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1 d growth arrest in the central region of the epiphyses.
2 gatively regulates secondary ossification of epiphyses.
3 h Blount disease and slipped capital femoral epiphyses.
4 d the degree of fusion between diaphyses and epiphyses.
5 o investigate if vascular injury in immature epiphyses affects cartilage repair outcomes of matrix-as
6 nal features, such as short stature and cone epiphyses, also suggest an underlying defect in endochon
7                     The physeal cartilage of epiphyses and apophyses is the weakest structure in the
8 by delayed and irregular ossification of the epiphyses and early-onset osteoarthritis.
9  scans were obtained by pQCT from the distal epiphyses and from the diaphyses of the tibia in each le
10 liferating pool of chondroblasts between the epiphyses and metaphyses of future long bones.
11 tyspondyly, generalized abnormalities of the epiphyses and metaphyses, and a distinctive lacy appeara
12 hort stature, hip abnormalities, cone-shaped epiphyses and premature closure of growth plates reflect
13 cluding thimble-like middle phalanges, coned epiphyses, and carpal and tarsal fusions.
14 SCs and putative HSC niches in the calvaria, epiphyses, and diaphyses, at steady state or after HSC t
15 etatarsals and calcanei, small distal tibial epiphyses, and thickened ischia.
16 ial attention to articular bone surfaces and epiphyses, are analyzed.
17 ssues of uptake were the proximal and distal epiphyses, at 0.33-0.62%ID/g.
18  of Phd2 on endochondral ossification of the epiphyses by conditionally deleting the Phd2 gene in ost
19 ion of punctate focal mineralization in bone epiphyses during neonatal age and infancy.
20                                      Femoral epiphyses from 5-week-old wild-type mice were avulsed an
21 al skeleton, forelimbs, and hind limbs, with epiphyses fused, indicate that it was a mature adult.
22 es in bone parameters in the proximal tibial epiphyses in 5 week old mice.
23  and subsequently in the chondrocytes of the epiphyses in a graded distribution that decreased toward
24                           In 36 newborn lamb epiphyses (including cartilage of the epiphysis and phys
25 e (normalized to tissue volume) in long bone epiphyses, indicating that Phd2 expressed in chondrocyte
26 omography to measure trabecular bone of limb epiphyses (long bone articular ends) in modern humans an
27 aken from both the femoral heads and humeral epiphyses of a 51-y-old male subject.
28 on, blood vessel invasion is impaired in the epiphyses of Dmp1(-/-) mice.
29                The proximal and distal femur epiphyses of mice are both weight-bearing structures der
30 eriosteum, tendons, and endosteum within the epiphyses of the long bones adjacent to articular joints
31 adiographic features often restricted to the epiphyses of the long bones.
32                                       Normal epiphyses, physes, and metaphyses of piglets were evalua
33 tively, and those to the proximal and distal epiphyses were 141 and 43.4 mGy/MBq, respectively.
34                                              Epiphyses were categorized into five types on the basis
35  skeletal defects including scoliosis, large epiphyses, wide growth plates and supernumerary distal l