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-HBCD was biotransformed to two mercapturic acid pathw

3 ss-siRNAs combine the simplicity and favorable biodistri

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

5 nsive codon mutagenesis library of the TEM-1 ss-lactamase gene.

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

7 relations found, one could predict [(1)O(2)](ss) within a factor of 4 using a300 alone.

8 )O(2) steady-state concentrations ([(1)O(2)](ss)).

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

10 Introduction of test sequences containing 3' ss into monocistronic luciferase reporter vectors widely

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

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

13 3-angstrom resolution, revealing that the 3' ss is mainly recognized through non-Watson-Crick base pa

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

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

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

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

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

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

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

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

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

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

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

25 19% in eyes with PDR (0.020 +/- 0.005 mm(3), ss = -0.01, P = .01) compared to controls (0.025 +/- 0.0

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

27 s/U1 base-pairing, we estimate that 10,248 5'ss ( approximately 5% of human 5'ss) in 6577 genes use b

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

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

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

31 at 10,248 5'ss ( approximately 5% of human 5'ss) in 6577 genes use bulge registers.

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

33 scriptome-wide free-energy calculations of 5'ss/U1 base-pairing, we estimate that 10,248 5'ss ( appro

34 cells, we now demonstrate that many other 5'ss are recognized via noncanonical base-pairing register

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

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

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

38 involving bulged nucleotides on either the 5'ss or U1 RNA strand, which we term "bulge registers." By

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

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

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

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

43 Indeed, we successfully detected, a ss-deoxynucleic acid (DNA) variant of cyclin D1 mRNA usi

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

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

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

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

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

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

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

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

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

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

54 tidase that degrades insulin and the amyloid ss-protein and is strongly implicated in the pathogenesi

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

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

57 Digests of alpha-casein and ss-casein were analyzed by EDTA-1D-RP-nanoUPLC, 2D-RP/RP

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

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

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

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

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

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

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

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

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

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

68 inhibition of human huntingtin expression by ss-siRNAs that target the expanded CAG repeats within th

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

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

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

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

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

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

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

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

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

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

79 and a nanorod core capped with complementary ss-DNA molecules.

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

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

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

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

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

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

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

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

88 n response of a secondary single-strand DNA (ss-DNA) to the unhybridized part of the target much like

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 We show that a further SNP, -14009T>G (ss 820486563), is significantly associated with lactose-

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

113 1, respectively, all P < .001) and glaucoma (ss = -6.8 to -5.6, P </= .009, and -0.75 to -0.69, P </=

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

115 High ss-catenin activity driven by specific CTNNB1 mutations

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

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

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

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

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

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

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

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

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

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

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

127 se results have four broad implications: (i) ss-siRNAs will not always behave similarly to analogous

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

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

130 ectivity of anti-CAG oligonucleotides; (iii) ss-siRNAs can function through multiple mechanisms and;

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 s = -0.533; P = 0.001), portal inflammation (ss = 0.291; P = 0.030), and absence of an ileocecal valv

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

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

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

139 nctional numeracy more than six years later (ss = 0.195, p = .0014) controlling for intelligence, wor

140 e analysis, age-adjusted small bowel length (ss = -0.533; P = 0.001), portal inflammation (ss = 0.291

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

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

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

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

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

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

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

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

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

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

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

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

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

154 nanorod for nanorods with a high density of ss-DNA molecules was quantified through a combination of

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

156 mice demonstrating pharmacological effect of ss-siRNA.

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

158 R1a which engender distinct functionality of ss-arrestins.

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

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

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

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

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

164 ing, or otherwise optimizing, the loading of ss-DNA in monolayers on gold nanorods could be a useful

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

166 The number of ss-DNA molecules per nanorod for nanorods with a high de

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

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

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

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

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

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

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

174 ble to use chemical modification to optimize ss-siRNA properties and improve their potential for drug

175 peptides were identified in either alpha- or ss-casein sample.

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

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

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

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

180 When different AAV capsids packaging ss/scDNA varying in length from 72 to 123% of wild-type

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

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

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

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

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

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

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

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

189 atic islets, including the insulin producing ss-cells.

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

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

192 ith markers of epithelial junction proteins (ss-catenin and connexin 43), of stromal keratocytes (CD3

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

194 ors of ataxin-3 expression and then redesign ss-siRNAs to optimize their selectivity.

195 ger transcriptional repressor that regulates ss expression.

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

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

198 Single-stranded silencing RNAs (ss-siRNAs) provide an alternative approach to gene silen

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

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

201 Hybridization of the secondary ss-DNA tagged to gold nanoparticles amplified as well as

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

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

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

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

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

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

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

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

210 Extended-spectrum ss-lactamase (ESBL)-producing Enterobacteriaceae isolate

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

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

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

214 s 1 was first identified as a single-strand (ss) DNA-binding protein.

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

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

217 1, and developed RPA-coated single stranded (ss) DNA.

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

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

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

221 ase translocation over long single-stranded (ss) DNA (>200 nt) with no apparent secondary structure.

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

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

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

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

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

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

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

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

230 on of lesions in persistent single-stranded (ss) DNA has been recently found in several types of canc

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

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

233 this coupling is reduced in single-stranded (ss) DNA sequences.

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

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

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

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

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

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

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

241 rst forming a filament on a single-stranded (ss) DNA.

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

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

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

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

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

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

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

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

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

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

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

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

254 tive and tunable loading of single-stranded (ss-DNA) molecules onto gold nanorods was achieved throug

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

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

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

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

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

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

261 es, i.e., Deltai as a function of the target ss-ODN concentration was studied.

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

263 as been difficult to examine the role of TGF-ss in post-natal tooth development due to perinatal leth

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

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

266 We demonstrate here that ss-siRNAs are allele-selective inhibitors of ataxin-3 ex

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

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

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

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

271 onfirmed in transgenic plants expressing the ss-glucuronidase reporter gene fused to the NtPDR1 promo

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

273 th about 19% of enzymes dissociated from the ss/dsDNA junction after translocating across the ssDNA r

274 tetraphosphopeptides were identified in the ss-casein sample.

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 mutations that each confer resistance to the ss-lactamase inhibitor tazobactam.

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

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

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

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

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

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

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

288 particles was easily displaced by thiolated ss-DNA, forming a tunable density of single-stranded DNA

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

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

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

292 wing ventricular injection of Cholera toxin, ss subunit (CTss), a tracer frequently used in brain cir

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

294 = 0.030), and absence of an ileocecal valve (ss = 0.267; P = 0.048) were predictive for fibrosis stag

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

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

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

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

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

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