戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 able P conditions, we conducted a microbiota reconstitution experiment.
2 sufficient to confer STI-571 resistance in a reconstitution experiment.
3 or the assembly of the NLRP3 inflammasome in reconstitution experiment.
4 mi1 subunit also stimulates Top3 activity in reconstitution experiments.
5 es, human hepatoma cell lines and telomerase reconstitution experiments.
6 ough a methodological series of knockout and reconstitution experiments.
7 sh multilineage hematopoiesis in competitive reconstitution experiments.
8  subjected the purified monomers to in vitro reconstitution experiments.
9 on of chlamydial protective antigens through reconstitution experiments.
10 ral CoQ10 content, were chosen for depletion/reconstitution experiments.
11 aches: antibody interception experiments and reconstitution experiments.
12 nstability (CIN) in vivo using hematopoietic reconstitution experiments.
13 m component, and its effect was validated by reconstitution experiments.
14 r was Pol epsilon able to extend a D-loop in reconstitution experiments.
15  bitterness and astringency by means of wine reconstitution experiments.
16 ild-type and mutant proteins in inflammasome reconstitution experiments.
17 ultured tracheal SMC and verified by in vivo reconstitution experiments.
18 ight considerations for designing condensate reconstitution experiments.
19 topoietic cells were excluded by bone marrow reconstitution experiments.
20 rrent interpretation of the classic omission-reconstitution experiments.
21  the tubulin-blocked state in single-channel reconstitution experiments.
22 ctivation by InsP(3) in planar lipid bilayer reconstitution experiments.
23 d MPK substrates were validated by in planta reconstitution experiments.
24                In many cases, in biochemical reconstitution experiments, a complex distribution of ol
25                                  In in vitro reconstitution experiments, acetylation was sufficient t
26                      Here we use biochemical reconstitution experiments alongside genetic and structu
27                                     In vitro reconstitution experiments also indicated that sequences
28                                     In vitro reconstitution experiments also show that the associatio
29                                     In vitro reconstitution experiments also support that TLR2 mediat
30               Here we use in vivo condensate reconstitution experiments and coarse-grained molecular
31 al analysis results, we designed biochemical reconstitution experiments and demonstrated that DNA syn
32             We use a minimal physical model, reconstitution experiments and in silico simulations to
33 id composition used for bilayer formation in reconstitution experiments and increases with the increa
34 ) pathogenic T cells (CD4(+Path) T cells) in reconstitution experiments and most efficiently ablated
35 es of plaque vulnerability using bone marrow reconstitution experiments and pharmacological targeting
36 diolipin stabilizes UCP1, as demonstrated by reconstitution experiments and thermostability assays, i
37                               Using in vitro reconstitution experiments and total internal reflection
38 eling studies, chemical-rescue-based partial reconstitution experiments, and chemical model studies t
39                                              Reconstitution experiments antagonized IGF-I-mediated MA
40 es of protein binding inferred from omission-reconstitution experiments are thought to preclude certa
41 ngeability with hTERT in in vitro telomerase reconstitution experiments, as mTERT produces strong tel
42                                     In vitro reconstitution experiments, as well as analysis of CRISP
43                          Crossed bone marrow reconstitution experiments between A/J and MHC congenic
44                               In biochemical reconstitution experiments, both response elements are a
45                                       In p53-reconstitution experiments, cell-cycle arrest, apoptosis
46                                    In marrow reconstitution experiments, coexpression of both genes p
47                                By reciprocal reconstitution experiments, comparing wild-type versus P
48                         We show by cell-free reconstitution experiments, computer simulations, and th
49 t are consistent with this location and with reconstitution experiments conducted with isolated perip
50                         Biochemical in vitro reconstitution experiments confirmed electron transport
51                                 Heterologous reconstitution experiments confirmed the formation of TR
52                                   Serum-free reconstitution experiments confirmed the involvement of
53                                     In vitro reconstitution experiments confirmed the requirement for
54 sed on accessibility to Fe(2+) chelators and reconstitution experiments, consistent with dynamic iron
55                                           In reconstitution experiments, CRAF R391W, but not CRAF WT,
56  these structures, combined with biochemical reconstitution experiments, cross-linking mass spectrome
57                                          Our reconstitution experiments delineate the minimal sets of
58                                              Reconstitution experiments demonstrate linearity of ASE
59                           In vitro chromatin reconstitution experiments demonstrate that H1.8 inhibit
60                                      Lastly, reconstitution experiments demonstrate that Jak2 is not
61                                              Reconstitution experiments demonstrate that Ppr covalent
62                         Remarkably, in vitro reconstitution experiments demonstrate that Wapl forms a
63 entified and immunoneutralizing antibody and reconstitution experiments demonstrated IL-8 is a critic
64                                     In vitro reconstitution experiments demonstrated that CENP-E-depe
65                      Interestingly, in vitro reconstitution experiments demonstrated that NIK was act
66                                       Medium reconstitution experiments demonstrated that spent mediu
67                                     In vitro reconstitution experiments demonstrated that the 53-kDa
68                                              Reconstitution experiments demonstrated that the additio
69                                      Soluble reconstitution experiments demonstrated that the chimeri
70                                    Moreover, reconstitution experiments demonstrated that the peptide
71                                  Fetal liver reconstitution experiments demonstrated that the require
72                                  Competitive reconstitution experiments demonstrated that Zfp36l2 KO
73 ctivity of Spo0A in vivo and, using in vitro reconstitution experiments, determine that they stimulat
74 sponsible for inhibition of LH1 formation in reconstitution experiments, different regions (N-terminu
75                                           In reconstitution experiments, either whole splenocytes, T
76 for AP release; however, immunodepletion and reconstitution experiments establish that it is necessar
77                                     In vitro reconstitution experiments established that the soluble
78                                        Metal reconstitution experiments examining the reaction kineti
79    This model is supported by the results of reconstitution experiments expressing recombinant TARS1,
80              Taken together, these microbial reconstitution experiments formally establish that a def
81                                  Bone marrow reconstitution experiments further mapped the effect of
82                                              Reconstitution experiments further reveal that ApoER2-R9
83                                  Competitive reconstitution experiments further showed that fetal liv
84                                  Bone marrow reconstitution experiments further supported an intrinsi
85 arrow transplantation and platelet depletion/reconstitution experiments generating mice with selectiv
86 -substrate network, whereas lack of in vitro reconstitution experiments has impeded insights into the
87 way for eukaryotic RNA polymerases, in vitro reconstitution experiments have been carried out with re
88 inhibit Ca(2+) uptake in imaging assays, and reconstitution experiments have been equivocal.
89                          Our recent in vitro reconstitution experiments have demonstrated that Cytosk
90 marrow (BM) have been described, irradiation-reconstitution experiments have failed to reveal defects
91                                              Reconstitution experiments have suggested that N-ethylma
92                                   Holoenzyme reconstitution experiments identified a new sigma factor
93                                  Bone marrow reconstitution experiments identified that many of the h
94                                        These reconstitution experiments illustrate Koch's postulate b
95 d optical tweezers to observe in a cell-free reconstitution experiment in real time a long-sought SNA
96                           Cell depletion and reconstitution experiments in a DSS-induced colitis mode
97 s as shown by overexpression, knockdown, and reconstitution experiments in cell culture models.
98      In this report, we conducted nucleosome reconstitution experiments in conjunction with high-thro
99  examine this question, we have used genetic reconstitution experiments in mice.
100                                Knockdown and reconstitution experiments in mouse and human breast can
101                                              Reconstitution experiments in non-hematopoietic cells sh
102                 Through loss-of-function and reconstitution experiments in pups, we showed that NK ce
103 ant of HP68 in mammalian cells and depletion-reconstitution experiments in the cell-free system, we d
104                                              Reconstitution experiments in the JAK1-deficient cells d
105                                           In reconstitution experiments in the same cell line all fou
106                                     Further, reconstitution experiments in total head homogenates sho
107                     However, in heterologous reconstitution experiments in vitro with RNase P subunit
108                                              Reconstitution experiments in which LDLR variants were i
109                                              Reconstitution experiments in which non-polysomal mRNA-b
110                         We performed in vivo reconstitution experiments in which ST8Sia IV(-/-) proge
111                                    Depletion-reconstitution experiments in Xenopus laevis egg extract
112                                              Reconstitution experiments in yeast demonstrated that LG
113                                 Our in vitro reconstitution experiments indeed identified a 5' nick-d
114                                              Reconstitution experiments indicate that both STG-1 and
115                                              Reconstitution experiments indicate that MPN/MDS and mye
116                                       Direct reconstitution experiments indicate that NK cytotoxic ac
117                                              Reconstitution experiments indicate that nucleotide and
118                                       Recent reconstitution experiments indicate that one of these, R
119                            Mixed bone marrow reconstitution experiments indicate that sbb2(a) is expr
120                                              Reconstitution experiments indicate that specific functi
121                               These in vitro reconstitution experiments indicate that there is a pref
122 4Fe-4S and 3Fe-4S clusters, and the in vitro reconstitution experiment indicated an iron-sulfur scaff
123                                              Reconstitution experiments indicated that CCND1 and p53
124                                  Bone marrow reconstitution experiments indicated that the mechanism
125                      In planar lipid bilayer reconstitution experiments, InsP3R1 activation by InsP3
126                                           In reconstitution experiments, lysophosphatidic acid comple
127                                  In in vitro reconstitution experiments, NiV particles provided time-
128                            Using bone marrow reconstitution experiments of lethally irradiated hosts,
129 NMR, and resonance Raman spectroscopies with reconstitution experiments of the apoprotein with protoh
130                                              Reconstitution experiments on cardiolipin-containing mem
131                       Combined with in vitro reconstitution experiments, our data show that the polym
132                                     In vitro reconstitution experiment proves that MMP-13, but not it
133 dings, together with the results of previous reconstitution experiments, reduce the number of possibl
134                          Tensional force and reconstitution experiments reveal a mechanosensory funct
135                                  Competitive reconstitution experiments reveal that fucoidan also eli
136                 Data obtained in bone marrow reconstitution experiments reveal that interleukin-1beta
137                                              Reconstitution experiments reveal that symplekin, previo
138                                              Reconstitution experiments revealed an important role fo
139 from infected HeLa cell lysates and in vitro reconstitution experiments revealed evidence for ubiquit
140 t for T-bet in these subsets and competitive reconstitution experiments revealed roles for T-bet in m
141               Lentiviral shRNA knockdown and reconstitution experiments revealed that both a function
142                                              Reconstitution experiments revealed that Hunk is suffici
143                                  Bone marrow reconstitution experiments revealed that infection with
144                                              Reconstitution experiments revealed that Munc18-1, Munc1
145                                  Biophysical reconstitution experiments revealed that non-enzymatic a
146 ith recombinant kinase, and kinase depletion-reconstitution experiments revealed that Ser1232 in eIF4
147                                     However, reconstitution experiments revealed that the catalytic a
148 urther mechanistic studies using bone marrow reconstitution experiments revealed that the increased d
149                         In vitro and in vivo reconstitution experiments revealed that the minimal com
150                                  Biochemical reconstitution experiments revealed that the polyubiquit
151  In this work, 30S ribosomal subunit kinetic reconstitution experiments revealed that thermodynamic d
152                                     In vitro reconstitution experiments revealed the critical and spe
153   The results from both in vivo and in vitro reconstitution experiments show increased activity level
154                                  Competitive reconstitution experiments show that average levels of 0
155                                      In vivo reconstitution experiments show that CLPs and CMPs can r
156                                  Biochemical reconstitution experiments show that EMC can directly me
157                                  Bone marrow reconstitution experiments show that Nlrp3 gene expressi
158                                  Bone marrow reconstitution experiments show that Nogo in myeloid cel
159                                     Finally, reconstitution experiments show that the association of
160                                              Reconstitution experiments show that the binding pocket
161                                              Reconstitution experiments show that the helicase activi
162                                  Bone marrow reconstitution experiments show that the PC defect is B-
163                             Bone marrow (BM) reconstitution experiments showed monocyte-dependent qua
164                             The results from reconstitution experiments showed that aged bone marrow
165                                       Enzyme reconstitution experiments showed that both microsomal a
166                                  Bone marrow reconstitution experiments showed that gammadelta T cell
167                                     In vitro reconstitution experiments showed that like AV, but in c
168                    Pharmacological and lipid reconstitution experiments showed that new synapses form
169 ilateral inhibition of suckling and hormonal reconstitution experiments showed that TGFbeta3 inductio
170                                              Reconstitution experiments showed that the formation of
171                                  Biochemical reconstitution experiments showed that the two intronic
172                                     Promoter reconstitution experiments showed that this novel elemen
173                                              Reconstitution experiments showed that, for the Sir2/Sir
174                                              Reconstitution experiments showed tight interactions bet
175 yond the nucleolus, consistent with in vitro reconstitution experiments showing that SRP19 must bind
176                                              Reconstitution experiments suggest that EP2 receptors pr
177                                              Reconstitution experiments suggest that the discrepancy
178                                 Our in vitro reconstitution experiments suggest that the Z-ring consi
179                                              Reconstitution experiments suggest that, although OB-R m
180                         Results of depletion/reconstitution experiments suggested that KuAg does not
181                                       In the reconstitution experiments, SV40 DNA was allowed to inte
182           Here, we show using functional GFP reconstitution experiments that Kenyon cells and dopamin
183            We show using in vivo bone marrow reconstitution experiments that ligand-independent activ
184 llular source for this mediator, we find via reconstitution experiments that mast cells are a dispens
185 as cell autonomous, because in a competitive reconstitution experiment the knockout-derived cells pro
186 de RNAi screening approaches and biochemical reconstitution experiments, the basic machinery of FGF2
187                                           In reconstitution experiments, the mitochondrial cytochrome
188  whole frequency range accessible in channel reconstitution experiments, the noise power spectrum is
189 vivo fluorescence spectroscopy, and in vitro reconstitution experiments, this study demonstrates that
190                             By extending the reconstitution experiment to include the guanine nucleot
191 e have used structural probing and molecular reconstitution experiments to examine the structures for
192 Dyn2 KO cell line and performed knockout and reconstitution experiments to explore the isoform- and s
193           We have now used fractionation and reconstitution experiments to functionally identify cell
194 cipitation-coupled western blot and in vitro reconstitution experiments to show that HSP70-2 interact
195             We performed BAC mutagenesis and reconstitution experiments to test the hypothesis that t
196                                              Reconstitution experiments to unravel essential componen
197 opy (cryo-EM), protein structure prediction, reconstitution experiments, tRNA sequencing, and other s
198 mpaired in the LTalpha-/- mice, we performed reconstitution experiments using a hapten/carrier system
199                                           In reconstitution experiments using purified proteasomes an
200                                  Biochemical reconstitution experiments using purified proteins revea
201                                              Reconstitution experiments using recombinant proteins an
202 e was essential in promoting angiogenesis as reconstitution experiments using Src-transformed FAK-nul
203                                              Reconstitution experiments utilizing exogenous recombina
204                                      Through reconstitution experiments, we demonstrate here that TIN
205 lusions based on nonphysiological nucleosome reconstitution experiments, we find that the histone ami
206                                      Through reconstitution experiments, we have defined more precise
207               Through live cell and in vitro reconstitution experiments, we have discovered a major s
208 synthesis, functional genetics and enzymatic reconstitution experiments, we show that this previously
209                                           In reconstitution experiments, we showed that human DNA pol
210                          Using depletion and reconstitution experiments, we showed that IL-4-responsi
211                                Depletion and reconstitution experiments were consistent with a suppre
212 sensitization model was used and bone marrow reconstitution experiments were performed to test the re
213 sensitization model was used and bone marrow reconstitution experiments were performed to test the re
214                   In this study, biochemical reconstitution experiments were used to gain insight int
215 tional activity in an in vitro transcription reconstitution experiment, whereas the L protein in peak
216                                              Reconstitution experiments with a chemically synthesized
217                             Using microbiota reconstitution experiments with a set of immunocompromis
218                     Herein, we used in vitro reconstitution experiments with chemically synthesized,
219                    Here, we combine in vitro reconstitution experiments with computational modeling t
220 onstructs, coimmunoprecipitation, functional reconstitution experiments with deletion mutants, and pe
221                                              Reconstitution experiments with different fusion assays
222                                              Reconstitution experiments with different RIP mutants fu
223                 We perform in vitro motility reconstitution experiments with high-resolution particle
224                                              Reconstitution experiments with mutant MAP65-1 proteins
225                                              Reconstitution experiments with pertussis toxin-insensit
226                                     In vitro reconstitution experiments with proteins from both M. ca
227 ng in a mouse knockout model and biochemical reconstitution experiments with pure proteins, we find t
228                                     In vitro reconstitution experiments with purified cyt b6f and rec
229                            Using bone marrow reconstitution experiments with purified PIGA(-) cells w
230                                              Reconstitution experiments with purified proteins indica
231 otubule polymerization rates in cells and in reconstitution experiments with purified tubulin.
232                                              Reconstitution experiments with recombinant interleukin
233                                           In reconstitution experiments with recombinantly expressed
234                                              Reconstitution experiments with the individual genes dem
235               A combination of knockdown and reconstitution experiments with wild type and a PDZ doma
236 trated in vitro using blocking antibody, and reconstitution experiments with wild-type and mutant Fcg
237      Affinity chromatography and biochemical reconstitution experiments with Xenopus egg extracts ide
238                             Renaturation and reconstitution experiments with Zn(2+) ions failed to pr

 
Page Top