ライフサイエンスコーパス: perivascular niche

1 l carcinomas (HNSCC) close to blood vessels (perivascular niche).

2 ma stem-like cells (MSLC) accumulated in the perivascular niche.

3 n and contribution to GSC maintenance in the perivascular niche.

4 ting that quiescent HSCs are maintained by a perivascular niche.

5 ifferentiation as long as they reside in the perivascular niche.

6 o-resistant medulloblastoma cells occupy the perivascular niche.

7 neuronal progenitor cell interactions in the perivascular niche.

8 roportion of surviving MSCs integrating in a perivascular niche.

9 vascular pericytes that may actively remodel perivascular niches.

10 growth factor secretion and are enriched in perivascular niches.

11 cancer cells (GSCs) that home to specialized perivascular niches.

12 When an HSPC arrives in the perivascular niche, a group of endothelial cells remodel

13 sed in the tumor cell niches compared to the perivascular niche across multiple regions in GBM patien

14 Stem-like glioma cells reside within a perivascular niche and display hallmark radiation resist

15 ellular niches in bone marrow: HSCs occupy a perivascular niche and early lymphoid progenitors occupy

16 s within skin injuries, where they home to a perivascular niche and generate alternatively activated,

17 ling axis as crucial for exploitation of the perivascular niche and identify potential therapeutic ta

18 Because GSCs often reside in perivascular niches and may undergo mesenchymal differen

19 Interactions with the adjacent perivascular niche are an important driver of malignancy

20 critical function in morphogenesis of these perivascular niches as well as in melanoma tumorigenicit

21 Haematopoietic stem cells (HSCs) reside in a perivascular niche but the specific location of this nic

22 te that the upper bulge is associated with a perivascular niche during the establishment and maintena

23 genes induced rapid release of GICs from the perivascular niche, followed by tumor regression.

24 We sought to determine whether there is a perivascular niche for hair follicle stem cells.

25 The perivascular niche for neurogenesis was first reported a

26 of GTPases in endosteal/osteoblastic versus perivascular niche function.

27 Here, we report that SCC cells within the perivascular niche have undergone epithelial to mesenchy

28 oietic stem cells (HSCs) are maintained by a perivascular niche in bone marrow but it is unclear whet

29 ng VM and the morphogenesis of a specialized perivascular niche in melanoma.

30 Thus, HSCs reside in a perivascular niche in which multiple cell types express

31 in human tumors, suggesting the existence of perivascular niches in HNSCC.

32 nous matrices that are soft and 2D, like the perivascular niches in marrow rather than 3D or rigid, l

33 errogating the codependence of BTSCs and the perivascular niche may directly inform clinical approach

34 Mesenchymal stem cells (MSCs) reside in the perivascular niche of many organs, including kidney, lun

35 Evidence has emerged for macrophages in the perivascular niche of tumors regulating important proces

36 ether, these data suggest that in the glioma perivascular niche, osteopontin promotes stem cell-like

37 Some adult animals presented perivascular niches outside the V-SVZ.

38 f SHH-producing stromal cells that reside in perivascular niche (PVN), namely low-cycling astrocytes

39 thelial cells (EC) in what has been termed a perivascular niche, spurring investigation into the role

40 bpopulations are colocalized in melanomas in perivascular niches that contain CD144 (VE-cadherin)(+)

41 llum of children and contain stem cells in a perivascular niche thought to give rise to recurrence fo

42 reby enriching for deposition of MSLC in the perivascular niche through an HIF1alpha-dependent proces

43 (MSCs) are recruited from the endosteal and perivascular niche to become fibrosis-driving myofibrobl

44 The importance of the perivascular niche was further suggested by the fact tha

45 ming abilities, with the majority located in perivascular niches where GSCs are found.

46 Furthermore, YAP1 is found in cells of the perivascular niche, where proposed tumor-repopulating ce

47 netrant medulloblastoma originating from the perivascular niche, which exhibited abnormal blood vesse