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1 , proliferating germinal center centroblasts/centrocytes.
2 lls, CD5(+) B cells, and GC centroblasts and centrocytes.
3 , essentially as nonproliferative CXCR4(neg) centrocytes.
4 ated into a population with the phenotype of centrocytes after stimulation with CD40 ligand (CD40L) a
5                    Nevertheless, a subset of centrocytes and B cells in the subepithelium showed nucl
6 t murine Aicda(-/-) GC B cells accumulate as centrocytes and inefficiently generate plasma cells.
7 als for differentiation of centroblasts into centrocytes and resistance to B cell receptor-mediated a
8 we propose that the selection probability of centrocytes and the recycling probability of selected ce
9 GC founder cells, 0% of centroblasts, 13% of centrocytes, and 9% of memory B cells.
10  centroblasts, it extends to all isotypes in centrocytes, and it is extinct in memory B cells.
11  in ex vivo isolated tonsillar centroblasts, centrocytes, and memory B cells.
12 mRNA was only found in tonsil naive B cells, centrocytes, and to a lesser extent in centroblasts.
13 Annexin V, comprised mostly (93%) of CD77(-) centrocytes, and were enriched for CD69(+) cells.
14 es and the recycling probability of selected centrocytes are not constant but vary during the GC reac
15                    It has been proposed that centrocytes are selected in the light zone on the basis
16             Germinal center centroblasts and centrocytes as well as tonsillar memory B cells express
17 w that the frequent recycling of Ag-selected centrocytes back into centroblasts can lead to efficient
18                    Upon further culture, the centrocytes differentiated to memory B cells, a process
19 gest that Bcl-x rather than Bcl-2 may rescue centrocytes during selection in the germinal center.
20               Centroblasts differentiated to centrocytes during the culture period of 3 days as demon
21       Purified B-cell fractions enriched for centrocytes express high amounts of Bcl-x and relatively
22  transit (naive B cells --> centroblasts --> centrocytes --> memory B cells) by gene expression profi
23 blasts give rise to smaller nonproliferating centrocytes in the light zone that compete for binding a
24 henotypic characteristics of germinal center centrocytes, including a low level of surface Ig, a lack
25  GC dissociation, followed by the release of centrocytes into the periphery, is advantageous for gene
26 nterfollicular neoplastic B cells were small centrocyte-like cells with lower grade cytology and lowe
27 ation, the BCL1 3B3 cells differentiate into centrocyte-like cells, whereas the BCL1 5B1b cells blast
28  IRTA1 in marginal zone B cells and IRTA2 in centrocytes, marginal zone B cells, and immunoblasts.
29 the transition between DZ centroblast and LZ centrocyte phenotypes occurred independently of position
30 large numbers even when most of the selected centrocytes recycle back into centroblasts.
31 as follicle-center B cells (centroblasts and centrocytes) show weaker expression.
32 with focal germinal centers (GCs) containing centrocytes staining strongly for bcl-2 protein, whereas
33 he germinal center B-cell-like subclass; the centrocyte subtype had a superior prognosis compared wit
34  subtype had a complex genotype, whereas the centrocyte subtype had high TP53 mutation and insertion/
35 ement with the observed therapeutic outcome, centrocyte subtypes were estimated as being less resista
36       Centroblasts produce non-proliferating centrocytes that are thought to migrate to the light zon
37 o be a specialized niche comprised mostly of centrocytes that may be in transition between activation
38 on by AG490 prevented the transition from GC centrocytes to preplasmablast, suggesting that STAT3 is
39                Centroblasts then mature into centrocytes to undergo clonal selection.
40             The transition of centroblast to centrocyte was enhanced by BCR stimulation and IL-4.
41 sed in positive regulatory domain 1-positive centrocytes, which are negative for all the B cell trans

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