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 *

370 related articles for article (PubMed ID: 28300211)

  • 1. ALS Along the Axons - Expression of Coding and Noncoding RNA Differs in Axons of ALS models.
    Rotem N; Magen I; Ionescu A; Gershoni-Emek N; Altman T; Costa CJ; Gradus T; Pasmanik-Chor M; Willis DE; Ben-Dov IZ; Hornstein E; Perlson E
    Sci Rep; 2017 Mar; 7():44500. PubMed ID: 28300211
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Galectin-1 deficiency improves axonal swelling of motor neurones in SOD1(G93A) transgenic mice.
    Kobayakawa Y; Sakumi K; Kajitani K; Kadoya T; Horie H; Kira J; Nakabeppu Y
    Neuropathol Appl Neurobiol; 2015 Feb; 41(2):227-44. PubMed ID: 24707896
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An integrative miRNA-mRNA expression analysis identifies miRNA signatures associated with SOD1 and TARDBP patient-derived motor neurons.
    Dash BP; Freischmidt A; Weishaupt JH; Hermann A
    Hum Mol Genet; 2024 Jul; 33(15):1300-1314. PubMed ID: 38676626
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Axonal degeneration, distal collateral branching and neuromuscular junction architecture alterations occur prior to symptom onset in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Clark JA; Southam KA; Blizzard CA; King AE; Dickson TC
    J Chem Neuroanat; 2016 Oct; 76(Pt A):35-47. PubMed ID: 27038603
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis-causing mutations.
    Vaughan SK; Kemp Z; Hatzipetros T; Vieira F; Valdez G
    J Comp Neurol; 2015 Dec; 523(17):2477-94. PubMed ID: 26136049
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Axon-Seq Decodes the Motor Axon Transcriptome and Its Modulation in Response to ALS.
    Nijssen J; Aguila J; Hoogstraaten R; Kee N; Hedlund E
    Stem Cell Reports; 2018 Dec; 11(6):1565-1578. PubMed ID: 30540963
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration.
    Li J; Li T; Zhang X; Tang Y; Yang J; Le W
    Neurobiol Aging; 2014 Apr; 35(4):837-46. PubMed ID: 24126158
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Degeneration of axons in spinal white matter in G93A mSOD1 mouse characterized by NFL and α-internexin immunoreactivity.
    King AE; Blizzard CA; Southam KA; Vickers JC; Dickson TC
    Brain Res; 2012 Jul; 1465():90-100. PubMed ID: 22609817
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epothilone D accelerates disease progression in the SOD1
    Clark JA; Blizzard CA; Breslin MC; Yeaman EJ; Lee KM; Chuckowree JA; Dickson TC
    Neuropathol Appl Neurobiol; 2018 Oct; 44(6):590-605. PubMed ID: 29380402
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inhibition of collapsin response mediator protein-2 phosphorylation ameliorates motor phenotype of ALS model mice expressing SOD1G93A.
    Numata-Uematsu Y; Wakatsuki S; Nagano S; Shibata M; Sakai K; Ichinohe N; Mikoshiba K; Ohshima T; Yamashita N; Goshima Y; Araki T
    Neurosci Res; 2019 Feb; 139():63-68. PubMed ID: 30194029
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Overexpression of TDP-43 Protein in the Neuron and Oligodendrocyte Cells Causes the Progressive Motor Neuron Degeneration in the SOD1 G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.
    Lu Y; Tang C; Zhu L; Li J; Liang H; Zhang J; Xu R
    Int J Biol Sci; 2016; 12(9):1140-9. PubMed ID: 27570488
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The ALS-inducing factors, TDP43
    Vaughan SK; Sutherland NM; Zhang S; Hatzipetros T; Vieira F; Valdez G
    Sci Rep; 2018 Nov; 8(1):16582. PubMed ID: 30410094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.
    Hossaini M; Cardona Cano S; van Dis V; Haasdijk ED; Hoogenraad CC; Holstege JC; Jaarsma D
    J Neuropathol Exp Neurol; 2011 Aug; 70(8):662-77. PubMed ID: 21760539
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Progressive Degeneration and Inhibition of Peripheral Nerve Regeneration in the SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis.
    Deng B; Lv W; Duan W; Liu Y; Li Z; Ma Y; Zhang G; Song X; Cui C; Qi X; Li Y; Li C
    Cell Physiol Biochem; 2018; 46(6):2358-2372. PubMed ID: 29742495
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.
    Jaarsma D; Haasdijk ED; Grashorn JA; Hawkins R; van Duijn W; Verspaget HW; London J; Holstege JC
    Neurobiol Dis; 2000 Dec; 7(6 Pt B):623-43. PubMed ID: 11114261
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Caspase 6 has a protective role in SOD1(G93A) transgenic mice.
    Hogg MC; Mitchem MR; König HG; Prehn JH
    Biochim Biophys Acta; 2016 Jun; 1862(6):1063-73. PubMed ID: 26976329
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A CRMP4-dependent retrograde axon-to-soma death signal in amyotrophic lateral sclerosis.
    Maimon R; Ankol L; Gradus Pery T; Altman T; Ionescu A; Weissova R; Ostrovsky M; Tank E; Alexandra G; Shelestovich N; Opatowsky Y; Dori A; Barmada S; Balastik M; Perlson E
    EMBO J; 2021 Sep; 40(17):e107586. PubMed ID: 34190355
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Potassium channel abnormalities are consistent with early axon degeneration of motor axons in the G127X SOD1 mouse model of amyotrophic lateral sclerosis.
    Maglemose R; Hedegaard A; Lehnhoff J; Dimintiyanova KP; Moldovan M; Grøndahl L; Meehan CF
    Exp Neurol; 2017 Jun; 292():154-167. PubMed ID: 28322742
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterizing the multiple roles of FGF-2 in SOD1
    Kefalakes E; Böselt S; Sarikidi A; Ettcheto M; Bursch F; Naujock M; Stanslowsky N; Schmuck M; Barenys M; Wegner F; Grothe C; Petri S
    J Cell Physiol; 2019 May; 234(5):7395-7410. PubMed ID: 30370540
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.