These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

866 related articles for article (PubMed ID: 18842883)

  • 21. Transcriptional profiling in the lumbar spinal cord of a mouse model of amyotrophic lateral sclerosis: a role for wild-type superoxide dismutase 1 in sporadic disease?
    D'Arrigo A; Colavito D; Peña-Altamira E; Fabris M; Dam M; Contestabile A; Leon A
    J Mol Neurosci; 2010 Jul; 41(3):404-15. PubMed ID: 20177826
    [TBL] [Abstract][Full Text] [Related]  

  • 22. PACAP signaling exerts opposing effects on neuroprotection and neuroinflammation during disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Ringer C; Büning LS; Schäfer MK; Eiden LE; Weihe E; Schütz B
    Neurobiol Dis; 2013 Jun; 54():32-42. PubMed ID: 23466699
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Motor neuron degeneration promotes neural progenitor cell proliferation, migration, and neurogenesis in the spinal cords of amyotrophic lateral sclerosis mice.
    Chi L; Ke Y; Luo C; Li B; Gozal D; Kalyanaraman B; Liu R
    Stem Cells; 2006 Jan; 24(1):34-43. PubMed ID: 16099995
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Significance of aberrant glial cell phenotypes in pathophysiology of amyotrophic lateral sclerosis.
    Trias E; Ibarburu S; Barreto-Núñez R; Barbeito L
    Neurosci Lett; 2017 Jan; 636():27-31. PubMed ID: 27473942
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Necroptosis is dispensable for motor neuron degeneration in a mouse model of ALS.
    Wang T; Perera ND; Chiam MDF; Cuic B; Wanniarachchillage N; Tomas D; Samson AL; Cawthorne W; Valor EN; Murphy JM; Turner BJ
    Cell Death Differ; 2020 May; 27(5):1728-1739. PubMed ID: 31745214
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Protein-bound crotonaldehyde accumulates in the spinal cord of superoxide dismutase-1 mutation-associated familial amyotrophic lateral sclerosis and its transgenic mouse model.
    Shibata N; Kawaguchi M; Uchida K; Kakita A; Takahashi H; Nakano R; Fujimura H; Sakoda S; Ihara Y; Nobukuni K; Takehisa Y; Kuroda S; Kokubo Y; Kuzuhara S; Honma T; Mochizuki Y; Mizutani T; Yamada S; Toi S; Sasaki S; Iwata M; Hirano A; Yamamoto T; Kato Y; Sawada T; Kobayashi M
    Neuropathology; 2007 Feb; 27(1):49-61. PubMed ID: 17319283
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Magnetic resonance microimaging of the spinal cord in the SOD1 mouse model of amyotrophic lateral sclerosis detects motor nerve root degeneration.
    Cowin GJ; Butler TJ; Kurniawan ND; Watson C; Wallace RH
    Neuroimage; 2011 Sep; 58(1):69-74. PubMed ID: 21689764
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosis.
    Nardo G; Iennaco R; Fusi N; Heath PR; Marino M; Trolese MC; Ferraiuolo L; Lawrence N; Shaw PJ; Bendotti C
    Brain; 2013 Nov; 136(Pt 11):3305-32. PubMed ID: 24065725
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Microglial keratan sulfate epitope elicits in central nervous tissues of transgenic model mice and patients with amyotrophic lateral sclerosis.
    Foyez T; Takeda-Uchimura Y; Ishigaki S; Narentuya ; Zhang Z; Sobue G; Kadomatsu K; Uchimura K
    Am J Pathol; 2015 Nov; 185(11):3053-65. PubMed ID: 26362733
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Interfering with lysophosphatidic acid receptor edg2/lpa
    Gento-Caro Á; Vilches-Herrando E; García-Morales V; Portillo F; Rodríguez-Bey G; González-Forero D; Moreno-López B
    Neuropathol Appl Neurobiol; 2021 Dec; 47(7):1004-1018. PubMed ID: 33508894
    [TBL] [Abstract][Full Text] [Related]  

  • 31. In-vivo effects of knocking-down metabotropic glutamate receptor 5 in the SOD1
    Bonifacino T; Cattaneo L; Gallia E; Puliti A; Melone M; Provenzano F; Bossi S; Musante I; Usai C; Conti F; Bonanno G; Milanese M
    Neuropharmacology; 2017 Sep; 123():433-445. PubMed ID: 28645622
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Appearance of phagocytic microglia adjacent to motoneurons in spinal cord tissue from a presymptomatic transgenic rat model of amyotrophic lateral sclerosis.
    Sanagi T; Yuasa S; Nakamura Y; Suzuki E; Aoki M; Warita H; Itoyama Y; Uchino S; Kohsaka S; Ohsawa K
    J Neurosci Res; 2010 Sep; 88(12):2736-46. PubMed ID: 20648658
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Apolloni S; Amadio S; Montilli C; Volonté C; D'Ambrosi N
    Hum Mol Genet; 2013 Oct; 22(20):4102-16. PubMed ID: 23736299
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Actions of the antihistaminergic clemastine on presymptomatic SOD1-G93A mice ameliorate ALS disease progression.
    Apolloni S; Fabbrizio P; Amadio S; Volonté C
    J Neuroinflammation; 2016 Aug; 13(1):191. PubMed ID: 27549088
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The review of the methods to obtain non-neuronal cells to study glial influence on Amyotrophic Lateral Sclerosis pathophysiology at molecular level in vitro.
    Scorisa JM; Duobles T; Oliveira GP; Maximino JR; Chadi G
    Acta Cir Bras; 2010 Jun; 25(3):281-9. PubMed ID: 20498942
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis.
    El Oussini H; Bayer H; Scekic-Zahirovic J; Vercruysse P; Sinniger J; Dirrig-Grosch S; Dieterlé S; Echaniz-Laguna A; Larmet Y; Müller K; Weishaupt JH; Thal DR; van Rheenen W; van Eijk K; Lawson R; Monassier L; Maroteaux L; Roumier A; Wong PC; van den Berg LH; Ludolph AC; Veldink JH; Witting A; Dupuis L
    Acta Neuropathol; 2016 Mar; 131(3):465-80. PubMed ID: 26744351
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1.
    Tokuda E; Okawa E; Watanabe S; Ono S
    Hum Mol Genet; 2014 Mar; 23(5):1271-85. PubMed ID: 24163136
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The Chinese prescription Wen-Pi-Tang extract delays disease onset in amyotrophic lateral sclerosis model mice while attenuating the activation of glial cells in the spinal cord.
    Sekiya M; Ichiyanagi T; Ikeshiro Y; Yokozawa T
    Biol Pharm Bull; 2009 Mar; 32(3):382-8. PubMed ID: 19252282
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice.
    Turner BJ; Ackerley S; Davies KE; Talbot K
    Hum Mol Genet; 2010 Mar; 19(5):815-24. PubMed ID: 20008901
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Depletion of reduced glutathione enhances motor neuron degeneration in vitro and in vivo.
    Chi L; Ke Y; Luo C; Gozal D; Liu R
    Neuroscience; 2007 Feb; 144(3):991-1003. PubMed ID: 17150307
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 44.