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1 2) bound to presynaptic vesicles; and (3) as microaggregates.
2 preexisting receptor dimers are driven into microaggregates.
3 re unchanged compared with unmodified fAbeta microaggregates.
4 ains, we found cytoplasmic, but not nuclear, microaggregates.
5 n by increased numbers of leukocytes and RBC microaggregates.
6 centrations in macroaggregates as well as in microaggregates.
7 2% of residual C associated with minerals in microaggregates.
8 the OM and mineral constituents forming the microaggregates.
9 es (17.6 6.7 vs 5.2 2.3; p < 0.0001) and RBC microaggregates (0.90 1.12 vs 0.06 0.24; p < 0.0001) was
12 ti-Abeta-antibody-coated fAbeta (IgG-fAbeta) microaggregates and found that the uptake of the latter
13 t in nitrogen-bearing organic matter on soil microaggregates and suggested a strong role for chemo- o
14 hat of complement protein, C1q-coated fAbeta microaggregates, and found that the levels of uptake are
15 ruitment of nuclear proteins to intranuclear microaggregates, and subsequently to NI, may contribute
17 degradation of both types of modified fAbeta microaggregates are unchanged compared with unmodified f
20 3 forms insoluble intranuclear complexes, or microaggregates, before NI can be detected, implying a p
23 treated with these molecules still contained microaggregates, but these microaggregates were not tran
24 e airways, M. avium subsp. hominissuis forms microaggregates composed of 3 to 20 bacteria on human re
26 g of IgG-fAbeta is similar to that of fAbeta microaggregates, following an endosomal/lysosomal pathwa
27 the continued presence of fluorescent Abeta microaggregates for 4 days, microglia took up huge amoun
28 in both whole blood and PRP as a measure of microaggregate formation, using both citrate and hirudin
29 ilized extracellular domain of CD84 promoted microaggregate formation, while SAP-deficient platelets
32 a higher abundance of lignins in mineral and microaggregate fractions and suberin in the macroaggrega
33 f whole blood the platelet potential to form microaggregates in response to an agonist; second, the p
35 tioning of MOPC micelles (and to some extent microaggregates) into the membrane, while even up to 20
38 ied whether the gallbladder can modulate the microaggregates of cholesterol carriers, which may in tu
40 ysfunction preceded the detection of nuclear microaggregates of mutated huntingtin in striatal neuron
41 , bulk samples are usually fractionated into microaggregates or micrometer-sized single particles.
42 (ICL) of aged submacular Bruch's membrane as microaggregates or were expanded in culture until enough
49 ubretinal transplants of human fetal retinal microaggregate suspensions without postoperative systemi
50 colloids) and (ii) as building units of soil microaggregates that are occluded inside them (occluded
55 pared internalization by microglia of fAbeta microaggregates to that of anti-Abeta-antibody-coated fA
56 also compared the internalization of fAbeta microaggregates to that of complement protein, C1q-coate
58 f similar and less diverse C forms in intact microaggregates under long-term elevated CO(2) condition
59 murine microglia bind and internalize fAbeta microaggregates via the type A scavenger receptor, but d
60 at the majority of the internalized Abeta in microaggregates was undegraded 72 h after uptake, wherea
61 cent protein (eGFP)-C57BL/6 neonatal retinal microaggregates were injected into the vitreous of B10-R
62 s still contained microaggregates, but these microaggregates were not transported to microtubule orga
63 (red) that intercalate with DNA (green) form microaggregates with DNA generated by the polymerase cha
64 mpared the degradation by microglia of Abeta microaggregates with the degradation of two other protei