13 results on '"Gourdon, G"'
Search Results
2. FP.44 Exploring the role of MuscleBlind-Like proteins in the regulation of CaVB1 isoform expression in adult skeletal muscle
3. Apnées obstructives et mixtes chez le souriceau DMSXL, modèle de la forme congénitale de la maladie de Steinert
4. O.32Genome editing of expanded CTG repeats within the human DMPK gene reduces nuclear RNA foci in muscle of DM1 mice
5. P.278 - CRISPR/Cas9-mediated genome editing corrects splicing alterations in myotonic dystrophy type 1
6. G.P.90 - Neuroglial miscommunication in the cerebellum of a mouse model of myotonic dystrophy
7. O.6 Antisense approach for myotonic dystrophy
8. P1-19 Dérégulation de l’épissage de Tau par MBNL1 dans une Tauopathie
9. T.O.4 Ribozyme-based gene therapy reverses muscle atrophy in a mouse model of myotonic dystrophy
10. G.P.14.09 Functional characterization of skeletal muscles in DM1 mice
11. Role of Upstream DNase I Hypersensitive Sites in the Regulation of Human α Globin Gene Expression
12. The Mouse α-Globin Locus Regulatory Element
13. Un nouveau cas de dystrophie myotonique de Steinert congénitale de transmission paternelle
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