Search Results - "lysosomes"

The novel TFEB agonist desloratadine ameliorates hepatic steatosis by activating the autophagy-lysosome pathway by Jieru Lin, Chunhuan Huang, Jingye Zhao, Lu Li, Zhenwei Wu, Tingyu Zhang, Yuyin Li, Wei Li, Baoqiang Guo, Zhenxing Liu, Aipo Diao

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A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders by Karen A. Sanders, Dimitar K. Gavrilov, Devin Oglesbee, Kimiyo M. Raymond, Silvia Tortorelli, John J. Hopwood, Fred Lorey, Ramanath Majumdar, Charles A. Kroll, Amber M. McDonald, Jean M. Lacey, Coleman T. Turgeon, Justin N. Tucker, Hao Tang, Robert Currier, Grazia Isaya, Piero Rinaldo, Dietrich Matern

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Lysosomal acid lipase deficiency: A rarely recognised cause of dyslipidaemia and liver dysfunction by Marta Marín Andrés, Ignacio Ros Arnal, Jorge Javier Cebolla Sanz, Raquel Pérez Delgado, María Concepción García Jiménez

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Role of lysosomal enzymes released by alveolar macrophages in the pathogenesis of the acute phase of hypersensitivity pneumonitis by J. L. Pérez-Arellano, M. N. Barrios, T. Martín, M. L. Sánchez, J. M. González Buitrago, A. Jiménez

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Newborn Screening for Krabbe Disease and Other Lysosomal Storage Disorders: Broad Lessons Learned by Joseph J. Orsini, Michele Caggana

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Mesenchymal Stem Cell-Based Therapy for Lysosomal Storage Diseases and Other Neurodegenerative Disorders by Shaza S. Issa, Shaza S. Issa, Alisa A. Shaimardanova, Victor V. Valiullin, Albert A. Rizvanov, Valeriya V. Solovyeva

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The Importance of Assay Imprecision near the Screen Cutoff for Newborn Screening of Lysosomal Storage Diseases by Bruce H. Robinson, Michael H. Gelb

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Implementation of Second-Tier Tests in Newborn Screening for Lysosomal Disorders in North Eastern Italy by Alberto B. Burlina, Giulia Polo, Laura Rubert, Daniela Gueraldi, Chiara Cazzorla, Giovanni Duro, Leonardo Salviati, Alessandro P. Burlina

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mTOR hyperactivity mediates lysosomal dysfunction in Gaucher's disease iPSC-neuronal cells by Robert A. Brown, Antanina Voit, Manasa P. Srikanth, Julia A. Thayer, Tami J. Kingsbury, Marlene A. Jacobson, Marta M. Lipinski, Ricardo A. Feldman, Ola Awad

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Loss of lysosomal acid lipase results in mitochondrial dysfunction and fiber switch in skeletal muscles of mice by Alena Akhmetshina, Valentina Bianco, Ivan Bradić, Melanie Korbelius, Anita Pirchheim, Katharina B. Kuentzel, Thomas O. Eichmann, Helga Hinteregger, Dagmar Kolb, Hansjoerg Habisch, Laura Liesinger, Tobias Madl, Wolfgang Sattler, Branislav Radović, Simon Sedej, Ruth Birner-Gruenberger, Nemanja Vujić, Dagmar Kratky

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Implementation and results of a risk-sharing scheme for enzyme replacement therapy in lysosomal storage diseases by María Dolores Edo-Solsona, José Luis Poveda-Andrés, Isidro Vitoria-Miñana

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Light and Shadows in Newborn Screening for Lysosomal Storage Disorders: Eight Years of Experience in Northeast Italy by Vincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi, Andrea Puma, Christian Loro, Elena Porcù, Maria Stornaiuolo, Paolo Miglioranza, Leonardo Salviati, Alessandro P. Burlina, Alberto B. Burlina

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Wild-type and pathogenic forms of ubiquilin 2 differentially modulate components of the autophagy-lysosome pathways by Akiko Idera, Lisa M. Sharkey, Yuki Kurauchi, Keiichi Kadoyama, Henry L. Paulson, Hiroshi Katsuki, Takahiro Seki

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Toosendanin Induces Hepatocyte Damage by Inhibiting Autophagic Flux via TFEB-Mediated Lysosomal Dysfunction by Li Luo, Yonghong Liang, Yuanyuan Fu, Zhiyuan Liang, Jinfen Zheng, Jie Lan, Feihai Shen, Zhiying Huang

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Pharmaceutical Chaperones and Proteostasis Regulators in the Therapy of Lysosomal Storage Disorders: Current Perspective and Future Promises by Fedah E. Mohamed, Lihadh Al-Gazali, Fatma Al-Jasmi, Bassam R. Ali, Bassam R. Ali

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The Schistosome Esophagus Is a 'Hotspot' for Microexon and Lysosomal Hydrolase Gene Expression: Implications for Blood Processing. by R Alan Wilson, Xiao Hong Li, Sandy MacDonald, Leandro Xavier Neves, Juliana Vitoriano-Souza, Luciana C C Leite, Leonardo P Farias, Sally James, Peter D Ashton, Ricardo DeMarco, William Castro Borges

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Triptolide induces lysosomal-mediated programmed cell death in MCF-7 breast cancer cells by Owa C, Messina Jr ME, Halaby R

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Lysosomal alterations and decreased electrophysiological activity in CLN3 disease patient-derived cortical neurons by Sueanne Chear, Sharn Perry, Richard Wilson, Aidan Bindoff, Jana Talbot, Tyson L. Ware, Alexandra Grubman, James C. Vickers, Alice Pébay, Jonathan B. Ruddle, Anna E. King, Alex W. Hewitt, Anthony L. Cook

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Establishment of Cutoff Values for Newborn Screening of Six Lysosomal Storage Disorders by Tandem Mass Spectrometry by Ruotong Li, Liping Tian, Qing Gao, Yuanfang Guo, Gaijie Li, Yulin Li, Meng Sun, Yan Yan, Qing Li, Wenying Nie, Hui Zou

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Newborn Screening for Lysosomal Storage Disorders: Methodologies for Measurement of Enzymatic Activities in Dried Blood Spots by Michael H. Gelb, Zoltan Lukacs, Enzo Ranieri, Peter C. J. I. Schielen

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