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1 ouble basic residues also lodged in the cell membrane fraction.
2 ation of CD95 with the lipid raft-containing membrane fraction.
3 ins generally are most abundant in the inner membrane fraction.
4 howed that PAP-7A was highly enriched in the membrane fraction.
5 s Tiam1, and were primarily increased in the membrane fraction.
6 ty of WalJ(Spn) were recovered from the cell membrane fraction.
7 pA, but not PspF, mainly associated with the membrane fraction.
8 NARE Vam3, AP-3 shifts from the cytosol to a membrane fraction.
9 X-100-insoluble to the Triton X-100-soluble membrane fraction.
10 amounts of FtsK, FtsQ, FtsI, and FtsN in the membrane fraction.
11 n indicated that Frmpd1 stabilizes AGS3 in a membrane fraction.
12 , and KChIP3x are highly associated with the membrane fraction.
13 the analysis of an Escherichia coli enriched membrane fraction.
14 oteins (FPs) and FPs targeted to the nonraft membrane fraction.
15 rked reduction in the Triton X-100-resistant membrane fraction.
16 c reticulum, and the mitochondria-associated membrane fraction.
17 cantly lower NOS3 enrichment in the caveolar membrane fraction.
18 a positive regulatory protein of NOX, to the membrane fraction.
19 ys mutants were predominantly present in the membrane fraction.
20 iculum (RER) and vesicles present in a Golgi membrane fraction.
21 t is associated predominantly with the outer membrane fraction.
22 S, Rac1 was activated and relocalized to the membrane fraction.
23 tributed between the cytoplasm and the inner membrane fraction.
24 e plasma membrane but also with a less dense membrane fraction.
25 Orb2A is also found enriched in the synaptic membrane fraction.
26 (ICD), which was loosely associated with the membrane fraction.
27 olipids in parallel, using the same enriched membrane fraction.
28 lpha (PKCalpha) translocated from cytosol to membrane fraction.
29 ntitative proteomics of a tonoplast-enriched membrane fraction.
30 Endogenous EFA6R was present in the plasma membrane fraction.
31 bidopsis tissues and present in a microsomal membrane fraction.
32 on on the sites identified in the human lens membrane fraction.
33 cholesterol cofractionate with this buoyant membrane fraction.
34 tion to the purified mitochondria-associated membrane fraction.
35 , and oligomers are enriched in the synaptic membrane fraction.
36 amount of tight junction protein present in membrane fractions.
37 as SAUR63:HA was present in both soluble and membrane fractions.
38 ence, but both are present in nuclear and SR/membrane fractions.
39 forms are proposed to be localized in these membrane fractions.
40 umarate via fumarate reductase by suppressor membrane fractions.
41 The protein was localized in the membrane fractions.
42 f localization of proteins within lipid raft membrane fractions.
43 crose gradients, APM1 occurs in unique light membrane fractions.
44 dria, and ribosomes, were identified in both membrane fractions.
45 L-type Ca2+ channel alpha1 subunit in heart membrane fractions.
46 to be present in detergent-resistant, plasma membrane fractions.
47 inA and M7 are associated with each other in membrane fractions.
48 lar-weight polymer that was detected only in membrane fractions.
49 C class II compartment (MIIC) and the plasma membrane fractions.
50 receptor is retained in detergent-resistant membrane fractions.
51 aling increased PTEN phosphatase activity in membrane fractions.
52 e B neurons and enhanced PKC activity in the membrane fractions.
53 n) were found in detergent-soluble (nonraft) membrane fractions.
54 or determining SKase activity in subcellular membrane fractions.
55 GIRK3 was found primarily in higher-density membrane fractions.
56 Ca proteins were restricted to caveolin-poor membrane fractions.
57 eracts and colocalizes with cdk5 in cellular membrane fractions.
58 and cAbl are found basally in Cav1-enriched membrane fractions.
59 ntaxin 4, and TI-VAMP/VAMP7 were detected on membrane fractions.
60 zine-1-carboxylic acid in both cytosolic and membrane fractions.
61 rifugation was used to isolate cytosolic and membrane fractions.
62 ubunit of the sodium pump) from human kidney membrane fractions.
63 iled to recruit TRAF6 to detergent-insoluble membrane fractions.
64 -bound Abeta(4)(2) were recovered from brain membrane fractions.
65 nd allene oxide synthase (AOS) activities in membrane fractions.
66 d PACSIN 1 was found in neuronal cytosol and membrane fractions.
67 ers within extracellular, intracellular, and membrane fractions.
68 slocation of NET.NK1R complexes to raft-rich membrane fractions.
69 tochalasin B-stimulated neutrophils or their membrane fractions.
70 ased AKT2 phosphorylation in the cytosol and membrane fractions; 3) insulin increased AS160 localizat
71 to recruit p190B into a detergent-insoluble membrane fraction, a process that is accompanied by a de
72 ulated adenylyl cyclase activity in striatal membrane fractions, AC1/8 double-knock-out (DKO) mice do
73 membrane was significantly increased in the membrane fraction after differential centrifugation and
75 Galphas redistributes from raft- to nonraft-membrane fractions after chronic antidepressant treatmen
77 secretase complex in the detergent-insoluble membrane fraction along with its substrates, APP-CTFalph
78 MR2 and MTMR13 cofractionate in both a light membrane fraction and a cytosolic fraction; and (iii) MT
79 exes initially reside in a detergent-soluble membrane fraction and acquire detergent insolubility as
80 iation of ULBP1 with the detergent-resistant membrane fraction and caused a significant reduction of
81 alized exclusively in the target cell plasma membrane fraction and correspondingly were visualized at
82 he entire procedure--beginning with isolated membrane fraction and finishing with MS data acquisition
83 SphK activity was mainly associated with the membrane fraction and phosphorylated predominantly the D
85 ity pool of PI4KIIalpha in a separable dense membrane fraction and this response was further enhanced
86 ated by immunoprecipitation from solubilized membrane fractions and able to produce amyloid beta-pept
87 aglandin receptors stimulated PRG binding to membrane fractions and activated signaling to PKA, and t
88 iated phosphorylation we observe in isolated membrane fractions and co-localization of the beta2AR an
89 Through a rigorous isolation of "native" PD membrane fractions and comparative mass spectrometry-bas
90 or vasotocin led to increases in PKCalpha in membrane fractions and concurrent decreases in PKCalpha
91 sed amounts of both Csk and PTPN22 in T cell membrane fractions and decreased association of PTPN22 w
92 s but was not found within the intracellular membrane fractions and may represent a new member of the
94 with GAPDH and pyruvate kinase in rat heart membrane fractions and that Kir6.2 protein co-localize w
95 identify Rab27b in purified tubulovesicular membrane fractions and used immunoblot and immunofluores
96 analysis showed that SOK was copurified with membrane fractions and was exposed on the surface of S.
97 , MtAhpE was found to be associated with the membrane fraction, and since mycothiol is hydrophilic, d
98 418 (37%) only in secretory vesicle-enriched membrane fractions, and 127 (11%) in both fractions.
99 as the predominant S-nitrosylated protein in membrane fractions, and following isoproterenol and isch
100 at septin 7 is found in both cytoplasmic and membrane fractions, and immunofluorescence microscopy sh
101 us, equal distribution between cytosolic and membrane fractions, and increasing levels of protein exp
102 nogen-binding proteins were discerned in the membrane fractions, and only relatively minor difference
103 1087 in C. tepidum decreased SQR activity in membrane fractions, and the CT1087 mutant could not grow
104 Heme agarose captured ZnuD in enriched outer membrane fractions, and this binding was inhibited by ex
106 gpA-, RgpB-, and Kgp-immunoreactive bands in membrane fractions as well as the culture supernatant of
107 noprecipitated with mGlu5 in the hippocampal membrane fraction, as well as when overexpressed in huma
108 co-localized in lipid raft/caveolin-enriched membrane fractions, as determined by gradient centrifuga
109 myocytes, we detected Cav-3 in both buoyant membrane fractions (BF) and heavy/non-buoyant fractions
110 n association with the lipid raft-containing membrane fraction but also those of inactive CD95 molecu
111 to a 14-kDa protein of whole cells and their membrane fractions but not after protease treatment.
113 ls decreased the level of endogenous AGS3 in membrane fractions by approximately 50% and enhanced the
114 phosphorylation of the beta2AR in the washed membrane fraction caused minimal desensitization of ISO
116 sed phospho-VEGFR2 in whole cell lysates and membrane fractions compared with control siRNA-treated c
117 blotting of low-density, detergent-insoluble membrane fractions confirmed that tight junction protein
119 associated with sterol/sphingolipid-enriched membrane fractions containing BIG/TIR3 and partitions in
122 Upon dodecylmaltoside solubilization of the membrane fraction, Cx26M34A and Cx26V84L are stable as h
123 s reconstituted with proteins from the outer membrane fractions derived from bacteria in the mid- and
124 ng intact cells as a receptor source because membrane fractions derived from these cells failed to di
125 of lysed erythrocytes was localized to their membrane fraction, did not involve membrane lipids, heme
126 exists primarily in the Triton X-100-soluble membrane fraction, distinct from the Triton-insoluble fr
127 ocedure to prepare a raft-like intracellular membrane fraction enriched for the trans-Golgi network (
132 ed within HeLa cells and can be found in the membrane fraction following subcellular fractionation.
134 e extracts, GerD-FLAG was found in the inner membrane fraction from dormant spores and was present at
136 dy, we performed a proteomic analysis of the membrane fraction from latex bead-containing (LBC) phago
138 ge factor Tiam1 were found associated with a membrane fraction from which they co-immunoprecipitated
144 in Xenopus oocytes after microinjection with membrane fractions from either HH or control hypothalamu
147 ctivation, we isolated endoplasmic reticulum membrane fractions from long-term Western diet-fed wild
150 med by identification of endogenous ClC-4 in membrane fractions from mouse brain homogenate enriched
152 -dimensional gel electrophoresis of isolated membrane fractions from strain UA159 and three mutants (
154 vivo at the Ser-419 site in the soluble and membrane fractions from the leaves but not from the inte
155 the retinol dehydrogenase activities of skin membrane fractions from the Sdr16c5/Sdr16c6 double-knock
157 paring the protein profiles of cell wall and membrane fractions from wild-type and DeltasecA2 mutant
158 e protein composition of detergent-resistant membrane fractions from wildtype and mutant cells, consi
162 s, but its recovery in a detergent-insoluble membrane fraction has suggested possible raft associatio
164 and immunoadsorption to enrich for specific membrane fractions, here we show that, when parental Chi
165 sessed by immunofluorescence and low-density membrane fraction immunoblotting); iii) increased claudi
166 orylated BCAP is transiently enriched in the membrane fraction in response to LPS treatment, suggesti
167 on with actin filaments and F-actin-enriched membrane fractions in both intact macrophages and a nove
168 ter 4 (GLUT4) levels were detected in muscle membrane fractions in Cip4-null mice under insulin stimu
169 cells and found that CyPA is recruited into membrane fractions in HCV-replicating cells via an inter
170 d for the purification of Cyt b from PLB-985 membrane fractions in order to confirm the appropriate m
171 by measuring superoxide anion production in membrane fractions in the absence of cytosolic component
173 th membrane particulate and surface-enriched membrane fractions, indicating that oligomeric hRFC is e
174 rity of immunogenic proteins remained in the membrane fraction, individually picked total and immunog
176 on of Fc(epsilon)RI with detergent-resistant membrane fractions is inhibited by 1-butanol, which subv
177 ATP-stimulated release of MHC-II in these membrane fractions is observed within 15 min and results
179 We recently demonstrated that mixed plasma membrane fractions isolated from rat hepatocyte couplets
180 d for immunoprecipitation against hepatocyte membrane fractions, it bound to alpha2-Heremans-Schmid g
181 R agonists promote PP2A translocation to the membrane fraction, leading to the dephosphorylation of t
182 cyanobacteria, Western blotting of isolated membrane fractions located SynCaK mainly to the plasma m
183 lso termed mitochondrial detergent-resistant membrane fractions (mDRM), play a role as platforms for
188 c antibody to adaA reacted with the purified membrane fraction of acute group isolates by Western blo
189 al vaccine candidates, proteins in the outer membrane fraction of bacteria were separated by two-dime
192 ptionally upregulated and accumulated in the membrane fraction of deguelin-treated cells, as indicate
193 trimer" AcrB was expressed well in the inner membrane fraction of DeltaacrB DeltarecA strains, as a l
196 , specifically regulating the cascade when a membrane fraction of ERK is activated via a PKC-dependen
197 nine-binding proteins were isolated from the membrane fraction of F. nucleatum ATCC 23726 and identif
198 Non-dimensional steady-state solutions for membrane fraction of GTPase are presented in multidimens
199 itative proteomics analyses using the plasma membrane fraction of HeLa cells expressing either wild-t
201 on of DAG revealed that DAG increased in the membrane fraction of high fat-fed mice, leading to PKCep
203 nd was associated with the detergent-soluble membrane fraction of mature virions, consistent with two
206 g44 fusion was also shown to localize in the membrane fraction of P. aeruginosa independently from it
208 nd its corresponding activity are present in membrane fraction of RBL cells, 3) exogenous CIF (extrac
209 sicle formation, we found an increase in the membrane fraction of Sec16A, a key regulator of COPII ve
210 t PtlH is exclusively localized to the inner membrane fraction of the cell in a wild-type strain of B
211 rotein kinase C (PKC) epsilon isoform to the membrane fraction of the hearts and the protective effec
212 ric acid receptor regulation in the synaptic membrane fraction of the rat mPFC following extinction a
214 tigen were associated with the cytoplasm and membrane fraction of unstimulated platelets, and these f
215 localized to both the cytoplasmic and inner membrane fractions of a mutant strain of B. pertussis th
217 membrane-expressed DAT, but synaptic plasma membrane fractions of DAT-tg mice show only a 30% increa
218 2 and cytosolic phospholipase A2 activity in membrane fractions of fibroblasts derived from patients
219 al cells to obtain periplasm, cytoplasm, and membrane fractions of high purity, as demonstrated by We
221 ta1 subunit expression was reduced in plasma membrane fractions of human WFS1 mutant fibroblasts and
222 vity is often elevated in both cytosolic and membrane fractions of malignant breast tissue and correl
224 fusion proteins and extracted from purified membrane fractions of Nicotiana benthamiana or Arabidops
229 n neither increased localization into "light membrane" fractions of sucrose gradients nor decreased s
230 ts from soluble (cytosolic) and particulate (membrane) fractions of ventral C(4) spinal segments reve
231 nding was increased in cytosolic, but not in membrane, fractions of cerebral cortex by all drugs test
233 Intact and lysed erythrocytes and their membrane fraction or specific erythrocyte components wer
234 R has been detected in a detergent-resistant membrane fraction prepared from airway epithelial cells,
235 e AgCad1 protein was present in brush border membrane fractions prepared from larvae, and Cry4Ba toxi
238 m cattle immunized with the protective outer membrane fraction provides a rationale for including the
241 Kv1.5 with low-density, detergent-resistant membrane fractions requires coexpression with exogenous
242 are considered to take place in specialized membrane fractions resembling an interface between the p
246 lysis of CAPS1 immunoprecipitates from brain membrane fractions revealed that CAPS1 associates with a
247 itro phosphorylation experiments using Golgi membrane fractions showed that 7B2 could be phosphorylat
250 ls and HeLa cells, and analysis of rat liver membrane fractions showed that Slc35c2 is primarily colo
251 uantification of mature cleaved alphaENaC in membrane fractions showed that the number of channels di
252 t recruitment of miRNA target transcripts to membrane fractions, shows that miRNAs inhibit the transl
253 immunoprecipitated from cytosol and nonraft membrane fractions, suggesting a redirection of signal t
254 n in detergent insoluble lipid raft/caveolae membrane fractions, suggesting that caveolin localizes a
255 of beta-arrestin2 favors its distribution in membrane fractions, suggesting that ubiquitination incre
256 e, detection of DrDps2 in the D. radiodurans membrane fraction suggests that the N-terminus of the pr
257 , which after cell disruption give rise to a membrane fraction that can be separated from mature ICM
258 ow that these Lpt proteins can be found in a membrane fraction that contains inner and outer membrane
259 3 activity was increased particularly in the membrane fraction that harbors SREBP2 and caspase-2.
260 t the soluble PKCgamma was translocated into membrane fractions that contained Cx46, Cx50, and the li
261 hat, unlike cav-1, phospho-cav-1 enriches in membrane fractions that express FA proteins and localize
262 evels of SP-A binding to non-live mycoplasma membrane fractions that were dependent on the presence o
265 ensities across the plastid and the enriched membrane fraction under both normal and cold conditions.
266 f NET.NK1R complexes exclusively in non-raft membrane fractions under basal/unstimulated conditions.
269 neas, rhCNTFRalpha incorporation into the CE membrane fraction was demonstrated by Western blot analy
273 [(3)H]PGE(2) binding of W203A in broken cell membrane fractions was inhibited by addition of GTPgamma
275 t reduces cADPR and NAADP synthesis in mouse membrane fractions, was shown to bind to CD38 in docking
280 and glycolipids isolated from the same cell membrane fractions were analyzed in parallel using previ
281 oplast-enriched and plasma membrane-enriched membrane fractions were carried out to look at tissue-sp
282 RESEARCH DESIGN AND Mitochondrial matrix and membrane fractions were generated from liver, brain, hea
284 peptide ligands to CRFR1alpha and CRFR2beta membrane fractions were similar, in part, to the complex
286 ect translocation of Galphas to the non-raft membrane fraction, where it activates the cAMP-signaling
287 binant protein detected PleC and CckA in the membrane fraction, whereas it detected NtrY, NtrX, and P
288 70-kD protein in the A. thaliana chloroplast membrane fraction which migrated faster than the His-tag
289 respiratory metabolism are localized in the membrane fractions which include the outer membrane and
290 6), active caspase 8 is detected only in the membrane fraction, which contains both mitochondria and
291 ranslocation of PP2A from the cytosol to the membrane fraction, which corresponded with increased coi
293 EWRS1 translocates into detergent-resistant membrane fractions, which contain the viral replicase pr
294 ted that wtRPE65 predominantly exists in the membrane fraction, while both of the mutants are primari
295 ents revealed that gp16 partitioned into the membrane fraction, while gp20 and gp7 remained in the so
296 or alkaline carbonate prepares an insoluble membrane fraction whose buoyant density permits its flot
297 AS1411 and immunoprecipitation of the plasma membrane fraction with anti-nucleolin antibody demonstra
298 photoreceptor inner segments and bound to a membrane fraction with characteristics of endoplasmic re
300 in beta1-AR density in surface and T-tubule membrane fractions without a change in beta2-AR density;