Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects
10.1371/journal.pone.0180828
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sg-nus-scholar.10635-1611862024-04-04T01:11:22Z Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects Chang J.-C. Morton D.B. PHYSIOLOGY mutant protein proteasome TAR DNA binding protein DNA binding protein TDP-43 protein, human adult age aged animal experiment animal tissue Article behavior disorder controlled study cytoplasm developmental disorder Drosophila embryo female gene mutation genetic transcription genome heredity hTDP 43 gene immunoprecipitation longevity male nerve cell nonhuman protein function protein localization protein phosphorylation ubiquitination wild type aging animal cytology Drosophila melanogaster genetics growth, development and aging human longevity metabolism mutation phosphorylation physiology protein processing signal transduction taxis response transgene transgenic animal ubiquitination Aging Animals Animals, Genetically Modified DNA-Binding Proteins Drosophila melanogaster Female Humans Longevity Male Mutation Neurons Phosphorylation Protein Processing, Post-Translational Signal Transduction Taxis Response Transgenes Ubiquitination 10.1371/journal.pone.0180828 PLoS ONE 12 7 e0180828 2019-11-01T07:51:32Z 2019-11-01T07:51:32Z 2017 Article Chang J.-C., Morton D.B. (2017). Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects. PLoS ONE 12 (7) : e0180828. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0180828 19326203 https://scholarbank.nus.edu.sg/handle/10635/161186 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20191101 |
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mutant protein proteasome TAR DNA binding protein DNA binding protein TDP-43 protein, human adult age aged animal experiment animal tissue Article behavior disorder controlled study cytoplasm developmental disorder Drosophila embryo female gene mutation genetic transcription genome heredity hTDP 43 gene immunoprecipitation longevity male nerve cell nonhuman protein function protein localization protein phosphorylation ubiquitination wild type aging animal cytology Drosophila melanogaster genetics growth, development and aging human longevity metabolism mutation phosphorylation physiology protein processing signal transduction taxis response transgene transgenic animal ubiquitination Aging Animals Animals, Genetically Modified DNA-Binding Proteins Drosophila melanogaster Female Humans Longevity Male Mutation Neurons Phosphorylation Protein Processing, Post-Translational Signal Transduction Taxis Response Transgenes Ubiquitination |
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mutant protein proteasome TAR DNA binding protein DNA binding protein TDP-43 protein, human adult age aged animal experiment animal tissue Article behavior disorder controlled study cytoplasm developmental disorder Drosophila embryo female gene mutation genetic transcription genome heredity hTDP 43 gene immunoprecipitation longevity male nerve cell nonhuman protein function protein localization protein phosphorylation ubiquitination wild type aging animal cytology Drosophila melanogaster genetics growth, development and aging human longevity metabolism mutation phosphorylation physiology protein processing signal transduction taxis response transgene transgenic animal ubiquitination Aging Animals Animals, Genetically Modified DNA-Binding Proteins Drosophila melanogaster Female Humans Longevity Male Mutation Neurons Phosphorylation Protein Processing, Post-Translational Signal Transduction Taxis Response Transgenes Ubiquitination Chang J.-C. Morton D.B. Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
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10.1371/journal.pone.0180828 |
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PHYSIOLOGY |
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PHYSIOLOGY Chang J.-C. Morton D.B. |
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Chang J.-C. Morton D.B. |
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Chang J.-C. |
title |
Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
title_short |
Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
title_full |
Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
title_fullStr |
Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
title_full_unstemmed |
Drosophila lines with mutant and wild type human TDP-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
title_sort |
drosophila lines with mutant and wild type human tdp-43 replacing the endogenous gene reveals phosphorylation and ubiquitination in mutant lines in the absence of viability or lifespan defects |
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2019 |
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https://scholarbank.nus.edu.sg/handle/10635/161186 |
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1795374096138108928 |