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1 nt enabled the maintenance of functional and hyaline cartilage.
2 has a similar collagen phenotype to that of hyaline cartilage.
3 ble of alleviating necrosis at the centre of hyaline cartilage.
4 gical development of these distinct types of hyaline cartilage.
5 rogenesis into either permanent or transient hyaline cartilage.
7 -bearing unossified epiphyseal and articular hyaline cartilage and for the distal femoral and proxima
8 the long alpha1(IX) transcript expressed in hyaline cartilage and matched the predicted sequence of
9 tion of type II collagen is observed in both hyaline cartilages and is secondary to proteoglycan loss
11 al type II, IX, and XI collagen phenotype of hyaline cartilage, but the fibrils appear abnormally thi
13 ar (82 [25%] vs 21 [19%], P = .25); isolated hyaline cartilage defect (77 [23%] vs 20 [18%], P = .29)
16 , pigmentation was widespread throughout the hyaline cartilage in either granular composition or as b
18 cartilaginous condylar cartilage, similar to hyaline cartilage in long bones, directly transform into
19 disc and cartilage is different from that of hyaline cartilage in other diarthrodial joints, and litt
20 dely expressed, but high levels are found in hyaline cartilage in the adult, bone tissue in newborn m
24 maturation of articular chondrocytes in the hyaline cartilage of both developing and degenerated joi
27 The trilaminar appearance depicted within hyaline cartilage on MR images obtained with this sequen
29 over expression of type X collagen which, in hyaline cartilage structure is not characteristic of the
31 cruciate), elastic cartilage, meniscus, and hyaline cartilage were analyzed for NTTPHase activity (t
32 vitro under hypoxia (2.5% O2) produced more hyaline cartilage, which expressed typical articular car
33 jority of vertebrate species have a layer of hyaline cartilage within the fibrous sclera giving an ex
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