BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 24989250)

  • 1. CUL4A-DDB1-Rbx1 E3 ligase controls the quality of the PTS2 receptor Pex7p.
    Miyauchi-Nanri Y; Mukai S; Kuroda K; Fujiki Y
    Biochem J; 2014 Oct; 463(1):65-74. PubMed ID: 24989250
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional studies on human Pex7p: subcellular localization and interaction with proteins containing a peroxisome-targeting signal type 2 and other peroxins.
    Ghys K; Fransen M; Mannaerts GP; Van Veldhoven PP
    Biochem J; 2002 Jul; 365(Pt 1):41-50. PubMed ID: 11931631
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview.
    Purdue PE; Skoneczny M; Yang X; Zhang JW; Lazarow PB
    Neurochem Res; 1999 Apr; 24(4):581-6. PubMed ID: 10227689
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype.
    Braverman N; Chen L; Lin P; Obie C; Steel G; Douglas P; Chakraborty PK; Clarke JT; Boneh A; Moser A; Moser H; Valle D
    Hum Mutat; 2002 Oct; 20(4):284-97. PubMed ID: 12325024
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor.
    Motley AM; Hettema EH; Hogenhout EM; Brites P; ten Asbroek AL; Wijburg FA; Baas F; Heijmans HS; Tabak HF; Wanders RJ; Distel B
    Nat Genet; 1997 Apr; 15(4):377-80. PubMed ID: 9090382
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.
    Purdue PE; Zhang JW; Skoneczny M; Lazarow PB
    Nat Genet; 1997 Apr; 15(4):381-4. PubMed ID: 9090383
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PTS2 protein import into mammalian peroxisomes.
    Legakis JE; Terlecky SR
    Traffic; 2001 Apr; 2(4):252-60. PubMed ID: 11285135
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform.
    Barøy T; Koster J; Strømme P; Ebberink MS; Misceo D; Ferdinandusse S; Holmgren A; Hughes T; Merckoll E; Westvik J; Woldseth B; Walter J; Wood N; Tvedt B; Stadskleiv K; Wanders RJ; Waterham HR; Frengen E
    Hum Mol Genet; 2015 Oct; 24(20):5845-54. PubMed ID: 26220973
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.
    Mukai S; Ghaedi K; Fujiki Y
    J Biol Chem; 2002 Mar; 277(11):9548-61. PubMed ID: 11756410
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The import receptor Pex7p and the PTS2 targeting sequence.
    Lazarow PB
    Biochim Biophys Acta; 2006 Dec; 1763(12):1599-604. PubMed ID: 16996627
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular mechanisms of import of peroxisome-targeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL.
    Mukai S; Fujiki Y
    J Biol Chem; 2006 Dec; 281(49):37311-20. PubMed ID: 17040904
    [TBL] [Abstract][Full Text] [Related]  

  • 12. In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes.
    Miyata N; Hosoi K; Mukai S; Fujiki Y
    Biochim Biophys Acta; 2009 May; 1793(5):860-70. PubMed ID: 19264098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of a novel missense mutation of PEX7 gene in an Iranian patient with rhizomelic chondrodysplasia punctata type 1.
    Mohamadynejad P; Ghaedi K; Shafeghati Y; Salamian A; Tanhaie S; Karamali F; Rabiee F; Parivar K; Baharvand H; Nasr-Esfahani MH
    Gene; 2013 Apr; 518(2):461-6. PubMed ID: 23357221
    [TBL] [Abstract][Full Text] [Related]  

  • 14. PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.
    Braverman N; Steel G; Lin P; Moser A; Moser H; Valle D
    Genomics; 2000 Jan; 63(2):181-92. PubMed ID: 10673331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals.
    Honsho M; Hashiguchi Y; Ghaedi K; Fujiki Y
    J Biochem; 2011 Feb; 149(2):203-10. PubMed ID: 21047816
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The cytosolic peroxisome-targeting signal (PTS)-receptors, Pex7p and Pex5pL, are sufficient to transport PTS2 proteins to peroxisomes.
    Mukai S; Matsuzaki T; Fujiki Y
    Biochim Biophys Acta Mol Cell Res; 2019 Mar; 1866(3):441-449. PubMed ID: 30296498
    [TBL] [Abstract][Full Text] [Related]  

  • 17. C86Y: as a destructive homozygous mutation deteriorating Pex7p function causing rhizomelic chondrodysplasia punctata type I.
    Salamian A; Mohamadynejad P; Ghaedi K; Nejati AS; Shafeghati Y; Ahnak MB; Nematollahi M; Karbalaie K; Hadipour F; Baharvand H; Nasr-Esfahani MH
    Ann Clin Lab Sci; 2013; 43(1):76-80. PubMed ID: 23462609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata.
    Braverman N; Steel G; Obie C; Moser A; Moser H; Gould SJ; Valle D
    Nat Genet; 1997 Apr; 15(4):369-76. PubMed ID: 9090381
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14p.
    Otera H; Harano T; Honsho M; Ghaedi K; Mukai S; Tanaka A; Kawai A; Shimizu N; Fujiki Y
    J Biol Chem; 2000 Jul; 275(28):21703-14. PubMed ID: 10767286
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pex18p and Pex21p, a novel pair of related peroxins essential for peroxisomal targeting by the PTS2 pathway.
    Purdue PE; Yang X; Lazarow PB
    J Cell Biol; 1998 Dec; 143(7):1859-69. PubMed ID: 9864360
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.