BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

253 related articles for article (PubMed ID: 10930361)

  • 1. 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; 67(3):549-62. PubMed ID: 10930361
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 11(3):217-27. PubMed ID: 11823441
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. 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; 41(21):6798-804. PubMed ID: 12022884
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional studies of frataxin.
    Isaya G; O'Neill HA; Gakh O; Park S; Mantcheva R; Mooney SM
    Acta Paediatr Suppl; 2004 May; 93(445):68-71; discussion 72-3. PubMed ID: 15176725
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial intermediate peptidase and the yeast frataxin homolog together maintain mitochondrial iron homeostasis in Saccharomyces cerevisiae.
    Branda SS; Yang ZY; Chew A; Isaya G
    Hum Mol Genet; 1999 Jun; 8(6):1099-110. PubMed ID: 10332043
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 17(2):215-7. PubMed ID: 9326946
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Yeast frataxin sequentially chaperones and stores iron by coupling protein assembly with iron oxidation.
    Park S; Gakh O; O'Neill HA; Mangravita A; Nichol H; Ferreira GC; Isaya G
    J Biol Chem; 2003 Aug; 278(33):31340-51. PubMed ID: 12732649
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Low iron concentration and aconitase deficiency in a yeast frataxin homologue deficient strain.
    Foury F
    FEBS Lett; 1999 Aug; 456(2):281-4. PubMed ID: 10456324
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Yeast and human frataxin are processed to mature form in two sequential steps by the mitochondrial processing peptidase.
    Branda SS; Cavadini P; Adamec J; Kalousek F; Taroni F; Isaya G
    J Biol Chem; 1999 Aug; 274(32):22763-9. PubMed ID: 10428860
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Frataxin expression rescues mitochondrial dysfunctions in FRDA cells.
    Tan G; Chen LS; Lonnerdal B; Gellera C; Taroni FA; Cortopassi GA
    Hum Mol Genet; 2001 Sep; 10(19):2099-107. PubMed ID: 11590127
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial dysfunction in friedreich's ataxia.
    Lodi R; Taylor DJ; Schapira AH
    Biol Signals Recept; 2001; 10(3-4):263-70. PubMed ID: 11351132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Towards a structural understanding of Friedreich's ataxia: the solution structure of frataxin.
    Musco G; Stier G; Kolmerer B; Adinolfi S; Martin S; Frenkiel T; Gibson T; Pastore A
    Structure; 2000 Jul; 8(7):695-707. PubMed ID: 10903947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.
    Babcock M; de Silva D; Oaks R; Davis-Kaplan S; Jiralerspong S; Montermini L; Pandolfo M; Kaplan J
    Science; 1997 Jun; 276(5319):1709-12. PubMed ID: 9180083
    [TBL] [Abstract][Full Text] [Related]  

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

  • 16. A structural approach to understanding the iron-binding properties of phylogenetically different frataxins.
    Adinolfi S; Trifuoggi M; Politou AS; Martin S; Pastore A
    Hum Mol Genet; 2002 Aug; 11(16):1865-77. PubMed ID: 12140189
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 11(17):2025-36. PubMed ID: 12165564
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Friedreich ataxia: from GAA triplet-repeat expansion to frataxin deficiency.
    Patel PI; Isaya G
    Am J Hum Genet; 2001 Jul; 69(1):15-24. PubMed ID: 11391483
    [No Abstract]   [Full Text] [Related]  

  • 19. The yeast frataxin homologue mediates mitochondrial iron efflux. Evidence for a mitochondrial iron cycle.
    Radisky DC; Babcock MC; Kaplan J
    J Biol Chem; 1999 Feb; 274(8):4497-9. PubMed ID: 9988680
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Iron metabolism and mitochondrial abnormalities in Friedreich ataxia.
    Pandolfo M
    Blood Cells Mol Dis; 2002; 29(3):536-47; discussion 548-52. PubMed ID: 12547248
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.