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1 le for limb girdle muscular dystrophy 2B and Miyoshi myopathy.
2 mb girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopathy.
3 onal regulation at the mRNA level in DMD and Miyoshi myopathy.
4 e limb girdle muscular dystrophy type 2B and Miyoshi myopathy.
5 hy type 2B (LGMD2B) and its allelic disease, Miyoshi myopathy.
6 ients with a clinical diagnosis of LGMD2B or Miyoshi myopathy.
7 syndrome, limb-girdle muscle dystrophy, and Miyoshi myopathy.
8 mb-girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopathy.
9 ch codes for the protein dysferlin, underlie Miyoshi myopathy and limb-girdle muscular dystrophy 2B i
10 d in limb-girdle muscular dystrophy type 2B, Miyoshi myopathy, and distal anterior compartment myopat
12 Limb girdle muscular dystrophy type 2B and Miyoshi myopathy are clinically distinct forms of muscul
13 mmonly limb girdle muscular dystrophy 2B and Miyoshi myopathy, are degenerative myopathies caused by
15 , limb-girdle muscular dystrophy type 2B and Miyoshi myopathy, but the mechanism that leads to muscle
16 ing in limb girdle muscular dystrophy 2B and Miyoshi myopathy, concentrates in transverse tubules of
18 n limb-girdle muscular dystrophy type 2B and Miyoshi myopathy in humans and myopathy in A/J(dys-/-) a
19 n cause the progressive muscular dystrophies Miyoshi myopathy, limb girdle muscular dystrophy 2B, and
23 girdle muscular dystrophies types 2A and 2B, Miyoshi myopathy, nemaline myopathy, polymyositis, derma
25 ts with limb girdle muscular dystrophy 2B or Miyoshi myopathy, the findings obtained using the new as
26 g limb-girdle muscular dystrophy type 2L and Miyoshi myopathy type 3, although the pathogenic mechani
28 ay for limb girdle muscular dystrophy 2B and Miyoshi myopathy, which screens for dysferlin expression
29 n limb girdle muscular dystrophy type 2B and Miyoshi myopathy, with resulting plasma membrane abnorma
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