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Cell|June 25, 2011
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathiesJoseph R Mazzulli, You-Hai Xu, Ying Sun, et al.
BMC Genomics|January 13, 2011
Global gene expression profile progression in Gaucher disease mouse modelsYou-Hai Xu, Li Jia, Brian Quinn, et al.
Molecular Genetics and Metabolism|May 20, 2014
Reversal of advanced disease in lysosomal acid lipase deficient mice: a model for lysosomal acid lipase deficiency diseaseYing Sun, You-Hai Xu, Hong Du, et al.
Biochemical and Biophysical Research Communications|September 21, 2013
Fine-tuning of xylose metabolism in genetically engineered Saccharomyces cerevisiae by scattered integration of xylose assimilation genesQi Zuo, Xin-Qing Zhao, Liang Xiong, et al.
Human Molecular Genetics|March 7, 2014
Multiple pathogenic proteins implicated in neuronopathic Gaucher disease miceYou-hai Xu, Kui Xu, Ying Sun, et al.
Human Molecular Genetics|January 6, 2010
Neuronopathic Gaucher disease in the mouse: viable combined selective saposin C deficiency and mutant glucocerebrosidase (V394L) mice with glucosylsphingosine and glucosylceramide accumulation and progressive neurological deficitsYing Sun, Benjamin Liou, Huimin Ran, et al.
Human Molecular Genetics|October 1, 2015
Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse modelNupur Dasgupta, You-Hai Xu, Ronghua Li, et al.
Annals of Neurology|April 8, 2011
Acid β-glucosidase mutants linked to Gaucher disease, Parkinson disease, and Lewy body dementia alter α-synuclein processingValerie Cullen, S Pablo Sardi, Juliana Ng, et al.
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