Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. - Wikidata - wikimedia - TriplyDB

Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.

Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.

http://www.wikidata.org/entity/Q38299079

about

Systematic analysis of cis-elements in unstable mRNAs demonstrates that CUGBP1 is a key regulator of mRNA decay in muscle cells Deregulated microRNAs in myotonic dystrophy type 2 Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs.Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2.ClC1 chloride channel in myotonic dystrophy type 2 and ClC1 splicing in vitro.Myotonic dystrophy mouse models: towards rational therapy development.Altered Ca2+ homeostasis and endoplasmic reticulum stress in myotonic dystrophy type 1 muscle cells.LOX-1 and Its Splice Variants: A New Challenge for Atherosclerosis and Cancer-Targeted Therapies.(CCUG)n RNA toxicity in a Drosophila model of myotonic dystrophy type 2 (DM2) activates apoptosis.Molecular Effects of the CTG Repeats in Mutant Dystrophia Myotonica Protein Kinase Gene.

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P2860

Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.

http://www.wikidata.org/entity/Q38299079

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Gene expression analysis in my ...... ogenic pathway in DM1 and DM2.

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Gene Expression

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Gene expression analysis in my ...... ogenic pathway in DM1 and DM2.

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Emanuela Bonifazi

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Enzo Mancinelli

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Fabrizio Rinaldi

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Laura Vallo

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Michela Biancolella

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P2860

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

The CELF family of RNA binding proteins is implicated in cell-specific and developmentally regulated alternative splicing

Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells

Ion transport in human skeletal muscle cells: disturbances in myotonic dystrophy and Brody's disease

Identification of a zinc finger protein that binds to the sterol regulatory element

Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy

In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

Statistical implications of pooling RNA samples for microarray experiments

RNA leaching of transcription factors disrupts transcription in myotonic dystrophy

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

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13

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Giuseppe Novelli

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