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.
22. Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo. Kabashi E; Lin L; Tradewell ML; Dion PA; Bercier V; Bourgouin P; Rochefort D; Bel Hadj S; Durham HD; Vande Velde C; Rouleau GA; Drapeau P Hum Mol Genet; 2010 Feb; 19(4):671-83. PubMed ID: 19959528 [TBL] [Abstract][Full Text] [Related]
23. Different clinical and neuropathologic phenotypes of familial ALS with A315E TARDBP mutation. Fujita Y; Ikeda M; Yanagisawa T; Senoo Y; Okamoto K Neurology; 2011 Oct; 77(15):1427-31. PubMed ID: 21956716 [TBL] [Abstract][Full Text] [Related]
24. Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject. Mosca L; Lunetta C; Tarlarini C; Avemaria F; Maestri E; Melazzini M; Corbo M; Penco S Neurobiol Aging; 2012 Aug; 33(8):1846.e1-4. PubMed ID: 22398199 [TBL] [Abstract][Full Text] [Related]
25. High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis. Xu GR; Hu W; Zhan LL; Wang C; Xu LQ; Lin MT; Chen WJ; Wang N; Zhang QJ BMC Neurol; 2018 Apr; 18(1):35. PubMed ID: 29621978 [TBL] [Abstract][Full Text] [Related]
26. TARDBP in amyotrophic lateral sclerosis: identification of a novel variant but absence of copy number variation. Bäumer D; Parkinson N; Talbot K J Neurol Neurosurg Psychiatry; 2009 Nov; 80(11):1283-5. PubMed ID: 19864663 [TBL] [Abstract][Full Text] [Related]
27. Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. Synofzik M; Born C; Rominger A; Lummel N; Schöls L; Biskup S; Schüle C; Grasshoff U; Klopstock T; Adamczyk C Neurobiol Aging; 2014 May; 35(5):1212.e1-5. PubMed ID: 24300238 [TBL] [Abstract][Full Text] [Related]
37. Lower motor neuron involvement in TAR DNA-binding protein of 43 kDa-related frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Riku Y; Watanabe H; Yoshida M; Tatsumi S; Mimuro M; Iwasaki Y; Katsuno M; Iguchi Y; Masuda M; Senda J; Ishigaki S; Udagawa T; Sobue G JAMA Neurol; 2014 Feb; 71(2):172-9. PubMed ID: 24378564 [TBL] [Abstract][Full Text] [Related]
38. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002 [TBL] [Abstract][Full Text] [Related]