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1 alytic domain that is 63% identical to human myotonic dystrophy protein kinase and has protein kinase
2 elated (65%) within the kinase domain to the myotonic dystrophy protein kinase (DM-PK), as well as th
4 sion in the literature about the size of the myotonic dystrophy protein kinase (DMPK) and its localiz
5 e basis for a new type of instability of the myotonic dystrophy protein kinase (DMPK) gene in patient
9 to modify the TRE at the 3' end of the human myotonic dystrophy protein kinase (DMPK) transcripts.
12 G)n tract in the 3' UTR of the gene encoding myotonic dystrophy protein kinase (DMPK), which results
15 -coil domain reminiscent of eukaryotic DMPK (Myotonic Dystrophy Protein Kinase) family kinases such a
16 n the 3'-untranslated region (3'-UTR) of the myotonic dystrophy protein kinase gene ( DMPK ), remain
17 ent within the 3'-untranslated region of the myotonic dystrophy protein kinase gene alters mRNA produ
21 ated region (UTR) of DMPK, the gene encoding myotonic dystrophy protein kinase, induces the dominantl
22 let-repeat expansion region from a truncated myotonic dystrophy protein kinase transcript mimic in vi
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