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1 ands ( approximately 60 kDa) present in each subcellular fraction.
2 32, RIP accumulated in a detergent-insoluble subcellular fraction.
3 the endoplasmic reticulum-Golgi intermediate subcellular fraction.
4 ed protein is associated with the microsomal subcellular fraction.
5 hips differed according to age, isoform, and subcellular fraction.
6 function and is expressed in the particulate subcellular fraction.
7 re their activities in the lysosome-enriched subcellular fraction.
8 s found to associate with a tubulin-enriched subcellular fraction.
9 tro reaction containing this novel adipocyte subcellular fraction.
10 a levels, with reduced targeting to synaptic subcellular fractions.
11  the content of receptor subunits in various subcellular fractions.
12 hich results in significant contamination of subcellular fractions.
13  proteins and proteins from granule-enriched subcellular fractions.
14 ) complexes in isolated phagosomes and other subcellular fractions.
15 y and/or immunoblotting and enzyme assays of subcellular fractions.
16 and shape to the CaMKII clusters observed in subcellular fractions.
17 are differentially partitioned between these subcellular fractions.
18 st, PLDbeta was not detectable in any of the subcellular fractions.
19 by confocal microscopy and immunoblotting of subcellular fractions.
20 ent subcompartments of the Golgi, as well as subcellular fractions.
21 on could be reconstituted in Golgi- enriched subcellular fractions.
22  of protein phosphorylation were detected in subcellular fractions.
23 ts translocation from soluble to particulate subcellular fractions.
24 e in flavin biosynthesis, is present in both subcellular fractions.
25  arise from redistribution of proteins among subcellular fractions.
26 A) in RNA transcripts by analyzing different subcellular fractions.
27        Five cross-linked bands appear in all subcellular fractions.
28 kt immune complexes from lipid raft-enriched subcellular fractions.
29 esence or absence of M. tuberculosis and its subcellular fractions.
30 ons showed ASPA is an active monomer in both subcellular fractions.
31 d by Western blot analyses of four different subcellular fractions.
32 ively assess lipid compositions of cells and subcellular fractions.
33 nts that are commonly found as impurities in subcellular fractions.
34  the detection of cytoskeletal impurities in subcellular fractions.
35 nogold method, and by immunoblot analysis of subcellular fractions.
36 ns was found in substantial amounts in other subcellular fractions.
37 ibited a negligible contamination with other subcellular fractions (1-4%) and high degree of function
38 fraction was similar or higher than in other subcellular fractions after both the pulse and the chase
39 were primarily found in a cell wall-enriched subcellular fraction and correlated with the presence (o
40 nding of [3H]-DGR is most enriched in the P2 subcellular fraction and is heterogeneously distributed
41              Studies with well characterized subcellular fractions and by indirect immunofluorescence
42             Protein interaction studies used subcellular fractions and detergent lysates prepared fro
43 is a function of its presence among specific subcellular fractions and established that HMW1 is a per
44  thereof, was further evaluated by preparing subcellular fractions and examining them for the presenc
45                     We measured Cd and Se in subcellular fractions and found that larvae sequestered
46                                              Subcellular fractions and fractions enriched in photorec
47 uro2a cells by both Western blot analysis of subcellular fractions and immunofluorescence analysis.
48                     Western blot analysis of subcellular fractions and indirect immunofluorescence an
49 on microscopic evaluation of M. tuberculosis subcellular fractions and intact bacteria confirm that P
50  from this population of microtubule binding subcellular fractions and its cleavage was unaffected in
51  be translocated to the membrane and nuclear subcellular fractions and PKC-delta to be depleted from
52          Analysis of Mycobacterium smegmatis subcellular fractions and spheroplasts showed that LAM a
53  intact human embryonic kidney 293 cells and subcellular fractions and were correlated with the rate
54 were observed in both pellet and supernatant subcellular fractions and were regulated by Ric-8A in bo
55 f G proteins, associate with the particulate subcellular fraction, and are present in the nucleus.
56 d on immunofluorescence, Western blotting of subcellular fractions, and epitope tagging with enhanced
57 d a similar distribution of PGHS-1 and -2 in subcellular fractions, and product analysis using isozym
58 -labeled rRNA substrates were incubated with subcellular fractions, and the conversion of uridine to
59 ical VGLUT1 mRNA, striatal VGLUT1 protein in subcellular fractions, and the Vmax of striatal vesicula
60 imately 25 kd in hepatocyte lysates, hepatic subcellular fractions, and tissue extracts.
61 n of neutrophils by Western blot analyses of subcellular fractions as well as by RT-PCR analyses of n
62 o be highly enriched in a novel cytoskeletal subcellular fraction associated with plasma membranes.
63 HeLa cells increased the levels of SM in all subcellular fractions, but the change was most dramatic
64 olase activity associated with the ribosomal subcellular fraction by differential centrifugation.
65 as shown to be associated with the ribosomal subcellular fractions by differential centrifugation.
66  epsilon from the soluble to the particulate subcellular fraction, cell cycle arrest in G1 phase, and
67 soforms were more prevalent in the cytosolic subcellular fraction compared to the particulate fractio
68 otein expression changes, protein changes in subcellular fractions, components of protein complexes,
69 f an alternative proreceptor of 170 kDa in a subcellular fraction consistent with endoplasmic reticul
70 s an anchor to the microtubules for specific subcellular fractions containing amyloidogenic fragments
71 ytosol of viable cells, but was recovered in subcellular fractions containing secretory granule-local
72 tin-binding protein utrophin are enriched in subcellular fractions containing secretory granules.
73           Both nNOS and HAP1 are enriched in subcellular fractions containing synaptic vesicles.
74 characterize the expression of DM in vivo in subcellular fractions containing the IIPLC.
75  synaptoneurosome experiments show that this subcellular fraction contains a similar complement of sp
76                                 The isolated subcellular fraction contains less than 1% of the total
77            T hybridoma responses to isolated subcellular fractions demonstrated OVA (323-339):I-Ad co
78 eriments as well as Western blot analysis on subcellular fractions demonstrated that Odin is localize
79             Immunoblot analysis of rat liver subcellular fractions demonstrated that this protein was
80                 Western blot analysis of PMN subcellular fractions demonstrated the presence of pp1al
81                     Western blot analysis of subcellular fractions demonstrated translocation of BIG2
82 isoform could potentially be present in both subcellular fractions, depending on the calcium level of
83 xamined in a novel cell-free assay utilizing subcellular fractions derived from 3T3-L1 adipocytes.
84           Inactivated M. tuberculosis or its subcellular fractions did not result in A549 necrosis or
85                           Analysing distinct subcellular fractions (e.g. myofibrillar, sarcoplasmic,
86                            We also show that subcellular fractions enhancing disease-specific prion p
87 and MLC2 were overrepresented in a rat liver subcellular fraction enriched in canalicular membrane ve
88                     Moreover, we show that a subcellular fraction enriched in mitochondria is require
89 n the postsynaptic density (PSD) fraction, a subcellular fraction enriched in structures with the mor
90 and HAX-1 were over-represented in rat liver subcellular fractions enriched for canalicular membrane
91                 Further biochemical tests on subcellular fractions enriched for clathrin-coated vesic
92 und that ErbB receptors are present in brain subcellular fractions enriched for postsynaptic densitie
93                     Third, in immunoblots of subcellular fractions enriched with PVs from amastigote-
94 ism for Rad51 nuclear transport, we analyzed subcellular fractions for two other Rad51-interacting pr
95                  To identify these proteins, subcellular fractions free of bacteria were probed with
96 , we find that the amount of ionic copper in subcellular fractions from brain is similar in all three
97 nelles containing doxorubicin (DOX) in crude subcellular fractions from CCRF-CEM and CEM/C2 cell line
98      Further, immunoblot analyses of hepatic subcellular fractions from ethanol-damaged livers indica
99  of hNMT was also examined by immunoblotting subcellular fractions from HeLa cells transfected with p
100                                    Utilizing subcellular fractions from M. smegmatis and M. tuberculo
101                                 In contrast, subcellular fractions from macrophages that ingested zym
102            The delta opioid binding sites in subcellular fractions from NG108-15 cells were character
103 uorescence microscopy and enzyme analyses of subcellular fractions from ODC-overexpressing cells demo
104                                              Subcellular fractions from patient PMNs generated less O
105                       Immunoblot analyses of subcellular fractions from stably transfected CWSV1 cell
106                     Western blot analysis of subcellular fractions from sucrose equilibrium density g
107                   Previous investigations of subcellular fractions from suspension-cultured cells of
108                         PTPase activities in subcellular fractions from the nondiabetic obese subject
109                                         When subcellular fractions from toxin-sensitive cells were in
110      We exploited this property to isolate a subcellular fraction highly enriched in cAR1 by flotatio
111  decreased with advancing age in three brain subcellular fractions, homogenate, cytosol, and synaptic
112 reasing accumulation and distribution in two subcellular fractions (i.e., metallothionein-like protei
113  hippocampal PKCgamma concentrations in both subcellular fractions in comparison with young rats, and
114 entified as a component of myelin-containing subcellular fractions in proteomic studies and mutations
115 and OSBP2 detected the proteins in different subcellular fractions in the retinal monkey tissue.
116                      ROC operates in various subcellular fractions including microsomes, mitochondria
117 13, glycosylated Fap1 was present in all the subcellular fractions including the cytoplasm.
118 determine the lipids in liver homogenate and subcellular fractions, including mitochondria, light mit
119    The remaining isoforms are present across subcellular fractions, including nuclei and are soluble.
120                     Western blot analysis of subcellular fractions indicated enrichment of A2BP1 in t
121 ence localization and immunoblot analysis of subcellular fractions indicated that expressed Myc-Rab1B
122                      Biochemical analysis of subcellular fractions indicated that pro-caspase-8 was e
123 Association of PLC-gamma1 with the insoluble subcellular fraction is also enhanced in PDGF-stimulated
124                                              Subcellular fractions isolated from 32P-labeled hepatocy
125                                      Mammary subcellular fractions isolated from Rbp1(-/-) mice have
126 ctivity of native oPGHS-1 and partitioned in subcellular fractions like native oPGHS-1; however, the
127          Western blotting of M. tuberculosis subcellular fractions localized CFP32 predominantly to t
128 in conventional steady-state MFA, tissues or subcellular fractions must be dissected or biochemically
129 added big endothelin-1 (big ET-1) to ET-1 in subcellular fractions obtained by sucrose density gradie
130 nnel, were normally expressed in the correct subcellular fraction of both cell lines.
131      In vitro kinase assays, using different subcellular fractions of 3T3-L1 adipocytes, revealed tha
132                             T cell assays on subcellular fractions of Ag-pulsed macrophages detected
133                                           In subcellular fractions of Arabidopsis leaves, PLDalpha an
134        The relative distribution of GLUT4 in subcellular fractions of basal and insulin-stimulated IR
135  chain reaction and Western blot analysis of subcellular fractions of both cell types.
136 the increased uptake of [3H]LIGA 20 into the subcellular fractions of brain including cell nuclei.
137 another study on the distribution of ARF6 in subcellular fractions of Chinese hamster ovary (CHO) cel
138  blot analysis of the distribution of p50 in subcellular fractions of COS-1 cells shows that p50 is a
139 k2 can be phosphorylated at Thr68 by various subcellular fractions of HEK293 cells.
140                             We have analyzed subcellular fractions of HeLa and HCT116 cells and found
141                      Biochemical analyses of subcellular fractions of HeLa cells further demonstrate
142                               Immunoblots of subcellular fractions of hepatocytes showed enrichment o
143 n cancer cells but was notably absent in all subcellular fractions of HOSE cells.
144               Western immunoblot analysis of subcellular fractions of N. gonorrhoeae strain F62 and N
145 sylated polypeptides occurred in appropriate subcellular fractions of normal mouse tissues.
146                                  Analysis of subcellular fractions of pea leaves and red beet roots e
147       Proteomic analysis of sucrose-gradient subcellular fractions of platelets indicated that NBEAL2
148 CT-related reductase activity was assayed in subcellular fractions of PNS-derived membranes isolated
149 lved in the degradation of desaturase, liver subcellular fractions of rats that had undergone inducti
150                                              Subcellular fractions of resting cells that were positiv
151            Determination of PI4K activity in subcellular fractions of SH-SY5Y cells indicated that en
152 e (PP) 1 and 2A holoenzymes present in three subcellular fractions of skeletal muscle.
153 ochemical activity assays and immunoblots of subcellular fractions of sperm incubated with the sterol
154 membrane events of tyrosine phosphorylation, subcellular fractions of T cells were treated with the P
155                                           Of subcellular fractions of the anther homogenate, the two
156       Binding of [3H]PAF was investigated in subcellular fractions of the epithelia of bovine corneas
157                                           In subcellular fractions of the whole retina, osteonectin/S
158  Further biochemical characterization of the subcellular fractions of the wzy mutant demonstrated tha
159 P hydrolytic and cGMP hydrolytic activity in subcellular fractions of this tissue.
160 iated with paclitaxel resistance in discrete subcellular fractions of two drug-resistant sublines rel
161  "N1," which is present in membrane-enriched subcellular fractions of wild-type mice.
162 athways in obese cells by delivery of normal subcellular fractions offers a potential new tool for ce
163              Using binding assays on myocyte subcellular fractions or a fluorescent alpha1-AR antagon
164 resent in the microsomal, nuclear (P-1), and subcellular fractions (P-2).
165 s also detected in the organelle and nuclear subcellular fraction prepared from murine fibroblasts.
166 of the various GPI biosynthetic reactions in subcellular fractions prepared from homogenates of mamma
167 uantify proteins in a given proteome (cells, subcellular fractions, protein complexes, tissues or bod
168                       Proteomic profiling on subcellular fractions provides invaluable information re
169                                 iCLIP-seq of subcellular fractions revealed that Rbfox1 bound predomi
170            Immunoprecipitation of c-Cbl from subcellular fractions reveals that p85 is predominantly
171                   Immunoblot analysis of the subcellular fraction showed that the 24-kDa FGF-2 was pr
172 as a dimer, size-exclusion chromatography of subcellular fractions showed ASPA is an active monomer i
173  SC2A mitochondria than in VC, whereas other subcellular fractions showed little rate difference.
174                       Immunoblot analysis of subcellular fractions showed pantophysin present exclusi
175 ates of S-nitrosocysteine decay in different subcellular fractions showed selective association with
176                                          The subcellular fractions studied both showed high protein l
177 nslational assembly events require ATP and a subcellular fraction, suggesting a requirement for a cel
178        It yielded a soluble, multicomponent, subcellular fraction termed the 27K vaccine.
179 (FMRP) in these processes by use of synaptic subcellular fractions, termed synaptoneurosomes.
180 factor, and (c) a detergent-insensitive host subcellular fraction that can be depleted and reconstitu
181 l PS2 complexes were co-localized to a novel subcellular fraction that is distinctively positive for
182 n immunofluorescence and western blotting of subcellular fractions that CHD7 is also constitutively l
183  the distribution of 13 metabolites in three subcellular fractions that form a pellet at < 1,400 g, 1
184 g these isozymes in crude tissue extracts or subcellular fractions; that is, activity lost after incu
185  measurements of enzyme activity in resolved subcellular fractions to define mechanisms that potentia
186 d immunofluorescence and Western blotting of subcellular fractions to investigate the distribution of
187                   We report changes in three subcellular fractions: total soluble protein, chloroplas
188  Although I(kappa)B(alpha) was found in both subcellular fractions, treatment with IR resulted in the
189 still be targeted to a mitochondria-enriched subcellular fraction via Miro and Milton.
190  post-injury and calcineurin distribution in subcellular fractions was assayed by Western blot analys
191        Relative abundance of PKC isoforms in subcellular fractions was determined by immunoblot analy
192                         [3H]P1075 binding to subcellular fractions was highest in membranes enriched
193                              PKC activity in subcellular fractions was measured by peptide substrate
194                           PDE1C1 activity in subcellular fractions was quantified using a new PDE1-se
195 cence microscopy, and immunoblot analysis of subcellular fractions, we also demonstrate that the G185
196 hy, PKC activity and its distribution in the subcellular fraction were determined in cultured neonata
197                                              Subcellular fractions were also examined for the presenc
198                                              Subcellular fractions were assayed for the ability to mo
199 icroM PAF (1 min), and whole cell lysates or subcellular fractions were immunoprecipitated or slides
200 O(2)(-) was measured, whole-cell lysates and subcellular fractions were prepared, or the PMNs were fi
201 ey reduced the amount of NS3 and NS5A in the subcellular fraction where active HCV RNA replication co
202  involved in targeting hNMT to the ribosomal subcellular fraction where cotranslational N-myristoylat
203 nd in the chromatin bound and nuclear matrix subcellular fractions while the mutant product was mainl
204 d t-PA antigen were co-localized to the same subcellular fraction with a major peak at 1.4 M sucrose,
205  chromatographic separation of extracts from subcellular fractions with quantitative label-free prote
206 s were found at similar concentration in all subcellular fractions with the exception of a mitochondr
207 as measured by incubating active human liver subcellular fractions with thyroid hormones (T4 and rT3

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