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Journal Abstract Search

283 related items for PubMed ID: 25228069

  • 1. Widespread and efficient transduction of spinal cord and brain following neonatal AAV injection and potential disease modifying effect in ALS mice.
    Ayers JI, Fromholt S, Sinyavskaya O, Siemienski Z, Rosario AM, Li A, Crosby KW, Cruz PE, DiNunno NM, Janus C, Ceballos-Diaz C, Borchelt DR, Golde TE, Chakrabarty P, Levites Y.
    Mol Ther; 2015 Jan; 23(1):53-62. PubMed ID: 25228069
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  • 3. Widespread spinal cord transduction by intrathecal injection of rAAV delivers efficacious RNAi therapy for amyotrophic lateral sclerosis.
    Wang H, Yang B, Qiu L, Yang C, Kramer J, Su Q, Guo Y, Brown RH, Gao G, Xu Z.
    Hum Mol Genet; 2014 Feb 01; 23(3):668-81. PubMed ID: 24108104
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  • 5. GLT1 overexpression in SOD1(G93A) mouse cervical spinal cord does not preserve diaphragm function or extend disease.
    Li K, Hala TJ, Seetharam S, Poulsen DJ, Wright MC, Lepore AC.
    Neurobiol Dis; 2015 Jun 01; 78():12-23. PubMed ID: 25818008
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  • 7. Adeno-associated virus-delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model.
    Stoica L, Todeasa SH, Cabrera GT, Salameh JS, ElMallah MK, Mueller C, Brown RH, Sena-Esteves M.
    Ann Neurol; 2016 Apr 01; 79(4):687-700. PubMed ID: 26891182
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  • 9. Adeno-associated virus-mediated delivery of a recombinant single-chain antibody against misfolded superoxide dismutase for treatment of amyotrophic lateral sclerosis.
    Patel P, Kriz J, Gravel M, Soucy G, Bareil C, Gravel C, Julien JP.
    Mol Ther; 2014 Mar 01; 22(3):498-510. PubMed ID: 24394188
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  • 11. Therapeutic AAV9-mediated suppression of mutant SOD1 slows disease progression and extends survival in models of inherited ALS.
    Foust KD, Salazar DL, Likhite S, Ferraiuolo L, Ditsworth D, Ilieva H, Meyer K, Schmelzer L, Braun L, Cleveland DW, Kaspar BK.
    Mol Ther; 2013 Dec 01; 21(12):2148-59. PubMed ID: 24008656
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  • 13. AAV2/9-mediated overexpression of MIF inhibits SOD1 misfolding, delays disease onset, and extends survival in mouse models of ALS.
    Leyton-Jaimes MF, Kahn J, Israelson A.
    Proc Natl Acad Sci U S A; 2019 Jul 16; 116(29):14755-14760. PubMed ID: 31262807
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  • 17. Intrathecal delivery of AAV-NDNF ameliorates disease progression of ALS mice.
    Cheng W, Huang J, Fu XQ, Tian WY, Zeng PM, Li Y, Luo ZG.
    Mol Ther; 2023 Nov 01; 31(11):3277-3289. PubMed ID: 37766430
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  • 18. Differential effects of mutant SOD1 on protein structure of skeletal muscle and spinal cord of familial amyotrophic lateral sclerosis: role of chaperone network.
    Wei R, Bhattacharya A, Hamilton RT, Jernigan AL, Chaudhuri AR.
    Biochem Biophys Res Commun; 2013 Aug 16; 438(1):218-23. PubMed ID: 23886956
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