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

Journal Abstract Search


332 related items for PubMed ID: 11823441

  • 1. Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia.
    Cavadini P, O'Neill HA, Benada O, Isaya G.
    Hum Mol Genet; 2002 Feb 01; 11(3):217-27. PubMed ID: 11823441
    [Abstract] [Full Text] [Related]

  • 2. Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia.
    Adamec J, Rusnak F, Owen WG, Naylor S, Benson LM, Gacy AM, Isaya G.
    Am J Hum Genet; 2000 Sep 01; 67(3):549-62. PubMed ID: 10930361
    [Abstract] [Full Text] [Related]

  • 3. Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
    Rötig A, de Lonlay P, Chretien D, Foury F, Koenig M, Sidi D, Munnich A, Rustin P.
    Nat Genet; 1997 Oct 01; 17(2):215-7. PubMed ID: 9326946
    [Abstract] [Full Text] [Related]

  • 4. Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae.
    Cavadini P, Gellera C, Patel PI, Isaya G.
    Hum Mol Genet; 2000 Oct 12; 9(17):2523-30. PubMed ID: 11030757
    [Abstract] [Full Text] [Related]

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

  • 6. Physical evidence that yeast frataxin is an iron storage protein.
    Gakh O, Adamec J, Gacy AM, Twesten RD, Owen WG, Isaya G.
    Biochemistry; 2002 May 28; 41(21):6798-804. PubMed ID: 12022884
    [Abstract] [Full Text] [Related]

  • 7. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
    Puccio H, Simon D, Cossée M, Criqui-Filipe P, Tiziano F, Melki J, Hindelang C, Matyas R, Rustin P, Koenig M.
    Nat Genet; 2001 Feb 28; 27(2):181-6. PubMed ID: 11175786
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No 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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation.
    Cossée M, Puccio H, Gansmuller A, Koutnikova H, Dierich A, LeMeur M, Fischbeck K, Dollé P, Koenig M.
    Hum Mol Genet; 2000 May 01; 9(8):1219-26. PubMed ID: 10767347
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Maturation of wild-type and mutated frataxin by the mitochondrial processing peptidase.
    Koutnikova H, Campuzano V, Koenig M.
    Hum Mol Genet; 1998 Sep 01; 7(9):1485-9. PubMed ID: 9700204
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins.
    Mühlenhoff U, Richhardt N, Ristow M, Kispal G, Lill R.
    Hum Mol Genet; 2002 Aug 15; 11(17):2025-36. PubMed ID: 12165564
    [Abstract] [Full Text] [Related]

  • 19. Changes in mitochondrial glutathione levels and protein thiol oxidation in ∆yfh1 yeast cells and the lymphoblasts of patients with Friedreich's ataxia.
    Bulteau AL, Planamente S, Jornea L, Dur A, Lesuisse E, Camadro JM, Auchère F.
    Biochim Biophys Acta; 2012 Feb 15; 1822(2):212-25. PubMed ID: 22200491
    [Abstract] [Full Text] [Related]

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


    Page: [Next] [New Search]
    of 17.