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

12 (1-->4)-beta-D-xylanase, beta-D-mannosidase, endo-(1-->4)-beta-D-mannanase, alpha-D-xylosidase, beta-

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

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

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

16 .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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

34 3(S)Hyp residues, which are all down (Cgamma-endo), and the varphi/psi dihedral angles of the Xaa 3(S

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 1 functions as a dual Ca(2+) sensor for both endo- and exocytosis, potentially coupling these two com

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 0 enzyme engaged in the biotransformation of endo- and xenobiotics, including >50% of clinically rele

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

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

125 ation of several pharmacologically important endo- and xenobiotics.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

233 The endo- or exoproteolytic hydrolysis of simple peptides ca

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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