N. Pencea

Deficiency of a Glycogen Synthase-associated Protein, Epm2aip1, Causes Decreased Glycogen Synthesis and Hepatic Insulin Resistance*

C. Ackerley, P. Frankland, A. Wheeler, 2013, The Journal of Biological Chemistry.

Increased Laforin and Laforin Binding to Glycogen Underlie Lafora Body Formation in Malin-deficient Lafora Disease*

C. Ackerley, Peixiang Wang, B. Minassian, 2012, The Journal of Biological Chemistry.

PTG protein depletion rescues malin‐deficient Lafora disease in mouse

C. Ackerley, P. Frankland, J. Epp, 2014, Annals of neurology.

Inhibiting glycogen synthesis prevents lafora disease in a mouse model

C. Ackerley, P. Frankland, J. Epp, 2013, Annals of neurology.

PTG Depletion Removes Lafora Bodies and Rescues the Fatal Epilepsy of Lafora Disease

C. Ackerley, M. Cortez, A. Depaoli-Roach, 2011, PLoS genetics.

Early-onset Lafora body disease.

S. Scherer, C. Ackerley, Peixiang Wang, 2012, Brain : a journal of neurology.

Glycogen hyperphosphorylation underlies lafora body formation

C. Ackerley, Peixiang Wang, B. Minassian, 2010, Annals of neurology.

Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2

Carol J. Saunders, J. Vincent, Yuzhi Zhang, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Early-onset Lafora body disease.

S. Scherer, C. Ackerley, Peixiang Wang, 2012, Brain : a journal of neurology.