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1 on of dopamine and ketones in a PSR leads to the formation of 1,1'-disubstituted tetrahydroisoquinoli
2 axane host recognises dicarboxylates through the formation of 1:1 stoichiometric sandwich complexes.
5 f the ensuing salts with pyrrole, results in the formation of 5-alkoxy-5-phenyl dipyrromethane deriva
7 3' ends, suggesting that in mammalian cells, the formation of a 3' end for noncoding RNAs can be a co
8 e treatment with an isonitrile, which led to the formation of a base-stabilized B,N-containing methyl
9 ir resistance against classical antibiotics, the formation of a biofilm and the difficulty to eradica
13 iacetic acid (poly(pyrrole-NTA)) followed by the formation of a Cu (II) complex with the NTA function
15 demonstrated a lasing regime associated with the formation of a dynamic vapour nanobubble around the
18 the earliest folding events in biogenesis is the formation of a helix, an elementary structure that i
19 rget dsDNA (dsDNA-T), which in turn leads to the formation of a high density of PNA/DNA heteroduplexe
20 l)-1,3-butadiene and 1,4-benzoquinone led to the formation of a key intermediate with all four 4-brom
24 it combines two contingent events; first is the formation of a new molecule, and second its crystall
25 n is ZHOUPI dependent, is necessary both for the formation of a normal embryo sheath and for embryo-e
26 a signaling in chondrocytes is necessary for the formation of a pool or niche of osteoprogenitors tha
27 /PfRipr complex to basigin, a step linked to the formation of a pore between merozoites and erythrocy
28 h the phospholipid-rich membrane and support the formation of a pre-apatitic mineral phase, which was
29 , whose high affinity with platinum triggers the formation of a Pt-CO film that prevents the reaction
30 At its simplest, dormancy can be imposed by the formation of a simple physical barrier around the se
31 molecule such as ThT in selectively favoring the formation of a specific type of fibril by binding to
32 o membrane-bound H-Ras, which greatly speeds the formation of a stable, membrane-bound PI3Kalpha comp
33 how that the grain growth is associated with the formation of a strong near-Cu {112}<111> texture com
34 in some urodeles and teleosts, resulting in the formation of a structurally distinct replacement.
35 raazanaphthacene provided for the first time the formation of a supramolecular H-bonded polymeric rib
36 rode as mounted in the IR spectrometer cause the formation of a thin electrolyte layer between the in
37 evious kinetic studies provided evidence for the formation of a transient complex that precedes the s
38 arried out in acetonitrile solution revealed the formation of a transient with a lambdamax= 570 nm wi
39 entiation and cell-type identity, depends on the formation of a tripartite Snail/HOTAIR/EZH2 complex.
40 llin, slightly slows down but cannot inhibit the formation of a U-shaped Abeta(17-36) protofilament.
43 endent increases in Prosapip1 levels promote the formation of actin filaments, leading to changes in
48 erve extensive splicing diversity leading to the formation of altered open reading frames (ORFs) that
50 -templated aqueous self-assembly resulted in the formation of an endohedrally functionalized Fe(II)4L
51 Binding of S-peptide to S-protein results in the formation of an enzymatically active RNase-S protein
52 scopic and electronic transport evidence for the formation of an excitonic insulator gap in an invert
53 tor for coagulation factor X (FX), mediating the formation of an FX reservoir at the macrophage surfa
57 Tie2 dimerization and activation occurs via the formation of an intermolecular beta-sheet between th
58 tween helices V and VI, which may facilitate the formation of an intracellular binding site that enha
61 enzyme activities that collectively lead to the formation of Ang-(1-7) from Ang II, in both normal c
62 these constraints ( approximately 20%) drive the formation of approximately 99% all experimentally ca
63 architecture by coupling gravity sensing to the formation of auxin gradients that override a LAZY-in
64 able to establish which decorations underpin the formation of AVIs, the conditions promoting AVI form
66 Smo (SmoM2)-driven BCC mouse model prevented the formation of BCC through suppressing primary cilia f
67 of arylamines and the mechanistic study for the formation of benzoquinoline was described precisely.
72 This *CHO is the common intermediate for the formation of both CH4 and C2H4 These results suggest
73 zyme histone deacetylase 3 (Hdac3) regulates the formation of both lymphovenous valves, which maintai
74 s covalent modification of DNA, resulting in the formation of BPDE-N(2)-dG, an adduct formed between
76 s represents a simple, metal-free method for the formation of C3-borylated benzothiophenes and benzof
78 )C{(14)N} dipolar-recoupling NMR showed that the formation of carbonate or bicarbonate is excluded.
80 h Scar/WAVE and Ena/VASP proteins to promote the formation of cellular protrusions and to stimulate i
81 ensification of these flakes by SPS promoted the formation of charged grain boundaries, which led to
82 ns arise in multicellular communities, where the formation of chemical gradients leads to resource li
84 that transposons in maize may be involved in the formation of circRNAs and further modulate phenotypi
85 actor-encoding gene, nkx1-1, is required for the formation of circular fibres, oriented along the med
88 cture of a type IV pilin protein involved in the formation of competence-induced pili in Gram-positiv
91 rol afforded by our method is illustrated by the formation of concentric, pericentric and multicompar
94 face, leading to the removal of Ag atoms and the formation of covalently bonded zigzag poly(m-phenyle
95 The conversion of TCS and, in particular, the formation of DCDD was inhibited in the presence of A
96 Our data suggests that RARgamma initiates the formation of death signaling complexes by mediating
97 intense winter air-sea heat exchange drives the formation of deep waters and the surface circulation
98 ependent c-NHEJ significantly contributes to the formation of deletions and translocations in G1, whi
100 ent of relatively mature features, including the formation of dendritic spines and spontaneously acti
101 lar exchange with FA+ ions, thereby enabling the formation of dense and compact FASnI3 film with larg
102 ate cells (PSCs) plays a predominant role in the formation of desmoplastic reaction through the synth
104 ligand, dppm, used in the reaction promotes the formation of dinuclear palladium complexes, wherein
105 ng into hierarchical structures and leads to the formation of discrete nickel-seamed pyrogallol[4]are
106 l, well-defined density gradients results in the formation of distinct layered patterns, such as thos
108 On this basis, we propose a mechanism for the formation of doping-gradients toward grain boundarie
111 ediated reentrant phase transition can drive the formation of dynamic droplet substructures (vacuoles
112 bles sequential tumor cell killing, enhances the formation of effective immune synapses, and improves
114 nable, and cytokinesis takes place following the formation of elongated bipolar phragmoplast MT array
115 , unlike SBAs, BA compounds uniquely induced the formation of empty capsids that migrated more slowly
117 , phylogenetic linear mixed models show that the formation of families was associated with more produ
118 ., breaded frozen fish products) can lead to the formation of fatty acid esters of 2-monochloropropan
120 oxetane via Lewis acid-activation results in the formation of five- and six-membered unsaturated carb
125 RNA molecules cause the proteins involved in the formation of germ granules to coalesce into liquid d
127 of autoimmunity in murine models of lupus is the formation of germinal centers (GCs) in lymphoid tiss
128 onal deletion of T-bet from B cells impaired the formation of germinal centers and mitigated the deve
130 PCA and Kohonen self-organizing maps showed the formation of groups, corresponding to the fruit part
131 ained electrochemical results clearly proved the formation of H2O2 in the leaves of plants 3h after t
142 oxy/hydroxy groups, epoxides and aldehydes); the formation of hydroxides was clearly favoured over th
143 13)C values of 1.2 and 0.2% are achieved for the formation of hydroxyethyl propionate from hydroxyeth
144 dic event that damages plant tissues through the formation of ice crystals at or below freezing tempe
145 reactivity of free guanidine and arginine in the formation of imidazolinone derivatives, model system
146 s fusion protein or a chimeric cDNA leads to the formation of indolent liver tumors in mice that clos
148 d to determine effective molarities (EM) for the formation of intramolecular phenol-amide H-bonds as
149 e of an alkyne in lieu of an alkene leads to the formation of isoxazole under identical reaction cond
150 Here, we quantify BPA oxidation rates and the formation of its predominant product, 4-hydroxycumyl
151 e mechanism for this efficient separation is the formation of Jupiter, opening a gap in the disk and
152 and that the transformation we observed was the formation of Kirkendall voids due to the outward dif
154 resence of etched enamel surfaces and led to the formation of large, randomly distributed plate-like
157 icles, we find that ARF1 is also involved in the formation of long ( approximately 3 microm), thin (
158 Abeta aggregation states, which result from the formation of low molecular weight oligomers, high mo
159 The role of electrostatic interactions in the formation of lysozyme/LM pectin complexes is discuss
160 selective ring-closing metathesis system for the formation of macrocycles using a stereoretentive, ru
161 toddart describes how being able to template the formation of mechanically interlocked molecules has
164 article colloidal crystallization allows for the formation of micrometer-scale single-crystal body-ce
165 ication, aneuploidy, chromosome breakage and the formation of micronuclei by targeting cellular ligas
166 e critical density, a resistance peak due to the formation of microscopic domains of opposite spin or
168 s in a decrease in VE-Cad levels, leading to the formation of monolayers with decreased barrier funct
169 esting that higher Fe(2+) availability drove the formation of more Fe(2+)-Fur and, accordingly, more
170 loys, which we find to be more selective for the formation of multi-carbon products than pure copper.
171 igate the effectiveness of serrated teeth on the formation of multiple fiber bundles, three-dimension
172 , components of the THO/TREX complex, led to the formation of multiple megaspore mother cells, which
173 -binding proteins plays an important role in the formation of multiple membrane-less organelles invol
174 atine N-acetyltransferase (AgmNAT) catalyzes the formation of N-acetylagmatine from acetyl-CoA and ag
175 een different harmonin isoforms can regulate the formation of networks with Myo7a motors and coordina
179 660 +/- 290 s(-1), and the rate constant for the formation of -NHD2(+) from -NH2D(+) is 3330 +/- 270
180 (UA) can scavenge the peroxynitrite to avoid the formation of nitrotyrosine, which is formed from the
181 n these three factors is responsible for (i) the formation of non-IPR (isolated pentagon rule) exohed
184 widespread evolutionary strategy to prevent the formation of nonphysiological complexes by specializ
187 incided with the surface wind, implying that the formation of O3 was impacted by both exports of plum
189 ids, mammalian carnivores, and crocodiles in the formation of Oldowan zooarchaeological assemblages w
190 bsence of functional PNPLA1 in mice impaired the formation of omega-O-acylceramides and led to an acc
192 Chlorination of amino acids can result in the formation of organic monochloramines or organic dich
193 ads to the scission of C-I bonds followed by the formation of organometallic zigzag structures, consi
198 n of immature urothelial cells can result in the formation of persistent intracellular reservoirs tha
200 ith the calcium ionophore A23187 resulted in the formation of PGE2, 5-HETE, and LTB4 as the principal
202 exchange is kinetically viable and leads to the formation of phase-separated interlayers through a m
208 imizes theoretical capacity while inhibiting the formation of polysulfide intermediates that lead to
209 lide, the transition state (TS) energies for the formation of possible zwitterionic intermediates and
212 igations indicated that APLP1 is involved in the formation of protein-protein complexes that bridge t
216 ivation of o-methylbenzaldehydes, leading to the formation of reactive o-quinodimethanes (photoenols)
218 al in SMA promote DNA damage in part through the formation of RNA:DNA hybrid structures, leading to m
219 nine S-adenosyltransferase (MAT2A) catalyzes the formation of S-adenosylmethionine (SAM) from ATP and
220 ate that the SMC5/6 complex is essential for the formation of segregation-competent bivalents during
221 increase in the total particle counts due to the formation of self-nucleated metallic nanoparticles.
222 ture enables strong quantum confinement with the formation of self-trapped excited states that give e
223 eactivity at these sites is a consequence of the formation of sigma-holes, i.e., maxima in the surfac
224 n the replisome must be coordinated to avoid the formation of significant gaps in the nascent strands
225 r activity of ALA1/ALA2 may be necessary for the formation of similar invaginations for the synthesis
227 ing and atomistic simulations indicates that the formation of single SiNS arises from spontaneous del
228 igorously, little attention has been paid to the formation of single-layer WS2 and its layer dependen
229 into virions in the absence of Nef inhibits the formation of small fusion pores between viruses and
233 To study the possible roles of xyloglucan in the formation of soils, we analysed the xyloglucan conte
234 iabatic effects, coherences, and to describe the formation of species such as charge-transfer states
235 ifferentiation of T cells by contributing to the formation of stable and heritable transcriptional pa
236 ctivity of polyphenolic compounds leading to the formation of stable diketones e.g. 1,2-quinones.
237 hich interaction of KinG with SHR allows for the formation of stable movement complexes that facilita
238 as acetaldehyde and pyruvate participate in the formation of stable pigments during fermentation and
242 on protein as a "molecular mold" in enabling the formation of such hexagonal protein IX network that
244 he ring closure of the zwitterion leading to the formation of sultines was kinetically preferred over
245 in a TAS3 ta-siRNA-insensitive mutant led to the formation of supernumerary megaspore mother cells, s
251 omaterial-biomolecule interactions result in the formation of the biocorona (BC), which alters nanoma
252 ntiation event in mouse development leads to the formation of the blastocyst consisting of the inner
253 substrate dicyclotyrosine (cYY) and observed the formation of the cross-linked product mycocyclosin b
255 uct), while the slow reaction corresponds to the formation of the delta-adduct (the thermodynamic pro
256 ot the DH domain, plays an important role in the formation of the differential p210 and p190 Bcr-Abl
259 quitous loss of the protein uniquely affects the formation of the larval stem cell niches, without al
263 e, cycloheptene, and cyclooctene resulted in the formation of the seleniranium ions 7 (m/z = 225), 6
264 chemistry is a key consideration to modulate the formation of the serum protein corona (PC) and the r
265 protein 23 (SNAP-23), which in turn enables the formation of the SNARE complex to allow exosomes rel
266 zation of complementary DNA strands to model the formation of the SNARE four-helix bundle that mediat
270 Stimulation of cells with TNFalpha leads to the formation of the TNF-R1 signaling complex (TNF-RSC)
271 ling the molecular basis for how they impact the formation of the tripartite complex and disrupt mech
272 U2506 and U2585 of the 23S rRNA resulting in the formation of the U2506*G2583 wobble pair that was at
273 associated conformational changes needed for the formation of the unique carbon-carbon cross-link in
274 We further use the insight gained to explain the formation of the unusual structure of zeolite IPC-6.
276 stence of cross-seeding as a crucial step in the formation of the yeast prion [PSI (+)], formed by th
277 tudy was to identify relevant parameters for the formation of these process contaminants during the p
281 High-resolution microscopic imaging confirms the formation of TMD alloys and identifies a random dist
282 necessary to develop strategies that reduce the formation of toxic byproducts such as chloroform (CF
283 bonds in secondary aliphatic amines lead to the formation of trans-disubstituted beta-lactams in exc
286 thane as a conjunctive reagent, resulting in the formation of two C-C bonds at a single carbon center
287 oute, deformation twinning initiated through the formation of two stacking faults separated by a sing
288 truction with a single template up-regulates the formation of two templates in a predictable manner.
290 nzene degradation, which was associated with the formation of unreactive surface carbonato complexes.
292 lizing with virus tegument protein pp150 and the formation of vAC was compromised upon endocytic inhi
295 ement proteins with microtubules facilitates the formation of virus-associated replication complexes,
297 hat TFAM creates loops in a discrete region, the formation of which correlates with activation of HSP
298 ution of a (YbLD) complex in D2O resulted in the formation of [(YbLD)2Tbx] (x = 1 to 3) complexes tha
300 T, ZNF532, BRD4, EP300, and H3K27ac revealed the formation of ZNF532-NUT-associated hyperacetylated m
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