BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 17922512)

  • 1. Partial characterization of the proteome of the mouse striatum.
    Guo LT; Friedmann T; King CC
    Proteomics; 2007 Nov; 7(21):3867-9. PubMed ID: 17922512
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Golgi study of neuronal architecture in a genetic mouse model for Lesch-Nyhan disease.
    Mikolaenko I; Rao LM; Roberts RC; Kolb B; Jinnah HA
    Neurobiol Dis; 2005 Nov; 20(2):479-90. PubMed ID: 15908225
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of the dopamine defect in primary cultures of dopaminergic neurons from hypoxanthine phosphoribosyltransferase knockout mice.
    Smith DW; Friedmann T
    Mol Ther; 2000 May; 1(5 Pt 1):486-91. PubMed ID: 10933970
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Functional analysis of brain dopamine systems in a genetic mouse model of Lesch-Nyhan syndrome.
    Jinnah HA; Langlais PJ; Friedmann T
    J Pharmacol Exp Ther; 1992 Nov; 263(2):596-607. PubMed ID: 1432691
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Study of the adenosinergic system in the brain of HPRT knockout mouse (Lesch-Nyhan disease).
    Bertelli M; Cecchin S; Lapucci C; Jacomelli G; Jinnah HA; Pandolfo M; Micheli V
    Clin Chim Acta; 2006 Nov; 373(1-2):104-7. PubMed ID: 16793031
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Guanine nucleotide depletion induces differentiation and aberrant neurite outgrowth in human dopaminergic neuroblastoma lines: a model for basal ganglia dysfunction in Lesch-Nyhan disease.
    Messina E; Micheli V; Giacomello A
    Neurosci Lett; 2005 Feb; 375(2):97-100. PubMed ID: 15670649
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Altered membrane NTPase activity in Lesch-Nyhan disease fibroblasts: comparison with HPRT knockout mice and HPRT-deficient cell lines.
    Pinto CS; Jinnah HA; Shirley TL; Nyhan WL; Seifert R
    J Neurochem; 2005 Jun; 93(6):1579-86. PubMed ID: 15935074
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The biochemical basis of the neurobehavioral abnormalities in the Lesch-Nyhan syndrome: a hypothesis.
    Neychev VK; Mitev VI
    Med Hypotheses; 2004; 63(1):131-4. PubMed ID: 15193365
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Is ZMP the toxic metabolite in Lesch-Nyhan disease?
    López JM
    Med Hypotheses; 2008 Nov; 71(5):657-63. PubMed ID: 18710792
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Consequences of impaired purine recycling on the proteome in a cellular model of Lesch-Nyhan disease.
    Dammer EB; Göttle M; Duong DM; Hanfelt J; Seyfried NT; Jinnah HA
    Mol Genet Metab; 2015 Apr; 114(4):570-579. PubMed ID: 25769394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular, biochemical, and genetic characterization of a female patient with Lesch-Nyhan disease.
    Rinat C; Zoref-Shani E; Ben-Neriah Z; Bromberg Y; Becker-Cohen R; Feinstein S; Sperling O; Frishberg Y
    Mol Genet Metab; 2006 Mar; 87(3):249-52. PubMed ID: 16343967
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human neural stem cells: a model system for the study of Lesch-Nyhan disease neurological aspects.
    Cristini S; Navone S; Canzi L; Acerbi F; Ciusani E; Hladnik U; de Gemmis P; Alessandri G; Colombo A; Parati E; Invernici G
    Hum Mol Genet; 2010 May; 19(10):1939-50. PubMed ID: 20159777
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Purine nucleotide metabolism in cultured neurons and astroglia from HPRT-deficient knockout mice.
    Zoref-Shani E; Boer P; Brosh S; Pelled D; Bromberg Y; Sperling O
    Ital J Biochem; 2001; 50(1-2):9-13. PubMed ID: 12170582
    [No Abstract]   [Full Text] [Related]  

  • 14. [Physiopathology of neurological signs of hypoxanthine-guanine phosphoribosyltransferase deficiency].
    Torres-Jiménez R; Mateos-Antón F; Arcas-Martínez J; Pascual-Castroviejo I; García-Puig J
    Rev Neurol; 1998 Dec; 27(160):1050-4. PubMed ID: 9951034
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease.
    Göttle M; Prudente CN; Fu R; Sutcliffe D; Pang H; Cooper D; Veledar E; Glass JD; Gearing M; Visser JE; Jinnah HA
    Ann Neurol; 2014 Jul; 76(1):95-107. PubMed ID: 24891139
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Influence of age and strain on striatal dopamine loss in a genetic mouse model of Lesch-Nyhan disease.
    Jinnah HA; Jones MD; Wojcik BE; Rothstein JD; Hess EJ; Friedmann T; Breese GR
    J Neurochem; 1999 Jan; 72(1):225-9. PubMed ID: 9886073
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis.
    Ceballos-Picot I; Mockel L; Potier MC; Dauphinot L; Shirley TL; Torero-Ibad R; Fuchs J; Jinnah HA
    Hum Mol Genet; 2009 Jul; 18(13):2317-27. PubMed ID: 19342420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Decreased GTP-stimulated adenylyl cyclase activity in HPRT-deficient human and mouse fibroblast and rat B103 neuroblastoma cell membranes.
    Pinto CS; Seifert R
    J Neurochem; 2006 Jan; 96(2):454-9. PubMed ID: 16336632
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A human neuronal tissue culture model for Lesch-Nyhan disease.
    Shirley TL; Lewers JC; Egami K; Majumdar A; Kelly M; Ceballos-Picot I; Seidman MM; Jinnah HA
    J Neurochem; 2007 May; 101(3):841-53. PubMed ID: 17448149
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Proteomics- and transcriptomics-based screening of differentially expressed proteins and genes in brain of Wig rat: a model for attention deficit hyperactivity disorder (ADHD) research.
    Hirano M; Rakwal R; Shibato J; Sawa H; Nagashima K; Ogawa Y; Yoshida Y; Iwahashi H; Niki E; Masuo Y
    J Proteome Res; 2008 Jun; 7(6):2471-89. PubMed ID: 18457438
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.