BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

844 related articles for article (PubMed ID: 25779930)

  • 1. Suppression of adenosine 2a receptor (A2aR)-mediated adenosine signaling improves disease phenotypes in a mouse model of amyotrophic lateral sclerosis.
    Ng SK; Higashimori H; Tolman M; Yang Y
    Exp Neurol; 2015 May; 267():115-22. PubMed ID: 25779930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Changes in adenosine receptors and neurotrophic factors in the SOD1G93A mouse model of amyotrophic lateral sclerosis: Modulation by chronic caffeine.
    Rei N; Valente CA; Vaz SH; Farinha-Ferreira M; Ribeiro JA; Sebastião AM
    PLoS One; 2022; 17(12):e0272104. PubMed ID: 36516126
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Presymptomatic and symptomatic ALS SOD1(G93A) mice differ in adenosine A1 and A2A receptor-mediated tonic modulation of neuromuscular transmission.
    Nascimento F; Sebastião AM; Ribeiro JA
    Purinergic Signal; 2015 Dec; 11(4):471-80. PubMed ID: 26335190
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Endothelin-1 is over-expressed in amyotrophic lateral sclerosis and induces motor neuron cell death.
    Ranno E; D'Antoni S; Spatuzza M; Berretta A; Laureanti F; Bonaccorso CM; Pellitteri R; Longone P; Spalloni A; Iyer AM; Aronica E; Catania MV
    Neurobiol Dis; 2014 May; 65():160-71. PubMed ID: 24423643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hippocampal synaptic dysfunction in the SOD1
    Rei N; Rombo DM; Ferreira MF; Baqi Y; Müller CE; Ribeiro JA; Sebastião AM; Vaz SH
    Neuropharmacology; 2020 Jul; 171():108106. PubMed ID: 32311420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dysregulation of Steroid Hormone Receptors in Motor Neurons and Glia Associates with Disease Progression in ALS Mice.
    McLeod VM; Chiam MDF; Lau CL; Rupasinghe TW; Boon WC; Turner BJ
    Endocrinology; 2020 Sep; 161(9):. PubMed ID: 32621747
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Intranasal delivery of insulin and a nitric oxide synthase inhibitor in an experimental model of amyotrophic lateral sclerosis.
    Martinez JA; Francis GJ; Liu WQ; Pradzinsky N; Fine J; Wilson M; Hanson LR; Frey WH; Zochodne D; Gordon T; Toth C
    Neuroscience; 2008 Dec; 157(4):908-25. PubMed ID: 18951954
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Connexin 43 in astrocytes contributes to motor neuron toxicity in amyotrophic lateral sclerosis.
    Almad AA; Doreswamy A; Gross SK; Richard JP; Huo Y; Haughey N; Maragakis NJ
    Glia; 2016 Jul; 64(7):1154-69. PubMed ID: 27083773
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Extracellular ATP and the P2X7 receptor in astrocyte-mediated motor neuron death: implications for amyotrophic lateral sclerosis.
    Gandelman M; Peluffo H; Beckman JS; Cassina P; Barbeito L
    J Neuroinflammation; 2010 Jun; 7():33. PubMed ID: 20534165
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neuroprotective effects of the Sigma-1 receptor (S1R) agonist PRE-084, in a mouse model of motor neuron disease not linked to SOD1 mutation.
    Peviani M; Salvaneschi E; Bontempi L; Petese A; Manzo A; Rossi D; Salmona M; Collina S; Bigini P; Curti D
    Neurobiol Dis; 2014 Feb; 62():218-32. PubMed ID: 24141020
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 78():12-23. PubMed ID: 25818008
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GAB(A) receptors present higher affinity and modified subunit composition in spinal motor neurons from a genetic model of amyotrophic lateral sclerosis.
    Carunchio I; Mollinari C; Pieri M; Merlo D; Zona C
    Eur J Neurosci; 2008 Oct; 28(7):1275-85. PubMed ID: 18973555
    [TBL] [Abstract][Full Text] [Related]  

  • 13. System xC- is a mediator of microglial function and its deletion slows symptoms in amyotrophic lateral sclerosis mice.
    Mesci P; Zaïdi S; Lobsiger CS; Millecamps S; Escartin C; Seilhean D; Sato H; Mallat M; Boillée S
    Brain; 2015 Jan; 138(Pt 1):53-68. PubMed ID: 25384799
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Astrocytic production of nerve growth factor in motor neuron apoptosis: implications for amyotrophic lateral sclerosis.
    Pehar M; Cassina P; Vargas MR; Castellanos R; Viera L; Beckman JS; Estévez AG; Barbeito L
    J Neurochem; 2004 Apr; 89(2):464-73. PubMed ID: 15056289
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Milanese M; Giribaldi F; Melone M; Bonifacino T; Musante I; Carminati E; Rossi PI; Vergani L; Voci A; Conti F; Puliti A; Bonanno G
    Neurobiol Dis; 2014 Apr; 64():48-59. PubMed ID: 24361555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. An astrocyte regenerative response from vimentin-containing cells in the spinal cord of amyotrophic lateral sclerosis's disease-like transgenic (G93A SOD1) mice.
    Zhou Y; Lu Y; Fang X; Zhang J; Li J; Li S; Deng X; Yu Y; Xu R
    Neurodegener Dis; 2015; 15(1):1-12. PubMed ID: 25591625
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MicroNeurotrophins Improve Survival in Motor Neuron-Astrocyte Co-Cultures but Do Not Improve Disease Phenotypes in a Mutant SOD1 Mouse Model of Amyotrophic Lateral Sclerosis.
    Glajch KE; Ferraiuolo L; Mueller KA; Stopford MJ; Prabhkar V; Gravanis A; Shaw PJ; Sadri-Vakili G
    PLoS One; 2016; 11(10):e0164103. PubMed ID: 27716798
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Astrocyte-derived Jagged-1 mitigates deleterious Notch signaling in amyotrophic lateral sclerosis.
    Nonneman A; Criem N; Lewandowski SA; Nuyts R; Thal DR; Pfrieger FW; Ravits J; Van Damme P; Zwijsen A; Van Den Bosch L; Robberecht W
    Neurobiol Dis; 2018 Nov; 119():26-40. PubMed ID: 30010003
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 43.