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

PUBMED FOR HANDHELDS

Journal Abstract Search

220 related items for PubMed ID: 1511996

  • 1. Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes.
    Stanczak H, Kremser K, Singh AK, Ashcraft J, Stanley W, Singh I.
    Hum Hered; 1992; 42(3):172-8. PubMed ID: 1511996
    [Abstract] [Full Text] [Related]

  • 2. Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
    Shimozawa N, Suzuki Y, Tomatsu S, Tsukamoto T, Osumi T, Fujiki Y, Kamijo K, Hashimoto T, Kondo N, Orii T.
    Pediatr Res; 1996 May; 39(5):812-5. PubMed ID: 8726233
    [Abstract] [Full Text] [Related]

  • 3. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Aubourg P, Kremser K, Roland MO, Rocchiccioli F, Singh I.
    Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868
    [Abstract] [Full Text] [Related]

  • 4. Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.
    Zoeller RA, Allen LA, Santos MJ, Lazarow PB, Hashimoto T, Tartakoff AM, Raetz CR.
    J Biol Chem; 1989 Dec 25; 264(36):21872-8. PubMed ID: 2689450
    [Abstract] [Full Text] [Related]

  • 5. Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease.
    Singh I, Voigt RG, Sheikh FG, Kremser K, Brown FR.
    Biochem Mol Med; 1997 Aug 25; 61(2):198-207. PubMed ID: 9259985
    [Abstract] [Full Text] [Related]

  • 6. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
    Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A.
    Prog Clin Biol Res; 1990 Aug 25; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 7. Analysis of peroxisomes in lymphoblasts: Zellweger syndrome and a patient with a deletion in chromosome 7.
    Santos MJ, Moser AB, Drwinga H, Moser HW, Lazarow PB.
    Pediatr Res; 1993 May 25; 33(5):441-4. PubMed ID: 8511016
    [Abstract] [Full Text] [Related]

  • 8. [Peroxisome disorders].
    Hashimoto T, Kamijo K, Suzuki Y.
    Tanpakushitsu Kakusan Koso; 1988 Apr 25; 33(5):817-20. PubMed ID: 3270898
    [No Abstract] [Full Text] [Related]

  • 9. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.
    Poll-The BT, Skjeldal OH, Stokke O, Poulos A, Demaugre F, Saudubray JM.
    Hum Genet; 1989 Jan 25; 81(2):175-81. PubMed ID: 2463966
    [Abstract] [Full Text] [Related]

  • 10. Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy.
    Sandhir R, Khan M, Chahal A, Singh I.
    J Lipid Res; 1998 Nov 25; 39(11):2161-71. PubMed ID: 9799802
    [Abstract] [Full Text] [Related]

  • 11. Transformation and characterization of mutant human fibroblasts defective in peroxisome assembly.
    Okamoto H, Suzuki Y, Shimozawa N, Yajima S, Masuno M, Orii T.
    Exp Cell Res; 1992 Aug 25; 201(2):307-12. PubMed ID: 1639130
    [Abstract] [Full Text] [Related]

  • 12. A new peroxisomal beta-oxidation disorder in twin neonates: defective oxidation of both cerotic and pristanic acids.
    Christensen E, Pedersen SA, Leth H, Jakobs C, Schutgens RB, Wanders RJ.
    J Inherit Metab Dis; 1997 Sep 25; 20(5):658-64. PubMed ID: 9323560
    [Abstract] [Full Text] [Related]

  • 13. Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.
    Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Tager JM, van den Bosch H, Thomas GH.
    J Inherit Metab Dis; 1988 Sep 25; 11 Suppl 2():161-4. PubMed ID: 3141699
    [No Abstract] [Full Text] [Related]

  • 14. Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
    Roscher AA, Hoefler S, Hoefler G, Paschke E, Paltauf F, Moser A, Moser H.
    Pediatr Res; 1989 Jul 25; 26(1):67-72. PubMed ID: 2475849
    [Abstract] [Full Text] [Related]

  • 15. Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.
    Schutgens RB, Wanders RJ, Heymans HS, Schram AW, Tager JM, Schrakamp G, van den Bosch H.
    J Inherit Metab Dis; 1987 Jul 25; 10 Suppl 1():33-45. PubMed ID: 3119940
    [Abstract] [Full Text] [Related]

  • 16. Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation.
    Clayton PT, Lake BD, Hjelm M, Stephenson JB, Besley GT, Wanders RJ, Schram AW, Tager JM, Schutgens RB, Lawson AM.
    J Inherit Metab Dis; 1988 Jul 25; 11 Suppl 2():165-8. PubMed ID: 3141700
    [No Abstract] [Full Text] [Related]

  • 17. Late-onset generalized disorder of peroxisomes.
    Burdette DE, Kremser K, Fink JK, Pahan K, Stanley W, Singh I.
    Neurology; 1996 Mar 25; 46(3):829-31. PubMed ID: 8618694
    [Abstract] [Full Text] [Related]

  • 18. Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.
    Baumgartner MR, Verhoeven NM, Jakobs C, Roels F, Espeel M, Martinez M, Rabier D, Wanders RJ, Saudubray JM.
    Neurology; 1998 Nov 25; 51(5):1427-32. PubMed ID: 9818873
    [Abstract] [Full Text] [Related]

  • 19. Complementation analysis of patients with intact peroxisomes and impaired peroxisomal beta-oxidation.
    McGuinness MC, Moser AB, Poll-The BT, Watkins PA.
    Biochem Med Metab Biol; 1993 Apr 25; 49(2):228-42. PubMed ID: 8484962
    [Abstract] [Full Text] [Related]

  • 20. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
    Suzuki Y.
    No To Hattatsu; 1992 Mar 25; 24(2):194-7. PubMed ID: 1373633
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.