BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 9922452)

  • 1. Peroxisome synthesis in the absence of preexisting peroxisomes.
    South ST; Gould SJ
    J Cell Biol; 1999 Jan; 144(2):255-66. PubMed ID: 9922452
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.
    Slawecki ML; Dodt G; Steinberg S; Moser AB; Moser HW; Gould SJ
    J Cell Sci; 1995 May; 108 ( Pt 5)():1817-29. PubMed ID: 7544797
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
    Honsho M; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Am J Hum Genet; 1998 Dec; 63(6):1622-30. PubMed ID: 9837814
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family.
    McCollum D; Monosov E; Subramani S
    J Cell Biol; 1993 May; 121(4):761-74. PubMed ID: 8098333
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders.
    Wiemer EA; Nuttley WM; Bertolaet BL; Li X; Francke U; Wheelock MJ; Anné UK; Johnson KR; Subramani S
    J Cell Biol; 1995 Jul; 130(1):51-65. PubMed ID: 7790377
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1.
    Waterham HR; de Vries Y; Russel KA; Xie W; Veenhuis M; Cregg JM
    Mol Cell Biol; 1996 May; 16(5):2527-36. PubMed ID: 8628321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Yarrowia lipolytica gene PAY2 encodes a 42-kDa peroxisomal integral membrane protein essential for matrix protein import and peroxisome enlargement but not for peroxisome membrane proliferation.
    Eitzen GA; Aitchison JD; Szilard RK; Veenhuis M; Nuttley WM; Rachubinski RA
    J Biol Chem; 1995 Jan; 270(3):1429-36. PubMed ID: 7836411
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders.
    Wendland M; Subramani S
    J Clin Invest; 1993 Nov; 92(5):2462-8. PubMed ID: 7693762
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal.
    Walton PA; Gould SJ; Feramisco JR; Subramani S
    Mol Cell Biol; 1992 Feb; 12(2):531-41. PubMed ID: 1732729
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PER3, a gene required for peroxisome biogenesis in Pichia pastoris, encodes a peroxisomal membrane protein involved in protein import.
    Liu H; Tan X; Russell KA; Veenhuis M; Cregg JM
    J Biol Chem; 1995 May; 270(18):10940-51. PubMed ID: 7738036
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of peroxisomal membrane ghosts with an epitope-tagged integral membrane protein in yeast mutants lacking peroxisomes.
    Purdue PE; Lazarow PB
    Yeast; 1995 Sep; 11(11):1045-60. PubMed ID: 7502580
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein.
    Gärtner J; Chen WW; Kelley RI; Mihalik SJ; Moser HW
    Pediatr Res; 1991 Feb; 29(2):141-6. PubMed ID: 1673025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Enlarged peroxisomes are present in oleic acid-grown Yarrowia lipolytica overexpressing the PEX16 gene encoding an intraperoxisomal peripheral membrane peroxin.
    Eitzen GA; Szilard RK; Rachubinski RA
    J Cell Biol; 1997 Jun; 137(6):1265-78. PubMed ID: 9182661
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import.
    Chang CC; Warren DS; Sacksteder KA; Gould SJ
    J Cell Biol; 1999 Nov; 147(4):761-74. PubMed ID: 10562279
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
    Shimozawa N; Suzuki Y; Tomatsu S; Tsukamoto T; Osumi T; Fujiki Y; Kamijo K; Hashimoto T; Kondo N; Orii T
    Pediatr Res; 1996 May; 39(5):812-5. PubMed ID: 8726233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.
    Maxwell M; Bjorkman J; Nguyen T; Sharp P; Finnie J; Paterson C; Tonks I; Paton BC; Kay GF; Crane DI
    Mol Cell Biol; 2003 Aug; 23(16):5947-57. PubMed ID: 12897163
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.