يعرض 1 - 10 نتائج من 11 نتيجة بحث عن '"metabolism [Autophagosomes]"', وقت الاستعلام: 1.22s تنقيح النتائج
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    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.2020.02.060

    مصطلحات 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

    وصف الملف: Print

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    المصدر: Cell Death & Disease
    Cell death & disease 12(10), 854 (2021). doi:10.1038/s41419-021-04138-0
    Cell Death and Disease, Vol 12, Iss 10, Pp 1-16 (2021)

    وصف الملف: application/pdf

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    المصدر: Nat Commun
    Nature Communications 12(1), 3818 (2021). doi:10.1038/s41467-021-24007-w
    Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
    Nature Communications

    وصف الملف: application/pdf

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    المصدر: Autophagy
    Autophagy 17(8), 1947-1961 (2021). doi:10.1080/15548627.2020.1804677

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    المصدر: Cell Reports, Vol 17, Iss 4, Pp 1071-1086 (2016)
    Cell reports 17(4), 1071-1086 (2016). doi:10.1016/j.celrep.2016.09.058
    Cell Reports

    مصطلحات موضوعية: Male, Aging, genetics [SKP Cullin F-Box Protein Ligases], Transcription, Genetic, Muscle Proteins, Apoptosis, metabolism [Hippocampus], genetics [Muscle Proteins], Hippocampus, pathology [Ataxia], metabolism [Forkhead Box Protein O3], genetics [Homeostasis], Mice, pathology [Aging], genetics [Parkinson Disease], metabolism [Ubiquitin], complications [Movement Disorders], Fbxo32 protein, mouse, Homeostasis, lcsh:QH301-705.5, Mice, Knockout, protein homeostasis, Movement Disorders, Forkhead Box Protein O3, neurodegeneration, Brain, pathology [Nerve Degeneration], Parkinson Disease, genetics [Ataxia], metabolism [Autophagosomes], Up-Regulation, metabolism [Acyltransferases], Protein Binding, Proteasome Endopeptidase Complex, autophagy, metabolism [Muscle Proteins], FBXO32 protein, human, genetics [Mutation], Article, FBXO32, endophilin, Autophagy, deficiency [Acyltransferases], Animals, Humans, endocytosis, FoxO3 protein, mouse, ddc:610, metabolism [Proteasome Endopeptidase Complex], SKP Cullin F-Box Protein Ligases, Endophilin-A, Ubiquitin-Proteasome System, Ubiquitin, ataxia, Autophagosomes, metabolism [SKP Cullin F-Box Protein Ligases], pathology [Movement Disorders], pathology [Parkinson Disease], complications [Nerve Degeneration], pathology [Hippocampus], lcsh:Biology (General), metabolism [Brain], Mutation, Nerve Degeneration, Parkinson’s disease, genetics [Forkhead Box Protein O3], 2-acylglycerophosphate acyltransferase, next-generation sequencing, ubiquitin-proteasome system, Acyltransferases, HeLa Cells

    وصف الملف: Print-Electronic; application/pdf