戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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 and eventually to monomers as separated on a sucrose density gradient.
2 lex that sedimented at approximately 5S in a sucrose density gradient.
3 so be detected by co-sedimentation through a sucrose density gradient.
4  isolated between 1.17 and 1.21 g/cm(3) in a sucrose density gradient.
5  remains bound to liposomes centrifuged on a sucrose density gradient.
6  was detected only in the CRD fractions of a sucrose density gradient.
7  by centrifugation and further purified by a sucrose density gradient.
8 t detergent treatment, using a discontinuous sucrose density gradient.
9 se (RT) activity that banded at 1.15 g/ml in sucrose density gradients.
10 nit that is immature and migrates at 45 S in sucrose density gradients.
11 tudy (<380 nM), as judged by its mobility in sucrose density gradients.
12 insoluble protein recovered at the bottom of sucrose density gradients.
13 lexes toward the uncoiled lariat position in sucrose density gradients.
14 d with non-polysomal, but dense fractions on sucrose density gradients.
15 pulina hyodysenteriae by using discontinuous sucrose density gradients.
16 R1 by flotation of CHAPS lysates of cells in sucrose density gradients.
17  and comigrates with the outer dynein arm in sucrose density gradients.
18 lipid membranes as assessed by floatation in sucrose density gradients.
19 tionic lipid was confirmed and quantified on sucrose density gradients.
20 ts with known cytoplasmic dynein proteins in sucrose density gradients.
21 icated by aqueous two-phase partitioning and sucrose density gradients.
22 containing a known glycoprotein in flotation sucrose density gradients.
23 atalytically active following isolation from sucrose density gradients.
24  cofractionates with the outer dynein arm in sucrose density gradients.
25 M Na(2)CO(3) buffer and fractionated through sucrose density gradients.
26  associated with liposomes and aggregated on sucrose density gradients.
27 5 M KI, and copurifies with radial spokes in sucrose density gradients.
28  and fractionation of retinal lysates, using sucrose density gradients.
29 of 1.07 to l.14 as defined by flotation into sucrose density gradients.
30 ent; cores were isolated by sedimentation in sucrose density gradients.
31 o-sedimenting with caveolin and flotillin on sucrose density gradients.
32                                              Sucrose density gradient analyses revealed formation of
33                                              Sucrose density gradient analyses revealed that depletio
34                                              Sucrose density gradient analysis demonstrated that both
35                                              Sucrose density gradient analysis detected AP1B predomin
36                                              Sucrose density gradient analysis indicates that a signi
37                                              Sucrose density gradient analysis of in vitro translates
38                                 Furthermore, sucrose density gradient analysis revealed significantly
39                                              Sucrose density gradient analysis revealed that in antim
40 d with normal prostate epithelial cells, and sucrose density gradient analysis showed co-sedimentatio
41                                              Sucrose density gradient analysis showed that 96% of the
42                              High-resolution sucrose density gradient analysis showed that, while mut
43                                              Sucrose density gradient analysis was employed to determ
44 -free cytoplasmic complexes that copurify in sucrose density gradients and are stable in nonionic det
45 into the vesicle compartment as confirmed by sucrose density gradients and confocal immunofluorescent
46 as isolated as a low buoyant density band on sucrose density gradients and exhibited an increase in l
47      LC9 copurifies with outer arm dynein in sucrose density gradients and is missing only in those s
48 fferent PCDH15 and VLGR1 variants along with sucrose density gradients and the use of vesicle traffic
49  shift from middle to low density regions on sucrose density gradients) and cytosol fractions.
50 resh bovine brain and size fractionated on a sucrose density gradient, and a size-fractionated bovine
51              Yeast lysates were separated on sucrose density gradients, and fractions assayed for org
52 Deriphat-polyacrylamide gel electrophoresis, sucrose density gradients, and isolated PSII particles,
53 GN/endosome-resident SNAREs cofractionate in sucrose density gradients, and show similar solubility o
54 ist in membranes that float on discontinuous sucrose density gradients, and that methyl-beta-cyclodex
55  is found in the same fraction as 125I-Tf on sucrose density gradients, and this fraction can be spec
56 hia coli TonB was found to be distributed in sucrose density gradients approximately equally between
57 ibosome profiles upon centrifugation through sucrose density gradients, association of mutant 30 S su
58  high-speed centrifugation and sedimented in sucrose density gradients at the same bouyant density as
59                                           In sucrose density gradients, Bop1 from nuclear extracts co
60 y Triton insoluble membranes that floated in sucrose density gradients but was recruited to these mem
61 h these proteins and comigrated with them on sucrose density gradients, but it did not colocalize, co
62 ower sedimentation rate than native virus on sucrose density gradients, but the particles retained al
63 ndicated by immunofluorescence localization, sucrose density gradients, cell fractionation, and yeast
64     However, the splitting was observed with sucrose density gradient centrifugation (SDGC) without I
65                                        Using sucrose density gradient centrifugation and antibody pul
66                                     Instead, sucrose density gradient centrifugation and electron mic
67 ner and outer membranes were fractionated by sucrose density gradient centrifugation and identified b
68 wing both ATP-sensitive microtubule affinity/sucrose density gradient centrifugation and immunoprecip
69 ocytosis" into the light vesicle fraction in sucrose density gradient centrifugation assays, as did t
70 ecipitation, native gel electrophoresis, and sucrose density gradient centrifugation assays.
71          Immunoblotting of rafts isolated by sucrose density gradient centrifugation demonstrated rec
72                                              Sucrose density gradient centrifugation of a maize mitoc
73                                              Sucrose density gradient centrifugation of A6 cell deter
74 onocytogenes 100S ribosomes were observed by sucrose density gradient centrifugation of bacterial ext
75   Viral core-like complexes were isolated by sucrose density gradient centrifugation of detergent-tre
76 to ET-1 in subcellular fractions obtained by sucrose density gradient centrifugation of human umbilic
77                                              Sucrose density gradient centrifugation of large ribosom
78                                           By sucrose density gradient centrifugation of membranes, ho
79 gent-insoluble membrane fraction prepared by sucrose density gradient centrifugation of postnuclear f
80                                              Sucrose density gradient centrifugation of postnuclear s
81                                   Similarly, sucrose density gradient centrifugation of purified MAO
82                                              Sucrose density gradient centrifugation of the culture m
83                                              Sucrose density gradient centrifugation of the ribosomal
84                                Discontinuous sucrose density gradient centrifugation revealed NET in
85 Characterization of the circulating mRNAs by sucrose density gradient centrifugation revealed that th
86       Examination of lipid rafts isolated by sucrose density gradient centrifugation revealed the con
87                                              Sucrose density gradient centrifugation reveals two majo
88 se of internal ribosome entry mechanisms and sucrose density gradient centrifugation showed that BC1-
89                                              Sucrose density gradient centrifugation showed that expo
90        Separation of purified E1 proteins by sucrose density gradient centrifugation showed that the
91                                        Using sucrose density gradient centrifugation to analyze ribos
92 dily detected in outer membranes produced by sucrose density gradient centrifugation, but it is sarco
93          Mutant viral particles, purified by sucrose density gradient centrifugation, had low infecti
94                                              Sucrose density gradient centrifugation, immunoblot, and
95                            Enzymatic assays, sucrose density gradient centrifugation, immunoprecipita
96 nd when subjected to size-exclusion HPLC and sucrose density gradient centrifugation, in the presence
97 fferent approaches including gel filtration, sucrose density gradient centrifugation, pull-down of di
98                                        Using sucrose density gradient centrifugation, this study eval
99 pheroplasting and osmotic lysis, followed by sucrose density gradient centrifugation, which separated
100                                  As shown by sucrose density gradient centrifugation, WT gamma-PAK, S
101 enriched membranes with DodGlc2, followed by sucrose density gradient centrifugation, yielded a super
102 e steps of gel filtration chromatography and sucrose density gradient centrifugation.
103 eolae-enriched membrane fractions as seen by sucrose density gradient centrifugation.
104 um carbonate without detergent), followed by sucrose density gradient centrifugation.
105  cholesterol were incubated and subjected to sucrose density gradient centrifugation.
106           Oocysts were initially isolated by sucrose density gradient centrifugation.
107 bidopsis suspension-cultured cells following sucrose density gradient centrifugation.
108 ciated with centrosome fractions isolated by sucrose density gradient centrifugation.
109 ce of solubilized oligomers was confirmed by sucrose density gradient centrifugation.
110 response to insulin binding as determined by sucrose density gradient centrifugation.
111 n-insoluble membranes then were separated by sucrose density gradient centrifugation.
112 ans of their light buoyant densities through sucrose density gradient centrifugation.
113 s after disruption and initial separation by sucrose density gradient centrifugation.
114                                              Sucrose density-gradient centrifugation showed that the
115 wever, we show by chemical cross-linking and sucrose density-gradient centrifugation that in the abse
116 amination by aqueous two-phase partitioning, sucrose density-gradient centrifugation, and immunoelect
117 roteins by size exclusion chromatography and sucrose-density gradient centrifugation revealed that th
118  performed gel filtration chromatography and sucrose density gradient centrifugations in H(2)O and D(
119     We have used immunogold localization and sucrose density gradient cosedimentation analyses to con
120  Subcellular fractionation using equilibrium sucrose density gradients demonstrated decreased hyperph
121                                Result of the sucrose density gradient experiment suggests that Der in
122                                         Upon sucrose density gradient flotation, membrane- associated
123                                              Sucrose density gradient fractionation and gel filtratio
124                                Discontinuous sucrose density gradient fractionation and immunoconfoca
125                                       During sucrose density gradient fractionation of bovine retinas
126                                        Using sucrose density gradient fractionation of cell membranes
127                                              Sucrose density gradient fractionation of cytoplasmic ex
128                          Using discontinuous sucrose density gradient fractionation of post-nuclear s
129 f epitope-tagged versions of Upf proteins by sucrose density gradient fractionation of soluble lysate
130                                              Sucrose density gradient fractionation of the culture me
131                                              Sucrose density gradient fractionation of the purified c
132                                              Sucrose density gradient fractionation reveals that loss
133 th Gpa1 at the plasma membrane, as judged by sucrose density gradient fractionation.
134 n blot analysis of cell lysates separated by sucrose density gradient fractionation.
135                                              Sucrose-density gradient fractionation demonstrated that
136  form of CD39L4 by measuring the activity of sucrose density gradient fractions of monomers and parti
137 asts, as well as subcellular fractionations, sucrose density gradients, immunocytochemical labeling,
138 at Pixie associates with the 40 S subunit on sucrose density gradients in an ATP-dependent manner.
139 FP-modified Rab5 as a larger mass complex on sucrose density gradients indicates that it binds to oth
140 ediments with the product of the LF1 gene in sucrose density gradients, indicating that these protein
141                                           In sucrose density gradients, KIF3C sediments at two distin
142                          Its distribution on sucrose density gradients matched the absorbance profile
143  radiolabeling with [(3)H]palmitic acid, and sucrose density gradient membrane partitioning studies.
144                                      We used sucrose density gradients of nucleosomes prepared by par
145 65 recognized a protein of roughly 65 kDa in sucrose density gradient-purified HHV-7 preparations; tr
146 al detergent extraction and fractionation in sucrose density gradients revealed TcdB-induced redistri
147 as released from infected cells; analysis on sucrose density gradients revealed that the precursor se
148 ntact sites were analyzed using a continuous sucrose density gradient, revealing an apparent heteroge
149                             Sedimentation in sucrose density gradients reveals that large unilamellar
150                                              Sucrose density gradient sedimentation analysis indicate
151 cupied ER complex shows distinct behavior by sucrose density gradient sedimentation analysis.
152 ere expressed in COS-1 cells and analyzed by sucrose density gradient sedimentation and gel filtratio
153                   Two-phase partitioning and sucrose density gradient sedimentation established that
154                                      We used sucrose density gradient sedimentation to ascertain whet
155 on X-100 in combination with gel filtration, sucrose density gradient sedimentation, and gel electrop
156 nt outside the lipid rafts, as determined by sucrose density gradient sedimentation.
157 t and beta-mercaptoethanol, and subjected to sucrose density gradient sedimentation.
158  enzyme was constructed and characterized by sucrose-density gradient sedimentation, size-exclusion c
159                                              Sucrose density gradient separation and immunoblotting w
160                                              Sucrose density gradients show that EGO is not associate
161                Analysis of soluble hensin by sucrose density gradients showed that low density cells
162                    Sedimentation analysis in sucrose density gradients showed that the CSP epitope ac
163                   Subfractionation of LDM on sucrose density gradients shows that insulin significant
164                                        Using sucrose density gradient, size-exclusion chromatography,
165 s of LIV during rate-zonal centrifugation in sucrose density gradients, suggesting that the enzyme is
166 er proteins as its sedimentation behavior in sucrose density gradient suggests an association with th
167 ments (L and R-DNA-gp3) sedimented faster in sucrose density gradients than their proteinase K-treate
168 branes were subfractionated on discontinuous sucrose density gradients to equilibrium or under nonequ
169  study, we used equilibrium sedimentation in sucrose density gradients to separate PrP(Sc) aggregates
170                                           In sucrose density gradients, Triton X-100-solubilized CaR
171                                           In sucrose density gradients Trypanosoma brucei NOG1 co-sed
172                                        Using sucrose density gradient ultracentrifugation and a sensi
173 mmunoprecipitation, confocal microscopy, and sucrose density gradient ultracentrifugation in mice.
174 ligomeric state of the purified complexes by sucrose density gradient ultracentrifugation revealed th
175                                              Sucrose density gradient ultracentrifugation studies wer
176               We also employed discontinuous sucrose density gradient ultracentrifugation to show tha
177  combination of both confocal microscopy and sucrose density gradient ultracentrifugation, we show th
178 rification by agarose gel electrophoresis or sucrose density gradient ultracentrifugation.
179  separated from the protoplasmic cylinder by sucrose density gradient ultracentrifugation.
180 cell culture-grown HCV after purification by sucrose density gradient ultracentrifugation.
181          Carbonate treatment, sonication and sucrose density-gradient ultracentrifugation are subsequ
182                                           In sucrose density gradients, Vif cosediments with capsid p
183                                        Using sucrose density gradients we have found that human T cel
184                               However, using sucrose density gradients, we demonstrate that the assoc
185                                Discontinuous sucrose density gradients were used for fractionation of

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top