Suchergebnisse - "Autophagy genetics"
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1
Autoren: et al.
Quelle: Glia
Glia, vol. 73, no. 7, pp. 1383-1397Schlagwörter: Animals, Autophagy/physiology, Autophagy/genetics, Oligodendroglia/pathology, Oligodendroglia/ultrastructure, Oligodendroglia/metabolism, Apoptosis/physiology, Apoptosis/genetics, Aging/pathology, Myelin Sheath/pathology, Myelin Sheath/metabolism, Myelin Sheath/ultrastructure, Mice, Transgenic, Neurons/pathology, Neurons/ultrastructure, Mice, Knockout, Mice, Cognitive Dysfunction/pathology, Autophagy-Related Protein 5/genetics, Autophagy-Related Protein 5/metabolism, Mice, Inbred C57BL, Axons/pathology, CNS, aging, autophagy, myelin, neurodegeneration, Research Article
Dateibeschreibung: application/pdf
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2
Autoren: et al.
Quelle: Nucleic Acids Res
Schlagwörter: Autophagy / genetics, Saccharomyces cerevisiae Proteins, RNA, Messenger / metabolism, Ribosomes / metabolism, Saccharomyces cerevisiae, Ribosomes / genetics, Mitochondrial Proteins, Saccharomyces cerevisiae Proteins / genetics, Autophagy, Saccharomyces cerevisiae / metabolism, RNA, Messenger, Mitochondrial Proteins / genetics, Molecular Biology, Saccharomyces cerevisiae Proteins / metabolism, Membrane Proteins / genetics, RNA, Messenger / genetics, Mitochondria / metabolism, Ubiquitination, Membrane Proteins, Mitochondria, Mitochondria / genetics, Mitochondrial Proteins / metabolism, Saccharomyces cerevisiae / genetics, Ribosomes
Dateibeschreibung: application/pdf
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3
Autoren: et al.
Quelle: Frontiers in Bioscience-Landmark, Vol 30, Iss 9, p 38730 (2025)
Schlagwörter: aging/genetics, autophagy/genetics, transcription factor eb (tfeb)/microphthalmia-associated transcription factors (mitfs), forkhead box o (foxo) transcription factors/forkhead transcription factors, drug effects/therapeutic use, Biochemistry, QD415-436, Biology (General), QH301-705.5
Dateibeschreibung: electronic resource
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4
Autoren:
Quelle: Kraft, C & Reggiori, F 2024, 'Phagophore closure, autophagosome maturation and autophagosome fusion during macroautophagy in the yeast Saccharomyces cerevisiae', FEBS Letters, vol. 598, no. 1, pp. 73-83. https://doi.org/10.1002/1873-3468.14720
FEBS LettersSchlagwörter: autophagy, phagophore, Saccharomyces cerevisiae Proteins, Vacuoles/metabolism, Autophagosomes, Autophagy-Related Proteins, Atg proteins, Saccharomyces cerevisiae, dephosphorylation, Autophagy/genetics, Saccharomyces cerevisiae/genetics, Autophagy-Related Proteins/genetics, Macroautophagy, Vacuoles, Autophagy, Saccharomyces cerevisiae Proteins/genetics, Autophagosomes/metabolism, PAS
Dateibeschreibung: pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/37585559
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5
Autoren: et al.
Quelle: Nature
Foronda, H, Fu, Y, Covarrubias-Pinto, A, Bocker, H T, González, A, Seemann, E, Franzka, P, Bock, A, Bhaskara, R M, Liebmann, L, Hoffmann, M E, Katona, I, Koch, N, Weis, J, Kurth, I, Gleeson, J G, Reggiori, F, Hummer, G, Kessels, M M, Qualmann, B, Mari, M, Dikić, I & Hübner, C A 2023, 'Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy', Nature, vol. 618, no. 7964, pp. 402-410. https://doi.org/10.1038/s41586-023-06090-9
Nature : international weekly journal of science 618(7964), 402-410 (2023). doi:10.1038/s41586-023-06090-9Schlagwörter: Intracellular Membranes/metabolism, Sensory Receptor Cells/metabolism, Membrane Proteins/deficiency, Sensory Receptor Cells, Intracellular Signaling Peptides and Proteins, Ubiquitination, Membrane Proteins, Intracellular Membranes, Intracellular Signaling Peptides and Proteins/deficiency, Ubiquitinated Proteins/metabolism, Endoplasmic Reticulum, Endoplasmic Reticulum Stress, Ubiquitinated Proteins, Article, Autophagy/genetics, Mice, Autophagy, Animals, Humans, Endoplasmic Reticulum/metabolism
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/37225994
https://hdl.handle.net/11370/4e056284-6ae3-43c4-b90c-1b0de71e5902
https://research.rug.nl/en/publications/4e056284-6ae3-43c4-b90c-1b0de71e5902
https://doi.org/10.1038/s41586-023-06090-9
http://hdl.handle.net/21.11116/0000-000D-3376-5
http://hdl.handle.net/21.11116/0000-000E-7297-7
https://pure.au.dk/portal/en/publications/bd290813-3ee1-4acb-b3a8-f617e96473c3
https://publications.rwth-aachen.de/record/981862
https://pure.au.dk/portal/en/publications/bd290813-3ee1-4acb-b3a8-f617e96473c3
https://doi.org/10.1038/s41586-023-06090-9
https://pure.au.dk/ws/files/401311750/s41586-023-06090-9.pdf -
6
Autoren: et al.
Quelle: Autophagy
Chumpen Ramirez, S, Gómez-Sánchez, R, Verlhac, P, Hardenberg, R, Margheritis, E, Cosentino, K, Reggiori, F & Ungermann, C 2023, 'Atg9 interactions via its transmembrane domains are required for phagophore expansion during autophagy', Autophagy, vol. 19, no. 5, pp. 1459-1478. https://doi.org/10.1080/15548627.2022.2136340Schlagwörter: 0301 basic medicine, membrane contact site, Saccharomyces cerevisiae Proteins, Autophagosome, Autophagy-Related Proteins, Saccharomyces cerevisiae, Endoplasmic Reticulum, 03 medical and health sciences, Saccharomyces cerevisiae/metabolism, Autophagy, Humans, Autophagosomes/metabolism, lipid transfer, Endoplasmic Reticulum/metabolism, phagophore, Cryoelectron Microscopy, Autophagy-Related Proteins/metabolism, Autophagosomes, Membrane Proteins, Saccharomyces cerevisiae Proteins/metabolism, Lipids, scramblase, Autophagy/genetics, Membrane Proteins/metabolism, Research Paper
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/36354155
https://pure.au.dk/portal/en/publications/0a82622f-9058-4d37-931c-4c08c4289f37
http://www.scopus.com/inward/record.url?scp=85141984373&partnerID=8YFLogxK
https://doi.org/10.1080/15548627.2022.2136340
https://pure.au.dk/portal/en/publications/0a82622f-9058-4d37-931c-4c08c4289f37
https://pure.au.dk/ws/files/401873087/Atg9_interactions_via_its_transmembrane_domains_are_required_for_phagophore_expansion_during_autophagy.pdf -
7
Autoren: et al.
Quelle: Journal of Hepatology
Schlagwörter: Inflammation, Liver Cirrhosis, 0301 basic medicine, autophagy, 0303 health sciences, Carcinoma, Hepatocellular, NAFLD, NASH, autophagy, genetics, liver fibrosis, Biopsy, Liver Neoplasms, NASH, NAFLD, genetics, liver fibrosis, Autophagy-Related Protein 7, 3. Good health, Humans, Liver, Non-alcoholic Fatty Liver Disease, 03 medical and health sciences
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/35405176
https://hdl.handle.net/2434/926557
https://www.sciencedirect.com/science/article/pii/S0168827822002070?via=ihub#!
https://doi.org/10.1016/j.jhep.2022.03.031
https://hdl.handle.net/10447/582777
https://hdl.handle.net/10447/582777
https://doi.org/10.1016/j.jhep.2022.03.031
https://hdl.handle.net/11390/1229069
https://doi.org/10.1016/j.jhep.2022.03.031
https://hdl.handle.net/11591/473508
https://doi.org/10.1016/j.jhep.2022.03.031 -
8
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Cancer Commun (Lond)
Cancer Communications, Vol 42, Iss 8, Pp 716-749 (2022)Schlagwörter: 0301 basic medicine, Autophagy / genetics, autophagy, Lung Neoplasms, pancreatic cancer, Acetyl Coenzyme A / pharmacology, ACLY, Lung Neoplasms* / genetics, AMP-Activated Protein Kinases, epithelial‐to‐mesenchymal transition, Proto-Oncogene Proteins p21(ras), Mice, 03 medical and health sciences, Transcription Factors / genetics, Acetyl Coenzyme A, acetyl-coenzyme A, snail, Autophagy, metastasis, Animals, acetyl-snail, KRAS inhibitor, non‐small‐cell lung cancer, RC254-282, Neoplastic Processes, Mammals, 0303 health sciences, AMP-Activated Protein Kinases / metabolism, Proto-Oncogene Proteins p21(ras)* / genetics, CAMKK2, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Acetylation, Original Articles, 3. Good health, non-small-cell lung cancer, epithelial-to-mesenchymal transition, Snail Family Transcription Factors, acetyl‐coenzyme A, Snail Family Transcription Factors / metabolism, Transcription Factors
Dateibeschreibung: application/pdf
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9
Autoren: et al.
Quelle: Mol Psychiatry
Schlagwörter: 0301 basic medicine, 0303 health sciences, Amyloid beta-Peptides, Mitophagy, Review Article, Biochemistry, biophysics & molecular biology [F05] [Life sciences], Autophagy/genetics, Mitochondria, 3. Good health, Disease Models, Animal, 03 medical and health sciences, Alzheimer Disease, Mitochondria/metabolism, Autophagy, Animals, Humans, Alzheimer Disease/metabolism, Mitophagy/physiology, Amyloid beta-Peptides/metabolism, Biochimie, biophysique & biologie moléculaire [F05] [Sciences du vivant]
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10
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Autophagy
Schlagwörter: 0301 basic medicine, Autophagy / genetics, Receptors, Steroid, Mutation / genetics, Knockout, Mice, Transgenic, Deafness, Transgenic, Mice, 03 medical and health sciences, Receptors, Deafness* / genetics, Autophagy, Animals, Humans, Steroid* / genetics, hearing loss, DFNA67, Mice, Knockout, Sirolimus, rapamycin, Sirolimus / pharmacology, 3. Good health, HEK293 Cells, Mutation, OSBPL2, Mutant Proteins, Research Paper
Dateibeschreibung: application/pdf
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11
Autoren: et al.
Quelle: Machiraju, P, Srinivas, R, Kannan, R, George, R, Heymans, S, Mukhopadhyay, R & Ghosh, A 2024, 'Paired Transcriptomic Analyses of Atheromatous and Control Vessels Reveal Novel Autophagy and Immunoregulatory Genes in Peripheral Artery Disease', Cells, vol. 13, no. 15, 1269. https://doi.org/10.3390/cells13151269
Schlagwörter: atherosclerosis, autophagy, metanalysis, paired transcriptomics, peripheral artery disease, telomeric regulation, Humans, Autophagy/genetics, Peripheral Arterial Disease/genetics pathology, Gene Expression Profiling, Transcriptome/genetics, Plaque, Atherosclerotic/genetics pathology, Male, Female, Gene Regulatory Networks, Middle Aged, Aged, Gene Expression Regulation
Relation: info:eu-repo/semantics/altIdentifier/wos/001287019100001; info:eu-repo/semantics/altIdentifier/pissn/2073-4409
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12
Autoren: et al.
Quelle: Nat Commun
Nature Communications, Vol 14, Iss 1, Pp 1-19 (2023)
Nature communications, vol. 14, no. 1, pp. 3077Schlagwörter: Phagocytosis, Science, QH426 Genetics / genetika, Autophagy, Animals, Drosophila, örökléstan, Microtubule-Associated Proteins, Neuroglia, Drosophila/metabolism, Microtubule-Associated Proteins/metabolism, Phagocytosis/genetics, Autophagy/genetics, Axons/metabolism, Neuroglia/metabolism, Article, Axons
Dateibeschreibung: application/pdf; text
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/37248218
https://doaj.org/article/5d460e7087d74b4d9aa634afe10666ea
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_C5BF226268657
https://serval.unil.ch/notice/serval:BIB_C5BF22626865
https://serval.unil.ch/resource/serval:BIB_C5BF22626865.P001/REF.pdf -
13
Autoren: et al.
Quelle: Oxid Med Cell Longev
Oxidative medicine and cellular longevity, vol. 2020, pp. 8506572
Losmanová, Tereza; Janser, Félice A.; Humbert, Magali; Tokarchuk, Igor; Schläfli, Anna M.; Neppl, Christina; Schmid, Ralph; Tschan, Mario P.; Langer, Rupert; Berezowska, Sabina (2020). Chaperone-Mediated Autophagy Markers LAMP2A and HSC70 Are Independent Adverse Prognostic Markers in Primary Resected Squamous Cell Carcinomas of the Lung. Oxidative medicine and cellular longevity, 2020, p. 8506572. Hindawi 10.1155/2020/8506572 <http://dx.doi.org/10.1155/2020/8506572>Schlagwörter: Adult, Male, 0301 basic medicine, Lung Neoplasms, 610 Medicine & health, Chaperone-Mediated Autophagy, Kaplan-Meier Estimate, Disease-Free Survival, 03 medical and health sciences, Aged, Aged, 80 and over, Biomarkers/metabolism, Carcinoma, Squamous Cell/diagnosis, Carcinoma, Squamous Cell/mortality, Carcinoma, Squamous Cell/pathology, Chaperone-Mediated Autophagy/genetics, Female, HSC70 Heat-Shock Proteins/genetics, HSC70 Heat-Shock Proteins/metabolism, Humans, Lung Neoplasms/diagnosis, Lung Neoplasms/mortality, Lung Neoplasms/pathology, Lysosomal-Associated Membrane Protein 2/genetics, Lysosomal-Associated Membrane Protein 2/metabolism, Middle Aged, Prognosis, Proportional Hazards Models, Retrospective Studies, Lysosomal-Associated Membrane Protein 2, 0303 health sciences, HSC70 Heat-Shock Proteins, 3. Good health, Carcinoma, Squamous Cell, 570 Life sciences, biology, Biomarkers, Research Article
Dateibeschreibung: text/xhtml; application/pdf
Zugangs-URL: https://downloads.hindawi.com/journals/omcl/2020/8506572.pdf
https://pubmed.ncbi.nlm.nih.gov/33029283
https://serval.unil.ch/en/notice/serval:BIB_E70EE8341A34
https://serval.unil.ch/resource/serval:BIB_E70EE8341A34.P002/REF.pdf
https://europepmc.org/article/PMC/PMC7527932
https://boris.unibe.ch/146883/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527932
https://www.ncbi.nlm.nih.gov/pubmed/33029283
https://serval.unil.ch/notice/serval:BIB_E70EE8341A34
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_E70EE8341A348
https://serval.unil.ch/resource/serval:BIB_E70EE8341A34.P002/REF.pdf
https://boris.unibe.ch/146883/ -
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Autoren: et al.
Quelle: Banerjee, P, Mehta, A R, Nirujogi, R, Cooper, J, James, O G, Nanda, J, Longden, J, Burr, K, Salzinger, A, Paza, E, Newton, J, Story, D, Pal, S, Smith, C, Alessi, D, Selvaraj, B T, Priller, J & Chandran, S 2023, 'Cell-autonomous immune dysfunction driven by disrupted autophagy in C9orf72-ALS iPSC-derived microglia contributes to neurodegeneration', Science Advances, vol. 9, no. 16, eabq0651. https://doi.org/10.1126/sciadv.abq0651
Schlagwörter: Humans, Amyotrophic Lateral Sclerosis/genetics, Frontotemporal Dementia/genetics, Induced Pluripotent Stem Cells/metabolism, C9orf72 Protein/genetics, Microglia/metabolism, Autophagy/genetics
Dateibeschreibung: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/37083530; info:eu-repo/semantics/altIdentifier/pissn/2375-2548
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15
Autoren: et al.
Quelle: Neuron, vol. 111, no. 15, pp. 2329-2347.e7
Schlagwörter: Animals, Mice, Autophagy/genetics, Mitophagy, Macroautophagy, Aging, Brain, ER-phagy, aggrephagy, autophagic vesicles, degradome, proteomic profiling, synapse
Dateibeschreibung: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/37279748; info:eu-repo/semantics/altIdentifier/eissn/1097-4199; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_4C5AC55F5FC85; https://serval.unil.ch/notice/serval:BIB_4C5AC55F5FC8; https://serval.unil.ch/resource/serval:BIB_4C5AC55F5FC8.P001/REF.pdf
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Autoren: et al.
Quelle: Nature Communications 14(1), 870 (2023). doi:10.1038/s41467-023-36553-6
Schlagwörter: info:eu-repo/classification/ddc/500, Carrier Proteins: metabolism, Secretory Pathway, Proteomics, Protein Transport, Autophagosomes, Autophagy: genetics, Golgi Apparatus, Nerve Tissue Proteins: metabolism
Geographisches Schlagwort: DE
Relation: info:eu-repo/semantics/altIdentifier/issn/2041-1723; info:eu-repo/semantics/altIdentifier/pmid/pmid:36797266; https://pub.dzne.de/record/255139
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17
Autoren: et al.
Schlagwörter: Arabidopsis/metabolism, Arabidopsis Proteins/genetics, Arabidopsis Proteins/metabolism, Autophagy/genetics, Carbon/metabolism, Cell Membrane/metabolism, Gene Expression Regulation, Plant, Hypocotyl/genetics, Light, Lipids, Phytochrome/metabolism, Sterols/metabolism
Dateibeschreibung: application/pdf
Relation: Nature Communications; https://iris.unil.ch/handle/iris/245959; serval:BIB_FC24C76DB11B; 000867457000036
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18
Autoren: et al.
Schlagwörter: Autophagy/genetics, Caspases/chemistry, Caspases/genetics, Cell Death/genetics, Gene Expression Regulation, Enzymologic, Leishmania major/enzymology, Leishmania major/genetics, Models, Biological, Protein Structure, Tertiary, Protozoan Proteins/chemistry, Protozoan Proteins/genetics, Stress, Physiological
Dateibeschreibung: application/pdf
Relation: Cell Death & Disease; https://iris.unil.ch/handle/iris/140030; serval:BIB_97502941E4E6
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19
Autoren:
Schlagwörter: Animals, Apoptosis/genetics, Autophagy/genetics, Caenorhabditis elegans/genetics, Endocytosis/genetics, Gene Expression Regulation, Heat-Shock Response/genetics, Humans, Necrosis/genetics, Neurons/metabolism, Neurons/physiology, Apoptosis, Autophagy, Calpain, Cathepsin, Cell death, Endocytosis, Excitotoxicity, Heat shock, Heat stroke, Necrosis, Neurodegeneration, Stress
Relation: Methods in enzymology; https://iris.unil.ch/handle/iris/111936; serval:BIB_59AED9035B70; 000340439100006
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20
Autoren: et al.
Schlagwörter: Anemia/genetics, Autophagy/genetics, Erythroblasts/metabolism, Erythroblasts/ultrastructure, Erythropoiesis/genetics, Membrane Proteins/metabolism, MicroRNAs/genetics, MicroRNAs/metabolism, Mitochondria/genetics, Mitochondria/physiology, Mitochondrial Proteins/metabolism, Nuclear Proteins/genetics, Nuclear Proteins/metabolism, Repressor Proteins/genetics, Repressor Proteins/metabolism, Transcription Factors/metabolism
Dateibeschreibung: application/pdf
Relation: Science; https://iris.unil.ch/handle/iris/43140; serval:BIB_46F2FB0DD990; 000317657500055
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