These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 30672142)

  • 1. Association of the TBK1 mutation p.Ile334Thr with frontotemporal dementia and literature review.
    Yu H; Yu W; Luo SS; Yang YJ; Liu FT; Zhang Y; Chen Y; Sun YM; Wu JJ
    Mol Genet Genomic Med; 2019 Mar; 7(3):e547. PubMed ID: 30672142
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Genetic and clinical landscape of Chinese frontotemporal dementia: dominance of TBK1 and OPTN mutations.
    Nan H; Kim YJ; Chu M; Li D; Li J; Jiang D; Wu Y; Ohtsuka T; Wu L
    Alzheimers Res Ther; 2024 Jun; 16(1):127. PubMed ID: 38872230
    [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. 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]  

  • 6. Novel TBK1 variant associated with Frontotemporal Dementia overlap syndrome.
    Arshad F; Vengalil S; Nalini A; Polavarapu K; Shamim U; Jabeen S; Nagaraj C; Ramakrishnan S; Faruq M; Alladi S
    Acta Neurol Scand; 2022 Apr; 145(4):399-406. PubMed ID: 34841512
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel
    Lamb R; Rohrer JD; Real R; Lubbe SJ; Waite AJ; Blake DJ; Walters RJ; Lashley T; Revesz T; Holton JL; Morris HR
    Cold Spring Harb Mol Case Stud; 2019 Jun; 5(3):. PubMed ID: 31160356
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
    Pottier C; Bieniek KF; Finch N; van de Vorst M; Baker M; Perkersen R; Brown P; Ravenscroft T; van Blitterswijk M; Nicholson AM; DeTure M; Knopman DS; Josephs KA; Parisi JE; Petersen RC; Boylan KB; Boeve BF; Graff-Radford NR; Veltman JA; Gilissen C; Murray ME; Dickson DW; Rademakers R
    Acta Neuropathol; 2015 Jul; 130(1):77-92. PubMed ID: 25943890
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature.
    Swift IJ; Bocchetta M; Benotmane H; Woollacott IO; Shafei R; Rohrer JD
    Neurobiol Aging; 2021 Mar; 99():100.e9-100.e15. PubMed ID: 32980182
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Retinoic acid worsens ATG10-dependent autophagy impairment in TBK1-mutant hiPSC-derived motoneurons through SQSTM1/p62 accumulation.
    Catanese A; Olde Heuvel F; Mulaw M; Demestre M; Higelin J; Barbi G; Freischmidt A; Weishaupt JH; Ludolph AC; Roselli F; Boeckers TM
    Autophagy; 2019 Oct; 15(10):1719-1737. PubMed ID: 30939964
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.