Sentence examples for periphery tissues from inspiring English sources

In other situations of inflammation or tumor, CXCR3, ChemR23, and CCR6 are implicated to be involved in pDCs migration to periphery tissues.

These data suggest that CCR1 might play a role in recruitment of immature DCs to periphery tissues during both steady-state and inflammatory-state.

They include BRN1[ 66], BRN2 [ 66], SMB [ 67], FEZ [ 67] TOM7 [ 68], PTL2 [ 69] and TCP20 [ 70], which were recently identified as functioning coordinately in the stem cell niche and periphery tissues in root caps.

Several studies demonstrated the role of CCR7 in control of tissue-resident myeloid dendritic cells from periphery tissues such as skin and mucosa migration to draining LNs via the afferent lymphatics under inflammatory and steady-state conditions [ 34, 63].

It has been indicated that several chemokine receptors including CCR1, CCR2, CCR3, CCR5, CCR6, CCR7, CCR9, CCR10, CXCR3, CXCR4, CXCR5, and ChemR23 are involved in control of different subsets of DCs recruitment to periphery tissues and migration to secondary lymphoid tissues or migration within lymphoid tissues.

For cDCs, CCR7 plays a central role in the migration of mature DCs to the draining LNs via lymphatic vessels during both inflammation and steady-state conditions, with a multimodule signaling model that involved G αi, G αq, and G α12. CXCR4, CCR2, and CXCR5 have also been implicated to be involved in some subsets of cDCs migration from periphery tissues to draining LNs.

One of its main functions is to keep the balance of glucose inside the body by regulating the absorption and metabolism of glucose in the periphery tissue, as well as the production and storage of hepatic glycogen.

In particular, the hypothalamus has critical roles in sensing and integrating signals from the periphery tissue and effecting appropriate physiological changes to maintain metabolic homeostasis (Zoccoli et al., 2011).

Intratumoral LVD (hot spots were located at tumor center) and peritumoral LVD (hot spots were located at periphery tissue within 2 mm of tumor adjacent to the invasive front) were assessed separately [ 2, 7- 9].

We can see that at this periphery tissue architecture is distinct from more medial/older wood of lower intensity, in a manner which is aligned with g-fibre orientation (the "upper" part of the stem) but not overlapping with g-layers.

It was found that in some inflamed situations such as in psoriatic lesions, pDCs found in the lesions were nearly all CXCR3, indirectly implicated the possible role for CXCR3 in mediating the recruitment of pDCs into the periphery tissue and developing lesions in human [ 50].