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1. Preventing acute neurotoxicity of CNS therapeutic oligonucleotides with the addition of Ca2+ and Mg2+ in the formulation.

2. Nacc1 Mutation in Mice Models Rare Neurodevelopmental Disorder with Underlying Synaptic Dysfunction.

3. Towards Standardizing Nomenclature in Huntingtons Disease Research.

5. Contributors

7. Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington’s disease

8. Targeting Tau Mitigates Mitochondrial Fragmentation and Oxidative Stress in Amyotrophic Lateral Sclerosis

10. Preventing acute neurotoxicity of CNS therapeutic oligonucleotides with the addition of Ca2+ and Mg2+ in the formulation

11. A programmable dual-targeting siRNA scaffold supports potent two-gene modulation in the central nervous system

12. KEAP1-modifying small molecule reveals muted NRF2 signaling responses in neural stem cells from Huntington's disease patients

13. Promise and challenges of dystonia brain banking: establishing a human tissue repository for studies of X-Linked Dystonia-Parkinsonism

17. Serum Deprivation of Mesenchymal Stem Cells Improves Exosome Activity and Alters Lipid and Protein Composition

18. Behavioral deficits, early gliosis, dysmyelination and synaptic dysfunction in a mouse model of mucolipidosis IV

19. A programmable dual-targeting di-valent siRNA scaffold supports potent multi-gene modulation in the central nervous system

20. Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington’s disease

21. Age-Dependent Increase in Tau Phosphorylation at Serine 396 in Huntington’s Disease Prefrontal Cortex

25. SUMO-2 and PIAS1 Modulate Insoluble Mutant Huntingtin Protein Accumulation

27. A divalent siRNA chemical scaffold for potent and sustained modulation of gene expression throughout the central nervous system

29. Levels of Synaptic Proteins in Brain and Neurofilament Light Chain in Cerebrospinal Fluid and Plasma of OVT73 Huntington’s Disease Sheep Support a Prodromal Disease State

34. Age-dependent increase in tau phosphorylation at serine 396 in Huntington s disease pre-frontal cortex

35. Extended Nucleic Acid (exNA): A Novel, Biologically Compatible Backbone that Significantly Enhances Oligonucleotide Efficacy in vivo

38. Age-dependent increase in tau phosphorylation at serine 396 in Huntington’s disease pre-frontal cortex

39. Extended Nucleic Acid (exNA): A Novel, Biologically Compatible Backbone that Significantly Enhances Oligonucleotide Efficacy in vivo

48. Di-valent siRNA Mediated Silencing of MSH3 Blocks Somatic Repeat Expansion in Mouse Models of Huntington’s Disease

49. Chemical engineering of therapeutic siRNAs for allele-specific gene silencingin vivoin CNS

50. SUMO-2 and PIAS1 Modulate Insoluble Mutant Huntingtin Protein Accumulation

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