Trinucleotide Repeat Expansion Diseases, RNAi, and Cancer: Trends in Cancer
Trinucleotide Repeat Expansion The human genome contains tandem repeats of trinucleotides. Normally they occur in groups of 5–35 repeats. When their number exceeds a certain threshold and they occur in a gene or close to it, they cause diseases. Once ...
Expanded CAG repeats in the crosshairs | Nature Biotechnology
Repeat Expansion Disorders: Mechanisms and Therapeutics | SpringerLink
Repeat expansion diseases. - Abstract - Europe PMC
Continuous and Periodic Expansion of CAG Repeats in Huntington's Disease R6/1 Mice
Transmission of the expanded HD CAG repeat to female and male offspring... | Download Table
What is the Pathogenic CAG Expansion Length in Huntington's Disease? - IOS Press
Exploring the Potential of Small Molecule-Based Therapeutic Approaches for Targeting Trinucleotide Repeat Disorders | SpringerLink
Ziekte van Huntington - Wikipedia
Kinderneurologie.eu
Trinucleotide repeats: triggers for genomic disorders? | Genome Medicine | Full Text
Trinucleotide Repeat Disorders - an overview | ScienceDirect Topics
Repeat expansion diseases. - Abstract - Europe PMC
Repeat expansion diseases. - Abstract - Europe PMC
Molecular genetic analysis of trinucleotide repeat disorders (TRDs) in Indian population and application of repeat primed PCR - ScienceDirect
Frontiers | RNA-mediated pathogenic mechanisms in polyglutamine diseases and amyotrophic lateral sclerosis | Cellular Neuroscience
Comparison of CAG repeat expansions in blood and sperm DNA of an SCA7... | Download Scientific Diagram
PDF) Repeat expansion diseases
Exploring the Potential of Small Molecule-Based Therapeutic Approaches for Targeting Trinucleotide Repeat Disorders | SpringerLink
PDF) Origin and Expansion of Trinucleotide Repeats and Neurological Disorders
HTT gene CAG triplet repeat expansions in Huntington's disease (HD)... | Download Scientific Diagram
Repeat expansion disease: progress and puzzles in disease pathogenesis | Nature Reviews Genetics
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset - ScienceDirect
Shortening trinucleotide repeats using highly specific endonucleases: a possible approach to gene therapy?: Trends in Genetics
