ライフサイエンスコーパス: microaggregate

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 ti-Abeta-antibody-coated fAbeta (IgG-fAbeta) microaggregates and found that the uptake of the latter

6 hat of complement protein, C1q-coated fAbeta microaggregates, and found that the levels of uptake are

7 ruitment of nuclear proteins to intranuclear microaggregates, and subsequently to NI, may contribute

8 Primary RPE microaggregates (approximately 40,000 RPE cells) were in

9 degradation of both types of modified fAbeta microaggregates are unchanged compared with unmodified f

10 As visualized by confocal microscopy, microaggregates, as well as MBP-1, induced vimentin poly

11 rst step is ligand-induced formation of CD95 microaggregates at the cell surface.

12 3 forms insoluble intranuclear complexes, or microaggregates, before NI can be detected, implying a p

13 Using anti-MBP-1 immune serum, microaggregate binding to HEp-2 cells was significantly

14 The gene encoding microaggregate-binding protein 1 (MBP-1) (MAV_3013) is h

15 treated with these molecules still contained microaggregates, but these microaggregates were not tran

16 e airways, M. avium subsp. hominissuis forms microaggregates composed of 3 to 20 bacteria on human re

17 Nuclear microaggregates, defined as small huntingtin-positive pu

18 g of IgG-fAbeta is similar to that of fAbeta microaggregates, following an endosomal/lysosomal pathwa

19 the continued presence of fluorescent Abeta microaggregates for 4 days, microglia took up huge amoun

20 in both whole blood and PRP as a measure of microaggregate formation, using both citrate and hirudin

21 ilized extracellular domain of CD84 promoted microaggregate formation, while SAP-deficient platelets

22 MBP-1) (MAV_3013) is highly expressed during microaggregate formation.

23 egrilin), and turbidimetry is insensitive to microaggregate formation.

24 a higher abundance of lignins in mineral and microaggregate fractions and suberin in the macroaggrega

25 f whole blood the platelet potential to form microaggregates in response to an agonist; second, the p

26 istin to translocate gephyrin to submembrane microaggregates in transfected mammalian cells.

27 tioning of MOPC micelles (and to some extent microaggregates) into the membrane, while even up to 20

28 RPE microaggregates obtained from male cats were transplante

29 Microglia bind and internalize microaggregates of Abeta that resemble those present in

30 ied whether the gallbladder can modulate the microaggregates of cholesterol carriers, which may in tu

31 Murine microglia internalize microaggregates of fluorescently labeled or radioiodinat

32 ysfunction preceded the detection of nuclear microaggregates of mutated huntingtin in striatal neuron

33 , bulk samples are usually fractionated into microaggregates or micrometer-sized single particles.

34 (ICL) of aged submacular Bruch's membrane as microaggregates or were expanded in culture until enough

35 Serial imaging of microaggregates over 1 week demonstrated a heterogeneous

36 PS-COOH forms microaggregates (PDI > 0.4) in NSW, whereas PS-NH2 resul

37 ployed to identify genes associated with the microaggregate phenotype.

38 When present, nuclear microaggregates predominated in the striosomal compartme

39 The microaggregate species were resistant to proteinase K, p

40 ubretinal transplants of human fetal retinal microaggregate suspensions without postoperative systemi

41 The bound SSRBCs thereupon form microaggregates that obstruct/occlude up to 88% of tumor

42 After 0.02-microm filtration to remove microaggregates, the resulting reagent was highly unifor

43 Animal models have disproved the microaggregate theory of acute lung injury from blood tr

44 Binding of microaggregates to HEp-2 cells was inhibited by treatmen

45 pared internalization by microglia of fAbeta microaggregates to that of anti-Abeta-antibody-coated fA

46 also compared the internalization of fAbeta microaggregates to that of complement protein, C1q-coate

47 murine microglia bind and internalize fAbeta microaggregates via the type A scavenger receptor, but d

48 at the majority of the internalized Abeta in microaggregates was undegraded 72 h after uptake, wherea

49 cent protein (eGFP)-C57BL/6 neonatal retinal microaggregates were injected into the vitreous of B10-R

50 s still contained microaggregates, but these microaggregates were not transported to microtubule orga

51 (red) that intercalate with DNA (green) form microaggregates with DNA generated by the polymerase cha

52 mpared the degradation by microglia of Abeta microaggregates with the degradation of two other protei