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المؤلفون: Manoj Kumar, Manasa P Srikanth, Michela Deleidi, Penelope J Hallett, Ole Isacson, Ricardo A Feldman
المصدر: Human molecular genetics 32(11), 1888-1900 (2023). doi:10.1093/hmg/ddad025
مصطلحات موضوعية: Acid Ceramidase, metabolism [Parkinson Disease], Mechanistic Target of Rapamycin Complex 1, genetics [Glucosylceramidase], metabolism [Lysosomes], ddc:570, Genetics, Humans, metabolism [alpha-Synuclein], metabolism [Glucosylceramidase], Molecular Biology, Genetics (clinical), TOR Serine-Threonine Kinases, metabolism [Dopaminergic Neurons], genetics [Mechanistic Target of Rapamycin Complex 1], MTOR Inhibitors, General Medicine, genetics [TOR Serine-Threonine Kinases], genetics [Acid Ceramidase], metabolism [Induced Pluripotent Stem Cells], metabolism [Gaucher Disease], Mutation, genetics [alpha-Synuclein], alpha-Synuclein, Glucosylceramidase, metabolism [Acid Ceramidase]
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e623d80d2d569f3311782fe53a2d787
https://doi.org/10.1093/hmg/ddad025 -
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المؤلفون: Pascale Baden, Maria Jose Perez, Hariam Raji, Federico Bertoli, Stefanie Kalb, María Illescas, Fokion Spanos, Claudio Giuliano, Alessandra Maria Calogero, Marvin Oldrati, Hannah Hebestreit, Graziella Cappelletti, Kathrin Brockmann, Thomas Gasser, Anthony H. V. Schapira, Cristina Ugalde, Michela Deleidi
المصدر: Nature Communications 14(1), 1930 (2023). doi:10.1038/s41467-023-37454-4
مصطلحات موضوعية: Proteomics, Multidisciplinary, metabolism [Parkinson Disease], General Physics and Astronomy, metabolism [ATP-Dependent Proteases], General Chemistry, genetics [Energy Metabolism], metabolism [Mitochondria], General Biochemistry, Genetics and Molecular Biology, genetics [Glucosylceramidase], metabolism [Mitochondrial Proteins], metabolism [Lysosomes], Mitochondrial Proteins, ATP-Dependent Proteases, Mutation, alpha-Synuclein, Humans, Glucosylceramidase, ddc:500, metabolism [Glucosylceramidase], genetics [Mitochondria], metabolism [alpha-Synuclein], LONP1 protein, human
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27055f5aa48d03d5dd4db093bb00cd70
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المؤلفون: Daniel Erskine, David J. Koss, Johannes Attems, Viktor I. Korolchuk, Ian G. McKeith, Tiago F. Outeiro
المصدر: Acta Neuropathologica
Acta neuropathologica 141(4), 511-526 (2021). doi:10.1007/s00401-021-02266-7مصطلحات موضوعية: Mitochondrial Diseases, Context (language use), Disease, Review, Biology, Mitochondrion, pathology [Mitochondria], Pathology and Forensic Medicine, metabolism [Lysosomes], Alpha-synuclein, Cellular and Molecular Neuroscience, chemistry.chemical_compound, medicine, Autophagy, Dementia, Humans, ddc:610, metabolism [alpha-Synuclein], pathology [Lysosomal Storage Diseases], Synucleinopathies, pathology [Lewy Bodies], Lewy body, Catabolism, pathology [Hemochromatosis], metabolism [Lewy Bodies], metabolism [Mitochondria], medicine.disease, Lipid Metabolism, Cell biology, Mitochondria, Lysosomal Storage Diseases, metabolism [Lysosomal Storage Diseases], pathology [Mitochondrial Diseases], Lipid metabolism, chemistry, metabolism [Mitochondrial Diseases], Lewy Bodies, Neurology (clinical), Hemochromatosis, physiology [Lipid Metabolism], Lysosomes, metabolism [Hemochromatosis], pathology [Lysosomes]
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المؤلفون: Maik Liedtke, Christin Völkner, Andreas Hermann, Moritz J. Frech
المصدر: Cells, Vol 11, Iss 507, p 507 (2022)
Cells 11(3), 507 (2022). doi:10.3390/cells11030507
Cells; Volume 11; Issue 3; Pages: 507مصطلحات موضوعية: metabolism [Endosomes], induced pluripotent stem cells, QH301-705.5, Mitophagy, iPSCs, Niemann-Pick Disease, Type C, General Medicine, Endosomes, NPC2, NPC1, mitochondria, lysosomal storage disorder, metabolism [Lysosomes], metabolism [Niemann-Pick Disease, Type C], ddc:570, Autophagy, Humans, Biology (General), Lysosomes
وصف الملف: application/pdf
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المؤلفون: Carmen Klepka, Moritz Sandmann, Helma Tatge, Matthew Mangan, Annabel Arens, Daniel Henkel, Ralf Gerhard
المصدر: Molecular microbiology 117(2), 493-507 (2022). doi:10.1111/mmi.14864
مصطلحات موضوعية: metabolism [Bacterial Proteins], Clostridioides difficile, Bacterial Toxins, lysosome inhibition, autophagic flux, Microbiology, metabolism [Lysosomes], Clostridioides, Bacterial Proteins, ddc:570, Clostridioides difficile Toxin B, DQ-BSA assay, Lysosomes, Molecular Biology, metabolism [Bacterial Toxins]
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8af5bef71e9418fd4c0a2a3c1227bf30
https://pub.dzne.de/record/163585 -
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المؤلفون: Anika Reifschneider, Sophie Robinson, Bettina van Lengerich, Johannes Gnörich, Todd Logan, Steffanie Heindl, Miriam A Vogt, Endy Weidinger, Lina Riedl, Karin Wind, Artem Zatcepin, Ida Pesämaa, Sophie Haberl, Brigitte Nuscher, Gernot Kleinberger, Julien Klimmt, Julia K Götzl, Arthur Liesz, Katharina Bürger, Matthias Brendel, Johannes Levin, Janine Diehl‐Schmid, Jung Suh, Gilbert Di Paolo, Joseph W Lewcock, Kathryn M Monroe, Dominik Paquet, Anja Capell, Christian Haass
المصدر: The EMBO journal 41(4), e109108 (2022). doi:10.15252/embj.2021109108
مصطلحات موضوعية: Male, pharmacology [Antibodies], microglia, physiopathology [Brain], SYK protein, human, drug effects [Microglia], Monocytes, metabolism [Lysosomes], immunology [Antibodies], Progranulins, genetics [Membrane Glycoproteins], genetics [Receptors, Immunologic], Receptors, Immunologic, Mice, Knockout, Membrane Glycoproteins, General Neuroscience, neurodegeneration, Brain, metabolism [Receptors, Immunologic], metabolism [Syk Kinase], drug effects [Monocytes], Grn protein, mouse, frontotemporal lobar degeneration, Female, Microglia, immunology [Membrane Glycoproteins], deficiency [Progranulins], General Biochemistry, Genetics and Molecular Biology, Antibodies, lysosomes, Trem2 protein, mouse, ddc:570, progranulin, Animals, Humans, Syk Kinase, Molecular Biology, diagnostic imaging [Brain], immunology [Receptors, Immunologic], General Immunology and Microbiology, TREM2 protein, human, pathology [Frontotemporal Lobar Degeneration], metabolism [Frontotemporal Lobar Degeneration], physiology [Microglia], Mice, Inbred C57BL, Disease Models, Animal, Frontotemporal Lobar Degeneration, Lysosomes, metabolism [Membrane Glycoproteins], pathology [Lysosomes], metabolism [Monocytes]
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::561d67316e9f278a34f08b959e8dd608
https://pub.dzne.de/record/163471 -
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المؤلفون: Elisabeth Dinter, Diana Cozma, Björn H. Falkenburger, Theodora Saridaki, Eva M. Szegö, Anna Maria Hilverling
المصدر: Cellular and Molecular Neurobiology
Cellular and molecular neurobiology 42(1), 155-171 (2022). doi:10.1007/s10571-021-01116-0
Cellular and molecular neurobiology 42, 155-171 (2022). doi:10.1007/s10571-021-01116-0مصطلحات موضوعية: 0301 basic medicine, physiology [Autophagy], Autophagosome maturation, Autolysosome, Amphisomes, Autolysosomes, metabolism [Neurodegenerative Diseases], metabolism [Lysosomes], 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Lysosome, medicine, Autophagy, Humans, ddc:610, Original Research, α-Synuclein, LAMP1, Chemistry, Vesicle, Time-lapse microscopy, Autophagosomes, Microtubule organizing center, Neurodegenerative Diseases, Cell Biology, General Medicine, Cell biology, Vesicular transport protein, 030104 developmental biology, medicine.anatomical_structure, MTOC, HEK293 Cells, Lysosomes, 030217 neurology & neurosurgery, Intracellular
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85b5010f448c6f241c94a7823fe27b1c
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المصدر: The EMBO journal, 41(7):e110057
The EMBO journal 41(7), e110057 (2022). doi:10.15252/embj.2021110057مصطلحات موضوعية: autophagy, General Immunology and Microbiology, physiology [Autophagy], General Neuroscience, Autophagosomes, lysosomes, secretory trafficking, Golgi satellites, metabolism [Synapses], Endoplasmic Reticulum, metabolism [Autophagosomes], General Biochemistry, Genetics and Molecular Biology, metabolism [Lysosomes], metabolism [Endoplasmic Reticulum], ddc:570, Synapses, Autophagy, Proteostasis, Lysosomes, Molecular Biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa05bd6d8bb51a27119bc0d73478ae71
https://www.embopress.org/doi/full/10.15252/embj.2021110057#support-information-section -
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المؤلفون: Renato Domingues, Ricardo Sant’Anna, Anna Carolina Carvalho da Fonseca, Bruno K. Robbs, Debora Foguel, Tiago F. Outeiro
المصدر: Neurobiology of disease 168, 105696 (2022). doi:10.1016/j.nbd.2022.105696
Neurobiology of Diseaseمصطلحات موضوعية: metabolism [Lysosomes], Neurons, Neurology, Synucleinopathies, metabolism [Neurons], ddc:570, Disease Progression, alpha-Synuclein, Humans, metabolism [alpha-Synuclein], Lysosomes
وصف الملف: application/pdf
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المؤلفون: Bernd Knöll, Renate Lüllmann-Rauch, Paul Saftig, Christian Haass, Yasuo Uchiyama, Wolfgang Wurst, Renate Wanner, Anja Capell, Rudi D'Hooge, Georg Werner, Stijn Stroobants, Patrick Lüningschrör, Benedikt Wefers, Daniela Sinske, Soichiro Kakuta, Michael Sendtner, Benjamin Dombert, Markus Damme
المصدر: Cell Reports, Vol 30, Iss 10, Pp 3506-3519.e6 (2020)
Cell reports 30(10), 3506-3519.e6 (2020). doi:10.1016/j.celrep.2020.02.060مصطلحات موضوعية: 0301 basic medicine, MODIFIER, Vacuole, pathology [Facial Nerve], VARIANTS, Axonal Transport, metabolism [Lysosomes], 0302 clinical medicine, innervation [Muscles], Risk Factors, Axon, lcsh:QH301-705.5, genetics [Nerve Tissue Proteins], Mice, Knockout, Motor Neurons, DEMENTIA, Muscles, ultrastructure [Autophagosomes], ultrastructure [Axon Initial Segment], Frontotemporal lobar degeneration, metabolism [Autophagosomes], Cell biology, genetics [Membrane Proteins], Facial Nerve, medicine.anatomical_structure, genetics [Frontotemporal Lobar Degeneration], Life Sciences & Biomedicine, PROTEINS, Nerve Tissue Proteins, ultrastructure [Motor Neurons], Biology, General Biochemistry, Genetics and Molecular Biology, MECHANISMS, Lipofuscin, 03 medical and health sciences, pathology [Brain Stem], MOTILITY, Lysosome, Organelle, medicine, Animals, Genetic Predisposition to Disease, ddc:610, metabolism [Cell Nucleus], PROGRANULIN, deficiency [Membrane Proteins], Axon Initial Segment, Cell Nucleus, FRONTOTEMPORAL LOBAR DEGENERATION, Science & Technology, deficiency [Nerve Tissue Proteins], MUTATIONS, Autophagosomes, metabolism [Axon Initial Segment], Membrane Proteins, ultrastructure [Lysosomes], metabolism [Motor Neurons], Cell Biology, medicine.disease, Axon initial segment, Mice, Inbred C57BL, 030104 developmental biology, nervous system, lcsh:Biology (General), Axoplasmic transport, Frontotemporal Lobar Degeneration, Lysosomes, 030217 neurology & neurosurgery, Brain Stem
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