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.
272 related articles for article (PubMed ID: 15226307)
1. Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia. Edgar JM; McLaughlin M; Yool D; Zhang SC; Fowler JH; Montague P; Barrie JA; McCulloch MC; Duncan ID; Garbern J; Nave KA; Griffiths IR J Cell Biol; 2004 Jul; 166(1):121-31. PubMed ID: 15226307 [TBL] [Abstract][Full Text] [Related]
2. Genetic dissection of oligodendroglial and neuronal Plp1 function in a novel mouse model of spastic paraplegia type 2. Lüders KA; Patzig J; Simons M; Nave KA; Werner HB Glia; 2017 Nov; 65(11):1762-1776. PubMed ID: 28836307 [TBL] [Abstract][Full Text] [Related]
3. Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene. Edgar JM; McLaughlin M; Barrie JA; McCulloch MC; Garbern J; Griffiths IR Acta Neuropathol; 2004 Apr; 107(4):331-5. PubMed ID: 14745569 [TBL] [Abstract][Full Text] [Related]
4. Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients. Kasher PR; De Vos KJ; Wharton SB; Manser C; Bennett EJ; Bingley M; Wood JD; Milner R; McDermott CJ; Miller CC; Shaw PJ; Grierson AJ J Neurochem; 2009 Jul; 110(1):34-44. PubMed ID: 19453301 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Progressive white matter pathology in the spinal cord of transgenic mice expressing mutant (P301L) human tau. Lin WL; Zehr C; Lewis J; Hutton M; Yen SH; Dickson DW J Neurocytol; 2005 Dec; 34(6):397-410. PubMed ID: 16902761 [TBL] [Abstract][Full Text] [Related]
7. Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport. Ferreirinha F; Quattrini A; Pirozzi M; Valsecchi V; Dina G; Broccoli V; Auricchio A; Piemonte F; Tozzi G; Gaeta L; Casari G; Ballabio A; Rugarli EI J Clin Invest; 2004 Jan; 113(2):231-42. PubMed ID: 14722615 [TBL] [Abstract][Full Text] [Related]
8. Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias. Soderblom C; Blackstone C Pharmacol Ther; 2006 Jan; 109(1-2):42-56. PubMed ID: 16005518 [TBL] [Abstract][Full Text] [Related]
9. Proteolipid protein is required for transport of sirtuin 2 into CNS myelin. Werner HB; Kuhlmann K; Shen S; Uecker M; Schardt A; Dimova K; Orfaniotou F; Dhaunchak A; Brinkmann BG; Möbius W; Guarente L; Casaccia-Bonnefil P; Jahn O; Nave KA J Neurosci; 2007 Jul; 27(29):7717-30. PubMed ID: 17634366 [TBL] [Abstract][Full Text] [Related]
11. Alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid-mediated excitotoxic axonal damage is attenuated in the absence of myelin proteolipid protein. Fowler JH; Edgar JM; Pringle A; McLaughlin M; McCulloch J; Griffiths IR; Garbern JY; Nave KA; Dewar D J Neurosci Res; 2006 Jul; 84(1):68-77. PubMed ID: 16625661 [TBL] [Abstract][Full Text] [Related]
12. Oligodendrocyte development and differentiation in the rumpshaker mutation. Fanarraga ML; Sommer IU; Griffiths IR; Montague P; Groome NP; Nave KA; Schneider A; Brophy PJ; Kennedy PG Glia; 1993 Oct; 9(2):146-56. PubMed ID: 7503954 [TBL] [Abstract][Full Text] [Related]
13. Structural myelin defects are associated with low axonal ATP levels but rapid recovery from energy deprivation in a mouse model of spastic paraplegia. Trevisiol A; Kusch K; Steyer AM; Gregor I; Nardis C; Winkler U; Köhler S; Restrepo A; Möbius W; Werner HB; Nave KA; Hirrlinger J PLoS Biol; 2020 Nov; 18(11):e3000943. PubMed ID: 33196637 [TBL] [Abstract][Full Text] [Related]
14. Current concepts of PLP and its role in the nervous system. Griffiths I; Klugmann M; Anderson T; Thomson C; Vouyiouklis D; Nave KA Microsc Res Tech; 1998 Jun; 41(5):344-58. PubMed ID: 9672418 [TBL] [Abstract][Full Text] [Related]
15. Plp gene regulation in the developing murine optic nerve: correlation with oligodendroglial process alignment along the axons. Thomson CE; Vouyiouklis DA; Barrie JA; Wease KN; Montague P Dev Neurosci; 2005; 27(1):27-36. PubMed ID: 15886482 [TBL] [Abstract][Full Text] [Related]
16. Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination. Lappe-Siefke C; Goebbels S; Gravel M; Nicksch E; Lee J; Braun PE; Griffiths IR; Nave KA Nat Genet; 2003 Mar; 33(3):366-74. PubMed ID: 12590258 [TBL] [Abstract][Full Text] [Related]
17. The raft-associated protein MAL is required for maintenance of proper axon--glia interactions in the central nervous system. Schaeren-Wiemers N; Bonnet A; Erb M; Erne B; Bartsch U; Kern F; Mantei N; Sherman D; Suter U J Cell Biol; 2004 Aug; 166(5):731-42. PubMed ID: 15337780 [TBL] [Abstract][Full Text] [Related]
18. Rumpshaker: an X-linked mutation causing hypomyelination: developmental differences in myelination and glial cells between the optic nerve and spinal cord. Fanarraga ML; Griffiths IR; McCulloch MC; Barrie JA; Kennedy PG; Brophy PJ Glia; 1992; 5(3):161-70. PubMed ID: 1375190 [TBL] [Abstract][Full Text] [Related]
19. Modeling of axonal endoplasmic reticulum network by spastic paraplegia proteins. Yalçın B; Zhao L; Stofanko M; O'Sullivan NC; Kang ZH; Roost A; Thomas MR; Zaessinger S; Blard O; Patto AL; Sohail A; Baena V; Terasaki M; O'Kane CJ Elife; 2017 Jul; 6():. PubMed ID: 28742022 [TBL] [Abstract][Full Text] [Related]
20. Axon loss is responsible for chronic neurological deficit following inflammatory demyelination in the rat. Papadopoulos D; Pham-Dinh D; Reynolds R Exp Neurol; 2006 Feb; 197(2):373-85. PubMed ID: 16337942 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]