CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabolism linked to myotonic dystrophy type 1. Crystal structures of the RRM domains in complex with cognate RNAs (Teplova et al., 2010) reveal molecular details for the selectivity of CUGBP1 toward GU-rich mRNA elements
Myotonic dystrophy 2 (DM2) is a multisystem skeletal muscle disease caused by an expansion of tetran...
Myotonic dystrophy (DM) is associated with a (CTG) (n) triplet repeat expansion in the 3'-untranslat...
Myotonic dystrophy (DM) is associated with a (CTG) (n) triplet repeat expansion in the 3'-untranslat...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
SummaryCUG-binding protein 1 (CUGBP1) regulates multiple aspects of nuclear and cytoplasmic mRNA pro...
SummaryCUG-binding protein 1 (CUGBP1) regulates multiple aspects of nuclear and cytoplasmic mRNA pro...
Expansions of noncoding CUG and CCUG repeats in myotonic dystrophies type 1 (DM1) and DM2 cause comp...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
CUG-repeat binding protein 1 (CUGBP1) mediates selective mRNA decay by binding to GU-rich elements (...
Contains fulltext : 233612.pdf (Publisher’s version ) (Open Access)Radboud Univers...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];沒有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway...
Myotonic dystrophy type 1(DM1), the most common form of adult-onset muscular dystrophy, is caused by...
Myotonic dystrophy type 1(DM1), the most common form of adult-onset muscular dystrophy, is caused by...
Tracks containing CUG repeats are abundant in human gene transcripts. Their biological role includes...
Myotonic dystrophy 2 (DM2) is a multisystem skeletal muscle disease caused by an expansion of tetran...
Myotonic dystrophy (DM) is associated with a (CTG) (n) triplet repeat expansion in the 3'-untranslat...
Myotonic dystrophy (DM) is associated with a (CTG) (n) triplet repeat expansion in the 3'-untranslat...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
SummaryCUG-binding protein 1 (CUGBP1) regulates multiple aspects of nuclear and cytoplasmic mRNA pro...
SummaryCUG-binding protein 1 (CUGBP1) regulates multiple aspects of nuclear and cytoplasmic mRNA pro...
Expansions of noncoding CUG and CCUG repeats in myotonic dystrophies type 1 (DM1) and DM2 cause comp...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
CUG-repeat binding protein 1 (CUGBP1) mediates selective mRNA decay by binding to GU-rich elements (...
Contains fulltext : 233612.pdf (Publisher’s version ) (Open Access)Radboud Univers...
[[sponsorship]]生物醫學科學研究所[[note]]已出版;[SCI];沒有審查制度;具代表性[[note]]http://gateway.isiknowledge.com/gateway...
Myotonic dystrophy type 1(DM1), the most common form of adult-onset muscular dystrophy, is caused by...
Myotonic dystrophy type 1(DM1), the most common form of adult-onset muscular dystrophy, is caused by...
Tracks containing CUG repeats are abundant in human gene transcripts. Their biological role includes...
Myotonic dystrophy 2 (DM2) is a multisystem skeletal muscle disease caused by an expansion of tetran...
Myotonic dystrophy (DM) is associated with a (CTG) (n) triplet repeat expansion in the 3'-untranslat...
Myotonic dystrophy (DM) is associated with a (CTG) (n) triplet repeat expansion in the 3'-untranslat...
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