| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF02255787 |
| P698 | PubMed publication ID | 7570184 |
| P2093 | author name string | R Berger | |
| R M Wright | |||
| R H Brown | |||
| D Patterson | |||
| E Mezey | |||
| J E Repine | |||
| M Brownstein | |||
| G Harta | |||
| K P Clancy | |||
| P2860 | cites work | cDNA cloning, characterization, and tissue-specific expression of human xanthine dehydrogenase/xanthine oxidase | Q24320372 |
| Uric acid provides an antioxidant defense in humans against oxidant- and radical-caused aging and cancer: a hypothesis | Q24617394 | ||
| Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase | Q27731976 | ||
| Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis | Q28131805 | ||
| A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis | Q28240033 | ||
| GDNF: a potent survival factor for motoneurons present in peripheral nerve and muscle | Q28241629 | ||
| Genetics, ontogeny, and testosterone inducibility of aldehyde oxidase isozymes in the mouse: Evidence for two genetic loci (Aox-1 and Aox-2) closely linked on chromosome 1 | Q28593370 | ||
| Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation | Q29547561 | ||
| Mapping the whole human genome by fingerprinting yeast artificial chromosomes | Q31095563 | ||
| Molecular cloning of a cDNA coding for mouse liver xanthine dehydrogenase. Regulation of its transcript by interferons in vivo | Q33215516 | ||
| Assignment of human xanthine dehydrogenase gene to chromosome 2p22. | Q34316626 | ||
| Molecular cloning, tissue expression of human xanthine dehydrogenase | Q34337791 | ||
| Cloning of the cDNA encoding human xanthine dehydrogenase (oxidase): structural analysis of the protein and chromosomal location of the gene | Q34343692 | ||
| Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells | Q34529852 | ||
| Identification of the rat xanthine dehydrogenase/oxidase promoter | Q34832990 | ||
| Central Catecholamine Neuron Systems: Anatomy and Physiology of the Norepinephrine and Epinephrine Systems | Q38063416 | ||
| The macroglial cells of the rat optic nerve | Q38613297 | ||
| Dichotomy of the glial cell response to axonal injury and regeneration | Q38696481 | ||
| Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. | Q39064480 | ||
| The mechanism of conversion of rat liver xanthine dehydrogenase from an NAD+-dependent form (type D) to an O2-dependent form (type O) | Q39982769 | ||
| Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy | Q41809526 | ||
| Effects of catecholamines on spinal motoneurones and spinal reflex discharges in the isolated spinal cord of the newborn rat. | Q48511533 | ||
| Transduction of the modulatory effect of catecholamines at the mammalian motor neuron terminal | Q67914874 | ||
| Ethanol-induced iron mobilization: role of acetaldehyde-aldehyde oxidase generated superoxide | Q68479575 | ||
| Mapping of the mouse fibronectin gene (Fn-1) to chromosome 1: conservation of the Idh-1-Cryg-Fn-1 synteny group in mammals | Q69916153 | ||
| Nervenkitt: notes on the history of the concept of neuroglia | Q70070382 | ||
| Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity | Q70142305 | ||
| Localization of the squalene synthase gene (FDFT1) to human chromosome 8p22-p23.1. | Q72036658 | ||
| Mouse model found for ALS | Q72531766 | ||
| Mild ALS in Japan associated with novel SOD mutation | Q72751018 | ||
| Glia: the brain's other cells | Q72839540 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | amyotrophic lateral sclerosis | Q206901 |
| P304 | page(s) | 121-31 | |
| P577 | publication date | 1995-03-01 | |
| P1433 | published in | Somatic Cell and Molecular Genetics | Q7559232 |
| P1476 | title | Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis | |
| P478 | volume | 21 |
| Q37337058 | A(a)LS: Ammonia-induced amyotrophic lateral sclerosis |
| Q37444937 | Absolute quantification of aldehyde oxidase protein in human liver using liquid chromatography-tandem mass spectrometry |
| Q28293711 | Aldehyde Oxidase: An Enzyme of Emerging Importance in Drug Discovery |
| Q46967490 | Aldehyde oxidase activity and stability in water-miscible organic solvents. |
| Q34129222 | Cellular distribution, metabolism and regulation of the xanthine oxidoreductase enzyme system |
| Q33815515 | Characterization of superoxide production from aldehyde oxidase: an important source of oxidants in biological tissues |
| Q33180688 | Cloning of the cDNAs coding for two novel molybdo-flavoproteins showing high similarity with aldehyde oxidase and xanthine oxidoreductase |
| Q73116806 | Cynomolgus monkey liver aldehyde oxidase: extremely high oxidase activity and an attempt at purification |
| Q51991155 | Developmental changes of aldehyde oxidase activity in young Japanese children. |
| Q50534664 | Effect of Tea Beverages on Aldehyde Oxidase Activity |
| Q34547620 | Familial amyotrophic lateral sclerosis |
| Q22010749 | Human phosphoribosylformylglycineamide amidotransferase (FGARAT): regional mapping, complete coding sequence, isolation of a functional genomic clone, and DNA sequence analysis |
| Q36896845 | Isolation and characterization of the human aldehyde oxidase gene: conservation of intron/exon boundaries with the xanthine oxidoreductase gene indicates a common origin |
| Q35063758 | Mammalian molybdo-flavoenzymes, an expanding family of proteins: structure, genetics, regulation, function and pathophysiology |
| Q31813048 | Molecular cloning of the cDNA coding for mouse aldehyde oxidase: tissue distribution and regulation in vivo by testosterone |
| Q54378416 | Molecular cloning, refined chromosomal mapping and structural analysis of the human gene encoding aldehyde oxidase (AOX1), a candidate for the ALS2 gene. |
| Q37881916 | Molybdenum metabolism in the alga Chlamydomonas stands at the crossroad of those in Arabidopsis and humans. |
| Q24649235 | Purification and mechanism of human aldehyde oxidase expressed in Escherichia coli |
| Q28591706 | Purification of the aldehyde oxidase homolog 1 (AOH1) protein and cloning of the AOH1 and aldehyde oxidase homolog 2 (AOH2) genes. Identification of a novel molybdo-flavoprotein gene cluster on mouse chromosome 1 |
| Q34611497 | Revealing the complexity of a monogenic disease: rett syndrome exome sequencing |
| Q37033659 | Role of the molybdoflavoenzyme aldehyde oxidase homolog 2 in the biosynthesis of retinoic acid: generation and characterization of a knockout mouse |
| Q38751930 | Structure and function of mammalian aldehyde oxidases |
| Q71973647 | TAO1, a representative of the molybdenum cofactor containing hydroxylases from tomato |
| Q52647869 | TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD. |
| Q33207069 | The aldehyde oxidase gene cluster in mice and rats. Aldehyde oxidase homologue 3, a novel member of the molybdo-flavoenzyme family with selective expression in the olfactory mucosa. |
| Q33746582 | The four aldehyde oxidases of Drosophila melanogaster have different gene expression patterns and enzyme substrate specificities |
| Q36475086 | The mammalian aldehyde oxidase gene family |
| Q38315449 | The mouse aldehyde oxidase gene: molecular cloning, chromosomal mapping and functional characterization of the 5'-flanking region. |
| Q28569142 | cDNA cloning, sequencing, and characterization of male and female rat liver aldehyde oxidase (rAOX1). Differences in redox status may distinguish male and female forms of hepatic APX |
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