ライフサイエンスコーパス: marrow cavity

1 rogenitors form bone that does not contain a marrow cavity.

2 leading to a reduction in the length of the marrow cavity.

3 only wild-type vessels expand to create the marrow cavity.

4 one was thickened with narrowing of the bone marrow cavity.

5 ation of neoplastic plasma cells in the bone marrow cavity.

6 ect proximity to osteoblasts within the bone marrow cavity.

7 d the retention time of LNP-Cas9 in the bone marrow cavity.

8 modeling events on the bone surface from the marrow cavity.

9 one by increasing their mobility in the bone marrow cavity.

10 ant SV40 (rSV40)--directly into both femoral marrow cavities.

11 nduce ectopic adipocyte accumulation in bone marrow cavities.

12 Trabecular bone-the spongy bone inside marrow cavities-adapts to its mechanical environment dur

13 icles across bone trabeculae, endosteum, and marrow cavities and (b) a spatial model of the marrow ti

14 were dispersed throughout the periosteum and marrow cavity and could be identified in close appositio

15 y implicated in stem cell trafficking to the marrow cavity and shown to be expressed by cells within

16 Marrow cavity and trabecular chord length distributions

17 chondro-osseous junction, increased invasive marrow cavities, and suboptimal subchondral bone.

18 bone marrow during growth, the formation of marrow cavities, and the appearance of stromal cell type

19 at and minimal or no extension into the bone marrow cavity at MR imaging and normal plain radiographi

20 ent rely heavily on a single set of bone and marrow cavity chord-length distributions in which partic

21 marrow dose assessment are based on bone and marrow cavity chord-length distributions.

22 also showed an increased cellularity in the marrow cavity compared with the p27+/+.

23 with resorptive abilities, forming the bone marrow cavity during development.

24 This marrow cavity, essential to hematopoiesis and osteoclast

25 Marrow cavities from CB and BM ossicles included donor-d

26 e of ninein delays the formation of the bone marrow cavity in the prenatal tibia.

27 fully rescues the late formation of the bone marrow cavity in VHL mutant mice, though it does not aff

28 nance of osteoclasts, bone mass and the bone marrow cavity involve iterative fusion of circulating bl

29 ficant binding to bone on the inner walls of marrow cavities, liver avoidance, and anti-osteoporotic

30 ny tissue that forms before ovulation in the marrow cavities of birds as a calcium source for eggshel

31 ects) are uniformly localized throughout the marrow cavities of cancellous bone.

32 lly derived bone tissues lining the interior marrow cavities of portions of Tyrannosaurus rex (Museum

33 of adipocytes were inserted interior to the marrow cavities of the binary images, which were then co

34 Marrow cavities of the ossicles contained phenotypically

35 e spatial distributions of adipocytes in the marrow cavities of trabecular bone.

36 ve endings that innervate the periosteum and marrow cavity of murine long bones.

37 into athymic mice, either into femoral bone marrow cavities or into the systemic circulation via the

38 cations in growing long bones: excavation of marrow cavities permitting hematopoiesis in the marrow s

39 ough a cartilage intermediate and generate a marrow cavity populated by host-derived long-term recons

40 Two-photon intravital microscopy in bone marrow cavities showed that DCs formed stable antigen-de

41 ls results in a substantial increase in bone marrow cavity size due to upregulated osteoclast functio

42 d progenitor cells were markedly reduced and marrow cavities were occupied by adipocytes (yellow adip

43 The periosteum and the marrow cavity were each innervated by myelinated (NF200+

44 fter birth is largely restricted to the bone marrow cavity, where HSCs are associated closely with os

45 found almost exclusively in a subset of bone marrow cavities with bone-remodelling activity.