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 *

81 related articles for article (PubMed ID: 32253937)

  • 1. A novel mutation in
    Goldstein O; Kedmi M; Gana-Weisz M; Nefussy B; Vainer B; Fainmesser Y; Drory VE; Orr-Urtreger A
    Amyotroph Lateral Scler Frontotemporal Degener; 2020 May; 21(3-4):280-285. PubMed ID: 32253937
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese.
    Iida A; Kamei T; Sano M; Oshima S; Tokuda T; Nakamura Y; Ikegawa S
    Neurobiol Aging; 2012 Apr; 33(4):786-90. PubMed ID: 20675015
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypes in Swiss patients with familial ALS carrying TARDBP mutations.
    Czell D; Andersen PM; Morita M; Neuwirth C; Perren F; Weber M
    Neurodegener Dis; 2013; 12(3):150-5. PubMed ID: 23327806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A novel S379A TARDBP mutation associated to late-onset sporadic ALS.
    Sprovieri T; Ungaro C; Perrone B; Naimo GD; Spataro R; Cavallaro S; La Bella V; Conforti FL
    Neurol Sci; 2019 Oct; 40(10):2111-2118. PubMed ID: 31165305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS.
    Naruse H; Ishiura H; Mitsui J; Takahashi Y; Matsukawa T; Tanaka M; Doi K; Yoshimura J; Morishita S; Goto J; Toda T; Tsuji S
    J Neurol Neurosurg Psychiatry; 2019 May; 90(5):537-542. PubMed ID: 30355605
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis.
    Orrù S; Manolakos E; Orrù N; Kokotas H; Mascia V; Carcassi C; Petersen MB
    Clin Genet; 2012 Feb; 81(2):172-8. PubMed ID: 21418058
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
    van Blitterswijk M; van Es MA; Hennekam EA; Dooijes D; van Rheenen W; Medic J; Bourque PR; Schelhaas HJ; van der Kooi AJ; de Visser M; de Bakker PI; Veldink JH; van den Berg LH
    Hum Mol Genet; 2012 Sep; 21(17):3776-84. PubMed ID: 22645277
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The first case of the
    Corrado L; Pensato V; Croce R; Di Pierro A; Mellone S; Dalla Bella E; Salsano E; Paraboschi EM; Giordano M; Saraceno M; Mazzini L; Gellera C; D'Alfonso S
    Amyotroph Lateral Scler Frontotemporal Degener; 2020 May; 21(3-4):273-279. PubMed ID: 31852254
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
    Hou L; Jiao B; Xiao T; Zhou L; Zhou Z; Du J; Yan X; Wang J; Tang B; Shen L
    Sci Rep; 2016 Sep; 6():32478. PubMed ID: 27604643
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China.
    Xu F; Huang S; Li XY; Lin J; Feng X; Xie S; Wang Z; Li X; Zhu J; Lai H; Xu Y; Huang X; Yao X; Wang C
    BMC Med Genomics; 2022 Aug; 15(1):173. PubMed ID: 35932023
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindred.
    Williams KL; Durnall JC; Thoeng AD; Warraich ST; Nicholson GA; Blair IP
    J Neurol Neurosurg Psychiatry; 2009 Nov; 80(11):1286-8. PubMed ID: 19864664
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
    Daoud H; Valdmanis PN; Kabashi E; Dion P; Dupré N; Camu W; Meininger V; Rouleau GA
    J Med Genet; 2009 Feb; 46(2):112-4. PubMed ID: 18931000
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations.
    Corcia P; Valdmanis P; Millecamps S; Lionnet C; Blasco H; Mouzat K; Daoud H; Belzil V; Morales R; Pageot N; Danel-Brunaud V; Vandenberghe N; Pradat PF; Couratier P; Salachas F; Lumbroso S; Rouleau GA; Meininger V; Camu W
    Neurology; 2012 May; 78(19):1519-26. PubMed ID: 22539580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Comprehensive analysis of the mutation spectrum in 301 German ALS families.
    Müller K; Brenner D; Weydt P; Meyer T; Grehl T; Petri S; Grosskreutz J; Schuster J; Volk AE; Borck G; Kubisch C; Klopstock T; Zeller D; Jablonka S; Sendtner M; Klebe S; Knehr A; Günther K; Weis J; Claeys KG; Schrank B; Sperfeld AD; Hübers A; Otto M; Dorst J; Meitinger T; Strom TM; Andersen PM; Ludolph AC; Weishaupt JH;
    J Neurol Neurosurg Psychiatry; 2018 Aug; 89(8):817-827. PubMed ID: 29650794
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.
    Tsai CP; Soong BW; Lin KP; Tu PH; Lin JL; Lee YC
    Neurobiol Aging; 2011 Mar; 32(3):553.e13-21. PubMed ID: 20472325
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
    Kabashi E; Valdmanis PN; Dion P; Spiegelman D; McConkey BJ; Vande Velde C; Bouchard JP; Lacomblez L; Pochigaeva K; Salachas F; Pradat PF; Camu W; Meininger V; Dupre N; Rouleau GA
    Nat Genet; 2008 May; 40(5):572-4. PubMed ID: 18372902
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family.
    Praline J; Vourc'h P; Guennoc AM; Veyrat-Durebex C; Corcia P
    Amyotroph Lateral Scler; 2012 Jan; 13(1):155-7. PubMed ID: 21830990
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.