Works matching DE "LYSOSOMES"

Results: 4579
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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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    Genetically Controlled Lysosomal Entrapment of Superparamagnetic Ferritin for Multimodal and Multiscale Imaging and Actuation with Low Tissue Attenuation.

    Published in:
    Advanced Functional Materials, 2018, v. 28, n. 19, p. 1, doi. 10.1002/adfm.201706793
    By:
    • Massner, Christoph;
    • Sigmund, Felix;
    • Pettinger, Susanne;
    • Seeger, Markus;
    • Hartmann, Carolin;
    • Ivleva, Natalia P.;
    • Niessner, Reinhard;
    • Fuchs, Helmut;
    • de Angelis, Martin Hrabě;
    • Stelzl, Anja;
    • Koonakampully, Neha Lal;
    • Rolbieski, Hannes;
    • Wiedwald, Ulf;
    • Spasova, Marina;
    • Wurst, Wolfgang;
    • Ntziachristos, Vasilis;
    • Winklhofer, Michael;
    • Westmeyer, Gil G.
    Publication type:
    Article
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    Genetically Controlled Lysosomal Entrapment of Superparamagnetic Ferritin for Multimodal and Multiscale Imaging and Actuation with Low Tissue Attenuation.

    Published in:
    Advanced Functional Materials, 2018, v. 28, n. 19, p. N.PAG, doi. 10.1002/adfm.201706793
    By:
    • Massner, Christoph;
    • Sigmund, Felix;
    • Pettinger, Susanne;
    • Seeger, Markus;
    • Hartmann, Carolin;
    • Ivleva, Natalia P.;
    • Niessner, Reinhard;
    • Fuchs, Helmut;
    • de Angelis, Martin Hrabě;
    • Stelzl, Anja;
    • Koonakampully, Neha Lal;
    • Rolbieski, Hannes;
    • Wiedwald, Ulf;
    • Spasova, Marina;
    • Wurst, Wolfgang;
    • Ntziachristos, Vasilis;
    • Winklhofer, Michael;
    • Westmeyer, Gil G.
    Publication type:
    Article
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    Twenty-two novel mutations in the lysosomal α-glucosidase gene (GAA) underscore the genotype–phenotype correlation in glycogen storage disease type II (Communicated by Elizabeth Neufeld).

    Published in:
    Human Mutation, 2004, v. 23, n. 1, p. 47, doi. 10.1002/humu.10286
    By:
    • Monique M.P. Hermans;
    • Dik van Leenen;
    • Marian A. Kroos;
    • Clare E. Beesley;
    • Ans T. Van der Ploeg;
    • Hitoshi Sakuraba;
    • Ron Wevers;
    • Wim Kleijer;
    • Helen Michelakakis;
    • Edwin P. Kirk;
    • Janice Fletcher;
    • Nils Bosshard;
    • Lina Basel-Vanagaite;
    • Guy Besley;
    • Arnold J.J. Reuser
    Publication type:
    Article
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    Missorting of the Aquaporin-2 mutant E258K to multivesicular bodies/lysosomes in dominant NDI is associated with its monoubiquitination and increased phosphorylation by PKC but is due to the loss of E258.

    Published in:
    Pflügers Archiv: European Journal of Physiology, 2008, v. 455, n. 6, p. 1041, doi. 10.1007/s00424-007-0364-6
    By:
    • Kamsteeg, Erik-Jan;
    • Savelkoul, Paul J. M.;
    • Hendriks, Giel;
    • Konings, Irene B. M.;
    • Nivillac, Nicole M. I.;
    • Lagendijk, Anne Karine;
    • van der Sluijs, Peter;
    • Deen, Peter M. T.
    Publication type:
    Article
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    Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation.

    Published in:
    Acta Neuropathologica, 2023, v. 145, n. 6, p. 749, doi. 10.1007/s00401-023-02568-y
    By:
    • Filipello, Fabia;
    • You, Shih-Feng;
    • Mirfakhar, Farzaneh S.;
    • Mahali, Sidhartha;
    • Bollman, Bryan;
    • Acquarone, Mariana;
    • Korvatska, Olena;
    • Marsh, Jacob A.;
    • Sivaraman, Anirudh;
    • Martinez, Rita;
    • Cantoni, Claudia;
    • De Feo, Luca;
    • Ghezzi, Laura;
    • Minaya, Miguel A.;
    • Renganathan, Arun;
    • Cashikar, Anil G.;
    • Satoh, Jun-Ichi;
    • Beatty, Wandy;
    • Iyer, Abhirami K.;
    • Cella, Marina
    Publication type:
    Article
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    Tau immunotherapy is associated with glial responses in FTLD-tau.

    Published in:
    Acta Neuropathologica, 2021, v. 142, n. 2, p. 243, doi. 10.1007/s00401-021-02318-y
    By:
    • Kim, Boram;
    • Mikytuck, Bailey;
    • Suh, Eunran;
    • Gibbons, Garrett S.;
    • Van Deerlin, Vivianna M.;
    • Vaishnavi, Sanjeev N.;
    • Spindler, Meredith A.;
    • Massimo, Lauren;
    • Grossman, Murray;
    • Trojanowski, John Q.;
    • Irwin, David J.;
    • Lee, Edward B.
    Publication type:
    Article
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    Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease.

    Published in:
    Acta Neuropathologica, 2020, v. 140, n. 3, p. 341, doi. 10.1007/s00401-020-02181-3
    By:
    • Bandres-Ciga, S.;
    • Saez-Atienzar, S.;
    • Kim, J. J.;
    • Makarious, M. B.;
    • Faghri, F.;
    • Diez-Fairen, M.;
    • Iwaki, H.;
    • Leonard, H.;
    • Botia, J.;
    • Ryten, M.;
    • Hernandez, D.;
    • Gibbs, J. R.;
    • Ding, J.;
    • Gan-Or, Z.;
    • Noyce, A.;
    • Pihlstrom, L.;
    • Torkamani, A.;
    • Soltis, A. R.;
    • Dalgard, C. L.;
    • Scholz, S. W.
    Publication type:
    Article
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    The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice.

    Published in:
    Acta Neuropathologica, 2014, v. 128, n. 5, p. 705, doi. 10.1007/s00401-014-1289-8
    By:
    • Alves, Sandro;
    • Cormier-Dequaire, Florence;
    • Marinello, Martina;
    • Marais, Thibaut;
    • Muriel, Marie-Paule;
    • Beaumatin, Florian;
    • Charbonnier-Beaupel, Fanny;
    • Tahiri, Khadija;
    • Seilhean, Danielle;
    • Hachimi, Khalid;
    • Ruberg, Merle;
    • Stevanin, Giovanni;
    • Barkats, Martine;
    • Dunnen, Wilfred;
    • Priault, Muriel;
    • Brice, Alexis;
    • Durr, Alexandra;
    • Corvol, Jean-Christophe;
    • Sittler, Annie
    Publication type:
    Article