BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 12657685)

  • 1. Proteolipid protein gene mutation induces altered ventilatory response to hypoxia in the myelin-deficient rat.
    Miller MJ; Haxhiu MA; Georgiadis P; Gudz TI; Kangas CD; Macklin WB
    J Neurosci; 2003 Mar; 23(6):2265-73. PubMed ID: 12657685
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Processing of PLP in a model of Pelizaeus-Merzbacher disease/SPG2 due to the rumpshaker mutation.
    McLaughlin M; Barrie JA; Karim S; Montague P; Edgar JM; Kirkham D; Thomson CE; Griffiths IR
    Glia; 2006 May; 53(7):715-22. PubMed ID: 16506223
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus-Merzbacher disease.
    Karim SA; Barrie JA; McCulloch MC; Montague P; Edgar JM; Kirkham D; Anderson TJ; Nave KA; Griffiths IR; McLaughlin M
    Glia; 2007 Mar; 55(4):341-51. PubMed ID: 17133418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PLP/DM20 expression and turnover in a transgenic mouse model of Pelizaeus-Merzbacher disease.
    Karim SA; Barrie JA; McCulloch MC; Montague P; Edgar JM; Iden DL; Anderson TJ; Nave KA; Griffiths IR; McLaughlin M
    Glia; 2010 Nov; 58(14):1727-38. PubMed ID: 20629189
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neuronal expression of the proteolipid protein gene in the medulla of the mouse.
    Miller MJ; Kangas CD; Macklin WB
    J Neurosci Res; 2009 Oct; 87(13):2842-53. PubMed ID: 19479988
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of a PLP-overexpressing transgenic rat, a model for the connatal form of Pelizaeus-Merzbacher disease.
    Mayer JA; Larsen EC; Kondo Y; Duncan ID
    Neurobiol Dis; 2011 Nov; 44(2):231-8. PubMed ID: 21784154
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neural stem cells restore myelin in a demyelinating model of Pelizaeus-Merzbacher disease.
    Gruenenfelder FI; McLaughlin M; Griffiths IR; Garbern J; Thomson G; Kuzman P; Barrie JA; McCulloch ML; Penderis J; Stassart R; Nave KA; Edgar JM
    Brain; 2020 May; 143(5):1383-1399. PubMed ID: 32419025
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pelizaeus-Merzbacher disease.
    Koeppen AH; Robitaille Y
    J Neuropathol Exp Neurol; 2002 Sep; 61(9):747-59. PubMed ID: 12230321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The PLP mutants from mouse to man.
    Duncan ID
    J Neurol Sci; 2005 Feb; 228(2):204-5. PubMed ID: 15694207
    [No Abstract]   [Full Text] [Related]  

  • 10. Deletion of a splicing enhancer disrupts PLP1/DM20 ratio and myelin stability.
    Wang E; Dimova N; Sperle K; Huang Z; Lock L; McCulloch MC; Edgar JM; Hobson GM; Cambi F
    Exp Neurol; 2008 Dec; 214(2):322-30. PubMed ID: 18835559
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oligodendrocytes expressing exclusively the DM20 isoform of the proteolipid protein gene: myelination and development.
    Spörkel O; Uschkureit T; Büssow H; Stoffel W
    Glia; 2002 Jan; 37(1):19-30. PubMed ID: 11746780
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation in the myelin proteolipid protein gene alters BK and SK channel function in the caudal medulla.
    Mayer CA; Macklin WB; Avishai N; Balan K; Wilson CG; Miller MJ
    Respir Physiol Neurobiol; 2009 Dec; 169(3):303-14. PubMed ID: 19808102
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic background determines phenotypic severity of the Plp rumpshaker mutation.
    Al-Saktawi K; McLaughlin M; Klugmann M; Schneider A; Barrie JA; McCulloch MC; Montague P; Kirkham D; Nave KA; Griffiths IR
    J Neurosci Res; 2003 Apr; 72(1):12-24. PubMed ID: 12645075
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gait abnormalities and progressive myelin degeneration in a new murine model of Pelizaeus-Merzbacher disease with tandem genomic duplication.
    Clark K; Sakowski L; Sperle K; Banser L; Landel CP; Bessert DA; Skoff RP; Hobson GM
    J Neurosci; 2013 Jul; 33(29):11788-99. PubMed ID: 23864668
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system.
    Garbern JY
    J Neurol Sci; 2005 Feb; 228(2):201-3. PubMed ID: 15694206
    [No Abstract]   [Full Text] [Related]  

  • 16. Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvement.
    Inoue K; Tanaka H; Scaglia F; Araki A; Shaffer LG; Lupski JR
    Ann Neurol; 2001 Dec; 50(6):747-54. PubMed ID: 11761472
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1.
    Sima AA; Pierson CR; Woltjer RL; Hobson GM; Golden JA; Kupsky WJ; Schauer GM; Bird TD; Skoff RP; Garbern JY
    Acta Neuropathol; 2009 Oct; 118(4):531-9. PubMed ID: 19562355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C>A, Ala242Glu) at the 'jimpy(msd) codon' in the PLP gene.
    Seeman P; Paderova K; Benes V; Sistermans EA
    Int J Mol Med; 2002 Feb; 9(2):125-9. PubMed ID: 11786921
    [TBL] [Abstract][Full Text] [Related]  

  • 19. N-Methyl-D-aspartate receptor expression in the nucleus tractus solitarii and maturation of hypoxic ventilatory response in the rat.
    Ohtake PJ; Simakajornboon N; Fehniger MD; Xue YD; Gozal D
    Am J Respir Crit Care Med; 2000 Sep; 162(3 Pt 1):1140-7. PubMed ID: 10988143
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assembly of CNS myelin in the absence of proteolipid protein.
    Klugmann M; Schwab MH; Pühlhofer A; Schneider A; Zimmermann F; Griffiths IR; Nave KA
    Neuron; 1997 Jan; 18(1):59-70. PubMed ID: 9010205
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.