ライフサイエンスコーパス: lone

1 plied for distinguishing hydrogen-bonded and lone (17)O sites on the surface of silica gel; the one-d

2 Markovnikov directing effect is relieved and lone abstraction is observed, affording the 5-hydroxy-is

3 as to promote a social bond with the group's lone adult male.

4 and 2008, and those with a family history of lone AF (AF without preceding cardiovascular/endocrine d

5 udies conducted using 1,335 individuals with lone AF (cases) and 12,844 unaffected individuals (refer

6 ere identified in all subjects with familial lone AF (n = 33) as well as apparently unaffected family

7 5A coding region in 375 subjects with either lone AF (n=118) or AF associated with heart disease (n=2

8 rtery disease without MV disease (n=57), and lone AF (n=35).

9 association in two independent cohorts with lone AF (overall combined odds ratio = 1.52, 95% CI 1.40

10 ntified an association on chromosome 1q21 to lone AF (rs13376333, adjusted odds ratio = 1.56; P = 6.3

11 s, and anatomic remodeling) in patients with lone AF and are strong predictors of recurrent arrhythmi

12 terature are inconsistent so that studies of lone AF are not comparable.

13 Guidelines provide a vague definition of lone AF but do not provide direction about how much or w

14 In the lone AF cohort, 9 rare missense variants and 1 splice si

15 and 35.8%), increased, and the prevalence of lone AF decreased.

16 The IRRs for lone AF given an affected first- or second-degree relati

17 techniques have improved, the prevalence of lone AF has fallen.

18 Patients with lone AF have impaired myocardial energetics and subtle L

19 The IRR for lone AF in persons aged <40 years given a first-degree r

20 (AF) before age 60 years is associated with lone AF in relatives.

21 the intervening years is that definitions of lone AF in the literature are inconsistent so that studi

22 A family history of lone AF is associated with substantial risk of lone AF,

23 experience with the CMP in the treatment of lone AF over 2 decades and compares the original cut-and

24 Little is known about BNP in lone AF patients undergoing arrhythmia ablation.

25 predictive ability for thromboembolism among lone AF patients.

26 Risk In Communities Study, Cleveland Clinic Lone AF Study, Cardiovascular Health Study, and Rotterda

27 We followed up 726 patients with lone AF undergoing first-time arrhythmia ablation.

28 IRR for lone AF was 6.24 (95% CI: 2.59 to 15.0), given at least

29 We hypothesized that early-onset lone AF was associated with genetic variation in SCN5A.

30 TS3-associated variants in the patients with lone AF was much higher than expected, compared with the

31 ht patients underwent "cut and sew" Maze for lone AF with no other surgical indication.

32 therefore, recommended that use of the term "lone AF" be avoided.

33 In addition, the term "lone AF" is not invariably useful in making treatment de

34 ical variables (including age, hypertension, lone AF) failed to significantly predict response to AAD

35 es mellitus, or obstructive sleep apnea (ie, lone AF) undergoing ablation and 25 matched control subj

36 other cardiovascular disease or dysfunction (lone AF).

37 l enlargement and spontaneous AF, goats with lone AF, and patients with chronic AF.

38 Tc intervals was stronger for the outcome of lone AF, as evidenced by a hazard ratio of 2.32 (95% con

39 In a cohort of patients with early-onset lone AF, we identified a high prevalence of SCN5A mutati

40 ne AF is associated with substantial risk of lone AF, with the strongest risks associated with young

41 strongest with respect to the development of lone AF.

42 developed AF, of whom 1,467 (14%) developed lone AF.

43 actors may play a role in the development of lone AF.

44 CNN3), that associate with either typical or lone AF.

45 least 2 first-degree relatives affected with lone AF.

46 s of at least certain types of patients with lone AF.

47 nistic overlap between LQTS3 and early-onset lone AF.

48 -up, 9,507 persons were identified as having lone AF.

49 ere followed up until the first diagnosis of lone AF.

50 s sequenced in 192 patients with early-onset lone AF.

51 sk of recurrent arrhythmia after ablation of lone AF.

52 identify common genetic variants underlying lone AF.

53 sms for AF in patients categorized as having lone AF.

54 dy of 345 patients initially diagnosed with "lone" AF between 1992 and 2007.

55 (2)DS(2)-VASc score reliably identified the "lone" AF patients who were at "truly low risk" for throm

56 risk stratification schemes in a cohort of "lone" AF patients with a 12-year follow-up.

57 F ablation only or AF+AFL ablation than with lone AFL ablation.

58 growth modes are achieved which result in a lone Ag structure emanating from a single (100) Au facet

59 ne-rich superfamily, but the position of the lone alpha helix differs due to interactions with the un

60 cated rare variants in 25 different genes in lone and familial atrial fibrillation (AF) using linkage

61 d whether an individual's risk of developing lone atrial fibrillation (AF) before age 60 years is ass

62 Lone atrial fibrillation (AF) may reflect a subclinical

63 BNP) is abnormally elevated in patients with lone atrial fibrillation (AF).

64 n=34), persistent (n=37), or permanent (n=5) lone atrial fibrillation at initial diagnosis met inclus

65 perimental study investigating patients with lone atrial fibrillation identified six novel mutations

66 The long-term natural history of lone atrial fibrillation is unknown.

67 Overall survival of the 76 patients with lone atrial fibrillation was 92% and 68% at 15 and 30 ye

68 The historical origin of the term "lone atrial fibrillation" (AF) predates by 60 years our

69 helpers produced more direct offspring than lone breeders, some while still subordinate but most aft

70 that promotes cell-cell interaction, limits lone cell movement, and slows swarm expansion.

71 otably more resistant to collagenolysis than lone collagen monomers.

72 perons) and CO(2) fixation (cbbLS), a third, lone copy of amoC (amoC(3)), and two representative hous

73 Cross-clamp time in the lone Cox-Maze procedure patients was 44 +/- 21 minutes,

74 ited in SSA) by chemical modification of the lone cysteine residue (Cys(10)) through mixed disulfide

75 Come), including a lone dentist, Laudumiey, surgeon-dentist to His Majesty,

76 The best lone disease predictor was Concavity Min (Marfan syndrom

77 The lone, divergent copy of amoC (amoC(3)) was expressed onl

78 In Arabidopsis, SPIKE1 (SPK1) is the lone DOCK family GEF.

79 agment corresponding to cleavage between the lone double bond and the carboxyl group and defining the

80 boxyl group and defining the position of the lone double bond.

81 n to be significantly more emissive than the lone dye, with a concentration-independent emission and

82 explained by assuming the association of the lone electron pair at sulfur to the Co-alkyne complexes.

83 r is of the conventional type, involving the lone electron pair of an oxygen donor, the latter is per

84 ics and OP identification confirmed that the lone electron pair of the amine-N is the predominant sit

85 s along the short axis and bonds through the lone electron pair of the nitrogen atom instead, and bot

86 different types of hyperconjugation between lone electron pairs of nitrogen atoms and sigma*C-N orbi

87 n-shell structure with a single bond and two lone electrons on each terminal atom (biradical).

88 d in small airway epithelium of smokers with lone emphysema and normal spirometry (n = 13, p < 0.01)

89 M >/= 5.5 have not been identified, with the lone exception of an M = 6.9 quake remotely triggered by

90 The lone factor for twinning dependent on grain size is the

91 Glycine is the lone fast neurotransmitter for which a metabotropic path

92 Lone females or males suffer similar rates of predation,

93 tion in atrial fibrillation, with studies in lone forms of the arrhythmia suggesting a traditional mo

94 tallographic data reveal arginine 183 as the lone H-bond-donating residue in the distal pocket.

95 Stimulation of the lone inhibitory FgammacR, FcgammaRIIB, also has adverse

96 r open time, and less InsP3 sensitivity than lone InsP3Rs.

97 ion of methylation in the heart, enriched in lone intergenic CpGs and depleted from CpG islands aroun

98 strate methyl contact shifts that places the lone iron pi-spin in the d(xz) orbital, rather than the

99 nd between males in long-term pair-bonds and lone males in areas including the nucleus accumbens, ven

100 The five lone males were re-scanned 48 h after pairing with a fem

101 a lesion of the prefrontal cortex) and five lone males were scanned.

102 -ARP2/3 pathway and together they define the lone mechanism for ARP2/3 activation.

103 DAGK) and undecaprenol kinase (UDPK) are the lone members of a family of multispan membrane enzymes t

104 This lone N-terminal tyrosine, however, is not required for w

105 s preferentially the twix hydrogens over the lone ones.

106 ants, in 9 genes, previously associated with lone or familial AF.

107 Rare variants previously implicated in lone or familial forms of AF present on the exome chip a

108 --> sigma* orbital delocalization between a lone pair (n) of a (thio)amide donor and the antibonding

109 ong HB, involves charge transfer between the lone pair (n) of Y, and the sigma* orbital of E-X as emp

110 low-lying dark state, involving the nitrogen lone pair (nNpi*), does significantly participate in the

111 rt-butyl group (sterically driven) and the N-lone pair (stereoelectronically driven).

112 pair donors, and the sigma*Xe-O orbitals are lone pair acceptors.

113 ergy difference between the frontier silicon lone pair and 3p orbitals.

114 d the electron-rich character of the carbene lone pair and also enhanced the CO(2) binding energy to

115 The interactions between an oxygen lone pair and an aromatic ring are attractive at van der

116 bilizing interaction between a nitrogen atom lone pair and an aromatic sulfur system (nN --> sigma*S-

117 ive study of the interactions between oxygen lone pair and aromatic rings.

118 r conformations with H antiperiplanar to the lone pair and D gauche.

119 an be used to raise the energy of the anchor lone pair and increase conductance.

120 directional dipoles of the endocyclic oxygen lone pair and of the highly polar axial Si-O bond.

121 onic effects (repulsion between the nitrogen lone pair and polarized C-Pd bond at C2-/C6-positions an

122 icated weak interaction between the nitrogen lone pair and proximal radical center in angular 5,6-die

123 cceptor substituents delocalize the nitrogen lone pair and stabilize the reactant state of 2-azetines

124 is depends on the dihedral angle between the lone pair and the C-H, a further consequence is a prefer

125 favorable overlap between the diffuse ligand lone pair and the primarily 7s/6d acceptor orbitals on U

126 lized by an interaction between the nitrogen lone pair and the vacant pi* orbital.

127 ning pH-responsive species, namely, an amine lone pair as the electron donor and a cationic ring of m

128 d molecular orbital (HOMO)-with a Ge-centred lone pair as the HOMO-1.

129 ve electron-sharing bonds R-E-R and only one lone pair at atom E.

130 The sigma-lone pair at the divalent carbon is the HOMO of these sp

131 ly, resulting from the delocalization of the lone pair at the nucleophilic center, a sigma CC bond, a

132 of the bonding was attributed to the reduced lone pair bond weakening effect, LPBWE, upon substitutio

133 bond with one water molecule at the nitrogen lone pair but only weakly N-H donating hydrogen bonds.

134 ereochemical activity due to the Sn(2+) s(2) lone pair causes a crystallographically hidden, locally

135 plexes, increasing the energy of the N(beta) lone pair decreases the ligand-to-metal CT (LMCT) energy

136 educing anomeric power by diminishing either lone pair donor ability (solvent) or antibonding accepto

137 en atoms in these cases are valence electron lone pair donors, and the sigma*Xe-O orbitals are lone p

138 confirmation of unusual features including a lone pair effect on (3)J(PH), the negative coupling cons

139 ontrary to common wisdom, fluorine is a good lone pair electron donor toward geminal sigma bonds.

140 meanwhile, it is enhanced by the strength of lone pair electrons coordination with the heme iron.

141 Here we make use of the lone pair electrons found in most of 2D metal chalcogeni

142 The key role played by lone pair electrons in achieving this high efficiency in

143 ivation energies due to participation of the lone pair electrons in the cyclization reactions.

144 e consistent with donation from the nitrogen lone pair electrons into the carbonyl pi* orbital.

145 The lone pair electrons of an ortho-triazolo substituent pla

146 teract with the gold nanofingers through the lone pair electrons of pyridyl nitrogens, not through de

147 d to be dependent on the availability of the lone pair electrons of the pendant groups.

148 Stable s(2) lone pair electrons on heavy main-group elements in thei

149 l, and the excitation primarily derives from lone pair electrons on the oxygen atom of water molecule

150 tributed to sigma-donation of the isocyanide lone pair electrons to the surface.

151 tween the radical alpha-C-H and the nitrogen lone pair followed by hydrogen abstraction within the co

152 the coordination geometry selected to favor lone pair formation on Pb(2+) ions and electrostatically

153 hown by quantum mechanical calculations, its lone pair having an energy significantly lower than that

154 and manifold originating from the hybridized lone pair in nitrogen orbitals of the Phthalocyanine rin

155 addition, we analyze the role of a carbanion lone pair in the rearrangement step, concluding that it

156 in the acylated catalyst and an appropriate lone pair in the substrate.

157 For the amine/Au contact, the nitrogen lone pair interaction with the gold results in a hybrid

158 ron-donor amine moiety converts the nitrogen lone pair into a sigma bond and the HOMO into a lower-ly

159 int energy by delocalization of the nitrogen lone pair into the C-H antibonding orbital.

160 t is due to delocalization of the phosphorus lone pair into the vacant p-orbital at germanium.

161 f the amine is proposed to occur faster than lone pair inversion of the amine.

162 is larger for 2 than for 1, whereas no extra lone pair is available in 2.

163 stituent and inward rotation of the nitrogen lone pair is preferred.

164 iated with a dominant donation from a p-type lone pair localized on one of two iodine atoms, the sigm

165 In possessing a lone pair of electrons and an accessible vacant orbital,

166 MO is a Ge-C bonding combination between the lone pair of electrons on the germanium atom and the C-N

167 The lone pair of electrons on the silicon atom of (carbene)S

168 redominantly by the presence of the Sn 5s(2) lone pair of electrons rather than the steric or electro

169 , which show that pyridinic defects retain a lone pair of electrons that are capable of binding CO2.

170 The donor oxygen donates a lone pair of electrons to the sigma* orbital of acceptor

171 d involve two ammonia molecules in which the lone pair of one NH(3) becomes associated with the empty

172 omplexes in which gold(I) coordinates to the lone pair of oxygen.

173 ive interaction of the trityl group with the lone pair of the enamine nitrogen is supported by the fi

174 n involves coordination of the SmI(2) to the lone pair of the nitrile nitrogen followed by an inner s

175 e of the reagent for substrates in which the lone pair of the nitrogen is electron releasing and thus

176 i))-sigma*CC interactions between the p-type lone pair of the terminal oxygen and adjacent unfilled C

177 -donation is better represented by an oxygen lone pair on flat sites, whereas it is delocalized on bo

178 4(-) oxygens, typical of a sterically active lone pair on Pb(II).

179 state of the drug shows a highly delocalized lone pair on the amine nitrogen of the melphalan, which

180 ansfer (ET) via nucleophilic attack by its N lone pair on the C of CO(2), and finally (c) proton tran

181 tead: the nucleophilic attack of the carbene lone pair on the imino nitrogen (pathway "a") or on the

182 calcium ions electrostatically stabilize the lone pair on the nitrogen atom that forms during the iso

183 calculations revealed that the stereoactive lone pair on the Pb(2+) cation is critical to producing

184 he double substitution, R155K/D168A, and the lone pair on the quinoxaline in grazoprevir.

185 ndent interaction between sulfur or selenium lone pair orbitals and sigma-orbitals, especially Si-Si

186 c potential minimum, observed at the carbene lone pair region of NHC (V(min1)) as well as at the carb

187 We show that lone pair stereochemical activity due to the Sn(2+) s(2)

188 ic potential minimum (V(min)) at the carbene lone pair suggested that annelation of heterocycle to a

189 rotations, and the propensity for the Pb(2+) lone pair to express its stereochemistry.

190 d relatively weak pi donation from the amide lone pair to platinum and supports a 14-electron assignm

191 rbital, with back-donation from the Ge or Sn lone pair to the H(2) sigma* orbital.

192 These calculations reveal that the lone pair type orbitals on the halogen-bonded anion gove

193 es bind to the metal substrate through the O-lone pair while making H-bonds with neighboring molecule

194 rise from electron repulsion of the nitrogen lone pair with electron density from the butadiene moiet

195 y increasing orbital overlap of the nitrogen lone pair with the incipient oxyallyl cation, is coupled

196 he sigma-hole on bromobenzene (BrPh) and the lone pair(s) of Pz significantly lowers the energies of

197 teraction between K(+), the tryptamine NH(2) lone pair, and the indole ring in K(+)(Tryp) favors the

198 e radical prefers to align with the nitrogen lone pair, and this interaction leads to an A(1,3)-strai

199 anism involves Cu(II) binding to the amide N lone pair, decoupling it from >N-C horizontal lineO reso

200 eme pocket polarity and the accessibility of lone pair, Lewis base donors.

201 and various types of halogen bond acceptors (lone pair, pi and sigma bonds).

202 ation energy (E(aroma)), strength of carbene lone pair, proton affinity, and CuCl binding energy.

203 environment attributable to its stereoactive lone pair, which was qualitatively described by pseudopo

204 For cases where steric, lone pair-cation, and cation-pi effects have been invoke

205 Electronegative but lone pair-donating groups NR2, OR, and F stabilize the c

206 by the competition between ferroelectric Bi lone pair-driven A site displacement, chemical order of

207 nt pyrazine and quinoxaline units involves a lone pair-heteroarene interaction which is much stronger

208 witterionic transition states facilitated by lone pair-LUMO interactions between the migrating R grou

209 this selectivity reversal is the result of a lone pair-pi interaction between the substrate ligated b

210 PYCH dihedral angle theta (Y = O, N, C) and lone pair-PYC dihedral angle omega shows similar theta,o

211 izontal lineN(alpha) pi bond and the N(beta) lone pair.

212 a dark state (nOpi*) involving the carbonyl lone pair.

213 lly reactive boron p-orbital and/or nitrogen lone pair.

214 +) ion complexes that contain a stereoactive lone pair.

215 bond anti-periplanar relative to the carbene lone pair.

216 eactivity owing to the presence of the Nbeta lone pair.

217 t-enhanced reactivity of nucleophiles with a lone-pair adjacent to the attacking center-was recently

218 condary orbital effect role for the nitrogen lone-pair and hence the process is likely neither purely

219 ymmetry coordination environments favored by lone-pair cations.

220 demonstrates the large non-Karplus effect of lone-pair conformation on vicinal phosphorus-hydrogen co

221 cophore for nAChRs and suggest that nitrogen lone-pair directionality and steric factors may be impor

222 rom Fe(III)-N-O bending, which is induced by lone-pair donation to the N(NO) atom.

223 absence of a net charge, covalent bonds, or lone-pair donor groups.

224 he shift to be associated with the loss of a lone-pair donor interaction from the distal histidine th

225 ctric phase transition ascribed to the 6s(2) lone-pair effects of Bi(3+) at around 135 K, and a long-

226 ransfer transition involving donation of the lone-pair electron density on both Sb(III) and Sn(II) to

227 However, for substituents that stabilize by lone-pair electron donation, such as N or O centers, the

228 .82-0.85) and the NBO energy of the nitrogen lone-pair electrons of amines (N = 59, R(2) values of 0.

229 nergy, occupied orbitals associated with the lone-pair electrons on oxygen.

230 ressure-induced delocalization of non-bonded lone-pair electrons to sp(3)d(2) hybridization in two-di

231 ond acidity and basicity, polarizability and lone-pair electrons.

232 with (n-1)d(10)ns(0), d(0), or stereoactive lone-pair electrons.

233 become competitive with the commonly favored lone-pair interaction whenever the carbonyl group carrie

234 e of distinctly coexisting weak covalent and lone-pair interactions, give rise to cooperative structu

235 lar bond critical points and the oxygen atom lone-pair locations are discussed.

236 volving an antibonding, b(1), combination of lone-pair MOs, occur in forming all (CO)(2n) molecules f

237 al disconnections-one involving the nitrogen lone-pair orbital and the other the carbonyl carbon of t

238 p and on the excitation energy of the oxygen lone-pair orbital.

239 an antibonding, b(1g) combination of carbon lone-pair orbitals in four CO molecules and the b(2g) an

240 and a natural population analysis of natural lone-pair orbitals on the donor atoms support the mechan

241 f the oxyallyl LUMO with the carbonyl pi and lone-pair orbitals, making this reaction "hemipseudoperi

242 Basicities are enhanced by the lone-pair possessing atoms on the substituents' arms sta

243 uilibrium because the ion is destabilized by lone-pair repulsion.

244 The associated lone-pair stabilization of the transition state by Ox pr

245 F --> Te chelate motif supported by a strong lone-pair(F) --> sigma*(Te-C) donor-acceptor interaction

246 he alpha-C-H sigma* orbital and a heteroatom lone-pair, increasing the C-H BDE and destabilizing the

247 ined rings, electronegative substituents, or lone-pair-bearing heteronuclei.

248 This is particularly problematic for lone-pair-rich, semiconducting materials, such as phase-

249 e opposed by the Pauli repulsion between the lone pairs (n) of O(i-1) and the bonding orbital (pi) of

250 z trajectory, involves delocalization of the lone pairs (n) of the oxygen (O(i-1)) of a peptide bond

251 z trajectory, involves delocalization of the lone pairs (n) of the oxygen (O(i-1)) of a peptide bond

252 to minimize interactions between the oxygen lone pairs and the pi electrons.

253 mides, and esters, and particularly when the lone pairs are engaged in orthogonal hydrogen bonding (h

254 spectrum despite the fact that the nitrogen lone pairs are held in a perpendicular geometry that wou

255 re divalent E(0) compounds which possess two lone pairs at E.

256 However, in the case of the phenolates, the lone pairs do interact significantly.

257 even electron-rich aromatic rings and oxygen lone pairs exhibit attractive interactions.

258 nerates the favored diastereomer, the oxygen lone pairs from the substituent are closer to the cation

259 ased on the simple orbital mixing model, the lone pairs in a pair of neutral directly connected heter

260 The exo directed lone pairs in the latter are able to scavenge Lewis acid

261 = -0.83) and reinforces the notion that the lone pairs in these phenols are not readily available fo

262 part, stabilized by delocalization of the N lone pairs into the vacant p-orbital at carbon (or a hea

263 gma orbital by two, adjacent, sp(2) nitrogen lone pairs of electrons and stabilization of the carbene

264 peculiar electronic structure of 3 with two lone pairs of electrons at the Ge atom.

265 al AsQ(3) units with stereochemically active lone pairs of electrons on arsenic.

266 ich include n-pi* interactions involving the lone pairs of electrons on water oxygen atoms and the an

267 nteraction of two donor protons with the two lone pairs of oxygen.

268 a weak electrostatic interaction between the lone pairs of the nitrogen atoms and the positively char

269 at a rearrangement to one sigma bond and two lone pairs on sulfur is usually more favorable.

270 ed to parallel alignment of the stereoactive lone pairs on the I(5+) cations.

271 The latter bears two highly localized lone pairs on the phosphorus atom due to the LSi horizon

272 fect at present is hyperconjugation from the lone pairs on the ring heteroatom to the antibonding orb

273 is of DFT calculations, to the twisting of N lone pairs out of conjugation with the carbonyl pi orbit

274 abilized by charge transfers from the N or O lone pairs to the quinone's pi* orbitals.

275 on produces electron-rich heterocycles (four lone pairs) and features homoatomic sigma-bond heterolys

276 o the aromatic pi-system via the chalcogen p lone pairs, and greater overlaps among these components

277 d with in-plane interactions and/or in-plane lone pairs, LP(n-) and LP(n+).

278 nto the chemical-bonding network, as well as lone pairs, of the prototypical PCM, Ge2 Sb2 Te5 (GST).

279 ridines that operate with hydrogen bonds and lone pairs, respectively.

280 Electronegative substituents with lone pairs, such as halogen and oxygen, thus appear to d

281 ly pairwise electronic behavior of bonds and lone pairs.

282 ixing of the orbitals occupied by the oxygen lone pairs.

283 is weakened by delocalization of the oxygen lone pairs.

284 ion between C-Si or C-Sn bonds and chalcogen lone pairs.

285 xist between electron-rich arenes and oxygen lone pairs.

286 sity comprised of the three valence electron lone pairs.

287 ergistic effect of two types of stereoactive lone-pairs on Sb(III) and Sn(II) is critical for the cha

288 NT binding ability in liquid compared to the lone PEGM surface and 3-fold higher TNT binding compared

289 tating the localization of the remaining two lone pi-electrons on each of the end atoms, therefore in

290 CAVI is the lone secreted CA and exists in both saliva and the gastr

291 obilities in transistors made with Te as the lone semiconductor or from Te-organic multilayer semicon

292 cell-to-cell transmission, viruses behave as lone soldiers.

293 ed by bacterial pathogens transmitted by the lone star tick (Amblyomma americanum).

294 as a new subgroup, the type IIL enzymes, for Lone strand DNA modification.

295 ed in paradigms that involve searching for a lone target in a cluttered array or natural scene.

296 in APH-1 serves as a scaffold, anchoring the lone transmembrane helix from nicastrin and supporting t

297 er the interaction of QCN with TbHK1, as the lone Trp residue (Trp-177) was quenched under all condit

298 TWA and MA when compared with patients with lone TWA (median, 37 [interquartile range, 26-61] versus

299 uilding design and access, communication and lone working, provision of equipment and consumables, an

300 In contrast, our results show that Dpo4, the lone Y-family DNA polymerase in S. solfataricus, can fai