BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

309 related articles for article (PubMed ID: 21669930)

  • 1. A Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders.
    Mast FD; Li J; Virk MK; Hughes SC; Simmonds AJ; Rachubinski RA
    Dis Model Mech; 2011 Sep; 4(5):659-72. PubMed ID: 21669930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype.
    Maxwell MA; Nelson PV; Chin SJ; Paton BC; Carey WF; Crane DI
    Hum Genet; 1999; 105(1-2):38-44. PubMed ID: 10480353
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Peroxisomes are required for lipid metabolism and muscle function in Drosophila melanogaster.
    Faust JE; Manisundaram A; Ivanova PT; Milne SB; Summerville JB; Brown HA; Wangler M; Stern M; McNew JA
    PLoS One; 2014; 9(6):e100213. PubMed ID: 24945818
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Depletion of HNRNPA1 induces peroxisomal autophagy by regulating PEX1 expression.
    Park NY; Jo DS; Park SJ; Lee H; Bae JE; Hong Y; Kim JB; Kim YH; Park HJ; Choi JY; Lee HJ; Ryoo ZY; Lee HS; Kim JC; Lee EK; Cho DH
    Biochem Biophys Res Commun; 2021 Mar; 545():69-74. PubMed ID: 33545634
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Peroxisomal disorders.
    Raymond GV
    Curr Opin Pediatr; 1999 Dec; 11(6):572-6. PubMed ID: 10590918
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Peroxisome Biogenesis Disorders.
    Honsho M; Okumoto K; Tamura S; Fujiki Y
    Adv Exp Med Biol; 2020; 1299():45-54. PubMed ID: 33417206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders.
    Crane DI; Maxwell MA; Paton BC
    Hum Mutat; 2005 Sep; 26(3):167-75. PubMed ID: 16086329
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and molecular bases of peroxisome biogenesis disorders.
    Suzuki Y; Shimozawa N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Kondo N
    Genet Med; 2001; 3(5):372-6. PubMed ID: 11545691
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Human disorders of peroxisome metabolism and biogenesis.
    Waterham HR; Ferdinandusse S; Wanders RJ
    Biochim Biophys Acta; 2016 May; 1863(5):922-33. PubMed ID: 26611709
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.