BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 21830990)

  • 1. 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]  

  • 2. Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
    Rutherford NJ; Zhang YJ; Baker M; Gass JM; Finch NA; Xu YF; Stewart H; Kelley BJ; Kuntz K; Crook RJ; Sreedharan J; Vance C; Sorenson E; Lippa C; Bigio EH; Geschwind DH; Knopman DS; Mitsumoto H; Petersen RC; Cashman NR; Hutton M; Shaw CE; Boylan KB; Boeve B; Graff-Radford NR; Wszolek ZK; Caselli RJ; Dickson DW; Mackenzie IR; Petrucelli L; Rademakers R
    PLoS Genet; 2008 Sep; 4(9):e1000193. PubMed ID: 18802454
    [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. A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosis.
    Solski JA; Yang S; Nicholson GA; Luquin N; Williams KL; Fernando R; Pamphlett R; Blair IP
    Amyotroph Lateral Scler; 2012 Sep; 13(5):465-70. PubMed ID: 22424122
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enlarging clinical spectrum of FALS with TARDBP gene mutations: S393L variant in an Italian family showing phenotypic variability and relevance for genetic counselling.
    Origone P; Caponnetto C; Bandettini Di Poggio M; Ghiglione E; Bellone E; Ferrandes G; Mancardi GL; Mandich P
    Amyotroph Lateral Scler; 2010; 11(1-2):223-7. PubMed ID: 19714537
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.
    Kamada M; Maruyama H; Tanaka E; Morino H; Wate R; Ito H; Kusaka H; Kawano Y; Miki T; Nodera H; Izumi Y; Kaji R; Kawakami H
    J Neurol Sci; 2009 Sep; 284(1-2):69-71. PubMed ID: 19411082
    [TBL] [Abstract][Full Text] [Related]  

  • 7. TARDBP mutation analysis in TDP-43 proteinopathies and deciphering the toxicity of mutant TDP-43.
    Gendron TF; Rademakers R; Petrucelli L
    J Alzheimers Dis; 2013; 33 Suppl 1(Suppl 1):S35-45. PubMed ID: 22751173
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan.
    Tomiyama H; Kokubo Y; Sasaki R; Li Y; Imamichi Y; Funayama M; Mizuno Y; Hattori N; Kuzuhara S
    Mov Disord; 2008 Dec; 23(16):2344-8. PubMed ID: 18759352
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
    Del Bo R; Ghezzi S; Corti S; Pandolfo M; Ranieri M; Santoro D; Ghione I; Prelle A; Orsetti V; Mancuso M; Sorarù G; Briani C; Angelini C; Siciliano G; Bresolin N; Comi GP
    Eur J Neurol; 2009 Jun; 16(6):727-32. PubMed ID: 19236453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Mutant TDP-43 in motor neurons promotes the onset and progression of ALS in rats.
    Huang C; Tong J; Bi F; Zhou H; Xia XG
    J Clin Invest; 2012 Jan; 122(1):107-18. PubMed ID: 22156203
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [TDP-43 proteinopathies: ALS and frontotemporal dementias].
    Prudlo J
    Fortschr Neurol Psychiatr; 2009 Aug; 77 Suppl 1():S25-7. PubMed ID: 19685386
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.
    Corrado L; Ratti A; Gellera C; Buratti E; Castellotti B; Carlomagno Y; Ticozzi N; Mazzini L; Testa L; Taroni F; Baralle FE; Silani V; D'Alfonso S
    Hum Mutat; 2009 Apr; 30(4):688-94. PubMed ID: 19224587
    [TBL] [Abstract][Full Text] [Related]  

  • 15. TDP-43 mutation in familial amyotrophic lateral sclerosis.
    Yokoseki A; Shiga A; Tan CF; Tagawa A; Kaneko H; Koyama A; Eguchi H; Tsujino A; Ikeuchi T; Kakita A; Okamoto K; Nishizawa M; Takahashi H; Onodera O
    Ann Neurol; 2008 Apr; 63(4):538-42. PubMed ID: 18438952
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43.
    Godoy-Corchuelo JM; Ali Z; Brito Armas JM; Martins-Bach AB; García-Toledo I; Fernández-Beltrán LC; López-Carbonero JI; Bascuñana P; Spring S; Jimenez-Coca I; Muñoz de Bustillo Alfaro RA; Sánchez-Barrena MJ; Nair RR; Nieman BJ; Lerch JP; Miller KL; Ozdinler HP; Fisher EMC; Cunningham TJ; Acevedo-Arozena A; Corrochano S
    Neurobiol Dis; 2024 Apr; 193():106437. PubMed ID: 38367882
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TDP-43: a DNA and RNA binding protein with roles in neurodegenerative diseases.
    Warraich ST; Yang S; Nicholson GA; Blair IP
    Int J Biochem Cell Biol; 2010 Oct; 42(10):1606-9. PubMed ID: 20601083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial ALS with G298S mutation in TARDBP: a comparison of CSF tau protein levels with those in sporadic ALS.
    Nozaki I; Arai M; Takahashi K; Hamaguchi T; Yoshikawa H; Muroishi T; Noguchi-Shinohara M; Ito H; Itokawa M; Akiyama H; Kawata A; Yamada M
    Intern Med; 2010; 49(12):1209-12. PubMed ID: 20558945
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.