BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 10453730)

  • 1. Hereditary spastic paraplegia: mitochondrial metalloproteases of yeast.
    Pearce DA
    Hum Genet; 1999 Jun; 104(6):443-8. PubMed ID: 10453730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia.
    Atorino L; Silvestri L; Koppen M; Cassina L; Ballabio A; Marconi R; Langer T; Casari G
    J Cell Biol; 2003 Nov; 163(4):777-87. PubMed ID: 14623864
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein.
    Kremmidiotis G; Gardner AE; Settasatian C; Savoia A; Sutherland GR; Callen DF
    Genomics; 2001 Aug; 76(1-3):58-65. PubMed ID: 11549317
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.
    Nolden M; Ehses S; Koppen M; Bernacchia A; Rugarli EI; Langer T
    Cell; 2005 Oct; 123(2):277-89. PubMed ID: 16239145
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The human homologue of the yeast mitochondrial AAA metalloprotease Yme1p complements a yeast yme1 disruptant.
    Shah ZH; Hakkaart GA; Arku B; de Jong L; van der Spek H; Grivell LA; Jacobs HT
    FEBS Lett; 2000 Aug; 478(3):267-70. PubMed ID: 10930580
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification and characterization of AFG3L2, a novel paraplegin-related gene.
    Banfi S; Bassi MT; Andolfi G; Marchitiello A; Zanotta S; Ballabio A; Casari G; Franco B
    Genomics; 1999 Jul; 59(1):51-8. PubMed ID: 10395799
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia.
    Koppen M; Metodiev MD; Casari G; Rugarli EI; Langer T
    Mol Cell Biol; 2007 Jan; 27(2):758-67. PubMed ID: 17101804
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Promotion of mitochondrial membrane complex assembly by a proteolytically inactive yeast Lon.
    Rep M; van Dijl JM; Suda K; Schatz G; Grivell LA; Suzuki CK
    Science; 1996 Oct; 274(5284):103-6. PubMed ID: 8810243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional evaluation of paraplegin mutations by a yeast complementation assay.
    Bonn F; Pantakani K; Shoukier M; Langer T; Mannan AU
    Hum Mutat; 2010 May; 31(5):617-21. PubMed ID: 20186691
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification and characterization of YME1L1, a novel paraplegin-related gene.
    Coppola M; Pizzigoni A; Banfi S; Bassi MT; Casari G; Incerti B
    Genomics; 2000 May; 66(1):48-54. PubMed ID: 10843804
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
    Casari G; De Fusco M; Ciarmatori S; Zeviani M; Mora M; Fernandez P; De Michele G; Filla A; Cocozza S; Marconi R; Dürr A; Fontaine B; Ballabio A
    Cell; 1998 Jun; 93(6):973-83. PubMed ID: 9635427
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Alternative splicing of Spg7, a gene involved in hereditary spastic paraplegia, encodes a variant of paraplegin targeted to the endoplasmic reticulum.
    Mancuso G; Barth E; Crivello P; Rugarli EI
    PLoS One; 2012; 7(5):e36337. PubMed ID: 22563492
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.
    Pierson TM; Adams D; Bonn F; Martinelli P; Cherukuri PF; Teer JK; Hansen NF; Cruz P; Mullikin For The Nisc Comparative Sequencing Program JC; Blakesley RW; Golas G; Kwan J; Sandler A; Fuentes Fajardo K; Markello T; Tifft C; Blackstone C; Rugarli EI; Langer T; Gahl WA; Toro C
    PLoS Genet; 2011 Oct; 7(10):e1002325. PubMed ID: 22022284
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia.
    Rugarli EI; Langer T
    Trends Mol Med; 2006 Jun; 12(6):262-9. PubMed ID: 16647881
    [TBL] [Abstract][Full Text] [Related]  

  • 15. m-AAA proteases, mitochondrial calcium homeostasis and neurodegeneration.
    Patron M; Sprenger HG; Langer T
    Cell Res; 2018 Mar; 28(3):296-306. PubMed ID: 29451229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary spastic paraplegia: respiratory choke or unactivated substrate?
    Claypool SM; Koehler CM
    Cell; 2005 Oct; 123(2):183-5. PubMed ID: 16239134
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.
    Elleuch N; Depienne C; Benomar A; Hernandez AM; Ferrer X; Fontaine B; Grid D; Tallaksen CM; Zemmouri R; Stevanin G; Durr A; Brice A
    Neurology; 2006 Mar; 66(5):654-9. PubMed ID: 16534102
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absence of the mitochondrial AAA protease Yme1p restores F0-ATPase subunit accumulation in an oxa1 deletion mutant of Saccharomyces cerevisiae.
    Lemaire C; Hamel P; Velours J; Dujardin G
    J Biol Chem; 2000 Aug; 275(31):23471-5. PubMed ID: 10816574
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Investigation of mitochondrial function in hereditary spastic paraparesis.
    McDermott CJ; Taylor RW; Hayes C; Johnson M; Bushby KM; Turnbull DM; Shaw PJ
    Neuroreport; 2003 Mar; 14(3):485-8. PubMed ID: 12634509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ATP-dependent proteases controlling mitochondrial function in the yeast Saccharomyces cerevisiae.
    Van Dyck L; Langer T
    Cell Mol Life Sci; 1999 Nov; 56(9-10):825-42. PubMed ID: 11212342
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.