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1 I) chain and the C-terminal domain (COL1) of type IX collagen.
2 oding cartilage oligomeric matrix protein or type IX collagen.
3 ted for a primary myopathy and a mutation in type IX collagen.
5 en fibrils, including an exponential loss of type IX collagen along with its chondroitin sulfate side
8 a3) of the non-collagenous domain 2 (NC2) of type IX collagen are assembled to guide triple-helical s
10 of collagen type V/XI and the NC2 domain of type IX collagen both contribute to prominent stain-excl
14 owth plate phenotype with retention of TSP5, type IX collagen (Col9), and matrillin-3 in the rough en
15 rtilage oligomeric matrix protein (COMP) and type IX collagen (COL9A2 and COL9A3) have previously bee
16 Synthetic peptides of the three chains of type IX collagen consisting of the carboxyl-terminal end
17 biguously demonstrate that the NC2 domain of type IX collagen determines not only the chain compositi
18 evidence came from Western blot analysis of type IX collagen extracted by pepsin from fetal human ca
19 lysis of the cross-linking sites occupied in type IX collagen from nucleus pulposus showed that usage
20 ned the expression and the potential role of type IX collagen in bone restoration and remodeling.
22 t the disulfide-linked NC1 domain of chicken type IX collagen, indicating the correct formation of th
26 ments were harvested from wild-type (WT) and type IX collagen-knockout (Col9a1(-/-)) mice at 3, 6, an
29 inor component of vitreous collagen fibrils, type IX collagen, probably by virtue of its chondroitin
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