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JAMA Neurology|December 16, 2014
Massive CAG repeat expansion and somatic instability in maternally transmitted infantile spinocerebellar ataxia type 7Heather Trang, Sabrina Y Stanley, Paul Thorner, et al.
Biochemistry|April 14, 2012
The nucleotide sequence, DNA damage location, and protein stoichiometry influence the base excision repair outcome at CAG/CTG repeatsAgathi-Vasiliki Goula, Christopher E Pearson, Julie Della Maria, et al.
Nucleic Acids Research|October 18, 2002
Slipped-strand DNAs formed by long (CAG)*(CTG) repeats: slipped-out repeats and slip-out junctionsChristopher E Pearson, Mandy Tam, Yuh-Hwa Wang, et al.
Neurobiology of Disease|December 30, 2021
CAG repeat-binding small molecule improves motor coordination impairment in a mouse model of Dentatorubral-pallidoluysian atrophyYuhei Hasuike, Hana Tanaka, Terence Gall-Duncan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2025
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and review of the first 3 yearsKristin D Kernohan, Lauren Gallagher, Marie Pigeon, et al.
Nucleic Acids Research|November 6, 2010
Determinants of R-loop formation at convergent bidirectionally transcribed trinucleotide repeatsKaalak Reddy, Mandy Tam, Richard P Bowater, et al.
DNA Repair|December 12, 2012
Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissuesStéphanie Tomé, Jodie P Simard, Meghan M Slean, et al.
Nucleic Acids Research|August 23, 2014
Processing of double-R-loops in (CAG)·(CTG) and C9orf72 (GGGGCC)·(GGCCCC) repeats causes instabilityKaalak Reddy, Monika H M Schmidt, Jaimie M Geist, et al.
The Lancet. Neurology|October 25, 2020
Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapiesGalen E B Wright, Hailey Findlay Black, Jennifer A Collins, et al.
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