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141 related items for PubMed ID: 7570184

  • 1. Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis.
    Berger R, Mezey E, Clancy KP, Harta G, Wright RM, Repine JE, Brown RH, Brownstein M, Patterson D.
    Somat Cell Mol Genet; 1995 Mar; 21(2):121-31. PubMed ID: 7570184
    [Abstract] [Full Text] [Related]

  • 2. The human molybdenum hydroxylase gene family: co-conspirators in metabolic free-radical generation and disease.
    Wright RM, Repine JE.
    Biochem Soc Trans; 1997 Aug; 25(3):799-804. PubMed ID: 9388549
    [No Abstract] [Full Text] [Related]

  • 3. Properties of rabbit liver aldehyde oxidase and the relationship of the enzyme to xanthine oxidase and dehydrogenase.
    Turner NA, Doyle WA, Ventom AM, Bray RC.
    Eur J Biochem; 1995 Sep 01; 232(2):646-57. PubMed ID: 7556219
    [Abstract] [Full Text] [Related]

  • 4. The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22.
    Rytkönen EM, Halila R, Laan M, Saksela M, Kallioniemi OP, Palotie A, Raivio KO.
    Cytogenet Cell Genet; 1995 Sep 01; 68(1-2):61-3. PubMed ID: 7956361
    [Abstract] [Full Text] [Related]

  • 5. Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.
    Hosler BA, Sapp PC, Berger R, O'Neill G, Bejaoui K, Hamida MB, Hentati F, Chin W, McKenna-Yasek D, Haines JL, Patterson D, Horvitz HR, Brown RH, Day CB.
    Neurogenetics; 1998 Dec 01; 2(1):34-42. PubMed ID: 9933298
    [Abstract] [Full Text] [Related]

  • 6. Gene expression in Drosophila: post-translational modification of aldehyde oxidase and xanthine dehydrogenase.
    Finnerty V, McCarron M, Johnson GB.
    Mol Gen Genet; 1979 Apr 17; 172(1):37-43. PubMed ID: 286873
    [Abstract] [Full Text] [Related]

  • 7. Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis.
    Boukaftane Y, Khoris J, Moulard B, Salachas F, Meininger V, Malafosse A, Camu W, Rouleau GA.
    Can J Neurol Sci; 1998 Aug 17; 25(3):192-6. PubMed ID: 9706719
    [Abstract] [Full Text] [Related]

  • 8. Molecular cloning, refined chromosomal mapping and structural analysis of the human gene encoding aldehyde oxidase (AOX1), a candidate for the ALS2 gene.
    Wright RM, Weigel LK, Varella-Garcia M, Vaitaitis G, Repine JE.
    Redox Rep; 1997 Jun 17; 3(3):135-44. PubMed ID: 27406959
    [Abstract] [Full Text] [Related]

  • 9. Familial amyotrophic lateral sclerosis.
    Siddique T, Hentati A.
    Clin Neurosci; 1997 Jun 17; 3(6):338-47. PubMed ID: 9021255
    [Abstract] [Full Text] [Related]

  • 10. Cloning of the cDNA encoding human xanthine dehydrogenase (oxidase): structural analysis of the protein and chromosomal location of the gene.
    Ichida K, Amaya Y, Noda K, Minoshima S, Hosoya T, Sakai O, Shimizu N, Nishino T.
    Gene; 1993 Nov 15; 133(2):279-84. PubMed ID: 8224915
    [Abstract] [Full Text] [Related]

  • 11. Genetic control of aldehyde oxidase activity and cross-reacting-material in Drosophila melanogaster.
    Meidinger EM, Williamson JH.
    Can J Genet Cytol; 1978 Dec 15; 20(4):489-97. PubMed ID: 94842
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  • 15. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
    Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX.
    Nature; 1993 Mar 04; 362(6415):59-62. PubMed ID: 8446170
    [Abstract] [Full Text] [Related]

  • 16. The effects of molybate, tungstate and lxd on aldehyde oxidase and xanthine dehydrogenase in Drosophila melanogaster.
    Bentley MM, Williamson JH, Oliver MJ.
    Can J Genet Cytol; 1981 Mar 04; 23(4):597-609. PubMed ID: 6804069
    [Abstract] [Full Text] [Related]

  • 17. Isolation and characterization of the human aldehyde oxidase gene: conservation of intron/exon boundaries with the xanthine oxidoreductase gene indicates a common origin.
    Terao M, Kurosaki M, Demontis S, Zanotta S, Garattini E.
    Biochem J; 1998 Jun 01; 332 ( Pt 2)(Pt 2):383-93. PubMed ID: 9601067
    [Abstract] [Full Text] [Related]

  • 18. Genetic and developmental characterization of the aldox-2 locus of Drosophila melanogaster.
    Meidinger RG, Bentley MM.
    Biochem Genet; 1986 Oct 01; 24(9-10):683-99. PubMed ID: 3096310
    [Abstract] [Full Text] [Related]

  • 19. A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis.
    Rosen DR, Bowling AC, Patterson D, Usdin TB, Sapp P, Mezey E, McKenna-Yasek D, O'Regan J, Rahmani Z, Ferrante RJ.
    Hum Mol Genet; 1994 Jun 01; 3(6):981-7. PubMed ID: 7951249
    [Abstract] [Full Text] [Related]

  • 20. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
    Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C.
    Nat Genet; 1994 Jul 01; 7(3):425-8. PubMed ID: 7920663
    [Abstract] [Full Text] [Related]

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