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Ebiomedicine|December 20, 2020
Impaired autophagy: The collateral damage of lysosomal storage disordersRachel Myerowitz, Rosa Puertollano, Nina Raben
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 19, 2012
Autophagy and mitochondria in Pompe disease: nothing is so new as what has long been forgottenNina Raben, Amanda Wong, Evelyn Ralston, et al.
Molecular Genetics and Metabolism|January 27, 2009
Murine muscle cell models for Pompe disease and their use in studying therapeutic approachesShoichi Takikita, Rachel Myerowitz, Kristien Zaal, et al.
Rare Diseases (Austin, Tex.)|December 1, 2015
Pompe disease: Shared and unshared features of lysosomal storage disordersJeong-A Lim, Or Kakhlon, Lishu Li, et al.
Autophagy|March 12, 2015
Defects in calcium homeostasis and mitochondria can be reversed in Pompe diseaseJeong-A Lim, Lishu Li, Or Kakhlon, et al.
Autophagy|July 3, 2009
The values and limits of an in vitro model of Pompe disease: the best laid schemes o' mice an' menShoichi Takikita, Rachel Myerowitz, Cynthia Schreiner, et al.
Human Molecular Genetics|May 23, 2002
Molecular pathophysiology in Tay-Sachs and Sandhoff diseases as revealed by gene expression profilingRachel Myerowitz, Douglas Lawson, Hiroki Mizukami, et al.
Molecular Genetics and Metabolism|December 14, 2004
Global gene expression in a type 2 Gaucher disease brainRachel Myerowitz, Hiroki Mizukami, Kristine L Richardson, et al.
Autophagy|September 24, 2010
Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder--murine Pompe diseaseNina Raben, Cynthia Schreiner, Rebecca Baum, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 8, 2008
Aptamer-based endocytosis of a lysosomal enzymeChi-hong B Chen, Kenneth R Dellamaggiore, Christopher P Ouellette, et al.
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