BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 11396274)

  • 1. Neurochemistry of SOD1 and familial amyotrophic lateral sclerosis.
    Carrì MT; Ceroni M; Ferri A; Gabbianelli R; Casciati A; Costa A
    Funct Neurol; 2001; 16(1):73-82. PubMed ID: 11396274
    [No Abstract]   [Full Text] [Related]  

  • 2. Cell death in amyotrophic lateral sclerosis: interplay between neuronal and glial cells.
    Ferri A; Nencini M; Casciati A; Cozzolino M; Angelini DF; Longone P; Spalloni A; Rotilio G; Carrì MT
    FASEB J; 2004 Aug; 18(11):1261-3. PubMed ID: 15208263
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Normal complement of motor units in asymptomatic familial (SOD1 mutation) amyotrophic lateral sclerosis carriers.
    Aggarwal A; Nicholson G
    J Neurol Neurosurg Psychiatry; 2001 Oct; 71(4):478-81. PubMed ID: 11561030
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mouse motor neuron disease caused by truncated SOD1 with or without C-terminal modification.
    Watanabe Y; Yasui K; Nakano T; Doi K; Fukada Y; Kitayama M; Ishimoto M; Kurihara S; Kawashima M; Fukuda H; Adachi Y; Inoue T; Nakashima K
    Brain Res Mol Brain Res; 2005 Apr; 135(1-2):12-20. PubMed ID: 15857664
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial amyotrophic lateral sclerosis (FALS): Emerging hints from redox proteomics. Highlight commentary on: "Redox proteomics analysis of oxidatively modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis".
    Dalle-Donne I
    Free Radic Biol Med; 2007 Jul; 43(2):157-9. PubMed ID: 17603924
    [No Abstract]   [Full Text] [Related]  

  • 6. Detection method of the adjacent motor neuronal death in an in vitro co-culture model of familial ALS-associated Cu/Zn superoxide dismutase.
    Park KS; Kim HJ; Choi WJ; Kim M; Lee KW
    Biotechnol Lett; 2004 Aug; 26(15):1201-5. PubMed ID: 15289674
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria.
    Pasinelli P; Belford ME; Lennon N; Bacskai BJ; Hyman BT; Trotti D; Brown RH
    Neuron; 2004 Jul; 43(1):19-30. PubMed ID: 15233914
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Restricted expression of mutant SOD1 in spinal motor neurons and interneurons induces motor neuron pathology.
    Wang L; Sharma K; Deng HX; Siddique T; Grisotti G; Liu E; Roos RP
    Neurobiol Dis; 2008 Mar; 29(3):400-8. PubMed ID: 18054242
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.
    Subramaniam JR; Lyons WE; Liu J; Bartnikas TB; Rothstein J; Price DL; Cleveland DW; Gitlin JD; Wong PC
    Nat Neurosci; 2002 Apr; 5(4):301-7. PubMed ID: 11889469
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Good science shows the way. Highlight Commentary on "Redox proteomics analysis of oxidatively modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis".
    Estévez AG
    Free Radic Biol Med; 2007 Jul; 43(2):163-4. PubMed ID: 17603926
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Reduction of axonal caliber does not alleviate motor neuron disease caused by mutant superoxide dismutase 1.
    Nguyen MD; Larivière RC; Julien JP
    Proc Natl Acad Sci U S A; 2000 Oct; 97(22):12306-11. PubMed ID: 11050249
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).
    Howland DS; Liu J; She Y; Goad B; Maragakis NJ; Kim B; Erickson J; Kulik J; DeVito L; Psaltis G; DeGennaro LJ; Cleveland DW; Rothstein JD
    Proc Natl Acad Sci U S A; 2002 Feb; 99(3):1604-9. PubMed ID: 11818550
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Primary lateral sclerosis as a phenotypic manifestation of familial ALS.
    Brugman F; Wokke JH; Vianney de Jong JM; Franssen H; Faber CG; Van den Berg LH
    Neurology; 2005 May; 64(10):1778-9. PubMed ID: 15911810
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Motor neuron disease in transgenic mice with an H46R mutant SOD1 gene.
    Sasaki S; Nagai M; Aoki M; Komori T; Itoyama Y; Iwata M
    J Neuropathol Exp Neurol; 2007 Jun; 66(6):517-24. PubMed ID: 17549011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Retrograde axonal transport and motor neuron disease.
    Ström AL; Gal J; Shi P; Kasarskis EJ; Hayward LJ; Zhu H
    J Neurochem; 2008 Jul; 106(2):495-505. PubMed ID: 18384644
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Highlight Commentary on "Redox proteomics analysis of oxidatively modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis".
    Calabrese V
    Free Radic Biol Med; 2007 Jul; 43(2):160-2. PubMed ID: 17603925
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synaptic sprouting increases the uptake capacities of motoneurons in amyotrophic lateral sclerosis mice.
    Millecamps S; Nicolle D; Ceballos-Picot I; Mallet J; Barkats M
    Proc Natl Acad Sci U S A; 2001 Jun; 98(13):7582-7. PubMed ID: 11404466
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.