BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 9700204)

  • 1. 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]  

  • 2. Maturation of frataxin within mammalian and yeast mitochondria: one-step processing by matrix processing peptidase.
    Gordon DM; Shi Q; Dancis A; Pain D
    Hum Mol Genet; 1999 Nov; 8(12):2255-62. PubMed ID: 10545606
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 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. Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue.
    Wilson RB; Roof DM
    Nat Genet; 1997 Aug; 16(4):352-7. PubMed ID: 9241271
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. The in vivo mitochondrial two-step maturation of human frataxin.
    Schmucker S; Argentini M; Carelle-Calmels N; Martelli A; Puccio H
    Hum Mol Genet; 2008 Nov; 17(22):3521-31. PubMed ID: 18725397
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Frataxin gene of Friedreich's ataxia is targeted to mitochondria.
    Priller J; Scherzer CR; Faber PW; MacDonald ME; Young AB
    Ann Neurol; 1997 Aug; 42(2):265-9. PubMed ID: 9266741
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distinct roles for two N-terminal cleaved domains in mitochondrial import of the yeast frataxin homolog, Yfh1p.
    Gordon DM; Kogan M; Knight SA; Dancis A; Pain D
    Hum Mol Genet; 2001 Feb; 10(3):259-69. PubMed ID: 11159945
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 27(2):181-6. PubMed ID: 11175786
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.
    Campuzano V; Montermini L; Lutz Y; Cova L; Hindelang C; Jiralerspong S; Trottier Y; Kish SJ; Faucheux B; Trouillas P; Authier FJ; Dürr A; Mandel JL; Vescovi A; Pandolfo M; Koenig M
    Hum Mol Genet; 1997 Oct; 6(11):1771-80. PubMed ID: 9302253
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular pathogenesis of Friedreich ataxia.
    Pandolfo M
    Arch Neurol; 1999 Oct; 56(10):1201-8. PubMed ID: 10520935
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Deciphering the cause of Friedreich ataxia.
    Koenig M; Mandel JL
    Curr Opin Neurobiol; 1997 Oct; 7(5):689-94. PubMed ID: 9384553
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.