BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 25313866)

  • 21. Postnatal electrical and morphological abnormalities in lumbar motoneurons from transgenic mouse models of amyotrophic lateral sclerosis.
    Amendola J; Gueritaud JP; Lamotte d'Incamps B; Bories C; Liabeuf S; Allene C; Pambo-Pambo A; Durand J
    Arch Ital Biol; 2007 Nov; 145(3-4):311-23. PubMed ID: 18075124
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Progressive changes in synaptic inputs to motoneurons in adult sacral spinal cord of a mouse model of amyotrophic lateral sclerosis.
    Jiang M; Schuster JE; Fu R; Siddique T; Heckman CJ
    J Neurosci; 2009 Dec; 29(48):15031-8. PubMed ID: 19955354
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice.
    Kieran D; Hafezparast M; Bohnert S; Dick JR; Martin J; Schiavo G; Fisher EM; Greensmith L
    J Cell Biol; 2005 May; 169(4):561-7. PubMed ID: 15911875
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Downregulation of the potassium chloride cotransporter KCC2 in vulnerable motoneurons in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Fuchs A; Ringer C; Bilkei-Gorzo A; Weihe E; Roeper J; Schütz B
    J Neuropathol Exp Neurol; 2010 Oct; 69(10):1057-70. PubMed ID: 20838240
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice.
    Maatkamp A; Vlug A; Haasdijk E; Troost D; French PJ; Jaarsma D
    Eur J Neurosci; 2004 Jul; 20(1):14-28. PubMed ID: 15245475
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dynamic interplay between H-current and M-current controls motoneuron hyperexcitability in amyotrophic lateral sclerosis.
    Buskila Y; Kékesi O; Bellot-Saez A; Seah W; Berg T; Trpceski M; Yerbury JJ; Ooi L
    Cell Death Dis; 2019 Apr; 10(4):310. PubMed ID: 30952836
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS.
    Bernard-Marissal N; Moumen A; Sunyach C; Pellegrino C; Dudley K; Henderson CE; Raoul C; Pettmann B
    J Neurosci; 2012 Apr; 32(14):4901-12. PubMed ID: 22492046
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Early Hypoexcitability in a Subgroup of Spinal Motoneurons in Superoxide Dismutase 1 Transgenic Mice, a Model of Amyotrophic Lateral Sclerosis.
    Filipchuk A; Pambo-Pambo A; Gaudel F; Liabeuf S; Brocard C; Gueritaud JP; Durand J
    Neuroscience; 2021 May; 463():337-353. PubMed ID: 33556455
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The effect of peripheral nerve injury on disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Sharp PS; Dick JR; Greensmith L
    Neuroscience; 2005; 130(4):897-910. PubMed ID: 15652988
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutant SOD1(G93A) microglia are more neurotoxic relative to wild-type microglia.
    Xiao Q; Zhao W; Beers DR; Yen AA; Xie W; Henkel JS; Appel SH
    J Neurochem; 2007 Sep; 102(6):2008-2019. PubMed ID: 17555556
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Glycine receptor channels in spinal motoneurons are abnormal in a transgenic mouse model of amyotrophic lateral sclerosis.
    Chang Q; Martin LJ
    J Neurosci; 2011 Feb; 31(8):2815-27. PubMed ID: 21414903
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gender-specific perturbations in modulatory inputs to motoneurons in a mouse model of amyotrophic lateral sclerosis.
    Herron LR; Miles GB
    Neuroscience; 2012 Dec; 226():313-23. PubMed ID: 23000617
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Selective mitochondrial Ca2+ uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93A mouse model of amyotrophic lateral sclerosis.
    Fuchs A; Kutterer S; Mühling T; Duda J; Schütz B; Liss B; Keller BU; Roeper J
    J Physiol; 2013 May; 591(10):2723-45. PubMed ID: 23401612
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Compensatory changes in degenerating spinal motoneurons sustain functional sparing in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
    Giusto E; Codrich M; de Leo G; Francardo V; Coradazzi M; Parenti R; Gulisano M; Vicario N; Gulino R; Leanza G
    J Comp Neurol; 2020 Feb; 528(2):231-243. PubMed ID: 31364764
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Imbalanced excitatory to inhibitory synaptic input precedes motor neuron degeneration in an animal model of amyotrophic lateral sclerosis.
    Schütz B
    Neurobiol Dis; 2005 Oct; 20(1):131-40. PubMed ID: 16137574
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Differential vulnerability of cranial motoneurons in mouse models with motor neuron degeneration.
    Haenggeli C; Kato AC
    Neurosci Lett; 2002 Dec; 335(1):39-43. PubMed ID: 12457737
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Calreticulin levels determine onset of early muscle denervation by fast motoneurons of ALS model mice.
    Bernard-Marissal N; Sunyach C; Marissal T; Raoul C; Pettmann B
    Neurobiol Dis; 2015 Jan; 73():130-6. PubMed ID: 25277755
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Selective loss of alpha motoneurons innervating the medial gastrocnemius muscle in a mouse model of amyotrophic lateral sclerosis.
    Mohajeri MH; Figlewicz DA; Bohn MC
    Exp Neurol; 1998 Apr; 150(2):329-36. PubMed ID: 9527903
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.