BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 9021255)

  • 1. Familial amyotrophic lateral sclerosis.
    Siddique T; Hentati A
    Clin Neurosci; 1995-1996; 3(6):338-47. PubMed ID: 9021255
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular genetic basis of familial ALS.
    Siddique T; Nijhawan D; Hentati A
    Neurology; 1996 Oct; 47(4 Suppl 2):S27-34; discussion S34-5. PubMed ID: 8858048
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial amyotrophic lateral sclerosis.
    Siddique T; Nijhawan D; Hentati A
    J Neural Transm Suppl; 1997; 49():219-33. PubMed ID: 9266431
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
    Nakano R
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1546-8. PubMed ID: 8752459
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.
    Aguirre T; Matthijs G; Robberecht W; Tilkin P; Cassiman JJ
    Eur J Hum Genet; 1999 Jul; 7(5):599-602. PubMed ID: 10439968
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
    Rosen DR; Siddique T; Patterson D; Figlewicz DA; Sapp P; Hentati A; Donaldson D; Goto J; O'Regan JP; Deng HX
    Nature; 1993 Mar; 362(6415):59-62. PubMed ID: 8446170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pathogenic mechanisms in familial amyotrophic lateral sclerosis due to mutation of Cu, Zn superoxide dismutase.
    Gurney ME; Cutting FB; Zhai P; Andrus PK; Hall ED
    Pathol Biol (Paris); 1996 Jan; 44(1):51-6. PubMed ID: 8734301
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease.
    Tu PH; Gurney ME; Julien JP; Lee VM; Trojanowski JQ
    Lab Invest; 1997 Apr; 76(4):441-56. PubMed ID: 9111507
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses.
    Sato T; Yamamoto Y; Nakanishi T; Fukada K; Sugai F; Zhou Z; Okuno T; Nagano S; Hirata S; Shimizu A; Sakoda S
    J Neurol Sci; 2004 Mar; 218(1-2):79-83. PubMed ID: 14759637
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.
    Rouleau GA; Clark AW; Rooke K; Pramatarova A; Krizus A; Suchowersky O; Julien JP; Figlewicz D
    Ann Neurol; 1996 Jan; 39(1):128-31. PubMed ID: 8572658
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of three mutations in the Cu,Zn-superoxide dismutase (Cu,Zn-SOD) gene with familial amyotrophic lateral sclerosis: transduction of human Cu,Zn-SOD into PC12 cells by HIV-1 TAT protein basic domain.
    Chou CM; Huang CJ; Shih CM; Chen YP; Liu TP; Chen CT
    Ann N Y Acad Sci; 2005 May; 1042():303-13. PubMed ID: 15965076
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic inroads in familial ALS.
    Shaw PJ
    Nat Genet; 2001 Oct; 29(2):103-4. PubMed ID: 11586285
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gender difference in levels of Cu/Zn superoxide dismutase (SOD1) in cerebrospinal fluid of patients with amyotrophic lateral sclerosis.
    Frutiger K; Lukas TJ; Gorrie G; Ajroud-Driss S; Siddique T
    Amyotroph Lateral Scler; 2008 Jun; 9(3):184-7. PubMed ID: 18574763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
    Tan CF; Piao YS; Hayashi S; Obata H; Umeda Y; Sato M; Fukushima T; Nakano R; Tsuji S; Takahashi H
    Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [What is the role of the genetic survey in amyotrophic lateral sclerosis?].
    Camu W
    Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S91-4S95. PubMed ID: 17128094
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.
    Turner BJ; Talbot K
    Prog Neurobiol; 2008 May; 85(1):94-134. PubMed ID: 18282652
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disruption of the structure of the Golgi apparatus and the function of the secretory pathway by mutants G93A and G85R of Cu, Zn superoxide dismutase (SOD1) of familial amyotrophic lateral sclerosis.
    Stieber A; Gonatas JO; Moore JS; Bantly A; Yim HS; Yim MB; Gonatas NK
    J Neurol Sci; 2004 Apr; 219(1-2):45-53. PubMed ID: 15050437
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Superoxide dismutase--applications and relevance to human diseases.
    Noor R; Mittal S; Iqbal J
    Med Sci Monit; 2002 Sep; 8(9):RA210-5. PubMed ID: 12218958
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural discovery of small molecule binding sites in Cu-Zn human superoxide dismutase familial amyotrophic lateral sclerosis mutants provides insights for lead optimization.
    Antonyuk S; Strange RW; Hasnain SS
    J Med Chem; 2010 Feb; 53(3):1402-6. PubMed ID: 20067275
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis.
    Gestri D; Cecchi C; Tedde A; Latorraca S; Orlacchio A; Grassi E; Massaro AM; Liguri G; St George-Hyslop PH; Sorbi S
    Neurosci Lett; 2000 Aug; 289(3):157-60. PubMed ID: 10961653
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.