ライフサイエンスコーパス: ABP

1 ABP alone compared to no prep resulted in significantly

2 ABP monitoring was performed at baseline and after 4 and

3 to extract/preconcentrate 2-aminobiphenyl (2-ABP) dissolved in the water and demonstrate a new applic

4 itu quantitatively estimate the amounts of 2-ABP distributed into each intact NE.

5 partitioning is governed by extraction of 2-ABP inside NEs rather than its adsorption on the NE surf

6 were 260 and 375 kJ/kg for category 1 and 3 ABP respectively.

7 4-ABP-Hb adducts were quantitatively measured on 230 contr

8 4-ABP-hemoglobin (Hb) adducts are established biomarkers o

9 of the tobacco carcinogen 4-aminobiphenyl (4-ABP) were detected in human hepatocytes treated with 4-A

10 ]PDE); the aromatic amine 4-aminobiphenyl (4-ABP), N-(deoxyguanosin-8-yl)-4-aminobiphenyl (dG-C8-4-AB

11 nzo[a]pyrene (B[a]P), and 4-aminobiphenyl (4-ABP).

12 The sulfonamide adducts of PhIP and 4-ABP were identified, by liquid chromatography/mass spect

13 hereas N-(deoxyguanosin-8-yl)-4-ABP (dG-C8-4-ABP) was identified in one subject (30 adducts per 10 (9

14 deoxyguanosin-8-yl)-4-aminobiphenyl (dG-C8-4-ABP); the HAA 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyr

15 of carcinogens in tobacco smoke including 4-ABP, 2-amino-9H-pyrido[2,3-b]indole (AalphaC), and benzo

16 iated with neither bladder cancer risk nor 4-ABP-Hb adduct levels in male lifelong nonsmokers.

17 (Hb) adducts are established biomarkers of 4-ABP exposure in humans.

18 Levels of 4-ABP-Hb adducts varied by ETS exposure status among femal

19 detected in human hepatocytes treated with 4-ABP, and three DNA adducts of the cooked-meat carcinogen

20 y specimen, whereas N-(deoxyguanosin-8-yl)-4-ABP (dG-C8-4-ABP) was identified in one subject (30 addu

21 The high prevalence of abnormal ABP, including masked hypertension, and its association

22 BP), assess factors associated with abnormal ABP, and examine whether ambulatory hypertension is asso

23 determining the role and mechanism of actin-ABP interactions in these processes.

24 In addition, ABP-PEG-HCBP1 can protect biological activity of Ad agai

25 Nrf2(+/+) mice than in Nrf2(-/-) mice after ABP exposure.

26 otably, Nrf2 protected bladder cells against ABP in vitro.

27 Although Nrf2 protected mouse liver against ABP (which is metabolically activated in liver), the bla

28 r UGT activity may protect the liver against ABP, it increases bladder exposure to ABP.

29 y an arginine-grafted poly(disulfide amine) (ABP) polymer in infarcted rats preserves cardiac geometr

30 grafted bio-reducible poly(disulfide amine) (ABP) was incorporated into the poly(amido amine) (PAMAM)

31 defined by a central aminobenzylpiperidine (ABP) moiety, X-ray crystal structures of BACE mutant-dis

32 dilemma in defense against 4-aminobiphenyl (ABP), a major human bladder carcinogen from tobacco smok

33 tin, both of which are unique features among ABPs.

34 GSTABP-G) to target the "G site", and (2) an ABP designed to mimic a substrate molecule and have "H s

35 the rupture force of a complex formed by an ABP linking two quasiparallel actin filaments.

36 We directly analyzed ABP-labeled and unlabeled global MS data, revealing ABP

37 dult male Wistar rats were anaesthetized and ABP was monitored via a femoral arterial catheter.

38 erosclerosis measures in men and for AWT and ABP in women (p interaction <0.05 each).

39 the augmented CO2 chemoreflex (breathing and ABP) in SHRs, which indicates an important role for the

40 chemoreflex that affects both breathing and ABP.

41 ntly greater increases in OVLT discharge and ABP than icv infusion of equi-osmotic sorbitol.

42 d to assess the reliability of OBP, HBP, and ABP and evaluate their associations with left ventricula

43 OBP, HBP, and ABP assess somewhat distinct parameters.

44 The correlations among OBP, HBP, and ABP, corrected for regression dilution bias, were 0.74 t

45 thetic nerve activity (SNA), adrenal SNA and ABP than equi-osmotic sorbitol (2.0 osmol l(-1) ).

46 rease in OVLT cell discharge, lumbar SNA and ABP.

47 ificantly raised lumbar SNA, adrenal SNA and ABP.

48 TSTA exendin-4 expression system with SP and ABP polymer has a potential gene therapy for the treatme

49 Thus, the actins and ABPs appear to have evolved class-specific, protein-prot

50 ctions among the major classes of actins and ABPs, we ectopically coexpressed reproductive profilin (

51 We believe the inhibitor and ABPs will be useful for future investigation of calpains

52 The Absence of the nucleophile abolishes any ABP labeling.

53 e not been experimentally determined for any ABP.

54 The amounts of APAP-ABP adducts formed in vivo were greater, whereas the amo

55 tin-binding protein filamin-A (also known as ABP-280) cross-links actin into a dynamic three-dimensio

56 bove LLA) from dysfunctional autoregulation (ABP below the LLA).

57 ods distinguished functional autoregulation (ABP above LLA) from dysfunctional autoregulation (ABP be

58 tagenized enzyme, as only the beta-aziridine ABP can bind in its absence.

59 retaining beta-glucosidases, beta-aziridine ABPs do not.

60 lophellitol beta-epoxide- and beta-aziridine ABPs.

61 ticles via the specific interactions between ABP and aptamer, and sgRNA and Cas9 protein.

62 of the wavelet transform phase-shift between ABP and ICP.

63 ng of how the molecular interactions between ABPs and F-actin regulate the dynamic properties of the

64 EPO gene therapy delivered by a bioreducible ABP polymer provide insight into the lack of phEPO gene

65 Both ABP unfolding and conformational transition events were

66 by 19.5 +/- 3.8-fold through binding to both ABPs.

67 erences between clinic BP and ambulatory BP (ABP) in a community sample of employed adults in the New

68 office blood pressure (OBP), ambulatory BP (ABP), and home BP (HBP) can inform which is best for dia

69 or-to-liver ratio of the Ad DNA delivered by ABP or ABP5k was significantly elevated at 229- or 419-f

70 Animal byproducts (ABP) are unavoidable byproduct of meat production that a

71 )-thione (CPDT) significantly inhibits dG-C8-ABP formation in bladder cells and tissues but does not

72 -(deoxyguanosin-8-yl)-4-aminobiphenyl (dG-C8-ABP), the predominant ABP-DNA adduct formed in bladder c

73 processes that are independent of canonical ABPs.

74 ages shows that activated bee pollen carbon (ABP) is comprised of spiky, brain-like, and tiny spheres

75 Caspase ABPs provided direct readouts of the kinetics of apoptos

76 n more accurate when applied to the cleanest ABP waveforms.

77 ide amine)polymer (ABP) and PEG5k-conjugated ABP (ABP5k) in expectation of oncolytic effect caused by

78 ng a diuretic agent or >/=4 drugs): control (ABP <125/75 mm Hg without RH); pseudoresistance (ABP <12

79 We describe ABP design principles and use case studies to illustrate

80 poly(cystaminebisacrylamide-diaminohexane) (ABP) and polyamidoamine (PAMAM) was used to deliver anti

81 poly (cystaminebisacrylamide-diaminohexane) (ABP)-conjugated poly (amidoamine) (PAMAM) dendrimer (PAM

82 this assay by testing it with two different ABPs: filamin and alpha-actinin.

83 Each ABP is a heterodimer assembled as an ABPA subunit encode

84 Each ABP recording was used to create 10 CBFVs corresponding

85 reactivity and selectivity profiles for each ABP, we demonstrate our ability to widely profile the fu

86 ing a bioreducible polymeric carrier, either ABP or ABP-PEG 10, merits further testing as a potential

87 young kidney transplant recipients, elevated ABP is frequently unrecognized and undertreated.

88 extensively, the contribution of endothelial ABPs to the regulation of leukocyte adhesion and transen

89 recently published evidence that endothelial ABPs, such as cortactin, myosin, or alpha-actinin, regul

90 orescent beta-aziridine but not beta-epoxide ABPs identifies the acid/base residue in mutagenized enz

91 Whereas beta-epoxide ABPs require a protonated acid/base for irreversible inh

92 solated fifth repeat of the gelation factor (ABP-120) from Dictyostelium discoideum (ddFLN5) by NMR s

93 se in femoral vascular conductance (FVC, FBF/ABP) from baseline, respectively.

94 e (SVR) decreased (Spinotrapezius blood flow/ABP), indicating muscle vasodilatation.

95 ith any of the growing number of fluorescent ABPs to provide data for more effective disease monitori

96 lable, and developers and vendors of CO-from-ABP algorithms are invited to test their methods using t

97 O estimated by eight investigational CO-from-ABP algorithms, and CO(TD) as a reference.

98 meaningful comparison of alternative CO-from-ABP algorithms.

99 whereas the second approach affords a gate (ABP-F(4)) that we can close with UV light and open with

100 The first approach led to a gate (ABP-Me(4)) that remains closed all the time, whereas the

101 tion incompetent GFP-expressing ad, (Ad/GFP)-ABP-PEG-HCBP1, showed a hepatoma cancer specific uptake

102 Competition assays demonstrated that Ad/GFP-ABP-PEG-HCBP1-mediated transduction was specifically inh

103 on compared to either naked Ad/GFP or Ad/GFP-ABP.

104 ressure 146 +/- 19/82 +/- 12 mm Hg, and 24-h ABP 129 +/- 17/72 +/- 10 mm Hg.

105 25 mg daily, significantly reduced mean 24-h ABP as well as daytime and nighttime BP.

106 visits, and completed 3 weeks of HBP, 2 24-h ABP recordings, and a 2-dimensional echocardiogram.

107 hort duration of action, no significant 24-h ABP reduction was seen with HCTZ, 12.5 mg daily, which m

108 sits with mercury sphygmomanometry, and 24-h ABP were 0.938, 0.894, and 0.846 for systolic and 0.918,

109 ur groups were constituted by combining 24-h ABP with diagnosis of RH (office blood pressure >/=130/8

110 tivariable adjustment including OBP and 24-h ABP, 10 mm Hg higher systolic and diastolic HBP were ass

111 Compared with OBP (3 visits) or 24-h ABP, systolic and diastolic HBP (1 week) were more relia

112 d a significant (p < 0.01) reduction in 24-h ABP.

113 spontaneously hypertensive rats (SHRs), high ABP is associated with enhanced sympathetic nerve activi

114 The augmented CO2 chemoreflex and the high ABP are measureable in young SHRs (postnatal day 30-58)

115 chemoreflex and significantly lower the high ABP in adult SHRs.

116 e the augmented CO2 chemoreflex and the high ABP in young SHRs and normalize the augmented CO2 chemor

117 oreflex in young and adult SHRs and the high ABP in young SHRs and significantly lowers ABP in adult

118 veractive orexin system are linked with high ABP in both young (postnatal day 30-58) and adult SHRs (

119 (i) An augmented CO2 chemoreflex and higher ABP in SHRs are measureable at a young age and increase

120 5/75 mm Hg with RH); sustained hypertension (ABP >/=125/75 mm Hg without RH); and true resistance (AB

121 h as palm oil and soya bean meal because (i) ABP were considered wastes that do not incur the environ

122 urvey, we used multiple imputation to impute ABP-defined hypertension status for NHANES participants

123 ive 2K1C rats showed a profound elevation in ABP (Wistar: 98 +/- 4 mmHg vs. 2K1C: 147 +/- 8 mmHg; P <

124 During 8% O2 for 10 min, the falls in ABP and SVR were maintained, but RF, HR and MSNA waned t

125 revented the further progressive increase in ABP seen in 2K1C+sham CSD rats, with a between-group dif

126 The rise in ABP was associated with an increase in the low frequency

127 e we show that the crucial role for Scrib in ABP has remained obscure due to the compensatory functio

128 roved a valuable early marker of severity in ABP with clear advantages for prediction of LOS over Ran

129 f [Pyr(1) ]apelin-13 significantly increased ABP (9 +/- 1 mmHg) compared to saline (-1 +/- 2mmHg; P <

130 ce of sympathoexcitatory neurones, increases ABP and sympathetic nerve activity.

131 A surprising feature of the linked ABP motifs is that a set of six similar compounds has th

132 h ABP in young SHRs and significantly lowers ABP in adult SHRs.

133 rally hypothesized that the activity of many ABPs are temporally and spatially regulated by PIP(2); h

134 Combined MBP/ABP results in significantly lower rates of SSI, organ s

135 but does not seem to significantly modulate ABP-catalyzing UGT in liver.

136 ains 1 and 3, a common binding site for most ABPs.

137 The 13 genes include seven new ABP-like OBPs as well as the previously identified PBPs

138 No ABPs or inhibitors have been discovered that specificall

139 r HBP, neither systolic or diastolic OBP nor ABP was associated with LVMI.

140 The cadherin-NPRAP-ABP complexes also bound GluR2.

141 ABP from the cytosol to form cadherin-NPRAP-ABP complexes, dependent on NPRAP interaction with the A

142 The resulting cadherin-NPRAP-ABP/GRIP complexes serve as anchorages for AMPARs.

143 The oAd/ABP-PEG-HCBP1 demonstrated enhanced cancer cell killing

144 r cell killing efficacy in comparison to oAd/ABP complex.

145 The affinities of ABP fragments were improved by structure-guided chemistr

146 X-ray photoelectron spectroscopy analysis of ABP and ACP confirmed that both samples contain high lev

147 Nrf2 promoted conjugation of ABP with glucuronic acid in the liver, increasing urinar

148 practical approach to predict the course of ABP and should be further evaluated in larger trials.

149 IV were evaluated in vitro after delivery of ABP/TSTA-SP-exendin-4.

150 s suggest that the structure and dynamics of ABP may be adapted to exploit dynamic changes to reduce

151 etion from the LNG) and 2) the expression of ABP, which can quench reactive APAP metabolites and ther

152 Although glucuronidation of ABP and its metabolites is a detoxification process, the

153 ve, requiring only femtomoles (nanograms) of ABP-labeled enzymes.

154 ular, single-molecule assay, a wide range of ABP/actin interactions can be studied to better understa

155 ase studies to illustrate the application of ABPs to protease enzymology, discovery and development o

156 that may facilitate spatial localization of ABPs: binding of a short cross-linker protein to 2 actin

157 rate that membrane-interaction mechanisms of ABPs evolved to precisely fulfill their specific functio

158 Based on ABP data recorded during routine intensive care unit (IC

159 Compounds with one ABP bind independently to two separated AT sites.

160 ioreducible polymeric carrier, either ABP or ABP-PEG 10, merits further testing as a potential therap

161 Kv7 targeting (ankyrin G-binding peptide, or ABP) and other pharmacological tools, we show that axona

162 PAM-ABP and siRNA formed polyplexes with average diameter of

163 PAM-ABP formed compact nanosized polyplexes and showed low c

164 ted poly (amidoamine) (PAMAM) dendrimer (PAM-ABP) in hMSCs.

165 d on these results, this newly developed PAM-ABP polyplex is a promising delivery system for clinical

166 ection efficiency and VEGF expression of PAM-ABP using gWiz-Luc and pbeta-VEGF were higher than those

167 VEGF gene silencing efficiency of PAM-ABP/siRNA polyplexes was shown to be more effective than

168 y, dendrimer type bio-reducible polymer (PAM-ABP) which was synthesized using arginine grafted bio-re

169 molecular weight bio-reducible polymer, PAM-ABP, to overcome the limitations of the low molecular we

170 cell lines using bio-reducible polymer, PAM-ABP.

171 The newly synthesized PAM-ABP was studied to determine its efficacy as a gene deli

172 Our results suggest that PAM-ABP has the ability to deliver a therapeutic gene in hMS

173 The PAM-ABP demonstrated superior condensing ability for plasmid

174 The siRNA in the PAM-ABP/siRNA polyplex was released by 5mM DTT and heparin.

175 in patients with acute biliary pancreatitis (ABP).

176 y, competition between endocytic actin patch ABPs fimbrin Fim1 and cofilin Adf1 enhances their activi

177 nes in the anthocyanin biosynthetic pathway (ABP).

178 0 to 100 and abnormal birefringence pattern (ABP) as TSS <or= 79.

179 er (ABP)-PEG-HCBP1, by conjugating PEGylated ABP with HCBP1 peptides which has high affinity and sele

180 ompeting peptide, ankyrin G binding peptide (ABP) that disrupts axonal K(V)7/M-channel function, had

181 ed, one or two amidine-benzimidazole-phenyl (ABP) motifs were designed, synthesized, and evaluated fo

182 Furthermore, phEPO/ABP delivery induced prominent suppression on Ang II and

183 arct support the beneficial effects of phEPO/ABP administration.

184 The reduced infarct size of phEPO/ABP delivery was followed by decrease in fibrosis, prote

185 onate [APP](2-), and aminobutyl phosphonate [ABP](2-).

186 figuration, forming two ATP binding pockets (ABP) with the ATP molecules buried at the dimer interfac

187 ssential for epithelial apicobasal polarity (ABP) in Drosophila However, a conserved function for thi

188 d bioreducible poly(disulfide amine)polymer (ABP) and PEG5k-conjugated ABP (ABP5k) in expectation of

189 The arginine grafted bioreducible polymer (ABP) and its PEGylated version, ABP-PEG10, were utilized

190 ng an arginine-grafted bioreducible polymer (ABP), microbubbles (MBs), and ultrasound technology (US)

191 yctaminebisacrylamide-diaminohexane polymer (ABP) was used as a gene carrier.

192 , an arginine grafted bio-reducible polymer (ABP)-PEG-HCBP1, by conjugating PEGylated ABP with HCBP1

193 4-aminobiphenyl (dG-C8-ABP), the predominant ABP-DNA adduct formed in bladder cells and tissues, was

194 he use of oral antibiotic bowel preparation (ABP) has been practiced for decades but its use is also

195 Concomitantly, arterial pressure (ABP), fell and heart rate (HR) and respiratory frequency

196 rve activity (SNA), arterial blood pressure (ABP) and breathing.

197 nuous monitoring of arterial blood pressure (ABP) and intracranial pressure (ICP), were retrospective

198 ation (CSD) reduces arterial blood pressure (ABP) in SHR.

199 Real arterial blood pressure (ABP) measurements from 34 traumatic brain injury patient

200 mg daily, by 24-h ambulatory blood pressure (ABP) monitoring and evaluated efficacy.

201 greater increase in arterial blood pressure (ABP) than equi-osmotic mannitol/sorbitol.

202 The arterial blood pressure (ABP) was gradually reduced until it dropped to below the

203 sis of a peripheral arterial blood pressure (ABP) waveform has not been definitively identified.

204 de that can elevate arterial blood pressure (ABP) yet understanding of the mechanisms involved remain

205 lence of abnormal ambulatory blood pressure (ABP), assess factors associated with abnormal ABP, and e

206 anaesthetized rats, arterial blood pressure (ABP), femoral blood flow (FBF) and tension in the extens

207 rs by CO2 increases arterial blood pressure (ABP), sympathetic nerve activity and breathing.

208 .e., confirmed by ambulatory blood pressure [ABP] monitoring).

209 ated an activity-based small-molecule probe (ABP) to track target engagement in vivo.

210 Activity-based probes (ABPs) and peptide-based inhibitors are instrumental in t

211 Here, we designed activity-based probes (ABPs) based on an inhibitor of the main EV71 protease (3

212 nthesis of a suite of activity-based probes (ABPs) based on the general MAP inhibitor scaffold, besta

213 , we demonstrate that activity-based probes (ABPs) targeting cysteine cathepsins can be used in murin

214 We have developed two activity-based probes (ABPs) that characterize active GSTs in mammalian tissues

215 fluorescently labeled activity-based probes (ABPs) that covalently label active caspases in vivo.

216 t cyclophellitol-type activity-based probes (ABPs) that exploit this mechanism to covalently modify t

217 mphasis on the use of activity-based probes (ABPs) to detect protease activity.

218 These activity-based probes (ABPs) were synthesized with alkynes to harness the utili

219 rsible calpain family activity-based probes (ABPs), which retained the specificity of the stabilized

220 s traits and aboveground biomass production (ABP) were considered.

221 on to AMPA receptor (AMPAR)-binding protein (ABP) and the related glutamate receptor (GluR)-interacti

222 erone and salivary androgen-binding protein (ABP) in the LNG.

223 oxofilin, a monomeric actin-binding protein (ABP) involved in invasion.

224 nteraction of the arabinose-binding protein (ABP) with its ligand, d-galactose, using NMR relaxation

225 etween aptamer and aptamer-binding proteins (ABP), here we develop a lentiviral capsid-based bionanop

226 The salivary androgen-binding proteins (ABPs) are members of the secretoglobin gene family prese

227 etween fission yeast actin binding proteins (ABPs) for binding F-actin facilitates their sorting to d

228 ive and -insensitive actin-binding proteins (ABPs) on PC2(iv) channel function in a lipid bilayer sys

229 Actin-binding proteins (ABPs) regulate the assembly of actin filaments (F-actin)

230 In cells, actin-binding proteins (ABPs) sort to different regions to establish F-actin net

231 cells have multiple actin binding proteins (ABPs) that exist simultaneously to maintain the structur

232 actions with various actin-binding proteins (ABPs), actin plays an active role in many cellular proce

233 e activities of many actin-binding proteins (ABPs), including profilin, cofilin, Dia2, N-WASP, ezrin,

234 iscrete locations by actin-binding proteins (ABPs), including the formins and tropomyosins (Tms).

235 tin cytoskeleton via actin-binding proteins (ABPs).

236 o lack all canonical actin-binding proteins (ABPs).

237 teins (GOBPs) and antennal-binding proteins (ABPs).

238 ctin cytoskeleton by actin-binding proteins (ABPs).

239 <125/75 mm Hg without RH); pseudoresistance (ABP <125/75 mm Hg with RH); sustained hypertension (ABP

240 data set containing a large number of radial ABP waveform segments and contemporaneous reference CO b

241 7%) received MBP only, 1374 (5.89%) received ABP only, and 8855 (37.98%) received both preparations.

242 dult Wistar rats were instrumented to record ABP via telemetry, and then underwent CSD (n = 9) or sha

243 of Madin-Darby canine kidney cells recruited ABP from the cytosol to form cadherin-NPRAP-ABP complexe

244 CSD reduced ABP in 2K1C+CSD rats and prevented the further progressi

245 change in the filament's ability to regulate ABPs and myosin motor activity.

246 ies compared to those of previously reported ABPs.

247 5/75 mm Hg without RH); and true resistance (ABP >/=125/75 mm Hg with RH).

248 The resting ABP is higher in young SHRs (122 +/- 5 mmHg) than in age

249 eled and unlabeled global MS data, revealing ABP selectivity for glycoside hydrolase (GH) enzymes, in

250 ified alpha-actinin Ain1, a contractile ring ABP, as another Fim1 competitor.

251 erefore, the combination of contractile ring ABPs Ain1 and Cdc8 is capable of inhibiting Fim1's assoc

252 The putative role of the mouse salivary ABPs is that of pheromones mediating mate selection resu

253 does not appear to be critical in the scrib ABP phenotype.

254 d HT1080 cancer cells treated with oAd/shMet-ABP-PEG-HCBP1 complex had significantly decreased Met an

255 dividually, and created our innovative siRNA-ABP-MB (SAM) complexes.

256 These data indicate that specific ABP-PC2 complexes would confer distinct Ca(2+)-sensitive

257 se studies demonstrate that caspase-specific ABPs have the potential to be used for noninvasive imagi

258 or scaffold, bestatin, we generated specific ABPs for these two enzymes.

259 .015) and 12 (p = 0.020), nighttime systolic ABP was significantly lower in the chlorthalidone group

260 n cytoskeleton independently of known target ABPs.

261 to its lower charge transfer resistance than ABP.

262 no preparation and a lower rate of SSI than ABP alone.

263 Furthermore, we found that ABP was able to compete with GSH and cellular proteins f

264 nonymous substitution rates, suggesting that ABP might play a similar biological role in both systems

265 We demonstrate that ABPs targeting the cysteine cathepsins can be used in mu

266 The ABP dimers are secreted into the saliva of mice and then

267 The ABP ligands represent a new type of nonpeptidic BACE-1 i

268 The ABP, palladin, is essential for the maintenance of cell

269 The ABP-PEG-HCBP1-conjugated replication incompetent GFP-exp

270 Both the ABP and the ABP-PEG10 carriers demonstrated efficient transfection a

271 Both the ABP and the ABP-PEG10 carriers demonstrated efficient tr

272 sition had a larger predictive power for the ABP than species diversity and FDQ, indicating a primary

273 effect of exendin-4 was also observed in the ABP/TSTA/SP-exendin-4-treated mice groups, compared with

274 the other, at the 3,5,3',5'-positions of the ABP units to curtail binding by the CBPQT(4+) ring if no

275 y(ethylene glycol) (PEG) modification of the ABP was employed to inhibit the particle aggregation res

276 e the effects of functional diversity on the ABP in the Northern Tibetan alpine grasslands.

277 nal diversity were positively related to the ABP.

278 xes, dependent on NPRAP interaction with the ABP PDZ domain 2.

279 The distinct effect(s) of the ABPs on PC2(iv) channel function demonstrate that Ca(2+)

280 Derivatization of the ABPs, including reactive groups, acetylation of the glyc

281 identified host candidates that bind to the ABPs.

282 Therefore, ABPs targeting the cysteine cathepsins are potentially v

283 Two of these ABPs, filamin and alpha-actinin, have been extensively u

284 Thus, ABP could be involved with mate recognition and species

285 Thus, ABPs may serve as targets for novel treatment strategies

286 greater transfection efficiency compared to ABP alone.

287 ventive agents are used in humans exposed to ABP, especially in smokers.

288 gainst ABP, it increases bladder exposure to ABP.

289 Unexpectedly, compounds with two ABP motifs can bind strongly either as monomers or as co

290 s of two ubiquitin activity-based probes (Ub-ABPs) employing solid phase chemical ligation (SPCL).

291 xploitation of the 4,4'-azobiphenyloxy unit (ABP) as a light-operated gate, we decided to introduce (

292 riate interaction with endogenous vegetative ABPs.

293 n of these reproductive, but not vegetative, ABP isovariants suppressed the ectopic ACT1 expression p

294 ble polymer (ABP) and its PEGylated version, ABP-PEG10, were utilized to study the expression efficie

295 the limitations of the low molecular weight ABP.

296 to uncover the molecular principles by which ABPs interact with phosphoinositide-rich membranes.

297 after single intravenous administration with ABP/TSTA-SP-exendin-4.

298 oncolytic Ad (oAd; RdB/shMet) complexed with ABP-PEG-HCBP1 delivered oAd efficiently into hepatoma ca

299 In eyes with ABP, SLP-ECC had a significantly greater (all P <or= 0.0

300 iques to visualize the binding of actin with ABPs.