BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

362 related articles for article (PubMed ID: 18797452)

  • 21. Analysis of neurotrophic factors in limb and extraocular muscles of mouse model of amyotrophic lateral sclerosis.
    Harandi VM; Lindquist S; Kolan SS; Brännström T; Liu JX
    PLoS One; 2014; 9(10):e109833. PubMed ID: 25334047
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Specific Expression of Glial-Derived Neurotrophic Factor in Muscles as Gene Therapy Strategy for Amyotrophic Lateral Sclerosis.
    Mòdol-Caballero G; García-Lareu B; Herrando-Grabulosa M; Verdés S; López-Vales R; Pagès G; Chillón M; Navarro X; Bosch A
    Neurotherapeutics; 2021 Apr; 18(2):1113-1126. PubMed ID: 33786805
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Activation of mGlu3 metabotropic glutamate receptors enhances GDNF and GLT-1 formation in the spinal cord and rescues motor neurons in the SOD-1 mouse model of amyotrophic lateral sclerosis.
    Battaglia G; Riozzi B; Bucci D; Di Menna L; Molinaro G; Pallottino S; Nicoletti F; Bruno V
    Neurobiol Dis; 2015 Feb; 74():126-36. PubMed ID: 25434487
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Transplantation of Neural Progenitor Cells Expressing Glial Cell Line-Derived Neurotrophic Factor into the Motor Cortex as a Strategy to Treat Amyotrophic Lateral Sclerosis.
    Thomsen GM; Avalos P; Ma AA; Alkaslasi M; Cho N; Wyss L; Vit JP; Godoy M; Suezaki P; Shelest O; Bankiewicz KS; Svendsen CN
    Stem Cells; 2018 Jul; 36(7):1122-1131. PubMed ID: 29656478
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Systemic injection of AAV9-GDNF provides modest functional improvements in the SOD1
    Thomsen GM; Alkaslasi M; Vit JP; Lawless G; Godoy M; Gowing G; Shelest O; Svendsen CN
    Gene Ther; 2017 Apr; 24(4):245-252. PubMed ID: 28276446
    [TBL] [Abstract][Full Text] [Related]  

  • 26. GDNF is trophic for mouse motoneurons that express a mutant superoxide dismutase (SOD-1) gene.
    Derby ML; Giuliano R; Figlewicz DA; Bohn MC
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2000 Mar; 1(2):113-22. PubMed ID: 11467048
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mesenchymal stromal cells prolong the lifespan in a rat model of amyotrophic lateral sclerosis.
    Forostyak S; Jendelova P; Kapcalova M; Arboleda D; Sykova E
    Cytotherapy; 2011 Oct; 13(9):1036-46. PubMed ID: 21736505
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Human mesenchymal stem cell transplantation extends survival, improves motor performance and decreases neuroinflammation in mouse model of amyotrophic lateral sclerosis.
    Vercelli A; Mereuta OM; Garbossa D; Muraca G; Mareschi K; Rustichelli D; Ferrero I; Mazzini L; Madon E; Fagioli F
    Neurobiol Dis; 2008 Sep; 31(3):395-405. PubMed ID: 18586098
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Transplantation of human neural progenitor cells secreting GDNF into the spinal cord of patients with ALS: a phase 1/2a trial.
    Baloh RH; Johnson JP; Avalos P; Allred P; Svendsen S; Gowing G; Roxas K; Wu A; Donahue B; Osborne S; Lawless G; Shelley B; Wheeler K; Prina C; Fine D; Kendra-Romito T; Stokes H; Manoukian V; Muthukumaran A; Garcia L; Bañuelos MG; Godoy M; Bresee C; Yu H; Drazin D; Ross L; Naruse R; Babu H; Macklin EA; Vo A; Elsayegh A; Tourtellotte W; Maya M; Burford M; Diaz F; Patil CG; Lewis RA; Svendsen CN
    Nat Med; 2022 Sep; 28(9):1813-1822. PubMed ID: 36064599
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pericytes Extend Survival of ALS SOD1 Mice and Induce the Expression of Antioxidant Enzymes in the Murine Model and in IPSCs Derived Neuronal Cells from an ALS Patient.
    Coatti GC; Frangini M; Valadares MC; Gomes JP; Lima NO; Cavaçana N; Assoni AF; Pelatti MV; Birbrair A; de Lima ACP; Singer JM; Rocha FMM; Da Silva GL; Mantovani MS; Macedo-Souza LI; Ferrari MFR; Zatz M
    Stem Cell Rev Rep; 2017 Oct; 13(5):686-698. PubMed ID: 28710685
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Astrocytes show reduced support of motor neurons with aging that is accelerated in a rodent model of ALS.
    Das MM; Svendsen CN
    Neurobiol Aging; 2015 Feb; 36(2):1130-9. PubMed ID: 25443290
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Intravenous infusion of mesenchymal stem cells delays disease progression in the SOD1G93A transgenic amyotrophic lateral sclerosis rat model.
    Magota H; Sasaki M; Kataoka-Sasaki Y; Oka S; Ukai R; Kiyose R; Onodera R; Kocsis JD; Honmou O
    Brain Res; 2021 Apr; 1757():147296. PubMed ID: 33516815
    [TBL] [Abstract][Full Text] [Related]  

  • 33. How to Build and to Protect the Neuromuscular Junction: The Role of the Glial Cell Line-Derived Neurotrophic Factor.
    Stanga S; Boido M; Kienlen-Campard P
    Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33374485
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Neural induction with neurogenin 1 enhances the therapeutic potential of mesenchymal stem cells in an amyotrophic lateral sclerosis mouse model.
    Chan-Il C; Young-Don L; Heejaung K; Kim SH; Suh-Kim H; Kim SS
    Cell Transplant; 2013; 22(5):855-70. PubMed ID: 22472631
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice.
    Teuling E; van Dis V; Wulf PS; Haasdijk ED; Akhmanova A; Hoogenraad CC; Jaarsma D
    Hum Mol Genet; 2008 Sep; 17(18):2849-62. PubMed ID: 18579581
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Empty mesoporous silica particles significantly delay disease progression and extend survival in a mouse model of ALS.
    Leyton-Jaimes MF; Ivert P; Hoeber J; Han Y; Feiler A; Zhou C; Pankratova S; Shoshan-Barmatz V; Israelson A; Kozlova EN
    Sci Rep; 2020 Nov; 10(1):20675. PubMed ID: 33244084
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations.
    Jeon GS; Shim YM; Lee DY; Kim JS; Kang M; Ahn SH; Shin JY; Geum D; Hong YH; Sung JJ
    Mol Neurobiol; 2019 Mar; 56(3):2007-2021. PubMed ID: 29982983
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Human neural progenitors differentiate into astrocytes and protect motor neurons in aging rats.
    Das MM; Avalos P; Suezaki P; Godoy M; Garcia L; Chang CD; Vit JP; Shelley B; Gowing G; Svendsen CN
    Exp Neurol; 2016 Jun; 280():41-9. PubMed ID: 27032721
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Astrocytes from familial and sporadic ALS patients are toxic to motor neurons.
    Haidet-Phillips AM; Hester ME; Miranda CJ; Meyer K; Braun L; Frakes A; Song S; Likhite S; Murtha MJ; Foust KD; Rao M; Eagle A; Kammesheidt A; Christensen A; Mendell JR; Burghes AH; Kaspar BK
    Nat Biotechnol; 2011 Aug; 29(9):824-8. PubMed ID: 21832997
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Unchanged Neurotrophic Factors and Their Receptors Correlate With Sparing in Extraocular Muscles in Amyotrophic Lateral Sclerosis.
    Harandi VM; Gaied AR; Brännström T; Pedrosa Domellöf F; Liu JX
    Invest Ophthalmol Vis Sci; 2016 Dec; 57(15):6831-6842. PubMed ID: 28002846
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.