independent stochastic choices, interchr

135 roup was also found to have a higher initial ss value than the male control group (P = .040), and the

136 sic residues energetically steer an inverted ss 5'-flap through a gateway over FEN1's active site and

137 ntiate the actions of GABA secreted by islet ss-cells on GABAA-Rs and provide a new class of drugs fo

138 Lep(ss)-P85(H) also has improved peripheral PK but in a stri

139 Lep(ss)-P85(L) crosses the BBB using the leptin transporter,

140 ), containing one P85 chain and another, Lep(ss)-P85(H), containing multiple P85 chains.

141 ated two new leptin-P85 conjugates: one, Lep(ss)-P85(L), containing one P85 chain and another, Lep(ss

142 stabilized composite phase change materials (ss-CPCMs) through a facile self-assembly process using C

143 ze, but formed two hydroxylated metabolites; ss- and gamma-HBCD were both extensively metabolized via

144 In preclinical animal models, ss-CyFaP is visualized in draining lymph nodes of rats t

145 Chemically modified ss-siRNA targeting human apoC III mRNA demonstrated good

146 and ss-2 HPV types, but the biology of most ss-HPV types and their possible connections to human dis

147 inant role of neurons in driving the myocyte ss-adrenergic phenotype, where SHR cultures elicited hei

148 Myrtenylo-ss-D-glycopyranoside was the most resistant glycoside to

149 Novel ss-CPCMs composed of polyethylene glycol (PEG) and RMS w

150 ortex was found to be greater in children of ss mothers compared with children of ll mothers.

151 rmines the ultimate cellular consequences of ss-arrestin signaling.

152 The concentration dependence of ss-lap revealed significant signal changes at levels of

153 mice demonstrating pharmacological effect of ss-siRNA.

154 In this study, we studied the effects of ss-3 type HPV49 in a novel transgenic (Tg) mouse model,

155 R1a which engender distinct functionality of ss-arrestins.

156 -casting method for better immobilization of ss DNA while MWCNTs are incorporated into the zeolite-as

157 utation types, tumor phenotype, and level of ss-catenin activation in malignant transformation.

158 mpound heterodimers exhibit higher levels of ss- and dsDNA degradation activities than the homodimers

159 In benign tumors, we defined three levels of ss-catenin activation related to specific mutations: (1)

160 well as sensitivity to sub-lethal levels of ss-lap.

161 The metabolites of ss- and gamma-HBCD were largely distinct, and could poss

162 kinase and CircLigase, and polymerization of ss-cDNA to double-stranded cDNA (ds-cDNA) by Phi29 polym

163 this chip-based platform enabled tracking of ss-lap-induced DNA damage repair when biological criteri

164 The electrochemical response of MB on ss-DNA and duplex of miRNA/DNA was characterized by CV a

165 mma-aminobutyric acid receptors (GABA-Rs) on ss-cells can promote their survival and replication.

166 ibited aggregation, while recombinant PDI(oo-ss) potentiated aggregation.

167 his defect was rescued by recombinant PDI(oo-ss).

168 y a functional C-terminal CGHC motif [PDI(oo-ss)].

169 f HBCD diastereomers followed the rank order ss > gamma > alpha, and was >65% of that administered.

170 ding proteins at replication forks and other ss duplex junctions.

171 major factor for predicting K(max) outcome (ss coefficient = 0.709, P = .02), whereas age, sex, and

172 Overall, ss-catenin activity was higher in malignant mutated tumo

173 ile the autoimmune destruction of pancreatic ss-cells underlying type 1 diabetes (1D) development is

174 The beta genus of human papillomaviruses (ss-HPV) includes approximately 50 different viral types

175 ields the single sorbate-specific parameter (ss-LNL) model.

176 -induced cremaster arteriole injury, and PDI(ss-oo) mice had attenuated platelet accumulation in FeCl

177 In vitro aggregation of platelets from PDI(ss-oo) mice and PDI-null platelets was reduced; however,

178 acks a functional C-terminal CGHC motif [PDI(ss-oo) mice].

179 In human platelets, recombinant PDI(ss-oo) inhibited aggregation, while recombinant PDI(oo-s

180 d enzyme, enzyme type (cellulase, pectinase, ss-glucosidase), and hydrolysis time (1, 4, 8, 24 h) on

181 This simple but powerful ss-dsDNA architecture lays the foundation for informatio

182 ), the rates of formation (R(f)), and [PPRI](ss) of (3)DOM* and (1)O(2) linearly increased with incre

183 Laboratory measurements of [PPRI](ss) and apparent quantum yields (Phi) of three PPRIs ((3

184 steady-state concentrations of PPRIs ([PPRI](ss)) is critical to predicting the persistence of pollut

185 Relationships of a(440) with R(f), [PPRIs](ss), and R(a) were coupled with satellite-based a(440) a

186 oimmune attack against the insulin-producing ss cells which leads to chronic hyperglycemia.

187 lls, or exogenously administered, to promote ss-cell replication and survival.

188 ariant associations in the Estrogen Receptor-ss (ESR2) gene, as well as a set of rare and common vari

189 The purified enzyme specifically recognises ss-dsDNA junctions and possesses ssDNA-dependent ATPase,

190 ger transcriptional repressor that regulates ss expression.

191 The DSC results indicated that the PEG/RMS ss-CPCM was a promising candidate for building thermal e

192 indicated that the properties of the PEG/RMS ss-CPCMs are influenced by the adsorption limitation of

193 , senescence-associated ss-galactosidase (SA-ss-gal), and p16(INK4a) were increased 2-, 8-, and 20-fo

194 also significantly reduced in eyes with SDD (ss = -0.003, P = .007).

195 lexes revealed mechanisms of 5'-splice site (ss) recognition, branching, and intron release, but lack

196 luid (GCF) was collected for selected sites (ss) at baseline and 1, 3, and 6 months.

197 Nonmelanoma cancers may involve some ss-1 and ss-2 HPV types, but the biology of most ss-HPV

198 types that are subdivided into five species (ss-1 through ss-5).

199 correlation of this change with the specific ss-lap-induced redox cycle using rational controls.

200 ing a robust and reproducible site-specific (ss) labeling methodology to generate three constructs ((

201 This single-solute specific (ss-LNL) model (2 + n parameters) was demonstrated to fit

202 nally, ARGs, including the extended-spectrum ss-lactam- and aminoglycoside-resistance genes, were ide

203 Lastly, stabilized ss-catenin in Lgr5+ cells enhances mitotic activity and

204 formation specificity in both single strand (ss) and double strand (ds) DNA.

205 Escherichia coli single strand (ss) DNA binding (SSB) protein protects ssDNA intermediat

206 E. coli single strand (ss) DNA binding protein (SSB) is an essential protein th

207 form helicases that encircle single-strand (ss) DNA and initiate bidirectional forks.

208 ns can deaminate cytosines in single-strand (ss) DNA, which restricts human immunodeficiency virus ty

209 Escherichia coli single-strand (ss) DNA-binding protein (SSB) is an essential protein th

210 roteins specifically degraded single-strand (ss) RNAs in vitro; but neither miRNAs nor miRNA*s in viv

211 ctivation generated extensive single-strand (ss)DNA that exceeded the protective capacity of the ssDN

212 e-dimensional structures of single stranded (ss) DNA required for aptamer applications, focusing expl

213 1, and developed RPA-coated single stranded (ss) DNA.

214 and compare the response to single stranded (ss) target DNA.

215 FEN1 precisely cleaves single-stranded (ss) 5'-flaps one nucleotide into duplex (ds) DNA.

216 Titer-matched single-stranded (ss) and self-complementary (sc) AAV9 carrying the green

217 e (N6mA) methyl mark act on single-stranded (ss) and transiently-unpaired DNA.

218 ts A3G binding to substrate single-stranded (ss) DNA and CDA activity.

219 Single-stranded (ss) DNA aptamers with binding affinity to Listeria spp.

220 Eleven nucleotides of single-stranded (ss) DNA are bound within the C-tier of MCM2-7 AAA+ ATPas

221 activity of NPH I requires single-stranded (ss) DNA as a cofactor; however, the source of this cofac

222 Single-stranded (ss) DNA binding (SSB) proteins play central roles in DNA

223 h the increase of substrate single-stranded (ss) DNA binding by the N-terminal CD1 domain.

224 ne 32 protein (gp32) is the single-stranded (ss) DNA binding protein of the bacteriophage T4.

225 e lesions in long tracts of single-stranded (ss) DNA damaged by apolipoprotein B mRNA editing enzyme,

226 in controlling infection of single-stranded (ss) DNA geminiviruses and ssRNA viroids, respectively, b

227 fivefold vertex and induce single-stranded (ss) DNA genome ejection.

228 orks generates stretches of single-stranded (ss) DNA on both strands that are exposed to nucleolytic

229 Such studies often embed a single-stranded (ss) DNA region within a longer double-stranded (ds) DNA

230 ies is its ATP-driven 3'-5' single-stranded (ss) DNA translocation activity.

231 Single-stranded (ss) DNA viruses are a major component of the earth virom

232 om reverse-transcribing and single-stranded (ss) DNA viruses.

233 nternalize and to recombine single-stranded (ss) DNA with homologous resident duplex.

234 annealing of complementary single-stranded (ss) DNA, a crucial step in DNA synthesis, repair and rec

235 When unconstrained on single-stranded (ss) DNA, AID moves in random bidirectional short slides/

236 s a presynaptic filament on single-stranded (ss) DNA, which catalyses pairing with homologous double-

237 onserved C-terminal tail of single-stranded (ss) DNA-binding protein (SSB), which is known to bind Es

238 e addition of mitochondrial single-stranded (ss) DNA-binding protein both influences the ways Twinkle

239 Single-stranded (ss) DNA-binding proteins (SSBs) bind and protect ssDNA i

240 teria encode homooligomeric single-stranded (ss) DNA-binding proteins (SSBs) that coat and protect ss

241 Primases use single-stranded (ss) DNAs as templates to synthesize short oligoribonucle

242 During replication, single-stranded (ss) positive-sense RNA segments are packaged into the as

243 We target single-stranded (ss) regions of DNA-origami structures and remove them wi

244 Single-stranded (ss) RNA viruses infect all domains of life.

245 nvestigate the mechanism of single-stranded (ss) RNAs packaging during nascent capsid assembly.

246 me, the interaction of long single-stranded (ss) RNAs with cognate homologous double-stranded (ds) DN

247 ent studies have shown that single-stranded (ss) viral RNAs fold into more compact structures than ra

248 ivity of RecA when bound to single-stranded (ss)DNA as a nucleoprotein filament (RecA*).

249 Escherichia coli single-stranded (ss)DNA binding (SSB) protein mediates genome maintenance

250 Single-stranded (ss)DNA binding (SSB) proteins bind with high affinity to

251 o a 3' phosphate group on a single-stranded (ss)DNA break.

252 We have established single-stranded (ss)DNA curtain assays for measuring individual base trip

253 other APOBEC3 members, is a single-stranded (ss)DNA cytosine deaminase with antiviral activity.

254 gins yet must transition to single-stranded (ss)DNA for helicase action.

255 -assisted immobilization of single-stranded (ss)DNA on gold surfaces is achieved by applying a pulse-

256 Single-stranded (ss)DNA viruses are extremely widespread, infect diverse

257 ng domain (CTD) which binds single-stranded (ss)DNA, and the BRC repeats, which bind RAD51 and modula

258 Bacterial single-stranded (ss)DNA-binding proteins (SSB) are essential for the repl

259 ite G. ruber (W) morphotypes, sensu stricto (ss) and sensu lato (sl), has hypothesized differences in

260 These chips supported ss-lap-induced biological redox cycle and tracked subseq

261 s evaluated by percent signal suppression (% ss), which indicates the change in current after hybridi

262 rotransmission, akin to a smart pre-synaptic ss-blocker.

263 d with guide strand to design and synthesize ss-siRNAs containing various 5'-phosphate analogs.

264 ybridization between ss DNA probe and target ss DNA was detected by reduction in current, generated b

265 ntify wide range of the complementary target ss th-DNA in the range 5-240 ng mul(-1) with good linear

266 Four synthesized terpenyl-ss-D-glycopyranosides (geranyl, neryl, citronellyl, myrt

267 survival and tolerance were dependent on TGF-ss, indicating a role for induced Tregs.

268 te analog for ss-siRNA and demonstrates that ss-siRNA provides an alternative strategy for therapeuti

269 Taken together, these data show that ss-CyFaP is an accessible contrast agent for deep tissue

270 The ss-siRNA activity in vivo requires a metabolically stabl

271 The ss-zone, as a percentage of disc area, increased in size

272 types, including immune cells, EPOR and the ss-common receptor (CD131) form heteromers (the innate r

273 rved in an analogous Tg model expressing the ss-2 HPV38 E6 and E7 oncogenes at the same anatomic site

274 ving a cyclic voltammetric response from the ss-HSDNA/rGOae electrode in three different charges of t

275 how FEN1 selects for but does not incise the ss 5'-flap was enigmatic.

276 the structural and thermal properties of the ss-CPCMs.

277 of the biosensor due to hybridization of the ss-DNA with target DNA.

278 The effect of hydrodynamic diffusion of the ss-HSDNA/rGOae rotating disk electrode (RDE) toward AFB1

279 fect of ghrelin were mainly dependent on the ss-arrestin bound to the phosphorylated GHSR1a.

280 required to unwind the fork compared to the ss/ds junction, suggesting that binding to the fork lead

281 s reduced for the forked DNA compared to the ss/ds junction.

282 ng pattern similar to that observed with the ss/ds junction, consistent with disruption of the intera

283 uption of base pairing was observed with the ss/ds junction.

284 ions and amino acid substitutions within the ss-TRCP binding site (D32-S37).

285 The % ss is generally due to more redox molecules (e.g., methy

286 by rapid deterioration and reversal of the % ss polarity, suggesting an unexpected case of increased

287 oncentration of the grafting solution, the % ss displays peak performance at certain grafting solutio

288 The (ss)dual-5B1 demonstrated a remarkable capacity to deline

289 voltammetry from these chips at therapeutic ss-lap concentrations of high statistical significance o

290 e subdivided into five species (ss-1 through ss-5).

291 NA recognition that at its core is common to ss/ds translocases that act on DNA or RNA.

292 We show that CST binds preferentially to ss-dsDNA junctions, an activity that can explain the inc

293 only able measure total carotenoids as total ss-carotene, HPLC enables the determination of individua

294 However, the two ss alleles also average their frequency of expression th

295 nd temporal sector coefficient of variation (ss = 0.099, P < .01).

296 like planar gold (pl-Au) electrodes, where % ss reaches a steady state with increasing concentration

297 ared with DW diffusion-weighted imaging with ss-EPI single-shot echo-planar imaging , and it improved

298 aun02 in the LHb previously transfected with ss-galactosidase under control of the FosB promoter.

299 r Lgr6(+) cells as mediated by increased Wnt/ss-catenin activity.

300 Here, we demonstrate that the Wnt/ss-catenin effector Lef1 is required for the differentia

301 s show that lithium, an activator of the Wnt/ss-catenin signaling pathway, slows melanoma progression