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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

227 related items for PubMed ID: 1380672

  • 21. The molecular genetics of myelination: an update.
    Lemke G.
    Glia; 1993 Apr; 7(4):263-71. PubMed ID: 7686535
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Genetic background determines phenotypic severity of the Plp rumpshaker mutation.
    Al-Saktawi K, McLaughlin M, Klugmann M, Schneider A, Barrie JA, McCulloch MC, Montague P, Kirkham D, Nave KA, Griffiths IR.
    J Neurosci Res; 2003 Apr 01; 72(1):12-24. PubMed ID: 12645075
    [Abstract] [Full Text] [Related]

  • 24. 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 Apr 01; 145(3):24-6. PubMed ID: 7533932
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Transgenic and natural mouse models of proteolipid protein (PLP)-related dysmyelination and demyelination.
    Griffiths IR, Schneider A, Anderson J, Nave KA.
    Brain Pathol; 1995 Jul 01; 5(3):275-81. PubMed ID: 8520727
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C>A, Ala242Glu) at the 'jimpy(msd) codon' in the PLP gene.
    Seeman P, Paderova K, Benes V, Sistermans EA.
    Int J Mol Med; 2002 Feb 01; 9(2):125-9. PubMed ID: 11786921
    [Abstract] [Full Text] [Related]

  • 37. 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 01; 107(4):331-5. PubMed ID: 14745569
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. 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 01; 2(12):2187-9. PubMed ID: 7509234
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.