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227 related items for PubMed ID: 1380672

  • 1. Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene.
    Schneider A, Montague P, Griffiths I, Fanarraga M, Kennedy P, Brophy P, Nave KA.
    Nature; 1992 Aug 27; 358(6389):758-61. PubMed ID: 1380672
    [Abstract] [Full Text] [Related]

  • 2. Developmental expression of major myelin protein genes in the CNS of X-linked hypomyelinating mutant rumpshaker.
    Mitchell LS, Gillespie SC, McAllister F, Fanarraga ML, Kirkham D, Kelly B, Brophy PJ, Griffiths IR, Montague P, Kennedy PG.
    J Neurosci Res; 1992 Oct 27; 33(2):205-17. PubMed ID: 1280692
    [Abstract] [Full Text] [Related]

  • 3. 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 27; 9(2):146-56. PubMed ID: 7503954
    [Abstract] [Full Text] [Related]

  • 4. Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.
    Gow A, Friedrich VL, Lazzarini RA.
    J Neurosci Res; 1994 Apr 01; 37(5):574-83. PubMed ID: 7518006
    [Abstract] [Full Text] [Related]

  • 5. 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 Apr 01; 5(3):161-70. PubMed ID: 1375190
    [Abstract] [Full Text] [Related]

  • 6. Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene.
    Kagawa T, Ikenaka K, Inoue Y, Kuriyama S, Tsujii T, Nakao J, Nakajima K, Aruga J, Okano H, Mikoshiba K.
    Neuron; 1994 Aug 01; 13(2):427-42. PubMed ID: 7520255
    [Abstract] [Full Text] [Related]

  • 7. Lipophilin (PLP) gene in X-linked myelin disorders.
    Fahim S, Riordan JR.
    J Neurosci Res; 1986 Aug 01; 16(1):303-10. PubMed ID: 3746948
    [Abstract] [Full Text] [Related]

  • 8. The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice.
    Dautigny A, Mattei MG, Morello D, Alliel PM, Pham-Dinh D, Amar L, Arnaud D, Simon D, Mattei JF, Guenet JL.
    Nature; 1986 Aug 01; 321(6073):867-9. PubMed ID: 2425262
    [Abstract] [Full Text] [Related]

  • 9. New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher disease.
    Pratt VM, Trofatter JA, Larsen MB, Hodes ME, Dlouhy SR.
    Am J Med Genet; 1992 Jun 01; 43(3):642-6. PubMed ID: 1376553
    [Abstract] [Full Text] [Related]

  • 10. Proteolipid proteins: structure and genetic expression in normal and myelin-deficient mutant mice.
    Nave KA, Milner RJ.
    Crit Rev Neurobiol; 1989 Jun 01; 5(1):65-91. PubMed ID: 2670252
    [Abstract] [Full Text] [Related]

  • 11. In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease.
    Kleindorfer DO, Dlouhy SR, Pratt VM, Jones MC, Trofatter JA, Hodes ME.
    Am J Med Genet; 1995 Feb 13; 55(4):405-7. PubMed ID: 7539213
    [Abstract] [Full Text] [Related]

  • 12. Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder.
    Hudson LD, Puckett C, Berndt J, Chan J, Gencic S.
    Proc Natl Acad Sci U S A; 1989 Oct 13; 86(20):8128-31. PubMed ID: 2479017
    [Abstract] [Full Text] [Related]

  • 13. Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease.
    Cailloux F, Gauthier-Barichard F, Mimault C, Isabelle V, Courtois V, Giraud G, Dastugue B, Boespflug-Tanguy O.
    Eur J Hum Genet; 2000 Nov 13; 8(11):837-45. PubMed ID: 11093273
    [Abstract] [Full Text] [Related]

  • 14. 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 13; 53(7):715-22. PubMed ID: 16506223
    [Abstract] [Full Text] [Related]

  • 15. 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 13; 55(4):341-51. PubMed ID: 17133418
    [Abstract] [Full Text] [Related]

  • 16. The rumpshaker mutation in spastic paraplegia.
    Kobayashi H, Hoffman EP, Marks HG.
    Nat Genet; 1994 Jul 13; 7(3):351-2. PubMed ID: 7522741
    [No Abstract] [Full Text] [Related]

  • 17. Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease.
    Carango P, Funanage VL, Quirós RE, Debruyn CS, Marks HG.
    Ann Neurol; 1995 Oct 13; 38(4):610-7. PubMed ID: 7574457
    [Abstract] [Full Text] [Related]

  • 18. A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease.
    Pratt VM, Trofatter JA, Schinzel A, Dlouhy SR, Conneally PM, Hodes ME.
    Am J Med Genet; 1991 Jan 13; 38(1):136-9. PubMed ID: 1707231
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 41(5):344-58. PubMed ID: 9672418
    [Abstract] [Full Text] [Related]

  • 20. The fifth exon of the myelin proteolipid protein-coding gene is not utilized in the brain of jimpy mutant mice.
    Moriguchi A, Ikenaka K, Furuichi T, Okano H, Iwasaki Y, Mikoshiba K.
    Gene; 1987 Jun 01; 55(2-3):333-7. PubMed ID: 2444499
    [Abstract] [Full Text] [Related]

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