154 related articles for article (PubMed ID: 16616851)
1. Bioenergetic abnormalities in discrete cerebral motor pathways presage spinal cord pathology in the G93A SOD1 mouse model of ALS.
Browne SE; Yang L; DiMauro JP; Fuller SW; Licata SC; Beal MF
Neurobiol Dis; 2006 Jun; 22(3):599-610. PubMed ID: 16616851
[TBL] [Abstract][Full Text] [Related]
2. Degeneration of axons in spinal white matter in G93A mSOD1 mouse characterized by NFL and α-internexin immunoreactivity.
King AE; Blizzard CA; Southam KA; Vickers JC; Dickson TC
Brain Res; 2012 Jul; 1465():90-100. PubMed ID: 22609817
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Degeneration of corticospinal and bulbospinal systems in the superoxide dismutase 1(G93A G1H) transgenic mouse model of familial amyotrophic lateral sclerosis.
Zang DW; Cheema SS
Neurosci Lett; 2002 Oct; 332(2):99-102. PubMed ID: 12384220
[TBL] [Abstract][Full Text] [Related]
5. Depletion of reduced glutathione enhances motor neuron degeneration in vitro and in vivo.
Chi L; Ke Y; Luo C; Gozal D; Liu R
Neuroscience; 2007 Feb; 144(3):991-1003. PubMed ID: 17150307
[TBL] [Abstract][Full Text] [Related]
6. Altered glucose catabolism in the presynaptic and perisynaptic compartments of SOD1
Ravera S; Torazza C; Bonifacino T; Provenzano F; Rebosio C; Milanese M; Usai C; Panfoli I; Bonanno G
J Neurochem; 2019 Nov; 151(3):336-350. PubMed ID: 31282572
[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. Disease-related regressive alterations of forebrain cholinergic system in SOD1 mutant transgenic mice.
Crochemore C; Peña-Altamira E; Virgili M; Monti B; Contestabile A
Neurochem Int; 2005 Apr; 46(5):357-68. PubMed ID: 15737434
[TBL] [Abstract][Full Text] [Related]
9. Activation of Phosphotyrosine-Mediated Signaling Pathways in the Cortex and Spinal Cord of SOD1
Mallozzi C; Spalloni A; Longone P; Domenici MR
Neural Plast; 2018; 2018():2430193. PubMed ID: 30154836
[TBL] [Abstract][Full Text] [Related]
10. Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis.
Niessen HG; Debska-Vielhaber G; Sander K; Angenstein F; Ludolph AC; Hilfert L; Willker W; Leibfritz D; Heinze HJ; Kunz WS; Vielhaber S
Eur J Neurosci; 2007 Mar; 25(6):1669-77. PubMed ID: 17432958
[TBL] [Abstract][Full Text] [Related]
11. Presymptomatic activation of the PDGF-CC pathway accelerates onset of ALS neurodegeneration.
Lewandowski SA; Nilsson I; Fredriksson L; Lönnerberg P; Muhl L; Zeitelhofer M; Adzemovic MZ; Nichterwitz S; Lawrence DA; Hedlund E; Eriksson U
Acta Neuropathol; 2016 Mar; 131(3):453-64. PubMed ID: 26687981
[TBL] [Abstract][Full Text] [Related]
12. Characterization of the Mitochondrial Aerobic Metabolism in the Pre- and Perisynaptic Districts of the SOD1
Ravera S; Bonifacino T; Bartolucci M; Milanese M; Gallia E; Provenzano F; Cortese K; Panfoli I; Bonanno G
Mol Neurobiol; 2018 Dec; 55(12):9220-9233. PubMed ID: 29656361
[TBL] [Abstract][Full Text] [Related]
13. Expression of heat shock transcription factor 1 and its downstream target protein T-cell death associated gene 51 in the spinal cord of a mouse model of amyotrophic lateral sclerosis.
Mimoto T; Morimoto N; Miyazaki K; Kurata T; Sato K; Ikeda Y; Abe K
Brain Res; 2012 Dec; 1488():123-31. PubMed ID: 23063459
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Corticospinal motor neurons and related subcerebral projection neurons undergo early and specific neurodegeneration in hSOD1G⁹³A transgenic ALS mice.
Ozdinler PH; Benn S; Yamamoto TH; Güzel M; Brown RH; Macklis JD
J Neurosci; 2011 Mar; 31(11):4166-77. PubMed ID: 21411657
[TBL] [Abstract][Full Text] [Related]
16. Lack of changes in the PI3K/AKT survival pathway in the spinal cord motor neurons of a mouse model of familial amyotrophic lateral sclerosis.
Peviani M; Cheroni C; Troglio F; Quarto M; Pelicci G; Bendotti C
Mol Cell Neurosci; 2007 Apr; 34(4):592-602. PubMed ID: 17303436
[TBL] [Abstract][Full Text] [Related]
17. Relationship of oxygen radical-induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALS.
Hall ED; Andrus PK; Oostveen JA; Fleck TJ; Gurney ME
J Neurosci Res; 1998 Jul; 53(1):66-77. PubMed ID: 9670993
[TBL] [Abstract][Full Text] [Related]
18. Early signs of motoneuron vulnerability in a disease model system: Characterization of transverse slice cultures of spinal cord isolated from embryonic ALS mice.
Avossa D; Grandolfo M; Mazzarol F; Zatta M; Ballerini L
Neuroscience; 2006; 138(4):1179-94. PubMed ID: 16442737
[TBL] [Abstract][Full Text] [Related]
19. Absence of p53: no effect in a transgenic mouse model of familial amyotrophic lateral sclerosis.
Kuntz C; Kinoshita Y; Beal MF; Donehower LA; Morrison RS
Exp Neurol; 2000 Sep; 165(1):184-90. PubMed ID: 10964497
[TBL] [Abstract][Full Text] [Related]
20. Memantine prolongs survival in an amyotrophic lateral sclerosis mouse model.
Wang R; Zhang D
Eur J Neurosci; 2005 Nov; 22(9):2376-80. PubMed ID: 16262676
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
