ライフサイエンスコーパス: osteochondral

1 s a surrogate biomarker for success of shell osteochondral allograft implantation.

2 Many large centers have abandoned osteochondral allografts and resection arthrodesis for t

3 at the osteochondral junction were assessed (osteochondral angiogenesis).

4 PPI-2458 treatment reduced synovial and osteochondral angiogenesis, synovial inflammation, joint

5 ndral defects, including marrow stimulation, osteochondral auto- and allografting, and autologous cho

6 Under video microscopy, pairs of osteochondral blocks from each core were apposed, compre

7 ast number, suggestive of an early arrest of osteochondral bone formation.

8 lowing in vivo implantation of the bilayered osteochondral constructs in the dorsum of immunodeficien

9 Osteochondral cores from femoral condyles of cadaveric h

10 Human osteochondral cores from lateral femoral condyles, chara

11 The osteochondral cores from tissue donors were macroscopica

12 Osteochondral cores were harvested from the knees of cad

13 acterized by marked cartilage friability and osteochondral debonding.

14 ssue regeneration in a rabbit full-thickness osteochondral defect model.

15 d mitomycin-pretreated apoptotic ADSCs in an osteochondral defect of the left femur.

16 ble adipose-derived stem cells (ADSCs) in an osteochondral defect of the right femur and mitomycin-pr

17 ty cartilage fracture line, and fluid-filled osteochondral defect).

18 the same MSCs were injected in rats with an osteochondral defect, allowing MR monitoring of their en

19 In a critical-size rabbit osteochondral defect-repair model, the nanofibrous hollo

20 be misinterpreted as an articular erosion or osteochondral defect.

21 artilage architecture was established in rat osteochondral defects after treatment with chondrogenica

22 24.4 msec; P < .05) and could be tracked in osteochondral defects for 4 weeks.

23 eled cells were subsequently transplanted in osteochondral defects of 14 knees of seven athymic rats

24 ntly lower than those of matched implants in osteochondral defects of female rats (mean, 10.72 msec f

25 or mismatched stem cells were implanted into osteochondral defects of the knee joints of experimental

26 When implanted into rat osteochondral defects, acellular nanofiber scaffolds sup

27 Besides the pigmentation and osteochondral defects, usb1-knockdown caused defects in

28 spontaneous healing of focal chondral versus osteochondral defects.

29 etically engineered MDSCs implanted into rat osteochondral defects.

30 reasing shear, which eventually leads to the osteochondral degeneration.

31 For the 59 myotendinous and the 48 osteochondral diagnoses, the sensitivity, specificity, a

32 Osteochondral explants obtained from mature cattle were

33 he top layers of cartilage were removed from osteochondral explants, and the residual cartilage was a

34 subchondral cyst (six patients) or a single osteochondral fragment (two patients).

35 tion, and early motion are primary goals for osteochondral fragment preservation.

36 aled that GPR103-/- mice exhibited a thinned osteochondral growth plate, a thickening of trabecular b

37 ndinitis and tear, and suspected osseous and osteochondral injuries.

38 es tended to involve the inner aspect of the osteochondral interface with an associated osseous fragm

39 l junction, a diagonal-plane junction and an osteochondral interface.

40 Channels positive for vessels at the osteochondral junction were assessed (osteochondral angi

41 new bone formation in osteophytes and at the osteochondral junction, thereby contributing to radiolog

42 ited a high-intensity linear signal near the osteochondral junction, which was not visible on protein

43 hy, osteophytosis, and channels crossing the osteochondral junction.

44 y of evaluating abnormalities at or near the osteochondral junction.

45 n T2 in superficial region of interest in an osteochondral lesion = 50.0 msec +/- 10.2) in comparison

46 i.e., soft tissue lateral ankle impingement, osteochondral lesion, or partial peroneal tendon tear).

47 ation, 49.2 years +/- 12.7) with chondral or osteochondral lesions were prospectively collected and r

48 t modulation of focal adhesion formation and osteochondral lineage commitment was observed as a funct

49 growth factor that is highly specific to the osteochondral lineage, and has demonstrated robust induc

50 Six-millimeter-diameter chondral (n = 5) and osteochondral (n = 5, 3-4 mm deep into subchondral bone)

51 and CA(4+) to GAGs in cartilage (six bovine osteochondral plugs) were quantified by means of a modif

52 The osteochondral potential of the isolated cells was also a

53 primordium, in addition to mesoderm-derived osteochondral progenitors.

54 SWIFT enabled assessment of spontaneous osteochondral repair in an equine model.

55 ation tests were performed with fresh bovine osteochondral samples.

56 is very limited and pertains only to massive osteochondral surgery for trauma or malignancy, and is c

57 ontribute to biomechanical alteration of the osteochondral tissue and its subchondral bone plate comp

58 ding, increased hydraulic conductance of the osteochondral tissue and subchondral bone plate could ha

59 hypothesis was that hydraulic conductance of osteochondral tissue and subchondral bone plate increase

60 Hydraulic conductance of native osteochondral tissue and subchondral bone plate was high

61 chondral tissue repair and holds promise for osteochondral tissue engineering applications.

62 d/or insulin-like growth factor-1 (IGF-1) on osteochondral tissue regeneration in a rabbit full-thick

63 rticles (GMPs) and stem cell populations for osteochondral tissue regeneration.

64 yered composite hydrogels positively affects osteochondral tissue repair and holds promise for osteoc

65 distinctive hierarchical structure of native osteochondral tissue was utilized to investigate the eff

66 cteristics as seen in vascularized bones and osteochondral tissues.