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Journal Abstract Search

171 related items for PubMed ID: 2444499

  • 41.
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  • 42. A novel insertional mutation at exon VII of the myelin proteolipid protein gene in Pelizaeus-Merzbacher disease.
    Kurosawa K, Iwaki A, Miyake S, Imaizumi K, Kuroki Y, Fukumaki Y.
    Hum Mol Genet; 1993 Dec; 2(12):2187-9. PubMed ID: 7509234
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  • 43. 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; 33(2):205-17. PubMed ID: 1280692
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  • 44. Lipophilin (PLP) gene in X-linked myelin disorders.
    Fahim S, Riordan JR.
    J Neurosci Res; 1986 Oct; 16(1):303-10. PubMed ID: 3746948
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  • 45.
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  • 46. 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
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  • 49. Myelination in the jimpy mouse in the absence of proteolipid protein.
    Duncan ID, Hammang JP, Goda S, Quarles RH.
    Glia; 1989 Jun 01; 2(3):148-54. PubMed ID: 2526078
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  • 52. Developmentally regulated alternative splicing of brain myelin-associated glycoprotein mRNA is lacking in the quaking mouse.
    Fujita N, Sato S, Kurihara T, Inuzuka T, Takahashi Y, Miyatake T.
    FEBS Lett; 1988 May 23; 232(2):323-7. PubMed ID: 2454205
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  • 55. Analysis of myelin proteolipid protein and F0 ATPase subunit 9 in normal and jimpy CNS.
    Benjamins JA, Studzinski DM, Skoff RP.
    Neurochem Res; 1994 Aug 23; 19(8):1013-22. PubMed ID: 7528346
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  • 56. A point mutation at the X-chromosomal proteolipid protein locus in Pelizaeus-Merzbacher disease leads to disruption of myelinogenesis.
    Weimbs T, Dick T, Stoffel W, Boltshauser E.
    Biol Chem Hoppe Seyler; 1990 Dec 23; 371(12):1175-83. PubMed ID: 1708672
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  • 57. 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
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