ライフサイエンスコーパス: perifollicular

1 Therefore, we investigated how perifollicular adipocytes affect the physiology of human

2 icroscopy showed that the number and size of perifollicular adipocytes declined during anagen-catagen

3 - and MMP-9-expressing cells were present in perifollicular and dermal inflammatory infiltrates withi

4 nd CD200-deficient C57BL/6 mice, significant perifollicular and intrafollicular inflammation was obse

5 nd interdigitating cells) and present in few perifollicular and intrafollicular lymphoid blasts.

6 s of CD3+, CD4+ T cells were elevated in the perifollicular and papillary dermis although levels were

7 Perifollicular angiogenesis was temporally and spatially

8 d vascular-endothelial-growth-factor-induced perifollicular angiogenesis, whereas the catagen regress

9 issue, by cells associated with sinusoids in perifollicular areas of spleen tissue, and at very high

10 t and reduced KRT82 expression have elevated perifollicular CD8 infiltrates.

11 immune and hair keratin biomarkers and with perifollicular cellular infiltrates.

12 Perifollicular dermal preadipocytes in human acne and mo

13 63 expression within the HF infundibulum and perifollicular epidermis.

14 tumor microenvironmental differences between perifollicular FMF and dermal classic MF regions, we ana

15 lted in an increased binding of monocytes to perifollicular high endothelial venules (HEVs) of lymph

16 e inflamed skin revealed intrafollicular and perifollicular human CD4(+) cells near F4/80(+) mouse ma

17 Perifollicular IFN-gamma+ CD8 T cells were rare in secon

18 ns as a HF IP guardian, e.g., by stimulating perifollicular immunoinhibitory cells and suppressing IF

19 evidence that IL-17+ cells are found in the perifollicular infiltrate of comedones.

20 Nilotinib therapy may induce perifollicular inflammation and widespread persistent al

21 mice developed scarring alopecia and severe perifollicular inflammation.

22 e rs763035 variant, revealed staining in the perifollicular inflammatory infiltrate of rosacea for bo

23 cells and to have FOXP3-positive cells in a perifollicular location.

24 Biopsies revealed perifollicular lymphocytic inflammation and evidence of

25 Thus, perifollicular macrophages contribute to the activation

26 lar B cell areas and the absence of discrete perifollicular marginal and mantle zones; the formation

27 madelta regulatory T cells, NKT10 cells, and perifollicular mast cells, in maintaining physiologic ha

28 HEVs-AMN) was designed to create a favorable perifollicular microenvironment.

29 ulted in depigmented hair fiber regrowth and perifollicular neutrophil and eosinophil infiltrates but

30 demonstrated no tendency to localize to the perifollicular region, and were similarly distributed as

31 gregation of plasmacytoid DCs in the splenic perifollicular region, follicular translocation of MZ B

32 In the mutant spleen, the characteristic perifollicular rim marking the marginal zone (MZ), which

33 trating monocytes formed a subepithelial and perifollicular shield, recruiting neutrophil extracellul

34 acterized by focal inflammatory lesions with perifollicular T-cell infiltrates, reflecting the role o

35 CCR6-deficient B(mem) from the marginal and perifollicular to the follicular/germinal center area.

36 tudy aimed to quantify the cyclic changes of perifollicular vascularization and to characterize the b

37 icantly prolonged, associated with increased perifollicular vascularization and vascular proliferatio

38 We found a significant increase in perifollicular vascularization during the growth phase (

39 tinocytes of hair follicles strongly induced perifollicular vascularization, resulting in accelerated

40 heath keratinocytes, associated with reduced perifollicular vascularization.

41 ophages in humans are found primarily in the perifollicular zone, whereas in chimpanzees they also oc