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1 of SnCs as a therapeutic target for treating degenerative joint disease.
2 an turnover and cartilage degradation during degenerative joint disease.
3  whereby CSA may be an effective therapy for degenerative joint disease.
4 ut not in successfully treated infections or degenerative joint disease.
5 d function, and may serve as an indicator of degenerative joint disease.
6  the catabolic phenotype may protect against degenerative joint disease.
7  short stature, joint laxity and early-onset degenerative joint disease.
8 arthritis (OA) is an age-related progressive degenerative joint disease.
9 0 could modulate cartilage mineralization in degenerative joint diseases.
10 age is an early event in the pathogenesis of degenerative joint diseases.
11  resolved associated comorbidities were 6/14 degenerative joint disease, 9/10 gastroesophageal reflux
12                                              Degenerative joint disease, also known as osteoarthritis
13 ism by which synovitis could develop in both degenerative joint disease and spondylarthritis.
14 al phenotype in which surviving mice acquire degenerative joint diseases and tumors in multiple organ
15 Importantly, we observe no clinical signs of degenerative joint disease apart from mild, or in one ca
16 ltrating immune cells play a central role in degenerative joint disease associated with osteoarthriti
17                          Osteoarthritis is a degenerative joint disease characterized by a progressiv
18 bular joint (TMJ) disc displacement (DD) and degenerative joint disease (DJD) has never been conclusi
19 th and without reduction (DDwR and DDwoR) to degenerative joint disease (DJD), and patient-reported o
20                   Osteoarthritis is a common degenerative joint disease for which no disease-modifyin
21 esity comorbidity in these patients included degenerative joint disease, gastroesophageal reflux dise
22 ntial biologic therapies in the treatment of degenerative joint disease in the future.
23        A relationship with meniscal tear and degenerative joint disease independent of effusion was a
24 eritance, coalitions also can be acquired by degenerative joint disease, inflammatory arthritis, infe
25 n of Smad3 exon 8 (Smad3(ex8/ex8)) developed degenerative joint disease resembling human osteoarthrit
26 ifferentiation and results in development of degenerative joint disease resembling osteoarthritis in
27 ssive degradation of the cartilage matrix in degenerative joint diseases such as osteoarthritis.
28 the integrity of the cartilage matrix during degenerative joint diseases such as osteoarthritis.
29 ose released from articular cartilage during degenerative joint diseases such as osteoarthritis.
30                                              Degenerative joint diseases, such as arthritis, cause lo
31 rome, hypertension, gastroesophageal reflux, degenerative joint disease symptoms, type 2 diabetes mel
32                     Osteoarthritis (OA) is a degenerative joint disease that involves the destruction
33                          Osteoarthritis is a degenerative joint disease that ranks among the leading
34 a, hypoventilation, gastroesophageal reflux, degenerative joint disease, urinary incontinence, venous
35                                              Degenerative joint disease, which affects one-fifth of t
36 omologous recombination leads to early onset degenerative joint disease, which is revealed by simulta
37                          Osteoarthritis is a degenerative joint disease whose molecular mechanism is
38 steoarthritis (OA) is a prevalent, heritable degenerative joint disease with a substantial public hea

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