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1 that were homozygous for V194D and null for matrilin 1.
2 ed aggregates and caused the co-retention of matrilin 1.
3 nt on the formation of hetero-oligomers with matrilin 1.
4 ndrocytes in the cartilage anlagen expresses matrilin-1.
5 directed toward the cartilage matrix protein matrilin-1.
6 de corresponding to the C-terminal domain of matrilin-1.
10 not dependent on hetero-oligomerization with matrilin 1, and that the total ablation of matrilin 1 ex
11 ain organization to cartilage matrix protein/matrilin-1, but information on the protein structure is
16 h matrilin 1, and that the total ablation of matrilin 1 expression has no impact on disease severity
17 n of early chondrocytes that do not activate matrilin-1 expression rather than by redifferentiation f
18 that, in primary chondrocyte cultures, CMP (matrilin-1) forms a filamentous network, which is made u
20 nase gene has been targeted to exon 1 of the matrilin-1 gene (Matn1) to investigate the origins of ar
21 e chondrocytes did not turn on expression of matrilin-1 in contrast to the other chondrocytes of the
23 appears to function in the matrix linked to matrilin-1 in the form of disulfide-bonded heteromeric m
26 expression at about 15 h post-fertilization, matrilin-1 is present throughout the zebrafish embryo wi
29 us angiogenesis inhibitors, we have purified matrilin-1 (MATN-1) and have demonstrated, for the first
31 of matrilin 1 would abolish the formation of matrilin 1/matrilin 3 hetero-oligomers, eliminate the se
35 derived from cells that have never expressed matrilin-1 whereas the remainder of the chondrocytes in
36 investigate the hypothesis that deletion of matrilin 1 would abolish the formation of matrilin 1/mat
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