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1 found that Gag and YB-1 localize together in cytoplasmic granules.
2 also resulted in the accumulation of DEF6 in cytoplasmic granules.
3 ing migration and are also able to roll past cytoplasmic granules.
4 ast cells (MCs) is their hTryptase-beta-rich cytoplasmic granules.
5 lizes with endogenous RIP1 at characteristic cytoplasmic granules.
6 ning two proteins localized predominantly to cytoplasmic granules.
7 y enzymes released into the vacuole from the cytoplasmic granules.
8 ation, IFNgamma production, and expulsion of cytoplasmic granules.
9 ecific PAS-diastase-resistant electron-dense cytoplasmic granules.
10 egmented nuclei and myeloperoxidase-positive cytoplasmic granules.
11 perforin, granzyme A, and granzyme B, within cytoplasmic granules.
12  exocytosis of lytic molecules stored within cytoplasmic granules.
13 f the cancer cells contained Glut-1 positive cytoplasmic granules.
14 ress bFGF mRNA and protein that localizes to cytoplasmic granules.
15 arge-cell histology and frequently contained cytoplasmic granules.
16 n proteases and other mediators in mast cell cytoplasmic granules; an important role for mast cells i
17 s together with an enhanced random motion of cytoplasmic granules and a reduction of cytoplasmic stif
18  required for the recruitment of Gemin2 into cytoplasmic granules and enhanced Gemin2 stability.
19                 Eo-MDSC exhibit eosinophilic cytoplasmic granules and express CD11b, the eosinophil m
20 o cells with recognizable and characteristic cytoplasmic granules and granule proteins.
21  In contrast, mNXF7 localizes exclusively to cytoplasmic granules and, despite its overall conserved
22 response, release of allergic mediators from cytoplasmic granules, and synthesis of cytokines and che
23 ture and exhibit hnRNP A2/B1 localization to cytoplasmic granules as well as exacerbated changes in g
24 iogenic amines that are stored in the cells' cytoplasmic granules as well as the production of lipid
25 of stress-response genes and accumulation of cytoplasmic granules associated with RNA-binding protein
26 throughout the cell but rat8-2p localized to cytoplasmic granules at nonpermissive temperature that a
27 ls loaded with periodic acid-Schiff-positive cytoplasmic granules began to appear singularly in some
28 uggesting that the enzyme is targeted to the cytoplasmic granules by a mechanism other than the manno
29                   cel-1(RNAi) embryos formed cytoplasmic granules characteristic of a phenocluster of
30  secretory granule contents and retention of cytoplasmic granule containers in the absence of entire
31 ction, low myeloperoxidase activity, and low cytoplasmic granule content, which accounts for their lo
32 eal Paneth cells was strong and specific for cytoplasmic granules, demonstrating that this microbicid
33 k staining with a few rAbs against nuclei or cytoplasmic granules in neurons, glia, and inflammatory
34 ger-containing protein that localizes to the cytoplasmic granules in NK cells.
35 discovered that RNA2 is recruited into large cytoplasmic granules in the absence of B2, whereas the d
36 nt protein (GFP)-tagged VHL also appeared as cytoplasmic granules in vitro and was colocalized with a
37               The protein PCM-1 localizes to cytoplasmic granules known as "centriolar satellites" th
38 umulate MCT1-CD147 complexes in the specific cytoplasmic granules known to undergo crystallization.
39 nd protein is synthesized and is targeted to cytoplasmic granule membranes.
40       Human eosinophils contain within their cytoplasmic granules multiple preformed proteins, includ
41 V was shown to induce the formation of large cytoplasmic granules, named inclusion bodies, for genome
42  the periodic acid-Schiff-diastase-resistant cytoplasmic granules of ASPS are strongly immunoreactive
43 ntimicrobial peptide-amide isolated from the cytoplasmic granules of bovine neutrophils that contains
44 ntimicrobial peptide-amide isolated from the cytoplasmic granules of bovine neutrophils.
45 s, a family of serine proteases contained in cytoplasmic granules of cytotoxic T lymphocytes and natu
46          Granulysin, a peptide stored in the cytoplasmic granules of human natural killer cells and c
47                                          The cytoplasmic granules of mammalian neutrophils contain se
48 ture 169 amino acid protein is stored in the cytoplasmic granules of neutrophils and eosinophils but
49        Neutrophil serine proteases (NSPs) in cytoplasmic granules of neutrophils are regarded as impo
50 ppeared to be due to up-regulation of MIF in cytoplasmic granules of neutrophils via activation of th
51       The bacterium Ralstonia eutropha forms cytoplasmic granules of polyhydroxybutyrate that are a s
52 within 3 h after infection, in small uniform cytoplasmic granules raising the possibility that vhs co
53 duction, these proteins were retained within cytoplasmic granules rather than being secreted into PV1
54 quires the action of neutrophils, which have cytoplasmic granules replete with antibiotic proteins an
55                     These findings show that cytoplasmic granule secretion from MCs that occurs in re
56  Abeta-like immunoreactivity within the same cytoplasmic granules, suggesting that uptake of lipids m
57 1 colocalized with centrosomal components in cytoplasmic granules surrounding nascent centrioles.
58 ogy, huntingtin was associated with punctate cytoplasmic granules that at the ultrastructural level r
59 osphomimic resulted in the formation of DEF6 cytoplasmic granules that co-localized with decapping en
60 us to the cytoplasm, where it accumulated in cytoplasmic granules that colocalized with Trim32.
61 mmunication during inflammation by secreting cytoplasmic granules that contain diverse mediators.
62 ytes are characterized by their inclusion of cytoplasmic granules that fuse with the plasma membrane
63 s a novel component of centriolar satellites-cytoplasmic granules that serve as recruitment sites for
64         While both 519 proteins are found in cytoplasmic granules, the 9-kDa form is also present in
65 is also associated with the translocation of cytoplasmic granules to the cell surface and alignment j
66      The association of MMTV Gag and YB-1 in cytoplasmic granules was not disrupted by cycloheximide
67  in development and is localized in distinct cytoplasmic granules where its target mRNA can be detect
68 rglomerular mesangial cells exhibit numerous cytoplasmic granules, which are reminiscent of renin-pro
69                     atALKBH9B accumulates in cytoplasmic granules, which colocalize with siRNA bodies
70    Cultured DeltadblGATA eosinophils contain cytoplasmic granules with immunoreactive major basic pro
71 en relocated from a nuclear location to form cytoplasmic granules with N(pro).
72 otein/nanos1 mRNA complex that is present in cytoplasmic granules with the translational repression p
73        Defensins are normally sequestered in cytoplasmic granules with their primary site of action i

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