BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 11405337)

  • 1. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.
    Suzuki Y; Shimozawa N; Imamura A; Fukuda S; Zhang Z; Orii T; Kondo N
    J Inherit Metab Dis; 2001 Apr; 24(2):151-65. PubMed ID: 11405337
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Temperature sensitivity in peroxisome assembly processes characterizes milder forms of peroxisome biogenesis disorders.
    Osumi T; Imamura A; Tsukamoto T; Fujiwara C; Hashiguchi N; Shimozawa N; Suzuki Y; Kondo N
    Cell Biochem Biophys; 2000; 32 Spring():165-70. PubMed ID: 11330043
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.
    Nito K; Kamigaki A; Kondo M; Hayashi M; Nishimura M
    Plant Cell Physiol; 2007 Jun; 48(6):763-74. PubMed ID: 17478547
    [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. Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.
    Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Wanders RJ; Kondo N
    Pediatr Res; 2000 Oct; 48(4):541-5. PubMed ID: 11004248
    [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. Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
    Tamura S; Matsumoto N; Imamura A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Biochem J; 2001 Jul; 357(Pt 2):417-26. PubMed ID: 11439091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.
    Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Kondo N
    Brain Dev; 2000 Jan; 22(1):8-12. PubMed ID: 10761827
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Metabolic control of peroxisome abundance.
    Chang CC; South S; Warren D; Jones J; Moser AB; Moser HW; Gould SJ
    J Cell Sci; 1999 May; 112 ( Pt 10)():1579-90. PubMed ID: 10212151
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.
    Faust PL; Banka D; Siriratsivawong R; Ng VG; Wikander TM
    J Inherit Metab Dis; 2005; 28(3):369-83. PubMed ID: 15868469
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism.
    Gootjes J; Schmohl F; Mooijer PA; Dekker C; Mandel H; Topcu M; Huemer M; Von Schütz M; Marquardt T; Smeitink JA; Waterham HR; Wanders RJ
    Hum Mutat; 2004 Aug; 24(2):130-9. PubMed ID: 15241794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders.
    Law KB; Bronte-Tinkew D; Di Pietro E; Snowden A; Jones RO; Moser A; Brumell JH; Braverman N; Kim PK
    Autophagy; 2017 May; 13(5):868-884. PubMed ID: 28521612
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.
    Shimozawa N; Nagase T; Takemoto Y; Ohura T; Suzuki Y; Kondo N
    Am J Med Genet A; 2003 Jul; 120A(1):40-3. PubMed ID: 12794690
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.
    Walter C; Gootjes J; Mooijer PA; Portsteffen H; Klein C; Waterham HR; Barth PG; Epplen JT; Kunau WH; Wanders RJ; Dodt G
    Am J Hum Genet; 2001 Jul; 69(1):35-48. PubMed ID: 11389485
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function.
    Li X; Baumgart E; Morrell JC; Jimenez-Sanchez G; Valle D; Gould SJ
    Mol Cell Biol; 2002 Jun; 22(12):4358-65. PubMed ID: 12024045
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.
    Liu Y; Björkman J; Urquhart A; Wanders RJ; Crane DI; Gould SJ
    Am J Hum Genet; 1999 Sep; 65(3):621-34. PubMed ID: 10441568
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.