BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 18702691)

  • 1. Sex-specific behavioural effects of environmental enrichment in a transgenic mouse model of amyotrophic lateral sclerosis.
    Stam NC; Nithianantharajah J; Howard ML; Atkin JD; Cheema SS; Hannan AJ
    Eur J Neurosci; 2008 Aug; 28(4):717-23. PubMed ID: 18702691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel behavioural characteristics of the superoxide dismutase 1 G93A (SOD1
    Kreilaus F; Guerra S; Masanetz R; Menne V; Yerbury J; Karl T
    Genes Brain Behav; 2020 Feb; 19(2):e12604. PubMed ID: 31412164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Motor neuron dysfunction in a mouse model of ALS: gender-dependent effect of P2X7 antagonism.
    Cervetto C; Frattaroli D; Maura G; Marcoli M
    Toxicology; 2013 Sep; 311(1-2):69-77. PubMed ID: 23583883
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Behavioural effects of cage systems on the G93A Superoxide Dismutase 1 transgenic mouse model for amyotrophic lateral sclerosis.
    Guerra S; Chung R; Yerbury J; Karl T
    Genes Brain Behav; 2021 Jun; 20(5):e12735. PubMed ID: 33871173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient.
    Niessen HG; Angenstein F; Sander K; Kunz WS; Teuchert M; Ludolph AC; Heinze HJ; Scheich H; Vielhaber S
    Exp Neurol; 2006 Oct; 201(2):293-300. PubMed ID: 16740261
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Significance of behavioural tests in a transgenic mouse model of amyotrophic lateral sclerosis (ALS).
    Knippenberg S; Thau N; Dengler R; Petri S
    Behav Brain Res; 2010 Nov; 213(1):82-7. PubMed ID: 20450936
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice.
    Teuling E; van Dis V; Wulf PS; Haasdijk ED; Akhmanova A; Hoogenraad CC; Jaarsma D
    Hum Mol Genet; 2008 Sep; 17(18):2849-62. PubMed ID: 18579581
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Serial in vivo imaging of transplanted allogeneic neural stem cell survival in a mouse model of amyotrophic lateral sclerosis.
    Srivastava AK; Gross SK; Almad AA; Bulte CA; Maragakis NJ; Bulte JWM
    Exp Neurol; 2017 Mar; 289():96-102. PubMed ID: 28038988
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Therapeutic immunization with a glatiramer acetate derivative does not alter survival in G93A and G37R SOD1 mouse models of familial ALS.
    Haenggeli C; Julien JP; Mosley RL; Perez N; Dhar A; Gendelman HE; Rothstein JD
    Neurobiol Dis; 2007 Apr; 26(1):146-52. PubMed ID: 17276077
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effects of environmental enrichment on the amyotrophic lateral sclerosis mouse model.
    Sorrells AD; Corcoran-Gomez K; Eckert KA; Fahey AG; Hoots BL; Charleston LB; Charleston JS; Roberts CR; Markowitz H
    Lab Anim; 2009 Apr; 43(2):182-90. PubMed ID: 19246505
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A role for the urokinase-type plasminogen activator system in amyotrophic lateral sclerosis.
    Glas M; Popp B; Angele B; Koedel U; Chahli C; Schmalix WA; Anneser JM; Pfister HW; Lorenzl S
    Exp Neurol; 2007 Oct; 207(2):350-6. PubMed ID: 17716658
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early motor and electrophysiological changes in transgenic mouse model of amyotrophic lateral sclerosis and gender differences on clinical outcome.
    Alves CJ; de Santana LP; dos Santos AJ; de Oliveira GP; Duobles T; Scorisa JM; Martins RS; Maximino JR; Chadi G
    Brain Res; 2011 Jun; 1394():90-104. PubMed ID: 21354109
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ascending neuropathology in the CNS of a mutant SOD1 mouse model of amyotrophic lateral sclerosis.
    Leichsenring A; Linnartz B; Zhu XR; Lübbert H; Stichel CC
    Brain Res; 2006 Jun; 1096(1):180-95. PubMed ID: 16737688
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The effect of peripheral nerve injury on disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Sharp PS; Dick JR; Greensmith L
    Neuroscience; 2005; 130(4):897-910. PubMed ID: 15652988
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Increased anxiety-like behavior and selective learning impairments are concomitant to loss of hippocampal interneurons in the presymptomatic SOD1(G93A) ALS mouse model.
    Quarta E; Bravi R; Scambi I; Mariotti R; Minciacchi D
    J Comp Neurol; 2015 Aug; 523(11):1622-38. PubMed ID: 25684566
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Optimal methods to characterize the G93A mouse model of ALS.
    Miana-Mena FJ; Muñoz MJ; Yagüe G; Mendez M; Moreno M; Ciriza J; Zaragoza P; Osta R
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Mar; 6(1):55-62. PubMed ID: 16036427
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Muscle-derived but not centrally derived transgene GDNF is neuroprotective in G93A-SOD1 mouse model of ALS.
    Li W; Brakefield D; Pan Y; Hunter D; Myckatyn TM; Parsadanian A
    Exp Neurol; 2007 Feb; 203(2):457-71. PubMed ID: 17034790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protective effects of heat shock protein 27 in a model of ALS occur in the early stages of disease progression.
    Sharp PS; Akbar MT; Bouri S; Senda A; Joshi K; Chen HJ; Latchman DS; Wells DJ; de Belleroche J
    Neurobiol Dis; 2008 Apr; 30(1):42-55. PubMed ID: 18255302
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.