Add to ORKGContains fulltext : 233612.pdf (Publisher’s version ) (Open Access)Radboud University, 11 juni 2021Promotor : Wieringa, B. Co-promotor : Wansink, D.G.242 p
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
g.oxfordjournals.org/ D ow nloaded from 2 Myotonic dystrophy type 1 (DM1) is a neuromuscular disorde...
New discoveries showing the key role of RNAs in diseases such as cancer and neurodegenerative disord...
29 p. A THESIS Presented to the Department of Chemistry and the Clark Honors College of the Universi...
Expansions of noncoding CUG and CCUG repeats in myotonic dystrophies type 1 (DM1) and DM2 cause comp...
Tracks containing CUG repeats are abundant in human gene transcripts. Their biological role includes...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
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...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
Contains fulltext : 89133.pdf (publisher's version ) (Closed access)Myotonic dystr...
Aberrant RNA structure plays a central role in the molecular mechanisms guided by repeat RNAs in dis...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN025572 / BLDSC - British Library D...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
Myotonic dystrophy type 1 is caused by abnor-mal expansion of a CTG-trinucleotide repeat in the gene...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
g.oxfordjournals.org/ D ow nloaded from 2 Myotonic dystrophy type 1 (DM1) is a neuromuscular disorde...
New discoveries showing the key role of RNAs in diseases such as cancer and neurodegenerative disord...
29 p. A THESIS Presented to the Department of Chemistry and the Clark Honors College of the Universi...
Expansions of noncoding CUG and CCUG repeats in myotonic dystrophies type 1 (DM1) and DM2 cause comp...
Tracks containing CUG repeats are abundant in human gene transcripts. Their biological role includes...
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CT...
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...
Myotonic dystrophy (DM)—the most common form of muscular dystrophy in adults, affecting 1/8,000 indi...
Contains fulltext : 89133.pdf (publisher's version ) (Closed access)Myotonic dystr...
Aberrant RNA structure plays a central role in the molecular mechanisms guided by repeat RNAs in dis...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN025572 / BLDSC - British Library D...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
Myotonic dystrophy type 1 is caused by abnor-mal expansion of a CTG-trinucleotide repeat in the gene...
CUG-binding protein 1 (CUGBP1) is a ubiquitous RNA-binding protein implicated in altered RNA metabol...
g.oxfordjournals.org/ D ow nloaded from 2 Myotonic dystrophy type 1 (DM1) is a neuromuscular disorde...
New discoveries showing the key role of RNAs in diseases such as cancer and neurodegenerative disord...