BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 20637744)

  • 1. Ultrastructural diversity of inclusions and aggregations in the lumbar spinal cord of SOD1-G93A transgenic mice.
    Guo Y; Li C; Wu D; Wu S; Yang C; Liu Y; Wu H; Li Z
    Brain Res; 2010 Sep; 1353():234-44. PubMed ID: 20637744
    [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. Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation.
    Zhang B; Tu P; Abtahian F; Trojanowski JQ; Lee VM
    J Cell Biol; 1997 Dec; 139(5):1307-15. PubMed ID: 9382875
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosis.
    Marcuzzo S; Bonanno S; Figini M; Scotti A; Zucca I; Minati L; Riva N; Domi T; Fossaghi A; Quattrini A; Galbardi B; D'Alessandro S; Bruzzone MG; García-Verdugo JM; Moreno-Manzano V; Mantegazza R; Bernasconi P
    Exp Neurol; 2017 Jul; 293():43-52. PubMed ID: 28351750
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An astrocyte regenerative response from vimentin-containing cells in the spinal cord of amyotrophic lateral sclerosis's disease-like transgenic (G93A SOD1) mice.
    Zhou Y; Lu Y; Fang X; Zhang J; Li J; Li S; Deng X; Yu Y; Xu R
    Neurodegener Dis; 2015; 15(1):1-12. PubMed ID: 25591625
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS.
    Shan X; Vocadlo D; Krieger C
    Neurosci Lett; 2009 Jul; 458(2):70-4. PubMed ID: 19379791
    [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. Ultrastructure of blood-brain barrier and blood-spinal cord barrier in SOD1 mice modeling ALS.
    Garbuzova-Davis S; Haller E; Saporta S; Kolomey I; Nicosia SV; Sanberg PR
    Brain Res; 2007 Jul; 1157():126-37. PubMed ID: 17512910
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.
    Tu PH; Raju P; Robinson KA; Gurney ME; Trojanowski JQ; Lee VM
    Proc Natl Acad Sci U S A; 1996 Apr; 93(7):3155-60. PubMed ID: 8610185
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transcriptional profiling in the lumbar spinal cord of a mouse model of amyotrophic lateral sclerosis: a role for wild-type superoxide dismutase 1 in sporadic disease?
    D'Arrigo A; Colavito D; Peña-Altamira E; Fabris M; Dam M; Contestabile A; Leon A
    J Mol Neurosci; 2010 Jul; 41(3):404-15. PubMed ID: 20177826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity.
    Bendotti C; Calvaresi N; Chiveri L; Prelle A; Moggio M; Braga M; Silani V; De Biasi S
    J Neurol Sci; 2001 Oct; 191(1-2):25-33. PubMed ID: 11676989
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Endocannabinoids accumulate in spinal cord of SOD1 G93A transgenic mice.
    Witting A; Weydt P; Hong S; Kliot M; Moller T; Stella N
    J Neurochem; 2004 Jun; 89(6):1555-7. PubMed ID: 15189359
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.
    Bruijn LI; Becher MW; Lee MK; Anderson KL; Jenkins NA; Copeland NG; Sisodia SS; Rothstein JD; Borchelt DR; Price DL; Cleveland DW
    Neuron; 1997 Feb; 18(2):327-38. PubMed ID: 9052802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurovascular unit pathology is observed very early in disease progression in the mutant SOD1
    Yoshikawa M; Aizawa S; Oppenheim RW; Milligan C
    Exp Neurol; 2022 Jul; 353():114084. PubMed ID: 35439439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Magnetic resonance microimaging of the spinal cord in the SOD1 mouse model of amyotrophic lateral sclerosis detects motor nerve root degeneration.
    Cowin GJ; Butler TJ; Kurniawan ND; Watson C; Wallace RH
    Neuroimage; 2011 Sep; 58(1):69-74. PubMed ID: 21689764
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GAB(A) receptors present higher affinity and modified subunit composition in spinal motor neurons from a genetic model of amyotrophic lateral sclerosis.
    Carunchio I; Mollinari C; Pieri M; Merlo D; Zona C
    Eur J Neurosci; 2008 Oct; 28(7):1275-85. PubMed ID: 18973555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Metallothionein expression is altered in a transgenic murine model of familial amyotrophic lateral sclerosis.
    Gong YH; Elliott JL
    Exp Neurol; 2000 Mar; 162(1):27-36. PubMed ID: 10716886
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.