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Journal Abstract Search

199 related items for PubMed ID: 9482656

  • 21. Proteolipid protein gene: Pelizaeus-Merzbacher disease in humans and neurodegeneration in mice.
    Woodward K, Malcolm S.
    Trends Genet; 1999 Apr; 15(4):125-8. PubMed ID: 10203813
    [Abstract] [Full Text] [Related]

  • 22. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.
    Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O.
    Nat Genet; 1994 Mar; 6(3):257-62. PubMed ID: 8012387
    [Abstract] [Full Text] [Related]

  • 23. Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease.
    Ellis D, Malcolm S.
    Nat Genet; 1994 Apr; 6(4):333-4. PubMed ID: 7519941
    [No Abstract] [Full Text] [Related]

  • 24. Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease.
    Wang PJ, Hwu WL, Lee WT, Wang TR, Shen YZ.
    Pediatr Neurol; 1997 Sep; 17(2):125-8. PubMed ID: 9367291
    [Abstract] [Full Text] [Related]

  • 25. Pelizaeus-Merzbacher disease presenting as spinal muscular atrophy: clinical and molecular studies.
    Kaye EM, Doll RF, Natowicz MR, Smith FI.
    Ann Neurol; 1994 Dec; 36(6):916-9. PubMed ID: 7998780
    [Abstract] [Full Text] [Related]

  • 26. 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; 8(11):837-45. PubMed ID: 11093273
    [Abstract] [Full Text] [Related]

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

  • 28. Rabbit paralytic tremor phenotype--a plp1 gene mutation as a model of human Pelizaeus-Merzbacher disease.
    Sypecka J, Domańska-Janik K.
    Acta Neurobiol Exp (Wars); 2005 Nov; 65(2):221-9. PubMed ID: 15960310
    [Abstract] [Full Text] [Related]

  • 29. Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestations.
    Inoue K, Osaka H, Imaizumi K, Nezu A, Takanashi J, Arii J, Murayama K, Ono J, Kikawa Y, Mito T, Shaffer LG, Lupski JR.
    Ann Neurol; 1999 May; 45(5):624-32. PubMed ID: 10319885
    [Abstract] [Full Text] [Related]

  • 30. Myelin proteolipid protein mutation in the rabbit: a new model of Pelizaeus-Merzbacher disease.
    Tosic M, Dolivo M, Domanska-Janik K, Matthieu JM.
    Schweiz Arch Neurol Psychiatr (1985); 1994 May; 145(3):24-6. PubMed ID: 7533932
    [Abstract] [Full Text] [Related]

  • 31. A de novo mutation (C755T; Ser252Phe) in exon 6 of the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease.
    Hodes ME, Aydanian A, Dlouhy SR, Whelan DT, Heshka T, Ronen G.
    Clin Genet; 1998 Sep; 54(3):248-9. PubMed ID: 9788732
    [No Abstract] [Full Text] [Related]

  • 32. 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 Sep; 55(2-3):333-7. PubMed ID: 2444499
    [Abstract] [Full Text] [Related]

  • 33. Pelizaeus-Merzbacher disease: a point mutation in exon 6 of the proteolipid protein (PLP) gene.
    Pratt VM, Dlouhy SR, Hodes ME.
    Clin Genet; 1995 Feb; 47(2):99-100. PubMed ID: 7541731
    [Abstract] [Full Text] [Related]

  • 34. The PLP mutants from mouse to man.
    Duncan ID.
    J Neurol Sci; 2005 Feb 15; 228(2):204-5. PubMed ID: 15694207
    [No Abstract] [Full Text] [Related]

  • 35. Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein.
    Gencic S, Abuelo D, Ambler M, Hudson LD.
    Am J Hum Genet; 1989 Sep 15; 45(3):435-42. PubMed ID: 2773936
    [Abstract] [Full Text] [Related]

  • 36. Disrupted proteolipid protein trafficking results in oligodendrocyte apoptosis in an animal model of Pelizaeus-Merzbacher disease.
    Gow A, Southwood CM, Lazzarini RA.
    J Cell Biol; 1998 Feb 23; 140(4):925-34. PubMed ID: 9472043
    [Abstract] [Full Text] [Related]

  • 37. 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 23; 86(20):8128-31. PubMed ID: 2479017
    [Abstract] [Full Text] [Related]

  • 38. Pelizaeus-Merzbacher disease: three novel mutations and implication for locus heterogeneity.
    Osaka H, Kawanishi C, Inoue K, Onishi H, Kobayashi T, Sugiyama N, Kosaka K, Nezu A, Fujii K, Sugita K, Kodama K, Murayama K, Murayama S, Kanazawa I, Kimura S.
    Ann Neurol; 1999 Jan 23; 45(1):59-64. PubMed ID: 9894878
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. Pelizaeus-Merzbacher disease: a novel mutation in the 5'-untranslated region of the proteolipid protein gene.
    Kawanishi C, Sugiyama N, Osaka H, Inoue K, Suzuki K, Onishi H, Yamada Y, Nezu A, Kimura S, Kosaka K.
    Hum Mutat; 1996 Jun 01; 7(4):355-7. PubMed ID: 8723686
    [No Abstract] [Full Text] [Related]

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