146 related articles for article (PubMed ID: 33439438)
1. Myeloid TBK1 Deficiency Induces Motor Deficits and Axon Degeneration Through Inflammatory Cell Infiltration.
Duan W; Yi L; Tian Y; Huang HP; Li Z; Bi Y; Guo M; Li Y; Liu Y; Ma Y; Song X; Liu Y; Li C
Mol Neurobiol; 2021 May; 58(5):2435-2446. PubMed ID: 33439438
[TBL] [Abstract][Full Text] [Related]
2. Deletion of Tbk1 disrupts autophagy and reproduces behavioral and locomotor symptoms of FTD-ALS in mice.
Duan W; Guo M; Yi L; Zhang J; Bi Y; Liu Y; Li Y; Li Z; Ma Y; Zhang G; Liu Y; Song X; Li C
Aging (Albany NY); 2019 Apr; 11(8):2457-2476. PubMed ID: 31039129
[TBL] [Abstract][Full Text] [Related]
3. Heterozygous
Brenner D; Sieverding K; Bruno C; Lüningschrör P; Buck E; Mungwa S; Fischer L; Brockmann SJ; Ulmer J; Bliederhäuser C; Philibert CE; Satoh T; Akira S; Boillée S; Mayer B; Sendtner M; Ludolph AC; Danzer KM; Lobsiger CS; Freischmidt A; Weishaupt JH
J Exp Med; 2019 Feb; 216(2):267-278. PubMed ID: 30635357
[TBL] [Abstract][Full Text] [Related]
4. TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts.
Le Ber I; De Septenville A; Millecamps S; Camuzat A; Caroppo P; Couratier P; Blanc F; Lacomblez L; Sellal F; Fleury MC; Meininger V; Cazeneuve C; Clot F; Flabeau O; LeGuern E; Brice A;
Neurobiol Aging; 2015 Nov; 36(11):3116.e5-3116.e8. PubMed ID: 26476236
[TBL] [Abstract][Full Text] [Related]
5. Association between TBK1 mutations and risk of amyotrophic lateral sclerosis/frontotemporal dementia spectrum: a meta-analysis.
Cui R; Tuo M; Li P; Zhou C
Neurol Sci; 2018 May; 39(5):811-820. PubMed ID: 29349657
[TBL] [Abstract][Full Text] [Related]
6. The Loss of TBK1 Kinase Activity in Motor Neurons or in All Cell Types Differentially Impacts ALS Disease Progression in SOD1 Mice.
Gerbino V; Kaunga E; Ye J; Canzio D; O'Keeffe S; Rudnick ND; Guarnieri P; Lutz CM; Maniatis T
Neuron; 2020 Jun; 106(5):789-805.e5. PubMed ID: 32220666
[TBL] [Abstract][Full Text] [Related]
7. Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis.
Scekic-Zahirovic J; Oussini HE; Mersmann S; Drenner K; Wagner M; Sun Y; Allmeroth K; Dieterlé S; Sinniger J; Dirrig-Grosch S; René F; Dormann D; Haass C; Ludolph AC; Lagier-Tourenne C; Storkebaum E; Dupuis L
Acta Neuropathol; 2017 Jun; 133(6):887-906. PubMed ID: 28243725
[TBL] [Abstract][Full Text] [Related]
8. TBK1: a new player in ALS linking autophagy and neuroinflammation.
Oakes JA; Davies MC; Collins MO
Mol Brain; 2017 Feb; 10(1):5. PubMed ID: 28148298
[TBL] [Abstract][Full Text] [Related]
9. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
Kobayakawa Y; Sakumi K; Kajitani K; Kadoya T; Horie H; Kira J; Nakabeppu Y
Neuropathol Appl Neurobiol; 2015 Feb; 41(2):227-44. PubMed ID: 24707896
[TBL] [Abstract][Full Text] [Related]
10. Functional and structural consequences of TBK1 missense variants in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Gurfinkel Y; Polain N; Sonar K; Nice P; Mancera RL; Rea SL
Neurobiol Dis; 2022 Nov; 174():105859. PubMed ID: 36113750
[TBL] [Abstract][Full Text] [Related]
11. TBK1 Suppresses RIPK1-Driven Apoptosis and Inflammation during Development and in Aging.
Xu D; Jin T; Zhu H; Chen H; Ofengeim D; Zou C; Mifflin L; Pan L; Amin P; Li W; Shan B; Naito MG; Meng H; Li Y; Pan H; Aron L; Adiconis X; Levin JZ; Yankner BA; Yuan J
Cell; 2018 Sep; 174(6):1477-1491.e19. PubMed ID: 30146158
[TBL] [Abstract][Full Text] [Related]
12. TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
van der Zee J; Gijselinck I; Van Mossevelde S; Perrone F; Dillen L; Heeman B; Bäumer V; Engelborghs S; De Bleecker J; Baets J; Gelpi E; Rojas-García R; Clarimón J; Lleó A; Diehl-Schmid J; Alexopoulos P; Perneczky R; Synofzik M; Just J; Schöls L; Graff C; Thonberg H; Borroni B; Padovani A; Jordanova A; Sarafov S; Tournev I; de Mendonça A; Miltenberger-Miltényi G; Simões do Couto F; Ramirez A; Jessen F; Heneka MT; Gómez-Tortosa E; Danek A; Cras P; Vandenberghe R; De Jonghe P; De Deyn PP; Sleegers K; Cruts M; Van Broeckhoven C; Goeman J; Nuytten D; Smets K; Robberecht W; Damme PV; Bleecker J; Santens P; Dermaut B; Versijpt J; Michotte A; Ivanoiu A; Deryck O; Bergmans B; Delbeck J; Bruyland M; Willems C; Salmon E; Pastor P; Ortega-Cubero S; Benussi L; Ghidoni R; Binetti G; Hernández I; Boada M; Ruiz A; Sorbi S; Nacmias B; Bagnoli S; Sorbi S; Sanchez-Valle R; Llado A; Santana I; Rosário Almeida M; Frisoni GB; Maetzler W; Matej R; Fraidakis MJ; Kovacs GG; Fabrizi GM; Testi S
Hum Mutat; 2017 Mar; 38(3):297-309. PubMed ID: 28008748
[TBL] [Abstract][Full Text] [Related]
13. ALS-associated TBK1 variant p.G175S is defective in phosphorylation of p62 and impacts TBK1-mediated signalling and TDP-43 autophagic degradation.
Foster AD; Downing P; Figredo E; Polain N; Stott A; Layfield R; Rea SL
Mol Cell Neurosci; 2020 Oct; 108():103539. PubMed ID: 32835772
[TBL] [Abstract][Full Text] [Related]
14. FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees.
Brenner D; Müller K; Lattante S; Yilmaz R; Knehr A; Freischmidt A; Ludolph AC; Andersen PM; Weishaupt JH
Neurogenetics; 2022 Jan; 23(1):59-65. PubMed ID: 34518945
[TBL] [Abstract][Full Text] [Related]
15. TBK1 variants in Chinese patients with amyotrophic lateral sclerosis: Genetic analysis and clinical features.
Zhao B; Jiang Q; Lin J; Wei Q; Li C; Hou Y; Cao B; Zhang L; Ou R; Liu K; Yang T; Xiao Y; Shang H
Eur J Neurol; 2023 Oct; 30(10):3079-3089. PubMed ID: 37422901
[TBL] [Abstract][Full Text] [Related]
16. A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice.
Brenner D; Sieverding K; Srinidhi J; Zellner S; Secker C; Yilmaz R; Dyckow J; Amr S; Ponomarenko A; Tunaboylu E; Douahem Y; Schlag JS; Rodríguez Martínez L; Kislinger G; Niemann C; Nalbach K; Ruf WP; Uhl J; Hollenbeck J; Schirmer L; Catanese A; Lobsiger CS; Danzer KM; Yilmazer-Hanke D; Münch C; Koch P; Freischmidt A; Fetting M; Behrends C; Parlato R; Weishaupt JH
J Exp Med; 2024 May; 221(5):. PubMed ID: 38517332
[TBL] [Abstract][Full Text] [Related]
17. Progressive Degeneration and Inhibition of Peripheral Nerve Regeneration in the SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis.
Deng B; Lv W; Duan W; Liu Y; Li Z; Ma Y; Zhang G; Song X; Cui C; Qi X; Li Y; Li C
Cell Physiol Biochem; 2018; 46(6):2358-2372. PubMed ID: 29742495
[TBL] [Abstract][Full Text] [Related]
18. Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.
Freischmidt A; Müller K; Ludolph AC; Weishaupt JH; Andersen PM
JAMA Neurol; 2017 Jan; 74(1):110-113. PubMed ID: 27892983
[TBL] [Abstract][Full Text] [Related]
19. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
Van Mossevelde S; van der Zee J; Gijselinck I; Engelborghs S; Sieben A; Van Langenhove T; De Bleecker J; Baets J; Vandenbulcke M; Van Laere K; Ceyssens S; Van den Broeck M; Peeters K; Mattheijssens M; Cras P; Vandenberghe R; De Jonghe P; Martin JJ; De Deyn PP; Cruts M; Van Broeckhoven C;
Brain; 2016 Feb; 139(Pt 2):452-67. PubMed ID: 26674655
[TBL] [Abstract][Full Text] [Related]
20. ALS- and FTD-associated missense mutations in TBK1 differentially disrupt mitophagy.
Harding O; Evans CS; Ye J; Cheung J; Maniatis T; Holzbaur ELF
Proc Natl Acad Sci U S A; 2021 Jun; 118(24):. PubMed ID: 34099552
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
