ライフサイエンスコーパス: endo-

1 ported (up to 98:2 enantiomer ratio and >98% endo).

2 cs of apurinic/apyrimidinic endonuclease (AP endo).

3 dolin-1-one (E-5-exo), and isoquinolinone (6-endo).

4 ion with bacteria-derived endoglycosidase S (EndoS).

5 served sequence in the effector Endosulfine (Endos).

6 exon 4 of Sirt1 in endothelial cells (Sirt1(endo-/-)).

7 as I(Kr) density was similar between Epi and Endo (0.31+/-0.05 versus 0.36+/-0.07 pA/pF) at 20 mV.

8 I(P)(ENDO) (0.34 +/- 0.04 pA/pF, n = 17) was smaller than I(P

9 37e than in the absence of the additive (exo/endo = 1:5.7).

10 decreased with administration of esmolol (v(endo) 1.4+/-0.2 cm/s [P<0.05]; SR 6+/-1 s(-1) [P<0.01]).

11 590+/-140 ms) and nonsustained focal waves (Endo: 1.2% versus Epi: 1.6%, P=0.669) were also observed

12 , I(Ks) densities were larger in Epi than in Endo (1.1+/-0.1 versus 0.43+/-0.07 pA/pF), whereas I(Kr)

13 (1-->4)-beta-D-xylanase, beta-D-mannosidase, endo-(1-->4)-beta-D-mannanase, alpha-D-xylosidase, beta-

14 all hydrolases screened: beta-D-xylosidase, endo-(1-->4)-beta-D-xylanase, beta-D-mannosidase, endo-(

15 Suppression or overexpression of endo-(1-->4)beta-D-glucanase activity has no detectable

16 (APD25) are reduced in hypertrophy (control: endo, 11.4+/-0.9 ms; mid, 8.2+/-0.9 ms; epi, 5.1+/-0.4 m

17 .2+/-0.9 ms; epi, 5.1+/-0.4 ms; hypertrophy: endo, 11.6+/-0.9 ms; mid, 10.4+/-0.8 ms; epi, 7.8+/-0.6

18 ) was lower in EPI (7 +/- 2 mM, n = 31) than ENDO (12 +/- 3 mM, n = 29), with MID being intermediate

19 rolonged in subepicardial myocytes (control: endo, 126+/-7 ms; epi, 96+/-10 ms; hypertrophy: endo, 91

20 ocardial (MID) (2.84 pA/pF) and endocardial (ENDO) (2.21 pA/pF) cells.

21 Only the endo-[2 + 2] (syn-3) transition state was located for cy

22 endo-2-exo-3-dihydroxynorbornane bearing a 5-endo-[2,2-bis(trifluoromethyl)hydroxyethyl] substituent

23 Transient rotations (Endo: 22% versus Epi: 19.2%, P=0.169; mean duration: 590

24 Both exo (21) and endo (27) isomers of the metabolite 2 were prepared via

25 e of fluorinated sugar rings for either a 2'-endo, 3'-exo (South), or a 3'-endo,2'-exo (North) confor

26 Epi: 46.8%, P=0.0194) and single wavefronts (Endo: 31.3% versus Epi: 28.1%, P=0.129) were the dominan

27 A high-density 3D Endo (321+/-93 sites mapped) and Epi (302+/-158 sites ma

28 roducts formed upon addition of bromine to 3-endo-, 4-, and 5-methyl- and 3-endo-phenyl-substituted N

29 ation from intermediate rac-5 leading to the endo-[4 + 2] (endo-2) and exo-[2 + 2] (anti-3) cycloaddu

30 The transition state for endo-[4 + 2] cycloaddition (endo-2TS, DeltaH(double dagg

31 Disorganized activity (Endo: 41.3% versus Epi: 46.8%, P=0.0194) and single wave

32 s in ligand protonation and the formation of endo (4a) and exo (4b) isomers of trans-[HFe(PNHP)(dmpm)

33 examples reveal the general concept that all endo-[6+4] cycloadditions are ambimodal.

34 o, 126+/-7 ms; epi, 96+/-10 ms; hypertrophy: endo, 91+/-6 ms; epi, 108+/-7 ms).

35 are symptoms associated with endometriosis (ENDO), a common condition among women that is characteri

36 here that Rad23 can bind Ho-endonuclease (Ho-endo), a nuclear protein that initiates mating-type swit

37 GAS secretes EndoS, an endoglycosidase that specifically cleaves the

38 re generated by site-directed mutagenesis of EndoS (an endoglycosidase from Streptococcus pyogenes )

39 in 10 healthy mice to measure endocardial (v(endo)) and epicardial systolic velocities and SR.

40 ndo), UA VSM, omental artery endothelium (OA endo), and OA VSM proteins were isolated and ERalpha and

41 3(S)Hyp residues, which are all down (Cgamma-endo), and the varphi/psi dihedral angles of the Xaa 3(S

42 tiarrhythmic drug therapy after endocardial (ENDO) and adjuvant epicardial (EPI) substrate modificati

43 report the results of combined endocardial (Endo) and Epi VT ablation and conducting channel (CC) el

44 PD) and high Vmax compared with endocardial (Endo) and epicardial (Epi) cells.

45 [K(+)](o) from 5.4 to 15 mM caused both I(P)(ENDO) and I(P)(EPI) to increase, but the ratio remained

46 dividual sugars in equilibrium between S (2'-endo) and N (3'-endo) conformations, with S being prefer

47 ter endotoxin challenge, decreases in both v(endo) and SR were detected before decreases in shortenin

48 d trip cyclization is a sequence of 5-exo, 6-endo, and 5-exo cyclizations in which the last radical c

49 enynes are suitable substrates, and 5-exo, 5-endo, and 6-exo cyclizations lead to outstanding enantio

50 nd 1,2-dioxacanes through 6-endo/exo, 7-endo/endo, and 8-endo/endo pathways.

51 VF did not terminate in the Epi, Endo, and control groups (P<0.001).

52 ully internally coordinated with all phenyls endo, and lithium is close to one terminal allyl carbon.

53 ancy under natural conditions, namely para-, endo-, and ecodormancy in summer, fall, and winter, resp

54 hree well-defined phases of dormancy, para-, endo-, and ecodormancy.

55 ytotoxic to human tumor cell lines of ecto-, endo-, and mesodermal origin.

56 phohydrolase (RppH), allowing access to both endo- and 5' exoribonucleases.

57 ford, without any significant selectivity, 6-endo- and 5-endo-substituted bicyclic lactone cycloadduc

58 semble in designer cellulosomes alongside an endo- and an exo-cellulase also converted to the cellulo

59 PBPs), rather than with low-molecular-weight endo- and carboxypeptidases, indicating that MreC might

60 and proteins demonstrates conservation among endo- and ectoparasitoids within the Apocrita (e.g., thi

61 Simultaneous intraoperative mapping of endo- and epicardial lateral right atrium wall was perfo

62 ned by asynchronous activation of the atrial endo- and epicardial layer and transmurally propagating

63 [ARVC]) with sustained VT underwent combined endo- and epicardial mapping.

64 Intraoperative mapping of the endo- and epicardial right atrial wall was performed dur

65 high-resolution mapping of the right atrial endo- and epicardial wall during AF in humans.

66 W indicate that muscular connections between endo- and epicardium underlie EBW and that a slight degr

67 , and similar densities were observed in the endo- and epicardium.

68 lidine incorporated lobelane analogues, endo,endo- and exo,exo-2,6-cis-diphenethyl-1-azabicyclo-[2.2.

69 The mesylate derivatives of endo- and exo-2-hydroxy-2-phenylbicyclo[2.2.1]heptan-3-o

70 es, the major oxidation products (>75%) were endo- and exo-2-norcaranol.

71 earch has been applied to design a series of endo- and exo-3-(pyridin-3-yl)bicyclo[2.2.1]heptan-2-ami

72 substituted bicyclo[1.1.0]but-2-ylmethanols (endo- and exo-9) from 1,3-butadiene has been developed.

73 , ActE secretes a suite of enzymes including endo- and exo-cellulases, CBM33 polysaccharide-monooxyge

74 ell-suited to generate diversity at both the endo- and exo-cyclic fragments formed during the ring-cl

75 In the absence of the catalyst, both endo- and exo-cycloisomerizations have been calculated t

76 Endo- and exo-cycloisomerizations of 4-pentyn-1-ol have

77 We used endo- and exo-metabolomics data to show that the thermod

78 y using micrococcal nuclease, which has both endo- and exo-nuclease activity, to fragment the chromat

79 methylmaleimide, and that similar amounts of endo- and exo-products are obtained.

80 Both endo- and exo-ring-protonated isomers are calculated to

81 oxide-opening cascade that incorporates both endo- and exo-selective epoxide openings, each directed

82 Loqs-PD promotes both endo- and exo-siRNA production by Dicer-2.

83 ne with 2-cyclohexenone to give a mixture of endo- and exo-trans-6-amino-5-phenylbicyclo[2.2.2]octan-

84 thermocellum is a multiprotein complex with endo- and exocellulase, xylanase, beta-glucanase, and ac

85 rally known that a team of enzymes including endo- and exocellulases as well as cellobiases are requi

86 terms of the functional differences between endo- and exocellulases.

87 14 patients with severe developmental delay, endo- and exocrine dysfunction, impairment of the sensor

88 ain relief, quality of life [QoL]), medical (endo- and exocrine function), and clinical (reoperation)

89 the sensory and autonomic nervous system and endo- and exocrine glands.

90 zoidal-shaped Ag(5) moiety via Ag-N bonds to endo- and exocyclic nitrogens of cytosine and adenine.

91 monella-containing vacuole labeled with both endo- and exocytic markers.

92 king along microtubules and through the cell endo- and exocytic pathways can be next visualized via l

93 AnxA6), regulates membrane trafficking along endo- and exocytic pathways.

94 Hrs-2 acts to provide communication between endo- and exocytic processes.

95 We compared synaptic vesicle proteins, endo- and exocytosis cofactors, cytoskeleton components,

96 tion-induced bilayer dynamics reminiscent of endo- and exocytosis in cells.

97 affold proteins involved in synaptic vesicle endo- and exocytosis near their site of action.

98 Live cell imaging studies revealed endo- and exocytosis of F-UiO and endosome acidification

99 While it is known that endo- and exocytosis regulate the cell membrane area in

100 ms in which transport, receptor interaction, endo- and exocytosis, and degradation occur together.

101 1 functions as a dual Ca(2+) sensor for both endo- and exocytosis, potentially coupling these two com

102 equired for normal rates of synaptic vesicle endo- and exocytosis.

103 e membrane trafficking events mediating B2AR endo- and exocytosis.

104 e recently been implicated in the control of endo- and exocytosis.

105 nd organization of the actin cytoskeleton to endo- and exocytosis.

106 phate (IPn) recognition domains important in endo- and exocytosis.

107 y protein kinases occurs mainly by regulated endo- and exocytosis; (ii) it is independent of consensu

108 cling endosome, which acts as a nexus in the endo- and exocytotic networks.

109 ave been developed to study the formation of endo- and exogenous DNA adducts.

110 ure and exposing the tissue cells to various endo- and exogenous factors, including bacterial toxins.

111 These displayed endo- and exoglucanase activity on the beta-1,3-1,6-gluc

112 Native virus deglycosylation by endo- and exoglycosidases dramatically reduced cytokine

113 The purified UL12.5 exhibited both endo- and exonuclease activities but was less active tha

114 Specifically, we show that the endo- and exonuclease activities of the exosome are both

115 SBR), detection, and signaling; yet, how its endo- and exonuclease activities regulate DSBR by nonhom

116 Artemis is a vertebrate nuclease with both endo- and exonuclease activities that acts on a wide ran

117 e been identified for the protein, including endo- and exonuclease activities, interaction with the H

118 l data show that this CR3 motif affects both endo- and exonuclease activity in vivo and both the nucl

119 c subunit of an Escherichia coli enzyme with endo- and exonuclease activity, SbcCD.

120 ecB1-929CD enzyme has lost the single-strand endo- and exonuclease and the double-strand exonuclease

121 Artemis is a diverse endo- and exonuclease, and creating a unified model for

122 exhibits greatly increased susceptibility to endo- and exonucleases but retains a full complement of

123 However, some noncoding RNA classes use endo- and exonucleases to achieve functionality.

124 bases embedded in duplex DNA and activating endo- and exonucleases to remove the mismatch.

125 te source, a phenotype dependent on secreted endo- and exonucleases.

126 nsidered bifunctional RNases possessing both endo- and exonucleolytic activities.

127 tion of pyrophosphorolysis as well as in the endo- and exonucleolytic cleavage of the nascent RNA.

128 o the molecular principles governing diverse endo- and exonucleolytic cleavage specificities of membe

129 e flap junctions, unifying the mechanisms of endo- and exonucleolytic processing.

130 Ribosomal processing requires a series of endo- and exonucleolytic steps for the production of mat

131 rnal cleavages in plasma proteins created by endo- and exopeptidases, providing information about the

132 o free amino acids by the combined action of endo- and exopeptidases.

133 l cells, is catalyzed by specific subsets of endo- and exoribonucleases that together recycle RNA fra

134 rokaryotic cells involves the action of both endo- and exoribonucleases.

135 l part of gene regulation that involves both endo- and exoribonucleases.

136 pacers (ITS1 and ITS2), which are removed by endo- and exoribonucleolytic steps to produce mature rRN

137 annihilation and that this is true for both endo- and exothermic singlet fission materials.

138 ns of OEG ensheathment and variations of the endo- and perineurium formed by olfactory nerve fibrobla

139 N. gonorrhoeae to infect and invade both the endo- and the ectocervix of the normal uterine cervix.

140 s capable of infecting and invading both the endo- and the ectocervix.

141 These results were compared with lavage and endo- and transbronchial biopsy studies in normal contro

142 lipids, and carbohydrates and by detoxifying endo- and xenobiotic components, the liver plays an impo

143 rplay between RORalpha and LXR in regulating endo- and xenobiotic genes, which may have broad implica

144 computer program termed Discovery of General Endo- and Xenobiotics (DoGEX) was developed, which uses

145 0 enzyme engaged in the biotransformation of endo- and xenobiotics, including >50% of clinically rele

146 on of a wide variety of structurally diverse endo- and xenobiotics, including many therapeutic agents

147 cts the cardiomyocyte by mediating efflux of endo- and xenobiotics.

148 ation of several pharmacologically important endo- and xenobiotics.

149 tted to the metabolism of chemically diverse endo- and xenobiotics.

150 conjugation of reduced glutathione (GSH) to endo- and xenobiotics.

151 presentatives of that family possessing only endo- and, in few cases, endo/exo-cellulase activities,

152 the replacement by RRP1 is coupled with the endo- and/or exo-ribonucleolytic cleavage of pre-rRNA re

153 I-TevI cleavage site (CS) and IS implicates endo- and/or exonuclease activities to resect the DNA se

154 airs at the CpG steps in the stem; (iii) C2'-endo, anti conformations for all the nucleotides.

155 e nucleotides in (CTG)5 and (CTG)6 adopt C2'-endo, anti conformations.

156 nosine is C3'-endo, syn, and cytidine is C2'-endo, anti.

157 approximately 2-fold) in female base but not endo-, apex or male myocytes.

158 nt experimentally confirm the [3 x mu-H, 2 x endo] arrangement for 9 also.

159 tes were isolated from basal subendocardial (endo), basal midmyocardial (mid), and apical subepicardi

160 P/dt(max) (r2=0.79 for SR and r2= 0.69 for v(endo); both P<0.0001).

161 e in NCX current density (P<0.05) limited to ENDO (by 202%) and MID (by 76%) but not EPI myocytes (P=

162 Equilibrium constants (Keq = [C2'-endo]/[C3'-endo]) for C2'-endo-C3'-endo interconversion

163 te conformation was determined to be syn-C2'-endo (ca. 80%).

164 R for lymphatic capillary endothelium (R(endo)), calculated from lymph/subsynovial concentration

165 current (Ito) in EPI but not in endocardial (ENDO) cardiomyocytes of UNx rats led to a decreased tran

166 d APD90 of M but abbreviated that of EPI and ENDO, causing a persistent increase in TDR; Torsade de P

167 LQT3) prolonged APD90 of M more than EPI and ENDO, causing increases in QT and TDR.

168 P) from epicardial (EPI), M and endocardial (ENDO) cells and a transmural electrocardiogram were simu

169 icular epicardial (EPI) than in endocardial (ENDO) cells.

170 roliferation and -migration observed in LKB1(endo-/-) cells.

171 The shapes of the inward (endo) CH surfaces determine the dynamic behavior, changi

172 ected C3'-endo, except sugar 2, which is C2'-endo, characteristic of B-form sugars.

173 Using expressed fragments of EndoS, circular dichroism of the isolated CBM, and a CBM

174 between non-helical (C2-endo) to helical (C3-endo) conformations during formation of two distinct exc

175 in equilibrium between S (2'-endo) and N (3'-endo) conformations, with S being preferred.

176 V(endo) correlated closely with sonomicrometer-measured ve

177 are considerable lower in energy than their "endo" counterparts, with the "exo-entended" conformation

178 flow, and less tissue hypoxia than TbetaRII(endo+/+) counterparts.

179 Endo, CR, and Vasc but not MIS FBR performed significant

180 The key second (6-endo) cyclization produces two stereoisomers, one of whi

181 rs are also identified for the S -type (C2'- endo) deoxyadenosine conformations that occur in R32 and

182 evealed that the mode of cyclization (exo vs endo) depends on the protecting group on nitrogen, the o

183 isomeric exocyclic (1-exo) and endocyclic (1-endo) dienolates.

184 sum of their isolated components (E(inc) = E(endo) - E(cage) - E(x)) and to their exohedral isomer en

185 their exohedral isomer energies (E(isom) = E(endo) - E(exo)).

186 an 88-kDa secreted protein, endoglycosidase (Endo) E, which is most likely responsible for this activ

187 plex, but shows that the sugar pucker is O4'-endo (East conformation), intermediate between the South

188 g angiostatin (PCI-Angio) or endostatin (PCI-Endo) effectively reduced angiogenesis using an in vivo

189 Three protonated isomers are formed (endo/endo, endo/exo, or exo/exo), which differ in the positio

190 Specifically, we show that (i) EndoS (endoglycosidase S) cleaves only complex-type glyc

191 All the RNA sugars are the expected C3'-endo, except sugar 2, which is C2'-endo, characteristic

192 e dielectric constant of the solvent and the endo/ exo ratio is found, but more polar solvents lead t

193 However, its aggressive endo-/exo-nuclease activities make MNase-seq unreliable

194 This 42 kDa endo-/exonuclease, FEN-1, is highly homologous to human

195 ochemical assays revealed that scTat-D is an endo-/exonuclease.

196 ving methyl iodide proceed from the concave (endo) face of the bicyclo[4.3.0]nonene ring system.

197 During M phase, Endosulfine (Endos) family proteins are phosphorylated by Greatwall k

198 minimally invasive (MIS), and 12 Endocrine (Endo) fellowships.

199 This enzyme is known to possess 5'-flap endo- (FEN) and 5'-3' exo- (EXO) nuclease activities.

200 Equilibrium constants (Keq = [C2'-endo]/[C3'-endo]) for C2'-endo-C3'-endo interconversion at 25 degre

201 creased with administration of dobutamine (v(endo) from 2.2+/-0.3 to 3.8+/-0.2 cm/s [P<0.01]; SR from

202 o protons [Fe(III)-bound C5-OH(exo) and C5-H(endo)] from camphor.

203 ealed the partial 3'-OH polarization and H3'-endo-->exo ribosyl configuration at the spMTAN transitio

204 voltage was essentially identical in EPI and ENDO (half-maximal activation at 9-10 mM [Na(+)](i) or a

205 al and eucaryotic sequences similar to these endo- (HII and III) and exoribonucleases (II, PH and D).

206 erally decreased with increasing doses of rh-Endo; however, the effects were complex and in some anal

207 rived alkenyl sulfides were submitted to a 6-endo [I(+)]-induced cyclization, and the resulting 2-deo

208 erichia coli DNA glycosylases, endonuclease (endo) III and endo VIII, which recognize oxidized pyrimi

209 Endonuclease (Endo) III and formamidopyrimidine-N-glycosylase (Fpg) ar

210 e evaluated recombinant human endostatin (rh-Endo) in a phase I trial designed to assess safety, phar

211 al enzyme endo-beta-N-acetylglucosaminidase (EndoS) induced a dominant suppression of immune complex

212 the critical combination of factors C4-(exo/endo), intraresidue H-bonding, stereoelectronic (R/S) an

213 Endometriosis (ENDO) is a disorder in which vascularized growths of end

214 Apurinic/apyrimidinic endonuclease (AP endo) is a key enzyme in oxidative damage DNA repair.

215 Apurinic/apyrimidinic endonuclease (AP endo) is a key enzyme in the repair of oxidatively damag

216 human apurinic/apyrimidinic endonuclease (AP endo) is a major factor in the maintenance of the integr

217 Apurinic/apyrimidinic endonuclease (AP endo) is believed to play a critical role in repair of o

218 Endoglycosidase S (EndoS) is a glycoside-hydrolase secreted by the bacteriu

219 ndoglycosidase from Streptococcus pyogenes , EndoS, is complementary to other known endoglycosidases

220 nsmural NCX gradient, from EPI (greatest) to ENDO (least), is disrupted in heart failure.

221 Thus, AP endo, like uracil DNA glycosylase, behaves in a quasi pr

222 complex can easily escape from intracellular endo-/lyso-somal compartments and release the gene load

223 that PorB increases the level of OVA in the endo-/lysosomal cellular compartment of BMDCs, increases

224 ndergoes pH-dependent disassembly within the endo-/lysosomal compartment, thereby exposing hidden dom

225 xG motifs in the transfer of vDNA across the endo-/lysosomal membrane.

226 Apurinic/apyrimidinic endonuclease (AP endo) makes a single nick 5' to a DNA abasic site.

227 angiogenic potential compared with TbetaRII(endo+/+) mice under basal conditions.

228 ozygous TGF-beta receptor knockout (TbetaRII(endo+/-)) mice to explore whether curtailed TGF-beta sig

229 or unilateral ureteral obstruction, TbetaRII(endo+/-) mice exhibited less tubulointerstitial fibrosis

230 ndothelial cell-specific LKB1-knockout (LKB1(endo-/-)) mice by crossbreeding vascular endothelial-cad

231 Tumors implanted in LKB1(endo-/-) mice but not macrophage-specific LKB1-knockout

232 nic folic acid-induced nephropathy) in Sirt1(endo-/-) mice resulted in robust acute renal functional

233 Under basal conditions, Sirt1(endo-/-) mice showed impaired endothelium-dependent vaso

234 In the kidneys of Sirt1(endo-/-) mice, impaired angiogenesis, reduced matrilytic

235 thelial cells but not in macrophages in LKB1(endo-/-) mice.

236 Consistently, LKB1(endo-/-) mouse tissues including the lung, skin, kidney

237 cess, we investigated Drosophila endophilin (endo) mutants.

238 ablated the Tgf-beta type I receptor Alk5 in endo-, myo- and epicardial lineages using the Tie2-Cre,

239 entricular epicardial (Epi) and endocardial (Endo) myocytes.

240 on in both epicardial (Epi) and endocardial (Endo) myocytes.

241 ves which are biased toward a "Northern" (3'-endo, N) sugar ring pucker were deaminated up to 65-fold

242 he nucleotide sugar moieties adopting a C3'- endo (N) conformation.

243 ssary for the sugar pucker to adjust to a 3'-endo (N-type) conformation to remain in the ADA substrat

244 ve repuckering of the 5'-G sugar ring to C3'-endo (N-type) conformation, retention of C2'-endo (S-typ

245 d repuckering of the 5'-G sugar rings to C3'-endo (N-type), retention of C2'-endo (S-type) conformati

246 the predominate C2'-endo (S-type) to the C3'-endo (N-type).

247 SSGSV bypass (n=621), AC bypass (n=236), and ENDO (n=923) procedures.

248 , in contrast to the previously reported C3'-endo (North conformation) described for the original 2.7

249 distinct sugar conformations by using a 3'- endo (north) 2'-fluoro-2'-deoxyribofuranosyl thymine (1)

250 he effect of monomer stereochemistry (exo vs endo) of two types of ester substituted monomers was als

251 xt/Endo), PDC with an Ext/Endo (PDC with Ext/Endo), or Ext/Endo without PDC (Ext/Endo without PDC).

252 hree classes of PBPs catalyze either trans-, endo-, or carboxypeptidase activities on the peptidoglyc

253 In this way, the molecule is converted to an endo- or an exoligand, possessing a concave or convex ar

254 oselectivity to be modulated to favor either endo- or exo-ester adducts.

255 These cationic 2-azadienes participate in endo- or exo-selective [4 + 2] cycloadditions with elect

256 pling of neuronal CB1Rs, after activation by endo- or exocannabinoids such as the marijuana component

257 Covalent binding of endo- or exogenous chemicals to DNA results in the forma

258 spectrometry before and after treatment with endo- or exoglycosidases or with alkaline phosphatase.

259 chemical library to discover specific MRE11 endo- or exonuclease inhibitors.

260 d to reveal the substrate specificity of any endo- or exopeptidase using liquid chromatography-tandem

261 The endo- or exoproteolytic hydrolysis of simple peptides ca

262 stion that UGT8 is involved in metabolism of endo- or xenobiotics.

263 and/or endodontic treatment (PDC without Ext/Endo), PDC with an Ext/Endo (PDC with Ext/Endo), or Ext/

264 ment (PDC without Ext/Endo), PDC with an Ext/Endo (PDC with Ext/Endo), or Ext/Endo without PDC (Ext/E

265 radiation, leading to two regioisomeric (exo/endo) photoproducts with complete chemoselectivity (excl

266 rane whorls in both vacuoles and the sarco- (endo-) plasmic reticulum, findings suggestive of a toxic

267 Furthermore, sarco(endo)-plasmic reticulum (Ca[2+] + Mg2+)-ATPase (SERCA) a

268 We show that Drosophila alpha-endosulfine (endos) plays a key role in this process.

269 llylic ring expansion to yield the formal "6-endo" products with aromatization via stereoelectronical

270 velopment of aromatic character along the "6-endo" reaction path is modulated via Au-complexation to

271 ), mid myocardium (MID), and subendocardium (ENDO), respectively.

272 schemia deemed eligible for either Bypass or Endo, revascularization resulted in significant and clin

273 or the DNA-like C-2'-endo form over the C-3'-endo (RNA-like) conformation, which suggests a potential

274 e than those that preferred a "Southern" (2'-endo, S) conformation.

275 endo (N-type) conformation, retention of C2'-endo (S-type) 3'-G sugar ring conformation, and anti ori

276 rings to C3'-endo (N-type), retention of C2'-endo (S-type) conformation for the 3'-G sugar rings, and

277 e pucker transition from the predominate C2'-endo (S-type) to the C3'-endo (N-type).

278 osphate receptor (IP3R), thereby linking the endo-/sarcoplasmic reticulum to the plasma membrane.

279 uction takes place with oxygen bound on the "endo" side ("dock-in") of the molecule.

280 2)O or D(2)O buffer, both ENDOR H(exo) and H(endo) signals are absent.

281 ation, these hosts can exchange an interior (endo) situated metal binding site for an exterior (exo)

282 o-2'-deoxyribofuranosyl thymine (1) or a 2'- endo (south) 2'-fluoro-2'-deoxyarabinofuranosyl thymine

283 Furthermore, similar to women with ENDO, such rats exhibit reduced fertility and increased

284 he nucleotide conformation; guanosine is C3'-endo, syn, and cytidine is C2'-endo, anti.

285 ower in cells isolated from the endocardial (Endo) than the epicardial (Epi) surface of the LV wall.

286 al trial of recombinant human endostatin (rh-Endo) that examined potential surrogates for response to

287 are evaluated by comparing their energies (E(endo)) to the sum of their isolated components (E(inc) =

288 mpanying transitions between non-helical (C2-endo) to helical (C3-endo) conformations during formatio

289 (P < 0.005) during para- to endo-dormant and endo- to eco-dormant transitions, respectively.

290 these stress-associated signals induced the endo- to ecodormancy transition and growth competence.

291 When crown buds transitioned from endo- to ecodormancy, the ABA metabolites PA and DPA dec

292 thout detectable cellulase activity (exo- or endo- type).

293 (EPI), midmyocardial (MID), and endocardial (ENDO) ventricular myocytes.

294 rized bovine glomerular endothelial cells (G/endo) was studied.

295 to 95 %) and regioselectivities (5-exo vs. 6-endo) were achieved through catalyst control and sequent

296 es, the highest stereoselectivities (>or=89% endo) were observed with 5-methyl or 6-methyl substituen

297 tes in M cells (P < .05 compared with Epi or Endo) when CL changed from 400 to 1000 ms.

298 nsient-state kinetics with purified human AP endo, which had been expressed in Escherichia coli.

299 pathogens, secretes a large endoglycosidase, EndoS, which removes carbohydrates in a highly specific

300 within plant microbiomes, i.e., endophytes ("endo" = within, "phyte" = plant), can significantly modi