These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


890 related items for PubMed ID: 22705440

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway.
    Matsuzaki T, Fujiki Y.
    J Cell Biol; 2008 Dec 29; 183(7):1275-86. PubMed ID: 19114594
    [Abstract] [Full Text] [Related]

  • 3. Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions.
    Fujiki Y, Matsuzono Y, Matsuzaki T, Fransen M.
    Biochim Biophys Acta; 2006 Dec 29; 1763(12):1639-46. PubMed ID: 17069900
    [Abstract] [Full Text] [Related]

  • 4. Peroxisome biogenesis and human peroxisome-deficiency disorders.
    Fujiki Y.
    Proc Jpn Acad Ser B Phys Biol Sci; 2016 Dec 29; 92(10):463-477. PubMed ID: 27941306
    [Abstract] [Full Text] [Related]

  • 5. Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation.
    Matsuzono Y, Matsuzaki T, Fujiki Y.
    J Cell Sci; 2006 Sep 01; 119(Pt 17):3539-50. PubMed ID: 16895967
    [Abstract] [Full Text] [Related]

  • 6. Pex3p-dependent peroxisomal biogenesis initiates in the endoplasmic reticulum of human fibroblasts.
    Toro AA, Araya CA, Córdova GJ, Arredondo CA, Cárdenas HG, Moreno RE, Venegas A, Koenig CS, Cancino J, Gonzalez A, Santos MJ.
    J Cell Biochem; 2009 Aug 15; 107(6):1083-96. PubMed ID: 19479899
    [Abstract] [Full Text] [Related]

  • 7. Peroxisome biogenesis and peroxisome biogenesis disorders.
    Fujiki Y.
    FEBS Lett; 2000 Jun 30; 476(1-2):42-6. PubMed ID: 10878247
    [Abstract] [Full Text] [Related]

  • 8. The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step.
    Pinto MP, Grou CP, Alencastre IS, Oliveira ME, Sá-Miranda C, Fransen M, Azevedo JE.
    J Biol Chem; 2006 Nov 10; 281(45):34492-502. PubMed ID: 16980692
    [Abstract] [Full Text] [Related]

  • 9. In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19p.
    Matsuzono Y, Fujiki Y.
    J Biol Chem; 2006 Jan 06; 281(1):36-42. PubMed ID: 16280322
    [Abstract] [Full Text] [Related]

  • 10. Assembly of Peroxisomal Membrane Proteins via the Direct Pex19p-Pex3p Pathway.
    Liu Y, Yagita Y, Fujiki Y.
    Traffic; 2016 Apr 06; 17(4):433-55. PubMed ID: 26777132
    [Abstract] [Full Text] [Related]

  • 11. Peroxisome biogenesis in mammalian cells.
    Fujiki Y, Okumoto K, Mukai S, Honsho M, Tamura S.
    Front Physiol; 2014 Apr 06; 5():307. PubMed ID: 25177298
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction.
    Sato Y, Shibata H, Nakano H, Matsuzono Y, Kashiwayama Y, Kobayashi Y, Fujiki Y, Imanaka T, Kato H.
    J Biol Chem; 2008 Mar 07; 283(10):6136-44. PubMed ID: 18174172
    [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 07; 67(4):976-81. PubMed ID: 10968777
    [Abstract] [Full Text] [Related]

  • 15. Peroxisome membrane biogenesis: the stage is set.
    Schliebs W, Kunau WH.
    Curr Biol; 2004 May 25; 14(10):R397-9. PubMed ID: 15186768
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of peroxisomal biogenesis disorders caused by defects in peroxisomal matrix protein import.
    Nagotu S, Kalel VC, Erdmann R, Platta HW.
    Biochim Biophys Acta; 2012 Sep 25; 1822(9):1326-36. PubMed ID: 22617146
    [Abstract] [Full Text] [Related]

  • 17. The N-domain of Pex22p can functionally replace the Pex3p N-domain in targeting and peroxisome formation.
    Halbach A, Rucktäschel R, Rottensteiner H, Erdmann R.
    J Biol Chem; 2009 Feb 06; 284(6):3906-16. PubMed ID: 19017643
    [Abstract] [Full Text] [Related]

  • 18. 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 24; 268(3):704-10. PubMed ID: 10679269
    [Abstract] [Full Text] [Related]

  • 19. Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.
    Fransen M, Wylin T, Brees C, Mannaerts GP, Van Veldhoven PP.
    Mol Cell Biol; 2001 Jul 24; 21(13):4413-24. PubMed ID: 11390669
    [Abstract] [Full Text] [Related]

  • 20. Import of peroxisomal matrix and membrane proteins.
    Subramani S, Koller A, Snyder WB.
    Annu Rev Biochem; 2000 Jul 24; 69():399-418. PubMed ID: 10966464
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 45.