BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 25848921)

  • 1. Motor neuron disease: loss-of-function mutations in TBK1 can cause familial ALS.
    Chase A
    Nat Rev Neurol; 2015 May; 11(5):246. PubMed ID: 25848921
    [No Abstract]   [Full Text] [Related]  

  • 2. Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
    Freischmidt A; Wieland T; Richter B; Ruf W; Schaeffer V; Müller K; Marroquin N; Nordin F; Hübers A; Weydt P; Pinto S; Press R; Millecamps S; Molko N; Bernard E; Desnuelle C; Soriani MH; Dorst J; Graf E; Nordström U; Feiler MS; Putz S; Boeckers TM; Meyer T; Winkler AS; Winkelman J; de Carvalho M; Thal DR; Otto M; Brännström T; Volk AE; Kursula P; Danzer KM; Lichtner P; Dikic I; Meitinger T; Ludolph AC; Strom TM; Andersen PM; Weishaupt JH
    Nat Neurosci; 2015 May; 18(5):631-6. PubMed ID: 25803835
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. TBK1 is associated with ALS and ALS-FTD in Sardinian patients.
    Borghero G; Pugliatti M; Marrosu F; Marrosu MG; Murru MR; Floris G; Cannas A; Occhineri P; Cau TB; Loi D; Ticca A; Traccis S; Manera U; Canosa A; Moglia C; Calvo A; Barberis M; Brunetti M; Gibbs JR; Renton AE; Errichiello E; Zoledziewska M; Mulas A; Qian Y; Din J; Pliner HA; Traynor BJ; Chiò A;
    Neurobiol Aging; 2016 Jul; 43():180.e1-5. PubMed ID: 27156075
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes.
    Wilke C; Baets J; De Bleecker JL; Deconinck T; Biskup S; Hayer SN; Züchner S; Schüle R; De Jonghe P; Synofzik M
    Neurobiol Aging; 2018 Feb; 62():244.e9-244.e13. PubMed ID: 29137817
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TBK1 haploinsufficiency in ALS and FTD compromises membrane trafficking.
    Lu Y; Almeida S; Gao FB
    Acta Neuropathol; 2021 Jul; 142(1):217-221. PubMed ID: 34081168
    [No Abstract]   [Full Text] [Related]  

  • 10. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.
    Gijselinck I; Van Mossevelde S; van der Zee J; Sieben A; Philtjens S; Heeman B; Engelborghs S; Vandenbulcke M; De Baets G; Bäumer V; Cuijt I; Van den Broeck M; Peeters K; Mattheijssens M; Rousseau F; Vandenberghe R; De Jonghe P; Cras P; De Deyn PP; Martin JJ; Cruts M; Van Broeckhoven C;
    Neurology; 2015 Dec; 85(24):2116-25. PubMed ID: 26581300
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A Pair of Siblings with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis and a Novel Thr462Lysfs Mutation in the TBK1 Gene].
    Schönecker S; Brendel M; van der Zee J; van Broeckhoven C; Rominger A; Danek A; Levin J
    Fortschr Neurol Psychiatr; 2016 Aug; 84(8):494-8. PubMed ID: 27570907
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic analysis of CHCHD10 in French familial amyotrophic lateral sclerosis patients.
    Teyssou E; Chartier L; Albert M; Bouscary A; Antoine JC; Camdessanché JP; Rotolo F; Couratier P; Salachas F; Seilhean D; Millecamps S
    Neurobiol Aging; 2016 Jun; 42():218.e1-3. PubMed ID: 27095681
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial primary lateral sclerosis or dementia associated with Arg573Gly
    Gómez-Tortosa E; Van der Zee J; Ruggiero M; Gijselinck I; Esteban-Pérez J; García-Redondo A; Borrego-Hernández D; Navarro E; Sainz MJ; Pérez-Pérez J; Cruts M; Van Broeckhoven C; Guerrero-López R;
    J Neurol Neurosurg Psychiatry; 2017 Nov; 88(11):996-997. PubMed ID: 28365590
    [No Abstract]   [Full Text] [Related]  

  • 14. Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin.
    Williams KL; McCann EP; Fifita JA; Zhang K; Duncan EL; Leo PJ; Marshall M; Rowe DB; Nicholson GA; Blair IP
    Neurobiol Aging; 2015 Dec; 36(12):3334.e1-3334.e5. PubMed ID: 26350399
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic coherence between hereditary amyotrophic lateral sclerosis and frontotemporal dementia].
    Gjerde KV; Tysnes OB
    Tidsskr Nor Laegeforen; 2014 Feb; 134(3):302-6. PubMed ID: 24518478
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel homozygous mutation in TBK1 gene causing ALS-FTD.
    Libonati L; Ceccanti M; Cambieri C; Colavito D; Moret F; Fiorini I; Inghilleri M
    Neurol Sci; 2022 Mar; 43(3):2101-2104. PubMed ID: 35028775
    [No Abstract]   [Full Text] [Related]  

  • 17. Human TBK1: A Gatekeeper of Neuroinflammation.
    Ahmad L; Zhang SY; Casanova JL; Sancho-Shimizu V
    Trends Mol Med; 2016 Jun; 22(6):511-527. PubMed ID: 27211305
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ALS due to a novel TBK1 mutation in Brazil.
    Gondim FAA; Fernandes JMA; Marques Júnior W
    Amyotroph Lateral Scler Frontotemporal Degener; 2022 Nov; 23(7-8):620-622. PubMed ID: 35118923
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort.
    Verheijen J; van der Zee J; Gijselinck I; Van den Bossche T; Dillen L; Heeman B; Gómez-Tortosa E; Lladó A; Sanchez-Valle R; Graff C; Pastor P; Pastor MA; Benussi L; Ghidoni R; Binetti G; Clarimon J; de Mendonça A; Gelpi E; Tsolaki M; Diehl-Schmid J; Nacmias B; Almeida MR; Borroni B; Matej R; Ruiz A; Engelborghs S; Vandenberghe R; De Deyn PP; Cruts M; Van Broeckhoven C; Sleegers K; ;
    Neurobiol Aging; 2018 Feb; 62():245.e1-245.e7. PubMed ID: 29146049
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.