14 results on '"Laganiere, Janet"'
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2. Valproic acid is protective in cellular and worm models of oculopharyngeal muscular dystrophy
3. Transit Defect of Potassium-Chloride Co-transporter 3 Is a Major Pathogenic Mechanism in Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum
4. Cellular expression of the K+–Cl− cotransporter KCC3 in the central nervous system of mouse
5. Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophy
6. Transgenic expression of an expanded (GCG) 13 repeat PABPN1 leads to weakness and coordination defects in mice
7. Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II
8. Cytoplasmic Targeting of Mutant Poly(A)-Binding Protein Nuclear 1 Suppresses Protein Aggregation and Toxicity in Oculopharyngeal Muscular Dystrophy
9. Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy
10. Schwannomin Isoform-1 Interacts with Syntenin via PDZ Domains
11. Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice
12. hnRNP A1 and A/B Interaction with PABPN1 in Oculopharyngeal Muscular Dystrophy
13. Oligomerization of polyalanineexpanded PABPN1 facilitates nuclear protein aggregation that is associatedwith cell death.
14. Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice
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