408 related articles for article (PubMed ID: 18815260)
1. Absence of 2-hydroxylated sphingolipids is compatible with normal neural development but causes late-onset axon and myelin sheath degeneration.
Zöller I; Meixner M; Hartmann D; Büssow H; Meyer R; Gieselmann V; Eckhardt M
J Neurosci; 2008 Sep; 28(39):9741-54. PubMed ID: 18815260
[TBL] [Abstract][Full Text] [Related]
2. Myelination in the absence of UDP-galactose:ceramide galactosyl-transferase and fatty acid 2 -hydroxylase.
Meixner M; Jungnickel J; Grothe C; Gieselmann V; Eckhardt M
BMC Neurosci; 2011 Mar; 12():22. PubMed ID: 21366909
[TBL] [Abstract][Full Text] [Related]
3. Central nervous system dysfunction in a mouse model of FA2H deficiency.
Potter KA; Kern MJ; Fullbright G; Bielawski J; Scherer SS; Yum SW; Li JJ; Cheng H; Han X; Venkata JK; Khan PA; Rohrer B; Hama H
Glia; 2011 Jul; 59(7):1009-21. PubMed ID: 21491498
[TBL] [Abstract][Full Text] [Related]
4. A mammalian fatty acid hydroxylase responsible for the formation of alpha-hydroxylated galactosylceramide in myelin.
Eckhardt M; Yaghootfam A; Fewou SN; Zöller I; Gieselmann V
Biochem J; 2005 May; 388(Pt 1):245-54. PubMed ID: 15658937
[TBL] [Abstract][Full Text] [Related]
5. Decreased turnover of the CNS myelin protein Opalin in a mouse model of hereditary spastic paraplegia 35.
Hardt R; Jordans S; Winter D; Gieselmann V; Wang-Eckhardt L; Eckhardt M
Hum Mol Genet; 2021 Jan; 29(22):3616-3630. PubMed ID: 33215680
[TBL] [Abstract][Full Text] [Related]
6. Absence of functional peroxisomes from mouse CNS causes dysmyelination and axon degeneration.
Hulshagen L; Krysko O; Bottelbergs A; Huyghe S; Klein R; Van Veldhoven PP; De Deyn PP; D'Hooge R; Hartmann D; Baes M
J Neurosci; 2008 Apr; 28(15):4015-27. PubMed ID: 18400901
[TBL] [Abstract][Full Text] [Related]
7. Alterations in the oligodendrocyte lineage, myelin, and white matter in adult mice lacking the chemokine receptor CXCR2.
Padovani-Claudio DA; Liu L; Ransohoff RM; Miller RH
Glia; 2006 Oct; 54(5):471-83. PubMed ID: 16886211
[TBL] [Abstract][Full Text] [Related]
8. Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS.
Traka M; Wollmann RL; Cerda SR; Dugas J; Barres BA; Popko B
J Neurosci; 2008 Nov; 28(45):11537-49. PubMed ID: 18987190
[TBL] [Abstract][Full Text] [Related]
9. Cyclin dependent kinase 5 is required for the normal development of oligodendrocytes and myelin formation.
Yang Y; Wang H; Zhang J; Luo F; Herrup K; Bibb JA; Lu R; Miller RH
Dev Biol; 2013 Jun; 378(2):94-106. PubMed ID: 23583582
[TBL] [Abstract][Full Text] [Related]
10. Axonal swellings and degeneration in mice lacking the major proteolipid of myelin.
Griffiths I; Klugmann M; Anderson T; Yool D; Thomson C; Schwab MH; Schneider A; Zimmermann F; McCulloch M; Nadon N; Nave KA
Science; 1998 Jun; 280(5369):1610-3. PubMed ID: 9616125
[TBL] [Abstract][Full Text] [Related]
11. Myelinogenesis and axonal recognition by oligodendrocytes in brain are uncoupled in Olig1-null mice.
Xin M; Yue T; Ma Z; Wu FF; Gow A; Lu QR
J Neurosci; 2005 Feb; 25(6):1354-65. PubMed ID: 15703389
[TBL] [Abstract][Full Text] [Related]
12. Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking.
Patzig J; Kusch K; Fledrich R; Eichel MA; Lüders KA; Möbius W; Sereda MW; Nave KA; Martini R; Werner HB
Glia; 2016 Jan; 64(1):155-74. PubMed ID: 26393339
[TBL] [Abstract][Full Text] [Related]
13. Reversal of non-hydroxy:alpha-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose:ceramide galactosyltransferase.
Fewou SN; Büssow H; Schaeren-Wiemers N; Vanier MT; Macklin WB; Gieselmann V; Eckhardt M
J Neurochem; 2005 Jul; 94(2):469-81. PubMed ID: 15998297
[TBL] [Abstract][Full Text] [Related]
14. Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons.
Yool DA; Klugmann M; McLaughlin M; Vouyiouklis DA; Dimou L; Barrie JA; McCulloch MC; Nave KA; Griffiths IR
J Neurosci Res; 2001 Jan; 63(2):151-64. PubMed ID: 11169625
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. The deletion of dicer in mature myelinating glial cells causes progressive axonal degeneration but not overt demyelination in adult mice.
Li T; Wang J; Wang H; Yang Y; Wang S; Huang N; Wang F; Gao X; Niu J; Li Z; Mei F; Xiao L
Glia; 2018 Sep; 66(9):1960-1971. PubMed ID: 29726608
[TBL] [Abstract][Full Text] [Related]
17. The role of oligodendrocytes and myelin on axon maturation in the developing rat retinofugal pathway.
Colello RJ; Pott U; Schwab ME
J Neurosci; 1994 May; 14(5 Pt 1):2594-605. PubMed ID: 7514208
[TBL] [Abstract][Full Text] [Related]
18. Myelin sheath decompaction, axon swelling, and functional loss during chronic secondary degeneration in rat optic nerve.
Payne SC; Bartlett CA; Harvey AR; Dunlop SA; Fitzgerald M
Invest Ophthalmol Vis Sci; 2012 Sep; 53(10):6093-101. PubMed ID: 22879411
[TBL] [Abstract][Full Text] [Related]
19. Early ultrastructural defects of axons and axon-glia junctions in mice lacking expression of Cnp1.
Edgar JM; McLaughlin M; Werner HB; McCulloch MC; Barrie JA; Brown A; Faichney AB; Snaidero N; Nave KA; Griffiths IR
Glia; 2009 Dec; 57(16):1815-24. PubMed ID: 19459211
[TBL] [Abstract][Full Text] [Related]
20. Age-Dependent Increase in Schmidt-Lanterman Incisures and a Cadm4-Associated Membrane Skeletal Complex in Fatty Acid 2-hydroxylase Deficient Mice: a Mouse Model of Spastic Paraplegia SPG35.
Jordans S; Hardt R; Becker I; Winter D; Wang-Eckhardt L; Eckhardt M
Mol Neurobiol; 2022 Jul; 59(7):3969-3979. PubMed ID: 35445918
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]