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4. Mislocalization of Nup62 Contributes to TDP-43 Proteinopathy in ALS/FTLD. Nag N; Tripathi T ACS Chem Neurosci; 2022 Sep; 13(17):2544-2546. PubMed ID: 36001801 [TBL] [Abstract][Full Text] [Related]
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6. A novel Drosophila model of TDP-43 proteinopathies: N-terminal sequences combined with the Q/N domain induce protein functional loss and locomotion defects. Langellotti S; Romano V; Romano G; Klima R; Feiguin F; Cragnaz L; Romano M; Baralle FE Dis Model Mech; 2016 Jun; 9(6):659-69. PubMed ID: 27101846 [TBL] [Abstract][Full Text] [Related]
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9. Channel nuclear pore complex subunits are required for transposon silencing in Munafò M; Lawless VR; Passera A; MacMillan S; Bornelöv S; Haussmann IU; Soller M; Hannon GJ; Czech B Elife; 2021 Apr; 10():. PubMed ID: 33856346 [TBL] [Abstract][Full Text] [Related]
10. PABPN1 suppresses TDP-43 toxicity in ALS disease models. Chou CC; Alexeeva OM; Yamada S; Pribadi A; Zhang Y; Mo B; Williams KR; Zarnescu DC; Rossoll W Hum Mol Genet; 2015 Sep; 24(18):5154-73. PubMed ID: 26130692 [TBL] [Abstract][Full Text] [Related]
11. Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies. Miguel L; Frébourg T; Campion D; Lecourtois M Neurobiol Dis; 2011 Feb; 41(2):398-406. PubMed ID: 20951205 [TBL] [Abstract][Full Text] [Related]
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13. RNA binding mediates neurotoxicity in the transgenic Drosophila model of TDP-43 proteinopathy. Ihara R; Matsukawa K; Nagata Y; Kunugi H; Tsuji S; Chihara T; Kuranaga E; Miura M; Wakabayashi T; Hashimoto T; Iwatsubo T Hum Mol Genet; 2013 Nov; 22(22):4474-84. PubMed ID: 23804749 [TBL] [Abstract][Full Text] [Related]
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18. TDP-43 induces mitochondrial damage and activates the mitochondrial unfolded protein response. Wang P; Deng J; Dong J; Liu J; Bigio EH; Mesulam M; Wang T; Sun L; Wang L; Lee AY; McGee WA; Chen X; Fushimi K; Zhu L; Wu JY PLoS Genet; 2019 May; 15(5):e1007947. PubMed ID: 31100073 [TBL] [Abstract][Full Text] [Related]
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