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1 avenue for treating advanced intervertebral disc disease.
2 D3 may serve a critical role in degenerative disc disease.
3 toration of cell numbers during degenerative disc disease.
4 ADAMTS-5 protein expression with severity of disc disease.
5 loping biological therapies for degenerative disc disease.
6 ge of a new form of therapy for degenerative disc disease.
7 that may be important in the pathogenesis of disc disease.
8 ed expression of NOTCH genes in degenerative disc disease.
10 e studies show an association between lumbar disc disease and mutations of genes encoding the alpha-2
12 s a key role in pathogenesis of degenerative disc disease by promoting aggrecan degradation by ADAMTS
14 enetic mutations in disorders such as lumbar disc disease, further investigation of the interaction b
16 Low back pain associated with degenerative disc disease is optimally treated with distraction of th
17 reed (PBonferroni = 0.01) and intervertebral disc disease (IVDD) across breeds (PBonferroni = 4.0 x 1
19 ing IL-1beta and TNF-alpha activities during disc disease may restore NOTCH signaling and nucleus pul
20 g this transcription factor for treatment of disc disease must spare osmoprotective, prosurvival, and
21 ere procured from patients with degenerative disc disease (n = 25) or herniated IVDs (n = 12); nondeg
24 lternative for the treatment of degenerative disc disease that is more logistically convenient than t
25 provide potential therapies for degenerative disc disease, which is the major cause of lower back pai
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