ライフサイエンスコーパス: breaking of

1 energy and chemistry, involve the making or breaking of a bond between carbon, nitrogen and oxygen.

2 r different catalytic motifs to catalyze the breaking of a carbon-carbon bond in a nonnatural substra

3 response to a local perturbation such as the breaking of a chemical bond or the absorption of a photo

4 chemical and physical processes such as the breaking of a chemical bond or the vibrational motion of

5 ndeed, in contrast to the discrete case, the breaking of a continuous symmetry leads to the emergence

6 ooperative, which could be a function of the breaking of a critical interaction.

7 The translational symmetry breaking of a crystal at its surface may form two-dimens

8 ng between residues 216-225 that enables the breaking of a hydrogen bond in subsite S(3).

9 tners either (i) through thermally activated breaking of a hydrogen bond that creates a dangling hydr

10 r chiral inversion that does not require the breaking of a metal-sulfur bond at the metal-ligand inte

11 ibozyme-substrate complex that result in the breaking of a phosphodiester bond.

12 Breaking of a single tether caused a reproducible forwar

13 As the concentration is lowered, breaking of achiral symmetry in the director configurati

14 orque generation facilitates chiral symmetry breaking of actomyosin flows and drives organismal left-

15 s involving hydrocarbons (homolytic C-C bond breaking of alkanes, progressive insertions of triplet m

16 ence of the plastic phase which involved the breaking of all hydrogen bonds, and modeling of small cl

17 Blocking the formation, growth, and breaking of amyloid fibrils by synthetic nanosystems cou

18 The latter implies that a breaking of an existing hydrogen-bond network in homogen

19 transitions that the compounds induced: (i) breaking of an interaction between Tyr-223 and Arg-187 i

20 We find that the barrier crossing involves breaking of an interhelical hydrogen bond between helix5

21 The first stage corresponds to breaking of As-O bonds at the particle surface, and the

22 single walker, which require the making and breaking of As-S bonds, and occur in aqueous solution at

23 rane-associated polarity crescent defined by BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) and

24 In Arabidopsis, BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) is

25 The BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) pro

26 In the Arabidopsis stomatal lineage, BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL) reg

27 A second polarity marker, BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE (BASL), al

28 vior of a tissue cell polarity protein BASL (BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE) in the si

29 pic expression of the stomatal protein BASL (BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE) reveals a

30 The polar localization of POLAR requires BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE.

31 he transformation are proposed which require breaking of at least one in six of the covalent bonds th

32 he intrinsic strength that governs a uniform breaking of atomic bonds in perfect graphene.

33 Drawing parallels to the symmetry breaking of atomic orbitals used to explain the periodic

34 n a structural rearrangement of the loop and breaking of autoinhibitory interactions.

35 ich could have important implications on the breaking of B cell central tolerance in autoimmunity.

36 the patient-oncologist encounter during the breaking of bad news, comprising essential aspects of th

37 The breaking of bilateral symmetry in most vertebrates is cr

38 computational model tracks the formation and breaking of bonds between platelets and treats the throm

39 and electronics on the gradual weakening and breaking of bonds was studied by investigating bridgehea

40 etal complexes that result in the making and breaking of C-N, C-O and C-S bonds via fundamental organ

41 agnetic moments from the c-axis leads to the breaking of C3 rotation symmetry, and thus, a small band

42 hanges in Fe-carbide covalency or stretching/breaking of carbide-Fe bonds.

43 In summary, symmetry breaking of cell contractility on a soft collagen gel pr

44 imately 0.25 eV and intra-unit cell symmetry breaking of charge distribution in individual alpha-RuCl

45 allows us to observe with clear evidence the breaking of chemical bonds between the ligands and the C

46 he surface orientation and the formation and breaking of chemical bonds.

47 atic and twist-bend nematic with spontaneous breaking of chiral symmetry is crucially dependent on th

48 emerging as a result of spontaneous symmetry breaking of clock/counterclockwise rotation of self-asse

49 These factors disfavor the breaking of conjugation by oxa-conjugate addition.

50 of superconducting qubits is affected by the breaking of Cooper pairs of electrons(4-6).

51 particles-the excitations resulting from the breaking of Cooper pairs-should exist.

52 The breaking of crystal symmetry in TCIs is predicted to imp

53 Selective breaking of degenerate energy levels is a well-known too

54 out external concentrations necessitates the breaking of detailed balance and consumption of energy,

55 With a model, we show how the breaking of detailed balance can also be quantified in s

56 robes to quantify entropy production and the breaking of detailed balance, little is known about the

57 imental observations of spontaneous symmetry breaking of dissipative optical solitons.

58 s thought to be related to the formation and breaking of disulfide bonds.

59 e inputs from the environment to promote the breaking of dormancy.

60 Breaking of either interaction triggers slow inactivatio

61 oscopic split-phase interface (MSPI) by dual breaking of electron cloud and space structure symmetry

62 ress has been made in understanding both the breaking of embryonic L-R symmetry and how the Nodal-Pit

63 nhanced germination, implicating gerS in the breaking of endospore dormancy in vivo.

64 emonstrated a strong capability for C-C bond breaking of ethanol than pure Pt and intermetallic Pt/Sn

65 rupture propagation could be promoted by the breaking of fault asperities in a cascading sequence.

66 est that the imaged subevents are due to the breaking of fault asperities-stronger spots or pins on t

67 weak antilocalization signatures as well as breaking of fourfold spin-valley symmetry, consistent wi

68 actor exceeds alpha(C), spontaneous symmetry breaking of fraction of cooperators presents itself betw

69 phase transitions occurs by the spontaneous breaking of fundamental symmetries.

70 ion in SHAM + CN, potentiation (i.e. domancy-breaking) of germination occurs.

71 paradigmatic system in which the making and breaking of H-bonds in a highly anharmonic potential ene

72 sufficient to observe repeated formation and breaking of helical structure, which we found to occur o

73 on, in an SW-defective (5,5) BNNT results in breaking of hydrogen bonding with neighboring water mole

74 in forced unfolding in TI I27 is largely the breaking of hydrogen bonds and hydrophobic interactions

75 Specifically, the focus is on breaking of hydrogen bonds following excitation of an in

76 consistent with the view that formation and breaking of hydrogen bonds in such water chains is a lim

77 water molecule clusters and the weakening or breaking of hydrogen bonds within clusters is introduced

78 ich is characterized by first stretching and breaking of hydrogen bonds, followed by deformation of c

79 e two main responsible IgG receptors for the breaking of immune tolerance of microglia.

80 Autoimmunity results from the breaking of immune tolerance, leading to inflammation an

81 of perpendicular magnetization requires the breaking of in-plane symmetry, which can be artificially

82 gistic effects of the Si:-->Ni moiety in the breaking of incredibly strong B-O bonds.

83 thelial NF-kappaB activation orchestrate the breaking of inhalational tolerance and allergic antigen

84 ore, our data suggest that the formation and breaking of inter- and intradomain salt bridges control

85 g of FN-III(10) A and B-strands and precedes breaking of inter-strand hydrogen bonds between F and G-

86 aled that covalent linkage leads to symmetry breaking of interfacial interactions.

87 and global climate, largely results from the breaking of internal gravity waves--disturbances propaga

88 A primary driver of deep-ocean mixing is breaking of internal tides generated via interactions of

89 trary, the unfolding process starts with the breaking of interstrand hydrogen bonds.

90 Thus, the breaking of intersubunit contacts occurs on a time scale

91 the backbone amides that contributes to the breaking of intrabackbone hydrogen bonds.

92 ch necessarily involves the energy intensive breaking of intramolecular hydrogen bonds, provides a ph

93 ey to lattice instability, which governs the breaking of inversion symmetry and induces ferroelectric

94 Engineering and enhancing the breaking of inversion symmetry in solids-that is, allowi

95 ucture, with ferroelectricity resulting from breaking of inversion symmetry in the latter.

96 rmolecular ion hopping through formation and breaking of ion-associations involving four polymerized

97 ation of iridium hydride, accompanied by the breaking of iridium-support bonds.

98 tivistic electrons are generated through the breaking of large-amplitude relativistic plasma waves cr

99 unrecognized function of PCP in the initial breaking of lateral symmetry.

100 cells along the anterior-posterior axis for breaking of left-right symmetry.

101 These characteristics include breaking of local particle-hole symmetry, a diameter nea

102 , a photon Devil's staircase, induced by the breaking of long-range translation symmetry, can emerge.

103 xing, harmonic beam steering or shaping, and breaking of Lorentz reciprocity.

104 ntified here: the intentional and systematic breaking of lower limbs.

105 gh-resistance domain walls, arising from the breaking of magnetic point group symmetry strongly coupl

106 criterion identifies a new kind of symmetry breaking--of magnetic translations--where nonvanishing c

107 ation of sulfur from the thiol complexes via breaking of mercury-sulfur bonds as in an alkylation rea

108 and acetyl species indeed helps the C-O bond breaking of methoxy species and therefore the direct eth

109 ifically of tau proteins leads to mechanical breaking of microtubules at high strain rates, whereas e

110 nodules to bands may result from a symmetry breaking of mineral dissolution and precipitation trigge

111 edge that pivots to enforce rapid making and breaking of miRNA:target base pairs in the 3' half of th

112 twisting energy, resulting in a spontaneous breaking of mirror symmetry; the chiral twisted state pe

113 age traces revealed details of evolution and breaking of molecular junctions.

114 Ammonia oxidation requires not only the breaking of multiple strong N-H bonds but also controlle

115 rmalities of the myelin sheaths included the breaking of myelin at several locations, a splitting and

116 ation of unfolding of disordered domains and breaking of native cross-links at different stages of st

117 only by promoting the formation but also the breaking of Nepsilon-(gamma-glutamyl)lysine isopeptides.

118 ecifically, we demonstrate that the symmetry breaking of network connectivity constitutes a timescale

119 resolution permits direct observation of the breaking of nuclear spin degeneracy for the 1S0 and 3P0

120 olled protocols, and simultaneous making and breaking of olefinic moieties.

121 oses the catalytic loop concertedly with the breaking of one of the two C-O bonds of CO2 and with pro

122 ting that mate change by pair members and/or breaking of pair bonds by unmated individuals is more fr

123 T phases is characterized by the spontaneous breaking of parity symmetry and the disappearance of per

124 ectric dipole moments in molecules require a breaking of parity symmetry.

125 Such a process is universal with the breaking of parity-inversion and time-reversal symmetry

126 for diversity and spatial-temporal symmetry breaking of pattern formation.

127 iated killing of endothelial cells indicated breaking of peripheral immune tolerance against this sel

128 single IV dose up to 15 mg/kg, resulting in breaking of peripheral immune tolerance to self-tissues

129 Breaking of peripheral T-cell tolerance to allergens can

130 Chiral symmetry breaking of phonons plays an essential role in emergent

131 lated electron-hole pair diagrams illustrate breaking of pi-conjugation in three-arm dendrimers due t

132 larization control, the spontaneous symmetry breaking of polarization states could be used for polari

133 tes and catalyzes hydride transfer, enabling breaking of polyethylene C-C bonds and forming C-C bonds

134 establish a unified picture of the symmetry breaking of polymethine dyes in fluid solution.

135 he ligand is undocked from the binding site, breaking of protein-disaccharide H-bonds takes place in

136 The selective breaking of PT symmetry can be used to systematically en

137 r mechanisms governing the establishment and breaking of radial symmetry at the gynoecium apex (style

138 al side of the embryo, providing the initial breaking of radial symmetry.

139 DCvC relies on the reversible formation and breaking of rather strong covalent bonding within molecu

140 which relies on the reversible formation and breaking of rather strong covalent bonds within molecule

141 essive numbers illustrate why the making and breaking of RBCs is at the heart of iron physiology, pro

142 rute force attack fails to ensure the timely breaking of robust encryption.

143 representing intra-unit-cell nematicity: the breaking of rotational symmetry by the electronic struct

144 Electronic nematicity, the spontaneous breaking of rotational symmetry, has emerged as a key in

145 Nematicity, spontaneous breaking of rotational symmetry, is a ubiquitous phenome

146 In many biological cases, the breaking of sacrificial bonds has been found to be rever

147 Furthermore, GVHD results in the breaking of self tolerance, resulting in the emergence o

148 sing an endogenous tumor antigen resulted in breaking of self-tolerance and long-term survival.

149 These findings indicate that breaking of self-tolerance in mHgIA requires signaling v

150 Then, helix packing is destabilized by breaking of several side chains involved in hydrogen bon

151 h parameters that typically lead to symmetry breaking of signalling states between neighbouring cells

152 d that this barrier is due to the concurrent breaking of six interstrand hydrogen bonds (H-bonds) bet

153 field, which is below the threshold for bond breaking of solvent molecules, leads to significant orde

154 An example is the breaking of spatial translational symmetry, which underl

155 Proteases are enzymes that catalyse the breaking of specific peptide bonds in proteins and polyp

156 d radiative transfer, which reveals that the breaking of spherical symmetry is a critical factor in d

157 multiferroics induced by inversion-symmetry-breaking of spin order.

158 After breaking of spore dormancy, Ctr6 localizes to the vacuol

159 mays) causes significant yield losses due to breaking of stalk tissue below the ear node before harve

160 a strong magnetic field exhibits spontaneous breaking of SU(4) symmetry.

161 The breaking of sublattice symmetry in doped graphene can ha

162 e propose that the origin of this gap is the breaking of sublattice symmetry owing to the graphene-su

163 nother class of metamaterials that shows the breaking of 'supersymmetry'(23,24) causing only antisoli

164 is underscores the importance of spontaneous breaking of symmetries, Fermi surface reconstruction, an

165 ctricity in any material through appropriate breaking of symmetry at surfaces and artificial nanostru

166 Megf8(C193R) mouse mutants show normal breaking of symmetry at the node, but Nodal signaling fa

167 Spontaneous breaking of symmetry in liquid crystal (LC) films often

168 nvolves cilia as essential components in the breaking of symmetry, an asymmetric signaling cascade, a

169 body interactions often induce a spontaneous breaking of symmetry.

170 ly narrow pH range; they exhibit spontaneous breaking of symmetry; and homochirality emerges through

171 ass starch of degradation processes also the breaking of the 1-6 glycosidic bonds, limiting oxidation

172 Most importantly, the symmetry breaking of the 4-MPBA molecule upon fructose binding le

173 es within a MEL zeolite framework allows the breaking of the above model.

174 Breaking of the alpha-carbonyl C-C bond in proline appea

175 Elongator induces symmetry breaking of the anaphase midzone by selectively stabiliz

176 ucture and dynamics that take place with the breaking of the Asp-His hydrogen bond in the catalytic t

177 The explicit breaking of the axial symmetry by quantum fluctuations g

178 rvature and is found to be associated with a breaking of the axisymmetry of the membrane.

179 and tertiary amines by direct photochemical breaking of the benzylic C-N bond.

180 Finally, we reveal that the breaking of the bilayer topology is accompanied by the n

181 tion, in the absence of enzyme, involves the breaking of the C O bond facilitated by intramolecular p

182 KIE study revealed that the breaking of the C-H bond of alcohol might be the rate-li

183 of 1.04 +/- 0.01 was measured, showing that breaking of the C-S bond in the substrate Me-S-CoM is th

184 le bond toward C1, resulting in preferential breaking of the C1-C3 bond.

185 Unlike in C60, in doped fullerenes, the breaking of the cage spherical symmetry makes super atom

186 ayer atomic registry results in both a local breaking of the carbon sublattice symmetry and a long-ra

187 rect evidence for the time-reversal symmetry breaking of the charge order remains elusive.

188 a subtle quantum phenomenon that denotes the breaking of the classical chiral symmetry by quantum flu

189 Breaking of the closed octamer symmetry may be a common

190 f Rho primarily proceeds through spontaneous breaking of the covalent linkage between opsin and 11-ci

191 Such breaking of the cubic symmetry can only be ascribed to t

192 Breaking of the cubic symmetry in the Fe film deposited

193 glutamate is due to two motions: Spontaneous breaking of the D1 dimer interface and hyperextension of

194 nsistent with the outward rotation of H6 and breaking of the dark-state Glu134(3.49)-Arg135(3.50)-Glu

195 ation to the In(III) center, and concomitant breaking of the dimer into monomeric porphyrin species,

196 This was assigned mainly to the breaking of the direct hydrogen bonds between the alpha

197 Breaking of the DNA-RNA polymerase-mRNA-ribosome-membran

198 The mechanical breaking of the donor-acceptor interactions responsible

199 The aggregation occurs via symmetry breaking of the enantiopure intrinsically C2-symmetric m

200 n state, the rate-determining step, involves breaking of the exocyclic P-O bond where a metal-ligated

201 embrane and axoneme alterations, followed by breaking of the flagellar membrane connected to the tryp

202 ffective Meissner effect without requiring a breaking of the gauge symmetry.

203 te is stabilized by lithium-induced symmetry breaking of the H phase MoS(2).

204 es trans-cis isomerization, which results in breaking of the H-bond between Glu46 and the chromophore

205 However, the breaking of the H-bond between strands A' and G needs to

206 that such mutations result in the transient breaking of the helix at the site of mutation but with n

207 Rotational symmetry breaking of the host crystal in the form of electronic n

208 rovides a potential molecular mechanism: the breaking of the hydrogen bond between the side chains of

209 ogresses, we find a sequential weakening and breaking of the hydrogen bonds between the ATP molecule

210 This activity profile and the breaking of the hydrogen-bonding chain at the active sit

211 During vertebrate embryo development, the breaking of the initial bilateral symmetry is translated

212 ental confirmation of such a BCD induced via breaking of the interfacial symmetry remains elusive.

213 CB2 binding pocket is sufficient to trigger breaking of the intracellular TMH3/6 ionic lock and the

214 ucial step for the complex formation was the breaking of the intramolecular hydrogen bond in urea der

215 rmational switches in beta(2)AR, namely, the breaking of the ionic lock between R131(3.50) at the int

216 odopsin and other class A GPCRs, namely, the breaking of the ionic lock between R135(3.50) at the int

217 typal model, rhodopsin, such as the apparent breaking of the ionic lock that stabilizes the inactive

218 idized state, which results in the transient breaking of the iron-methionine-sulfur bond and sufficie

219 morphological changes are caused by symmetry breaking of the irreducible building blocks, with the fo

220 y more advanced in the transition state than breaking of the isoxazolyl N-O bond.

221 Here we present a study of local symmetry breaking of the lattice structure on the picosecond time

222 ing-dependent three-fold rotational-symmetry breaking of the local density of states in TBG, with the

223 ectedly large flexoelectric response exhibit breaking of the macroscopic centric symmetry through inh

224 rt effect is mainly governed by the symmetry breaking of the material systems and is gaining extensiv

225 tice scattering are intertwined resulting in breaking of the Matthiessen's rule with increasing EES.

226 bly and those where axons are injured due to breaking of the microtubules.

227 p (>C=NH), most likely to MnB, is coupled to breaking of the MnB-(mu-H2O) bond, forming a terminal aq

228 effects within the microchannel and not from breaking of the nematic ordering.

229 simulations reveal the spontaneous symmetry breaking of the Ni coordination environment after Li ext

230 reaction coordinates of the reaction are the breaking of the O-O bond of H2O2 and the formation of th

231 y acids or H(2) O(2) : reactions that entail breaking of the O-O bond to form a Fe(V) =O fragment.

232 rocenyl units and the imine pai system since breaking of the orbital symmetry results in allowed tran

233 ization into a diamond lattice, implying the breaking of the original chemical bonds.

234 r equilibrated SMO complex exhibits complete breaking of the pi-cation interaction between R451(6.32)

235 ensities just above a threshold required for breaking of the plasma wave.

236 Due to the intrinsic symmetry breaking of the process, the concept can be used to gene

237 Higgs mechanism, i.e., spontaneous symmetry breaking of the quantum vacuum, is a cross-disciplinary

238 -entry pathway, which involves formation and breaking of the salt bridge between side chains of Arg(8

239 is that this large dipole moment drives the breaking of the salt bridges between the two monomer sub

240 property of the interface that leads to the breaking of the scaling relations.

241 onal Theory simulations trace changes in the breaking of the scaling relationship for the Tafel HER m

242 ation of a trigonal intermediate and then by breaking of the scissile bond between the beta- and gamm

243 t enter the binding pocket and assist in the breaking of the shielded hydrogen bonds.

244 opening at the Fermi level and an additional breaking of the six-fold rotational symmetry, which pers

245 duced by C(2) symmetry and z-mirror symmetry breaking of the slanted nanograting, STOV is generated t

246 r(2)O(7)/Dy(2)Ti(2)O(7) heterostructure, the breaking of the spin-ice rule in insulating Dy(2)Ti(2)O(

247 wrinkle-to-crumple transition marks symmetry-breaking of the stress in highly bendable sheets.

248 I copper species that appears results from a breaking of the strong antiferromagnetic coupling of the

249 place as the arrival of MPT(+) triggers the breaking of the strong Fe-H(delta-)...H(delta+)-O dihydr

250 es is "anticorrelated" in the sense that the breaking of the T252-G248 hydrogen bond is concurrent wi

251 The sequential breaking of the tandem hydrophobic constrictions on the

252 al MTs detach from MT bundles via sequential breaking of the tau-tau bonds.

253 hus a macroscopic witness of the progressive breaking of the tetrahedral hydrogen bond network that m

254 ing magnetic anisotropy, consistent with the breaking of the threefold valley degeneracy.

255 changes and cannot be fully accounted for by breaking of the top contact, we argue that the cause is

256 tilted outward at the tip end, leading to a breaking of the trimerous symmetry and distortion at a r

257 -dependent DFT calculations predict that the breaking of the two strong Ru-O bonds and the formation

258 The spinners emerge via spontaneous breaking of the uniaxial symmetry of the energizing magn

259 lifted degeneracy, associated with symmetry-breaking of the water environment.

260 r role except in the case of gold, for which breaking of the weak Au-S bond that tethers the monolaye

261 he 4f Wyckoff sites of P63/mmc) layers, with breaking of the weakly bonded Al-Ti4f.

262 sequence of transitions as distinct symmetry breakings of the shape and the stress field.

263 Conversely, the corresponding sequential breaking of these bonds is driven by rotation of the sha

264 Designed symmetry breaking of these giant tetrahedra introduces precise po

265 ies and the intrinsic orientational symmetry-breaking of these materials gives rise to a host of intr

266 e failure of conscious access results in the breaking of this chain and a subsequent slow decay of th

267 Breaking of this filament during cell division was obser

268 We suggest that the breaking of this interaction may be the rate-determining

269 ransient (a)cyclic oxocarbenium cations, the breaking of three single C(sp(3))-O bonds, and the forma

270 Breaking of Ti-O bonds is found to have little effect on

271 The breaking of time reversal symmetry (TRS) in three-dimens

272 The breaking of time-reversal symmetry (TRS) in topological

273 es, the Kelvin and Yanai modes, owing to the breaking of time-reversal symmetry by Earth's rotation.

274 this fluctuation corresponds to spontaneous breaking of time-reversal symmetry in the system.

275 rength of the deformations, temperature, and breaking of time-reversal symmetry were also investigate

276 owing to their unusual lattice geometry and breaking of time-reversal symmetry(14,15).

277 Mathematically they require breaking of time-reversal symmetry, typically achieved u

278 t application of external magnetic fields or breaking of time-reversal symmetry.

279 ses are linked and what role RV plays in the breaking of tolerance in regulatory T (Treg) cells is un

280 The breaking of tolerance or unresponsiveness to self-antige

281 ge for tumor immunologists has thus been the breaking of tolerance to cancer antigens.

282 To understand the role of T cells in the breaking of tolerance, an anti-DNA site-specific transge

283 leads to operator complex destabilization by breaking of toxin dimers.

284 Using the analogy of crystals in space, the breaking of translational symmetry in time and the emerg

285 h states were intimately associated with the breaking of translational symmetry(1,2), resulting in th

286 As a result of the spontaneous breaking of translational symmetry, a Goldstone mode eme

287 It involves the breaking of two backbone hydrogen bonds that anchor the

288 rs, the geared motion involves the concerted breaking of two hydrogen bonds.

289 e but small relative yield that involves the breaking of two molecular bonds and the formation of a n

290 t imaging of charge state-dependent symmetry breaking of two prototypical atomic quantum emitters in

291 eta-strands A' and G that is preceded by the breaking of two to three hydrogen bonds between strands

292 s, the main transition was identified as the breaking of van der Waals interactions between the acyl

293 ion (SFG) spectroscopy to probe the symmetry-breaking of water molecules at a charged silica surface

294 ket in a step-wise process involving (i) the breaking of water-mediated hydrogen bonds and van der Wa

295 tailed analysis of DNA stretching shows that breaking of Watson-Crick bonds is not necessary for the

296 A observed in our simulations occurs without breaking of Watson-Crick bonds.

297 metastable configurations that form from the breaking of weak bonds between metals and underlying hig

298 ts are stretched after being released by the breaking of weak bonds, called sacrificial bonds.

299 cier calving triggers internal tsunamis, the breaking of which drives vigorous mixing.

300 on of dand5 is a central process in symmetry breaking of Xenopus, zebrafish and mouse.