A CAG repeat-targeting artificial miRNA lowers the mutant huntingtin level in the YAC128 model of Huntington's disease: Molecular Therapy - Nucleic Acids
Molecular Genesis Huntington's Disease Illustration Expansion Cag Trinucleotide Sequence Htt Stock Photo by ©katerynakon 474065062
Huntington disease: MedlinePlus Genetics
Molecular genesis of Huntington's disease, illustration. Expansion of the CAG trinucleotide sequence in the htt gene causes production of mutated Huntingtin protein leading to neurodegeneration, atrophy of brain basal ganglia, involuntary movements
Selective suppression of polyglutamine-expanded protein by lipid nanoparticle-delivered siRNA targeting CAG expansions in the mouse CNS: Molecular Therapy - Nucleic Acids
What is the Pathogenic CAG Expansion Length in Huntington's Disease? - IOS Press
mHTT Protein: The Fundamental Cause of Huntington's Disease
Huntington's disease: prevention and current innovations in treatment - Personalize My Medicine
In silico designing of putative peptides for targeting pathological protein Htt in Huntington's disease - ScienceDirect
Cartoon model of Cag proteins. A: The N-terminal portion of... | Download Scientific Diagram
Huntington's Disease Research: Shutting down the mutant gene – HudsonAlpha Institute for Biotechnology
A Pathogenic Mechanism in Huntington's Disease Involves Small CAG-Repeated RNAs with Neurotoxic Activity | PLOS Genetics
The expanded CAG repeat in the huntingtin gene as target for therapeutic RNA modulation throughout the HD mouse brain | PLOS ONE
Molecular Genesis Huntington's Disease Illustration Expansion Cag Trinucleotide Sequence Htt Stock Photo by ©katerynakon 474065032
Structure and putative protein binding properties of the CAG repeats... | Download Scientific Diagram
IJMS | Free Full-Text | Decreased Interactions between Calmodulin and a Mutant Huntingtin Model Might Reduce the Cytotoxic Level of Intracellular Ca2+: A Molecular Dynamics Study
Frontiers | Protein Aggregation Inhibitors as Disease-Modifying Therapies for Polyglutamine Diseases
Discovery of a potent small molecule inhibiting Huntington's disease (HD) pathogenesis via targeting CAG repeats RNA and Poly Q protein | Scientific Reports
Suppression of Mutant Protein Expression in SCA3 and SCA1 Mice Using a CAG Repeat-Targeting Antisense Oligonucleotide: Molecular Therapy - Nucleic Acids
The importance of CagA protein in Helicobacter Pylori infection
Uninterrupted CAG repeat drives striatum-selective transcriptionopathy and nuclear pathogenesis in human Huntingtin BAC mice - ScienceDirect
Stem cells reveal developmental defects in Huntington's disease | The Stem Cellar
Huntington disease: MedlinePlus Genetics
Huntington disease: MedlinePlus Genetics
PolyQ-independent toxicity associated with novel translational products from CAG repeat expansions | bioRxiv
DNA Repair: Hot Topic in Huntington's Research – European Huntington Association
Huntingtin - Wikipedia
