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1 e CaD fragment had no effect on the yield of sedimentable actin, nor did it affect the actin ATPase a
2 re but appear morphologically similar to the sedimentable aggregates into which they eventually matur
3 fer fluorescence is due to self-quenching in sedimentable aggregates or micelles which upon interacti
4 cell and presumably in motor neurons to form sedimentable aggregates.
5 of neuroblastoma cells leads to formation of sedimentable aggregates.
6 ndergo slow structural rearrangement to form sedimentable aggregates.
7 dicating that soluble aggregates mature into sedimentable aggregates.
8 eins were investigated in HMPC as well as in sedimentable and non-sedimentable fractions recovered af
9 ptimal clathrin binding and the formation of sedimentable assemblies.
10 bicans membranes remained largely intact and sedimentable at CHAPS concentrations (4%) where >90% of
11 appearance of PY-STAT3 in the cav-1-enriched sedimentable cytoplasmic fraction, suggesting that these
12 M ATP at pH 6.5 resulted in the formation of sedimentable enzyme and a 70% loss of enzyme activity.
13 of the enzyme resulted in the formation of a sedimentable enzyme due to self-association.
14 enzyme lost only 30% of its activity, and no sedimentable enzyme was detected.
15 ATP at pH 7.5 resulted in the formation of a sedimentable enzyme with a 33% loss in enzyme activity.
16 t in a loss of activity or the production of sedimentable enzyme, even though the stoichiometry of au
17 aline reaction pH lead to the formation of a sedimentable enzyme.
18 self-association to form large aggregates of sedimentable enzyme.
19                                   Insoluble, sedimentable fibrils contribute to SEVI-mediated enhance
20 ufficient to convert soluble protofibrils to sedimentable fibrils.
21 ed Soi1p existed in a detergent-insensitive, sedimentable form.
22  cells, were sequestered in a salt-resistant sedimentable fraction rather than released to the cytoso
23  protein aggregates observed in HMPC and the sedimentable fraction were mainly composed of lactoferri
24  protein aggregates observed in HMPC and the sedimentable fraction were mainly composed of lactoferri
25 amples (99.22% +/- 1.46%) was present in the sedimentable fraction.
26 transfer of NGF back from nonsedimentable to sedimentable fractions and to a remasking of the previou
27 recently found to be largely associated with sedimentable fractions of adult rat brain and treatments
28 d in HMPC as well as in sedimentable and non-sedimentable fractions recovered after ultracentrifugati
29 ced and half of the antigen was recovered in sedimentable fractions.
30 ctionated, a substantial amount of FBPase is sedimentable in the high speed pellet, suggesting that F
31 hondrial and ER membranes, and the levels of sedimentable insoluble SOD1 aggregates were significantl
32 found that DLP1 protein alone assembled into sedimentable macromolecular structures in the presence o
33 atic increase in bulk STAT3 association with sedimentable membranes.
34 tein is released from cells at low levels in sedimentable particles that have a density similar to th