BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

78 related articles for article (PubMed ID: 27464601)

  • 1. Impairment of SOD1-G93A motility is linked to mitochondrial movement in axons of hippocampal neurons.
    Bae JR; Kim SH
    Arch Pharm Res; 2016 Aug; 39(8):1144-50. PubMed ID: 27464601
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Calcium dysregulation, mitochondrial pathology and protein aggregation in a culture model of amyotrophic lateral sclerosis: mechanistic relationship and differential sensitivity to intervention.
    Tradewell ML; Cooper LA; Minotti S; Durham HD
    Neurobiol Dis; 2011 Jun; 42(3):265-75. PubMed ID: 21296666
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Milanese M; Giribaldi F; Melone M; Bonifacino T; Musante I; Carminati E; Rossi PI; Vergani L; Voci A; Conti F; Puliti A; Bonanno G
    Neurobiol Dis; 2014 Apr; 64():48-59. PubMed ID: 24361555
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
    Kobayakawa Y; Sakumi K; Kajitani K; Kadoya T; Horie H; Kira J; Nakabeppu Y
    Neuropathol Appl Neurobiol; 2015 Feb; 41(2):227-44. PubMed ID: 24707896
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Increased axonal mitochondrial mobility does not slow amyotrophic lateral sclerosis (ALS)-like disease in mutant SOD1 mice.
    Zhu YB; Sheng ZH
    J Biol Chem; 2011 Jul; 286(26):23432-40. PubMed ID: 21518771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Impairment of axonal transport in the axon hillock and the initial segment of anterior horn neurons in transgenic mice with a G93A mutant SOD1 gene.
    Sasaki S; Warita H; Abe K; Iwata M
    Acta Neuropathol; 2005 Jul; 110(1):48-56. PubMed ID: 15920660
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Axonal mitochondrial clusters containing mutant SOD1 in transgenic models of ALS.
    Sotelo-Silveira JR; Lepanto P; Elizondo V; Horjales S; Palacios F; Martinez-Palma L; Marin M; Beckman JS; Barbeito L
    Antioxid Redox Signal; 2009 Jul; 11(7):1535-45. PubMed ID: 19344250
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypoxia causes autophagic stress and derangement of metabolic adaptation in a cell model of amyotrophic lateral sclerosis.
    Cimini S; Rizzardini M; Biella G; Cantoni L
    J Neurochem; 2014 May; 129(3):413-25. PubMed ID: 24359187
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.
    Li QX; Mok SS; Laughton KM; McLean CA; Volitakis I; Cherny RA; Cheung NS; White AR; Masters CL
    Aging Cell; 2006 Apr; 5(2):153-65. PubMed ID: 16626394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Zinc pre-treatment enhances NMDAR-mediated excitotoxicity in cultured cortical neurons from SOD1(G93A) mouse, a model of amyotrophic lateral sclerosis.
    Nutini M; Frazzini V; Marini C; Spalloni A; Sensi SL; Longone P
    Neuropharmacology; 2011 Jun; 60(7-8):1200-8. PubMed ID: 21056589
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Olfactory ensheathing cell transplantation into spinal cord prolongs the survival of mutant SOD1(G93A) ALS rats through neuroprotection and remyelination.
    Li Y; Bao J; Khatibi NH; Chen L; Wang H; Duan Y; Huang H; Zhou C
    Anat Rec (Hoboken); 2011 May; 294(5):847-57. PubMed ID: 21416627
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosis.
    Nardo G; Iennaco R; Fusi N; Heath PR; Marino M; Trolese MC; Ferraiuolo L; Lawrence N; Shaw PJ; Bendotti C
    Brain; 2013 Nov; 136(Pt 11):3305-32. PubMed ID: 24065725
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trehalose decreases mutant SOD1 expression and alleviates motor deficiency in early but not end-stage amyotrophic lateral sclerosis in a SOD1-G93A mouse model.
    Li Y; Guo Y; Wang X; Yu X; Duan W; Hong K; Wang J; Han H; Li C
    Neuroscience; 2015 Jul; 298():12-25. PubMed ID: 25841320
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Overexpression of human mutated G93A SOD1 changes dynamics of the ER mitochondria calcium cycle specifically in mouse embryonic motor neurons.
    Lautenschläger J; Prell T; Ruhmer J; Weidemann L; Witte OW; Grosskreutz J
    Exp Neurol; 2013 Sep; 247():91-100. PubMed ID: 23578819
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ultrastructural study of mitochondria in the spinal cord of transgenic mice with a G93A mutant SOD1 gene.
    Sasaki S; Warita H; Murakami T; Abe K; Iwata M
    Acta Neuropathol; 2004 May; 107(5):461-74. PubMed ID: 15029445
    [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. Altered miRNA expression is associated with neuronal fate in G93A-SOD1 ependymal stem progenitor cells.
    Marcuzzo S; Kapetis D; Mantegazza R; Baggi F; Bonanno S; Barzago C; Cavalcante P; Kerlero de Rosbo N; Bernasconi P
    Exp Neurol; 2014 Mar; 253():91-101. PubMed ID: 24365539
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dysregulation of iron protein expression in the G93A model of amyotrophic lateral sclerosis.
    Hadzhieva M; Kirches E; Wilisch-Neumann A; Pachow D; Wallesch M; Schoenfeld P; Paege I; Vielhaber S; Petri S; Keilhoff G; Mawrin C
    Neuroscience; 2013 Jan; 230():94-101. PubMed ID: 23178912
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cell culture models to investigate the selective vulnerability of motoneuronal mitochondria to familial ALS-linked G93ASOD1.
    Raimondi A; Mangolini A; Rizzardini M; Tartari S; Massari S; Bendotti C; Francolini M; Borgese N; Cantoni L; Pietrini G
    Eur J Neurosci; 2006 Jul; 24(2):387-99. PubMed ID: 16903849
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.