BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

224 related articles for article (PubMed ID: 15509539)

  • 1. Dysregulation of stathmin, a microtubule-destabilizing protein, and up-regulation of Hsp25, Hsp27, and the antioxidant peroxiredoxin 6 in a mouse model of familial amyotrophic lateral sclerosis.
    Strey CW; Spellman D; Stieber A; Gonatas JO; Wang X; Lambris JD; Gonatas NK
    Am J Pathol; 2004 Nov; 165(5):1701-18. PubMed ID: 15509539
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aggregates of mutant protein appear progressively in dendrites, in periaxonal processes of oligodendrocytes, and in neuronal and astrocytic perikarya of mice expressing the SOD1(G93A) mutation of familial amyotrophic lateral sclerosis.
    Stieber A; Gonatas JO; Gonatas NK
    J Neurol Sci; 2000 Aug; 177(2):114-23. PubMed ID: 10980307
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Stathmin 1/2-triggered microtubule loss mediates Golgi fragmentation in mutant SOD1 motor neurons.
    Bellouze S; Baillat G; Buttigieg D; de la Grange P; Rabouille C; Haase G
    Mol Neurodegener; 2016 Jun; 11(1):43. PubMed ID: 27277231
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Over-expression of Hsp27 does not influence disease in the mutant SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Krishnan J; Vannuvel K; Andries M; Waelkens E; Robberecht W; Van Den Bosch L
    J Neurochem; 2008 Sep; 106(5):2170-83. PubMed ID: 18624915
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice.
    Maatkamp A; Vlug A; Haasdijk E; Troost D; French PJ; Jaarsma D
    Eur J Neurosci; 2004 Jul; 20(1):14-28. PubMed ID: 15245475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models.
    Kato S; Kato M; Abe Y; Matsumura T; Nishino T; Aoki M; Itoyama Y; Asayama K; Awaya A; Hirano A; Ohama E
    Acta Neuropathol; 2005 Aug; 110(2):101-12. PubMed ID: 15983830
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragmentation of the Golgi apparatus in neurodegenerative diseases and cell death.
    Gonatas NK; Stieber A; Gonatas JO
    J Neurol Sci; 2006 Jul; 246(1-2):21-30. PubMed ID: 16545397
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Regional Differences in Heat Shock Protein 25 Expression in Brain and Spinal Cord Astrocytes of Wild-Type and SOD1
    San Gil R; Clarke BE; Ecroyd H; Kalmar B; Greensmith L
    Cells; 2021 May; 10(5):. PubMed ID: 34069691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Protein oxidative damage in a transgenic mouse model of familial amyotrophic lateral sclerosis.
    Andrus PK; Fleck TJ; Gurney ME; Hall ED
    J Neurochem; 1998 Nov; 71(5):2041-8. PubMed ID: 9798929
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heat shock factor 1 over-expression protects against exposure of hydrophobic residues on mutant SOD1 and early mortality in a mouse model of amyotrophic lateral sclerosis.
    Lin PY; Simon SM; Koh WK; Folorunso O; Umbaugh CS; Pierce A
    Mol Neurodegener; 2013 Nov; 8():43. PubMed ID: 24256636
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
    Watanabe M; Dykes-Hoberg M; Culotta VC; Price DL; Wong PC; Rothstein JD
    Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS.
    Zhai J; Lin H; Canete-Soler R; Schlaepfer WW
    Hum Mol Genet; 2005 Sep; 14(18):2629-40. PubMed ID: 16079151
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus.
    Stieber A; Gonatas JO; Gonatas NK
    J Neurol Sci; 2000 Feb; 173(1):53-62. PubMed ID: 10675580
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease.
    Mourelatos Z; Gonatas NK; Stieber A; Gurney ME; Dal Canto MC
    Proc Natl Acad Sci U S A; 1996 May; 93(11):5472-7. PubMed ID: 8643599
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heat-shock protein 105 interacts with and suppresses aggregation of mutant Cu/Zn superoxide dismutase: clues to a possible strategy for treating ALS.
    Yamashita H; Kawamata J; Okawa K; Kanki R; Nakamizo T; Hatayama T; Yamanaka K; Takahashi R; Shimohama S
    J Neurochem; 2007 Sep; 102(5):1497-1505. PubMed ID: 17403032
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Differential inductions of small heat shock protein 27 and 1-Cys peroxiredoxin in reactive astrocytes in sulfatide-deficient mouse spinal cord.
    Suzuki A; Yamaguchi Y; Hoshi T; Hayashi A; Baba H
    J Neurosci Res; 2007 Jul; 85(9):1921-32. PubMed ID: 17510974
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Upregulation of HSP27 in a transgenic model of ALS.
    Vleminckx V; Van Damme P; Goffin K; Delye H; Van Den Bosch L; Robberecht W
    J Neuropathol Exp Neurol; 2002 Nov; 61(11):968-74. PubMed ID: 12430713
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential effects of mutant SOD1 on protein structure of skeletal muscle and spinal cord of familial amyotrophic lateral sclerosis: role of chaperone network.
    Wei R; Bhattacharya A; Hamilton RT; Jernigan AL; Chaudhuri AR
    Biochem Biophys Res Commun; 2013 Aug; 438(1):218-23. PubMed ID: 23886956
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis.
    Urushitani M; Sik A; Sakurai T; Nukina N; Takahashi R; Julien JP
    Nat Neurosci; 2006 Jan; 9(1):108-18. PubMed ID: 16369483
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.