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Publications by Michael Sandstrom

Silencing of the Mutant Huntingtin Gene Through CRISPR-Cas9 Improves the Mitochondrial Biomarkers in an in Vitro Model of Huntington’s Disease

Cell Transplantation

Transplantation

Biomedical Engineering

English

Related publications

Inhibition of Aggregation of Mutant Huntingtin by Nucleic Acid Aptamers in Vitro and in a Yeast Model of Huntington’s Disease

English

Genistein Induces Degradation of Mutant Huntingtin in Fibroblasts From Huntington’s Disease Patients

Metabolic Brain Disease

Molecular Neuroscience

English

PIAS1 Regulates Mutant Huntingtin Accumulation and Huntington’s Disease-Associated Phenotypes in Vivo

English

In Vitro CRISPR/Cas9-Directed Gene Editing to Model LRRK2 G2019S Parkinson’s Disease in Common Marmosets

Scientific Reports

Multidisciplinary

English

Huntington’s Disease: From the Physiological Function of Huntingtin to the Disease

English

Huntingtin Lowering Strategies for Disease Modification in Huntington’s Disease

English

An in Vitro Perspective on the Molecular Mechanisms Underlying Mutant Huntingtin Protein Toxicity

Cell Death and Disease

Molecular Neuroscience

Cancer Research

English

130. Gene Editing of the AAVS1 Locus With CRISPR/Cas9

Molecular Therapy

Molecular Medicine

Molecular Biology

English

Targeting N-Terminal Huntingtin With a Dual-sgRNA Strategy by CRISPR/Cas9

BioMed Research International

Molecular Biology

English