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1 - and MMP-9-expressing cells were present in perifollicular and dermal inflammatory infiltrates withi
2 nd CD200-deficient C57BL/6 mice, significant perifollicular and intrafollicular inflammation was obse
4 s of CD3+, CD4+ T cells were elevated in the perifollicular and papillary dermis although levels were
6 d vascular-endothelial-growth-factor-induced perifollicular angiogenesis, whereas the catagen regress
7 issue, by cells associated with sinusoids in perifollicular areas of spleen tissue, and at very high
9 lted in an increased binding of monocytes to perifollicular high endothelial venules (HEVs) of lymph
10 e inflamed skin revealed intrafollicular and perifollicular human CD4(+) cells near F4/80(+) mouse ma
15 e rs763035 variant, revealed staining in the perifollicular inflammatory infiltrate of rosacea for bo
19 lar B cell areas and the absence of discrete perifollicular marginal and mantle zones; the formation
20 ulted in depigmented hair fiber regrowth and perifollicular neutrophil and eosinophil infiltrates but
21 demonstrated no tendency to localize to the perifollicular region, and were similarly distributed as
22 gregation of plasmacytoid DCs in the splenic perifollicular region, follicular translocation of MZ B
23 In the mutant spleen, the characteristic perifollicular rim marking the marginal zone (MZ), which
24 acterized by focal inflammatory lesions with perifollicular T-cell infiltrates, reflecting the role o
25 CCR6-deficient B(mem) from the marginal and perifollicular to the follicular/germinal center area.
26 tudy aimed to quantify the cyclic changes of perifollicular vascularization and to characterize the b
27 icantly prolonged, associated with increased perifollicular vascularization and vascular proliferatio
29 tinocytes of hair follicles strongly induced perifollicular vascularization, resulting in accelerated
31 ophages in humans are found primarily in the perifollicular zone, whereas in chimpanzees they also oc
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