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1 s the joining of complementary DNA ends in a cell free system.
2 n-can be recapitulated in vitro with a yeast cell-free system.
3 titis C virus IRES-mediated translation in a cell-free system.
4 ficantly decreased protein production in the cell-free system.
5 us type 1 (HIV-1) reverse transcriptase in a cell-free system.
6  These findings were partially mimicked in a cell-free system.
7 terial cloning because it amplifies DNA in a cell-free system.
8 2E1 (CYP2E1) and as purified components in a cell-free system.
9 rdiomyocyte culture after characterizing the cell-free system.
10 hout the biological reductant ascorbate in a cell-free system.
11 lso increased caspase-3 and -9 cleavage in a cell-free system.
12 acterized their deubiquitinase activity in a cell-free system.
13 ansfected and infected cell lysates and in a cell-free system.
14 n metabolism in HaCaT keratinocytes and in a cell-free system.
15 gation by forming an Abeta-heme complex in a cell-free system.
16 n-dUTP near the sites of its initiation in a cell-free system.
17 amino acid-fed and -deficient cells and in a cell-free system.
18 ent regulation of the V(D)J recombinase in a cell-free system.
19 o failed to alter HCV capsid assembly in the cell-free system.
20  capsid assembly in this highly reproducible cell-free system.
21  levels of infectivity can be generated in a cell-free system.
22 gocytophilum rapidly detoxifies O(2)(-) in a cell-free system.
23 a vacuole biogenesis was analyzed by using a cell-free system.
24 e than that of native alphaB-crystallin in a cell-free system.
25 g by apo-nNOS to form the active enzyme in a cell-free system.
26 istance for reporter mRNA translation in the cell-free system.
27 , which spontaneously hydrolyze in a defined cell-free system.
28 NAs could support protein translation in the cell-free system.
29 inhibitors of Tat-induced transcription in a cell-free system.
30 cy virus type 1 (HIV-1) capsid assembly in a cell-free system.
31 nstrate that this interaction can occur in a cell-free system.
32  in cells, as was observed previously in the cell-free system.
33 o were found to inhibit RNA synthesis in the cell-free system.
34 igand-dependent IL-10E1 phosphorylation in a cell-free system.
35 y, it completely blocks DNA end joining in a cell-free system.
36 ransduction is likely to be preserved in the cell-free system.
37 r co-receptor can be expressed in an E. coli cell-free system.
38 HMG2) also reproduce B12/23 restriction in a cell-free system.
39 ect can be reversed by addition of dATP in a cell-free system.
40 ciently than in the absence of survivin in a cell-free system.
41  inhibition of the cell cycle by MCM3AP in a cell-free system.
42 block holo-dependent caspase activation in a cell-free system.
43 ctly with aSyn in both intact cells and in a cell-free system.
44  shown to degrade glutathione in yeast and a cell-free system.
45 ngle-strand deoxyribonucleic acid (DNA) in a cell-free system.
46 mpared to fresh garlic extract in vitro in a cell-free system.
47 was heterologously expressed in a eukaryotic cell-free system.
48 ibit EGFR or other related receptor TKs in a cell-free system.
49 peroxide generation or elastase release in a cell-free system.
50 hol), whereas dA adducts predominated in the cell-free system.
51 anel of 25 pre-selected protein kinases in a cell-free system.
52 ferred pathway of ICL repair in a vertebrate cell-free system.
53 OL-dependent ubiquitination of the LDLR in a cell-free system.
54 to cognate precursor peptide in cellular and cell free systems.
55 ential advantages for protein elaboration in cell free systems.
56 ds (>mg ml(-1)) of proteins from the present cell-free systems.
57 ivity both in pancreatic cancer cells and in cell-free systems.
58 we have analyzed its interaction with Bax in cell-free systems.
59 mic instability on microtubules assembled in cell-free systems.
60 ompetitive affinity to TfR evaluated in cell/cell-free systems.
61 d to assess DNA binding and transcription in cell-free systems.
62 0 are targeted by p300HAT for acetylation in cell-free systems.
63 e monitored PHD activity both in vivo and in cell-free systems.
64  shock protein A and apomyoglobin (apoMb) in cell-free systems.
65 available to characterize target proteins in cell-free systems.
66 tic activity, and processing were defined in cell-free systems.
67  receptor-ligand interaction in cells and in cell-free systems.
68 2 and integrin alpha5beta1 was determined in cell-free systems.
69 interfered with the formation of hemozoin in cell-free systems.
70 ing cytoplasmic dynein that can be formed in cell-free systems.
71  alkylates and interstrand crosslinks DNA in cell-free systems.
72 synthesis in both prokaryotic and eukaryotic cell-free systems.
73 ound directly to integrin alpha(v)beta(3) in cell-free systems.
74 S936, a mechanism-based inhibitor of NQO1 in cell-free systems.
75 ns similar to those needed for DNA damage in cell-free systems.
76 kinase activity to Elk1 in both cellular and cell-free systems.
77 ions inside Chlamydia-infected cells than in cell-free systems.
78 examine directly protein-RNA interactions in cell-free systems.
79 ke GPCRs by coupling them to ion channels in cell-free systems.
80 ity were accurately reproduced in Tg mice or cell-free systems.
81 tion by Mdm2-MdmX E3 complex in cells and in cell-free systems.
82 tory elements using Escherichia coli extract cell-free systems.
83 ctase 2 (NQO2) for use either in cellular or cell-free systems.
84  and are equally attractive as reporters for cell-free systems.
85 escribed HIV-1 assembly intermediates in the cell-free system (10S, 80-150S, and 500S).
86                                         In a cell-free system, addition of actin to in vitro-generate
87 degraded by the 26S proteasomal pathway in a cell-free system, albeit not in an S-allele-specific man
88                                           In cell-free systems, Alix directly interacts with F-actin
89                Importantly, we show that the cell-free system allows for the rapid (2 h) identificati
90                     Additionally, the use of cell-free systems allows the selection of proteins that
91                                          The cell-free system also replicated the full-length TBSV ge
92                Caspase-3 activates AN34 in a cell-free system, although caspase-3 cannot cleave Ape1
93 aracterization of this antibody using both a cell-free system and a cell model system of apoptosis de
94 ract with AIF either in intact cells or in a cell-free system and furthermore, failed to prevent nucl
95 tes post-translationally with HIV-1 Gag in a cell-free system and human T cells infected with HIV-1.
96                     We found that, both in a cell-free system and in cells, NO/SNO donors such as S-n
97 ts suggest that NDV F protein made both in a cell-free system and in Cos-7 cells may exist in two top
98 t YY1 physically interacts with AR both in a cell-free system and in cultured cells.
99 s spectrometry and mutagenesis analyses in a cell-free system and in gliomas cells identified Tyr-7 a
100  interaction and for glycogen synthesis in a cell-free system and in intact cells.
101 potently reduces Abeta production in the N2a cell-free system and in intact N2a cells.
102 element AU-rich element 1 of bcl-2 mRNA in a cell-free system and in MCF-7 cells.
103 8 residue and associates with Ubc9 both in a cell-free system and in virus-infected BCBL-1 cells.
104 ditis virus (EMCV) and poliovirus IRESs in a cell-free system and in virus-infected HeLa cells.
105 cts with integrin alpha(v)beta(5), both in a cell-free system and on the cell surface of rat lung fib
106                Inhibition of the trypanosome cell-free system and recombinant rat GlcNAc-PI de-N-acet
107  SNAP also blocked caspase 9 activation in a cell-free system and reversibly inhibited catalytic acti
108 periments are consistent with those from the cell-free system and strongly suggest that ara-G is phos
109 at HIV-2 Gag associates with human HP68 in a cell-free system and that Gag proteins of HIV-2, simian
110 fects of these mutations on RNA binding in a cell-free system and TTP-induced mRNA instability in cel
111 e mechanisms governing EB/tau interaction in cell-free systems and cellular models.
112                                        Using cell-free systems and different cellular models, we show
113 e of the critical residues identified in the cell-free systems and exploring the limit of CPAF's tole
114 ther biological networks behave similarly in cell-free systems and in cells.
115  CP is essential for actin-based motility in cell-free systems and in Dictyostelium.
116 ge activity toward its effector Rap1 both in cell-free systems and in intact cells.
117 domain Bax or Bak, or BH3-only Bim or Bad in cell-free systems and in intact human cancer cells, free
118 y co-immunoprecipitation studies, using both cell-free systems and mammalian cells, and the specific
119                          Binding analyses in cell-free systems and on the cell membrane demonstrate t
120 bition of NQO2 activity was assessed in both cell-free systems and the human leukemia K562 cell line.
121 roplatelet formation can be recapitulated in cell-free systems and their biochemistry evaluated; the
122 (TcdB) has been studied extensively by using cell-free systems and tissue culture, but, like many bac
123                                      We used cell-free systems and ultimately a vesicular reconstitut
124 M2 promotes the ubiquitination of FOXO1 in a cell-free system, and its knockdown by small interfering
125 n from HSP2 has been reported only once in a cell-free system, and never when recombinant proteins ha
126 e demonstrated both in intact cells and in a cell-free system, and proteasome inhibition or Huwe1 sil
127 stranded RNA-dependent protein kinase PKR in cell-free systems, and within latently infected B-cell l
128                          Capsids produced in cell-free systems are also indistinguishable from capsid
129                                              Cell-free systems are appealing alternative environments
130 olesterol (FC) bilayer membranes in cell and cell-free systems are compared.
131                       Commercially available cell-free systems are freeze dried onto paper, enabling
132               Ro106-9920 was identified in a cell-free system as a time-dependent inhibitor of Ikappa
133     The GSMs modulate Abeta both in cell and cell-free systems as well as lower amyloidogenic Abeta42
134                                      In this cell-free system, as in mammalian cells, capsid assembly
135 activation by recruitment in a reconstituted cell-free system, assembled entirely from a defined numb
136                                         In a cell-free system, ATP hydrolysis by the v-ATPase was nec
137 l tombusvirus of plants, we have developed a cell-free system based on a Saccharomyces cerevisiae ext
138 c reticulum (ER) has been reconstituted in a cell-free system based on interphase Xenopus egg extract
139                                         In a cell-free system based on the immunoglobulin heavy chain
140                          Here, we describe a cell-free system based on Xenopus egg extracts that supp
141 is known to mediate actin/MT interactions in cell-free systems but the role of tau in regulating cyto
142  vitro-translated MCL-1 can be degraded in a cell-free system by the 20S proteasome.
143 n vitro method to generate DNA templates for cell-free systems, bypassing the need for DNA template g
144 alternate forward engineering paradigm using cell-free systems can thus accurately capture cellular b
145                          We have developed a cell-free system capable of processing and joining nonco
146 alytically less efficient than intact PE3 in cell-free systems, co-expression in live cells transfect
147                        We have established a cell-free system competent for replication in which all
148 cate cell-bound system and (ii) a simplistic cell-free system composed of a single cohesin-containing
149 ated kinase 2 (PAK-2) was recapitulated in a cell-free system consisting of in vitro-transcribed RNA,
150  import of phytochromes can be analyzed in a cell-free system consisting of isolated nuclei of the un
151 ause direct inhibition of PARP activity in a cell-free system containing PARP and NAD(+) but did coun
152 % of HCV core protein synthesized de novo in cell-free systems containing rabbit reticulocyte lysate
153 tly, we demonstrate that characterization in cell-free systems correlates and is reflective of perfor
154                                         In a cell-free system, CPAF activity is both necessary and su
155        Second, addition of wortmannin to the cell-free system demonstrated that Nef activation of PAK
156  Experiments in both breast cancer cells and cell-free systems demonstrated that niclosamide possesse
157                                            A cell-free system depleted of intersectin failed to suppo
158 this question by imaging growing asters in a cell-free system derived from eggs, where asters grew to
159                 We previously used a soluble cell-free system derived from Xenopus eggs to investigat
160                                              Cell-free systems designed to perform complex chemical c
161 y to proteasome-dependent degradation in the cell-free system did not increase.
162   However, increasing amounts of Alpha2 in a cell-free system disrupted the formation of Dab1-Lis1 co
163 elieve that these data are unattainable in a cell-free system due to the poor replication of these CR
164                                   Our unique cell-free system enables complete control and manipulati
165 r additional cloning steps, which makes this cell-free system fast and efficient.
166       Nucleotides 6-9 inhibited oxidation in cell-free systems (Fe(II)-H2O2), as detected by ESR (IC5
167 s study also illustrates the utility of this cell-free system for investigating hypotheses of recepto
168  contribute to mRNA turnover, we developed a cell-free system for mRNA turnover using the trypanosome
169                    This protocol describes a cell-free system for studying vertebrate centromere and
170      These membrane fractions were used in a cell-free system for the analysis of HCV RNA replication
171                             We established a cell-free system from individual Drosophila melanogaster
172                              By the use of a cell-free system from Xenopus eggs that reproduces the m
173 emonstration of an ion channel in eukaryotic cell-free system has a large potential for future applic
174                              In summary, the cell-free system has defined several RNA turnover steps
175 t progress in propagating TSE infectivity in cell-free systems has effectively ruled out the involvem
176 th both intact cells and a kinase-dependent, cell-free system have suggested that protein kinase C ca
177                               Experiments in cell-free systems have demonstrated that the VP5 cleavag
178 tively blocked gamma-secretase activity in a cell-free system (IC50 = 30 nM).
179 T bundles and 2D MT bundles may assemble, in cell free systems in the presence of counter-ions, revea
180 capsid assembly and RNA encapsidation in the cell-free system in a manner similar to that seen in mam
181 ailed to directly inhibit Cdc2 activity in a cell-free system in spite of direct association between
182 tivation of the oxidase in a semirecombinant cell-free system in the absence of an amphiphilic activa
183              An analysis of GPIs formed in a cell-free system in the presence and absence of glucosam
184                                      Using a cell-free system in vitro, we evaluated the action of DM
185 spase-3 and -8 in liver homogenates and in a cell-free system in vitro.
186                We have developed a mammalian cell-free system in which HBc is expressed at physiologi
187                        We have established a cell-free system in which mitochondria derived from viru
188                   Recently, we established a cell-free system in which over 60% of full-length HCV co
189 action between two molecular systems using a cell-free system in which polystyrene microspheres funct
190 mechanism of apoB degradation, we employed a cell-free system in which proteasome-dependent degradati
191                               We developed a cell-free system in which TTP and its related proteins s
192          RacC stimulates F-actin assembly in cell-free systems in a WASP-dependent manner.
193 f the time-course of protein expression in a cell-free system, in conjunction with the development of
194                                      Using a cell-free system, in vitro-translated 35S-labeled KLF4 p
195           The addition of purified RatA to a cell-free system inhibited the formation of 70S ribosome
196  addition of phosphorylated p40(PHOX) to the cell-free system inhibits NADPH oxidase activated by pro
197                  Studies were performed in a cell-free system involving endothelial PM sheets and iso
198                  As demonstrated herein, the cell-free system is a new and important tool in the inve
199 amma-secretase generation of Abeta in an N2a cell-free system is ATP dependent.
200 single-protein production can be achieved in cell-free systems, it is not easy to completely suppress
201 A replication in a Xenopus egg extract based cell-free system, leading to the expectation that the pr
202                                         This cell-free system lends itself to use in protein immunode
203 lar requirements for capsid formation, these cell-free systems make a mechanistic dissection of HCV c
204                                         In a cell-free system, Mediator directly and substantially in
205 stabilization of oligomeric intermediates in cell-free systems, no studies have examined the effects
206                                           In cell-free systems, Nrdp1 has ubiquitin ligase (E3) activ
207                                         In a cell-free system, obatoclax induced an activating confor
208                            Furthermore, in a cell-free system of IKK complex activation by TRAF6 (TNF
209                                              Cell-free systems offer several advantages over traditio
210 ence on translational efficiency in either a cell-free system or cell culture, indicating that any AG
211 n adaptors, whereas functional studies using cell-free systems or intact cells have demonstrated the
212            Interaction with soluble CAR in a cell-free system, or with CAR on the surfaces of transfe
213 metry of the nuclear transport factor 2 in a cell-free system over a broad concentration range.
214                                           In cell-free systems, p53R2 did not oxidize a reactive oxyg
215 tochrome c-induced caspase-3 activation in a cell-free system, particularly in the presence of H(2)O(
216 lcytosine (used as a substrate for dCK) in a cell-free system; phosphorylation of this compound by dG
217                                           In cell-free systems, polyamides have been shown to regulat
218 s were able to inhibit RNA synthesis in this cell-free system, presumably through chain termination,
219 ng ability on par with other flavonoids in a cell-free system, Proxison is orders of magnitude more p
220  purified Pyk2 can be activated by acid in a cell-free system, Pyk2 may serve as the pH sensor that i
221                                         In a cell-free system, recombinant PKC-zeta phosphorylates LK
222                                           In cell-free systems, recombinant IRE1alpha endonucleolytic
223 at stabilizes microtubules in neurons and in cell-free systems regulates actin-microtubule interactio
224                                              Cell-free systems represent a promising approach to quic
225 at autophosphorylation of Chk2 produced in a cell-free system requires trans phosphorylation by a wor
226  transfer of heavy chains to hyaluronan in a cell-free system, restore the expansion of Tnfip6-null c
227     Oscillation periods in cells matched the cell-free system results for all networks tested.
228                           Additionally, in a cell-free system, resveratrol directly induced the depol
229       However, examination of apoptosis in a cell-free system revealed a block in chromatin condensat
230                On the basis of studies using cell-free systems, ribosomal frameshifting can explain t
231                                          The cell-free system should now allow for the definition of
232     Altogether, tombusvirus replicase in the cell-free system showed features remarkably similar to t
233                                          The cell-free system showed high template specificity, since
234                                          Yet cell-free systems showed that recognition was mediated o
235 failed to induce PPARdelta binding to DRE in cell-free system, suggesting that cPLA2alpha-mediated AA
236 omolar concentration in both intact-cell and cell-free systems, suggesting that these inhibitors targ
237 ADPH oxidase regulation using whole cell and cell-free systems suggests that the toxins do not exert
238 animal myocytes, E. coli, and the wheat germ cell-free system than Mbs from terrestrial mammals.
239 hat generates active PS, we used a mammalian cell-free system that allows de novo human PS NTF and CT
240 nts of PCD, we have developed an Arabidopsis cell-free system that can be used to monitor biochemical
241                       We also confirmed in a cell-free system that ER-alpha is an inhibitory regulato
242 ecular level, we have recently established a cell-free system that initiates chromosomal DNA replicat
243                         In addition, using a cell-free system that makes both G and SG RNA, we show t
244                       In this paper, using a cell-free system that recapitulates end synapsis and DNA
245 erstand these processes, we have developed a cell-free system that recapitulates these early steps of
246                            Here we present a cell-free system that reconstitutes fragmentation of pur
247                                      Using a cell-free system that synthesizes both SG and G RNA, we
248                       mES Ex provide a novel cell-free system that uses the immense regenerative powe
249 e it has been predicted from some studies of cell-free systems that mutations may occur with a freque
250 the agent, the prion, can be replicated in a cell-free system, that it can be generated de novo, and
251                        We characterized in a cell-free system the 'repressilator', a three-node synth
252 ous studies, however, we demonstrate that in cell-free systems the mode of action of selected NSAIDs
253 Because these studies are primarily based on cell-free systems, the role of the ubiquitin ligase acti
254                Here we describe the use of a cell-free system to characterize the effect of T Ag on p
255 ole in this process, we used a reconstituted cell-free system to define the precise contribution of p
256 ramide's inhibitory effect on PLD, we used a cell-free system to examine PLD activity and translocati
257                In this study, we have used a cell-free system to examine the requirements for microtu
258      Here, we used an Escherichia coli-based cell-free system to express a MOMP protein from the mous
259                                      Using a cell-free system to initiate replication within G1-phase
260                  Here we use a reconstituted cell-free system to investigate the mechanism and extent
261                     We previously employed a cell-free system to investigate the nature of the vesicl
262                               We developed a cell-free system to recapitulate cytokinesis signaling u
263 mbly during replication and provide a facile cell-free system to study capsid assembly under physiolo
264 ning and plasmid transport, we established a cell-free system to study plasmid partition reactions in
265 ility to function as reporters in completely cell-free systems to allow for the extremely rapid and s
266 5-bisphosphate (PIP(2)) levels in intact and cell-free systems to provide electrophysiological and bi
267 e surfactants in commercial Escherichia coli cell-free systems to rapidly produce milligram quantitie
268                                   Using this cell-free system together with a variety of pharmacologi
269 protein was monitored in an Escherichia coli cell-free system under different experimental conditions
270                            We show here in a cell-free system using incorporation of radioactive guan
271 studied the lipin 1beta enzyme activity in a cell-free system using PA/Triton X-100 mixed micelles as
272  of regulated recombinase accessibility in a cell-free system using plasmid substrates assembled into
273 ed the interface of the Bcl-2 homodimer in a cell-free system using site-specific photocross-linking.
274 n of TR1 by the IQs was studied in detail in cell-free systems using purified enzyme.
275 een characterized, either in living cells or cell-free systems, using radioactive compounds for quant
276 ic ability of radiomimetics to cleave DNA in cell-free systems, varying in activity from 2-fold (desc
277                                            A cell free system was developed, and a succession of comp
278 ated by immunoprecipitation and studied in a cell-free system was activated and phosphorylated at aci
279 fully replicating the TBSV replicon RNA, the cell-free system was also capable of generating TBSV RNA
280                                          The cell-free system was capable of performing a complete re
281                                          The cell-free system was used to analyze the mechanism of Ne
282                                      Using a cell-free system we show that hypersensitivity does not
283                               Using in vitro cell free systems, we demonstrated that apratoxin A prev
284                                Here, using a cell-free system, we demonstrate that although recombina
285  depletion-reconstitution experiments in the cell-free system, we demonstrate that HP68 is essential
286                                       With a cell-free system, we demonstrated the conversion of meth
287                                      Using a cell-free system, we have directly and systematically in
288                                      Using a cell-free system, we recently identified the phosphoinos
289                                      Using a cell-free system, we showed that FANCI-FANCD2 is require
290                                  Using these cell-free systems, we show that HCV capsid assembly is i
291 parum proteins prepared using the wheat germ cell-free system (WGCFS).
292 le, inhibits protein synthesis in an E. coli cell-free system, whereas the addition of PemI, the anti
293  factors or conditions not yet reproduced in cell-free systems which contribute to fidelity during re
294                                         In a cell-free system with externally added DHA, nearly 70% o
295                                    We used a cell-free system with pure Escherichia coli components t
296                                         In a cell-free system with purified transport factors alpha-s
297                 PKR autophosphorylation in a cell-free system with recombinant NLRP3, apoptosis-assoc
298 ng properties of eight TCR/pMHC couples in a cell-free system with single bond resolution.
299 on (O2.-) production in a reconstituted Nox1 cell-free system, with no effect on Nox2-, Nox4-, Nox5-,
300 y, VapC-mt4 inhibited protein synthesis in a cell-free system without cleaving the corresponding mRNA

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