ライフサイエンスコーパス: condyle

1 samples from the medial and lateral femoral condyle).

2 lar neck in 4 female miniature pigs (one per condyle).

3 steoarthritis-like changes in the mandibular condyle.

4 e niche in the temporomandibular joint (TMJ) condyle.

5 of the secondary cartilage at the mandibular condyle.

6 and bone marrow edema in the lateral femoral condyle.

7 ltering the fibrocartilaginous nature of the condyle.

8 with the posterior non-weight-bearing medial condyle.

9 sulting structure fails to separate from the condyle.

10 properties by osmotic loading of the femoral condyle.

11 e fibrous and cartilaginous zones of the TMJ condyle.

12 into the shape of a cadaver human mandibular condyle.

13 ution of signal intensity changes within the condyle.

14 al tibial plateau and of the lateral femoral condyle.

15 ateral tibial plateau or the lateral femoral condyle.

16 and maxilla, with sparing of the mandibular condyles.

17 boys and girls or between medial and lateral condyles.

18 long the weight-bearing region and posterior condyles.

19 t-bearing articular cartilage of the femoral condyles.

20 +/- 2.4 versus 10.6 +/- 1.5), medial femoral condyle (22.8 +/- 2.9 versus 12.6 +/- 1.3), lateral femo

21 2.3+/-2.0 versus 10.4+/-0.8), medial femoral condyle (25.8+/-1.8 versus 15.9+/-1.9), and lateral femo

22 /- 2.9 versus 12.6 +/- 1.3), lateral femoral condyle (26.7 +/- 2.6 versus 16.2 +/- 1.9), and radial s

23 -1.8 versus 15.9+/-1.9), and lateral femoral condyle (27+/-1.9 versus 18.9+/-2.4).

24 the VPT at the MTP joint and lateral femoral condyle, after adjustment for age, sex, body mass index,

25 lagen and for the formation of the coronoid, condyle and angular processes.

26 our work provides the evidence that the TMJ condyle and disc develop independently of the mandibular

27 Remarkably, condyle and disc formation are not affected in these mut

28 ous tissue positioned between the mandibular condyle and glenoid fossa of the temporal bone, with imp

29 Gli2, which is expressed specifically in the condyle and in the disk of the developing TMJ.

30 ity of cartilage loss in the lateral femoral condyle and lateral tibial plateau and bone marrow edema

31 and bone marrow edema in the medial femoral condyle and medial tibial plateau.

32 e of impingement between the lateral femoral condyle and the posterior aspect of the patellar ligamen

33 They were observed in all grade 2 condyles and some grade 2 tibiae, but never in grade 0-1

34 parately from the medial and lateral femoral condyles and tibial plateaus of cynomolgus monkeys at th

35 condyle, two occurred in the lateral femoral condyle, and one occurred in the medial trochlea.

36 e digestion products of normal human femoral condyle articular cartilage and of purified aggrecan wer

37 higher in the weight-bearing anterior medial condyle as compared with the posterior non-weight-bearin

38 tants lacked the temporomandibular joint and condyle, but had a mandibular remnant that displayed abn

39 niofacial structures--such as the mandibular condyle, calvarial bone, cranial suture, and subcutaneou

40 his study was that a human-shaped mandibular condyle can be tissue-engineered from rat mesenchymal st

41 recorded, and samples of the medial femoral condyle cartilage and the synovial tissue adjacent to th

42 and reliably assess indicators of mandibular condyle cartilage pathology in mice.

43 man osteochondral cores from lateral femoral condyles, characterized as normal or mildly degenerated

44 parent BV/TV, Tb.N, and Tb.Sp in the femoral condyles could be used to differentiate healthy patients

45 Careful clinical evaluation of the condyle coupled with appropriate radiographic interpreta

46 aluation of the tissue-engineered mandibular condyle demonstrated two stratified layers of histogenes

47 s is common in both long bone and mandibular condyle development and during bone fracture repair.

48 strate that DDR2 is necessary for normal TMJ condyle development and homeostasis and that these DDR2

49 ant glenoid fossa, disc, synovial cells, and condyles displayed higher Hyaluronan synthase 2 expressi

50 By 6 months of age, mutant condyles displayed osteoarthritic degradation with apica

51 In FgfR3(P244R) mutants, the condyles displayed reduced levels of Ihh expression, H4C

52 tempted to analyze strain on the neck of the condyle during normal mastication and during simulated f

53 Condyle explants or dispersed chondrocytes were cultured

54 Medial femoral condyle flaps were elevated in 18 pigs.

55 e dorsum of immunodeficient mice, mandibular condyles formed de novo.

56 Mutant condyles from 3-month-old mice were narrow and flat alon

57 Mutant condyles had a rough and flattened bone surface, accompa

58 ments showed increased mandibular length and condyle head length following I-PTH treatment.

59 ntent in the cartilage of the medial femoral condyle in damaged and contralateral knees, but did not

60 rected more anteriorly along the neck of the condyle in that position.

61 re obtained from the central lateral femoral condyles in 11 patients undergoing total knee replacemen

62 .36 percent among those who received femoral condyles in particular.

63 on strains were significantly lower with the condyles in the anterior position compared with the othe

64 he femoral shaft immediately proximal to the condyles in the unstable limb was consistently wider (me

65 l mechanical properties of 22 pig mandibular condyles in three loading directions at a mean strain ra

66 ge flattening in posterior region of femoral condyle (in 16, 16, and nine patients).

67 zone adjacent to subchondral bone of femoral condyle (in zero, zero, and 26 patients), (c) pseudolami

68 e, signal intensity in the posterior femoral condyles increased and became progressively more focal.

69 at two distinct steps in disk morphogenesis, condyle initiation, and disk-condyle separation and prov

70 upon location, these results verify that the condyle is strongest and stiffest under compressive load

71 architecture suggest that the pig mandibular condyle is strongest when loaded supero-inferiorly, and

72 The impact of mandibular distraction on condyles is poorly understood.

73 BMLs on the lateral and medial femoral condyle, lateral and medial aspect of the tibial plateau

74 splay aberrant TMJ development such that the condyle loses its growth-plate-like cellular organizatio

75 weight-bearing regions of the medial femoral condyle (M1 and M4, respectively).

76 rts-medicine tissues (i.e., tendons, femoral condyles, menisci) from Tissue Bank A and 0.36 percent a

77 posterior surface of the posteromedial tibia condyle, merged with fibers from the semimembranosus ten

78 slie) mice revealed a developmental delay in condyle mineralization, as measured by micro-computed to

79 details, such as the presence of the dentary condyle of the mammalian jaw hinge and the postdentary t

80 Osteochondral cores from femoral condyles of cadaveric human donors were harvested.

81 ified in cartilage obtained from the femoral condyles of immature bovines, using immunoblotting, and

82 cular surface of unilateral proximal humeral condyles of skeletally mature rabbits was surgically exc

83 lculated in posterior regions of the femoral condyle on images obtained with each sequence; Wilcoxon

84 Samples of intact cartilage (condyles, patellofemoral groove, and proximal tibia) lyi

85 for both the medial and the lateral femoral condyles (r = 0.71 and r = 0.77, respectively; P < .001)

86 morphogenesis, condyle initiation, and disk-condyle separation and provide a molecular framework for

87 etrical mandibular incisure, medially placed condyle, small superior medial pterygoid tubercle, mesia

88 roaches for replacing degenerated mandibular condyles suffer from deficiencies such as donor site mor

89 the temporomandibular joint (TMJ) mandibular condyle that generates cartilage anlagen, which is subse

90 ain components of the TMJ are the mandibular condyle, the glenoid fossa of the temporal bone, and a f

91 nteen lesions occurred in the medial femoral condyle, two occurred in the lateral femoral condyle, an

92 Although the mechanical properties of the condyle vary depending upon location, these results veri

93 variation of the lateral and medial femoral condyle was indicative of the extent of the disease.

94 removed from lesions of the tali and femoral condyles was analyzed for type IIB collagen messenger RN

95 the hypertrophic chondrocyte zone in the cKO condyles was considerably larger than in wild-type mice.

96 The condition of the femoral condyles was determined by scanning electron microscopy

97 ssion in cartilage obtained from the femoral condyles was quantified by enzyme-linked immunosorbent a

98 of the articular cartilage from the femoral condyle were determined, and collagenolytic activity in

99 ess (sigma u) in the anterior regions of the condyle were greater than those in the posterior.

100 perficial and deeper layers of human femoral condyles were cultured with and without IL-1 in the pres

101 In contrast, the femoral condyles were fibrillated in all 12 of the sedentary ham

102 Fresh cadaveric canine femoral condyles were subjected to 20-25-MPa impact injury.