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1 iate more frequently at G.C sites during the polymerization reaction.
2 nity (K(d)=6.81 microm), thus initiating the polymerization reaction.
3 gh an increase in the apparent V(max) of the polymerization reaction.
4 action has provided on the mechanisms of the polymerization reaction.
5 ll requires the presence of TAF-I during the polymerization reaction.
6 omoting pyrophosphorolysis that reverses the polymerization reaction.
7  by affecting other residues involved in the polymerization reaction.
8 eptides, KfiA and KfiC, to catalyze the same polymerization reaction.
9 c pyrophosphate which is an inhibitor of the polymerization reaction.
10 t over the last 50 years on this fundamental polymerization reaction.
11 ptide monomers into dimers that nucleate the polymerization reaction.
12 nk this to the exothermicity of the ethylene polymerization reaction.
13  nanometer-sized pores via a Pictet-Spengler polymerization reaction.
14 icroemulsion, significantly accelerating the polymerization reaction.
15 leoside triphosphates (dNTPs) to control the polymerization reaction.
16 electron acceptors during the photocatalytic polymerization reaction.
17 abilization in alkaline solutions leading to polymerization reaction.
18  surface of MTs and tubulin rings during the polymerization reaction.
19 res with FtsZ assembly but also reverses the polymerization reaction.
20 by photolithography, in the same step as the polymerization reaction.
21 quential additions of lactide monomer to the polymerization reaction.
22 lent catalysts for the formaldehyde (CH(2)O) polymerization reaction.
23 rmed amyloid fibrils implicating a nucleated polymerization reaction.
24  of several elementary steps for the forward polymerization reaction.
25 r a better understanding of the mechanism of polymerization reactions.
26 eration (chemiluminescence) is used to drive polymerization reactions.
27  dependence on the E2 component of ubiquitin polymerization reactions.
28 ups that could potentially prevent or quench polymerization reactions.
29 rmediates present in nickel-catalyzed olefin polymerization reactions.
30 ed as porous templates to exert control over polymerization reactions.
31 s have been synthesized using solution-phase polymerization reactions.
32 plify the screening of potentially prebiotic polymerization reactions.
33 ch separate reconstructive and amplification polymerization reactions.
34 ogenation, alkene isomerization, and radical polymerization reactions.
35 zed, characterized, and explored in ethylene polymerization reactions.
36 lso discussed, including their corresponding polymerization reactions.
37 talyst to achieve logic gating of controlled polymerization reactions.
38 initiator), as typically observed for living polymerization reactions.
39 ic catalysts without homogeneous analogs for polymerization reactions.
40 gulation of initiation in nitroxide-mediated polymerization reactions.
41 sequential polycondensation and free radical polymerization reactions.
42 -by-step in an iterative fashion, and not by polymerization reactions.
43 mical alternative to standard cross-coupling polymerization reactions.
44 ining sequence-controlled polymers in simple polymerization reactions.
45 olarized NMR for quantifying early events in polymerization reactions.
46 litate replication by relatively inefficient polymerization reactions.
47  other contaminants capable of similar redox/polymerization reactions.
48 issolution DNP an attractive method to study polymerization reactions.
49 , a 4M1P-appended ligand was isolated from a polymerization reaction (50:1 monomer:catalyst) by colum
50   Thus, wild-type Thg1 catalyzes a templated polymerization reaction acting in the reverse direction
51 ployment of a purge-free controlled/"living" polymerization reaction, activators generated by electro
52 rotects them from undesirable hydrolysis and polymerization reactions, allowing them to achieve their
53                             The topochemical polymerization reaction also displays excellent function
54                                          The polymerization reaction and its regulation have been stu
55 ymerization in solution) and controlling the polymerization reaction and properties of these novel ma
56 n of primers is achieved using an isothermal polymerization reaction and quantified by fluorescence r
57 we review the general characteristics of the polymerization reaction and recent approaches that have
58                                     Suitable polymerization reaction and synthetic strategy are both
59 ins declined almost tenfold, probably due to polymerization reactions and copigmentation.
60 nched polymers are obtained through one-step polymerization reactions and exhibit properties that are
61 o opportunities of using force to manipulate polymerization reactions and tune the physiochemical pro
62 nearly 60nm, obtained through an emulsion co-polymerization reaction, and the MB alone were evaluated
63 ium (Pd) clusters that are formed during the polymerization reaction, and there is increasing evidenc
64 ; they remain in the soluble fraction of the polymerization reaction, and they increase the amount of
65  benzene derivatives through dehydration and polymerization reactions, and may possess several possib
66                            Surface-initiated polymerization reactions are a powerful tool to generate
67                              Photo-initiated polymerization reactions are an alternative means of gen
68 pelago motifs and the occurrence of cracking/polymerization reactions are central in the production o
69 s is a significant challenge, since cationic polymerization reactions are highly sensitive to chain-t
70                                          The polymerization reactions are specific and controlled, in
71                                        Basic polymerization reactions are the cornerstones of synthet
72 oxygen-free environment when classic radical polymerization reactions are used in signal amplificatio
73 roducts of polymer degradation or incomplete polymerization reactions, are the first species to leach
74                                       Plasma polymerization reaction at atmospheric pressure has been
75 u(III) solutions by a surface-enhanced redox/polymerization reaction at the muscovite (001) basal pla
76 se starting materials facilitated performing polymerization reactions at large scales (4 L), yielding
77                                          The polymerization reactions at the filopodial tip require t
78 on of amorphous polymer, a by-product of the polymerization reactions, at the interface.
79 le light-triggered quantitative topochemical polymerization reaction based on a conjugated dye molecu
80                               A non-covalent polymerization reaction between macromolecular monomers,
81 ser scanning, and Raman microscopy while the polymerization reaction between the BMEP primers and hyd
82  of these two specific bindings advances the polymerization reaction by K4CP.
83 dding sonicated preformed CsgA fibers to the polymerization reaction can significantly shorten the du
84 ameters tightly controlled in solution-based polymerization reactions can seamlessly be translated in
85 sslinking methods in addition to interfacial polymerization reaction chemistry and conditions.
86  early RMGI development, acid-base and light-polymerization reactions compete with and inhibit one an
87                                              Polymerization reactions conducted inside cells must be
88              The crystal environment of this polymerization reaction controlled both the molecular an
89                      In this reversal of the polymerization reaction, deoxynucleotides in DNA are con
90 y dilute, but in experimental simulations of polymerization reactions dilute solutions of activated m
91  added cofactors, did not affect the rate of polymerization reactions during storage.
92                            Template-directed polymerization reactions enable the accurate storage and
93              Detailed kinetic studies of the polymerization reaction enabled integral and nonintegral
94       The in situ gold reduction promote the polymerization reaction, enlarging the effective surface
95 id to the carbohydrate recognition site, the polymerization reaction entered a highly processive phas
96 tion to elongation for the RNA-dependent RNA polymerization reaction, explain the role of the noncata
97 s sufficient for complete termination of the polymerization reaction for a short template mediated by
98                                          The polymerization reaction for the synthesis of polymer NPs
99 rt mainly focuses on the summary of suitable polymerization reactions for colloidal polymer derived p
100 ate hydrolysis may be necessary to drive the polymerization reaction forward.
101 eotide polymerases at different steps of the polymerization reaction has provided on the mechanisms o
102        However, the totality of topochemical polymerization reactions has failed to produce ultra-hig
103  that the glycosyl donor and acceptor in the polymerization reaction have distinct lipid requirements
104 tutorial review explains how photo-initiated polymerization reactions have been used in a conditional
105  attempts to demonstrate plausibly prebiotic polymerization reactions have met with limited success.
106                                 Topochemical polymerization reactions hold the promise of producing u
107  the isothermal circular strand displacement polymerization reaction (ICSDPR) initiated with miRNA-14
108 s paper should be applicable to a variety of polymerization reactions in aqueous solution.
109 tions are a key factor in cluster growth and polymerization reactions in ionizing environments such a
110 of amphiphilic compounds could have promoted polymerization reactions in prebiotic conditions, giving
111                                              Polymerization reactions in which RnqPD and the prion do
112  stable adducts, and reduction of late-stage polymerization reactions, increasing accumulation of cyc
113 d polyacrylate gel were prepared by inducing polymerization reaction inside long glass or Tygon tubin
114 intrinsic microporosity (PIM), prepared by a polymerization reaction involving the formation of Troge
115              The primary interaction of this polymerization reaction is between the newly exposed N-t
116                                          The polymerization reaction is catalysed by a pincer complex
117                                 Notably, the polymerization reaction is confined epitaxially to the c
118        Thus, the deltaH for the condensation polymerization reaction is dependent on the crystal pack
119                              Surprising, the polymerization reaction is not reciprocal as natural nuc
120           Specifically, a controlled radical polymerization reaction is triggered after the capture o
121           Specifically, a controlled radical polymerization reaction is triggered after the capture o
122  in bis(imino)pyridine iron catalyzed olefin polymerization reactions is also presented.
123 e reactivity of the propagating chain end in polymerization reactions is crucial for achieving well-d
124 lling the chain growth process in non-living polymerization reactions is difficult because chain term
125 l structure compression and pressure-induced polymerization reaction kinetics of two polycyclic 1:1 a
126           We report on a stepwise on-surface polymerization reaction leading to oriented graphene nan
127 sight into this solid-state polycondensation polymerization reaction may be gained from the single-cr
128                            We speculate that polymerization reactions may be occurring at depth withi
129  stereocontrol mechanism governing these new polymerization reactions mediated by chiral metalloceniu
130                                              Polymerization reactions occur readily in the presence o
131                              We suggest that polymerization reactions occurred in the atmosphere as i
132      Herein, we demonstrate the topochemical polymerization reaction of a family of para-azaquinodime
133 [4 + 4] reactions, Diels-Alder reactions and polymerization reactions of acetylene molecules.
134                                   Unlike the polymerization reactions of DNA and RNA and polypeptide
135                                         Such polymerization reactions of polyphenolic antioxidants ca
136 es does not enter into the radical coupling (polymerization) reactions of lignification.
137 nal transitions in the APD during nucleation-polymerization reactions or/and in the presence of actin
138 method may be extendable to monitoring other polymerization reactions previously overlooked for lack
139                                   During the polymerization reaction, primase tolerated substantial m
140                                              Polymerization reactions proceed rapidly to completion o
141                                          The polymerization reaction proceeds regioselectively with t
142        Addition of 3.47 mM (0.1%) SDS to the polymerization reaction produced Abeta42 fibrils that we
143                    Real-time measurements on polymerization reactions provide both mechanistic and ki
144                              In nucleic acid polymerization reaction, pyrophosphorolysis is the rever
145 he central termination sequence (CTS) on the polymerization reaction: reduction of burst amplitude in
146 acterization challenges amongst topochemical polymerization reactions, representing a critical step t
147 nd may be involved in yet unknown nucleotide polymerization reactions required for maintenance of chr
148  acid, NaOH and HCl to initiate and stop the polymerization reaction, respectively, which makes the a
149 When included into a thrombin-induced fibrin polymerization reaction, rFnbA strongly inhibited fibrin
150 lymer cages as a confined reaction space for polymerization reactions such as atom transfer radical p
151                                 Unlike other polymerization reactions that can be performed in water
152 s to develop models of potentially prebiotic polymerization reactions that cannot be studied easily u
153 uced a colored precipitate suggestive of the polymerization reactions that characterize microbial mel
154 the initiation step of a cascade of aromatic polymerization reactions that eventually convert PAHs to
155 ucture and counterion pairing, thus enabling polymerization reactions that proceeded with remarkable
156 y complex, multi-step synthetic pathways and polymerization reactions that rely on air-sensitive cata
157  tuning the concentration of MAA monomers in polymerization reaction the concentration of surface -CO
158 cted concentration dependence of a nucleated polymerization reaction, the addition of preformed amylo
159                                   During the polymerization reaction, the polymers undergo a phase tr
160  conjunction with kinetic data regarding the polymerization reaction, these data indicate that UDP-Gl
161 y adjusting the oxidative environment of the polymerization reaction through the addition of a strong
162 ear increase of copolymer Mw with increasing polymerization reaction time.
163 he amplification inherent in a radical chain polymerization reaction to detect molecular recognition.
164 nascent base pair in the active site for the polymerization reaction to occur, thus overcoming these
165 h a rate constant of 0.39 h(-1), causing the polymerization reaction to stall before complete templat
166 ynthetic strategies based on typical one-pot polymerization reactions to demonstrate the growth of bu
167 elective initiation of atom-transfer radical polymerization reactions to form an addressable polymer
168 dase (GOx) to water/solvent mixtures enables polymerization reactions to proceed in extremely low vol
169 talysts enable exquisite control over alkene polymerization reactions to produce new materials with u
170 monstrated the concept of using free-radical polymerization reactions to provide signal amplification
171 esses design and syntheses of ILMs and their polymerization reactions to yield PILs and PIL-based mat
172 polymer NPs can be synthesized in a one-step polymerization reaction using commercially available rea
173 les by in vivo enzyme-catalyzed chain growth polymerization reactions using activated monomers that h
174  linkages, which are favored in nonenzymatic polymerization reactions using similarly activated ribon
175  demonstrate switching of controlled radical polymerization reactions using temperature "LOW"/"HIGH",
176 of selective recognition and of initiating a polymerization reaction was central to obtaining high se
177 amic photoswitching of dispersity during the polymerization reaction was demonstrated.
178                                          The polymerization reaction was followed either by an increa
179 ea, a tyrosinase inhibitor; the (HO)2IndCOOH polymerization reaction was inhibited by superoxide dism
180                                          The polymerization reaction was initiated by exposing crysta
181 effects of photocaged nucleosides on the DNA polymerization reaction was investigated, finding that m
182   A component of the mechanism of the cyclic polymerization reaction was probed by isolation and full
183                                          The polymerization reaction was simultaneously monitored by
184               The chain-growth nature of the polymerization reaction was utilized to produce well-def
185 cture, while the phenyl ester formed in bulk polymerization reactions was not detected.
186                                              Polymerization reactions were efficient for all five dif
187 sing a technically expedient, photoinitiated polymerization reaction whereby a approximately 2 to 10-
188 sing a technically expedient, photoinitiated polymerization reaction whereby an oxygen-sensitive poly
189  process using a dedicated 'module' for each polymerization reaction, which specifies the unit to be
190               Here, we demonstrate a radical polymerization reaction whose initiation is controlled b
191 rlying principles that govern these types of polymerization reactions will be enumerated as a paradig
192 mbining two sequential atom-transfer radical polymerization reactions with a click reaction.
193                    Surprisingly, in chain co-polymerization reactions with a second donor, this thiol
194 could be utilized to induce asymmetric photo-polymerization reactions with high enantioselectivity an
195    Here we demonstrate that illuminating tau polymerization reactions with laser light and measuring
196 onomer that undergoes UV-catalyzed thiol-ene polymerization reactions with polythiol comonomers to af
197                                          The polymerization reaction yields highly conjugated backbon

 
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