BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

443 related articles for article (PubMed ID: 31500113)

  • 1. Gene Therapy for ALS-A Perspective.
    Cappella M; Ciotti C; Cohen-Tannoudji M; Biferi MG
    Int J Mol Sci; 2019 Sep; 20(18):. PubMed ID: 31500113
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Approaches to Gene Modulation Therapy for ALS.
    Meijboom KE; Brown RH
    Neurotherapeutics; 2022 Jul; 19(4):1159-1179. PubMed ID: 36068427
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model.
    Biferi MG; Cohen-Tannoudji M; Cappelletto A; Giroux B; Roda M; Astord S; Marais T; Bos C; Voit T; Ferry A; Barkats M
    Mol Ther; 2017 Sep; 25(9):2038-2052. PubMed ID: 28663100
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Beyond the Traditional Clinical Trials for Amyotrophic Lateral Sclerosis and The Future Impact of Gene Therapy.
    Cappella M; Pradat PF; Querin G; Biferi MG
    J Neuromuscul Dis; 2021; 8(1):25-38. PubMed ID: 33074186
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. In vivo genome editing improves motor function and extends survival in a mouse model of ALS.
    Gaj T; Ojala DS; Ekman FK; Byrne LC; Limsirichai P; Schaffer DV
    Sci Adv; 2017 Dec; 3(12):eaar3952. PubMed ID: 29279867
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 116(29):14755-14760. PubMed ID: 31262807
    [TBL] [Abstract][Full Text] [Related]  

  • 8. From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis.
    Alrafiah AR
    In Vivo; 2018; 32(5):983-998. PubMed ID: 30150420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene Therapy in Amyotrophic Lateral Sclerosis.
    Fang T; Je G; Pacut P; Keyhanian K; Gao J; Ghasemi M
    Cells; 2022 Jun; 11(13):. PubMed ID: 35805149
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gene therapy for ALS: A review.
    Amado DA; Davidson BL
    Mol Ther; 2021 Dec; 29(12):3345-3358. PubMed ID: 33839324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosis.
    Nizzardo M; Simone C; Falcone M; Riboldi G; Rizzo F; Magri F; Bresolin N; Comi GP; Corti S
    Cell Mol Life Sci; 2012 May; 69(10):1641-50. PubMed ID: 22094924
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Intracerebroventricular Delivery in Mice for Motor Neuron Diseases.
    Nizzardo M; Rizzuti M
    Methods Mol Biol; 2017; 1565():229-239. PubMed ID: 28364247
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Therapeutic tools for familial ALS.
    Camu W; De La Cruz E; Esselin F
    Rev Neurol (Paris); 2023; 179(1-2):49-53. PubMed ID: 36503675
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dysregulation of AMPA receptor subunit expression in sporadic ALS post-mortem brain.
    Gregory JM; Livesey MR; McDade K; Selvaraj BT; Barton SK; Chandran S; Smith C
    J Pathol; 2020 Jan; 250(1):67-78. PubMed ID: 31579943
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial Amyotrophic Lateral Sclerosis].
    Suzuki N; Nishiyama A; Kato M; Warita H; Aoki M
    Brain Nerve; 2019 Nov; 71(11):1169-1181. PubMed ID: 31722303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gene Therapy for ALS: progress and prospects.
    Azzouz M
    Biochim Biophys Acta; 2006; 1762(11-12):1122-7. PubMed ID: 16806843
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Risk Factors and Emerging Therapies in Amyotrophic Lateral Sclerosis.
    Nowicka N; Juranek J; Juranek JK; Wojtkiewicz J
    Int J Mol Sci; 2019 May; 20(11):. PubMed ID: 31141951
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Viral delivery of antioxidant genes as a therapeutic strategy in experimental models of amyotrophic lateral sclerosis.
    Nanou A; Higginbottom A; Valori CF; Wyles M; Ning K; Shaw P; Azzouz M
    Mol Ther; 2013 Aug; 21(8):1486-96. PubMed ID: 23732987
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 23(3):668-81. PubMed ID: 24108104
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Gene-specific treatment approaches in amyotrophic lateral sclerosis in the present and future].
    Brenner D; Freischmidt A; Ludolph AC; Weishaupt JH
    Nervenarzt; 2020 Apr; 91(4):287-293. PubMed ID: 32076756
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.