Works matching DE "LYSOSOMES"


Results: 4725
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    DISFUNÇÃO DA AUTOFAGIA LISOSSOMAL E SEU PAPEL NO DESENVOLVIMENTO DA OBESIDADE.

    Published in:
    Revista Foco (Interdisciplinary Studies Journal), 2025, v. 18, n. 4, p. 1, doi. 10.54751/revistafoco.v18n4-109
    By:
    • Vitor da Costa, Orbenia;
    • Freire de Oliveira, Kaylane;
    • Pereira Pinto, Maria Clara;
    • Gomes Marques, Clayton Cleone;
    • de Medeiros Dantas, Tatiany;
    • Bezerra Vieira, Fillipe;
    • Bezerra do Nascimento, Francisca Paloma;
    • Pinel Neto, Orlando;
    • Cavalcante de Lira, Rafaelle
    Publication type:
    Article
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    A Voltage-Gated Calcium Channel Regulates Lysosomal Fusion with Endosomes and Autophagosomes and Is Required for Neuronal Homeostasis.

    Published in:
    PLoS Biology, 2015, v. 13, n. 3, p. 1, doi. 10.1371/journal.pbio.1002103
    By:
    • Tian, Xuejun;
    • Gala, Upasana;
    • Zhang, Yongping;
    • Shang, Weina;
    • Nagarkar Jaiswal, Sonal;
    • di Ronza, Alberto;
    • Jaiswal, Manish;
    • Yamamoto, Shinya;
    • Sandoval, Hector;
    • Duraine, Lita;
    • Sardiello, Marco;
    • Sillitoe, Roy V.;
    • Venkatachalam, Kartik;
    • Fan, Hengyu;
    • Bellen, Hugo J.;
    • Tong, Chao
    Publication type:
    Article
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    Lysosomal ROS formation.

    Published in:
    Redox Report, 2005, v. 10, n. 4, p. 199, doi. 10.1179/135100005X70170
    By:
    • Nohl, Hans;
    • Gille, Lars
    Publication type:
    Article
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    TAP and TAP-like — Brothers in arms?

    Published in:
    Naunyn-Schmiedeberg's Archives of Pharmacology, 2006, v. 372, n. 6, p. 444, doi. 10.1007/s00210-005-0028-z
    By:
    • Zhao, Chenguang;
    • Tampé, Robert;
    • Abele, Rupert
    Publication type:
    Article
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    Small fibre neuropathy in Fabry disease: a human-derived neuronal in vitro disease model and pilot data.

    Published in:
    Brain Communications, 2024, v. 6, n. 2, p. 1, doi. 10.1093/braincomms/fcae095
    By:
    • Klein, Thomas;
    • Grüner, Julia;
    • Breyer, Maximilian;
    • Schlegel, Jan;
    • Schottmann, Nicole Michelle;
    • Hofmann, Lukas;
    • Gauss, Kevin;
    • Mease, Rebecca;
    • Erbacher, Christoph;
    • Finke, Laura;
    • Klein, Alexandra;
    • Klug, Katharina;
    • Karl-Schöller, Franziska;
    • Vignolo, Bettina;
    • Reinhard, Sebastian;
    • Schneider, Tamara;
    • Günther, Katharina;
    • Fink, Julian;
    • Dudek, Jan;
    • Maack, Christoph
    Publication type:
    Article
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    Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.

    Published in:
    Brain Communications, 2021, v. 3, n. 4, p. 1, doi. 10.1093/braincomms/fcab245
    By:
    • Bott, Laura C.;
    • Forouhan, Mitra;
    • Lieto, Maria;
    • Sala, Ambre J.;
    • Ellerington, Ruth;
    • Johnson, Janel O.;
    • Speciale, Alfina A.;
    • Criscuolo, Chiara;
    • Filla, Alessandro;
    • Chitayat, David;
    • Alkhunaizi, Ebba;
    • Shannon, Patrick;
    • Nemeth, Andrea H.;
    • Angelucci, Francesco;
    • Wooi Fang Lim;
    • Striano, Pasquale;
    • Zara, Federico;
    • Helbig, Ingo;
    • Muona, Mikko;
    • Courage, Carolina
    Publication type:
    Article
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