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- 英文名:
Myotonic Dystrophy Protein Kinase (DMPK) fragment; Epitope: coil
- 库存:
999
- 供应商:
博奥派克
- 规格:
Supernatant 1ml
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文献和实验Repair of Myotonic Dystrophy Protein Kinase (DMPK) Transcripts by Trans-Splicing Ribozymes
cellular functions in diseased cells. The purpose of this chaper is to present the methodology that can be used to repair mutations responsible for myotonic dystrophy. The design and construction of group I intron ribozymes and their transfection
Use of Animal Models to Understand Human Muscular Dystrophy
(myotonic dystrophy protein kinase [DMPK]) in myotonic dystrophy (DM) (5 ), and mutations in a novel nuclear protein in Emery-Dreifuss MD (6 ).
Real-Time RT-PCR for CTG Repeat-Containing Genes
Myotonic dystrophy (DM1) is a neuromuscular disorder caused by a CTGn expansion in the 3′-untranslated region (UTR) of myotonic dystrophy protein kinase (DMPK ). SIX5 is a homeodomain gene located just downstream of the repeat, and myotonic
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