160 related articles for article (PubMed ID: 11555629)
1. Protective effects of cardiotrophin-1 adenoviral gene transfer on neuromuscular degeneration in transgenic ALS mice.
Bordet T; Lesbordes JC; Rouhani S; Castelnau-Ptakhine L; Schmalbruch H; Haase G; Kahn A
Hum Mol Genet; 2001 Sep; 10(18):1925-33. PubMed ID: 11555629
[TBL] [Abstract][Full Text] [Related]
2. Neuroprotective effects of glial cell line-derived neurotrophic factor mediated by an adeno-associated virus vector in a transgenic animal model of amyotrophic lateral sclerosis.
Wang LJ; Lu YY; Muramatsu S; Ikeguchi K; Fujimoto K; Okada T; Mizukami H; Matsushita T; Hanazono Y; Kume A; Nagatsu T; Ozawa K; Nakano I
J Neurosci; 2002 Aug; 22(16):6920-8. PubMed ID: 12177190
[TBL] [Abstract][Full Text] [Related]
3. Therapeutic benefits of cardiotrophin-1 gene transfer in a mouse model of spinal muscular atrophy.
Lesbordes JC; Cifuentes-Diaz C; Miroglio A; Joshi V; Bordet T; Kahn A; Melki J
Hum Mol Genet; 2003 Jun; 12(11):1233-9. PubMed ID: 12761038
[TBL] [Abstract][Full Text] [Related]
4. Glycoprotein nonmetastatic melanoma protein B ameliorates skeletal muscle lesions in a SOD1G93A mouse model of amyotrophic lateral sclerosis.
Nagahara Y; Shimazawa M; Tanaka H; Ono Y; Noda Y; Ohuchi K; Tsuruma K; Katsuno M; Sobue G; Hara H
J Neurosci Res; 2015 Oct; 93(10):1552-66. PubMed ID: 26140698
[TBL] [Abstract][Full Text] [Related]
5. Increased survival and function of SOD1 mice after glial cell-derived neurotrophic factor gene therapy.
Acsadi G; Anguelov RA; Yang H; Toth G; Thomas R; Jani A; Wang Y; Ianakova E; Mohammad S; Lewis RA; Shy ME
Hum Gene Ther; 2002 Jun; 13(9):1047-59. PubMed ID: 12067438
[TBL] [Abstract][Full Text] [Related]
6. L-carnitine suppresses the onset of neuromuscular degeneration and increases the life span of mice with familial amyotrophic lateral sclerosis.
Kira Y; Nishikawa M; Ochi A; Sato E; Inoue M
Brain Res; 2006 Jan; 1070(1):206-14. PubMed ID: 16412993
[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. Expression of adenovirus-mediated E. coli lacZ gene in skeletal muscles and spinal motor neurons of transgenic mice with a mutant superoxide dismutase gene.
Warita H; Abe K; Setoguchi Y; Itoyama Y
Neurosci Lett; 1998 May; 246(3):153-6. PubMed ID: 9792615
[TBL] [Abstract][Full Text] [Related]
9. Intramuscular grafts of myoblasts genetically modified to secrete glial cell line-derived neurotrophic factor prevent motoneuron loss and disease progression in a mouse model of familial amyotrophic lateral sclerosis.
Mohajeri MH; Figlewicz DA; Bohn MC
Hum Gene Ther; 1999 Jul; 10(11):1853-66. PubMed ID: 10446925
[TBL] [Abstract][Full Text] [Related]
10. Macrophage-mediated inflammation and glial response in the skeletal muscle of a rat model of familial amyotrophic lateral sclerosis (ALS).
Van Dyke JM; Smit-Oistad IM; Macrander C; Krakora D; Meyer MG; Suzuki M
Exp Neurol; 2016 Mar; 277():275-282. PubMed ID: 26775178
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors.
Haase G; Kennel P; Pettmann B; Vigne E; Akli S; Revah F; Schmalbruch H; Kahn A
Nat Med; 1997 Apr; 3(4):429-36. PubMed ID: 9095177
[TBL] [Abstract][Full Text] [Related]
14. VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model.
Azzouz M; Ralph GS; Storkebaum E; Walmsley LE; Mitrophanous KA; Kingsman SM; Carmeliet P; Mazarakis ND
Nature; 2004 May; 429(6990):413-7. PubMed ID: 15164063
[TBL] [Abstract][Full Text] [Related]
15. Increased motoneuron survival and improved neuromuscular function in transgenic ALS mice after intraspinal injection of an adeno-associated virus encoding Bcl-2.
Azzouz M; Hottinger A; Paterna JC; Zurn AD; Aebischer P; Büeler H
Hum Mol Genet; 2000 Mar; 9(5):803-11. PubMed ID: 10749988
[TBL] [Abstract][Full Text] [Related]
16. Spinal subpial delivery of AAV9 enables widespread gene silencing and blocks motoneuron degeneration in ALS.
Bravo-Hernandez M; Tadokoro T; Navarro MR; Platoshyn O; Kobayashi Y; Marsala S; Miyanohara A; Juhas S; Juhasova J; Skalnikova H; Tomori Z; Vanicky I; Studenovska H; Proks V; Chen P; Govea-Perez N; Ditsworth D; Ciacci JD; Gao S; Zhu W; Ahrens ET; Driscoll SP; Glenn TD; McAlonis-Downes M; Da Cruz S; Pfaff SL; Kaspar BK; Cleveland DW; Marsala M
Nat Med; 2020 Jan; 26(1):118-130. PubMed ID: 31873312
[TBL] [Abstract][Full Text] [Related]
17. Progressive impairment of CaV1.1 function in the skeletal muscle of mice expressing a mutant type 1 Cu/Zn superoxide dismutase (G93A) linked to amyotrophic lateral sclerosis.
Beqollari D; Romberg CF; Dobrowolny G; Martini M; Voss AA; Musarò A; Bannister RA
Skelet Muscle; 2016; 6():24. PubMed ID: 27340545
[TBL] [Abstract][Full Text] [Related]
18.
Miyoshi S; Tezuka T; Arimura S; Tomono T; Okada T; Yamanashi Y
EMBO Mol Med; 2017 Jul; 9(7):880-889. PubMed ID: 28490573
[TBL] [Abstract][Full Text] [Related]
19. Dihydrotestosterone ameliorates degeneration in muscle, axons and motoneurons and improves motor function in amyotrophic lateral sclerosis model mice.
Yoo YE; Ko CP
PLoS One; 2012; 7(5):e37258. PubMed ID: 22606355
[TBL] [Abstract][Full Text] [Related]
20. Time course of preferential motor unit loss in the SOD1 G93A mouse model of amyotrophic lateral sclerosis.
Hegedus J; Putman CT; Gordon T
Neurobiol Dis; 2007 Nov; 28(2):154-64. PubMed ID: 17766128
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
