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1 ) perivascular population, and contribute to cartilage repair.
2 reases contribution of Gdf5-lineage cells to cartilage repair.
3 esting their potential utility for articular cartilage repair.
4 an chondrocyte function and a new target for cartilage repair.
5 ential in engineered cartilage formation and cartilage repair.
6 n the nanoscale for application to articular cartilage repair.
7 nce in formulating effective stem cell-based cartilage repair.
8 iation and of cell replacement therapies for cartilage repair.
9 e application of growth factors to articular cartilage repair.
10 tor involved in chondrogenesis and articular cartilage repair.
11 s in vitro and in vivo and enhance articular cartilage repair.
12 practical utility for tissue engineering and cartilage repair.
13 rtilage lubrication, can inhibit integrative cartilage repair.
14 rphologic assessment of the knee joint after cartilage repair.
15 CPII, both of which are putative markers of cartilage repair.
16 se PHD-2 may represent a relevant target for cartilage repair.
17 elf-assembling peptide hydrogel scaffold for cartilage repair and developed a method to encapsulate c
19 itional MR imaging techniques for imaging of cartilage repair and their application to longitudinal s
21 ulin-like growth factor 1 (IGF-1) stimulates cartilage repair but is not a practical therapy due to i
23 are an attractive allogeneic cell source for cartilage repair, but their clinical translation has bee
24 ro and improved the persistence of articular cartilage repair by preventing vascularization and bone
25 se effects of NO may result in impairment of cartilage repair, by interfering with the extracellular
26 ant issue affecting the use of stem cells in cartilage repair, especially with regard to the persiste
29 ransplantation revealed significantly better cartilage repair in animals that received BMP-4-transduc
30 have previously found that the capacity for cartilage repair in human adult articular chondrocytes i
31 d mesenchymal stem cells (MSCs) and enhances cartilage repair in mouse osteoarthritis (OA) models.
35 enge in choosing an appropriate scaffold for cartilage repair is the identification of a material tha
37 lopment of tissue engineering approaches for cartilage repair or regeneration for the treatment of jo
42 the efficacy of pharmacologic treatments and cartilage repair strategies, but noninvasive techniques
43 drocytes group achieved substantially better cartilage repair than the chondrocytes-alone group that
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