Homepage About Dr. Pearson Research Projects Publications Staff Page Photo Page Links Links
Selected Publications
 Pubmed Search for Dr. CE Pearson
   Page 10   

Matsuura T, Fang P, Pearson CE, Jayakar P, Ashizawa T, Roa BB, Nelson DL. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier? American Journal of Human Genetics. 2006 January; 78(1):125-9.


Nichol Edamura K, Pearson CE. DNA methylation and replication: implications for the deletion hotspot region of FMR1. Human Genetics. 2005 November; 118(2):301-4.


Pearson CE, Nichol Edamura K, Cleary JD. Repeat instability: mechanisms of dynamic mutations. Nature Reviews Genetics. 2005 October; 6(10):729-42. Review.

\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\'ad infinitum iteratio\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\' by John D. Cleary and Christopher E. Pearson, adapted by Tom Wilson

Panigrahi GB, Lau R, Montgomery SE, Leonard MR, Pearson CE. Slipped (CTG) (CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair. Nature Structural Molecular Biology. 2005 August; 12(8):654-62.


Cleary JD, Pearson CE. Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability. Trends in Genetics. 2005 May; 21(5):272-80.


Nichol Edamura K, Leonard MR, Pearson CE. Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells. American Journal of Human Genetics. 2005 February; 76(2):302-11.


Mulvihill DJ, Nichol Edamura K, Hagerman KA, Pearson CE, Wang YH. Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome. Journal of Biological Chemistry. 2005 February; 280(6):4498-503.


Yang Z, Lau R, Marcadier JL, Chitayat D, Pearson CE. Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cells. American Journal of Human Genetics. 2003 November; 73(5):1092-105.

  Page 10   
Current Openings