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In silico designing of putative peptides for targeting pathological protein Htt in Huntington's disease - ScienceDirect
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A CAG repeat-targeting artificial miRNA lowers the mutant huntingtin level in the YAC128 model of Huntington's disease: Molecular Therapy - Nucleic Acids
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Structure and putative protein binding properties of the CAG repeats... | Download Scientific Diagram
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Molecular Genesis Huntington's Disease Illustration Expansion Cag Trinucleotide Sequence Htt Stock Photo by ©katerynakon 474065062
A Pathogenic Mechanism in Huntington's Disease Involves Small CAG-Repeated RNAs with Neurotoxic Activity | PLOS Genetics
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Frontiers | Protein Aggregation Inhibitors as Disease-Modifying Therapies for Polyglutamine Diseases
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Huntington's Disease Research: Shutting down the mutant gene – HudsonAlpha Institute for Biotechnology
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Selective suppression of polyglutamine-expanded protein by lipid nanoparticle-delivered siRNA targeting CAG expansions in the mouse CNS: Molecular Therapy - Nucleic Acids
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Molecular Genesis Huntington's Disease Illustration Expansion Cag Trinucleotide Sequence Htt Stock Photo by ©katerynakon 474065032
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