BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 35932552)

  • 1. Hypomorphic mutation of PEX3 with peroxisomal mosaicism reveals the oscillating nature of peroxisome biogenesis coupled with differential metabolic activities.
    Takashima S; Fujita H; Toyoshi K; Ohba A; Hirata Y; Shimozawa N; Oh-Hashi K
    Mol Genet Metab; 2022; 137(1-2):68-80. PubMed ID: 35932552
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
    Muntau AC; Mayerhofer PU; Paton BC; Kammerer S; Roscher AA
    Am J Hum Genet; 2000 Oct; 67(4):967-75. PubMed ID: 10958759
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The biochemical basis of mitochondrial dysfunction in Zellweger Spectrum Disorder.
    Nuebel E; Morgan JT; Fogarty S; Winter JM; Lettlova S; Berg JA; Chen YC; Kidwell CU; Maschek JA; Clowers KJ; Argyriou C; Chen L; Wittig I; Cox JE; Roh-Johnson M; Braverman N; Bonkowsky J; Gygi SP; Rutter J
    EMBO Rep; 2021 Oct; 22(10):e51991. PubMed ID: 34351705
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease.
    Fujiki Y; Yagita Y; Matsuzaki T
    Biochim Biophys Acta; 2012 Sep; 1822(9):1337-42. PubMed ID: 22705440
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biochemical and genetic characterization of an unusual mild PEX3-related Zellweger spectrum disorder.
    Bjørgo K; Fjær R; Mørk HH; Ferdinandusse S; Falkenberg KD; Waterham HR; Øye AM; Sikiric A; Amundsen SS; Kulseth MA; Selmer K
    Mol Genet Metab; 2017 Aug; 121(4):325-328. PubMed ID: 28673549
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes.
    Nakayama M; Sato H; Okuda T; Fujisawa N; Kono N; Arai H; Suzuki E; Umeda M; Ishikawa HO; Matsuno K
    PLoS One; 2011; 6(8):e22984. PubMed ID: 21826223
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities.
    Wang XM; Yik WY; Zhang P; Lu W; Huang N; Kim BR; Shibata D; Zitting M; Chow RH; Moser AB; Steinberg SJ; Hacia JG
    Stem Cell Res Ther; 2015 Aug; 6():158. PubMed ID: 26319495
    [TBL] [Abstract][Full Text] [Related]  

  • 8. PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
    Ghaedi K; Honsho M; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Am J Hum Genet; 2000 Oct; 67(4):976-81. PubMed ID: 10968777
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder.
    Berendse K; Ebberink MS; Ijlst L; Poll-The BT; Wanders RJ; Waterham HR
    Orphanet J Rare Dis; 2013 Sep; 8():138. PubMed ID: 24016303
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.
    Muntau AC; Holzinger A; Mayerhofer PU; Gärtner J; Roscher AA; Kammerer S
    Biochem Biophys Res Commun; 2000 Feb; 268(3):704-10. PubMed ID: 10679269
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis.
    Krause C; Rosewich H; Woehler A; Gärtner J
    Hum Mol Genet; 2013 Oct; 22(19):3844-57. PubMed ID: 23716570
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
    Yik WY; Steinberg SJ; Moser AB; Moser HW; Hacia JG
    Hum Mutat; 2009 Mar; 30(3):E467-80. PubMed ID: 19105186
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis.
    South ST; Sacksteder KA; Li X; Liu Y; Gould SJ
    J Cell Biol; 2000 Jun; 149(7):1345-60. PubMed ID: 10871277
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Newly identified milder phenotype of peroxisome biogenesis disorder caused by mutated PEX3 gene.
    Matsui S; Funahashi M; Honda A; Shimozawa N
    Brain Dev; 2013 Oct; 35(9):842-8. PubMed ID: 23245813
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Peroxisome biogenesis disorders.
    Steinberg SJ; Dodt G; Raymond GV; Braverman NE; Moser AB; Moser HW
    Biochim Biophys Acta; 2006 Dec; 1763(12):1733-48. PubMed ID: 17055079
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondria as emergency landing for abandoned peroxins.
    Vögtle FN; Meisinger C
    EMBO Rep; 2021 Oct; 22(10):e53790. PubMed ID: 34414648
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Accurate and live peroxisome biogenesis evaluation achieved by lentiviral expression of a green fluorescent protein fused to a peroxisome targeting signal 1.
    Demaret T; Courtoy GE; Ravau J; Van Der Smissen P; Najimi M; Sokal EM
    Histochem Cell Biol; 2020 May; 153(5):295-306. PubMed ID: 32124009
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Quantitative Proteomics and Differential Protein Abundance Analysis after the Depletion of PEX3 from Human Cells Identifies Additional Aspects of Protein Targeting to the ER.
    Zimmermann R; Lang S; Lerner M; Förster F; Nguyen D; Helms V; Schrul B
    Int J Mol Sci; 2021 Dec; 22(23):. PubMed ID: 34884833
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.
    Nguyen T; Bjorkman J; Paton BC; Crane DI
    J Cell Sci; 2006 Feb; 119(Pt 4):636-45. PubMed ID: 16449325
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders.
    Brosius U; Gärtner J
    Cell Mol Life Sci; 2002 Jun; 59(6):1058-69. PubMed ID: 12169017
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.