Ralston, Evelyn

Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease.

Raben, N., Hill, V., Shea, L., Takikita, S., Baum, R., Mizushima, N., Ralston, E., & Plotz, P. (2008) · Human Molecular Genetics

Lysosomal Storage Disorders ResearchAutophagy in Disease and Therapy

Cited by 352

Expression of the adrenoleukodystrophy protein in the human and mouse central nervous system

Fouquet, F., Zhou, J. M., Ralston, E., Murray, K., Troalen, F., Magal, E., Robain, O., Dubois-Dalcq, M., & Aubourg, P. (1997) · Neurobiology of Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 115

Fiber Type Conversion by PGC-1α Activates Lysosomal and Autophagosomal Biogenesis in Both Unaffected and Pompe Skeletal Muscle

Takikita, S., Schreiner, C., Baum, R., Xie, T., Ralston, E., Plotz, P. H., & Raben, N. (2010) · PLoS ONE

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 60