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 *

218 related articles for article (PubMed ID: 19094180)

  • 1. Loss of translation elongation factor (eEF1A2) expression in vivo differentiates between Wallerian degeneration and dying-back neuronal pathology.
    Murray LM; Thomson D; Conklin A; Wishart TM; Gillingwater TH
    J Anat; 2008 Dec; 213(6):633-45. PubMed ID: 19094180
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid loss of motor nerve terminals following hypoxia-reperfusion injury occurs via mechanisms distinct from classic Wallerian degeneration.
    Baxter B; Gillingwater TH; Parson SH
    J Anat; 2008 Jun; 212(6):827-35. PubMed ID: 18510509
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy mice.
    Mi W; Beirowski B; Gillingwater TH; Adalbert R; Wagner D; Grumme D; Osaka H; Conforti L; Arnhold S; Addicks K; Wada K; Ribchester RR; Coleman MP
    Brain; 2005 Feb; 128(Pt 2):405-16. PubMed ID: 15644421
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Progressive loss of motor neuron function in wasted mice: effects of a spontaneous null mutation in the gene for the eEF1 A2 translation factor.
    Newbery HJ; Gillingwater TH; Dharmasaroja P; Peters J; Wharton SB; Thomson D; Ribchester RR; Abbott CM
    J Neuropathol Exp Neurol; 2005 Apr; 64(4):295-303. PubMed ID: 15835265
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synaptic withdrawal following nerve injury is influenced by postnatal maturity, muscle-specific properties, and the presence of underlying pathology in mice.
    Mole AJ; Bell S; Thomson AK; Dissanayake KN; Ribchester RR; Murray LM
    J Anat; 2020 Aug; 237(2):263-274. PubMed ID: 32311115
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Axotomy-dependent and -independent synapse elimination in organ cultures of Wld(s) mutant mouse skeletal muscle.
    Parson SH; Ribchester RR; Davie N; Gandhi NP; Malik RQ; Gillingwater TH; Thomson D
    J Neurosci Res; 2004 Apr; 76(1):64-75. PubMed ID: 15048930
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Axonal and neuromuscular synaptic phenotypes in Wld(S), SOD1(G93A) and ostes mutant mice identified by fiber-optic confocal microendoscopy.
    Wong F; Fan L; Wells S; Hartley R; Mackenzie FE; Oyebode O; Brown R; Thomson D; Coleman MP; Blanco G; Ribchester RR
    Mol Cell Neurosci; 2009 Dec; 42(4):296-307. PubMed ID: 19683573
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The relationship of neuromuscular synapse elimination to synaptic degeneration and pathology: insights from WldS and other mutant mice.
    Gillingwater TH; Ribchester RR
    J Neurocytol; 2003; 32(5-8):863-81. PubMed ID: 15034273
    [TBL] [Abstract][Full Text] [Related]  

  • 9. eEF1A2 and neuronal degeneration.
    Abbott CM; Newbery HJ; Squires CE; Brownstein D; Griffiths LA; Soares DC
    Biochem Soc Trans; 2009 Dec; 37(Pt 6):1293-7. PubMed ID: 19909265
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss.
    White MA; Lin Z; Kim E; Henstridge CM; Pena Altamira E; Hunt CK; Burchill E; Callaghan I; Loreto A; Brown-Wright H; Mead R; Simmons C; Cash D; Coleman MP; Sreedharan J
    Acta Neuropathol Commun; 2019 Oct; 7(1):166. PubMed ID: 31661035
    [TBL] [Abstract][Full Text] [Related]  

  • 12. In vivo characterization of the role of tissue-specific translation elongation factor 1A2 in protein synthesis reveals insights into muscle atrophy.
    Doig J; Griffiths LA; Peberdy D; Dharmasaroja P; Vera M; Davies FJ; Newbery HJ; Brownstein D; Abbott CM
    FEBS J; 2013 Dec; 280(24):6528-40. PubMed ID: 24460877
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Haploinsufficiency for translation elongation factor eEF1A2 in aged mouse muscle and neurons is compatible with normal function.
    Griffiths LA; Doig J; Churchhouse AM; Davies FC; Squires CE; Newbery HJ; Abbott CM
    PLoS One; 2012; 7(7):e41917. PubMed ID: 22848658
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Activity-dependent degeneration of axotomized neuromuscular synapses in Wld S mice.
    Brown R; Hynes-Allen A; Swan AJ; Dissanayake KN; Gillingwater TH; Ribchester RR
    Neuroscience; 2015 Apr; 290():300-20. PubMed ID: 25617654
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The neuroprotective factor Wlds does not attenuate mutant SOD1-mediated motor neuron disease.
    Vande Velde C; Garcia ML; Yin X; Trapp BD; Cleveland DW
    Neuromolecular Med; 2004; 5(3):193-203. PubMed ID: 15626820
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Atrophy and degeneration in sciatic nerve of presymptomatic mice carrying the Huntington's disease mutation.
    Wade A; Jacobs P; Morton AJ
    Brain Res; 2008 Jan; 1188():61-8. PubMed ID: 18062944
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Progressive Motor Deficit is Mediated by the Denervation of Neuromuscular Junctions and Axonal Degeneration in Transgenic Mice Expressing Mutant (P301S) Tau Protein.
    Yin Z; Valkenburg F; Hornix BE; Mantingh-Otter I; Zhou X; Mari M; Reggiori F; Van Dam D; Eggen BJL; De Deyn PP; Boddeke E
    J Alzheimers Dis; 2017; 60(s1):S41-S57. PubMed ID: 28222529
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Calpains mediate axonal cytoskeleton disintegration during Wallerian degeneration.
    Ma M; Ferguson TA; Schoch KM; Li J; Qian Y; Shofer FS; Saatman KE; Neumar RW
    Neurobiol Dis; 2013 Aug; 56():34-46. PubMed ID: 23542511
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Programmed axon death, synaptic dysfunction and the ubiquitin proteasome system.
    Coleman MP; Ribchester RR
    Curr Drug Targets CNS Neurol Disord; 2004 Jun; 3(3):227-38. PubMed ID: 15180483
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differential protection of neuromuscular sensory and motor axons and their endings in Wld(S) mutant mice.
    Oyebode OR; Hartley R; Singhota J; Thomson D; Ribchester RR
    Neuroscience; 2012 Jan; 200():142-58. PubMed ID: 22062136
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.