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8 examples:

Huntington's disease is caused by a mutant huntingtin (HTT) gene that contains an expanded tract of poly(CAG) repeats.
(Nature Reviews Genetics, )

Huntington's disease (HD) is caused by an expanded CAG repeat in huntingtin (HTT) and is characterized by tau deposition.
(Nature Reviews Neuroscience, )

Coexpression network analyses reveal 13 striatal and 5 cortical modules that are highly correlated with CAG length and age.
(Nature Neuroscience, )

The most prevalent SCAs (SCA1, SCA2, SCA3, SCA6 and SCA7) are caused by expansion of a glutamine-encoding CAG repeat in the affected gene.
(Nature Reviews Neuroscience, )

Huntington disease (HD) is caused by the expansion of a CAG repeat tract in the gene encoding huntingtin (HTT), resulting in aggregation of a toxic mutant HTT protein (mHTT).
(Nature Reviews Drug Discovery, )

Huntington disease (HD) is a progressive autosomal-dominant neurodegenerative disorder caused by a CAG trinucleotide-repeat-expansion mutation in the huntingtin (HTT)-encoding gene.
(Nature Reviews Drug Discovery, )

To gain insight into how mutant huntingtin (mHtt) CAG repeat length modifies Huntington's disease pathogenesis, the authors profiled mRNA in over 600 brain and peripheral tissue samples from Huntington's disease knock-in mice with increasing CAG repeat lengths.
(Nature Neuroscience, )

In mice bearing the creERT2-ODD transgene driven by either the ubiquitous CAG promoter or the cardiomyocyte-specific α myosin heavy chain promoter, we identify a rare population of hypoxic cardiomyocytes that display characteristics of proliferative neonatal cardiomyocytes, such as smaller size, mononucleation and lower oxidative DNA damage.
(Nature, )

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