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SLAS Discovery : Advancing Life Sciences R & D|July 18, 2017
Tissue Localization of Glycosphingolipid Accumulation in a Gaucher Disease Mouse Brain by LC-ESI-MS/MS and High-Resolution MALDI Imaging Mass SpectrometryE Ellen Jones, Wujuan Zhang, Xueheng Zhao, et al.
Ebiomedicine|February 4, 2018
Chitinase-3-like Protein 1: A Progranulin Downstream Molecule and Potential Biomarker for Gaucher DiseaseJinlong Jian, Yuehong Chen, Rossella Liberti, et al.
European Journal of Pediatrics|December 17, 2003
Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statementsGregory A Grabowski, Generoso Andria, Antonio Baldellou, et al.
European Journal of Pediatrics|December 17, 2003
Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoringAntonio Baldellou, Generoso Andria, Pauline E Campbell, et al.
Human Molecular Genetics|August 5, 2024
Intrinsic link between PGRN and Gba1 D409V mutation dosage in potentiating Gaucher diseaseYi Lin, Xiangli Zhao, Benjamin Liou, et al.
Human Molecular Genetics|December 18, 2009
Specific saposin C deficiency: CNS impairment and acid beta-glucosidase effects in the mouseYing Sun, Huimin Ran, Matt Zamzow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2009
Dose-response relationships for enzyme replacement therapy with imiglucerase/alglucerase in patients with Gaucher disease type 1Gregory A Grabowski, Katherine Kacena, J Alexander Cole, 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|May 16, 2008
Neurological deficits and glycosphingolipid accumulation in saposin B deficient miceYing Sun, David P Witte, Huimin Ran, et al.
Human Molecular Genetics|March 1, 2013
Tissue-specific effects of saposin A and saposin B on glycosphingolipid degradation in mutant miceYing Sun, Matt Zamzow, Huimin Ran, et al.
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