Jodie P. Simard

发表

Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation.

C. E. Pearson, P. Haentjens, K. Sermon, 2011, Human molecular genetics.

MSH3 Polymorphisms and Protein Levels Affect CAG Repeat Instability in Huntington's Disease Mice

Greg W. Clark, E. Tillier, C. E. Pearson, 2013, PLoS genetics.

Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age.

A. Morton, R. Beyer, C. E. Pearson, 2014, Human molecular genetics.

Human Mismatch Repair Protein hMutLα Is Required to Repair Short Slipped-DNAs of Trinucleotide Repeats*

C. E. Pearson, M. Slean, Jodie P. Simard, 2012, The Journal of Biological Chemistry.

Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich’s ataxia

S. Schiffmann, M. Pandolfo, C. E. Pearson, 2012, Disease Models & Mechanisms.

Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues.

C. E. Pearson, M. Slean, Jodie P. Simard, 2013, DNA repair.

Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSβ, but clustered slip-outs are poorly repaired

O. Gileadi, C. E. Pearson, M. Slean, 2010, Proceedings of the National Academy of Sciences.

FRDA. Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich’s

S. Schiffmann, M. Pandolfo, C. E. Pearson, 2013 .

Overexpression of HSP70 inhibits cofilin phosphorylation and promotes lymphocyte migration in heat-stressed cells

Jodie P. Simard, Alan P Kraguljac, D. D. Mosser, 2011, Journal of Cell Science.