Pages that link to "Q35078193"
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The following pages link to Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2. (Q35078193):
Displaying 14 items.
- Expanded CCUG repeat RNA expression in Drosophila heart and muscle trigger Myotonic Dystrophy type 1-like phenotypes and activate autophagocytosis genes. (Q30854929) (← links)
- MBNL proteins and their target RNAs, interaction and splicing regulation. (Q34248811) (← links)
- Competition between RNA-binding proteins CELF1 and HuR modulates MYC translation and intestinal epithelium renewal (Q35621945) (← links)
- Clinical aspects, molecular pathomechanisms and management of myotonic dystrophies (Q38209927) (← links)
- Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism (Q39012035) (← links)
- Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects (Q39081415) (← links)
- Biomolecular diagnosis of myotonic dystrophy type 2: a challenging approach. (Q39333700) (← links)
- Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle. (Q41702661) (← links)
- Relation of genomic variants for Alzheimer disease dementia to common neuropathologies (Q42029540) (← links)
- rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences. (Q55087601) (← links)
- Myotonic Dystrophies: Targeting Therapies for Multisystem Disease (Q57812794) (← links)
- (CTG)n repeat-mediated dysregulation of MBNL1 and MBNL2 expression during myogenesis in DM1 occurs already at the myoblast stage. (Q64900419) (← links)
- Of Mice and Men: Advances in the Understanding of Neuromuscular Aspects of Myotonic Dystrophy. (Q64989527) (← links)
- Myotonic Dystrophy and Developmental Regulation of RNA Processing (Q88453318) (← links)