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

223 related items for PubMed ID: 10586251

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
    Patel PI, Roa BB, Welcher AA, Schoener-Scott R, Trask BJ, Pentao L, Snipes GJ, Garcia CA, Francke U, Shooter EM, Lupski JR, Suter U.
    Nat Genet; 1992 Jun; 1(3):159-65. PubMed ID: 1303228
    [Abstract] [Full Text] [Related]

  • 9. Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation.
    Giambonini-Brugnoli G, Buchstaller J, Sommer L, Suter U, Mantei N.
    Neurobiol Dis; 2005 Apr; 18(3):656-68. PubMed ID: 15755691
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Expression of myelin proteins in the adult heterozygous Trembler mouse.
    Vallat JM, Sindou P, Garbay B, Preux PM, Anani T, Richard L, Diot M.
    Acta Neuropathol; 1999 Sep; 98(3):281-7. PubMed ID: 10483786
    [Abstract] [Full Text] [Related]

  • 14. Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A.
    Valentijn LJ, Baas F, Wolterman RA, Hoogendijk JE, van den Bosch NH, Zorn I, Gabreëls-Festen AW, de Visser M, Bolhuis PA.
    Nat Genet; 1992 Dec; 2(4):288-91. PubMed ID: 1303281
    [Abstract] [Full Text] [Related]

  • 15. Transgenic mouse models of CMT1A and HNPP.
    Suter U, Nave KA.
    Ann N Y Acad Sci; 1999 Sep 14; 883():247-53. PubMed ID: 10586249
    [Abstract] [Full Text] [Related]

  • 16. Depleting endogenous neurotrophin-3 enhances myelin formation in the Trembler-J mouse, a model of a peripheral neuropathy.
    Liu N, Varma S, Tsao D, Shooter EM, Tolwani RJ.
    J Neurosci Res; 2007 Oct 14; 85(13):2863-9. PubMed ID: 17628499
    [Abstract] [Full Text] [Related]

  • 17. PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells.
    Colby J, Nicholson R, Dickson KM, Orfali W, Naef R, Suter U, Snipes GJ.
    Neurobiol Dis; 2000 Dec 14; 7(6 Pt B):561-73. PubMed ID: 11114256
    [Abstract] [Full Text] [Related]

  • 18. Many facets of the peripheral myelin protein PMP22 in myelination and disease.
    Naef R, Suter U.
    Microsc Res Tech; 1998 Jun 01; 41(5):359-71. PubMed ID: 9672419
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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