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You searched for: Author/Creator Gillis, Tammy

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1. A22 Medium-sized spiny neurons diversity in Huntington's disease pathology. (12th September 2022)

3. Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease. Issue 2 (5th February 2015)

4. High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgrounds. (27th February 2017)

5. Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs. Issue 3 (11th January 2021)

6. Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levels. (6th February 2017)

7. Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1. (7th July 2020)

8. Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder. (26th February 2015)

9. Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out. (2nd September 2020)