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1 ction a small amount of LPS was found in the paracortex.
2 icients than naive T lymphocytes in the deep paracortex.
3 tical ridge, poorly accessing the lymph node paracortex.
4 ecreased the speed of locomotion in the deep paracortex.
5 nuses, with reduced abundance in the deep LN paracortex.
6 tor T cells localized exclusively within the paracortex.
7 169(-/-) mice but penetrated deeper into the paracortex.
8 network regulated naive T cell access to the paracortex and also supported and defined the limits of
9 cific CD4 T cells redistributed to the outer paracortex and interacted with CD11b(+), but not CD8(+)
10 sule of the lymph node from migrating to the paracortex and interposing between T cells.
11 ation, infected cells were identified in the paracortex and subcapsular sinus of the draining interna
12 ompetent mangabeys but were seen in both the paracortex and the germinal center of SIV-infected macaq
13 e rapidly degraded in the subcapsular sinus, paracortex, and interfollicular regions, whereas low pro
14 lutaminase is expressed at low levels in the paracortex around primary follicles but is markedly up-r
15 aining lymph nodes, where they reside in the paracortex as interdigitating dendritic cells (IDCs).
16 he prodrug accumulated in the MLN cortex and paracortex at 5 and 10 h following administration and wa
17                     This localization in the paracortex by CD8 T cells was followed by intranodal mig
18  with T cell retention within the lymph node paracortex due to disrupted CXCR3 chemokine gradient for
19 ection, they were confined to the lymph node paracortex in immune-competent mangabeys but were seen i
20 ual expressed CXCL10 and CXCL11 mRNAs in the paracortex, including venules, as detected by in situ hy
21                               The lymph node paracortex is composed of a network of fibroblastic reti
22  specific cells in the lymph node cortex and paracortex is difficult.
23 ere located mainly in the outer edges of the paracortex near the B cell-rich follicles.
24  DC migration from peripheral tissues to the paracortex of draining lymph nodes.
25    Naive T lymphocyte locomotion in the deep paracortex of the LN required a perfusion rate of >13 mi
26                                       In the paracortex, p24-positive multinucleated lymphocytes with
27 f soluble molecules to distinct sites in the paracortex, particularly the high endothelial venule.
28 dominately in extrafollicular regions of the paracortex that contain T-lymphocytes and macrophages.
29 ormly distributed throughout the T cell-rich paracortex, whereas CD11b(+) dendritic cells were locate
30 re and CD138(+) plasma cells residing in the paracortex, which expressed IgE, IgG, and IgM but not Ig
31 with vaccinia virus-infected cells in the LN paracortex, which led to T cell activation in the LN int
32  to follicles, whereas T cells remain in the paracortex, with each lymphocyte type showing apparently