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 *

131 related articles for article (PubMed ID: 23040663)

  • 1. E6-AP association promotes SOD1 aggresomes degradation and suppresses toxicity.
    Mishra A; Maheshwari M; Chhangani D; Fujimori-Tonou N; Endo F; Joshi AP; Jana NR; Yamanaka K
    Neurobiol Aging; 2013 Apr; 34(4):1310.e11-23. PubMed ID: 23040663
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mahogunin ring finger 1 confers cytoprotection against mutant SOD1 aggresomes and is defective in an ALS mouse model.
    Chhangani D; Endo F; Amanullah A; Upadhyay A; Watanabe S; Mishra R; Yamanaka K; Mishra A
    Neurobiol Dis; 2016 Feb; 86():16-28. PubMed ID: 26607786
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. CHIP promotes proteasomal degradation of familial ALS-linked mutant SOD1 by ubiquitinating Hsp/Hsc70.
    Urushitani M; Kurisu J; Tateno M; Hatakeyama S; Nakayama K; Kato S; Takahashi R
    J Neurochem; 2004 Jul; 90(1):231-44. PubMed ID: 15198682
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ALS-linked mutant SOD1 proteins promote Aβ aggregates in ALS through direct interaction with Aβ.
    Jang JY; Cho H; Park HY; Rhim H; Kang S
    Biochem Biophys Res Commun; 2017 Nov; 493(1):697-707. PubMed ID: 28864422
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.
    Kerman A; Liu HN; Croul S; Bilbao J; Rogaeva E; Zinman L; Robertson J; Chakrabartty A
    Acta Neuropathol; 2010 Mar; 119(3):335-44. PubMed ID: 20111867
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dorfin ameliorates phenotypes in a transgenic mouse model of amyotrophic lateral sclerosis.
    Sone J; Niwa J; Kawai K; Ishigaki S; Yamada S; Adachi H; Katsuno M; Tanaka F; Doyu M; Sobue G
    J Neurosci Res; 2010 Jan; 88(1):123-35. PubMed ID: 19610091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dorfin-CHIP chimeric proteins potently ubiquitylate and degrade familial ALS-related mutant SOD1 proteins and reduce their cellular toxicity.
    Ishigaki S; Niwa J; Yamada S; Takahashi M; Ito T; Sone J; Doyu M; Urano F; Sobue G
    Neurobiol Dis; 2007 Feb; 25(2):331-41. PubMed ID: 17157513
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS.
    Robertson J; Sanelli T; Xiao S; Yang W; Horne P; Hammond R; Pioro EP; Strong MJ
    Neurosci Lett; 2007 Jun; 420(2):128-32. PubMed ID: 17543992
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.
    Jaarsma D; Haasdijk ED; Grashorn JA; Hawkins R; van Duijn W; Verspaget HW; London J; Holstege JC
    Neurobiol Dis; 2000 Dec; 7(6 Pt B):623-43. PubMed ID: 11114261
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Elevation of the Hsp70 chaperone does not effect toxicity in mouse models of familial amyotrophic lateral sclerosis.
    Liu J; Shinobu LA; Ward CM; Young D; Cleveland DW
    J Neurochem; 2005 May; 93(4):875-82. PubMed ID: 15857390
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutant SOD1-induced neuronal toxicity is mediated by increased mitochondrial superoxide levels.
    Zimmerman MC; Oberley LW; Flanagan SW
    J Neurochem; 2007 Aug; 102(3):609-18. PubMed ID: 17394531
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity.
    Niwa J; Ishigaki S; Hishikawa N; Yamamoto M; Doyu M; Murata S; Tanaka K; Taniguchi N; Sobue G
    J Biol Chem; 2002 Sep; 277(39):36793-8. PubMed ID: 12145308
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Co-chaperone CHIP associates with mutant Cu/Zn-superoxide dismutase proteins linked to familial amyotrophic lateral sclerosis and promotes their degradation by proteasomes.
    Choi JS; Cho S; Park SG; Park BC; Lee DH
    Biochem Biophys Res Commun; 2004 Aug; 321(3):574-83. PubMed ID: 15358145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Formation of advanced glycation end-product-modified superoxide dismutase-1 (SOD1) is one of the mechanisms responsible for inclusions common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutation, and transgenic mice expressing human SOD1 gene mutation.
    Kato S; Nakashima K; Horiuchi S; Nagai R; Cleveland DW; Liu J; Hirano A; Takikawa M; Kato M; Nakano I; Sakoda S; Asayama K; Ohama E
    Neuropathology; 2001 Mar; 21(1):67-81. PubMed ID: 11304045
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA.
    Wang J; Xu G; Slunt HH; Gonzales V; Coonfield M; Fromholt D; Copeland NG; Jenkins NA; Borchelt DR
    Neurobiol Dis; 2005 Dec; 20(3):943-52. PubMed ID: 16046140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. TNF receptor-associated factor 6 interacts with ALS-linked misfolded superoxide dismutase 1 and promotes aggregation.
    Semmler S; Gagné M; Garg P; Pickles SR; Baudouin C; Hamon-Keromen E; Destroismaisons L; Khalfallah Y; Chaineau M; Caron E; Bayne AN; Trempe JF; Cashman NR; Star AT; Haqqani AS; Durcan TM; Meiering EM; Robertson J; Grandvaux N; Plotkin SS; McBride HM; Vande Velde C
    J Biol Chem; 2020 Mar; 295(12):3808-3825. PubMed ID: 32029478
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice.
    Wong M; Martin LJ
    Hum Mol Genet; 2010 Jun; 19(11):2284-302. PubMed ID: 20223753
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Parkin Protects Against Misfolded SOD1 Toxicity by Promoting Its Aggresome Formation and Autophagic Clearance.
    Yung C; Sha D; Li L; Chin LS
    Mol Neurobiol; 2016 Nov; 53(9):6270-6287. PubMed ID: 26563499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.