The DMWD protein from the myotonic dystrophy (DM1) gene region is developmentally regulated and is present most prominently in synapse-dense brain areas

Author:

Westerlaken Jolanda H.A.M,Van der Zee Catharina E.E.M,Peters Wilma,Wieringa Bé

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference36 articles.

1. Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat;Alwazzan;Hum. Mol. Genet.,1999

2. Developmental changes in expression of myotonic dystrophy protein kinase in the rat central nervous system;Balasubramanyam;J. Comp. Neurol.,1998

3. Interaction cloning: identification of a helix-loop-helix zipper protein that interacts with c-Fos;Blanar;Science,1992

4. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat;Boucher;Hum. Mol. Genet.,1995

5. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992

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