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Journal Abstract Search

214 related items for PubMed ID: 7910611

  • 1. Differential protein import deficiencies in human peroxisome assembly disorders.
    Motley A, Hettema E, Distel B, Tabak H.
    J Cell Biol; 1994 May; 125(4):755-67. PubMed ID: 7910611
    [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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Abnormality in catalase import into peroxisomes leads to severe neurological disorder.
    Sheikh FG, Pahan K, Khan M, Barbosa E, Singh I.
    Proc Natl Acad Sci U S A; 1998 Mar 17; 95(6):2961-6. PubMed ID: 9501198
    [Abstract] [Full Text] [Related]

  • 5. The import receptor for the peroxisomal targeting signal 2 (PTS2) in Saccharomyces cerevisiae is encoded by the PAS7 gene.
    Rehling P, Marzioch M, Niesen F, Wittke E, Veenhuis M, Kunau WH.
    EMBO J; 1996 Jun 17; 15(12):2901-13. PubMed ID: 8670791
    [Abstract] [Full Text] [Related]

  • 6. Import of the peroxisomal targeting signal type 2 protein 3-ketoacyl-coenzyme a thiolase into glyoxysomes.
    Johnson TL, Olsen LJ.
    Plant Physiol; 2003 Dec 17; 133(4):1991-9. PubMed ID: 14630959
    [Abstract] [Full Text] [Related]

  • 7. Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.
    Zhang JW, Lazarow PB.
    J Cell Biol; 1996 Feb 17; 132(3):325-34. PubMed ID: 8636211
    [Abstract] [Full Text] [Related]

  • 8. An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes.
    Braverman N, Dodt G, Gould SJ, Valle D.
    Hum Mol Genet; 1998 Aug 17; 7(8):1195-205. PubMed ID: 9668159
    [Abstract] [Full Text] [Related]

  • 9. Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence.
    Purdue PE, Lazarow PB.
    J Cell Biol; 1996 Aug 17; 134(4):849-62. PubMed ID: 8769411
    [Abstract] [Full Text] [Related]

  • 10. 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 17; 130(1):51-65. PubMed ID: 7790377
    [Abstract] [Full Text] [Related]

  • 11. Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.
    Otera H, Okumoto K, Tateishi K, Ikoma Y, Matsuda E, Nishimura M, Tsukamoto T, Osumi T, Ohashi K, Higuchi O, Fujiki Y.
    Mol Cell Biol; 1998 Jan 17; 18(1):388-99. PubMed ID: 9418886
    [Abstract] [Full Text] [Related]

  • 12. PTS2 protein import into mammalian peroxisomes.
    Legakis JE, Terlecky SR.
    Traffic; 2001 Apr 17; 2(4):252-60. PubMed ID: 11285135
    [Abstract] [Full Text] [Related]

  • 13. Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1.
    Motley A, Lumb MJ, Oatey PB, Jennings PR, De Zoysa PA, Wanders RJ, Tabak HF, Danpure CJ.
    J Cell Biol; 1995 Oct 17; 131(1):95-109. PubMed ID: 7559790
    [Abstract] [Full Text] [Related]

  • 14. Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.
    Ebberink MS, Mooyer PA, Koster J, Dekker CJ, Eyskens FJ, Dionisi-Vici C, Clayton PT, Barth PG, Wanders RJ, Waterham HR.
    Hum Mutat; 2009 Jan 17; 30(1):93-8. PubMed ID: 18712838
    [Abstract] [Full Text] [Related]

  • 15. Isolation of peroxisome assembly mutants from Saccharomyces cerevisiae with different morphologies using a novel positive selection procedure.
    Van der Leij I, Van den Berg M, Boot R, Franse M, Distel B, Tabak HF.
    J Cell Biol; 1992 Oct 17; 119(1):153-62. PubMed ID: 1356111
    [Abstract] [Full Text] [Related]

  • 16. The methylotrophic yeast Hansenula polymorpha contains an inducible import pathway for peroxisomal matrix proteins with an N-terminal targeting signal (PTS2 proteins).
    Faber KN, Haima P, Gietl C, Harder W, Ab G, Veenhuis M.
    Proc Natl Acad Sci U S A; 1994 Dec 20; 91(26):12985-9. PubMed ID: 7809160
    [Abstract] [Full Text] [Related]

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  • 18. Pex20p functions as the receptor for non-PTS1/non-PTS2 acyl-CoA oxidase import into peroxisomes of the yeast Yarrowia lipolytica.
    Chang J, Rachubinski RA.
    Traffic; 2019 Jul 20; 20(7):504-515. PubMed ID: 31042004
    [Abstract] [Full Text] [Related]

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  • 20. Pex20p of the yeast Yarrowia lipolytica is required for the oligomerization of thiolase in the cytosol and for its targeting to the peroxisome.
    Titorenko VI, Smith JJ, Szilard RK, Rachubinski RA.
    J Cell Biol; 1998 Jul 27; 142(2):403-20. PubMed ID: 9679140
    [Abstract] [Full Text] [Related]

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